Standard

Structure of 2-chloro-3-phenylbenzoic acid. / Boyarskiy, V. P.; Fonari, M. S.; Suwinska, K.; Simonov, Yu A.

в: Journal of Structural Chemistry, Том 50, № 3, 07.2009, стр. 585-587.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Boyarskiy, VP, Fonari, MS, Suwinska, K & Simonov, YA 2009, 'Structure of 2-chloro-3-phenylbenzoic acid', Journal of Structural Chemistry, Том. 50, № 3, стр. 585-587. https://doi.org/10.1007/s10947-009-0091-2

APA

Boyarskiy, V. P., Fonari, M. S., Suwinska, K., & Simonov, Y. A. (2009). Structure of 2-chloro-3-phenylbenzoic acid. Journal of Structural Chemistry, 50(3), 585-587. https://doi.org/10.1007/s10947-009-0091-2

Vancouver

Boyarskiy VP, Fonari MS, Suwinska K, Simonov YA. Structure of 2-chloro-3-phenylbenzoic acid. Journal of Structural Chemistry. 2009 Июль;50(3):585-587. https://doi.org/10.1007/s10947-009-0091-2

Author

Boyarskiy, V. P. ; Fonari, M. S. ; Suwinska, K. ; Simonov, Yu A. / Structure of 2-chloro-3-phenylbenzoic acid. в: Journal of Structural Chemistry. 2009 ; Том 50, № 3. стр. 585-587.

BibTeX

@article{bbd6e9cf13af469fb83d5e1fd2929048,
title = "Structure of 2-chloro-3-phenylbenzoic acid",
abstract = "The carbonylation reaction of 2,3-dichlorobiphenyl proceeds with a substitution of the chlorine atom in position 3 and results in the formation of 2-chloro-3-phenylbenzoic acid. The structure of this acid is revealed by single crystal XRD. It is determined by steric interactions of substituents in positions 2,4,2′, and 6′, a stable carboxyl supramolecular synthon, and weak interactions with the participation of the carbonyl oxygen atom and the chlorine atom.",
keywords = "Aromatic carbonic acids, Carbonylation, Crystal structure, Polychlorobiphenyls, Synthesis",
author = "Boyarskiy, {V. P.} and Fonari, {M. S.} and K. Suwinska and Simonov, {Yu A.}",
note = "Funding Information: The work was supported by RFBR and the Academy of Sciences of the Republic of Moldova, Project 08-03-90104",
year = "2009",
month = jul,
doi = "10.1007/s10947-009-0091-2",
language = "English",
volume = "50",
pages = "585--587",
journal = "Journal of Structural Chemistry",
issn = "0022-4766",
publisher = "Springer Nature",
number = "3",

}

RIS

TY - JOUR

T1 - Structure of 2-chloro-3-phenylbenzoic acid

AU - Boyarskiy, V. P.

AU - Fonari, M. S.

AU - Suwinska, K.

AU - Simonov, Yu A.

N1 - Funding Information: The work was supported by RFBR and the Academy of Sciences of the Republic of Moldova, Project 08-03-90104

PY - 2009/7

Y1 - 2009/7

N2 - The carbonylation reaction of 2,3-dichlorobiphenyl proceeds with a substitution of the chlorine atom in position 3 and results in the formation of 2-chloro-3-phenylbenzoic acid. The structure of this acid is revealed by single crystal XRD. It is determined by steric interactions of substituents in positions 2,4,2′, and 6′, a stable carboxyl supramolecular synthon, and weak interactions with the participation of the carbonyl oxygen atom and the chlorine atom.

AB - The carbonylation reaction of 2,3-dichlorobiphenyl proceeds with a substitution of the chlorine atom in position 3 and results in the formation of 2-chloro-3-phenylbenzoic acid. The structure of this acid is revealed by single crystal XRD. It is determined by steric interactions of substituents in positions 2,4,2′, and 6′, a stable carboxyl supramolecular synthon, and weak interactions with the participation of the carbonyl oxygen atom and the chlorine atom.

KW - Aromatic carbonic acids

KW - Carbonylation

KW - Crystal structure

KW - Polychlorobiphenyls

KW - Synthesis

UR - http://www.scopus.com/inward/record.url?scp=70350681103&partnerID=8YFLogxK

U2 - 10.1007/s10947-009-0091-2

DO - 10.1007/s10947-009-0091-2

M3 - Article

AN - SCOPUS:70350681103

VL - 50

SP - 585

EP - 587

JO - Journal of Structural Chemistry

JF - Journal of Structural Chemistry

SN - 0022-4766

IS - 3

ER -

ID: 87472131