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Issue 32, 2019
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Structural diversity of the complexes of monovalent metal d10 ions with macrocyclic aggregates of iso-tellurazole N-oxides

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Abstract

The reactions of iso-tellurazole N-oxides with monocations of the coinage metals yielded a family of coordination complexes with a remarkable variety of compositions and structures. All new species were identified by single-crystal X-ray diffraction. In all cases, the macrocyclic aggregation of the organo-chalcogen heterocycles through Te⋯O chalcogen bonding interactions is preserved and the metal ions are coordinated by tellurium. Copper and gold formed complexes with the tetramers. The lighter element acquired a κ4Te,κ1O pentacoordinated square pyramidal structure with a triflate anion in the apical position. The preference of the heavier metal for a linear κ1Te,κ1Cl coordination geometry permitted the formation of a binuclear complex. Silver demonstrated a unique preference for coordinating to the hexamer; two distinct examples showed a structure with a pair of endocyclic κ2Te,κ2O metal ions bridged by two triflate anions; the other two chalcogen atoms are located at trans-annular positions and each coordinates a κ1Te,κ1O,κ1C silver ion, also bonded to an aromatic carbon and another triflate anion.

Graphical abstract: Structural diversity of the complexes of monovalent metal d10 ions with macrocyclic aggregates of iso-tellurazole N-oxides

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Article information


Submitted
30 Apr 2019
Accepted
17 Jul 2019
First published
17 Jul 2019

New J. Chem., 2019,43, 12601-12608
Article type
Paper

Structural diversity of the complexes of monovalent metal d10 ions with macrocyclic aggregates of iso-tellurazole N-oxides

J. Wang, P. C. Ho, J. F. Britten, V. Tomassetti and I. Vargas-Baca, New J. Chem., 2019, 43, 12601
DOI: 10.1039/C9NJ02217A

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