Discrete and polymeric, mono- and dinuclear silver complexes of a macrocyclic tetraoxime ligand with AgI-AgI
Shohei Tashiro1, Jun-ichiro Tanihira, Mihoko Yamada
1Department of Chemistry, Graduate School of Science, the University of Tokyo, Tokyo, Japan. tashiro@chem.s.u-tokyo.ac.jp
Abstract:
Macrocyclic compounds that can bind cationic species efficiently and selectively with their cyclic cavities have great potential as excellent chemosensors for metal ions. Recently, we have developed a tetraoxime-type tetraazamacrocyclic ligand 1 formed through a facile one-pot cyclization reaction. Aiming to explore and bring out the potential of the tetraoxime macrocycle 1 as a chelating sensor, we report herein the preparation of several kinds of silver complexes of 1 and their unique coordination structures determined by single-crystal X-ray diffraction analyses. As a result, the formation of two kinds of discrete structures, monomeric complexes [Ag(1)X] (X = counter anions) and a dimeric complex [Ag2(1)2]X2, and two kinds of polymeric structures from a mononuclear complex, [Ag(1)]nXn, and from a dinuclear complex, [Ag2(1)X2]n, was demonstrated. In the resulting complexes, the structurally flexible macrocyclic ligand 1 was found to provide several different coordination modes. Notably, in some silver complexes of 1, AgI-AgI interactions were observed with different AgI-AgI distances which depend on the kind of counter anions and the chemical composition.
More Related Videos
Related Concept Videos
Complexation Equilibria: The Chelate Effect
Complexometric Titration: Ligands
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
EDTA: Chemistry and Properties
Formation of Complex Ions
Complexation Equilibria: Factors Influencing Stability of Complexes


