Tai Lin's research while affiliated with The University of Edinburgh and other places

Salicylaldehyde hydrazones are weaker copper extractants than their oxime derivatives, which are used in hydrometallurgical processes to recover ∼20% of the world's copper. Their strength, based on the extraction equilibrium constant Ke, can be increased by nearly three orders of magnitude by incorporating electron-withdrawing or hydrogen-bond acceptor groups (X) ortho to the phenolic OH group of the salicylaldehyde unit. Density functional theory calculations suggest that the effects of the 3-X substituents arise from a combination of their influence on the acidity of the phenol in the pH-dependent equilibrium, Cu²⁺+2Lorg→[Cu(L-H)2]org+2H⁺, and on their ability to 'buttress' interligand hydrogen bonding by interacting with the hydrazone N-H donor group. X-ray crystal structure determination and computed structures indicate that in both the solid state and the gas phase, coordinated hydrazone groups are less planar than coordinated oximes and this has an adverse effect on intramolecular hydrogen-bond formation to the neighbouring phenolate oxygen atoms.

Combining cation- and anion-binding functionalities in a salen-type extractant leads to multiple loading of ZnCl(2). Zn(ii) cations are bound by the salen N(2)O(2)(2-) donor set, and chlorozincate anions are associated with protonated pendant amine groups.