Proton magnetic relaxation in solid poly(L-alanine), poly(L-leucine), poly(L-valine), and polyglycine

✍ Scribed by E. R. Andrew; R. Gaspar Jr.; W. Venart

• Publisher: Wiley (John Wiley & Sons)
• Year: 1978
• Tongue: English
• Weight: 632 KB
• Volume: 17
• Category: Article
• ISSN: 0006-3525
• DOI: 10.1002/bip.1978.360170808

✦ Synopsis

Abstract

Molecular motion in solid poly(L‐alanine), Poly(L‐leucine), poly(L‐valine), and polyglycine has been investigated through measurement of the portion spin‐lattice relaxation time at 30 and 60 MHz between 110 and 350°K. Rapid random reoriention of sied‐chain methyl groups provides the dominent source of relaxation in the first three; activation energies are 10.5 ± 1 1, 8.5 ± 1 kJ/mol, respectively, significantly lower than in the monomeric crystals. Relaxation times in poyglycine are two orders of magnitude longer than in the monomeric crystals. Relaxation times in polyglycine, significantly lower than in the monomeric crystals. Relaxation times in polyglycine are two orders of magnitude longer and are attributed mainly to segmental motions of the polymer chains. Evidence of nonexponential recovery of nuclear magnetization was encountered in the first three homopolyamino acids but not in polylycine, and was attributed to the correlated time to characterize these motions gave quite good agreement with the data; some improvement was obtained for two polymers using a Cole‐Davidson distribution of correlation times. For biopolymers using a Cole‐Davidson distribution of correlation times. For biopolymers generally it is concluded that rapid methyl group reorientation is a common dynamical feature and an important source of nuclear magnetic relaxation.