{"title":"Study of tribenzo[<i>b</i>,<i>d</i>,<i>f</i>]azepine as donor in D-A photocatalysts.","authors":"Katy Medrano-Uribe, Jorge Humbrías-Martín, Luca Dell'Amico","doi":"10.3762/bjoc.21.76","DOIUrl":null,"url":null,"abstract":"<p><p>Since the discovery of donor-acceptor (D-A) type molecules in the field of materials science, they have found great applicability in the field of photocatalysis. Most of these compounds are based on complex D-A-D structures or multi-D-A systems, such as 4CzIPN. Whereas these systems have been widely studied and applied as photocatalysts, simpler D-A structures remain less explored. Nevertheless, the simplicity of D-A structures makes them the ideal structures to further understand the structure-property relationship of D-A molecules for optimizing their photocatalytic performance by simpler modification of the different D-A subunits. In particular, D-A structures featuring sulfur-based acceptors and nitrogen donors have gained increasing attention for their use as photoredox catalysts. This study introduces a new family of D-A molecules by exploring various sulfur-based acceptors and nitrogen donors, including a novel tribenzo[<i>b,d,f</i>]azepine (TBA) unit and 5<i>H</i>-dibenz[<i>b,f</i>]azepine (IMD). Our findings demonstrate that these simple D-A structures exhibit promising photocatalytic properties, comparable to those of more complex D-A-D systems.</p>","PeriodicalId":8756,"journal":{"name":"Beilstein Journal of Organic Chemistry","volume":"21 ","pages":"935-944"},"PeriodicalIF":2.2000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12117207/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Beilstein Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3762/bjoc.21.76","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Since the discovery of donor-acceptor (D-A) type molecules in the field of materials science, they have found great applicability in the field of photocatalysis. Most of these compounds are based on complex D-A-D structures or multi-D-A systems, such as 4CzIPN. Whereas these systems have been widely studied and applied as photocatalysts, simpler D-A structures remain less explored. Nevertheless, the simplicity of D-A structures makes them the ideal structures to further understand the structure-property relationship of D-A molecules for optimizing their photocatalytic performance by simpler modification of the different D-A subunits. In particular, D-A structures featuring sulfur-based acceptors and nitrogen donors have gained increasing attention for their use as photoredox catalysts. This study introduces a new family of D-A molecules by exploring various sulfur-based acceptors and nitrogen donors, including a novel tribenzo[b,d,f]azepine (TBA) unit and 5H-dibenz[b,f]azepine (IMD). Our findings demonstrate that these simple D-A structures exhibit promising photocatalytic properties, comparable to those of more complex D-A-D systems.
期刊介绍:
The Beilstein Journal of Organic Chemistry is an international, peer-reviewed, Open Access journal. It provides a unique platform for rapid publication without any charges (free for author and reader) – Platinum Open Access. The content is freely accessible 365 days a year to any user worldwide. Articles are available online immediately upon publication and are publicly archived in all major repositories. In addition, it provides a platform for publishing thematic issues (theme-based collections of articles) on topical issues in organic chemistry.
The journal publishes high quality research and reviews in all areas of organic chemistry, including organic synthesis, organic reactions, natural product chemistry, structural investigations, supramolecular chemistry and chemical biology.