Synthesis, structure and π-expansion of tris(4,5-dehydro-2,3:6,7-dibenzotropone).

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC Beilstein Journal of Organic Chemistry Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI:10.3762/bjoc.21.1
Yongming Xiong, Xue Lin Ma, Shilong Su, Qian Miao
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Abstract

The polycyclic skeleton of tris(4,5-dehydro-2,3:6,7-dibenzotropone) is a key structural fragment in carbon schwarzites, a theoretical form of negatively curved carbon allotrope. This report presents a new synthesis of this compound using a Ni-mediated Yamamoto coupling reaction and structural analysis of it with X-ray crystallography. Interestingly, it is observed that tris(4,5-dehydro-2,3:6,7-dibenzotropone) crystallized from its solution in hexane resulting in colorless and yellow crystal polymorphs, where it adopts conformations of approximate C s and C 2 symmetry, respectively. Furthermore, expanding its π-skeleton through the Barton-Kellogg and Scholl reactions led to the successful synthesis of a curved polycyclic arene containing three heptagons and two pentagons.

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三(4,5-脱氢-2,3:6,7-二苯并苯托酮)的合成、结构及π扩张。
tris(4,5-脱氢-2,3:6,7-二苯并tropone)的多环骨架是碳schwarzite中的一个关键结构片段,是负弯曲碳同素异形体的一种理论形式。本文报道了用镍介导的山本偶联反应合成该化合物的新方法,并用x射线晶体学对其进行了结构分析。有趣的是,我们观察到tris(4,5-脱氢-2,3:6,7-二苯并托酮)在己烷溶液中结晶,形成无色和黄色的晶体多晶,其中它分别采用近似的C s和C 2对称构象。此外,通过Barton-Kellogg和Scholl反应扩展其π骨架,成功合成了含有三个七面体和两个五边形的弯曲多环芳烃。
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来源期刊
CiteScore
4.90
自引率
3.70%
发文量
167
审稿时长
1.4 months
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.
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