Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone

Standard

Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone. / Oplachko, Maria V.; Smolentsev, Artem B.; Magin, Ilya M. и др.

в: Physical Chemistry Chemical Physics, Том 22, № 9, 07.03.2020, стр. 5220-5228.

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

Harvard

Oplachko, MV, Smolentsev, AB, Magin, IM, Pozdnyakov, IP , Nichiporenko, VA, Grivin, VP, Plyusnin, VF, Vyazovkin, VV, Yanshole, VV, Parkhats, MV, Yadykov, AV, Shirinian, VZ & Glebov, EM 2020, 'Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone', Physical Chemistry Chemical Physics, Том. 22, № 9, стр. 5220-5228. https://doi.org/10.1039/c9cp05744g

APA

Oplachko, M. V., Smolentsev, A. B., Magin, I. M., Pozdnyakov, I. P., Nichiporenko, V. A., Grivin, V. P., Plyusnin, V. F., Vyazovkin, V. V., Yanshole, V. V., Parkhats, M. V., Yadykov, A. V., Shirinian, V. Z., & Glebov, E. M. (2020). Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone. Physical Chemistry Chemical Physics, 22(9), 5220-5228. https://doi.org/10.1039/c9cp05744g

Vancouver

Oplachko MV, Smolentsev AB, Magin IM, Pozdnyakov IP , Nichiporenko VA, Grivin VP и др. Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone. Physical Chemistry Chemical Physics. 2020 март 7;22(9):5220-5228. doi: 10.1039/c9cp05744g

Author

Oplachko, Maria V. ; Smolentsev, Artem B. ; Magin, Ilya M. и др. / Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone. в: Physical Chemistry Chemical Physics. 2020 ; Том 22, № 9. стр. 5220-5228.

BibTeX

@article{11b255d18b7e493381d517901d53d03a,

title = "Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone",

abstract = "A mechanistic study of the photochromic properties and photodegradation processes of an asymmetrical diarylcyclopentenone bearing thiophene and benzothiophene units using stationary photolysis, nanosecond laser flash photolysis and time-resolved luminescence was performed. It was found that the light-induced reversible isomerization of (3-(2,5-dimethyltiophen-3-il)-2-(2-methyl-1-benzylthiophen-3-il)cyclopent-2-en-1-one, compound 1) from open to closed form is a common photochromic transformation inherent to diarylethenes, while the photodegradation process proceeds in two ways. The first is a formal 1,2-dyotropic rearrangement, proceeding without the participation of oxygen. The second is the oxygen-dependent mechanism involving the excitation of the open form 1A into the triplet state, quenching of the latter by dissolved oxygen, and oxidation of the initial compound by singlet oxygen.",

author = "Oplachko, {Maria V.} and Smolentsev, {Artem B.} and Magin, {Ilya M.} and Pozdnyakov, {Ivan P.} and Nichiporenko, {Vladislav A.} and Grivin, {Vjacheslav P.} and Plyusnin, {Victor F.} and Vyazovkin, {Vladimir V.} and Yanshole, {Vadim V.} and Parkhats, {Marina V.} and Yadykov, {Anton V.} and Shirinian, {Valerii Z.} and Glebov, {Evgeni M.}",

year = "2020",

month = mar,

day = "7",

doi = "10.1039/c9cp05744g",

language = "English",

volume = "22",

pages = "5220--5228",

journal = "Physical Chemistry Chemical Physics",

issn = "1463-9076",

publisher = "Royal Society of Chemistry",

number = "9",

}

RIS

TY - JOUR

T1 - Mechanism of photochromic transformations and photodegradation of an asymmetrical 2,3-diarylcyclopentenone

AU - Oplachko, Maria V.

AU - Smolentsev, Artem B.

AU - Magin, Ilya M.

AU - Pozdnyakov, Ivan P.

AU - Nichiporenko, Vladislav A.

AU - Grivin, Vjacheslav P.

AU - Plyusnin, Victor F.

AU - Vyazovkin, Vladimir V.

AU - Yanshole, Vadim V.

AU - Parkhats, Marina V.

AU - Yadykov, Anton V.

AU - Shirinian, Valerii Z.

AU - Glebov, Evgeni M.

PY - 2020/3/7

Y1 - 2020/3/7

N2 - A mechanistic study of the photochromic properties and photodegradation processes of an asymmetrical diarylcyclopentenone bearing thiophene and benzothiophene units using stationary photolysis, nanosecond laser flash photolysis and time-resolved luminescence was performed. It was found that the light-induced reversible isomerization of (3-(2,5-dimethyltiophen-3-il)-2-(2-methyl-1-benzylthiophen-3-il)cyclopent-2-en-1-one, compound 1) from open to closed form is a common photochromic transformation inherent to diarylethenes, while the photodegradation process proceeds in two ways. The first is a formal 1,2-dyotropic rearrangement, proceeding without the participation of oxygen. The second is the oxygen-dependent mechanism involving the excitation of the open form 1A into the triplet state, quenching of the latter by dissolved oxygen, and oxidation of the initial compound by singlet oxygen.

AB - A mechanistic study of the photochromic properties and photodegradation processes of an asymmetrical diarylcyclopentenone bearing thiophene and benzothiophene units using stationary photolysis, nanosecond laser flash photolysis and time-resolved luminescence was performed. It was found that the light-induced reversible isomerization of (3-(2,5-dimethyltiophen-3-il)-2-(2-methyl-1-benzylthiophen-3-il)cyclopent-2-en-1-one, compound 1) from open to closed form is a common photochromic transformation inherent to diarylethenes, while the photodegradation process proceeds in two ways. The first is a formal 1,2-dyotropic rearrangement, proceeding without the participation of oxygen. The second is the oxygen-dependent mechanism involving the excitation of the open form 1A into the triplet state, quenching of the latter by dissolved oxygen, and oxidation of the initial compound by singlet oxygen.

UR - http://www.scopus.com/inward/record.url?scp=85081094174&partnerID=8YFLogxK

U2 - 10.1039/c9cp05744g

DO - 10.1039/c9cp05744g

M3 - Article

C2 - 32091057

AN - SCOPUS:85081094174

VL - 22

SP - 5220

EP - 5228

JO - Physical Chemistry Chemical Physics

JF - Physical Chemistry Chemical Physics

SN - 1463-9076

IS - 9

ER -

ID: 23738855