<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Du J</submitter><funding>RCUK | Engineering and Physical Sciences Research Council (EPSRC)</funding><funding>European Research Council</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>5649</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8463702</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Determining the nature and extent of covalency of early actinide chemical bonding is a fundamentally important challenge. Recently, X-ray absorption, electron paramagnetic, and nuclear magnetic resonance spectroscopic studies have probed actinide-ligand covalency, largely confirming the paradigm of early actinide bonding varying from ionic to polarised-covalent, with this range sitting on the continuum between ionic lanthanide and more covalent d transition metal analogues. Here, we report measurement of the covalency of a terminal uranium(VI)-nitride by &lt;sup>15&lt;/sup>N nuclear magnetic resonance spectroscopy, and find an exceptional nitride chemical shift and chemical shift anisotropy. This redefines the &lt;sup>15&lt;/sup>N nuclear magnetic resonance spectroscopy parameter space, and experiment</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Exceptional uranium(VI)-nitride triple bond covalency from &lt;sup>15&lt;/sup>N nuclear magnetic resonance spectroscopy and quantum chemical analysis.</pubmed_title><pmcid>PMC8463702</pmcid><funding_grant_id>EP/N021932/1</funding_grant_id><funding_grant_id>EP/S033181/1</funding_grant_id><funding_grant_id>EP/M027015/1</funding_grant_id><funding_grant_id>612724</funding_grant_id><funding_grant_id>EP/K024000/1</funding_grant_id><funding_grant_id>EP/V007580/1</funding_grant_id><pubmed_authors>Berryman VEJ</pubmed_authors><pubmed_authors>Kaltsoyannis N</pubmed_authors><pubmed_authors>Adams RW</pubmed_authors><pubmed_authors>Du J</pubmed_authors><pubmed_authors>Liddle ST</pubmed_authors><pubmed_authors>Seed JA</pubmed_authors><pubmed_authors>Lee D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exceptional uranium(VI)-nitride triple bond covalency from &lt;sup>15&lt;/sup>N nuclear magnetic resonance spectroscopy and quantum chemical analysis.</name><description>Determining the nature and extent of covalency of early actinide chemical bonding is a fundamentally important challenge. Recently, X-ray absorption, electron paramagnetic, and nuclear magnetic resonance spectroscopic studies have probed actinide-ligand covalency, largely confirming the paradigm of early actinide bonding varying from ionic to polarised-covalent, with this range sitting on the continuum between ionic lanthanide and more covalent d transition metal analogues. Here, we report measurement of the covalency of a terminal uranium(VI)-nitride by &lt;sup>15&lt;/sup>N nuclear magnetic resonance spectroscopy, and find an exceptional nitride chemical shift and chemical shift anisotropy. This redefines the &lt;sup>15&lt;/sup>N nuclear magnetic resonance spectroscopy parameter space, and experiment</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-07T00:10:27.594Z</modification><creation>2025-04-04T19:44:51.24Z</creation></dates><accession>S-EPMC8463702</accession><cross_references><pubmed>34561448</pubmed><doi>10.1038/s41467-021-25863-2</doi></cross_references></HashMap>