The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry Full article
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Journal of Structural Chemistry
ISSN: 0022-4766 , E-ISSN: 1573-8779 |
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| Output data | Year: 2006, Volume: 47, Number: 4, Pages: 663-667 Pages count : 5 DOI: 10.1007/s10947-006-0353-1 | ||||||
| Tags | NMR; photoisomerization; 1-aryloxyanthraquinones; photochemistry; UV spectrophotometry; anthraquinones; photo-induced molecular dynamics | ||||||
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Abstract:
It has been stated by H-1 NMR and UV spectrophotometry that 1-(4-tert-butil-phenoxy)-2-cetylamino-9, 10-anthraquinone photoisomerizes to 9-(4-terf-butylphenoxy)-2-cetylamino-1,10-anthraquinon with quantum yield phi = 0.4 +/- 0.1 under light excitation in the absorption band region in the UV/visible spectrum range with the maximum lambda = 441 nm.
Cite:
Babailov S.P.
, Klimenko L.S.
, Mainagashev I.Y.
The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry
Journal of Structural Chemistry. 2006. V.47. N4. P.663-667. DOI: 10.1007/s10947-006-0353-1 WOS Scopus РИНЦ OpenAlex
The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry
Journal of Structural Chemistry. 2006. V.47. N4. P.663-667. DOI: 10.1007/s10947-006-0353-1 WOS Scopus РИНЦ OpenAlex
Original:
Бабайлов С.П.
, Клименко Л.С.
, Майнагашев И.Я.
Исследование фотоизомеризации 1-арилоксиантрахинонов по данным спектроскопии ямр и уф спектрофотометрии
Журнал структурной химии (J STRUCT CHEM+). 2006. Т.47. №4. С.682-686. РИНЦ
Исследование фотоизомеризации 1-арилоксиантрахинонов по данным спектроскопии ямр и уф спектрофотометрии
Журнал структурной химии (J STRUCT CHEM+). 2006. Т.47. №4. С.682-686. РИНЦ
Dates:
| Published print: | Jul 1, 2006 |
Identifiers:
| Web of science: | WOS:000243492300010 |
| Scopus: | 2-s2.0-33846034498 |
| Elibrary: | 13514510 |
| OpenAlex: | W1998443277 |