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One “Click” access to self-complementary molecular modules for halogen bonding†
G. Cavallo,T. Pilati,G. Resnati,A. Scrivanti,M. Aversa,E. Cariati
RSC Advances Pub Date : 04/06/2016 00:00:00 , DOI:10.1039/C6RA05341F
Abstract

Novel D–π–A push–pull chromophores were synthesized in good yields by CuAAc coupling of 4-X-2,3,5,6-tetrafluorophenyl-1-azides (X = H, Br, I) with 4-ethynyl-dimethylaniline. Thanks to the self-complementary binding sites at the molecular ends, the iodo derivative self-organizes in the solid state forming head-to-tail halogen-bonded one-dimensional unlimited chains. The second-order NLO properties of the iodo compound have been investigated by the solution-phase electric field induced second-harmonic generation method (EFISH).

Graphical abstract: One “Click” access to self-complementary molecular modules for halogen bonding
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