Phosphite ligands derived from distally and proximally substituted dipropyloxy calix[4]arenes and their palladium complexes: Solution dynamics, solid-state structures and catalysis

Abstract

Two bisphosphite ligands, 25,27-bis-(2,2′-biphenyldioxyphosphinoxy)-26,28-dipropyloxy- p-tert-butyl calix[4]arene ( 3) and 25,26-bis-(2,2′-biphenyldioxyphosphinoxy)-27,28-dipropyloxy- p-tert-butyl calix[4]arene ( 4) and two monophosphite ligands, 25-hydroxy-27-(2,2′-biphenyldioxyphosphinoxy)-26,28-dipropyloxy- p-tert-butyl calix[4]arene ( 5) and 25-hydroxy-26-(2,2′-biphenyldioxyphosphinoxy)-27,28-dipropyloxy- p-tert-butyl calix[4]arene ( 6) have been synthesized. Treatment of (allyl) palladium precursors [(η 3-1,3-R,R′-C 3H 4)Pd(Cl)] 2 with ligand 3 in the presence of NH 4PF 6 gives a series of cationic allyl palladium complexes ( 3a– 3d). Neutral allyl complexes ( 3e– 3g) are obtained by the treatment of the allyl palladium precursors with ligand 3 in the absence of NH 4PF 6. The cationic allyl complexes [(η 3-C 3H 5)Pd( 4)]PF 6 ( 4a) and [(η 3-Ph 2C 3H 3)Pd( 4)]PF 6 ( 4b) have been synthesized from the proximally (1,2-) substituted bisphosphite ligand 4. Treatment of ligand 4 with [Pd(COD)Cl 2] gives the palladium dichloride complex, [PdCl 2( 4)] ( 4c). The solid-state structures of [{(η 3-1-CH 3-C 3H 4)Pd(Cl)} 2( 3)] ( 3f) and [PdCl 2( 4)] ( 4c) have been determined by X-ray crystallography; the calixarene framework in 3f adopts the pinched cone conformation whereas in 4c, the conformation is in between that of cone and pinched cone. Solution dynamics of 3f has been studied in detail with the help of two-dimensional NMR spectroscopy. The solid-state structures of the monophosphite ligands 5 and 6 have also been determined; the calix[4]arene framework in both molecules adopts the cone conformation. Reaction of the monophosphite ligands ( 5, 6) with (allyl) palladium precursors, in the absence of NH 4PF 6, yield a series of neutral allyl palladium complexes ( 5a– 5c; 6a– 6d). Allyl palladium complexes of proximally substituted ligand 6 showed two diastereomers in solution owing to the inherently chiral calix[4]arene framework. Ligands 3, 6 and the allyl palladium complex 3f have been tested for catalytic activity in allylic alkylation reactions.