<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ramachandran MRK</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Alexander von Humboldt-Stiftung</funding><funding>Nemzeti Kutat?si Fejleszt?si ?s Innov?ci?s Hivatal</funding><funding>Magyar Tudom?nyos Akad?mia</funding><pagination>4639-4646</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8941515</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(11)</volume><pubmed_abstract>Anionic 1,4-dihydro-1,4-diphosphinines were synthesized from tricyclic 1,4-diphosphinines and isolated as blue powdery salts M[&lt;b>2a&lt;/b>-&lt;b>2c&lt;/b>]. Reaction of solutions of these monoanions with iodomethane led to &lt;i>P&lt;/i>-methylated compounds &lt;b>3a&lt;/b>-&lt;b>3c&lt;/b>. An oxidation/reduction cycle was examined, starting from solutions of K[&lt;b>2a&lt;/b>] via P-P coupled product &lt;b>4a&lt;/b> and back to K[&lt;b>2a&lt;/b>], and the recyclability and redox chemistry of this cycle were confirmed by experimental and simulated cyclic voltammetry analysis, which is proposed as a potential 2-electron cathode for rechargeable cells. TD-DFT studies were used to examine species that might be involved in the process.</pubmed_abstract><journal>Inorganic chemistry</journal><pubmed_title>Reversible Redox Chemistry of Anionic Imidazole-2-thione-Fused 1,4-Dihydro-1,4-diphosphinines.</pubmed_title><pmcid>PMC8941515</pmcid><funding_grant_id>STR 441/52-1</funding_grant_id><funding_grant_id>TKP2021/BME-NVA-02</funding_grant_id><pubmed_authors>Kelemen Z</pubmed_authors><pubmed_authors>Gal D</pubmed_authors><pubmed_authors>Ramachandran MRK</pubmed_authors><pubmed_authors>Streubel RK</pubmed_authors><pubmed_authors>Nyulaszi L</pubmed_authors><pubmed_authors>Boere RT</pubmed_authors><pubmed_authors>Majumdar M</pubmed_authors><pubmed_authors>Schnakenburg G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reversible Redox Chemistry of Anionic Imidazole-2-thione-Fused 1,4-Dihydro-1,4-diphosphinines.</name><description>Anionic 1,4-dihydro-1,4-diphosphinines were synthesized from tricyclic 1,4-diphosphinines and isolated as blue powdery salts M[&lt;b>2a&lt;/b>-&lt;b>2c&lt;/b>]. Reaction of solutions of these monoanions with iodomethane led to &lt;i>P&lt;/i>-methylated compounds &lt;b>3a&lt;/b>-&lt;b>3c&lt;/b>. An oxidation/reduction cycle was examined, starting from solutions of K[&lt;b>2a&lt;/b>] via P-P coupled product &lt;b>4a&lt;/b> and back to K[&lt;b>2a&lt;/b>], and the recyclability and redox chemistry of this cycle were confirmed by experimental and simulated cyclic voltammetry analysis, which is proposed as a potential 2-electron cathode for rechargeable cells. TD-DFT studies were used to examine species that might be involved in the process.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-18T15:07:00.129Z</modification><creation>2025-04-07T01:42:56.849Z</creation></dates><accession>S-EPMC8941515</accession><cross_references><pubmed>35258281</pubmed><doi>10.1021/acs.inorgchem.1c03620</doi></cross_references></HashMap>