Abstract
The in situ reactions of MCH2Ph (M = Na, K or Rb) with C6H11NH2 in toluene followed by the addition of the appropriate stoichiometric quantity of Sb(NMe2)3 gave the new heterobimetallic antimony(III)/alkali metal complexes [{Sb2(NC6H11)4}2Na 4] and M[{(C6H11NH)Sb(μ-NC6H11) 2}2Sb]·2thf (M = K or Rb). Comparison of the crystal structures of these species with those of the lithium complexes [{Sb2(NC6H11)4}2Li 4] and Li[{(C6H11NH)-Sb(μ-NC6H11) 2}2Sb] reveals that the geometries of these heterobimetallic cages are fundamentally dictated by the rigidity of the [Sb2(NC6H11)4]2- and [{(C6H11NH)Sb(μ-NC6H11) 2}2Sb]- anions.
| Original language | English |
|---|---|
| Pages (from-to) | 1389-1394 |
| Number of pages | 6 |
| Journal | Journal of the Chemical Society - Dalton Transactions |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 21 Apr 1998 |
ASJC Scopus subject areas
- General Chemistry
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Dive into the research topics of 'Co-ordination of heavier alkali metals by polyimido antimony(III) ligands; syntheses and structures of [{Sb2(NC6H11)4}2M 4] (M = Li or Na), Li[{(Me2N)Sb(μ-NC6H11)2} 2Sb]'. Together they form a unique fingerprint.Cite this
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