Abstract

Two cadmium(II) coordination polymers, with thiocyanate and pyridine-based ligands e.g., 3-acetamidopyridine (3-Acpy) and niazid (nicotinic acid hydrazide, nia), namely one-dimensional {[Cd(SCN)2(3-Acpy)]}n (1) and two-dimensional {[Cd(SCN)2(nia)]}n (2), are prepared in the mixture of water and ethanol. The adjacent cadmium(II) ions in 1 are bridged by two N,S-thiocyanate ions and an N,O-bridging 3-Acpy molecule, forming infinite one-dimensional polymeric chains, which are assembled by the intermolecular N–H∙∙∙S hydrogen bonds in one direction and by the intermolecular S∙∙∙S chalcogen bonds in another direction. Within the coordination network of 2, the adjacent cadmium(II) ions are bridged by N,S-thiocyanate ions in one direction and by N,O,N’-chelating and bridging nia molecules in another direction. The coordination networks of 2 are assembled by the intermolecular N–H∙∙∙S and N–H∙∙∙N hydrogen bonds and S∙∙∙S chalcogen bonds. Being the only supramolecular interactions responsible for assembling the polymer chains of 1 in the particular direction, the chalcogen S∙∙∙S bonds are more significant in the structure of 1, whilst the chalcogen S∙∙∙S bonds which act in cooperation with the N–H∙∙∙S and N–H∙∙∙N hydrogen bonds are of less significance in the structure of 2.

Highlights

  • Not yet as established and studied as hydrogen and halogen bonding, chalcogen bonding (ChB) has recently gained more attention as an important supramolecular interaction with possible applications in biochemistry, crystal engineering, the design of new materials, and catalysis [1,2,3,4,5]

  • Nitrate tetrahydrate and sodium coordination polymers in this study werethiocyanate obtained by u from the water–ethanol mixture yielded a 1-D coordination polymer idopyridine (3-Acpy) and niazide ligands

  • The neighboring cadmium(II) ions are bridged by two thiocyanate ions and one 3-Acpy ligand, into a polymeric chain of 1

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Summary

Introduction

Not yet as established and studied as hydrogen and halogen bonding, chalcogen bonding (ChB) has recently gained more attention as an important supramolecular interaction with possible applications in biochemistry, crystal engineering, the design of new materials, and catalysis [1,2,3,4,5]. Chalcogen bond donor D is a Lewis acid and acceptor A is a Lewis base, while Ch is a chalcogen atom (of group 16). Understood from the crystal structures of various chalcogenated compounds for some time, the chalcogen bonds did not gain desired importance and become relevant supramolecular interactions in crystal engineering, in the way that halogen bonds did [4,6]

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