Aggregation effects in visible light flavin photocatalysts: Synthesis, structure and catalytic activity of 10-arylflavins
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F13%3A43895601" target="_blank" >RIV/60461373:22310/13:43895601 - isvavai.cz</a>
Alternative codes found
RIV/60461373:22810/13:43895601
Result on the web
<a href="http://dx.doi.org/10.1002/chem.201202488" target="_blank" >http://dx.doi.org/10.1002/chem.201202488</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/chem.201202488" target="_blank" >10.1002/chem.201202488</a>
Alternative languages
Result language
angličtina
Original language name
Aggregation effects in visible light flavin photocatalysts: Synthesis, structure and catalytic activity of 10-arylflavins
Original language description
A series of 10-arylflavins (10-phenyl- (2a), 10-(2,6-dimethylphenyl)- (2b), 10-(2,6-diethylphenyl)- (2c), 10-(2,6-diisopropylphenyl)- (2d), 10-(2-tert-butylphenyl)- (2e), and 10-(2,6-dimethylphenyl)-3-methyl- (2f) isoalloxazine) was prepared as potentially non-aggregating flavin photocatalysts. The investigation of their structures in the crystalline phase combined with 1H-DOSY NMR experiments in CD3CN, CD3CN/D2O 1:1 and in D2O confirm reduced ability of 10-arylflavins 2 to form aggregates in comparisonwith tetra-O-acetyl riboflavin (1). 10-Arylflavins 2a-2d do not interact by interactions, which are restricted by 10-phenyl ring oriented perpendicularly to the isoalloxazine skeleton. On the other hand, N(3)-H---O hydrogen bonds have been detected in their crystal structures. In the structure of 10-aryl-3-methylflavin (2f) with substituted N(3) position, weak C-H---O bonds and weak interactions have been found. 10-Arylflavins 2 were tested as photoredox catalysts for the aerial oxidati
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—
Result continuities
Project
—
Continuities
S - Specificky vyzkum na vysokych skolach
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Chemistry A European Journal
ISSN
0947-6539
e-ISSN
—
Volume of the periodical
19
Issue of the periodical within the volume
3
Country of publishing house
DE - GERMANY
Number of pages
10
Pages from-to
1066-1075
UT code for WoS article
000313263300033
EID of the result in the Scopus database
—