Standard

Sarcosine and betaine crystals upon cooling : Structural motifs unstable at high pressure become stable at low temperatures. / Kapustin, E. A.; Minkov, V. S.; Boldyreva, E. V.

In: Physical Chemistry Chemical Physics, Vol. 17, No. 5, 07.02.2015, p. 3534-3543.

Research output: Contribution to journalArticlepeer-review

Harvard

APA

Vancouver

Kapustin EA, Minkov VS, Boldyreva EV. Sarcosine and betaine crystals upon cooling: Structural motifs unstable at high pressure become stable at low temperatures. Physical Chemistry Chemical Physics. 2015 Feb 7;17(5):3534-3543. doi: 10.1039/c4cp05094k

Author

Kapustin, E. A. ; Minkov, V. S. ; Boldyreva, E. V. / Sarcosine and betaine crystals upon cooling : Structural motifs unstable at high pressure become stable at low temperatures. In: Physical Chemistry Chemical Physics. 2015 ; Vol. 17, No. 5. pp. 3534-3543.

BibTeX

@article{ae7bc77102ff4daba97359c5eddfe2f2,
title = "Sarcosine and betaine crystals upon cooling: Structural motifs unstable at high pressure become stable at low temperatures",
abstract = "The crystal structures of N-methyl derivatives of the simplest amino acid glycine, namely sarcosine (C3H7NO2) and betaine (C5H11NO2), were studied upon cooling by single-crystal X-ray diffraction and single-crystal polarized Raman spectroscopy. The effects of decreasing temperature and increasing hydrostatic pressure on the crystal structures were compared. In particular, we have studied the behavior upon cooling of those structural motifs in the crystals, which are involved in structural rearrangement during pressure-induced phase transitions. In contrast to their high sensitivity to hydrostatic compression, the crystals of both sarcosine and betaine are stable to cooling down to 5 K. Similarly to most α-amino acids, the crystal structures of the two compounds are most rigid upon cooling in the direction of the main structural motif, namely head-to-tail chains (linked via the strongest N-H⋯O hydrogen bonds and dipole-dipole interactions in the case of sarcosine, or exclusively by dipole-dipole interactions in the case of betaine). The anisotropy of linear strain in betaine does not differ much upon cooling and on hydrostatic compression, whereas this is not the case for sarcosine. Although the interactions between certain structural motifs in sarcosine and betaine weaken as a result of phase transitions induced by pressure, the same interactions strengthen when volume reduction results from cooling.",
author = "Kapustin, {E. A.} and Minkov, {V. S.} and Boldyreva, {E. V.}",
year = "2015",
month = feb,
day = "7",
doi = "10.1039/c4cp05094k",
language = "English",
volume = "17",
pages = "3534--3543",
journal = "Physical Chemistry Chemical Physics",
issn = "1463-9076",
publisher = "Royal Society of Chemistry",
number = "5",

}

RIS

TY - JOUR

T1 - Sarcosine and betaine crystals upon cooling

T2 - Structural motifs unstable at high pressure become stable at low temperatures

AU - Kapustin, E. A.

AU - Minkov, V. S.

AU - Boldyreva, E. V.

PY - 2015/2/7

Y1 - 2015/2/7

N2 - The crystal structures of N-methyl derivatives of the simplest amino acid glycine, namely sarcosine (C3H7NO2) and betaine (C5H11NO2), were studied upon cooling by single-crystal X-ray diffraction and single-crystal polarized Raman spectroscopy. The effects of decreasing temperature and increasing hydrostatic pressure on the crystal structures were compared. In particular, we have studied the behavior upon cooling of those structural motifs in the crystals, which are involved in structural rearrangement during pressure-induced phase transitions. In contrast to their high sensitivity to hydrostatic compression, the crystals of both sarcosine and betaine are stable to cooling down to 5 K. Similarly to most α-amino acids, the crystal structures of the two compounds are most rigid upon cooling in the direction of the main structural motif, namely head-to-tail chains (linked via the strongest N-H⋯O hydrogen bonds and dipole-dipole interactions in the case of sarcosine, or exclusively by dipole-dipole interactions in the case of betaine). The anisotropy of linear strain in betaine does not differ much upon cooling and on hydrostatic compression, whereas this is not the case for sarcosine. Although the interactions between certain structural motifs in sarcosine and betaine weaken as a result of phase transitions induced by pressure, the same interactions strengthen when volume reduction results from cooling.

AB - The crystal structures of N-methyl derivatives of the simplest amino acid glycine, namely sarcosine (C3H7NO2) and betaine (C5H11NO2), were studied upon cooling by single-crystal X-ray diffraction and single-crystal polarized Raman spectroscopy. The effects of decreasing temperature and increasing hydrostatic pressure on the crystal structures were compared. In particular, we have studied the behavior upon cooling of those structural motifs in the crystals, which are involved in structural rearrangement during pressure-induced phase transitions. In contrast to their high sensitivity to hydrostatic compression, the crystals of both sarcosine and betaine are stable to cooling down to 5 K. Similarly to most α-amino acids, the crystal structures of the two compounds are most rigid upon cooling in the direction of the main structural motif, namely head-to-tail chains (linked via the strongest N-H⋯O hydrogen bonds and dipole-dipole interactions in the case of sarcosine, or exclusively by dipole-dipole interactions in the case of betaine). The anisotropy of linear strain in betaine does not differ much upon cooling and on hydrostatic compression, whereas this is not the case for sarcosine. Although the interactions between certain structural motifs in sarcosine and betaine weaken as a result of phase transitions induced by pressure, the same interactions strengthen when volume reduction results from cooling.

UR - http://www.scopus.com/inward/record.url?scp=84921639305&partnerID=8YFLogxK

U2 - 10.1039/c4cp05094k

DO - 10.1039/c4cp05094k

M3 - Article

AN - SCOPUS:84921639305

VL - 17

SP - 3534

EP - 3543

JO - Physical Chemistry Chemical Physics

JF - Physical Chemistry Chemical Physics

SN - 1463-9076

IS - 5

ER -

ID: 25438726