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Synthesis of Two-Photon Absorbing Unsymmetrical Fluorenyl-Based Chromophores

2006; American Chemical Society; Volume: 18; Issue: 20 Linguagem: Inglês

10.1021/cm061406z

1520-5002

Alma R. Morales, Kevin D. Belfield, Joel M. Hales, Eric W. Van Stryland, David J. Hagan,

Nonlinear Optical Materials Research

Unsymmetrical fluorenyl-based chromophores, flanked on either side by electron-acceptor (A) and/or electron-donating (D) groups, separated by conjugated (π) moieties, were synthesized. Heck coupling and Wittig reactions were utilized to prepare target fluorene derivatives that possess very high solubility in organic solvents, high thermal stability (up to 395 °C), and generally high fluorescence quantum yields (0.6−0.9). The systematic alteration of the structural design allowed for investigation of numerous factors that affect the optical nonlinearity, as well as probing effects of molecular symmetry, solvent polarity, strengths of electron donating and/or withdrawing end groups, and π-conjugation length. A detailed spectroscopic study of these molecules, including absorption, fluorescence emission, excitation, and excitation anisotropy, was conducted. Two-photon absorption (2PA) cross sections (δ) were determined by a nonlinear transmission method employing a femtosecond white-light continuum (WLC) pump−probe method, with all compounds exhibiting high two-photon absorption under femtosecond excitation. Compound 3 had a peak 2PA cross section, δ, of 1093 × 10-50 cm4 s photon-1 molecule-1 at 828 nm. In addition, excitation anisotropy studies permitted the determination of the spectral position of the S0 → S1 and S0 → S2 electronic transitions.