scholarly journals Photoisomerization reaction of CH2BrI following A-band and B-band photoexcitation in the solution phase: Transient resonance Raman observation of the iso-CH2I–Br photoproduct

2000 ◽  
Vol 113 (8) ◽  
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Author(s):  
Xuming Zheng ◽  
David Lee Phillips
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Takashi Kikukawa ◽  
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Haruki Yamaryo ◽  
Yuta Saito ◽  
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1999 ◽  
Vol 19 (1-4) ◽  
pp. 237-243
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Luc Jacquet ◽  
John M. Kelly ◽  
...  

Transient resonance Raman (TR2) spectroscopy has been used to investigate the metalligand charge-transfer (MLCT) excited states of Ru(II) polypyridyl complexes inDNAand in homogeneous solution. In DNA, complexes of the type [Ru(L)2(L′)]2+ were studied, where L=2, 2’-bipyridyl (bpy), 1,4, 5, 8-tetraazaphenanthrene (tap), and L′ dipyrido [3,2:a-2′ ,3′:c]-phenazine (dppz) or 1,4,5,8,9,12-hexaazatriphenylene (HAT). For [Ru(bpy)2(HAT)]2+, the enhancement pattern of vibrational modes in the TR2 spectra attributable to reduced HAT⋅− in the triplet MLCT state suggest perturbations to the intraligand transition of HAT⋅− in the presence of DNA. Transient RR spectra for [Ru(tap)2(dppz)]2+ are indicative of formation of the species RunII(tap⋅−)(tap)(dppz) by electron transfer from DNA to the triplet MLCT state of the complex.TR2 spectra for complexes of the type, [(Ru(bpy)2)n(L)]2+ , n=1, 2 where L=a triazole bridging ligand, illustrate the use of the technique as a probe of the response of MLCT states to the electronic environment.


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