{"title":"Synthesis of Acenaphthene Fused Dithiaporphyrin(3.1.1.1)s and N-Fused Triphyrin(3.1.1)s in One-Pot Condensation.","authors":"Vratta Grover, Shubham Tiwari, Mangalampalli Ravikanth","doi":"10.1002/asia.202401203","DOIUrl":null,"url":null,"abstract":"<p><p>Two different types of novel nonaromatic acenaphthene fused macrocycles such as acenaphthene fused dithiaporphyrin(3.1.1.1)s and acenaphthene fused N-fused triphyrin(3.1.1)s were synthesized in one pot condensation reaction using 5,6-dibromoacenaphthene as a key precursor. The X-ray analysis revealed the oval core-shaped structure for dithiaporphyrin(3.1.1.1)s and intramolecular ring fusion in N-Fused triphyrin(3.1.1)s. The NMR, absorption and DFT studies suggested the non-aromatic nature of both macrocycles which absorb strongly in visible-NIR region. Both macrocycles were stable under electrochemical conditions and showed their electron-rich nature.</p>","PeriodicalId":145,"journal":{"name":"Chemistry - An Asian Journal","volume":" ","pages":"e202401203"},"PeriodicalIF":3.5000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - An Asian Journal","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1002/asia.202401203","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Two different types of novel nonaromatic acenaphthene fused macrocycles such as acenaphthene fused dithiaporphyrin(3.1.1.1)s and acenaphthene fused N-fused triphyrin(3.1.1)s were synthesized in one pot condensation reaction using 5,6-dibromoacenaphthene as a key precursor. The X-ray analysis revealed the oval core-shaped structure for dithiaporphyrin(3.1.1.1)s and intramolecular ring fusion in N-Fused triphyrin(3.1.1)s. The NMR, absorption and DFT studies suggested the non-aromatic nature of both macrocycles which absorb strongly in visible-NIR region. Both macrocycles were stable under electrochemical conditions and showed their electron-rich nature.
期刊介绍:
Chemistry—An Asian Journal is an international high-impact journal for chemistry in its broadest sense. The journal covers all aspects of chemistry from biochemistry through organic and inorganic chemistry to physical chemistry, including interdisciplinary topics.
Chemistry—An Asian Journal publishes Full Papers, Communications, and Focus Reviews.
A professional editorial team headed by Dr. Theresa Kueckmann and an Editorial Board (headed by Professor Susumu Kitagawa) ensure the highest quality of the peer-review process, the contents and the production of the journal.
Chemistry—An Asian Journal is published on behalf of the Asian Chemical Editorial Society (ACES), an association of numerous Asian chemical societies, and supported by the Gesellschaft Deutscher Chemiker (GDCh, German Chemical Society), ChemPubSoc Europe, and the Federation of Asian Chemical Societies (FACS).