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New Spin Probes : Tri- and Hexacationic Derivatives of Stable Tetrathiatriarylmethyl Radicals. / Trukhin, D. V.; Rogozhnikova, O. Yu; Troitskaya, T. I. и др.

в: Russian Journal of Organic Chemistry, Том 55, № 3, 01.03.2019, стр. 296-301.

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

Harvard

Trukhin, DV, Rogozhnikova, OY, Troitskaya, TI, Kuzhelev, AA, Amosov, EV, Halpern, HJ, Koval’, VV & Tormyshev, VM 2019, 'New Spin Probes: Tri- and Hexacationic Derivatives of Stable Tetrathiatriarylmethyl Radicals', Russian Journal of Organic Chemistry, Том. 55, № 3, стр. 296-301. https://doi.org/10.1134/S1070428019030035

APA

Trukhin, D. V., Rogozhnikova, O. Y., Troitskaya, T. I., Kuzhelev, A. A., Amosov, E. V., Halpern, H. J., Koval’, V. V., & Tormyshev, V. M. (2019). New Spin Probes: Tri- and Hexacationic Derivatives of Stable Tetrathiatriarylmethyl Radicals. Russian Journal of Organic Chemistry, 55(3), 296-301. https://doi.org/10.1134/S1070428019030035

Vancouver

Trukhin DV, Rogozhnikova OY, Troitskaya TI, Kuzhelev AA, Amosov EV, Halpern HJ и др. New Spin Probes: Tri- and Hexacationic Derivatives of Stable Tetrathiatriarylmethyl Radicals. Russian Journal of Organic Chemistry. 2019 март 1;55(3):296-301. doi: 10.1134/S1070428019030035

Author

Trukhin, D. V. ; Rogozhnikova, O. Yu ; Troitskaya, T. I. и др. / New Spin Probes : Tri- and Hexacationic Derivatives of Stable Tetrathiatriarylmethyl Radicals. в: Russian Journal of Organic Chemistry. 2019 ; Том 55, № 3. стр. 296-301.

BibTeX

@article{0ad8316383d44b51a617c39490d1639c,
title = "New Spin Probes: Tri- and Hexacationic Derivatives of Stable Tetrathiatriarylmethyl Radicals",
abstract = "The reaction of Finland trityl with tertiary aliphatic alcohols containing a terminal tertiary amino group, followed by quaternization of the amino groups, afforded new highly polar tri- and hexacationic derivatives. The obtained compounds are characterized by a sharp singlet signal in the EPR spectrum and are soluble in water over a wide pH range.",
keywords = "cationic derivatives of Finland trityl, EPR, spin probes, stable triarylmethyl radicals",
author = "Trukhin, {D. V.} and Rogozhnikova, {O. Yu} and Troitskaya, {T. I.} and Kuzhelev, {A. A.} and Amosov, {E. V.} and Halpern, {H. J.} and Koval{\textquoteright}, {V. V.} and Tormyshev, {V. M.}",
year = "2019",
month = mar,
day = "1",
doi = "10.1134/S1070428019030035",
language = "English",
volume = "55",
pages = "296--301",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "3",

}

RIS

TY - JOUR

T1 - New Spin Probes

T2 - Tri- and Hexacationic Derivatives of Stable Tetrathiatriarylmethyl Radicals

AU - Trukhin, D. V.

AU - Rogozhnikova, O. Yu

AU - Troitskaya, T. I.

AU - Kuzhelev, A. A.

AU - Amosov, E. V.

AU - Halpern, H. J.

AU - Koval’, V. V.

AU - Tormyshev, V. M.

PY - 2019/3/1

Y1 - 2019/3/1

N2 - The reaction of Finland trityl with tertiary aliphatic alcohols containing a terminal tertiary amino group, followed by quaternization of the amino groups, afforded new highly polar tri- and hexacationic derivatives. The obtained compounds are characterized by a sharp singlet signal in the EPR spectrum and are soluble in water over a wide pH range.

AB - The reaction of Finland trityl with tertiary aliphatic alcohols containing a terminal tertiary amino group, followed by quaternization of the amino groups, afforded new highly polar tri- and hexacationic derivatives. The obtained compounds are characterized by a sharp singlet signal in the EPR spectrum and are soluble in water over a wide pH range.

KW - cationic derivatives of Finland trityl

KW - EPR

KW - spin probes

KW - stable triarylmethyl radicals

UR - http://www.scopus.com/inward/record.url?scp=85065466101&partnerID=8YFLogxK

U2 - 10.1134/S1070428019030035

DO - 10.1134/S1070428019030035

M3 - Article

AN - SCOPUS:85065466101

VL - 55

SP - 296

EP - 301

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 3

ER -

ID: 20030694