Molecular structures of thymidine isomers isolated in low-temperature inert matrices
Biological Systems at Low Temperatures
DOI (Low Temperature Physics):
https://doi.org/10.1063/1.1614199Ключові слова:
PACS: 33.15.–e, 67.80.CxАнотація
The Fourier transform infrared spectra of 2`-deoxyribonucleoside — thymidine (dT) in low-temperature Ar matrices are obtained in the range 4000–1300 cm–1. It is determined that anti-conformers of thymidine are dominant. The ribose rings of the main anti-conformers dT_a0, dT_a1 are in the C2`-endo conformation, but the ribose rings of minor anti-conformers dT_a2, dT_a3 have the C3`-endo conformation, stabilized by intramolecular hydrogen bonds O3`H…O5` and O5`H…O3`, respectively. The main syn-conformer dT_s2 is stabilized by the intramolecular hydrogen bond O5`H…O2 and has C2`-endo conformation of the ribose ring.
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Опубліковано
2003-09-01
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(1)
A.Yu. Ivanov, S.A. Krasnokutski, and G.G. Sheina, Molecular structures of thymidine isomers isolated in low-temperature inert matrices: Biological Systems at Low Temperatures, Low Temp. Phys. 29, (2003) [Fiz. Nizk. Temp. 29, 1065-1070, (2003)] DOI: https://doi.org/10.1063/1.1614199.
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