2005
DOI: 10.1016/j.chemphys.2004.10.028
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Femtosecond photoelectron spectroscopy of trans-stilbene above the reaction barrier

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Cited by 28 publications
(34 citation statements)
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“…Consistent with our experimental results, we were able to confirm that the absorption wavelength redshifts and the oscillator strength increase for molecules with larger charge-transfer character. Similar to the well-known photoisomerisation process of stilbene [18][19][20], one electron from the HOMO (with π bonding character with respect to 4 the vinyl C=C bond) is excited to the respective anti-bonding LUMO, reducing the C=C bond order and facilitating bond rotation in all combretastatins. However, we observed that the elongation of the central C=C bond on excitation was slightly larger for derivatives of low charge-transfer character, while the relaxation energies for the fluorescence from the S 1 surface to the ground state were higher.…”
Section: Introductionmentioning
confidence: 88%
“…Consistent with our experimental results, we were able to confirm that the absorption wavelength redshifts and the oscillator strength increase for molecules with larger charge-transfer character. Similar to the well-known photoisomerisation process of stilbene [18][19][20], one electron from the HOMO (with π bonding character with respect to 4 the vinyl C=C bond) is excited to the respective anti-bonding LUMO, reducing the C=C bond order and facilitating bond rotation in all combretastatins. However, we observed that the elongation of the central C=C bond on excitation was slightly larger for derivatives of low charge-transfer character, while the relaxation energies for the fluorescence from the S 1 surface to the ground state were higher.…”
Section: Introductionmentioning
confidence: 88%
“…Photoinduced gelation by stilbene oxalyl amide compounds was described (116). Femtosecond photoelectron spectroscopy was employed to study the excitation of trans-stilbene above the isomerization reaction barrier (117). Data on the temperature dependence of the azulene (I) effect on the Ph 2 CO sensitized photoisomerization of stilbenes in PhMe, C 6 H 6 , Me3COH, and MeCN were shown to be consistent with the formation of identical stilbene triplets from the two isomers (118).…”
Section: Stilbenesmentioning
confidence: 97%
“…Time-dependent density functional theory (TD-DFT) calculations, together with simulations of the electron energy distribution, allowed to estimate selective photoelectron energies of the S 0 , S 1 , S 2 , and D 0 electronic states (Figure 3.3) [24].…”
Section: Through Double-bond Twisting (Saltiel) Mechanismmentioning
confidence: 99%
“…Femtosecond photoelectron spectroscopy was employed to study the excitation of trans-stilbene above the isomerization reaction barrier [82]. Apart from the S 1 contribution, evidence of a second electronic state was found on the basis of two different transients measured across the photoelectron spectrum.…”
Section: Viscosity Effectmentioning
confidence: 99%