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Anisotropy of the polarizability and steric structure of 1,2-diarylaziridines. / Arbuzov, B. A.; Vul'fson, S. G.; Kostikov, R. R.; Monetina, L. A.; Khlebnikov, A. F.; Vereshchagin, A. N.

In: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, Vol. 24, No. 6, 01.06.1975, p. 1199-1202.

Research output: Contribution to journal › Article › peer-review

Harvard

Arbuzov, BA, Vul'fson, SG, Kostikov, RR, Monetina, LA, Khlebnikov, AF & Vereshchagin, AN 1975, 'Anisotropy of the polarizability and steric structure of 1,2-diarylaziridines', Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, vol. 24, no. 6, pp. 1199-1202. https://doi.org/10.1007/BF00922045

APA

Arbuzov, B. A., Vul'fson, S. G., Kostikov, R. R., Monetina, L. A., Khlebnikov, A. F., & Vereshchagin, A. N. (1975). Anisotropy of the polarizability and steric structure of 1,2-diarylaziridines. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 24(6), 1199-1202. https://doi.org/10.1007/BF00922045

Vancouver

Arbuzov BA, Vul'fson SG, Kostikov RR, Monetina LA, Khlebnikov AF, Vereshchagin AN. Anisotropy of the polarizability and steric structure of 1,2-diarylaziridines. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1975 Jun 1;24(6):1199-1202. https://doi.org/10.1007/BF00922045

Author

Arbuzov, B. A. ; Vul'fson, S. G. ; Kostikov, R. R. ; Monetina, L. A. ; Khlebnikov, A. F. ; Vereshchagin, A. N. / Anisotropy of the polarizability and steric structure of 1,2-diarylaziridines. In: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1975 ; Vol. 24, No. 6. pp. 1199-1202.

BibTeX

@article{629f866e4b6c4105a06c365e37fc25da,
title = "Anisotropy of the polarizability and steric structure of 1,2-diarylaziridines",
abstract = "1. A graphical method was proposed for the conformational analysis of aromatic compounds, based on a comparison of the molar Kerr constants of p-substituted aryl derivatives - the method of {"}isoconstant maps.{"} 2. A trans-configuration of aziridines - adducts of dichlorocarbene with certain benzylidine anilines - was established on the basis of the dipole moments. 3. Structures with C- and N-aryl substitution are noticeably distorted in comparison with the simplest analogs.",
author = "Arbuzov, {B. A.} and Vul'fson, {S. G.} and Kostikov, {R. R.} and Monetina, {L. A.} and Khlebnikov, {A. F.} and Vereshchagin, {A. N.}",
year = "1975",
month = jun,
day = "1",
doi = "10.1007/BF00922045",
language = "English",
volume = "24",
pages = "1199--1202",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer Nature",
number = "6",

}

RIS

TY - JOUR

T1 - Anisotropy of the polarizability and steric structure of 1,2-diarylaziridines

AU - Arbuzov, B. A.

AU - Vul'fson, S. G.

AU - Kostikov, R. R.

AU - Monetina, L. A.

AU - Khlebnikov, A. F.

AU - Vereshchagin, A. N.

PY - 1975/6/1

Y1 - 1975/6/1

N2 - 1. A graphical method was proposed for the conformational analysis of aromatic compounds, based on a comparison of the molar Kerr constants of p-substituted aryl derivatives - the method of "isoconstant maps." 2. A trans-configuration of aziridines - adducts of dichlorocarbene with certain benzylidine anilines - was established on the basis of the dipole moments. 3. Structures with C- and N-aryl substitution are noticeably distorted in comparison with the simplest analogs.

AB - 1. A graphical method was proposed for the conformational analysis of aromatic compounds, based on a comparison of the molar Kerr constants of p-substituted aryl derivatives - the method of "isoconstant maps." 2. A trans-configuration of aziridines - adducts of dichlorocarbene with certain benzylidine anilines - was established on the basis of the dipole moments. 3. Structures with C- and N-aryl substitution are noticeably distorted in comparison with the simplest analogs.

UR - http://www.scopus.com/inward/record.url?scp=34250399485&partnerID=8YFLogxK

U2 - 10.1007/BF00922045

DO - 10.1007/BF00922045

M3 - Article

AN - SCOPUS:34250399485

VL - 24

SP - 1199

EP - 1202

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 6

ER -

ID: 28244847