Pyrrole-Based New Diphosphines: Pd and Ni Complexes Bearing the PNP Pincer Ligand

Kumar, Shanish ; Mani, Ganesan ; Mondal, Sukanta ; Chattaraj, Pratim Kumar (2012) Pyrrole-Based New Diphosphines: Pd and Ni Complexes Bearing the PNP Pincer Ligand Inorganic Chemistry, 51 (22). pp. 12527-12539. ISSN 0020-1669

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Official URL: http://doi.org/10.1021/ic301967r

Related URL: http://dx.doi.org/10.1021/ic301967r

Abstract

A new class of diphosphine PNP pincer ligand, 2,5-bis(diphenylphosphinomethyl)pyrrole 2, was synthesized by the reaction between Ph2PH and 2,5-bis(dimethylaminomethyl)pyrrole in 90% yield. The analogous reaction of Ph2PH with 1,9-bis(dimethylaminomethyl)diphenyldipyrrolylmethane readily afforded a PNNP type diphosphine ligand, 1,9-bis(diphenylphosphinomethyl)diphenyldipyrrolylmethane 5 in 92% yield. These phosphine compounds were oxidized with H2O2 and S8 to give the corresponding phosphoryl and thiophosphoryl compounds 6–9 in very good yields. The reaction of the PNP pincer ligand 2 with [PdCl2(PhCN)2] in the presence of Et3N afforded the mononuclear Pd(II) complex, [PdCl{C4H2N-2,5-(CH2PPh2)2-κ3PNP}] 10 in 87% yield. Conversely, treatment of 2 with [PdCl2(PhCN)2] in the absence of Et3N gave the dinuclear Pd(II) complex [Pd2Cl4{μ-C4H3N-2,5-(CH2PPh2)2-κ2PP}2], the structure which is proposed based on the spectroscopic data. When 2 was treated with Pd(0) precursor [Pd2(dba)3]·CHCl3 the dinuclear Pd(I) complex [Pd2{μ-C4H2N-2,5-(CH2PPh2)2-κ2PN,κ1P}2], 12, was obtained in 23% yield. The formation of complex 12 is solvent dependent, which transforms into complex 10 in CDCl3 as studied by variable temperature 1H and 31P NMR methods. Treatment of 2 with [Ni(OAc)2]·4H2O gave the mononuclear Ni(II) pincer complex [Ni(OAc){C4H2N-2,5-(CH2PPh2)2-κ3PNP}], 13, which upon treatment with an excess of LiCl or LiBr or KI afforded the respective halide ion substituted Ni(II) complexes, [NiX{C4H2N-2,5-(CH2PPh2)2-κ3PNP}] (X = Cl, Br, and I), 14–16, in very good yields. The structures of 5, 2,5-bis(diphenylphosphorylmethyl)pyrrole 6, 10, 12, and 14–16 were determined by the single crystal X-ray diffraction method. In the structure of 12, two short contacts between the diagonally positioned Pd and P atoms are observed. To understand these weak interactions, density functional theory (DFT) calculations were done and an interaction MO diagram is presented.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society
ID Code:133793
Deposited On:30 Dec 2022 08:41
Last Modified:30 Dec 2022 08:41

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