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Electron-Deficient Pt2M2Pt2 Hexanuclear Metal Strings (M = Pt, Pd) Supported by Triphosphine Ligands

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journal contribution
posted on 28.04.2014, 00:00 by Eri Goto, Rowshan Ara Begum, Chiaki Ueno, Aya Hosokawa, Chie Yamamoto, Kanako Nakamae, Bunsho Kure, Takayuki Nakajima, Takashi Kajiwara, Tomoaki Tanase
Electron-deficient Pt2M2Pt2 hexanuclear clusters, [Pt4M2(μ-dpmp)4(XylNC)2]­(PF6)4 (M = Pt (7), Pd (8); dpmp = bis­((diphenylphosphino)­methyl)­phenylphosphine), were synthesized by oxidation of hydride-bridged hexanuclear clusters [Pt4M2(μ-H)­(μ-dpmp)4(XylNC)2]­(PF6)3 (M = Pt (2), Pd (3)) and were revealed to involve a linearly ordered Pt2M2Pt2 array joined by delocalized bonding interactions with 84 cluster valence electrons, which are discussed on the basis of DFT calculations. The central M–M distances of 7 and 8 are significantly reduced upon the apparent loss of a hydride unit from the M–H–M central part of 2 and 3, indicating that the bonding electrons in the adjacent M–Pt bonds migrate into the central M–M bond to result in a dynamic structural change during two-electron oxidation of the hexanuclear metal strings. A similar Pt6 complex terminated by two iodide anions, [Pt6I2(μ-dpmp)4]­(PF6)2 (9), was synthesized from [Pt6(μ-H)­I2(μ-dpmp)4]­(PF6) (5) by treatment with [Cp2Fe]­[PF6]. Complexes 7 and 8 were readily reacted with the neutral two-electron donors XylNC, CO, and phosphines to afford the trinuclear complexes [Pt2M­(μ-dpmp)2(XylNC)­L]­(PF6)2 (M = Pt, L = XylNC (1a), CO (10), PPh3 (11); M = Pd, L = XylNC (1b)) through cleavage of the electron-deficient central M–M bond. When complex 7 was reacted with the diphosphines (PP) trans-Ph2PCHCHPPh2 (dppen) and Ph2P­(CH2)2PPh2 (dppe), the diphosphine was inserted into the central M–M bond to afford [(XylNC)­Pt3(μ-dpmp)2(PP)­Pt3(μ-dpmp)2(XylNC)]­(PF6)4 (12), which was transformed by treatment with another 1 equiv of diphosphine into the asymmetric trinuclear complexes [Pt3(μ-dpmp)2(XylNC)­(PP)]­(PF6)2 (13). A further ligand exchange reaction of 13a (PP = trans-dppen) provided the diphosphine-terminated symmetrical Pt3 complex [Pt3(μ-dpmp)2(L)2]­(PF6)2 (L = trans-dppen (14a)). Complexes 7 and 8 were also reacted with [AuCl­(PPh3)] to yield the Pt2MAu heterotetranuclear complexes [Pt2MAuCl­(μ-dpmp)2(PPh3)­(XylNC)]­(PF6)2 (M = Pt (15), Pd (16)), in which the Pt2M trinuclear fragment is inserted into the Au–Cl bond in a 1,1-fashion on the central M atoms of the Pt2M2Pt2 string.

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