Tuning the photophysical and NLO properties of β-diketonates derived from coumarin-triphenylamine-chalcones: Effect of the BF2 group

Herein the synthesis of three difluoroboron β-diketonate complexes ( 7a-c ) and one chalcone ( 7d ) with coumarin and triphenylamine fragments is described. The effect of the inclusion of the difluoroboron (BF 2 ) group and a phenyl linker on the photophysical properties, intramolecular charge transfer (ICT) and nonlinear optical (NLO) properties was studied. These dyes exhibited excellent ICT properties due to their A-π-D and D-π-A-π-D type push-pull configuration. Thus, all compounds presented a strong solvatochromism, given the absorption and emission maxima shifted to red because of the increase in the polarity of the medium. In addition to this, 7a-d showed the formation of a twisted intramolecular charge transfer (TICT) state, which quenched fluorescence in polar solvents. Compounds 7a , 7b and 7d exhibited aggregation-induced emission (AIE) in MeCN/H 2 O mixtures, while 7c did not have this behavior. In addition, all compounds showed emission in the solid state. Using DFT and TD-DFT calculations, the molecular geometries of the ground state S 0 and the first excited state S 1 were elucidated, which confirmed the formation of a TICT state. Furthermore, the theoretical and experimental absorption electronic transitions were correlated by testing different functionals: B3LYP, CAM-B3LYP, PBE0, wB97XD, HSEH1PBE and M062X. Frontier molecular orbitals (FOMs) and molecular electrostatic potentials (MEPs) supported the ICT from the donor to the acceptor group. The global reactivity descriptors were studied and the NLO properties were predicted by calculating first ( β tot ) and second-order ( γ ave ) hyperpolarizabilities, revealing that 7a-d would present promising NLO behavior.