Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
L-Cysteine Nitrates. / Giester, G.; Ghazaryan, V. V.; Minkov, V. S. и др.
в: Journal of Structural Chemistry, Том 64, № 5, 05.2023, стр. 917-931.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - L-Cysteine Nitrates
AU - Giester, G.
AU - Ghazaryan, V. V.
AU - Minkov, V. S.
AU - Boldyreva, E. V.
AU - Petrosyan, A. M.
N1 - This work was supported in part by a research grant matsc-3822 from the Armenian National Science and Education Fund (ANSEF) based in New York, USA. This work was supported by the RA MES State Committee of Science and Russian Foundation for Basic Research (RF) in the frames of the joint research projects SCS 15RF-007 and RFBR 15-53-05023. Публикация для корректировки.
PY - 2023/5
Y1 - 2023/5
N2 - The formation of salts in the L-cysteine–HNO3–H2O system was studied yielding three representatives as single crystals: anhydrous L-cysteinium nitrate (L-CysH)NO3 (I) and two new salts (L-CysH⋯L-Cys)NO3 (II) and (L-CysH⋯L-Cys)NO3∙0.5H2O (III) with the dimeric (L-CysH⋯L-Cys) cation. (I), (II) and (III) crystallize in space groups P212121, P21 and I2, respectively. Dimeric cations in (II) and (III) were formed by very short O–H⋯O hydrogen bonds with R(O⋯O) distances of 2.440(2) Å and 2.4352(17) Å, respectively. Infrared and Raman spectra of (I–III) were registered and discussed in relation to crystal structures. Characteristics of dimeric cations are compared with those in the previously obtained compounds of L-CysH(L-CysH⋯L-Cys)F(F⋯HF), (L-CysH⋯L-Cys)Cl, (L-CysH⋯L-Cys)Br and (L-CysH⋯L-Cys)I·0.5H2O.
AB - The formation of salts in the L-cysteine–HNO3–H2O system was studied yielding three representatives as single crystals: anhydrous L-cysteinium nitrate (L-CysH)NO3 (I) and two new salts (L-CysH⋯L-Cys)NO3 (II) and (L-CysH⋯L-Cys)NO3∙0.5H2O (III) with the dimeric (L-CysH⋯L-Cys) cation. (I), (II) and (III) crystallize in space groups P212121, P21 and I2, respectively. Dimeric cations in (II) and (III) were formed by very short O–H⋯O hydrogen bonds with R(O⋯O) distances of 2.440(2) Å and 2.4352(17) Å, respectively. Infrared and Raman spectra of (I–III) were registered and discussed in relation to crystal structures. Characteristics of dimeric cations are compared with those in the previously obtained compounds of L-CysH(L-CysH⋯L-Cys)F(F⋯HF), (L-CysH⋯L-Cys)Cl, (L-CysH⋯L-Cys)Br and (L-CysH⋯L-Cys)I·0.5H2O.
KW - L-cysteine
KW - crystal structure
KW - dimeric cation
KW - nitrates
KW - short hydrogen bonds
KW - vibrational spectra
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85160930687&origin=inward&txGid=a177550191c27510d2922fafcee97d6f
UR - https://www.mendeley.com/catalogue/f676ca73-fb09-368e-afe7-106897acba05/
U2 - 10.1134/S0022476623050104
DO - 10.1134/S0022476623050104
M3 - Article
VL - 64
SP - 917
EP - 931
JO - Journal of Structural Chemistry
JF - Journal of Structural Chemistry
SN - 0022-4766
IS - 5
ER -
ID: 59646995