VIBRATIONAL-SPECTRA OF N-ACETYLGLYCINE OLIGOMERS .2. RAMAN-SCATTERINGSTUDY OF SELECTIVELY C-DEUTERIATED OLIGOMERS WITH POLYGLYCINE-I-TYPE AND POLYGLYCINE-II-TYPE STRUCTURES
H. Etori et al., VIBRATIONAL-SPECTRA OF N-ACETYLGLYCINE OLIGOMERS .2. RAMAN-SCATTERINGSTUDY OF SELECTIVELY C-DEUTERIATED OLIGOMERS WITH POLYGLYCINE-I-TYPE AND POLYGLYCINE-II-TYPE STRUCTURES, Journal of the Chemical Society. Faraday transactions, 93(2), 1997, pp. 313-319
Citations number
27
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
Selectively C-deuteriated N-acetylglycine trimer and tetramer acid typ
es have been synthesized, and their two crystalline modifications, sol
id-A and solid-B [which correspond in structure to polyglycine (PG) II
and I, respectively] have been prepared. Raman scattering spectra hav
e been measured for a series of these glycine oligomers, and the CH2-
and CD2-characteristic modes have been investigated in detail. Assignm
ent of the CH2-characteristic bands to each CH2 group in the oligomers
has been carried out successfully. In particular, the results obtaine
d from the CD2 stretch region show that N- and C-terminal glycine resi
dues for the PGI- and PGII-type trimers and tetramers are all in very
similar environments and that the glycine residues which are sandwiche
d between the two terminal residues are also in a similar environment
for both the trimers and the tetramers.