四苯基乙烯取代亚酞菁的合成及其光物理性质

IF 0.9 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY
Taniyuki Furuyama, Sho Shitanda, T. Fukumura, N. Kobayashi
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引用次数: 0

摘要

合成了四苯基亚乙基取代的邻苯二甲腈和相应的亚酞菁。单取代和二取代邻苯二甲腈可以通过典型的SNAr反应制备。邻苯二甲腈的晶体结构表明,大体积的四苯乙烯部分抑制了分子间的[式:见正文]-[式:见正文]相互作用。通过硼模板化邻苯二甲腈的大环化反应,获得了在周边和轴向位置被四苯乙烯取代的亚酞菁。酞菁在THF/水混合溶剂中表现出典型的聚集诱导发射行为,而亚酞菁的荧光强度随着水含量的增加而降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and photophysical properties of subphthalocyanine substituted with tetraphenylethylene moieties
Tetraphenylethylene-substituted phthalonitriles and corresponding subphthalocyanines have been synthesized. Mono- and di-substituted phthalonitriles could be prepared by a typical SNAr reaction. The crystallographic structures of phthalonitriles indicated that intermolecular [Formula: see text]-[Formula: see text] interactions were suppressed by the bulky tetraphenylethylene moieties. Subphthalocyanines substituted with tetraphenylethylenes at peripheral and axial positions were obtained by boron-templated macrocyclization of phthalonitriles. Phthalonitriles showed typical aggregation-induced-emission behavior in THF/water mixed solvents, while fluorescence intensities of subphthalocyanines were decreased with increasing water content.
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来源期刊
CiteScore
2.10
自引率
20.00%
发文量
62
审稿时长
1 months
期刊介绍: The Journal of Porphyrins and Phthalocyanines (JPP) covers research in the chemistry, physics, biology and technology of porphyrins, phthalocyanines and related macrocycles. Research papers, review articles and short communications deal with the synthesis, spectroscopy, processing and applications of these compounds.
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