Trapping of ZnCl2 by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties

Chem Commun (Camb). 2020 Apr 30;56(35):4769-4772. doi: 10.1039/d0cc01887b.

Abstract

We report the syntheses of two new organotin sulfide clusters with heteroaromatic substituents. A phenanthroline-functionalized tin sulfide cluster [(RPhenSn)4S6] (1; RPhen = CMe2CH2C(Me)N-NC(H)C12H7N2) and a bipyridyl-terminated cluster [(R4-bipySn)4S6] (2; R4-bipy = CMe2CH2C(Me)N-NC(H)-4-C10H7N2) were obtained from reactions of the hydrazone-functionalized organotin sulfide cluster [(RNSn)4S6] (RN = CMe2CH2C(Me)N-NH2) with 1,10-phenanthroline-5-carboxaldehyde or 2,2'-bipyridine-4-carbaldehyde. 1 and 2 were tested towards their capability of trapping metal ions by means of the terminal chelating ligands. The reaction of 2 with ZnCl2 afforded the cluster compound [(R4-bipyZnCl2Sn)4S6] (5), in which four ZnCl2 units are coordinated by the heteroaromatic organic groups. We discuss the structures and demonstrate the effect of ZnCl2 trapping on optical absorption and luminescence properties.