Chiral phosphine ligands derived from sugars. 15. Synthesis, structure andspectroscopic studies of platinum(II) complexes with chiral phosphine substituted carbohydrate ligands

Citation
Jc. Shi et al., Chiral phosphine ligands derived from sugars. 15. Synthesis, structure andspectroscopic studies of platinum(II) complexes with chiral phosphine substituted carbohydrate ligands, INORG CHIM, 290(1), 1999, pp. 121-126
Citations number
20
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANICA CHIMICA ACTA
ISSN journal
00201693 → ACNP
Volume
290
Issue
1
Year of publication
1999
Pages
121 - 126
Database
ISI
SICI code
0020-1693(19990630)290:1<121:CPLDFS>2.0.ZU;2-A
Abstract
The reactions of chiral P,O-bidentate methyl 4,6-O-benzylidene-n-deoxyl-n-( diphenylphino)-alpha-D-altropyranoside (n-Hmbpa, n = 2, 3) with [PtCl2(NCMe )(2)] gave the complexes trans-[PtCl2(n-Hmbpa)(2)] (1a: n = 2; 1b: n = 3). Treating the complexes 1a and 1b with NEt3 or NaOMe, only the corresponding mono(alkoxo)platinum(II) complex trans-[PtCl(3-mbpa)(3-Hmbpa)] (2b) can be isolated and characterized. The molecular structure of 1b has been determi ned by X-ray analysis and shows the pyrano-ring of the ligand 3-Hmbpa in a slightly distorted chair conformation. As the oxygen donor coordinating to the Pt(II) center to form the five-membered P:O chelating alkoxoplatinum(II ) complex 2b, the pyrano-ring of the ligand 3-mbpa results in a boat confor mation suggested by the NMR spectra. (C) 1999 Elsevier Science S.A. All rig hts reserved.