Diastereomeric metallatetrahedron complexes of the type Re-2(MPPh3)(M ' PPh3)(mu-PCy2)(CO)(7)(-)-thiocamphanate (M = Ag, Au, M ' = Cu, Ag, Au): synthesis, structure and CD data

Citation
Hj. Haupt et al., Diastereomeric metallatetrahedron complexes of the type Re-2(MPPh3)(M ' PPh3)(mu-PCy2)(CO)(7)(-)-thiocamphanate (M = Ag, Au, M ' = Cu, Ag, Au): synthesis, structure and CD data, J CHEM S DA, (22), 2001, pp. 3329-3336
Citations number
29
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
ISSN journal
14727773 → ACNP
Issue
22
Year of publication
2001
Pages
3329 - 3336
Database
ISI
SICI code
1472-7773(2001):22<3329:DMCOTT>2.0.ZU;2-#
Abstract
Four pairs of diastereomeric metallatetrahedron complexes of the type Re-2( MPPh3)(M'PPh3) (mu -PCy2)(CO)(7) (-)-thiocamphanate have been synthesized, with identical (M = M' = Au (5a, 5b) and Ag (6a, 6b)) and with mixed coinag e metals (M = Au, M' = Ag (8a, 8b) and Cu (9a, 9b)). After separation, the absolute configuration was determined by single crystal X-ray crystallograp hy for 6a, 8a and 9a. In agreement with solution (P-31 and H-1 NMR) spectra l data, the thiocamphanate acts as a mu -S bridging bidentate ligand along the Re-coinage metal edge; in the mixed coinage metal complexes coordinatio n involves the lower homologue of the coinage metals. Signs of the long wav elength absorption bands in the CD spectra were found to correlate with the counter (A) or clockwise (C) configuration of the chiral transition metal core.