Three new push-pull molecules having either pyridyl or N,N-dimethylanilino groups as electron-donor moieties and the p-iodo-tetrafluorophenyl ring as an electron-acceptor group have been synthesized and their single crystal X-ray structures are reported. Halogen bonding drives the self-assembly of these molecules in the solid state giving rise to head-to-tail halogen-bonded infinite polar chains which crystallize in an antiparallel arrangement. The three new nonlinear optical (NLO)-phores synthesized show high hyperpolarizabilities at the molecular level in solution. Rationalization of the obtained NLO measurements is supported by molecular modeling calculations.
Self-complementary nonlinear optical-phores targeted to halogen bond-driven self-assembly of electro-optic materials / E. Cariati, G. Cavallo, A. Forni, G. Leem, P. Metrangolo, F. Meyer, T. Pilati, G. Resnati, S. Righetto, G. Terraneo, E. Tordin. - In: CRYSTAL GROWTH & DESIGN. - ISSN 1528-7483. - 11:12(2011), pp. 5642-5648. [10.1021/cg201194a]
Self-complementary nonlinear optical-phores targeted to halogen bond-driven self-assembly of electro-optic materials
E. Cariati
;S. Righetto;E. TordinUltimo
2011
Abstract
Three new push-pull molecules having either pyridyl or N,N-dimethylanilino groups as electron-donor moieties and the p-iodo-tetrafluorophenyl ring as an electron-acceptor group have been synthesized and their single crystal X-ray structures are reported. Halogen bonding drives the self-assembly of these molecules in the solid state giving rise to head-to-tail halogen-bonded infinite polar chains which crystallize in an antiparallel arrangement. The three new nonlinear optical (NLO)-phores synthesized show high hyperpolarizabilities at the molecular level in solution. Rationalization of the obtained NLO measurements is supported by molecular modeling calculations.File | Dimensione | Formato | |
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