Uzelmeier Calvin E, Smucker Bradley W, Reinheimer Eric W, Shatruk Mikhail, O'Neal Amanda W, Fourmigué Marc, Dunbar Kim R
Department of Chemistry, Texas A and M University, College Station, TX 77842-3012, USA.
Dalton Trans. 2006 Nov 28(44):5259-68. doi: 10.1039/b610659e. Epub 2006 Oct 19.
Reactions of 3,4-dimethyl-3',4'-bis(diphenylphosphino)tetrathiafulvalene, o-P2, with BF(4) salts of Fe(ii), Co(ii), Ni(II), Pd(II), and Pt(II) yield complexes of general formula [M(o-P2)(2)]BF(4). Similar reactions between o-P2 and AgSbF(6) or AgPF(6) produced the salts [Ag(o-P2)(2)][X] where X = SbF(6) or PF(6). The resulting compounds were fully characterized by (1)H and (31)P{(1)H} NMR, infrared and electronic absorption spectroscopies, cyclic voltammetry, FAB-MS and single-crystal X-ray diffraction. The paramagnetic Co(II) compound exhibits an S = 3/2 state with large spin-orbit coupling contribution at higher temperatures and an effective S' = 1/2 state below 20 K. Electrochemical studies of the compounds indicate that the two functionalized TTF ligands are not in electronic communication and that they essentially behave as isolated redox centers.
3,4 - 二甲基 - 3',4'-双(二苯基膦基)四硫富瓦烯(邻 - P2)与铁(II)、钴(II)、镍(II)、钯(II)和铂(II)的[BF₄]⁻盐反应生成通式为[M(邻 - P2)₂][BF₄]₂的配合物。邻 - P2与AgSbF₆或AgPF₆之间的类似反应生成盐[Ag(邻 - P2)₂][X],其中X = [SbF₆]⁻或[PF₆]⁻。所得化合物通过¹H和³¹P{¹H}核磁共振、红外和电子吸收光谱、循环伏安法、快原子轰击质谱和单晶X射线衍射进行了全面表征。顺磁性的钴(II)化合物在较高温度下表现出具有大自旋 - 轨道耦合贡献的S = 3/2态,在20 K以下表现出有效S' = 1/2态。这些化合物的电化学研究表明,两个功能化的TTF配体没有电子通信,它们基本上表现为孤立的氧化还原中心。