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Imido Analogues of Common Oxo Anions: A New Episode in the Chemistry of Cluster Compounds
Author(s) -
Brask Justin K.,
Chivers Tristram
Publication year - 2001
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/1521-3773(20011105)40:21<3960::aid-anie3960>3.0.co;2-u
Subject(s) - homoleptic , chemistry , denticity , ternary operation , cluster (spacecraft) , alkali metal , main group element , metal , transition metal , block (permutation group theory) , stereochemistry , crystallography , computational chemistry , inorganic chemistry , crystal structure , organic chemistry , catalysis , programming language , geometry , mathematics , computer science
Oxo anions of p‐ and d‐block elements, for example, SiO 4 4− , PO 4 3− , SO 4 2− , and CrO 4 2− , are commonly encountered species. The full or partial replacement of the oxo ligands by isoelectronic imido (NR) groups generates homoleptic polyimido anions of the type [E(NR) x ] z − or heteroleptic imidooxo anions with the general formula [O y E(NR) x − y ] z − (where E=main group element or transition metal). The alkali metal derivatives of this new class of anions form ternary or quaternary cluster systems, respectively. The structures of these clusters can be rationalized in terms of the self‐assembly of fundamental building blocks. An understanding of the factors that control this process may allow the design of functional materials with specific properties. In addition, these anions are attracting attention as multidentate ligands with unique electronic and stereochemical properties that may engender novel metal‐centered chemistry.