4,4′,4″-(苯-1,3,5-三(乙炔-2,1-二基))三(1-甲基吡啶-1-鎓)碘化物

IF 0.6 Q4 CHEMISTRY, ORGANIC Molbank Pub Date : 2023-11-08 DOI:10.3390/m1742
Lorenza Romagnoli, Andrea D’Annibale, Alessandro Latini
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引用次数: 0

摘要

尽管人们已经知道了很长时间,但由于其特殊的氧化还原和电荷转移特性,季4,4 ' -联吡啶盐(或称viologens)仍然是一类非常鼓舞人心的化合物。然而,含有多个吡啶环的更复杂的结构,也由共轭基团间隔,允许更广泛的合成变异性和其特性的可调性。本文所描述的化合物是一个星形的完全共轭分子,由三个甲基化的吡啶环通过一个三键间隔连接到一个中心苯核,它是由现成的构建块合成的,代表了一个相当简单的多吡啶扩展的分子模型;对其紫外可见吸收光谱和荧光光谱进行了研究。
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4,4′,4″-(Benzene-1,3,5-triyltris(ethyne-2,1-diyl))tris(1-methylpyridin-1-ium) Iodide
Despite having been known for a long time, quaternary 4,4′-bipyridinium salts, or viologens, are still a highly inspiring class of compounds, thanks to their peculiar redox and charge transfer properties. However, more complex structures containing multiple pyridinium rings, also interspaced by conjugated moieties, allow an even wider synthetic variability and tunability of their characteristics. The compound described herein is a star-shaped, fully conjugated molecule with three methylated pyridinium rings connected by a triple bond spacer to a central benzene core, which was synthesized from readily available building blocks, representing a quite simple model of multi-pyridyl extended viologen; its UV–visible absorption and fluorescence spectra have also been investigated.
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来源期刊
Molbank
Molbank Chemistry-Physical and Theoretical Chemistry
CiteScore
0.70
自引率
33.30%
发文量
174
审稿时长
11 weeks
期刊介绍: •organic synthesis •biosynthesis •extraction and purification •natural product derivatives •structural elucidation (X-ray crystallography, NMR, etc.)
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