Ji Yong, Zhang Rui, Li Yu-Jia, Li Yi-Zhi, Zuo Jing-Lin, You Xiao-Zeng
Coordination Chemistry Institute and the State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, People's Republic of China.
Inorg Chem. 2007 Feb 5;46(3):866-73. doi: 10.1021/ic061882r.
A series of new platinum(II) complexes containing both 4,4'-di-tert-butyl-2,2'-bipyridine (dbbpy) and the extended tetrathiafulvalenedithiolate ligands have been prepared and characterized. These complexes include [Pt(dbbpy)(C8H4S8)] (1; C8H4S82- = 2-{(4,5-ethylenedithio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate), [Pt(dbbpy)(ptdt)] (2; ptdt = 2-{(4,5-cyclopentodithio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate), [Pt(dbbpy)(mtdt)] (3; mtdt = 2-{(4,5-methylethylenedithio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate), [Pt(dbbpy)(btdt)] (4; btdt = benzotetrathiafulvalenedithiolate), [Pt(dbbpy)(C8H6S8)] (5; C8H6S82- = 2-{4,5-bis(methylthio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate), [Pt(dbbpy)(3O-C6S8)] (6; 3O-C6S82- = 2-{4,5-dithia-(3',6',9'-trioxaundecyl)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate), and [Pt(dbbpy)(4O-C6S8)] (7; 4O-C6S82- = 2-{4,5-dithia-(3',6',9',12'-tetraoxatetradecyl)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate). The crystal structures of a new ligand precursor (2-[4,5-dithia-(3',6',9',12'-tetraoxatetradecyl)-1,3-dithiol-2-ylidene]-4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiole, IIIc) and complexes 5-7 have been determined by X-ray crystallography. Complexes 1-7 show intense electronic absorption bands in the UV-vis region due to the intramolecular mixed metal/ligand-to-ligand charge-transfer transition, and they display significant solvatochromic behavior. Redox properties of these compounds have been investigated by cyclic voltammetry, and complex 7 shows a significant response for Na+ ions with a large positive shift of ca. 45 mV.
一系列同时含有4,4'-二叔丁基-2,2'-联吡啶(dbbpy)和扩展的四硫富瓦烯二硫醇盐配体的新型铂(II)配合物已被制备并表征。这些配合物包括[Pt(dbbpy)(C8H4S8)](1;C8H4S82- = 2-{(4,5-亚乙基二硫基)-1,3-二硫醇-2-亚基}-1,3-二硫醇-4,5-二硫醇盐)、[Pt(dbbpy)(ptdt)](2;ptdt = 2-{(4,5-环戊二硫基)-1,3-二硫醇-2-亚基}-1,3-二硫醇-4,5-二硫醇盐)、[Pt(dbbpy)(mtdt)](3;mtdt = 2-{(4,5-甲基亚乙基二硫基)-1,3-二硫醇-2-亚基}-1,3-二硫醇-4,5-二硫醇盐)、[Pt(dbbpy)(btdt)](4;btdt = 苯并四硫富瓦烯二硫醇盐)、[Pt(dbbpy)(C8H6S8)](5;C8H6S82- = 2-{4,5-双(甲硫基)-1,3-二硫醇-2-亚基}-1,3-二硫醇-4,5-二硫醇盐)、[Pt(dbbpy)(3O-C6S8)](6;3O-C6S82- = 2-{4,5-二硫杂-(3',6',9'-三氧杂十一烷基)-1,3-二硫醇-2-亚基}-1,3-二硫醇-4,5-二硫醇盐)和[Pt(dbbpy)(4O-C6S8)](7;4O-C6S82- = 2-{4,5-二硫杂-(3',6',9',12'-四氧杂十四烷基)-1,3-二硫醇-2-亚基}-1,3-二硫醇-4,5-二硫醇盐)。通过X射线晶体学确定了一种新的配体前体(2-[4,5-二硫杂-(3',6',9',12'-四氧杂十四烷基)-1,3-二硫醇-2-亚基]-4,5-双(2-氰基乙硫基)-1,3-二噻吩,IIIc)以及配合物5 - 7的晶体结构。配合物1 - 7在紫外 - 可见区域显示出强烈的电子吸收带,这归因于分子内混合金属/配体到配体的电荷转移跃迁,并且它们表现出显著的溶剂化显色行为。通过循环伏安法研究了这些化合物的氧化还原性质,配合物7对Na+离子显示出显著响应,其正向大位移约为45 mV。