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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 10958-10969 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A resonance Raman intensity analysis is performed on the intramolecular charge-transfer molecule 1-aza-adamantane-4-ylidenemalononitrile in acetonitrile solution. We explore the extent to which changes in molecular structure upon charge transfer can be obtained from resonance Raman intensity analysis, and extend the analysis method for charge-transfer excitation to take into account the possible influence of nearby locally excited states. Absolute scattering cross sections are measured at five excitation wavelengths spanning both the charge-transfer band at 324 nm and the lowest locally excited band at 231 nm, and the absorption spectra and resonance Raman intensities are modeled self-consistently to obtain the mode-specific reorganization energies accompanying electronic excitation to both states. Interference effects between the two states are considered but are found to be of minimal importance for this particular charge-transfer molecule. The reorganization parameters in terms of dimensionless normal coordinates are converted to actual bond length and bond angle changes by making use of a previously developed ground-state normal mode analysis and by comparing with electronic structure calculations on models for the donor and acceptor ends to reduce the indeterminacy in the signs of the dimensionless displacements. The geometry changes upon excitation to the LE state are dominated by lengthening of the ethylenic C(Double Bond)C bond, while for CT excitation the distortions are distributed over the donor, acceptor, and adamantane bridge, with a smaller C(Double Bond)C bond length change. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 121-135 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Time-dependent perturbation theory, together with a (minimal) molecular model consisting of three energy levels (S0,S1,S3), is used to investigate the spectroscopy and the dynamics of fast time resolved, two-photon, two-color, pump–probe experiments, involving the direct S0→S1 two-photon excitation of α-NPO. In particular the theory is used to examine the aitch-theta-dependence of the fluorescence signal from the S1 state, where aitch-theta is the angle between the polarization vectors of the pump and probe lasers, for fixed (zero) time delay between the laser pulses. It is predicted, in contradistinction to the cos2 aitch-theta dependence of the fluorescence signal from the S2 state of azulene arising from the sequential two-photon S0→S1→S2 transition, that the signal from the S1 state of α-NPO can vary between pure cos2 aitch-theta and pure cos4 aitch-theta dependencies and that secondary maxima in the signal, as a function of aitch-theta, can occur for certain laser intensities. Also reported is a new series of experiments for α-NPO, motivated by the theory, that yields results for the fluorescence intensity of the S1 state, as a function of aitch-theta and laser intensity, in agreement with the theoretical predictions. Comparison of experiment and theory is used to estimate the relative orientations of the relevant transition and permanent dipole moments, and the transition moment between the S1 and S3 states of α-NPO. The important role played by the permanent dipoles of the S0 and S1 states, and the importance of including averages over the relative laser phase, the jitter in the time-delay, and the orientations of the absorbing molecules, is emphasized in the theoretical analysis of the problem. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 96 (1992), S. 7904-7908 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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