Abstract
Two novel macrocyclic tetra-imine-diphenol Schiff base (H2L1 and H2L2) were synthesized by [2 + 2] cyclocondensation of ortho-aminophenyl diamines [1,2-bis(2′-aminophenoxy)benzene (I) and 1,2-bis(2′-aminophenoxy)-4-t-butylbenzene (II)] with 2,6-diformyl-4-methylphenol. Two novel tetra-amine-diphenol macrocycles (H2L3 and H2L4) have been obtained by reduction of the imine analogs with NaBH4 in MeOH/CHCl3.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
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
