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).

One "click" access to self-complementary molecular modules for halogen bonding / G. Cavallo, P. Metrangolo, T. Pilati, G. Resnati, A. Scrivanti, M. Aversa, E. Cariati. - In: RSC ADVANCES. - ISSN 2046-2069. - 6:43(2016), pp. 36723-36727. [10.1039/c6ra05341f]

One "click" access to self-complementary molecular modules for halogen bonding

E. Cariati
Ultimo
2016

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).
chemical engineering (all); chemistry (all)
Settore CHIM/03 - Chimica Generale e Inorganica
2016
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/388365
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