Abstract
Asymmetric 2-p-nitrophenyl-5-naphthylmethylene-1,3,4-oxadiazole and 2-p-aminophenyl-5-naphthylmethylene-1,3,4-oxadiazole were synthesized and characterized by IR、1HNMR and MS analysis, and their optical properties were detected using UV-vis absorption spectroscopy and fluorescence spectroscopy. The existence of electron-withdrawing oxadiazole units causes a significant bathochromic shift of the UV absorption maximum. The largest UV-absorption peak of target compounds is in the range of 298-317 nm, and a new emission band at 402 nm is formed. The fluorescence intensity is gradually enhanced, which strengthens the intramolecular charge transfer effect between the electron-withdrawing oxadiazole and electron-donating aniline.
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 call
