<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Soejima K</submitter><funding>Iketani Science and Technology Foundation</funding><funding>Ministry of Education, Culture, Sports, Science and Technology</funding><funding>Kumamoto University</funding><funding>Japan Society for the Promotion of Science</funding><pagination>35892-35898</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12477679</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(43)</volume><pubmed_abstract>Exploring new compounds that exhibit spin-state switching under external stimuli is crucial for advancing materials science. However, the feasibility of combining π-conjugated moieties with Co(ii)-terpy cation units &lt;i>via&lt;/i> an ethynyl group has not yet been investigated. This approach represents a hybridization strategy wherein distinct functional moieties are incorporated into a single coordination metal complex to achieve multifunctionality. In this study, we synthesised a series of Co(ii)-terpyridine complexes [Co(R-ethynyl-terpy)&lt;sub>2&lt;/sub>](BF&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub> (R = phenyl for 1, naphthyl for 2, anthracenyl for 3, and pyrenyl for 4), resolved their crystal structures and packing arrangements, and evaluated their magnetic properties using a superconducting quantum interference device magnetometer. These Co(ii)-based complexes exhibited thermal spin-crossover behaviour in the solid state. Although complexes 1-4 were luminescent in solution, only complexes 3 and 4 emitted dual monomer and excimer fluorescence in solution due to their substituted π-conjugated moieties. Our findings are expected to serve as a platform for the synthesis of magnetically functional coordination metal compounds based on Co(ii) ions for the potential development of photophysical materials.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Observation of spin-crossover behaviour in Co(ii)-terpyridine complexes possessing π-conjugated substations.</pubmed_title><pmcid>PMC12477679</pmcid><funding_grant_id>JP24K01502</funding_grant_id><funding_grant_id>JPMXS0320200363</funding_grant_id><funding_grant_id>JP24K08449</funding_grant_id><pubmed_authors>Zenno H</pubmed_authors><pubmed_authors>Soejima K</pubmed_authors><pubmed_authors>Miyake K</pubmed_authors><pubmed_authors>Hayami S</pubmed_authors><pubmed_authors>Sekine Y</pubmed_authors><pubmed_authors>Kiba K</pubmed_authors><pubmed_authors>Yamaguchi Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Observation of spin-crossover behaviour in Co(ii)-terpyridine complexes possessing π-conjugated substations.</name><description>Exploring new compounds that exhibit spin-state switching under external stimuli is crucial for advancing materials science. However, the feasibility of combining π-conjugated moieties with Co(ii)-terpy cation units &lt;i>via&lt;/i> an ethynyl group has not yet been investigated. This approach represents a hybridization strategy wherein distinct functional moieties are incorporated into a single coordination metal complex to achieve multifunctionality. In this study, we synthesised a series of Co(ii)-terpyridine complexes [Co(R-ethynyl-terpy)&lt;sub>2&lt;/sub>](BF&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub> (R = phenyl for 1, naphthyl for 2, anthracenyl for 3, and pyrenyl for 4), resolved their crystal structures and packing arrangements, and evaluated their magnetic properties using a superconducting quantum interference device magnetometer. These Co(ii)-based complexes exhibited thermal spin-crossover behaviour in the solid state. Although complexes 1-4 were luminescent in solution, only complexes 3 and 4 emitted dual monomer and excimer fluorescence in solution due to their substituted π-conjugated moieties. Our findings are expected to serve as a platform for the synthesis of magnetically functional coordination metal compounds based on Co(ii) ions for the potential development of photophysical materials.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T23:29:15.945Z</modification><creation>2026-05-03T03:11:14.849Z</creation></dates><accession>S-EPMC12477679</accession><cross_references><pubmed>41030305</pubmed><doi>10.1039/d4ra08657k</doi></cross_references></HashMap>