Abstract
A number of aryloxazol-5-ones were synthesized by condensation of aromatic aldehydes with hippuric acid and substituted hippuric acids. Most of the products have intense luminescence in the solid state; all of them have luminescence in toluene at 77°K. Lengthening of the conjugation chain in the oxazolone molecules leads to a shift in their luminescence to the long-wave region. The compound that contains a conjugated system including two oxazolone rings also luminesces intensely in toluene at room temperature.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
