Journal of Physical Chemistry A, Vol.103, No.50, 10730-10736, 1999
Subpicosecond ring opening of 7-dehydrocholesterol studied by ultrafast spectroscopy
The photoinitiated electrocyclic ring opening of 7-dehydrocholesterol (DHC) Co form previtamin D-3 was studied in methanol solution with femtosecond transient absorption spectroscopy. The molecules were excited at 265 nm and probed at 20 wavelengths ranging from 261 to 650 nm. A sizable absorption signal decaying on a 0.95 +/- 0.10 ps time scale was seen at all probe wavelengths from 470 to 650 nm. This absorption is assigned to an S-1 --> S-n transition that peaks near 470 nm, Thus, the S-1 state has a lifetime of 0.95 ps, while the initially prepared St state has a lifetime less than or equal to 0.1 ps, Data obtained with probe wavelengths in the ultraviolet yielded a subpicosecond (0.4-1.0 ps) component corresponding to the lifetime of the S-1 state. This data set also exhibits a 1-5 ps wavelength-dependent component assigned to vibrational cooling, and a 100 +/- 20 ps component assigned to rotational isomerization of the photoproduct to achieve a thermal distribution of rotamers. No further dynamics are seen for time delays of up to 1 ns. Agreement between the static difference spectrum and the absorption difference observed in the kinetic data at 300 ps indicates that there are no significant longer-time dynamics.
Keywords:FEMTOSECOND TRANSIENT ABSORPTION;UV RESONANCE RAMAN;PREVITAMIN-D;VITAMIN-D;1;3-CYCLOHEXADIENE;PHOTOCHEMISTRY;WAVELENGTH;CYCLOHEXANE;DYNAMICS;CIS