Synthesis of Unsymmetrical Alkyloxy/Aryloxy-azaphthalocyanines Based on a Transetherification Reaction

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F11%3A10100598" target="_blank" >RIV/00216208:11160/11:10100598 - isvavai.cz</a>
Result on the web
<a href="http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201100689/pdf" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201100689/pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ejoc.201100689" target="_blank" >10.1002/ejoc.201100689</a>

Result language
angličtina
Original language name
Synthesis of Unsymmetrical Alkyloxy/Aryloxy-azaphthalocyanines Based on a Transetherification Reaction
Original language description
Synthesis of unsymmetrical aryloxy substited azaphthalocyanines was presented for the first ime. The method employs a side reaction that occurs during cyclotetramerization - a transetherification of peripheral substituents. New compounds were characterized also from the point of view of photophysical and photochemical properties and showed good quantum yields of fluorescence and singlet oxygen.
Czech name
—
Czech description
—

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Project
<a href="/en/project/GAP207%2F11%2F1200" target="_blank" >GAP207/11/1200: Red emitting photoinduced charge transfer sensors from the group of azaphthalocyanines</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Result description