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Sarcosine and Betaine Crystals upon Cooling: Structural Motifs Unstable at High Pressure Become Stable at Low Temperatures Full article

Journal PCCP: Physical Chemistry Chemical Physics
ISSN: 1463-9076 , E-ISSN: 1463-9084
Output data Year: 2015, Volume: 17, Number: 5, Pages: 3534-3543 Pages count : 10 DOI: 10.1039/c4cp05094k
Tags ATOMIC DISPLACEMENT PARAMETERS; III AMMINE COMPLEXES; X-RAY-DIFFRACTION; HYDROGEN-BONDS; L-ALANINE; AMINO-ACIDS; DL-ALANINE; PHASE-TRANSITIONS; ALPHA-POLYMORPH; LATTICE STRAIN
Authors Kapustin E.A. 1,2 , Minkov V.S. 1,3 , Boldyreva E.V. 1,3
Affiliations
1 Novosibirsk State University, Pirogov street, 2, Novosibirsk, Russian Federation
2 Department of Chemistry, University of California, Berkeley, CA, United States
3 Institute of Solid State Chemistry and Mechanochemistry SB RAS, Kutateladze street, 18, Novosibirsk, Russian Federation

Funding (2)

1 The Ministry of Education and Science of the Russian Federation 1828
2 Russian Foundation for Basic Research 12-03-31145 (01201272812)

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
Cite: 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
PCCP: Physical Chemistry Chemical Physics. 2015. V.17. N5. P.3534-3543. DOI: 10.1039/c4cp05094k WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Nov 4, 2014
Accepted: Dec 16, 2014
Published online: Dec 16, 2014
Identifiers:
Web of science: WOS:000348203200065
Scopus: 2-s2.0-84921639305
Elibrary: 23968831
Chemical Abstracts: 2014:2132916
Chemical Abstracts (print): 162:176355
OpenAlex: W2000884878
Citing:
DB Citing
Web of science 12
Scopus 12
OpenAlex 12
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