The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry

S. P. Babailov, L. S. Klimenko, I. Ya Mainagashev

Результат исследований: Материалы для журналаСтатья

1 цитирование (Scopus)

Выдержка

It has been stated by 1H NMR and UV spectrophotometry that 1-(4-tert-butil-phenoxy)-2-cetylamino-9,10-anthraquinone photoisomerizes to 9-(4-tert-butylphenoxy)-2-cetylamino-1,10-anthraquinon with quantum yield φ = 0.4 ±0.1 under light excitation in the absorption band region in the UV/visible spectrum range with the maximum λ = 441 nm.

Язык оригиналаАнглийский
Страницы (с-по)663-667
Число страниц5
ЖурналJournal of Structural Chemistry
Том47
Номер выпуска4
DOI
СостояниеОпубликовано - июл 2006
Опубликовано для внешнего пользованияДа

Отпечаток

Photoisomerization
anthraquinones
Spectrophotometry
Quantum yield
spectrophotometry
visible spectrum
Nuclear magnetic resonance spectroscopy
Absorption spectra
Nuclear magnetic resonance
absorption spectra
nuclear magnetic resonance
spectroscopy
excitation
9,10-anthraquinone

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Physical and Theoretical Chemistry

Цитировать

The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry. / Babailov, S. P.; Klimenko, L. S.; Mainagashev, I. Ya.

В: Journal of Structural Chemistry, Том 47, № 4, 07.2006, стр. 663-667.

Результат исследований: Материалы для журналаСтатья

Babailov, S. P. ; Klimenko, L. S. ; Mainagashev, I. Ya. / The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry. В: Journal of Structural Chemistry. 2006 ; Том 47, № 4. стр. 663-667.
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KW - Photo-induced molecular dynamics

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KW - Photoisomerization

KW - UV spectrophotometry

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