<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Garci F</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Tunisian Ministry of Higher Education and Scientific Research</funding><pagination>731</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9866386</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(2)</volume><pubmed_abstract>Two isomeric 2-bromomethylpyridine Cu(II) complexes [Cu(C&lt;sub>6&lt;/sub>H&lt;sub>9&lt;/sub>NBr)&lt;sub>2&lt;/sub>(NO&lt;sub>3&lt;/sub>)&lt;sub>2&lt;/sub>] with 2-bromo-5-methylpyridine (L&lt;sup>1&lt;/sup>) and 2-bromo-4-methylpyridine (L&lt;sup>2&lt;/sup>) were synthesized as air-stable blue materials in good yields. The crystal structures were different with [Cu(L&lt;sup>1&lt;/sup>)&lt;sub>2&lt;/sub>(NO&lt;sub>3&lt;/sub>)&lt;sub>2&lt;/sub>] (&lt;b>CuL&lt;sup>1&lt;/sup>&lt;/b>) crystallizing in the monoclinic space group &lt;i>P&lt;/i>2&lt;sub>1&lt;/sub>/c, while the 4-methyl derivative &lt;b>CuL&lt;sup>2&lt;/sup>&lt;/b> was solved and refined in triclinic &lt;i>P&lt;/i>1¯. The orientation of the Br substituents in the molecular structure (&lt;i>anti&lt;/i> (&lt;b>CuL&lt;sup>1&lt;/sup>&lt;/b>) vs. &lt;i>syn&lt;/i> (&lt;b>CuL&lt;sup>2&lt;/sup>&lt;/b>) conformations) and the geometry around Cu(II) in an overall 4 + 2 distorted c</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Structure, Optical and Magnetic Properties of Two Isomeric 2-Bromomethylpyridine Cu(II) Complexes [Cu(C&lt;sub>6&lt;/sub>H&lt;sub>9&lt;/sub>NBr)&lt;sub>2&lt;/sub>(NO&lt;sub>3&lt;/sub>)&lt;sub>2&lt;/sub>] with Very Different Binding Motives.</pubmed_title><pmcid>PMC9866386</pmcid><funding_grant_id>DI 1788/2-1</funding_grant_id><funding_grant_id>Hammouda Chebbi</funding_grant_id><pubmed_authors>Garci F</pubmed_authors><pubmed_authors>Disch S</pubmed_authors><pubmed_authors>Chebbi H</pubmed_authors><pubmed_authors>Sebastian SS</pubmed_authors><pubmed_authors>Ruschewitz U</pubmed_authors><pubmed_authors>Haseloer A</pubmed_authors><pubmed_authors>Klein A</pubmed_authors><pubmed_authors>Rochels L</pubmed_authors><pubmed_authors>Rouzbeh N</pubmed_authors><pubmed_authors>Anthony ET</pubmed_authors><pubmed_authors>Zid MF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structure, Optical and Magnetic Properties of Two Isomeric 2-Bromomethylpyridine Cu(II) Complexes [Cu(C&lt;sub>6&lt;/sub>H&lt;sub>9&lt;/sub>NBr)&lt;sub>2&lt;/sub>(NO&lt;sub>3&lt;/sub>)&lt;sub>2&lt;/sub>] with Very Different Binding Motives.</name><description>Two isomeric 2-bromomethylpyridine Cu(II) complexes [Cu(C&lt;sub>6&lt;/sub>H&lt;sub>9&lt;/sub>NBr)&lt;sub>2&lt;/sub>(NO&lt;sub>3&lt;/sub>)&lt;sub>2&lt;/sub>] with 2-bromo-5-methylpyridine (L&lt;sup>1&lt;/sup>) and 2-bromo-4-methylpyridine (L&lt;sup>2&lt;/sup>) were synthesized as air-stable blue materials in good yields. The crystal structures were different with [Cu(L&lt;sup>1&lt;/sup>)&lt;sub>2&lt;/sub>(NO&lt;sub>3&lt;/sub>)&lt;sub>2&lt;/sub>] (&lt;b>CuL&lt;sup>1&lt;/sup>&lt;/b>) crystallizing in the monoclinic space group &lt;i>P&lt;/i>2&lt;sub>1&lt;/sub>/c, while the 4-methyl derivative &lt;b>CuL&lt;sup>2&lt;/sup>&lt;/b> was solved and refined in triclinic &lt;i>P&lt;/i>1¯. The orientation of the Br substituents in the molecular structure (&lt;i>anti&lt;/i> (&lt;b>CuL&lt;sup>1&lt;/sup>&lt;/b>) vs. &lt;i>syn&lt;/i> (&lt;b>CuL&lt;sup>2&lt;/sup>&lt;/b>) conformations) and the geometry around Cu(II) in an overall 4 + 2 distorted c</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-05-29T20:01:44.743Z</modification><creation>2024-11-06T14:19:34.806Z</creation></dates><accession>S-EPMC9866386</accession><cross_references><pubmed>36677789</pubmed><doi>10.3390/molecules28020731</doi></cross_references></HashMap>