Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 663-667 |
| Number of pages | 5 |
| Journal | Journal of Structural Chemistry |
| Volume | 47 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Jul 2006 |
| Externally published | Yes |
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Keywords
- 1-aryloxyanthraquinones
- Anthraquinones
- NMR
- Photo-induced molecular dynamics
- Photochemistry
- Photoisomerization
- UV spectrophotometry
ASJC Scopus subject areas
- Inorganic Chemistry
- Physical and Theoretical Chemistry
Cite this
The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry. / Babailov, S. P.; Klimenko, L. S.; Mainagashev, I. Ya.
In: Journal of Structural Chemistry, Vol. 47, No. 4, 07.2006, p. 663-667.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - The study of photoisomerisation of 1-aryloxyanthraquinones by NMR spectroscopy and UV spectrophotometry
AU - Babailov, S. P.
AU - Klimenko, L. S.
AU - Mainagashev, I. Ya
PY - 2006/7
Y1 - 2006/7
N2 - 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.
AB - 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.
KW - 1-aryloxyanthraquinones
KW - Anthraquinones
KW - NMR
KW - Photo-induced molecular dynamics
KW - Photochemistry
KW - Photoisomerization
KW - UV spectrophotometry
UR - http://www.scopus.com/inward/record.url?scp=33846034498&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33846034498&partnerID=8YFLogxK
U2 - 10.1007/s10947-006-0353-1
DO - 10.1007/s10947-006-0353-1
M3 - Article
AN - SCOPUS:33846034498
VL - 47
SP - 663
EP - 667
JO - Journal of Structural Chemistry
JF - Journal of Structural Chemistry
SN - 0022-4766
IS - 4
ER -