Issue 32, 2019

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

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

Supplementary files

Article information

Article type
Paper
Submitted
30 4月 2019
Accepted
17 7月 2019
First published
17 7月 2019

New J. Chem., 2019,43, 12601-12608

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements