TY - JOUR
T1 - Pyridin-2-ylthiazolothiazoles – Synthesis and photophysical properties
AU - Cerqueira, Ana F. R.
AU - Neves, Maria G. P. M. S.
AU - Jorge Parola, A.
AU - Tomé, Augusto C.
N1 - info:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FQEQ-QOR%2F6160%2F2014/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/POR_CENTRO/SFRH%2FBD%2F135597%2F2018/PT#
info:eu-repo/grantAgreement/FCT/POR_CENTRO/SFRH%2FBD%2F135597%2F2018/PT#
PY - 2021/1
Y1 - 2021/1
N2 - Thiazolo[5,4-d]thiazoles are valuable materials for a range of technical and biological applications. They are used as chemosensors, electroluminescent materials, organic light-emitting diodes (OLEDs), in solar cells, in live-cell imaging, etc., and for those applications π-extended thiazolo[5,4-d]thiazole derivatives are particularly attractive. A convenient synthetic route to non-symmetrical thiazolo[5,4-d]thiazoles bearing styrylpyridyl or hetarylvinylpyridyl groups, and their absorption and emission properties, is reported.
AB - Thiazolo[5,4-d]thiazoles are valuable materials for a range of technical and biological applications. They are used as chemosensors, electroluminescent materials, organic light-emitting diodes (OLEDs), in solar cells, in live-cell imaging, etc., and for those applications π-extended thiazolo[5,4-d]thiazole derivatives are particularly attractive. A convenient synthetic route to non-symmetrical thiazolo[5,4-d]thiazoles bearing styrylpyridyl or hetarylvinylpyridyl groups, and their absorption and emission properties, is reported.
KW - Dyes
KW - Thiazolothiazoles
KW - Thiazolo[5,4-d]thiazoles
KW - Wittig reaction
UR - http://www.scopus.com/inward/record.url?scp=85119680494&partnerID=8YFLogxK
U2 - 10.1016/j.rechem.2021.100246
DO - 10.1016/j.rechem.2021.100246
M3 - Article
AN - SCOPUS:85119680494
SN - 2211-7156
VL - 3
JO - Results in Chemistry
JF - Results in Chemistry
M1 - 100246
ER -