<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lalli D</submitter><funding>Ministero dell???Istruzione, dell???Universit?? e della Ricerca</funding><funding>Universit?? degli Studi del Piemonte Orientale</funding><funding>European Cooperation in Science and Technology</funding><pagination>496-506</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8753608</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(1)</volume><pubmed_abstract>Typically, Ln(III) complexes are isostructural along the series, which enables studying one particular metal chelate to derive the structural features of the others. This is not the case for [Ln(AAZTA)(H&lt;sub>2&lt;/sub>O)&lt;i>&lt;sub>x&lt;/sub>&lt;/i>]&lt;sup>-&lt;/sup> (&lt;i>x&lt;/i> = 1, 2) systems, where structural variations along the series cause changes in the hydration number of the different metal complexes, and in particular the loss of one of the two metal-coordinated water molecules between Ho and Er. Herein, we present a &lt;sup>1&lt;/sup>H field-cycling relaxometry and &lt;sup>17&lt;/sup>O NMR study that enables accessing the different exchange dynamics processes involving the two water molecules bound to the metal center in the [Gd(AAZTA)(H&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub>]&lt;sup>-&lt;/sup> complex. The resulting picture sho</pubmed_abstract><journal>Inorganic chemistry</journal><pubmed_title>Surprising Complexity of the [Gd(AAZTA)(H&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub>]&lt;sup>-&lt;/sup> Chelate Revealed by NMR in the Frequency and Time Domains.</pubmed_title><pmcid>PMC8753608</pmcid><funding_grant_id>FAR2019</funding_grant_id><funding_grant_id>CA15209</funding_grant_id><funding_grant_id>PRIN 2017A2KEPL</funding_grant_id><pubmed_authors>Platas-Iglesias C</pubmed_authors><pubmed_authors>Carniato F</pubmed_authors><pubmed_authors>Tei L</pubmed_authors><pubmed_authors>Lalli D</pubmed_authors><pubmed_authors>Botta M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Surprising Complexity of the [Gd(AAZTA)(H&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub>]&lt;sup>-&lt;/sup> Chelate Revealed by NMR in the Frequency and Time Domains.</name><description>Typically, Ln(III) complexes are isostructural along the series, which enables studying one particular metal chelate to derive the structural features of the others. This is not the case for [Ln(AAZTA)(H&lt;sub>2&lt;/sub>O)&lt;i>&lt;sub>x&lt;/sub>&lt;/i>]&lt;sup>-&lt;/sup> (&lt;i>x&lt;/i> = 1, 2) systems, where structural variations along the series cause changes in the hydration number of the different metal complexes, and in particular the loss of one of the two metal-coordinated water molecules between Ho and Er. Herein, we present a &lt;sup>1&lt;/sup>H field-cycling relaxometry and &lt;sup>17&lt;/sup>O NMR study that enables accessing the different exchange dynamics processes involving the two water molecules bound to the metal center in the [Gd(AAZTA)(H&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub>]&lt;sup>-&lt;/sup> complex. The resulting picture sho</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-05-08T16:37:21.05Z</modification><creation>2026-04-08T00:08:55.741Z</creation></dates><accession>S-EPMC8753608</accession><cross_references><pubmed>34890182</pubmed><doi>10.1021/acs.inorgchem.1c03194</doi></cross_references></HashMap>