具有五烯并[1,2-b:4,5-b']二芴核心的扩展四硫杂戊烯--一种供体-受体多重氧化还原系统。

IF 2.9 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-11-20 DOI:10.1039/d4ob01755b
Jeppe Granhøj, Viktor Bliksted Roug Pedersen, Kurt V Mikkelsen, Mogens Brøndsted Nielsen
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引用次数: 0

摘要

通过引入大的五烯并[1,2-b:4,5-b']二芴作为中心多环芳烃分子,制备出了一种新型的扩展四硫富戊烯。该化合物是一个多氧化还原体系,可以可逆地呈现六种氧化还原状态(-1、0、+1、+2、+3、+4)。该化合物在可见光区域表现出很强的吸收能力,其末端吸收几乎达到 700 纳米。
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Extended tetrathiafulvalene with a pentaleno[1,2-b:4,5-b']difluorene core - a donor-acceptor multi-redox system.

A novel extended tetrathiafulvalene was prepared by introducing the large pentaleno[1,2-b:4,5-b']difluorene as a central polycyclic aromatic hydrocarbon moiety. This compound behaved as a multi-redox system that could take reversibly six redox states (-1, 0, +1, +2, +3, +4). The compound exhibited strong absorptions in the visible region with an end-absorption almost reaching to 700 nm.

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来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: The international home of synthetic, physical and biomolecular organic chemistry.
期刊最新文献
Direct synthesis of enone-hydrazones under solvent free and additive free conditions. Extended tetrathiafulvalene with a pentaleno[1,2-b:4,5-b']difluorene core - a donor-acceptor multi-redox system. Correction: Cu(II)-Mediated aerobic oxidative synthesis of sulfonated chromeno[4,3-c]pyrazol-4(2H)-ones. Cu(II)-catalyzed synthesis of N-sulfonated quinolin-2(1H)-one-3-carboxamides. Innovations in isocyanate synthesis for a sustainable future.
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