<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hardy M</submitter><funding>Evonik Stiftung</funding><funding>jürgen manchot stiftung</funding><funding>jsps program for advancing strategic international networks</funding><funding>European Research Council</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Jürgen Manchot Stiftung</funding><funding>deutsche forschungsgemeinschaft</funding><funding>evonik stiftung</funding><pagination>22562-22569</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8519129</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>60(41)</volume><pubmed_abstract>Using 4-(4'-pyridyl)aniline as a simple organic building block in combination with three different aldehyde components together with metal(II) salts gave three different Fe&lt;sub>8&lt;/sub> Pt&lt;sub>6&lt;/sub> -cubes and their corresponding Zn&lt;sub>8&lt;/sub> Pt&lt;sub>6&lt;/sub> analogues by employing the subcomponent self-assembly approach. Whereas the use of zinc(II) salts gave rise to diamagnetic cages, iron(II) salts yielded metallosupramolecular cages that show spin-crossover behaviour in solution. The spin-transition temperature T&lt;sub>1/2&lt;/sub> depends on the incorporated aldehyde component, giving a construction kit for the deliberate synthesis of spin-crossover compounds with tailored transition properties. Incorporation of 4-thiazolecarbaldehyde or N-methyl-2-imidazole-carbaldehyde yielded cages that undergo spin-crossover around room temperature whereas the cage obtained using 1H-4-imidazolecarbaldehyde shows a spin-transition at low temperatures. Three new structures were characterized by synchrotron X-ray diffraction and all structures were characterized by mass spectrometry, NMR and UV/Vis spectroscopy.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>A Family of Heterobimetallic Cubes Shows Spin-Crossover Behaviour Near Room Temperature.</pubmed_title><pmcid>PMC8519129</pmcid><funding_grant_id>SFB 813</funding_grant_id><funding_grant_id>ERC Consolidator grant 683083 RAMSES</funding_grant_id><funding_grant_id>683083</funding_grant_id><pubmed_authors>Weisbarth R</pubmed_authors><pubmed_authors>Lutzen A</pubmed_authors><pubmed_authors>Horiuchi S</pubmed_authors><pubmed_authors>Engeser M</pubmed_authors><pubmed_authors>Clever GH</pubmed_authors><pubmed_authors>Hardy M</pubmed_authors><pubmed_authors>Tessarolo J</pubmed_authors><pubmed_authors>Beck J</pubmed_authors><pubmed_authors>Holstein JJ</pubmed_authors><pubmed_authors>Struch N</pubmed_authors><pubmed_authors>Wagner N</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Family of Heterobimetallic Cubes Shows Spin-Crossover Behaviour Near Room Temperature.</name><description>Using 4-(4'-pyridyl)aniline as a simple organic building block in combination with three different aldehyde components together with metal(II) salts gave three different Fe&lt;sub>8&lt;/sub> Pt&lt;sub>6&lt;/sub> -cubes and their corresponding Zn&lt;sub>8&lt;/sub> Pt&lt;sub>6&lt;/sub> analogues by employing the subcomponent self-assembly approach. Whereas the use of zinc(II) salts gave rise to diamagnetic cages, iron(II) salts yielded metallosupramolecular cages that show spin-crossover behaviour in solution. The spin-transition temperature T&lt;sub>1/2&lt;/sub> depends on the incorporated aldehyde component, giving a construction kit for the deliberate synthesis of spin-crossover compounds with tailored transition properties. Incorporation of 4-thiazolecarbaldehyde or N-methyl-2-imidazole-carbaldehyde yielded cages that undergo spin-crossover around room temperature whereas the cage obtained using 1H-4-imidazolecarbaldehyde shows a spin-transition at low temperatures. Three new structures were characterized by synchrotron X-ray diffraction and all structures were characterized by mass spectrometry, NMR and UV/Vis spectroscopy.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-05-18T12:31:58.18Z</modification><creation>2025-05-18T12:31:58.18Z</creation></dates><accession>S-EPMC8519129</accession><cross_references><pubmed>34382295</pubmed><doi>10.1002/anie.202108792</doi></cross_references></HashMap>