Enhancement of the Large Stokes-Shifted Fluorescence Emission from the 2-(2‘-Hydroxyphenyl)benzoxazole Core in a Dendrimer
Citations Over TimeTop 20% of 2005 papers
Abstract
The photochemical properties of a series of newly synthesized dendrimers, 4-6, having a 2-(2'-hydroxyphenyl)benzoxazole (HBO) core, were studied in benzene. The fluorescence quantum yields (Phi(f)) were determined to be 0.022, 0.030, and 0.038 for 4, 5, and 6, respectively, increasing in higher generation dendrimers. With transient absorption spectroscopy, the quantum yields of the isomerization from the (E)-keto form ((1)K(E)*) to the (Z)-keto form ((1)K(Z)) (Phi(E)(-->)(Z)) and those of intersystem crossing (Phi(isc)) can be estimated. Whereas Phi(E)(-->)(Z) values decreased in higher generation dendrimers, Phi(isc) values were almost the same among 4-6. The quantum yields of nonradiative decay (Phi(nr)) increased in higher generation dendrimers. The dendrimer structure also affected the reverse tautomerization process.
Related Papers
- → Reaction of the 2-(bromodifluoromethyl)benzoxazole with tetrakis(dimethylamino)ethylene (TDAE) in the presence of aldehydes. A convenient synthesis of 2-(difluoromethyl)benzoxazole alcohols(1997)28 cited
- Studies of Catecholase Activities of N-donor Bidentates Ligands derivated from Benzoxazole with Copper (II) Salts(2019)
- → Syntheses of new benzoxazole derivatives(2011)10 cited
- Design, synthesis and screening of some novel benzoxazole based 1,3,4-oxadiazoles as potential antimicrobial agents(2013)
- → Cyanoacetylenes in a reaction with benzoxazole-2-thione and benzoxazol-2-one(1990)1 cited