双芴和环辛并[1,2,3-jk:6,5,4-j'k']二芴--新型多重氧化还原体系的合成

IF 1.7 4区化学 Q3 CHEMISTRY, ORGANIC

Synlett Pub Date : 2024-07-25 DOI:10.1055/a-2373-0422

Jonathan Kirschner Solberg Hansen, Mogens Brøndsted Nielsen

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引用次数: 0

摘要

在本文中，我们合成了一种新型 9,9'-联芴基扩展四硫富戊烯（TTF）的 E/Z 异构体混合物，发现该混合物很容易发生氧化二聚反应，生成一种 TTF 乙烯基对映体，其中两个二硫富戊烯单元连接到一个与联芴基核心融合的八元环上。这种化合物具有多重氧化还原行为，在循环伏安法条件下可产生六种电荷状态：-这种二阳离子对应于带有两个附加 1,3 二硫环的环辛基[1,2,3-jk:6,5,4-j'k']二芴。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Synthesis of Bifluorenylidene- and Cycloocta[1,2,3-jk:6,5,4-j'k']difluorene-Extended Tetrathiafulvalenes – Novel Multi-Redox Systems

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Synthesis of Bifluorenylidene- and Cycloocta[1,2,3-jk:6,5,4-j'k']difluorene-Extended Tetrathiafulvalenes – Novel Multi-Redox Systems

Herein, we present the synthesis of a novel 9,9’-bifluorenylidene-extended tetrathiafulvalene (TTF) as an E/Z isomeric mixture that was found to readily undergo an oxidative dimerization to furnish a TTF vinylogue with the two dithiafulvene units connected to an eight-membered ring fused to a bifluorenylidene core. This compound exhibited multi-redox behavior and was found to take six charge states under cyclic voltammetry conditions: -2, -1, 0, +1, +2, +3. The dication corresponds to a cycloocta[1,2,3-jk:6,5,4-j’k’]difluorene with two appended 1,3-dithiolium rings.

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来源期刊

Synlett 化学-有机化学

CiteScore

3.40

自引率

5.00%

发文量

369

审稿时长

1 months

期刊介绍： SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.