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Crystal structure of two paracetamol polymorphs at 20 K : A search for the "structure-property" relationship. / Druzhbin, D. A.; Drebushchak, T. N.; Min'kov, V. S. et al.

In: Journal of Structural Chemistry, Vol. 56, No. 2, 29.03.2015, p. 317-323.

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Druzhbin DA, Drebushchak TN, Min'kov VS, Boldyreva EV. Crystal structure of two paracetamol polymorphs at 20 K: A search for the "structure-property" relationship. Journal of Structural Chemistry. 2015 Mar 29;56(2):317-323. doi: 10.1134/S002247661502016X

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Druzhbin, D. A. ; Drebushchak, T. N. ; Min'kov, V. S. et al. / Crystal structure of two paracetamol polymorphs at 20 K : A search for the "structure-property" relationship. In: Journal of Structural Chemistry. 2015 ; Vol. 56, No. 2. pp. 317-323.

BibTeX

@article{7c078ce816094c99bdb28ea85d795d89,
title = "Crystal structure of two paracetamol polymorphs at 20 K: A search for the {"}structure-property{"} relationship",
abstract = "At a temperature of 20 K the crystal structures of two paracetamol polymorphs (monoclinic, form I, SPG P21/n and orthorhombic, form II, SPG Pbca) are solved by single crystal X-ray diffraction and a comparative analysis of the geometric characteristics of intra- and intermolecular interactions is performed. Polymorphous transformations were not observed until cooling to this temperature. It is shown that in form II hydrogen bonds remain longer than those in form I up to a temperature of 20 K, and the density of metastable form II remains higher than that of stable form I. At the same time, in form II, thermal parameters of nitrogen and oxygen atoms remain higher than those in form I. The features observed in the behavior of the heat capacity of both forms at temperatures below 100 K are not directly related to a change in the geometry of hydrogen bonds. The methyl group orientation determined from the electron density maps does not alter as compared to higher temperatures in both modifications. Thus, changes in the Raman spectra observed in the orthorhombic paracetamol form below 100 K are explained by the features of its dynamics rather than a change in the overall average orientation of the methyl group determined by X-ray diffraction.",
keywords = "hydrogen bonds, low temperatures, paracetamol, polymorphism, single crystal X-ray diffraction analysis",
author = "Druzhbin, {D. A.} and Drebushchak, {T. N.} and Min'kov, {V. S.} and Boldyreva, {E. V.}",
year = "2015",
month = mar,
day = "29",
doi = "10.1134/S002247661502016X",
language = "English",
volume = "56",
pages = "317--323",
journal = "Journal of Structural Chemistry",
issn = "0022-4766",
publisher = "Springer GmbH & Co, Auslieferungs-Gesellschaf",
number = "2",

}

RIS

TY - JOUR

T1 - Crystal structure of two paracetamol polymorphs at 20 K

T2 - A search for the "structure-property" relationship

AU - Druzhbin, D. A.

AU - Drebushchak, T. N.

AU - Min'kov, V. S.

AU - Boldyreva, E. V.

PY - 2015/3/29

Y1 - 2015/3/29

N2 - At a temperature of 20 K the crystal structures of two paracetamol polymorphs (monoclinic, form I, SPG P21/n and orthorhombic, form II, SPG Pbca) are solved by single crystal X-ray diffraction and a comparative analysis of the geometric characteristics of intra- and intermolecular interactions is performed. Polymorphous transformations were not observed until cooling to this temperature. It is shown that in form II hydrogen bonds remain longer than those in form I up to a temperature of 20 K, and the density of metastable form II remains higher than that of stable form I. At the same time, in form II, thermal parameters of nitrogen and oxygen atoms remain higher than those in form I. The features observed in the behavior of the heat capacity of both forms at temperatures below 100 K are not directly related to a change in the geometry of hydrogen bonds. The methyl group orientation determined from the electron density maps does not alter as compared to higher temperatures in both modifications. Thus, changes in the Raman spectra observed in the orthorhombic paracetamol form below 100 K are explained by the features of its dynamics rather than a change in the overall average orientation of the methyl group determined by X-ray diffraction.

AB - At a temperature of 20 K the crystal structures of two paracetamol polymorphs (monoclinic, form I, SPG P21/n and orthorhombic, form II, SPG Pbca) are solved by single crystal X-ray diffraction and a comparative analysis of the geometric characteristics of intra- and intermolecular interactions is performed. Polymorphous transformations were not observed until cooling to this temperature. It is shown that in form II hydrogen bonds remain longer than those in form I up to a temperature of 20 K, and the density of metastable form II remains higher than that of stable form I. At the same time, in form II, thermal parameters of nitrogen and oxygen atoms remain higher than those in form I. The features observed in the behavior of the heat capacity of both forms at temperatures below 100 K are not directly related to a change in the geometry of hydrogen bonds. The methyl group orientation determined from the electron density maps does not alter as compared to higher temperatures in both modifications. Thus, changes in the Raman spectra observed in the orthorhombic paracetamol form below 100 K are explained by the features of its dynamics rather than a change in the overall average orientation of the methyl group determined by X-ray diffraction.

KW - hydrogen bonds

KW - low temperatures

KW - paracetamol

KW - polymorphism

KW - single crystal X-ray diffraction analysis

UR - http://www.scopus.com/inward/record.url?scp=84934876968&partnerID=8YFLogxK

U2 - 10.1134/S002247661502016X

DO - 10.1134/S002247661502016X

M3 - Article

AN - SCOPUS:84934876968

VL - 56

SP - 317

EP - 323

JO - Journal of Structural Chemistry

JF - Journal of Structural Chemistry

SN - 0022-4766

IS - 2

ER -

ID: 25463068