Abstract
In previous studies[1,2] we considered the time-resolved resonance Raman (TRRR) spectra of 1,3,5-hexatriene (HT) in its lowest excited triplet state in order to obtain information about the geometry of the T1 intermediate and the mechanism of the cis-trans photoisomerization in T1.
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F. Negri, G. Orlandi, A.M. Brouwer, F.W. Langkilde, S. Møller and R. Wilbrandt, J. Phys. Chem. 95 (1991) (in press)
F.W. Langkilde, R. Wilbrandt, A.M. Brouwer, H.J.C. Jacobs, E. Negri and G. Orlandi, “Steric control of excited state molecular structure. Resonance Raman and absorption spectroscopy of 2-methyl- and 3-methyl-1,3,5-hexatriene in theT1 state” (submitted)
F.W. Langkilde, N.-H. Jensen, R. Wilbrandt, A.M. Brouwer and H.J.C. Jacobs, J. Phys. Chem. 91, 1029 (1987)
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© 1992 Springer-Verlag Berlin Heidelberg
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Wilbrandt, R., Møller, S., Langkilde, F.W., Brouwer, A.M., Negri, F., Orlandi, G. (1992). The Potential Energy Surface of the T1 State of 1,3,5-Hexatrienes and Methylated Derivatives: A Survey of Present Knowledge. In: Takahashi, H. (eds) Time-Resolved Vibrational Spectroscopy V. Springer Proceedings in Physics, vol 68. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84771-4_45
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DOI: https://doi.org/10.1007/978-3-642-84771-4_45
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