TY - JOUR
T1 - Photophysics of (1-butyl-4-(1H-inden-1-ylidene)-1,4-dihydropyridine (BIDP)
T2 - An experimental test for conical intersections
AU - Cogan, Semyon
AU - Kahan, Anat
AU - Zilberg, Shmuel
AU - Haas, Yehuda
PY - 2008/6/26
Y1 - 2008/6/26
N2 - Fluorescence experiments on (1-butyl-4-(1H-inden-1-ylidene)-1,4- dihydropyridine (BIDP) are reported in liquid and glassy solutions. The data indicate a fast decay in the fluid nonpolar, nonprotic solutions (decay times ∼0-12s) and rapid but considerably slower decay in polar ones. In frozen solutions (polar and nonpolar), the fluorescence quantum yield is much higher (near 0.5 and around 0.1 in polar and nonpolar glasses, respectively). The rapid nonradiative transitions in fluid solutions are assigned to internal conversion in both solvent classes, as intersystem crossing is much slower and no net reaction is observed. These results are in agreement with predictions made for the closely related (in terms of electronic structure) but simpler molecule cyclopentadienyl-1,4-dihydropyridine (CPDHP) for which an S 1/S0 conical intersection was recently proposed [Int. J. Quant. Chem. 2005, 702, 961]. The crossing of the two lowest singlet states is calculated to vanish in polar solvents such as methyl cyanide, leading to longer lifetime of Si of CPDHP. As BIDP has a very similar electronic structure, the model predicts a corresponding change in this larger molecule. The strong fluorescence observed in the glassy environments is rationalized by the hindering of the internal torsion required to reach the geometry of the conical intersection.
AB - Fluorescence experiments on (1-butyl-4-(1H-inden-1-ylidene)-1,4- dihydropyridine (BIDP) are reported in liquid and glassy solutions. The data indicate a fast decay in the fluid nonpolar, nonprotic solutions (decay times ∼0-12s) and rapid but considerably slower decay in polar ones. In frozen solutions (polar and nonpolar), the fluorescence quantum yield is much higher (near 0.5 and around 0.1 in polar and nonpolar glasses, respectively). The rapid nonradiative transitions in fluid solutions are assigned to internal conversion in both solvent classes, as intersystem crossing is much slower and no net reaction is observed. These results are in agreement with predictions made for the closely related (in terms of electronic structure) but simpler molecule cyclopentadienyl-1,4-dihydropyridine (CPDHP) for which an S 1/S0 conical intersection was recently proposed [Int. J. Quant. Chem. 2005, 702, 961]. The crossing of the two lowest singlet states is calculated to vanish in polar solvents such as methyl cyanide, leading to longer lifetime of Si of CPDHP. As BIDP has a very similar electronic structure, the model predicts a corresponding change in this larger molecule. The strong fluorescence observed in the glassy environments is rationalized by the hindering of the internal torsion required to reach the geometry of the conical intersection.
UR - http://www.scopus.com/inward/record.url?scp=84961980427&partnerID=8YFLogxK
U2 - 10.1021/jp7110296
DO - 10.1021/jp7110296
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AN - SCOPUS:84961980427
SN - 1089-5639
VL - 112
SP - 5604
EP - 5612
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 25
ER -