two n4-type schiff base ligands named n,n'-bis(2-pyridylmethylidene)-1,2-diiminoethane (l1) and n,n'-bis(2-pyridylmethylidene)-1,3-diiminopropane (l2) have been synthesized by the reaction of pyridine-2-carbaldehyde with ethylenediamine and propylenediamine, respectively. the binding abilities of l1 and l2 in dichloromethane towards cu2+, cd2+, co2+, ni2+, zn2+ and pb2+ ions were evaluated by p...

Two N4-type Schiff base ligands named N,N'-bis(2-pyridylmethylidene)-1,2-diiminoethane (L1) and N,N'-bis(2-pyridylmethylidene)-1,3-diiminopropane (L2) have been synthesized by the reaction of pyridine-2-carbaldehyde with ethylenediamine and propylenediamine, respectively. The binding abilities of L1 and L2 in dichloromethane towards Cu<...

A metal-free 16-membered N4-donor [1 + 1] Schiff-base macrocycle was isolated as HL(Pr)·2acid, by 1 : 1 condensation of diphenylamine-2,2'-dicarboxaldehyde (1), dipropylene triamine and an excess of either acetic or formic acid, or as HL(Pr)·(tosylic acid) when just one equivalent of tosylic acid was employed. Interestingly, the acid-free synthesis employed for the 14-membered analogue HL(Et) f...

A new family of Tetraazamacrocyclic Ru(II) complexes [RuCl2(L)] (where L = N4 donor macrocyclic ligands) have been synthesized by the reactions of [RuCl2(DMSO)4] with some of macrocyclic Schiff base ligands containing N4 donor groups. The complexes were characterized by elemental analysis, IR, H, C NMR, mass, electronic, molar conductance and magnetic susceptibility measurements. An octahedral ...

A component of the shikimate biosynthetic pathway, dehydroquinate dehydratase (DHQD) catalyzes the dehydration of 3-dehydroquniate (DHQ) to 3-dehydroshikimate. In the type I DHQD reaction mechanism a lysine forms a Schiff base intermediate with DHQ. The Schiff base acts as an electron sink to facilitate the catalytic dehydration. To address the mechanism of Schiff base formation, we determined ...