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• W2070105227 abstract "In a study of cross sections of the E = ƒ(χ1,χ2) side-chain conformational potential energy surface of the γL or c7eq backbone conformation of For-l-Phe-NH2, it was found that there are three conformations (g +, a and g −) due to rotation about the Cαχ1 Cβ bond. It should be emphasised that the γL backbone conformation is conserved during rotation about χ1. However, there is only one unique conformation along the rotation about the Cβχ2 Ph bond. The CH2Ph group showed greater stabilisation, with respect to hydrogen (Gly), than the CH3 (Ala) or CH2OH (Ser) substituents. The hydrogen-bonded CO (amide 1) vibrational frequency is split into two bands due to the coupling of the CO stretching and NH2 scissoring modes of motion. The other carbonyl, not involved in hydrogen bonding, has a characteristic single IR band with a relatively high frequency. The orientation of the Ph group has no appreciable effect on these vibrational frequencies." @default.
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• W2070105227 date "1996-09-01" @default.
• W2070105227 modified "2023-10-15" @default.
• W2070105227 title "Peptide models XIX: Side-chain conformational energy surface and amide I vibrational frequencies of N-formyl-l-phenylalaninamide (For-Phe-NH2) in its γL or γinv or C7eq backbone conformation" @default.
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• W2070105227 doi "https://doi.org/10.1016/s0166-1280(96)04548-4" @default.
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