Taniyuki Furuyama, Sho Shitanda, T. Fukumura, N. Kobayashi
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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.
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.