{"title":"使用 2-(二苯基膦)苯酚辅助配体实现光化学异构化以显著提高发光性能的异谱 C^N 环金属化铱配合物","authors":"Yuji Koga*, Kaori Torii, Yuji Yamada, Satoshi Kawata and Kouki Matsubara, ","doi":"10.1021/acs.organomet.4c00007","DOIUrl":null,"url":null,"abstract":"<p >A series of stable heteroleptic Ir complexes bearing a pair of 2-phenylpyridine as main ligands and 2-(diphenylphosphino)phenol as an auxiliary ligand were synthesized to achieve efficient luminescence upon photochemical isomerization. Photoisomerization of an <i>N,N-trans</i> isoform, where a pair of nitrogen atoms of 2-phenylpyridine ligands were located at the <i>trans</i> position, using a high-pressure Hg lamp successfully produced its <i>N,N</i>-<i>cis</i> isomer in solution. A fluorine substituent on 2-phenylpyridine accelerated photoisomerization, whereas a methyl group deactivated the photochemical reaction. Photoluminescence efficiencies of the obtained <i>N,N-cis</i> isomers were significantly higher than those of the <i>N,N-trans</i> isomers.</p>","PeriodicalId":56,"journal":{"name":"Organometallics","volume":"43 7","pages":"764–773"},"PeriodicalIF":2.9000,"publicationDate":"2024-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Heteroleptic C^N Cyclometalated Iridium Complexes Enabling Photochemical Isomerization To Remarkably Enhance Luminescent Performance Using 2-(Diphenylphosphino)phenol Auxiliary Ligand\",\"authors\":\"Yuji Koga*, Kaori Torii, Yuji Yamada, Satoshi Kawata and Kouki Matsubara, \",\"doi\":\"10.1021/acs.organomet.4c00007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A series of stable heteroleptic Ir complexes bearing a pair of 2-phenylpyridine as main ligands and 2-(diphenylphosphino)phenol as an auxiliary ligand were synthesized to achieve efficient luminescence upon photochemical isomerization. Photoisomerization of an <i>N,N-trans</i> isoform, where a pair of nitrogen atoms of 2-phenylpyridine ligands were located at the <i>trans</i> position, using a high-pressure Hg lamp successfully produced its <i>N,N</i>-<i>cis</i> isomer in solution. A fluorine substituent on 2-phenylpyridine accelerated photoisomerization, whereas a methyl group deactivated the photochemical reaction. Photoluminescence efficiencies of the obtained <i>N,N-cis</i> isomers were significantly higher than those of the <i>N,N-trans</i> isomers.</p>\",\"PeriodicalId\":56,\"journal\":{\"name\":\"Organometallics\",\"volume\":\"43 7\",\"pages\":\"764–773\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-03-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organometallics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.organomet.4c00007\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organometallics","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.organomet.4c00007","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Heteroleptic C^N Cyclometalated Iridium Complexes Enabling Photochemical Isomerization To Remarkably Enhance Luminescent Performance Using 2-(Diphenylphosphino)phenol Auxiliary Ligand
A series of stable heteroleptic Ir complexes bearing a pair of 2-phenylpyridine as main ligands and 2-(diphenylphosphino)phenol as an auxiliary ligand were synthesized to achieve efficient luminescence upon photochemical isomerization. Photoisomerization of an N,N-trans isoform, where a pair of nitrogen atoms of 2-phenylpyridine ligands were located at the trans position, using a high-pressure Hg lamp successfully produced its N,N-cis isomer in solution. A fluorine substituent on 2-phenylpyridine accelerated photoisomerization, whereas a methyl group deactivated the photochemical reaction. Photoluminescence efficiencies of the obtained N,N-cis isomers were significantly higher than those of the N,N-trans isomers.
期刊介绍:
Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.