Synthesis of Quinoline-Based Pt-Sb Complexes with L- or Z-Type Interaction: Ligand-Controlled Redox via Anion Transfer

喹啉基Pt-Sb配合物的合成及其L型或Z型相互作用:通过阴离子转移实现配体控制的氧化还原反应

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Abstract

A series of Pt-Sb complexes with two or three L-type quinoline side arms were prepared and studied. Two ligands, tri(8-quinolinyl)stibane (SbQ(3), Q = 8-quinolinyl, 1) and 8,8'-(phenylstibanediyl)diquinoline (SbQ(2)Ph, 2), were used to synthesize the Pt(II)-Sb(III) complexes (SbQ(3))PtCl(2) (3) and (SbQ(2)Ph)PtCl(2) (4). Chloride abstraction with AgOAc provided the bis-acetate complexes (SbQ(3))Pt(OAc)(2) (5) and (SbQ(2)Ph)Pt(OAc)(2) (6). To better understand the electronic effects of the Sb moiety, analogous bis-chloride complexes were oxidized to an overall formal oxidation state of +7 (i.e., Pt + Sb formal oxidation states = 7) using dichloro(phenyl)-λ(3)-iodane (PhICl(2)) and 3,4,5,6-tetrachloro-1,2-dibenzoquinone (o-chloranil) as two-electron oxidants. Depending on the oxidant, different conformational changes occur within the coordination sphere of Pt as confirmed by single-crystal X-ray diffraction and NMR spectroscopy. In addition, the nature of Pt-Sb interactions was evaluated via molecular and localized orbital calculations.

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