5-(9-(对甲苯基)-2,3,4,4a,9,9a-六氢-1H-1,4-甲烷咔唑-6-基)噻吩-2-甲醛

Molbank Pub Date : 2024-03-14 DOI:10.3390/m1792
N. Gudim, E. Knyazeva, O. Rakitin
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引用次数: 0

摘要

供体-π间隔物-受体(D-π-A)染料是设计有机染料敏化太阳能电池(DSSC)最具吸引力的结构之一。通常,这些敏化剂的关键中间体是含有醛基的 D-π 化合物,醛基通过 Knoevenagel 反应连接到锚受体基团上。本文通过铃木交叉偶联反应制备了 5-(9-(对甲苯基)-2,3,4,4a,9,9a-六氢-1H-1,4-甲烷咔唑-6-基)噻吩-2-甲醛。通过高分辨质谱、1H NMR、13C NMR、IR 和 UV-Vis 光谱分析,确定了新合成化合物的结构。该化合物将用于合成 DSSC 的敏化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
5-(9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-1,4-methanocarbazol-6-yl)thiophene-2-carbaldehyde
Donor–π spacer–acceptor (D–π–A) dyes are among the most attractive structures for the design of organic dye-sensitized solar cells (DSSCs). Typically, the key intermediates for these sensitizers are D–π compounds containing an aldehyde group to which an anchor acceptor group is attached via the Knoevenagel reaction. In this communication, 5-(9-(p-tolyl)-2,3,4,4a,9,9a-hexahydro-1H-1,4-methanocarbazol-6-yl)thiophene-2-carbaldehyde was prepared via the Suzuki cross-coupling reaction. The structure of the newly synthesized compound was established by means of high-resolution mass spectrometry, 1H NMR, 13C NMR, IR, and UV–Vis spectroscopy. The title compound would be used in the synthesis of sensitizers for DSSCs.
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