Solvent effects on the resonance Raman spectra of bacteriochlorophyll a cation radical
β Scribed by Yasuhito Misono; Ei-ichi Nishizawa; Leenawaty Limantara; Yasushi Koyama; Koichi Itoh
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 587 KB
- Volume
- 236
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Resonance Raman (RR) spectra were measured for the cation radical of bacteriochlorophyli a in acetone, methanol, dichloromethane and mixed solvents of acetone and methanol. The ring-breathing (C~-C m stretching) frequency of the radical (abbreviated as v~ +) was observed at 1601 cm-i in acetone (forming a penta-coordinated monomer), at 1587 cmin methanol (forming a hexa-coordinated monomer) and at 1600 cm -~ in dichioromethane (forming a penta-coordinated aggregate). The RR spectrum of the radical in dichloromethane is almost identical to the transient RR spectrum ascribed to 'the aggregated T~ species of Bchi a' formed in the particular solvent by Nishizawa, Limantara, Nanjou, Nagae, Kakuno and Koyama, indicating that their interpretation needs to be revised.
π SIMILAR VOLUMES
Solution \*sM-ENDOR and TRIPLE n~~~~+nce esperiments have been performed on the bacteriochlorophyll a (BChl a) zJ anion and cation radicals enriched in 25hIg. The 2shfg isotropic hyperfime coupling constants for BChl a\* and BChl ar have been determined. The vaIues are in good agreement with those o
## Abstract The chemical shifts of the __N__βmethyl signals for a number of thioβoxamide and oxamide derivatives are unambiguously determined in the solvents chloroform, carbon tetrachloride, benzene, chlorobenzene, __o__βdichlorobenzene and nitrobenzene. The ASIS effect is discussed. The temperatu