{"title":"u型二苯并氮炔环同型二聚体的合成及其光物理性质。","authors":"Naohiro Namba, , , Satoshi Minakata*, , and , Youhei Takeda*, ","doi":"10.1021/acs.orglett.5c03358","DOIUrl":null,"url":null,"abstract":"<p >A new class of cyclic π-extended heteroarylene oligomer─cyclic homodimer of U-shaped dibenzophenazinylene─has been successfully synthesized and characterized. NMR spectroscopy and DFT calculations implicated the unique topologies of the macrocycle. The cyclic dimer displays intense green-to-yellow fluorescence in both solution and the solid state. Remarkably, it shows acid-responsive color changes and a photoluminescence “turn-OFF” response upon protonation. The heteroaromatic macrocycle represents a versatile scaffold for the development of advanced optoelectronic materials and supramolecular host–guest systems.</p>","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"27 41","pages":"11480–11484"},"PeriodicalIF":5.0000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and Photophysical Properties of Cyclic Homodimer of U-Shaped Dibenzophenazinylene\",\"authors\":\"Naohiro Namba, , , Satoshi Minakata*, , and , Youhei Takeda*, \",\"doi\":\"10.1021/acs.orglett.5c03358\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A new class of cyclic π-extended heteroarylene oligomer─cyclic homodimer of U-shaped dibenzophenazinylene─has been successfully synthesized and characterized. NMR spectroscopy and DFT calculations implicated the unique topologies of the macrocycle. The cyclic dimer displays intense green-to-yellow fluorescence in both solution and the solid state. Remarkably, it shows acid-responsive color changes and a photoluminescence “turn-OFF” response upon protonation. The heteroaromatic macrocycle represents a versatile scaffold for the development of advanced optoelectronic materials and supramolecular host–guest systems.</p>\",\"PeriodicalId\":54,\"journal\":{\"name\":\"Organic Letters\",\"volume\":\"27 41\",\"pages\":\"11480–11484\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-10-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.orglett.5c03358\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Letters","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.orglett.5c03358","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthesis and Photophysical Properties of Cyclic Homodimer of U-Shaped Dibenzophenazinylene
A new class of cyclic π-extended heteroarylene oligomer─cyclic homodimer of U-shaped dibenzophenazinylene─has been successfully synthesized and characterized. NMR spectroscopy and DFT calculations implicated the unique topologies of the macrocycle. The cyclic dimer displays intense green-to-yellow fluorescence in both solution and the solid state. Remarkably, it shows acid-responsive color changes and a photoluminescence “turn-OFF” response upon protonation. The heteroaromatic macrocycle represents a versatile scaffold for the development of advanced optoelectronic materials and supramolecular host–guest systems.
期刊介绍:
Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.