{"id":6,"date":"2015-07-23T14:07:24","date_gmt":"2015-07-23T14:07:24","guid":{"rendered":"https:\/\/my.vanderbilt.edu\/schley\/publications\/"},"modified":"2025-07-10T21:37:50","modified_gmt":"2025-07-11T02:37:50","slug":"publications","status":"publish","type":"page","link":"https:\/\/my.vanderbilt.edu\/schley\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<h4>Categories<\/h4>\n<p><a href=\"#vanderbilt\">Work from our Group<\/a><br \/>\n<a href=\"#chapters\">Book Chapters and Perspectives<\/a><br \/>\n<a href=\"#collaborative\">Collaborative Publications<\/a><br \/>\n<a href=\"#prior\">Prior to Vanderbilt<\/a><\/p>\n<hr \/>\n<h4 id=\"vanderbilt\">Work from our Group<\/h4>\n<ol>\n<li><strong>Tandem Oligomerization-Hydrogenation Using Br\u00f8nsted Acidic Iridium Hydride Catalysts<\/strong><\/li>\n<p>Leitgeb, A. J.; Chapp, S. M.; Fast, C. D.; Fink, K. E.; Schley, N. D.<br \/>\n<em>Organometallics<\/em>, 2025.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.5c00160\">10.1021\/acs.organomet.5c00160<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/07\/isobutene.png\" alt=\"\" width=\"579\" height=\"260\" class=\"alignright size-full wp-image-538\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/07\/isobutene.png 579w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/07\/isobutene-300x135.png 300w\" sizes=\"auto, (max-width: 579px) 100vw, 579px\" \/><\/p>\n<p><a href=\"https:\/\/pubs.acs.org\/toc\/orlef7\/26\/29\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/orlef7.2024.26.issue-29.largecover.jpg\" alt=\"orlef7.2024.26.issue-29.largecover\" width=\"131\" height=\"175\" class=\"alignright size-full wp-image-492\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/orlef7.2024.26.issue-29.largecover.jpg 298w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/orlef7.2024.26.issue-29.largecover-225x300.jpg 225w\" sizes=\"auto, (max-width: 131px) 100vw, 131px\" \/><\/a><\/p>\n<li><strong>Bis(bicyclo[1.1.1]pentyl)chlorophosphine as a Precursor for the Preparation of Bis(bicyclo[1.1.1]pentyl)phosphines<\/strong><\/li>\n<p>Perry, G. L.; Schley, N. D.<br \/>\n<em>Org. Lett.<\/em>, 2024, 26, 29, 6071-6075.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.4c01190\">10.1021\/acs.orglett.4c01190<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chlorophos.png\" alt=\"chlorophos\" width=\"430\" height=\"263\" class=\"aligncenter size-full wp-image-430\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chlorophos.png 430w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chlorophos-300x183.png 300w\" sizes=\"auto, (max-width: 430px) 100vw, 430px\" \/><\/p>\n<li><strong>Tris(bicyclo[1.1.1]pentyl)phosphine: An Exceptionally Small Tri-<em><strong>tert<\/strong><\/em>-alkylphosphine and Its Bis-Ligated Pd(0) Complex<\/strong><\/li>\n<p>Perry, G. L.; Schley, N. D.<br \/>\n<em>J. Am. Chem. Soc.<\/em>, 2023, 145, 7005\u20137010.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.3c00885\">10.1021\/jacs.3c00885<\/a><br \/>\nHighlighted: <em>Org. Process Res. Dev.<\/em> 2023, 27, 6, 993\u20131002. DOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.oprd.3c00176\">10.1021\/acs.oprd.3c00176<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/bcp-650x399.png\" alt=\"bcp\" width=\"430\" height=\"264\" class=\"aligncenter size-full wp-image-390\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/bcp-650x399.png 650w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/bcp-300x184.png 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/bcp-768x471.png 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/bcp.png 1040w\" sizes=\"auto, (max-width: 430px) 100vw, 430px\" \/><\/p>\n<li><strong>Light-Promoted Transfer of an Iridium Hydride in Alkyl Ether Cleavage<\/strong><\/li>\n<p>Fast, C. D.; Schley, N. D.<br \/>\n<em>Organometallics<\/em>, 2021, 40, 3291\u20133297.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.1c00391\">10.1021\/acs.organomet.1c00391<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/photohydr.png\" alt=\"photohydr\" width=\"430\" height=\"195\" class=\"aligncenter size-full wp-image-350\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/photohydr.png 430w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/photohydr-300x136.png 300w\" sizes=\"auto, (max-width: 430px) 100vw, 430px\" \/><\/p>\n<li><strong>Selective demethylation of O-aryl glycosides by iridium-catalyzed hydrosilylation <\/strong><\/li>\n<p>Jones, C. A. H.; Schley, N. D.<br \/>\n<em>Chem. Commun.<\/em>, 2021, 57, 5953\u20135956.<br \/>\nDOI: <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/cc\/d1cc00496d\">10.1039\/D1CC00496D<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/carb_dem-1.png\" alt=\"carb_dem\" width=\"553\" height=\"167\" class=\"aligncenter size-full wp-image-321\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/carb_dem-1.png 553w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/carb_dem-1-300x91.png 300w\" sizes=\"auto, (max-width: 553px) 100vw, 553px\" \/><\/p>\n<li><strong>Reversible C(sp<sup>3<\/sup>)-Si Oxidative Addition of Unsupported Organosilanes: Effects of Silicon Substituents on Kinetics and Thermodynamics<\/strong><\/li>\n<p>Chapp, S. M.; Schley, N. D.<br \/>\n<em>J. Am. Chem. Soc.<\/em>, 2021, 143, 5534\u20135539.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.1c01564\">10.1021\/jacs.1c01564<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/silyl.png\" alt=\"silyl\" width=\"563\" height=\"212\" class=\"aligncenter size-full wp-image-322\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/silyl.png 563w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/silyl-300x113.png 300w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Ligand-Driven Advances in Iridium-Catalyzed sp<sup>3<\/sup> C\u2013H Borylation: 2,2\u2032-Dipyridylarylmethane<\/strong><\/li>\n<p>Jones, M. R.; Schley, N. D.<br \/>\n<em>Synlett<\/em>, 2021, 32, 845-850.<br \/>\nDOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-1344-1904\">10.1055\/a-1344-1904<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/synpac-1.png\" alt=\"synpac\" width=\"626\" height=\"200\" class=\"aligncenter size-full wp-image-333\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/synpac-1.png 626w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/synpac-1-300x96.png 300w\" sizes=\"auto, (max-width: 626px) 100vw, 626px\" \/><\/p>\n<li><strong>Product Inhibition in Nucleophilic Aromatic Substitution through DPPPent-Supported \u03c0-Arene Catalysis<\/strong><\/li>\n<p>Mueller, B. R. J.; Schley, N. D.<br \/>\n<em>Dalton Transactions<\/em>, 2020, 49, 10114\u201310119.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D0DT00786B\">10.1039\/D0DT00786B<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/arene-1.png\" alt=\"arene\" width=\"582\" height=\"165\" class=\"aligncenter size-full wp-image-324\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/arene-1.png 582w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/arene-1-300x85.png 300w\" sizes=\"auto, (max-width: 582px) 100vw, 582px\" \/><\/p>\n<li><strong>Selectivity and Mechanism of Iridium-Catalyzed Cyclohexyl Methyl Ether Cleavage<\/strong><\/li>\n<p>Fast, C. D.; Jones, C. A. H.; Schley, N. D.<br \/>\n<em>ACS Catalysis<\/em>, 2020, 10, 11, 6450\u20136456.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c01718\">10.1021\/acscatal.0c01718<\/a><br \/>\nFeatured at Organic-chemistry.org: <a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2021\/20September.shtm\">Highlights: Reduction<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/demeth.png\" alt=\"demeth\" width=\"554\" height=\"201\" class=\"aligncenter size-full wp-image-325\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/demeth.png 554w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/demeth-300x109.png 300w\" sizes=\"auto, (max-width: 554px) 100vw, 554px\" \/><\/p>\n<li><strong>Group-Transfer Reactions of a Cationic Iridium Alkoxycarbene Generated by Ether Dehydrogenation<\/strong><\/li>\n<p>Chapp, S. M.; Schley, N. D.<br \/>\n<em>Inorg. Chem.<\/em>, 2020, 59, 10, 7143\u20137149.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.inorgchem.0c00609\">10.1021\/acs.inorgchem.0c00609<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/grptransf.png\" alt=\"grptransf\" width=\"551\" height=\"206\" class=\"aligncenter size-full wp-image-326\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/grptransf.png 551w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/grptransf-300x112.png 300w\" sizes=\"auto, (max-width: 551px) 100vw, 551px\" \/><\/p>\n<li><strong>Iridium-Catalyzed sp<sup>3<\/sup> C\u2013H Borylation in Hydrocarbon Solvent Enabled by 2,2\u2032-Dipyridylarylmethane Ligands<\/strong><\/li>\n<p>Jones, M. R.; Fast, C. D.; Schley, N. D.<br \/>\n<em>J. Am. Chem. Soc.<\/em>, 2020, 142, 14, 6488-6492.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.0c00524\">10.1021\/jacs.0c00524<\/a><br \/>\nFeatured at Organic-chemistry.org: <a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2020\/26October.shtm\">Highlights: C-H functionalization<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/jonesboryl.png\" alt=\"jonesboryl\" width=\"571\" height=\"209\" class=\"aligncenter size-full wp-image-327\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/jonesboryl.png 571w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/jonesboryl-300x110.png 300w\" sizes=\"auto, (max-width: 571px) 100vw, 571px\" \/><\/p>\n<li><strong>Selective alkyl ether cleavage by cationic bis(phosphine)iridium complexes<\/strong><\/li>\n<p>Jones, C. A. H.; Schley, N. D.<br \/>\n<em>Org. Biomol. Chem.,<\/em> 2019. 17, 1744-1748.<br \/>\nDOI: <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/OB\/C8OB02298D#!divAbstract\">10.1039\/C8OB02298D<\/a><br \/>\n<em>Invited submission &#8211; New Talent, 2019.<\/em><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/debenzy-1.png\" alt=\"debenzy\" width=\"630\" height=\"153\" class=\"aligncenter size-full wp-image-332\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/debenzy-1.png 630w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/debenzy-1-300x73.png 300w\" sizes=\"auto, (max-width: 630px) 100vw, 630px\" \/><\/p>\n<li><strong>Formation of a Delocalized Iridium Benzylidene with Azaquinone Methide Character via Alkoxycarbene Cleavage<\/strong><\/li>\n<p>Zhang, Y.; Mueller, B. R. J.; Schley, N. D.<br \/>\n<em>Organometallics<\/em>, 2018, 37 (12), pp 1825\u20131828.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.organomet.8b00249\">10.1021\/acs.organomet.8b00249<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/azaqu.png\" alt=\"azaqu\" width=\"578\" height=\"156\" class=\"aligncenter size-full wp-image-329\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/azaqu.png 578w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/azaqu-300x81.png 300w\" sizes=\"auto, (max-width: 578px) 100vw, 578px\" \/><\/p>\n<li><strong>Evidence for reversible cyclometalation in alkane dehydrogenation and C-O bond cleavage at iridium bis(phosphine) complexes<\/strong><\/li>\n<p>Chapp, S. M.; Schley, N. D.<br \/>\n<em>Organometallics<\/em>, 2017, 36 (22), pp 4355\u20134358.<br \/>\nDOI: <a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.7b00676\">10.1021\/acs.organomet.7b00676<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/irallyl.png\" alt=\"irallyl\" width=\"566\" height=\"155\" class=\"aligncenter size-full wp-image-330\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/irallyl.png 566w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/irallyl-300x82.png 300w\" sizes=\"auto, (max-width: 566px) 100vw, 566px\" \/><\/p>\n<li><strong>Reversible alkoxycarbene formation by C\u2013H activation of ethers via discrete, isolable intermediates<\/strong><\/li>\n<p>Zhang, Y.; Schley, N. D.<br \/>\n<em>Chem. Commun.<\/em>, 2017, 53, 2130\u20132133.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/C6CC09838J\">10.1039\/C6CC09838J<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/dicarbene.png\" alt=\"dicarbene\" width=\"583\" height=\"152\" class=\"aligncenter size-full wp-image-331\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/dicarbene.png 583w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/dicarbene-300x78.png 300w\" sizes=\"auto, (max-width: 583px) 100vw, 583px\" \/><\/p>\n<hr \/>\n<h4 id=\"chapters\">Book Chapters and Perspectives<\/h4>\n<li><strong>(1,5-Cyclooctadiene)bis(2-Me-allyl)ruthenium(II)<\/strong><\/li>\n<p>Li, H.; Colacot, T. J; Schley, N. D.<br \/>\n<em>Encyclopedia of Reagents for Organic Synthesis<\/em>, 2021.<br \/>\nDOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/047084289X.rn01145.pub2\">10.1002\/047084289X.rn01145.pub2<\/a><\/p>\n<li><strong>Pioneers and Influencers in Organometallic Chemistry: Professor Robert Crabtree\u2019s Storied Career via an Unusual Journey to the Ivy League<\/strong><\/li>\n<p>Dobereiner, G. E.; Hazari, N.; Schley, N. D.<br \/>\n<em>Organometallics<\/em> 2021, 40, 295\u2013301.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.0c00797\">10.1021\/acs.organomet.0c00797<\/a><\/p>\n<hr \/>\n<h4 id=\"collaborative\">Collaborative Work<\/h4>\n<li><strong>Unlocking Chromium Decarboxylative Ligand-to-Metal Charge Transfer: Efficient and Redox-Neutral Allylation of Aldehydes Using Carboxylic Acids<\/strong><\/li>\n<p>Wu, S.\u2020; Jiao, Z.\u2020; Sung, A. T.; Faulhaber, A. B.; Schley, N. D.; Schuppe, A. W.<br \/>\n<em>J. Am. Chem. Soc.<\/em> 2025, 147, 26, 22759\u201322767.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/jacs.5c04691\">10.1021\/jacs.5c04691<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/07\/images_large_ja5c04691_0008.jpeg\" alt=\"\" width=\"512\" height=\"263\" class=\"aligncenter size-full wp-image-535\" \/><\/p>\n<li><strong>Photocatalyzed Epimerization of Quaternary Stereocenters<\/strong><\/li>\n<p>Wu, L.; McIntyre, B. N.; Wu, S.; Jiao, Z.; Fox, C. B.; Schley, N. D.; Schuppe, A. W.<br \/>\n<em>J. Am. Chem. Soc.<\/em> 2025, 147, 13, 11080\u201311088.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/jacs.4c16769\">10.1021\/jacs.4c16769<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_ja4c16769_0007.jpeg\" alt=\"\" width=\"409\" height=\"215\" class=\"aligncenter size-full wp-image-529\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_ja4c16769_0007.jpeg 1000w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_ja4c16769_0007-300x158.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_ja4c16769_0007-650x342.jpeg 650w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_ja4c16769_0007-768x404.jpeg 768w\" sizes=\"auto, (max-width: 409px) 100vw, 409px\" \/><\/p>\n<li><strong>Total Synthesis and Pharmacological Evaluation of Phochrodines A\u2013C<\/strong><\/li>\n<p>Bouchard, J. L.; Chang, S.; Krishnan, S.; Presley, C. C.; Boutaud, O.; Schley, N. D.; Engers, D. W.; Engers, J. L.; Lindsley, C. W.; Bender, A. M.;<br \/>\n<em>J. Nat. Prod.<\/em> 2025, 88, 4, 996\u20131003.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.jnatprod.5c00104\">10.1021\/acs.jnatprod.5c00104<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_np5c00104_0005.jpeg\" alt=\"\" width=\"483\" height=\"180\" class=\"aligncenter size-full wp-image-528\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_np5c00104_0005.jpeg 1000w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_np5c00104_0005-300x112.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_np5c00104_0005-650x242.jpeg 650w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/05\/images_large_np5c00104_0005-768x286.jpeg 768w\" sizes=\"auto, (max-width: 483px) 100vw, 483px\" \/><\/p>\n<li><strong>Synthesis, Structure, and Reactivity of Copper(I) Proazaphosphatrane Complexes<\/strong><\/li>\n<p>Hoskins-Harris, J. E.; Kotera, K.; Hoilette, D. A., Jr.; Apostolou, W. E.; Osenga, V. A.; Thomas, J. I.; Schley, N. D.; Donald, K. J.; Johnson, M. W.<br \/>\n<em>Inorg. Chem.<\/em> 2025, 64, 1132-1138.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.inorgchem.4c04779\">10.1021\/acs.inorgchem.4c04779<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/04\/images_large_ic4c04779_0008.jpeg\" alt=\"\" width=\"563\" height=\"136\" class=\"aligncenter size-full wp-image-516\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/04\/images_large_ic4c04779_0008.jpeg 1254w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/04\/images_large_ic4c04779_0008-300x72.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/04\/images_large_ic4c04779_0008-650x157.jpeg 650w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/04\/images_large_ic4c04779_0008-768x186.jpeg 768w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Diastereoselective dearomative cycloaddition of bicyclobutanes with pyridinium ylides: a modular approach to multisubstituted azabicyclo[3.1.1]heptanes<\/strong><\/li>\n<p>Dhake, K.; Woelk, K. J.; Krueckl, L. D. N.; Alberts, F.; Mutter, J.; Pohl, M. O.; Thomas, G. T.; Sharma, M.; Bjornerud-Brown, J.; Fern\u00e1ndez, N. P.; Schley, N. D.; Leitch, D. C.<br \/>\n<em>Chem. Commun.<\/em> 2024, 60, 13008-13011.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D4CC04730C\">10.1039\/D4CC04730C<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2025\/04\/aza-BCH.jpg\" alt=\"\" width=\"258\" height=\"212\" class=\"aligncenter size-full wp-image-517\" \/><\/p>\n<li><strong>Mechanisms and Site Selectivity of (Het)Ar\u2013X Oxidative Addition to Pd(0) Are Controlled by Frontier Molecular Orbital Symmetry<\/strong><\/li>\n<p>Lu, J.; Schley, N. D.; Paci, I.; Leitch, D. C.<br \/>\n<em>Organometallics<\/em> 2024, 43, 24, 3192\u20133203.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.organomet.4c00224\">10.1021\/acs.organomet.4c00224<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00224_0013.jpeg\" alt=\"images_large_om4c00224_0013\" width=\"563\" height=\"231\" class=\"aligncenter size-full wp-image-502\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00224_0013.jpeg 1000w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00224_0013-300x123.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00224_0013-768x316.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00224_0013-650x267.jpeg 650w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>A Thermally Stable, Alkene-Free Palladium Source for Oxidative Addition Complex Formation and High-Turnover Catalysis<\/strong><\/li>\n<p>Huang, J.; Ho, D. B.; Gaube, G.; Celuszak, H.; Becica, J.; Thomas, G. T.; Schley, N. D.; Leitch, D. C.<br \/>\n<em>Organometallics<\/em> 2024, 43, 20, 2403\u20132412.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.organomet.4c00125\">10.1021\/acs.organomet.4c00125<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00125_0009.jpeg\" alt=\"images_large_om4c00125_0009\" width=\"454\" height=\"263\" class=\"aligncenter size-full wp-image-500\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00125_0009.jpeg 958w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00125_0009-300x174.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00125_0009-768x445.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00125_0009-650x377.jpeg 650w\" sizes=\"auto, (max-width: 454px) 100vw, 454px\" \/><\/p>\n<li><strong>Alkene-Coordinated Palladium(0) Cross-Coupling Precatalysts: Comparing Oxidative Addition and Catalytic Reactivity for Dimethyl Fumarate and Maleic Anhydride Stabilizing Ligands<\/strong><\/li>\n<p>Thomas, G. T.; Litman, J. Z.; Ho, D. B.; Huang, J.; Blonska, K.; Schley, N. D.; Leitch, D. C.<br \/>\n<em>Organometallics<\/em> 2024, 43, 20, 2413\u20132426.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.organomet.4c00065\">10.1021\/acs.organomet.4c00065<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00065_0017.jpeg\" alt=\"images_large_om4c00065_0017\" width=\"554\" height=\"242\" class=\"aligncenter size-full wp-image-498\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00065_0017.jpeg 994w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00065_0017-300x131.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00065_0017-768x336.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om4c00065_0017-650x284.jpeg 650w\" sizes=\"auto, (max-width: 554px) 100vw, 554px\" \/><\/p>\n<li><strong>Five Hypotheses on the Origins of Temperature Dependence of 77Se NMR Shifts in Diselenides<\/strong><\/li>\n<p>Koziel, A. C.; Bortoli, M.; Tremblay, M.; Zhao, Y.; Orian, L.; Yang, Z. J.; Schley, N. D.; Macdonald, J. E.,<br \/>\n<em>Inorg. Chem.<\/em> 2024, 63, 12063-12072.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.inorgchem.4c01025\">10.1021\/acs.inorgchem.4c01025<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic4c01025_0009.jpeg\" alt=\"images_large_ic4c01025_0009\" width=\"563\" height=\"219\" class=\"aligncenter size-full wp-image-496\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic4c01025_0009.jpeg 1252w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic4c01025_0009-300x116.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic4c01025_0009-768x298.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic4c01025_0009-650x252.jpeg 650w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Rapid sp<sup>3<\/sup>-Enriched Scaffold Generation via a Selective Aziridine Amide Ring-Opening Reaction<\/strong><\/li>\n<p>Masahito, A.; Coleman, J. S.; Presley, C. C.; Schley, N. D.; Lindsley, C. W.<br \/>\n<em>J. Org. Chem.<\/em> 2024, 89, 5, 3500-3508.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.3c02952\">10.1021\/acs.joc.3c02952<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_jo3c02952_0008.jpg\" alt=\"images_large_jo3c02952_0008\" width=\"554\" height=\"287\" class=\"aligncenter size-full wp-image-441\" \/><\/p>\n<li><strong>Comparative Analysis of the Donor Properties of Isomeric Pyrrolyl Phosphine Ligands<\/strong><\/li>\n<p>Osenga, V. A.; Sykes, N. C.; Pa, S.; Bambha, M. K.; Schley, N. D.; Johnson, M. W.<br \/>\n<em>Organometallics<\/em> 2024, 43, 14-20.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.organomet.3c00467\">10.1021\/acs.organomet.3c00467<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om3c00467_0014.jpeg\" alt=\"images_large_om3c00467_0014\" width=\"563\" height=\"133\" class=\"aligncenter size-full wp-image-444\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om3c00467_0014.jpeg 1745w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om3c00467_0014-300x71.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om3c00467_0014-768x182.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om3c00467_0014-650x154.jpeg 650w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Enolate addition to bicyclobutanes enables expedient access to 2-oxo-bicyclohexane scaffolds<\/strong><\/li>\n<p>Woelk, K. J.; Dhake, K.; Schley, N. D.; Leitch, D. C.<br \/>\n<em>Chem. Commun.<\/em> 2023, 59, 13847-13850.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D3CC04234K\">10.1039\/D3CC04234K<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/Get.gif\" alt=\"Get\" width=\"378\" height=\"185\" class=\"aligncenter size-full wp-image-445\" \/><\/p>\n<li><strong>Vanol-Supported Lanthanide Complexes for Strong Circularly Polarized Luminescence at 1550 nm<\/strong><\/li>\n<p>Adewuyi, J. A.; Schley, N. D.; Ung, G.<br \/>\n<em>Chem. Eur. J.<\/em> 2023, 29, e202300800.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1002\/chem.202300800\">10.1002\/chem.202300800<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chem202300800-toc-0001-m.jpg\" alt=\"chem202300800-toc-0001-m\" width=\"487\" height=\"263\" class=\"aligncenter size-full wp-image-447\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chem202300800-toc-0001-m.jpg 648w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chem202300800-toc-0001-m-300x163.jpg 300w\" sizes=\"auto, (max-width: 487px) 100vw, 487px\" \/><\/p>\n<li><strong>Synthesis, characterization and absolute configurations of methyl ladderanoates<\/strong><\/li>\n<p>Harris, C. M.; Harris, T. M.; Stec, D. F.; Schley, N. D.; Johnson, J. L.; Covington, C. L.; Polavarapu, P. L.<br \/>\n<em>Chirality<\/em> 2023, 35, 49-57.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1002\/chir.23515\">10.1002\/chir.23515<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chir23515-toc-0001-m.jpg\" alt=\"chir23515-toc-0001-m\" width=\"554\" height=\"220\" class=\"aligncenter size-full wp-image-449\" \/><\/p>\n<li><strong>Spinolate Lanthanide Complexes for High Circularly Polarized Luminescence Metrics in the Visible and Near-Infrared<\/strong><\/li>\n<p>Willis, B.-A. N.; Schnable, D.; Schley, N. D.; Ung, G.<br \/>\n<em>J. Am. Chem. Soc.<\/em> 2022, 144, 22421-22425.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/jacs.2c10364\">10.1021\/jacs.2c10364<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c10364_0006.jpeg\" alt=\"images_large_ja2c10364_0006\" width=\"491\" height=\"263\" class=\"aligncenter size-full wp-image-450\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c10364_0006.jpeg 971w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c10364_0006-300x161.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c10364_0006-768x411.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c10364_0006-650x348.jpeg 650w\" sizes=\"auto, (max-width: 491px) 100vw, 491px\" \/><\/p>\n<li><strong>Reassessment of N<sub>2<\/sub> activation by low-valent Ti-amide complexes: a remarkable side-on bridged bis-N<sub>2<\/sub> adduct is actually an arene adduct<\/strong><\/li>\n<p>Huh, D. N.; Koby, R, F.; Stuart, Z. E.; Dunscomb, R. J.; Schley, N. D.; Tonks, I. A.<br \/>\n<em>Chem. Sci.<\/em> 2022, 13, 13330-13337.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D2SC04368H\">10.1039\/D2SC04368H<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/7c16e5f17bae5f9741ee6cc10dd05d32c70ec043.gif\" alt=\"7c16e5f17bae5f9741ee6cc10dd05d32c70ec043\" width=\"378\" height=\"165\" class=\"aligncenter size-full wp-image-452\" \/><\/p>\n<li><strong>Structure\u2013Activity Relationships for the <em><strong>N<\/strong><\/em>-Me- Versus <em><strong>N<\/strong><\/em>-H-Amide Modification to Macrocyclic <em><strong>ent<\/strong><\/em>-Verticilide Antiarrhythmics<\/strong><\/li>\n<p>Smith, A. N.; Thorpe, M. P.; Blackwell, D. J.; Batiste, S. M.; Hopkins, C. R.; Schley, N. D.; Knollmann, B. C.; Johnston, J. N.<br \/>\n<em>ACS Med. Chem. Lett. <\/em> 2022, 13, 1755-1762.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.2c00377\">10.1021\/acsmedchemlett.2c00377<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ml2c00377_0011.jpeg\" alt=\"images_large_ml2c00377_0011\" width=\"563\" height=\"257\" class=\"aligncenter size-full wp-image-453\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ml2c00377_0011.jpeg 629w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ml2c00377_0011-300x137.jpeg 300w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Circularly Polarized Luminescence from Uranyl Improves Resolution of Electronic Transitions<\/strong><\/li>\n<p>Schnable, D.; Schley, N. D.; Ung, G.<br \/>\n<em>J. Am. Chem. Soc.<\/em> 2022, 144, 10718-10722.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/jacs.2c03791\">10.1021\/jacs.2c03791<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c03791_0006.jpeg\" alt=\"images_large_ja2c03791_0006\" width=\"492\" height=\"263\" class=\"aligncenter size-full wp-image-455\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c03791_0006.jpeg 967w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c03791_0006-300x160.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c03791_0006-768x411.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c03791_0006-650x348.jpeg 650w\" sizes=\"auto, (max-width: 492px) 100vw, 492px\" \/><\/p>\n<li><strong>Strong Circularly Polarized Luminescence at 1550 nm from Enantiopure Molecular Erbium Complexes<\/strong><\/li>\n<p>Mukthar, N. F. M.; Schley, N. D.; Ung, G.<br \/>\n<em>J. Am. Chem. Soc.<\/em> 2022, 144, 6148-6153.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1021\/jacs.2c01134\">10.1021\/jacs.2c01134<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c01134_0007.jpeg\" alt=\"images_large_ja2c01134_0007\" width=\"491\" height=\"263\" class=\"aligncenter size-full wp-image-454\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c01134_0007.jpeg 935w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c01134_0007-300x161.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c01134_0007-768x412.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja2c01134_0007-650x348.jpeg 650w\" sizes=\"auto, (max-width: 491px) 100vw, 491px\" \/><\/p>\n<li><strong>Synthesis of bright water-soluble circularly polarized luminescence emitters as potential sensors<\/strong><\/li>\n<p>Adewuyi, J. A.; Schley, N. D.; Ung, G.<br \/>\n<em>Inorganic Chemistry Frontiers<\/em> 2022, 9, 1474-1480.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D1QI01398J\">10.1039\/D1QI01398J<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/D1QI01398J.gif\" alt=\"D1QI01398J\" width=\"352\" height=\"189\" class=\"aligncenter size-full wp-image-457\" \/><\/p>\n<li><strong>Trace Oxygen Affects Osmium Redox Polymer Synthesis for Wired Enzymatic Biosensors<\/strong><\/li>\n<p>Calhoun, M. C.; Stachurski, C. D.; Winn, S. L.; Gizzie, E.; Daniel, A. W.; Schley, N. D.; Cliffel, D. E.<br \/>\n<em>J. Electrochem. Soc.<\/em> 2022, 169, 016506.<br \/>\nDOI: <a href=\"http:\/\/doi.org\/10.1149\/1945-7111\/ac42a0\">10.1149\/1945-7111\/ac42a0<\/a><\/p>\n<li><strong>Fluorine-induced diastereodivergence discovered in an equally rare enantioselective syn-aza-Henry reaction<\/strong><\/li>\n<p>Bing, J. A.; Schley, N. D.; Johnston, J. N.<br \/>\n<em>Chemical Science<\/em> 2022, 13, 2614-2623.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D1SC05910F\">10.1039\/D1SC05910F<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/fdfcbb564a8f93bf18cd3122cbb6d125f04478c3.gif\" alt=\"fdfcbb564a8f93bf18cd3122cbb6d125f04478c3\" width=\"264\" height=\"189\" class=\"aligncenter size-full wp-image-458\" \/><\/p>\n<li><strong>Substituent Effect on the Circularly Polarized Luminescence of C1-Symmetric Carbene-Copper(I) Complexes<\/strong><\/li>\n<p>Braker, E. E.; Mukthar, N. F. M.; Schley, N. D.; Ung, G.<br \/>\n<em>ChemPhotoChem<\/em> 2021, 5, 902-905.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1002\/cptc.202100068\">10.1002\/cptc.202100068<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/cptc202100068-toc-0001-m.jpg\" alt=\"cptc202100068-toc-0001-m\" width=\"487\" height=\"263\" class=\"aligncenter size-full wp-image-459\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/cptc202100068-toc-0001-m.jpg 972w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/cptc202100068-toc-0001-m-300x162.jpg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/cptc202100068-toc-0001-m-768x415.jpg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/cptc202100068-toc-0001-m-650x351.jpg 650w\" sizes=\"auto, (max-width: 487px) 100vw, 487px\" \/><\/p>\n<li><strong>Synthesis and Cytotoxic Evaluation of Arimetamycin A and Its Daunorubicin and Doxorubicin Hybrids<\/strong><\/li>\n<p>Huseman, E. D.; Byl, J. A. W.; Chapp, S. M.; Schley, N. D.; Osheroff, N.; Townsend, S. D.<br \/>\n<em>ACS Central Science<\/em> 2021, 7, 1327-1337.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acscentsci.1c00040\">10.1021\/acscentsci.1c00040<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_oc1c00040_0010.jpeg\" alt=\"images_large_oc1c00040_0010\" width=\"447\" height=\"263\" class=\"aligncenter size-full wp-image-460\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_oc1c00040_0010.jpeg 922w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_oc1c00040_0010-300x176.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_oc1c00040_0010-768x451.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_oc1c00040_0010-650x382.jpeg 650w\" sizes=\"auto, (max-width: 447px) 100vw, 447px\" \/><\/p>\n<li><strong>Electronic structure analysis and reactivity of the bimetallic bis-titanocene vinylcarboxylate complex, [(Cp<sub>2<\/sub>Ti)<sub>2<\/sub>(O<sub>2<\/sub>C<sub>3<\/sub>TMS<sub>2<\/sub>)].<\/strong><\/li>\n<p>Huh, D. N.; Maity, A.; Van Trieste, G. P.; Schley, N. D.; Powers, D. C.; Tonks, I. A.<br \/>\n<em>Polyhedron<\/em> 2021, 207, 115368.<br \/>\nDOI: <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0277538721003508\">10.1016\/j.poly.2021.115368<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/1-s2.0-S0277538721003508-ga1.jpg\" alt=\"1-s2.0-S0277538721003508-ga1\" width=\"256\" height=\"245\" class=\"aligncenter size-full wp-image-461\" \/><\/p>\n<li><strong>Di(indenyl)beryllium<\/strong><\/li>\n<p>Koby, R. F.; Schley, N. D.; Hanusa, T. P.<br \/>\n<em>Angew. Chem. Int. Ed.<\/em> 2021, 60, 21174-21178.<br \/>\nDOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202107980\">10.1002\/anie.202107980<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie202107980-toc-0001-m.jpg\" alt=\"anie202107980-toc-0001-m\" width=\"272\" height=\"263\" class=\"aligncenter size-full wp-image-462\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie202107980-toc-0001-m.jpg 1296w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie202107980-toc-0001-m-300x290.jpg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie202107980-toc-0001-m-768x743.jpg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie202107980-toc-0001-m-650x629.jpg 650w\" sizes=\"auto, (max-width: 272px) 100vw, 272px\" \/><\/p>\n<li><strong>Mechanochemical Formation, Solution Rearrangements, and Catalytic Behavior of a Polymorphic Ca\/K Allyl Complex<\/strong><\/li>\n<p>Koby, R. F.; Doerr, A. M.; Rightmire, N. R.; Schley, N. D.; Brennessel, W. W.; Long, B. K.; Hanusa, T. P.<br \/>\n<em>Chem. Eur. J.<\/em> 2021, 27,8195-8202.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1002\/chem.202100589\">10.1002\/chem.202100589<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chem202100589-toc-0001-m.jpg\" alt=\"chem202100589-toc-0001-m\" width=\"440\" height=\"230\" class=\"aligncenter size-full wp-image-463\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chem202100589-toc-0001-m.jpg 440w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/chem202100589-toc-0001-m-300x157.jpg 300w\" sizes=\"auto, (max-width: 440px) 100vw, 440px\" \/><\/p>\n<li><strong>How important are the intermolecular hydrogen bonding interactions in methanol solvent for interpreting the chiroptical properties?<\/strong><\/li>\n<p>Polavarapu, P. L.; Santoro, E.; Covington, C. L.; Johnson, J. L.; Puente, A. R.; Schley, N. D.; Kallingathodi, Z.; Prakasan, P. C.; Haleema, S.; Thomas, A. A.; Ibnusaud, I.<br \/>\n<em>Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy<\/em> 2021, 247, 119094<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1016\/j.saa.2020.119094\">10.1016\/j.saa.2020.119094<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/1-s2.0-S1386142520310738-ga1.jpg\" alt=\"1-s2.0-S1386142520310738-ga1\" width=\"346\" height=\"199\" class=\"aligncenter size-full wp-image-464\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/1-s2.0-S1386142520310738-ga1.jpg 346w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/1-s2.0-S1386142520310738-ga1-300x173.jpg 300w\" sizes=\"auto, (max-width: 346px) 100vw, 346px\" \/><\/p>\n<li><strong>High circularly polarized luminescence brightness from analogues of Shibasaki&#8217;s lanthanide complexes.<\/strong><\/li>\n<p>Deng, M.; Schley, N. D.; Ung, G.<br \/>\n<em>Chem. Commun<\/em>. 2020, 56, 14813-14816<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D0CC06568D\">10.1039\/D0CC06568D<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/shibisaki.gif\" alt=\"shibisaki\" width=\"351\" height=\"189\" class=\"aligncenter size-full wp-image-465\" \/><\/p>\n<li><strong>Alkali-metal- and halide-free dinuclear mixed-valent samarium and europium complexes.<\/strong><\/li>\n<p>Mukthar, N. F. M.; Schley, N. D.; Ung, G.<br \/>\n<em>Dalton Transactions<\/em> 2020, 49, 16059-16061<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D0DT01095B\">10.1039\/D0DT01095B<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/europ.gif\" alt=\"europ\" width=\"354\" height=\"189\" class=\"aligncenter size-full wp-image-466\" \/><\/p>\n<li><strong>Systematic evaluation of the electronic effect of aluminum-containing ligands in iridium\u2013aluminum and rhodium\u2013aluminum bimetallic complexes<\/strong><\/li>\n<p>Charles, R. M.; Taylor, N. S.; Mercado, A. A.; Frost, C. E.; Yokley, T. W.; Eckenhoff, W. T.; Schley, N. D.; DeYonker, N. J.; Brewster, T. P.<br \/>\n<em>Dalton Transactions<\/em> 2020, 49, 13029-13043<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D0DT02472D\">10.1039\/D0DT02472D<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/bimet.gif\" alt=\"bimet\" width=\"378\" height=\"185\" class=\"aligncenter size-full wp-image-467\" \/><\/p>\n<li><strong>CO<sub>2<\/sub> Capture by 2-(Methylamino)pyridine Ligated Aluminum Alkyl Complexes.<\/strong><\/li>\n<p>Yokley, T. W.; Tupkar, H.; Schley, N. D.; DeYonker, N. J.; Brewster, T. P.<br \/>\n<em>Eur. J. Inorg. Chem.<\/em> 2020, 2020, 2958-2967.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1002\/ejic.202000437\">10.1002\/ejic.202000437<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/alum.jpg\" alt=\"alum\" width=\"563\" height=\"255\" class=\"aligncenter size-full wp-image-469\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/alum.jpg 591w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/alum-300x136.jpg 300w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Study and modular synthesis of unsymmetrical bis(phosphino)pyrrole ligands.<\/strong><\/li>\n<p>Fokwa, H. D.; Vidlak, J. F.; Weinberg, S. C.; Duplessis, I. D.; Schley, N. D.; Johnson, M. W.<br \/>\n<em>Dalton Transactions<\/em> 2020, 49, 9957-9960.<br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1039\/D0DT02063J\">10.1039\/D0DT02063J<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/pyrolyl.gif\" alt=\"pyrolyl\" width=\"378\" height=\"127\" class=\"aligncenter size-full wp-image-471\" \/><\/p>\n<li><strong>Circularly Polarized Luminescence from Enantiopure C<sub>2<\/sub>-Symmetrical Tetrakis(2-pyridylmethyl)-1,2-diaminocyclohexane Lanthanide Complexes.<\/strong><\/li>\n<p>Ayers, K. M.; Schley, N. D.; Ung, G.<br \/>\n<em>Inorg. Chem.<\/em> 2020, 59, 11, 7657\u20137665.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.inorgchem.0c00628\">10.1021\/acs.inorgchem.0c00628<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00628_0010.jpeg\" alt=\"images_large_ic0c00628_0010\" width=\"492\" height=\"263\" class=\"aligncenter size-full wp-image-470\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00628_0010.jpeg 852w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00628_0010-300x160.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00628_0010-768x410.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00628_0010-650x347.jpeg 650w\" sizes=\"auto, (max-width: 492px) 100vw, 492px\" \/><\/p>\n<li><strong>Synthesis of Enantiopure Lanthanide Complexes Supported by Hexadentate N,N\u2032-Bis(methylbipyridyl)bipyrrolidine and Their Circularly Polarized Luminescence.<\/strong><\/li>\n<p>Schnable, D.; Freedman, K.; Ayers, K. M.; Schley, N. D.; Kol, M.; Ung, G.<br \/>\n<em>Inorg. Chem.<\/em> 2020, 59, 8498-8504.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.inorgchem.0c00946\">10.1021\/acs.inorgchem.0c00946<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00946_0005.jpeg\" alt=\"images_large_ic0c00946_0005\" width=\"489\" height=\"263\" class=\"aligncenter size-full wp-image-473\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00946_0005.jpeg 1000w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00946_0005-300x161.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00946_0005-768x413.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic0c00946_0005-650x350.jpeg 650w\" sizes=\"auto, (max-width: 489px) 100vw, 489px\" \/><\/p>\n<li><strong>Algal Toxin Goniodomin A Binds Potassium Ion Selectively Yielding a Conformationally Altered Complex Having Biological Consequences.<\/strong><\/li>\n<p>Tainter, C. J.; Schley, N. D.; Harris, C. M.; Stec, D. F.; Song, A. K.; Balinski, A.; May, J. C.; McLean, J. A.; Reece, K. S.; Harris, T. M.,<br \/>\n<em>Journal of Natural Products<\/em>, 2020, 83, 4, 1069\u20131081.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.jnatprod.9b01094\">10.1021\/acs.jnatprod.9b01094<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np9b01094_0008.jpeg\" alt=\"images_large_np9b01094_0008\" width=\"563\" height=\"244\" class=\"aligncenter size-full wp-image-474\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np9b01094_0008.jpeg 1000w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np9b01094_0008-300x131.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np9b01094_0008-768x334.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np9b01094_0008-650x283.jpeg 650w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Synthesis and Electronic Characterization of Iridium-Aluminum and Rhodium-Aluminum Heterobimetallic Complexes Bridged by 3-Oxypyridine and 4-Oxypyridine.<\/strong><\/li>\n<p>Charles III, R. M.; Tupkar, H.; Helland, S. D.; Mercado, A. A.; Eckenhoff, W. T.; Schley, N. D.; DeYonker, N. J.; Brewster, T. P.<br \/>\n<em>Eur. J. Inorg. Chem. <\/em>2020, 2020, 1192-1198.<br \/>\nDOI: <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/ejic.201901317\">10.1002\/ejic.201901317<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/ejic201901317-toc-0001-m.jpg\" alt=\"ejic201901317-toc-0001-m\" width=\"431\" height=\"183\" class=\"aligncenter size-full wp-image-475\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/ejic201901317-toc-0001-m.jpg 431w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/ejic201901317-toc-0001-m-300x127.jpg 300w\" sizes=\"auto, (max-width: 431px) 100vw, 431px\" \/><\/p>\n<li><strong>An <em>\u03b7<sup>3<\/sup><\/em>-Bound Allyl Ligand on Magnesium in a Mechanochemically Generated Mg\/K Allyl Complex.<\/strong><\/li>\n<p>Koby, R. F.; Doerr, A. M.; Rightmire, N. R.; Schley, N. D.; Long, B. K.; Hanusa, T. P.<br \/>\n<em>Angew. Chem. Int. Ed. <\/em>2020, 59, 9542-9548.<br \/>\nDOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201916410\">10.1002\/anie.201916410<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie201916410-toc-0001-m.jpg\" alt=\"anie201916410-toc-0001-m\" width=\"296\" height=\"263\" class=\"aligncenter size-full wp-image-476\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie201916410-toc-0001-m.jpg 394w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie201916410-toc-0001-m-300x266.jpg 300w\" sizes=\"auto, (max-width: 296px) 100vw, 296px\" \/><\/p>\n<li><strong>Rhodium and iridium NNO-Scorpionate complexes: synthesis, structure, and reactivity with aluminum alkyls.<\/strong><\/li>\n<p>Yokley, T. W.; Schley, N. D.; Brewster, T. P.<br \/>\n<em>Inorg. Chim. Acta 2020, 506, 119529.<\/em><br \/>\nDOI: <a href=\"https:\/\/doi.org\/10.1016\/j.ica.2020.119529\">10.1016\/j.ica.2020.119529<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/1-s2.0-S0020169319315178-ga1.jpg\" alt=\"1-s2.0-S0020169319315178-ga1\" width=\"500\" height=\"181\" class=\"aligncenter size-full wp-image-477\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/1-s2.0-S0020169319315178-ga1.jpg 500w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/1-s2.0-S0020169319315178-ga1-300x109.jpg 300w\" sizes=\"auto, (max-width: 500px) 100vw, 500px\" \/><\/p>\n<li><strong>Yellow Circularly Polarized Luminescence from C<sub>1<\/sub>\u2010Symmetrical Copper(I) Complexes<\/strong><\/li>\n<p>Deng, M.; Mukthar, N. F. M.; Schley, N. D.; Ung, G.<br \/>\n<em>Angew. Chem. Int. Ed.<\/em>, 2020, 59,1228\u20131231.<br \/>\nDOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201913672\">10.1002\/anie.201913672<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie201913672-toc-0001-m.jpg\" alt=\"anie201913672-toc-0001-m\" width=\"432\" height=\"230\" class=\"aligncenter size-full wp-image-478\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie201913672-toc-0001-m.jpg 432w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/anie201913672-toc-0001-m-300x160.jpg 300w\" sizes=\"auto, (max-width: 432px) 100vw, 432px\" \/><\/p>\n<li><strong>Catalytic, Enantioselective Synthesis of Cyclic Carbamates from Dialkyl Amines by CO<sub>2<\/sub>-Capture: Discovery, Development, and Mechanism<\/strong><\/li>\n<p>Yousefi, R.; Struble, T. J.; Payne, J. L.; Vishe, M.; Schley, N. D.; Johnston, J. N.<br \/>\n<em>J. Am. Chem. Soc.<\/em>, 2019, 141 (1), 618-625.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.8b11793\">10.1021\/jacs.8b11793<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-117937_0011.jpeg\" alt=\"images_large_ja-2018-117937_0011\" width=\"526\" height=\"263\" class=\"aligncenter size-full wp-image-479\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-117937_0011.jpeg 850w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-117937_0011-300x150.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-117937_0011-768x384.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-117937_0011-650x325.jpeg 650w\" sizes=\"auto, (max-width: 526px) 100vw, 526px\" \/><\/p>\n<li><strong>Halide metathesis in overdrive: mechanochemical synthesis of a heterometallic group 1 allyl complex<\/strong><\/li>\n<p>Koby, R. F.; Rightmire, N. R.; Schley, N. D.; Hanusa, T. P.; Brennessel, W. W.<br \/>\n<em>Beilstein Journal of Organic Chemistry<\/em> 2019, 15, 1856-1863.<br \/>\nDOI: <a href=\"https:\/\/www.beilstein-journals.org\/bjoc\/articles\/15\/181\">10.3762\/bjoc.15.181<\/a><\/p>\n<li><strong>Monometallic lanthanide salicylhydrazone complexes exhibiting strong near-infrared luminescence<\/strong><\/li>\n<p>Ayers, K. M.; Schley, N. D.; Ung, G.<br \/>\n<em>Chem. Commun.<\/em>, 2019, 55, 8446\u20138449.<br \/>\nDOI: <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/cc\/c9cc03934a\">10.1039\/C9CC03934A<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/salicyl.gif\" alt=\"salicyl\" width=\"353\" height=\"189\" class=\"aligncenter size-full wp-image-480\" \/><\/p>\n<li><strong>Hydrogen Activation and Hydrogenolysis Facilitated By Late-Transition-Metal\u2013Aluminum Heterobimetallic Complexes.<\/strong><\/li>\n<p>Charles, R. M.; Yokley, T. W.; Schley, N. D.; DeYonker, N. J.; Brewster, T. P.<br \/>\n<em>Inorganic Chemistry<\/em>, 2019, 58, 12635-12645.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.inorgchem.9b01359\">10.1021\/acs.inorgchem.9b01359<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic9b01359_0011.jpeg\" alt=\"images_large_ic9b01359_0011\" width=\"481\" height=\"263\" class=\"aligncenter size-full wp-image-481\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic9b01359_0011.jpeg 868w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic9b01359_0011-300x164.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic9b01359_0011-768x420.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic9b01359_0011-650x356.jpeg 650w\" sizes=\"auto, (max-width: 481px) 100vw, 481px\" \/><\/p>\n<li><strong>Synthesis and characterization of rhodium\u2013aluminum heterobimetallic complexes tethered by a 1,3-bis(diphenylphosphino)-2-propanoxy group.<\/strong><\/li>\n<p>Li, Z.; Yokley, T. W.; Tran, S. L.; Zong, J.; Schley, N. D.; Brewster, T. P.<br \/>\n<em>Dalton Transactions<\/em>, 2019, 48, 8782-8790.<br \/>\nDOI: <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/dt\/c9dt00938h\">10.1039\/C9DT00938H<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/tetheredpropanoxy.gif\" alt=\"tetheredpropanoxy\" width=\"273\" height=\"189\" class=\"aligncenter size-full wp-image-482\" \/><\/p>\n<li><strong>Solid State Structures, Solution Behavior, and Luminescence of Simple Tetrakis(2-pyridylmethyl)ethylenediamine Lanthanide Complexes.<\/strong><\/li>\n<p>Ayers, K. M.; Schley, N. D.; Ung, G.<br \/>\n<em>European Journal of Inorganic Chemistry<\/em>, 2019, 2019, 3769-3775.<br \/>\nDOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ejic.201900609\">10.1002\/ejic.201900609<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/ejic201900609-toc-0001-m.jpg\" alt=\"ejic201900609-toc-0001-m\" width=\"431\" height=\"129\" class=\"aligncenter size-full wp-image-483\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/ejic201900609-toc-0001-m.jpg 431w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/ejic201900609-toc-0001-m-300x90.jpg 300w\" sizes=\"auto, (max-width: 431px) 100vw, 431px\" \/><\/p>\n<li><strong>Absolute Configurations of Naturally Occurring [5]-and [3]-Ladderanoic Acids: Isolation, Chiroptical Spectroscopy and Crystallography<\/strong><\/li>\n<p>Raghavan, V.; Johnson, J. L.; Stec, D. F.; Song, B.; Zajac, G.; Baranska, M.; Harris, C. M.; Schley, N. D.; Polavarapu, P. L.; Harris, T. M.<br \/>\n<em>Journal of Natural Products,<\/em> 2018, 81 (12), 2654\u20132666.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.jnatprod.8b00458\">10.1021\/acs.jnatprod.8b00458<\/a>.<br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np-2018-00458e_0015.jpeg\" alt=\"images_large_np-2018-00458e_0015\" width=\"563\" height=\"189\" class=\"aligncenter size-full wp-image-484\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np-2018-00458e_0015.jpeg 1000w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np-2018-00458e_0015-300x101.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np-2018-00458e_0015-768x257.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_np-2018-00458e_0015-650x218.jpeg 650w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Solvent Dependent Sensitization of Ytterbium and Neodymium via an Intramolecular Excimer<\/strong><\/li>\n<p>Deng, M.; Schley, N. D.; Ung, G.<br \/>\n<em>Inorg. Chem.<\/em> 2018, 57 (24), pp 15399\u201315405.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.inorgchem.8b02709\">10.1021\/acs.inorgchem.8b02709<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2018-02709a_0011.jpeg\" alt=\"images_large_ic-2018-02709a_0011\" width=\"547\" height=\"263\" class=\"aligncenter size-full wp-image-485\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2018-02709a_0011.jpeg 1000w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2018-02709a_0011-300x144.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2018-02709a_0011-768x369.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2018-02709a_0011-650x313.jpeg 650w\" sizes=\"auto, (max-width: 547px) 100vw, 547px\" \/><\/p>\n<li><strong>Mechanochemically driven transformations in organotin chemistry: stereochemical rearrangement, redox behavior, and dispersion-stabilized complexes<\/strong><\/li>\n<p>Koby, F. R.; Hanusa, T. P.*; Schley, N. D.<br \/>\n<em>J. Am. Chem. Soc.<\/em>, 2018, 140 (46), pp 15934\u201315942.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.8b09862\">10.1021\/jacs.8b09862<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-098623_0013.jpeg\" alt=\"images_large_ja-2018-098623_0013\" width=\"338\" height=\"263\" class=\"aligncenter size-full wp-image-486\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-098623_0013.jpeg 723w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-098623_0013-300x233.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ja-2018-098623_0013-650x505.jpeg 650w\" sizes=\"auto, (max-width: 338px) 100vw, 338px\" \/><\/p>\n<li><strong>Synthesis, Structure, and Reactivity of Palladium Proazaphosphatrane Complexes Invoked in C\u2013N Cross-Coupling.<\/strong><\/li>\n<p>Matthews, A. D.; Gravalis, G. M.; Schley, N. D.; Johnson, M. W.<br \/>\n<em>Organometallics<\/em> 2018, 37 (18), pp 3073\u20133078.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.organomet.8b00453\">10.1021\/acs.organomet.8b00453<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om-2018-00453u_0011.jpeg\" alt=\"images_large_om-2018-00453u_0011\" width=\"563\" height=\"210\" class=\"aligncenter size-full wp-image-487\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om-2018-00453u_0011.jpeg 979w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om-2018-00453u_0011-300x112.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om-2018-00453u_0011-768x286.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_om-2018-00453u_0011-650x242.jpeg 650w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<li><strong>Synthesis and Characterization of Heterobimetallic Iridium\u2013Aluminum and Rhodium\u2013Aluminum Complexes<\/strong><\/li>\n<p>Brewster, T. P.; Nguyen, T. H.; Li, Z.; Eckenhoff, W. T.; Schley, N. D.; DeYonker, N. J.<br \/>\n<em>Inorg. Chem.<\/em> 2018, 57 (3), pp 1148\u20131157.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/acs.inorgchem.7b02601\">10.1021\/acs.inorgchem.7b02601<\/a><br \/>\n<img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2017-02601k_0014.jpeg\" alt=\"images_large_ic-2017-02601k_0014\" width=\"563\" height=\"177\" class=\"aligncenter size-full wp-image-488\" srcset=\"https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2017-02601k_0014.jpeg 796w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2017-02601k_0014-300x94.jpeg 300w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2017-02601k_0014-768x241.jpeg 768w, https:\/\/cdn.vanderbilt.edu\/t2-my\/my-prd\/wp-content\/uploads\/sites\/1816\/2015\/07\/images_large_ic-2017-02601k_0014-650x204.jpeg 650w\" sizes=\"auto, (max-width: 563px) 100vw, 563px\" \/><\/p>\n<hr \/>\n<h4 id=\"prior\">Prior to Vanderbilt<\/h4>\n<li><strong>Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation.<\/strong><\/li>\n<p>Schley, N. D.; Fu, Gregory C.<br \/>\n<em>J. Am. Chem. Soc.<\/em>, 2014, 136 (47), 16588\u201316593.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ja508718m\">10.1021\/ja508718m<\/a><\/p>\n<li><strong>Hydrogen-Transfer Catalysis with Cp*Ir-III Complexes: The Influence of the Ancillary Ligands.<\/strong><\/li>\n<p>Hintermair, U.; Campos, J.; Brewster, T. P.; Pratt, L. M.; Schley, N. D.; Crabtree, R. H.<br \/>\n<em>ACS Catalysis <\/em>2014, 4, 99\u2013108.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/cs400834q\">10.1021\/cs400834q<\/a><\/p>\n<li><strong>Domain Structure for an Amorphous Iridium-Oxide Water-Oxidation Catalyst Characterized by X-Ray Pair Distribution Function Analysis.<\/strong><\/li>\n<p>Huang, J.; Blakemore, J. D.; Fazi, D.; Kokhan, O.; Schley, N. D.; Crabtree, R. H.; Brudvig, G. W.; Tiede, D. M.<br \/>\n<em>Phys. Chem. Chem. Phys<\/em>. 2014, 16, 1814\u20131819.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/C3CP54878C\">10.1039\/C3CP54878C<\/a><\/p>\n<li><strong>Characterization of an Amorphous Iridium Water-Oxidation Catalyst Electrodeposited from Organometallic Precursors.<\/strong><\/li>\n<p>Blakemore, J. D.; Mara, M. W.; Kushner-Lenhoff, M. N.; Schley, N. D.; Konezny, S. J.; Rivalta, I.; Negre, C. F. A.; Snoeberger, R. C.; Kokhan, O.; Huang, J.; Stickrath, A.; Tran, L. A.; Parr, M. L.; Chen, L. X.; Tiede, D. M.; Batista, V. S.; Crabtree, R. H.; Brudvig, G. W.<br \/>\n<em>Inorg. Chem<\/em>. 2013, 52, 1860\u20131871.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ic301968j\">10.1021\/ic301968j<\/a><\/p>\n<li><strong>Effects of Aqueous Buffers on Electrocatalytic Water Oxidation with an Iridium Oxide Material Electrodeposited in Thin Layers from an Organometallic Precursor.<\/strong><\/li>\n<p>Kushner-Lenhoff, M. N.; Blakemore, J. D.; Schley, N. D.; Crabtree, R. H.; Brudvig, G. W.<br \/>\n<em>Dalton Trans<\/em>. 2013, 42, 3617\u20133622.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/C2DT32326E\">10.1039\/C2DT32326E<\/a><\/p>\n<li><strong>Symmetrical Hydrogen Bonds in Iridium(III) Alkoxides with Relevance to Outer Sphere Hydrogen Transfer.<\/strong><\/li>\n<p>Schley, N. D.; Halbert, S.; Raynaud, C.; Eisenstein, O.; Crabtree, R. H.<br \/>\n<em>Inorg. Chem<\/em>. 2012, 51 (22), 12313\u201313323.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ic301601c\">10.1021\/ic301601c<\/a><\/p>\n<li><strong>Mild, Reversible Reaction of Iridium(III) Amido Complexes with Carbon Dioxide.<\/strong><\/li>\n<p>Dobereiner, G. E.; Wu, J.; Manas, M. G.; Schley, N. D.; Takase, M. K.; Crabtree, R. H.; Hazari, N.; Maseras, F.; Nova, A.<br \/>\n<em>Inorg. Chem<\/em>. 2012, 51 (18), 9683\u20139693.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ic300923c\">10.1021\/ic300923c<\/a><\/p>\n<li><strong>A Comparison of Amorphous Iridium Water-Oxidation Electrocatalysts Prepared from Soluble Precursors.<\/strong><\/li>\n<p>Blakemore, J. D.; Schley, N. D.; Kushner-Lenhoff, M. N.; Winter, A. M.; D\u2019Souza, F.; Crabtree, R. H.; Brudvig, G. W.<br \/>\n<em>Inorg. Chem<\/em>. 2012, 51 (14), 7749\u20137763.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ic300764f\">10.1021\/ic300764f<\/a><\/p>\n<li><strong>Ultrafast Photodriven Intramolecular Electron Transfer from an Iridium-Based Water-Oxidation Catalyst to Perylene Diimide Derivatives.<\/strong><\/li>\n<p>Vagnini, M. T.; Smeigh, A. L.; Blakemore, J. D.; Eaton, S. W.; Schley, N. D.; D\u2019Souza, F.; Crabtree, R. H.; Brudvig, G. W.; Co, D. T.; Wasielewski, M. R.<br \/>\n<em>Proc. Natl. Acad. Sci. U.S.A<\/em>. 2012, 109 (39), 15651\u201315656.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1073\/pnas.1202075109\">10.1073\/pnas.1202075109<\/a><\/p>\n<li><strong>Characterization of an Activated Iridium Water Splitting Catalyst Using Infrared Photodissociation of H<sub>2<\/sub> Tagged Ions.<\/strong><\/li>\n<p>Garand, E.; Fournier, J. A.; Kamrath, M. Z.; Schley, N. D.; Crabtree, R. H.; Johnson, M. A.<br \/>\n<em>Phys. Chem. Chem. Phys.<\/em> 2012, 14, 10109\u201310113.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/C2CP41490B\">10.1039\/C2CP41490B<\/a><\/p>\n<li><strong>Electron-Rich CpIr(biphenyl-2,2\u2032-diyl) Complexes with \u03c0-Accepting Carbon Donor Ligands.<\/strong><\/li>\n<p>Graeupner, J.; Brewster, T. P.; Blakemore, J. D.; Schley, N. D.; Thomsen, J. M.; Brudvig, G. W.; Hazari, N.; Crabtree, R. H.<br \/>\n<em>Organometallics <\/em>2012, 31, 7158\u20137164.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/om300696t\">10.1021\/om300696t<\/a><\/p>\n<li><strong>Axially Chiral Dimeric Ir and Rh Complexes Bridged by Flexible NHC Ligands.<\/strong><\/li>\n<p>Ashley, J. M.; Farnaby, J. H.; Hazari, N.*; Kim, K. E.; Luzik Jr, E. D.; Meehan, R, E.; Meyer, E. B.; Schley, N. D.; Schmeier T. J.; Tailor, A. N.<br \/>\n<em>Inorg. Chim. Acta<\/em>. 2012, 380, 399\u2013410.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1016\/j.ica.2011.11.034\">10.1016\/j.ica.2011.11.034<\/a><\/p>\n<li><strong>Oxidative Synthesis of Amides and Pyrroles via Dehydrogenative Alcohol Oxidation by Ruthenium Diphosphine Diamine Complexes.<\/strong><\/li>\n<p>Schley, N. D.; Dobereiner, G. E.; Crabtree, R. H.<br \/>\n<em>Organometallics <\/em>2011, 30 (15), 4174\u20134179.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/om2004755\">10.1021\/om2004755<\/a><\/p>\n<li><strong>Distinguishing Homogeneous from Heterogeneous Catalysis in Electrode-Driven Water Oxidation with Molecular Iridium Complexes.<\/strong><\/li>\n<p>Schley, N. D.; Blakemore, J. D.; Subbaiyan, N. K.; Incarvito, C. D.; D\u2019Souza, F.; Crabtree, R. H.; Brudvig, G. W.<br \/>\n<em>J. Am. Chem. Soc<\/em>. 2011, 133 (27), 10473\u201310481.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ja2004522\">10.1021\/ja2004522<\/a><br \/>\nHighlighted: Meyer, T. J., <em>Nat. Chem<\/em>. 2011, 3, 757\u2013758. DOI: <a href=\"http:\/\/dx.doi.org\/10.1038\/nchem.1161\">10.1038\/nchem.1161<\/a><\/p>\n<li><strong>Thiocyanate Linkage Isomerism in a Ruthenium Polypyridyl Complex.<\/strong><\/li>\n<p>Brewster, T. P.; Ding, W.; Schley, N. D.; Hazari, N.; Batista, V. S.; Crabtree, R. H.<br \/>\n<em>Inorg. Chem<\/em>. 2011, 50, 11938\u221211946.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ic200950e\">10.1021\/ic200950e<\/a><\/p>\n<li><strong>Iridium-Catalyzed Hydrogenation of N-Heterocyclic Compounds under Mild Conditions by an Outer Sphere Pathway.<\/strong><\/li>\n<p>Dobereiner, G. E.; Nova, A.; Schley, N. D.; Hazari, N.; Miller, S. J.; Eisenstein, O.; Crabtree, R. H.<br \/>\n<em>J. Am. Chem. Soc.<\/em> 2011, 133 (19), 7547\u20137562.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ja2014983\">10.1021\/ja2014983<\/a><\/p>\n<li><strong>An Iridium(IV) Species, [Cp*Ir(NHC)Cl]<sup>+<\/sup>, Related to a Water-Oxidation Catalyst.<\/strong><\/li>\n<p>Brewster, T. P.; Blakemore, J. D.; Schley, N. D.; Incarvito, C. D.; Hazari, N.; Brudvig, G. W.; Crabtree, R. H.<br \/>\n<em>Organometallics <\/em>2011, 30 (5), 965\u2013973.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/om101016s\">10.1021\/om101016s<\/a><\/p>\n<li><strong>An Experimental-Theoretical Study of the Factors That Affect the Switch between Ruthenium-Catalyzed Dehydrogenative Amide Formation versus Amine Alkylation.<\/strong><\/li>\n<p>Nova, A.; Balcells, D.; Schley, N. D.; Dobereiner, G. E.; Crabtree, R. H.; Eisenstein, O.<br \/>\n<em>Organometallics <\/em>2010, 29 (23), 6548\u20136558.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/om101015u\">10.1021\/om101015u<\/a><\/p>\n<li><strong>Anodic Deposition of a Robust Iridium-Based Water-Oxidation Catalyst from Organometallic Precursors.<\/strong><\/li>\n<p>Blakemore, J. D.; Schley, N. D.; Olack, G. W.; Incarvito, C. D.; Brudvig, G. W.; Crabtree, R. H.<br \/>\n<em>Chem. Sci<\/em>. 2011, 2 (1), 94\u201398.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/C0SC00418A\">10.1039\/C0SC00418A<\/a><\/p>\n<li><strong>Half-Sandwich Iridium Complexes for Homogeneous Water-Oxidation Catalysis.<\/strong><\/li>\n<p>Blakemore, J. D.; Schley, N. D.; Balcells, D.; Hull, J. F.; Olack, G. W.; Incarvito, C. D.; Eisenstein, O.; Brudvig, G. W.; Crabtree, R. H.<br \/>\n<em> J. Am. Chem. Soc<\/em>. 2010, 132 (45), 16017\u201316029.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ja104775j\">10.1021\/ja104775j<\/a><\/p>\n<li><strong>Cp* Iridium Complexes Give Catalytic Alkane Hydroxylation with Retention of Stereochemistry.<\/strong><\/li>\n<p>Zhou, M.; Schley, N. D.; Crabtree, R. H.<br \/>\n<em>J. Am. Chem. Soc<\/em>. 2010, 132 (36), 12550\u201312551.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ja1058247\">10.1021\/ja1058247<\/a><\/p>\n<li><strong>Acyl Protection Strategy for Synthesis of a Protic NHC Complex via N-Acyl Methanolysis.<\/strong><\/li>\n<p>Dobereiner, G. E.; Chamberlin, C. A.; Schley, N. D.; Crabtree, R. H.<br \/>\n<em>Organometallics <\/em>2010, 29 (21), 5728\u20135731.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/om100452g\">10.1021\/om100452g<\/a><\/p>\n<li><strong>Iridium and Ruthenium Complexes with Chelating N-Heterocyclic Carbenes: Efficient Catalysts for Transfer Hydrogenation, beta-Alkylation of Alcohols, and N-Alkylation of Amines.<\/strong><\/li>\n<p>Gnanamgari, D.; Sauer, E. L. O.; Schley, N. D.; Butler, C.; Incarvito, C. D.; Crabtree, R. H.<br \/>\n<em>Organometallics <\/em>2009, 28 (1), 321\u2013325.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/om800821q\">10.1021\/om800821q<\/a><\/p>\n<li><strong>Alcohol Cross-Coupling Reactions Catalyzed by Ru and Ir Terpyridine Complexes.<\/strong><\/li>\n<p>Gnanamgari, D.; Leung, C. H.; Schley, N. D.; Hilton, S. T.; Crabtree, R. H.<br \/>\n<em>Org. Biomol. Chem<\/em>. 2008, 6 (23), 4442\u20134445.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/B815547J\">10.1039\/B815547J<\/a><\/p>\n<li><strong>Isomeric Forms of Heavier Main Group Hydrides: Experimental and Theoretical Studies of the [Sn(Ar)H]<sub>2<\/sub> (Ar=terphenyl) System.<\/strong><\/li>\n<p>Rivard, E.; Fischer, R. C.; Wolf, R.; Peng, Y.; Merrill, W. A.; Schley, N. D.; Zhu, Z. L.; Pu, L.; Fettinger, J. C.; Teat, S. J.; Nowik, I.; Herber, R. H.; Takagi, N.; Nagase, S.; Power, P. P.<br \/>\n<em>J. Am. Chem. Soc<\/em>. 2007, 129 (51), 16197\u201316208.<br \/>\nDOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/ja076453m\">10.1021\/ja076453m<\/a><\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Categories Work from our Group Book Chapters and Perspectives Collaborative Publications Prior to Vanderbilt Work from our Group Tandem Oligomerization-Hydrogenation Using Br\u00f8nsted Acidic Iridium Hydride Catalysts Leitgeb, A. J.; Chapp, S. M.; Fast, C. D.; Fink, K. E.; Schley, N. D. Organometallics, 2025. DOI: 10.1021\/acs.organomet.5c00160 Bis(bicyclo[1.1.1]pentyl)chlorophosphine as a Precursor for the Preparation of Bis(bicyclo[1.1.1]pentyl)phosphines Perry,&#8230;<\/p>\n","protected":false},"author":4085,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"footnotes":""},"tags":[],"class_list":["post-6","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/pages\/6","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/users\/4085"}],"replies":[{"embeddable":true,"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/comments?post=6"}],"version-history":[{"count":138,"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/pages\/6\/revisions"}],"predecessor-version":[{"id":148,"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/pages\/6\/revisions\/148"}],"wp:attachment":[{"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/media?parent=6"}],"wp:term":[{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/my.vanderbilt.edu\/schley\/wp-json\/wp\/v2\/tags?post=6"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}