摘要
Three fluorescent quinazolines thiophen-2-yl-5,6-dihydrobenzo-[4,5]imidazo[1,2-c]quinazoline (1), pyridin-3-yl-5,6-dihydrobenzo-[4,5]imidazo-[1,2-c]quinazoline (2) and phenyl-5,5鈥?6,6鈥?dihydrobenzo-[4,4鈥?5,5鈥瞉imidazo-[1.1鈥?2-c,2鈥?c]quinazoline (3) have been synthesized. Structures of 1 and 3 have been authenticated crystallographically. Quinazolines 1-3 exhibit highly selective 鈥榦n-off鈥?switching for Hgup>2+up> ions. The fluorescence intensity displayed a linear relationship with respect to Hgup>2+up> concentration (0.1-1.0 渭M; Rup>2up> = 0.99) with detection limit of 2.0 脳 10up>鈭?up> M.