Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions. / Kuzhelev, Andrey A.; Tormyshev, Victor M.; Plyusnin, Victor F. и др.
в: Physical Chemistry Chemical Physics, Том 22, № 3, 21.01.2020, стр. 1019-1026.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
AU - Kuzhelev, Andrey A.
AU - Tormyshev, Victor M.
AU - Plyusnin, Victor F.
AU - Rogozhnikova, Olga Yu
AU - Edeleva, Mariya V.
AU - Veber, Sergey L.
AU - Bagryanskaya, Elena G.
PY - 2020/1/21
Y1 - 2020/1/21
N2 - During the last decades, persistent tris(2,3,5,6-tetrathiaaryl)methyl radicals (TAMs) have attracted much attention due to their applications in oximetry, EPR tomography, and as spin labels in pulsed dipolar EPR spectroscopy. Recently, researchers proposed to use TAM radicals as spin labels and/or a partner for photoinduced spin labels. Thus, the questions of their photochemical stability and mechanism of degradation under UV irradiation have become relevant and important. In this study, steady-state photolysis and flash photolysis of TAM radicals were investigated. A detailed mechanism of TAM phototransformations was proposed and confirmed by NMR, gel permeation chromatography, and mass-spectrometric analyses of the products.
AB - During the last decades, persistent tris(2,3,5,6-tetrathiaaryl)methyl radicals (TAMs) have attracted much attention due to their applications in oximetry, EPR tomography, and as spin labels in pulsed dipolar EPR spectroscopy. Recently, researchers proposed to use TAM radicals as spin labels and/or a partner for photoinduced spin labels. Thus, the questions of their photochemical stability and mechanism of degradation under UV irradiation have become relevant and important. In this study, steady-state photolysis and flash photolysis of TAM radicals were investigated. A detailed mechanism of TAM phototransformations was proposed and confirmed by NMR, gel permeation chromatography, and mass-spectrometric analyses of the products.
KW - NANOMETER DISTANCE MEASUREMENTS
KW - ELECTRON-SPIN RELAXATION
KW - TRITYL RADICALS
KW - TRIARYLMETHYL RADICALS
KW - DIPOLAR SPECTROSCOPY
KW - TRIPLET-STATE
KW - EPR
KW - LABELS
KW - OXYGEN
KW - POLARIZATION
UR - http://www.scopus.com/inward/record.url?scp=85078442725&partnerID=8YFLogxK
U2 - 10.1039/c9cp06213k
DO - 10.1039/c9cp06213k
M3 - Article
C2 - 31850431
AN - SCOPUS:85078442725
VL - 22
SP - 1019
EP - 1026
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
SN - 1463-9076
IS - 3
ER -
ID: 23263157