Electronic interactions in a branched chromophore investigated by nonlinear optical and time-resolved spectroscopy J. Chem. Phys. 120, 337 (2004); 10.1063/1.1630309Study of hyper-Rayleigh scattering and two-photon absorption induced fluorescence from crystal violet Three two-photon active boradiazaindacene derivatives named 2,6-di-͑phenylacetylenyl͒-1,3,5,7-tetramethyl-8-phenyl-4,4-difluoroboradiazaindacene ͑3a͒, 2,6-di-͑9-ethyl-9H-carbazole-3-ethynyl͒-1,3,5,7-tetramethyl-8-phenyl-4,4-difluoroboradiazaindacene ͑3b͒, and 2,6-di-͑4-N,N-diphenyl-phenylacetylenyl͒-1,3,5,7-tetramethyl-8-phenyl-4,4-difluoroboradiazaindacene ͑3c͒ in tetrahydrofuran solutions were systematically investigated by using the femtosecond laser spectroscopic techniques. The two-photon absorption cross sections of 3a, 3b and 3c were determined to be 29 GM, 46 GM, and 60 GM, respectively, increasing with the increase in strength of the electron-donor groups. The relaxation dynamics of the excited states measured by femtosecond pump-probe experiments reveal a broad region of stimulated radiation of the excited states and the different relaxation process happened in these compounds. The preliminary two-photon fluorescence imaging experiment show their good cell permeability, nontoxicity, and excellent two-photon fluorescence properties.