Variation of the Backbone Conjugation in NLO Model Compounds: Torsion-Angle-Restricted, Biphenyl-Based Push-Pull-Systems

Terminal piperidinyl- and nitro-functionalized biphenyls, bridged between the 2 and 2' positions by a variable number of methylene groups, are synthesized and fully characterized. These push-pull systems with defined and restricted torsion angles between their phenyl rings are ideal model compounds to investigate the influence of the chromophore's conjugation in nonlinear optic (NLO) responses. A general synthetic route that can be implemented to access these model compounds is reported, starting from dibromo or ditriflate biphenyls. Hartwig-Buchwald cross-coupling, a selective azacycloalkylation of diaminobiphenyls and a mild oxidation of primary amines to nitro groups in the presence of a tertiary amine summarizes the synthetic pathway towards the desired model compounds. NLO properties of the series of torsionally constrained push-pull biphenyls are collected by electric-field-induced second-harmonic generation (ERSH) experiments. The results agree qualitatively with semi-empirical simulations based on the AM1 Hamiltoman. A linear dependence of the quadratic response on the cos(2)(Phi) of the inter-aryl dihedral angle is observed, which points to oscillator strength loss as the dominant effect of increasing backbone twist.