![2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure](https://cnstatic.chemtradehub.com/structs/910/910788-24-8-5b70.webp "2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure")
Direct functionalization at the boron center of antiaromatic chloroborole
文献信息
发布日期
2008-07-30
DOI
10.1039/B808483A
影响因子
6.222
作者
Holger Braunschweig, Thomas Kupfer
查看原文
摘要
The presence of a reactive B–Cl bond allowed for the direct functionalization of the boron center in antiaromatic chloroborole ClBC4Ph4, thus allowing for a selective fine tuning of the optical properties of borole derivatives and facilitating a potential new approach toward the introduction of borole moieties into the backbone of organic π-conjugated frameworks.
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来源期刊
Chemical Communications
CiteScore:
8.6
自引率:
4.7%
年发文量:
2458
ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry
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