Chiral "P-N-P" ligands, (C20H12O2)PN(R)PY2 [R = CHMe2, Y = C6H5, OC6H5, OC6H4-4-Me, OC6H4-4-OMe or OC6H4-4-tBu] and their allyl palladium complexes

Mandal, Swadhin K. ; Nagana Gowda, G. A. ; Krishnamurthy, Setharampattu S. ; Stey, Thomas ; Stalke, Dietmar (2005) Chiral "P-N-P" ligands, (C20H12O2)PN(R)PY2 [R = CHMe2, Y = C6H5, OC6H5, OC6H4-4-Me, OC6H4-4-OMe or OC6H4-4-tBu] and their allyl palladium complexes Journal of Organometallic Chemistry, 690 (3). pp. 742-750. ISSN 0022-328X

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00223...

Related URL: http://dx.doi.org/10.1016/j.jorganchem.2004.09.082

Abstract

Chiral "P-N-P" ligands, (C20H12O2)PN(R)PY2 [R = CHMe2, Y = C6H5 (1), OC6H5 (2), OC6H4-4-Me (3), OC6H4-4-OMe (4) or OC6H4-4-tBu (5)] bearing the axially chiral 1,1'-binaphthyl-2,2'-dioxy moiety have been synthesised. Palladium allyl chemistry of two of these chiral ligands (1 and 2) has been investigated. The structures of isomeric η3-allyl palladium complexes, (R' = Me or Ph; Y = C6H5 or OC6H5) have been elucidated by high field two-dimensional NMR spectroscopy. The solid state structure of [Pd(η3-1,3-R'2-C3H3) κ2-(racemic)-(C20H12O2)PN(CHMe2)PPh2 ](PF6) has been determined by X-ray crystallography. Preliminary investigations show that the diphosphazanes, 1 and 2 function as efficient auxiliary ligands for catalytic allylic alkylation but give rise to only moderate levels of enantiomeric excess.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Chiral "P-N-P" Ligands; η3-allyl Palladium Complexes; NMR Spectroscopy; X-ray Crystal Structure; Allylic Alkylation
ID Code:17755
Deposited On:16 Nov 2010 12:44
Last Modified:08 Jun 2011 06:40

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