Coordination chemistry of homoatomic ligands of bismuth, selenium and tellurium
Research output: Contribution to journal › Review article › Contributed › peer-review
Contributors
Abstract
Multi-centre-bonds as well as conventional two-centre two-electron bonds are the basis for charged or uncharged homoatomic molecules of the heavy main-group elements bismuth, selenium and tellurium. In many cases these homoatomic species are not fairly isolated in the structures but make use of their paired or unpaired p-electrons and, if available, of their π-systems to establish (strong) heteropolar covalent donor bonds to metal cations. Such coordination can have retroactive effect on the bonding inside the ligand and even stabilises new homonuclear species such as the Bi104+ antiprism or the Te10-tricycle. Moreover, these homoatomic ligands can be highly connecting, since all of their atoms are potential donors. Here we give an overview of recent developments in the coordination chemistry of oligo- and polyatomic selenium, tellurium and bismuth ligands.
Details
Original language | English |
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Pages (from-to) | 1-10 |
Number of pages | 10 |
Journal | Coordination chemistry reviews |
Volume | 285 |
Publication status | Published - 5 Feb 2015 |
Peer-reviewed | Yes |
External IDs
ORCID | /0000-0002-2391-6025/work/159171973 |
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Keywords
ASJC Scopus subject areas
Keywords
- Bismuth, Homoatomic molecules, Polyanions, Polycations, Selenium, Tellurium