Resonance Raman Study of Short-Time Photodissociation Dynamics of the Charge-Transfer Band Absorption of Nitrobenzene in Cyclohexane Solution

2005 ◽  
Vol 109 (13) ◽  
pp. 3086-3093 ◽  
Author(s):  
Xin-Ming Zhu ◽  
Shu-Qiang Zhang ◽  
Xuming Zheng ◽  
David Lee Phillips
1999 ◽  
Vol 19 (1-4) ◽  
pp. 71-74 ◽  
Author(s):  
Xuming Zheng ◽  
David Lee Phillips

We have obtained A-band absorption resonance Raman spectra of 1-chloro-2- iodoethane in cyclohexane solution. We have done preliminary time-dependent wavepacket calculations to simulate the resonance Raman intensities and absorption spectrum in order to learn more about the short-time photodissociation dynamics. We compare our preliminary results for 1-chloro-2-iodoethane with previous resonance Raman results for iodoethane and find that there appears to be more motion along non- C—I stretch modes for 1-chloro-2-iodoethane than for iodoethane. This is consistent with results of TOF photofragment spectroscopy experiments which indicate much more internal excitation of the photoproducts from 1-chloro-2-iodoethane photodissociation than the photoproducts from iodoethane photodissociation.


1994 ◽  
Vol 48 (10) ◽  
pp. 1236-1241 ◽  
Author(s):  
Paola Deplano ◽  
Francesco A. Devillanova ◽  
John R. Ferraro ◽  
Maria Laura Mercuri ◽  
Vito Lippolis ◽  
...  

In resonance Raman (RR) spectroscopy, the laser excitation sources have often been found to be destructive towards polyiodides if compared with the milder conditions under which the Fourier transform Raman (FT-R) technique operates. In fact, our FT-R spectra of some model polyiodides—[(CH3)4N]I5 (I5− bent), [(C2H5)4N]I7, and [(CH3)4N]I9—are significantly different from the literature RR data, give evidence of decomposition of the samples in RR, and are in agreement, respectively, with the I− · 2I2, I3− · 2I2 and (I− · 2I2) · 2I2 descriptions. In addition to the above-cited cases, the FT-R spectra of (Mn(modtc)3]Is (modtc = morpholine carbodithioato) and (moH]I5 (moH = morpholinium) are reported. The crystal structures indicate that in these two compounds the I5 anions can be properly described as I− · 2I2 and I3− · I2, respectively, and FT-R spectra agree well with this formulation. Moreover, the first FT-R spectrum of an I164– anion in [mo2ttl]2I16, ([mo2ttl]2+ = 3,5-di( N-morpholinio)-1,2,4-trithiolane), whose X-ray structure shows a sequence of two I3− … I2 … I− ·I2 (I82–) interacting anions, is reported. A close correlation of the FT-Raman peaks with the molecular species, identified by the interatomic distances, is also observed in this case. Thus, a combination of X-ray structural data and FT-R data can provide a reasonable interpretation of the nature of the acceptor iodine moiety in charge-transfer polyiodide complexes.


FEBS Letters ◽  
1982 ◽  
Vol 138 (1) ◽  
pp. 29-32 ◽  
Author(s):  
Gary Williamson ◽  
Paul C. Engel ◽  
Yasuzo Nishina ◽  
Kiyoshi Shiga

1980 ◽  
Vol 87 (3) ◽  
pp. 831-839 ◽  
Author(s):  
Yasuzo NISHINA ◽  
Teizo KITAGAWA ◽  
Kiyoshi SHIGA ◽  
Hiroshi WATARI ◽  
Toshio YAMANO

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