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. CariatiUltimo
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).File | Dimensione | Formato | |
---|---|---|---|
RSC Advances16.pdf
Open Access dal 02/07/2017
Tipologia:
Post-print, accepted manuscript ecc. (versione accettata dall'editore)
Dimensione
363.31 kB
Formato
Adobe PDF
|
363.31 kB | Adobe PDF | Visualizza/Apri |
c6ra05341f.pdf
accesso aperto
Tipologia:
Publisher's version/PDF
Dimensione
399.56 kB
Formato
Adobe PDF
|
399.56 kB | Adobe PDF | Visualizza/Apri |
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.