<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Temerova D</submitter><funding>Academy of Finland</funding><pagination>19220-19231</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9727735</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(48)</volume><pubmed_abstract>The phosphonium-decorated phenanthro-imidazolyl pyridine ligand, &lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>Br, readily reacts with zinc(II) and cadmium(II) bromides to give inorganic-organic zero-dimensional compounds [&lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>ZnBr&lt;sub>2&lt;/sub>]&lt;sub>2&lt;/sub>[ZnBr&lt;sub>4&lt;/sub>] (&lt;b>1&lt;/b>) and [(&lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>)&lt;sub>2&lt;/sub>Cd&lt;sub>2&lt;/sub>Br&lt;sub>4&lt;/sub>][CdBr&lt;sub>4&lt;/sub>] (&lt;b>2&lt;/b>), respectively, upon crystallization. These salts are moderately fluorescent in the solid state under ambient conditions (λ&lt;sub>em&lt;/sub> = 458 nm, Φ&lt;sub>em&lt;/sub> = 0.11 for &lt;b>1&lt;/b>; λ&lt;sub>em&lt;/sub> = 460 nm, Φ&lt;sub>em&lt;/sub> = 0.13 for &lt;b>2&lt;/b>). Their emission results from spin-allowed electronic transitions localized on the organic component with the negligible effect of [MBr&lt;sub>4&lt;/sub>]&lt;sup>2-&lt;/sup> and MBr&lt;sub>2&lt;/sub> units. Contrary to ionic species &lt;b>1&lt;/b> and &lt;b>2&lt;/b>, lead(II) bromide affords a neutral and water-stable complex [(&lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>)&lt;sub>2&lt;/sub>Pb&lt;sub>3&lt;/sub>Br&lt;sub>8&lt;/sub>] (&lt;b>3&lt;/b>), showing weak room-temperature phosphorescence arising from spin-orbit coupling due to the heavy atom effect. The emission, which is substantially enhanced for the amorphous sample of &lt;b>3&lt;/b> (λ&lt;sub>em&lt;/sub> = 575 nm, Φ&lt;sub>em&lt;/sub> = 0.06), is assigned to the intraligand triplet excited state, which is a rare phenomenon among Pb(II) molecular materials.</pubmed_abstract><journal>Inorganic chemistry</journal><pubmed_title>Hybrid Inorganic-Organic Complexes of Zn, Cd, and Pb with a Cationic Phenanthro-diimine Ligand.</pubmed_title><pmcid>PMC9727735</pmcid><funding_grant_id>317903</funding_grant_id><funding_grant_id>340584</funding_grant_id><funding_grant_id>320166</funding_grant_id><pubmed_authors>Chou PT</pubmed_authors><pubmed_authors>Kinnunen N</pubmed_authors><pubmed_authors>Koshevoy IO</pubmed_authors><pubmed_authors>Kisel KS</pubmed_authors><pubmed_authors>Eskelinen T</pubmed_authors><pubmed_authors>Janis J</pubmed_authors><pubmed_authors>Karttunen AJ</pubmed_authors><pubmed_authors>Temerova D</pubmed_authors><pubmed_authors>Chou TC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hybrid Inorganic-Organic Complexes of Zn, Cd, and Pb with a Cationic Phenanthro-diimine Ligand.</name><description>The phosphonium-decorated phenanthro-imidazolyl pyridine ligand, &lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>Br, readily reacts with zinc(II) and cadmium(II) bromides to give inorganic-organic zero-dimensional compounds [&lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>ZnBr&lt;sub>2&lt;/sub>]&lt;sub>2&lt;/sub>[ZnBr&lt;sub>4&lt;/sub>] (&lt;b>1&lt;/b>) and [(&lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>)&lt;sub>2&lt;/sub>Cd&lt;sub>2&lt;/sub>Br&lt;sub>4&lt;/sub>][CdBr&lt;sub>4&lt;/sub>] (&lt;b>2&lt;/b>), respectively, upon crystallization. These salts are moderately fluorescent in the solid state under ambient conditions (λ&lt;sub>em&lt;/sub> = 458 nm, Φ&lt;sub>em&lt;/sub> = 0.11 for &lt;b>1&lt;/b>; λ&lt;sub>em&lt;/sub> = 460 nm, Φ&lt;sub>em&lt;/sub> = 0.13 for &lt;b>2&lt;/b>). Their emission results from spin-allowed electronic transitions localized on the organic component with the negligible effect of [MBr&lt;sub>4&lt;/sub>]&lt;sup>2-&lt;/sup> and MBr&lt;sub>2&lt;/sub> units. Contrary to ionic species &lt;b>1&lt;/b> and &lt;b>2&lt;/b>, lead(II) bromide affords a neutral and water-stable complex [(&lt;b>LP&lt;/b>&lt;sup>&lt;b>+&lt;/b>&lt;/sup>)&lt;sub>2&lt;/sub>Pb&lt;sub>3&lt;/sub>Br&lt;sub>8&lt;/sub>] (&lt;b>3&lt;/b>), showing weak room-temperature phosphorescence arising from spin-orbit coupling due to the heavy atom effect. The emission, which is substantially enhanced for the amorphous sample of &lt;b>3&lt;/b> (λ&lt;sub>em&lt;/sub> = 575 nm, Φ&lt;sub>em&lt;/sub> = 0.06), is assigned to the intraligand triplet excited state, which is a rare phenomenon among Pb(II) molecular materials.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-19T05:09:49.748Z</modification><creation>2025-04-19T05:09:49.748Z</creation></dates><accession>S-EPMC9727735</accession><cross_references><pubmed>36414241</pubmed><doi>10.1021/acs.inorgchem.2c02867</doi></cross_references></HashMap>