Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Nuclear Magnetic Resonance Spectra of Polyhydroxylated Fullerene C60(OH)n. / Mazur, A. S.; Karpunin, A. E.; Proskurina, O. V.; Gerasimov, V. I.; Pleshakov, I. V.; Matveev, V. V.; Kuz’min, Yu I.
в: Physics of the Solid State, Том 60, № 7, 01.07.2018, стр. 1468-1470.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
}
TY - JOUR
T1 - Nuclear Magnetic Resonance Spectra of Polyhydroxylated Fullerene C60(OH)n
AU - Mazur, A. S.
AU - Karpunin, A. E.
AU - Proskurina, O. V.
AU - Gerasimov, V. I.
AU - Pleshakov, I. V.
AU - Matveev, V. V.
AU - Kuz’min, Yu I.
PY - 2018/7/1
Y1 - 2018/7/1
N2 - Polyhydroxylated fullerene C60(OH)n (with an estimated number of hydroxyl groups n = 38–44) synthesized from pure fullerene by mixing a benzene solution of C60 with a NaOH aqueous solution in the presence of a catalyst was studied with 1H and 13C solid-state nuclear magnetic resonance. Possible features of the structure of a molecule shell were revealed from 1H NMR data. The 13C spectrum showed a peak splitting with an increase in temperature, which is probably due to fullerenol isomers.
AB - Polyhydroxylated fullerene C60(OH)n (with an estimated number of hydroxyl groups n = 38–44) synthesized from pure fullerene by mixing a benzene solution of C60 with a NaOH aqueous solution in the presence of a catalyst was studied with 1H and 13C solid-state nuclear magnetic resonance. Possible features of the structure of a molecule shell were revealed from 1H NMR data. The 13C spectrum showed a peak splitting with an increase in temperature, which is probably due to fullerenol isomers.
UR - http://www.scopus.com/inward/record.url?scp=85050296908&partnerID=8YFLogxK
U2 - 10.1134/S106378341807017X
DO - 10.1134/S106378341807017X
M3 - Article
AN - SCOPUS:85050296908
VL - 60
SP - 1468
EP - 1470
JO - Physics of the Solid State
JF - Physics of the Solid State
SN - 1063-7834
IS - 7
ER -
ID: 35748937