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首页> 外文期刊>Bulletin of the Chemical Society of Japan >Ion Pairs between Maleonitriledithiolato Complex Dianions of Cobalt and Nickel and Macrocyclic Ligand Complex Dications of Nickel (II)-Control of Intrapair Interaction through Ligand Modification
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Ion Pairs between Maleonitriledithiolato Complex Dianions of Cobalt and Nickel and Macrocyclic Ligand Complex Dications of Nickel (II)-Control of Intrapair Interaction through Ligand Modification

机译:在钴和镍的马来氮二硫代噻唑胺复合型的离子对和镍(II)镍(II)的大环配体复合物 - 通过配体改性的内部互动相互作用

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摘要

The ion pairs {[Ni(cyclam)]~(2+) [M(mnt)_2]~(2-)} (M = Co, Ni:1a,b), {[Ni(tmc)]~(2+)[M(mnt)_2]~(2-)} (M = Co, Ni:2a,b) and the solvent complexes {[Ni(cyclam)(dmso)_2]~(2+)[M(mnt)_2]~(2-)} (M = Co, Ni, mnt~(2-) = maleonitriledithiolato = (Z) 1,2-dicyano-1,2-ethylenedithiolato, cyclam = 1,4,8,11-tetraazacyclotetradecane, tmc = 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane) were isolated and structurally characterised. The nature of the macrocyclic ligand and the presence of coordinating solvents determine whether the dication is present as a tetra-, penta- or hexacoordinated complex. In 1a the tetracoordinated dications and dianions are arranged in a mixed stack structure; the absences of any short contacts and of a mutual ion pair charge transfer band indicate the absence of charge transfer interaction. The highly puckered cyclam ligand will prevent a close approach of the planar bis (maleonitriledithiolato) cobaltate (II). When cyclam is replaced by its tetramethyl derivative tmc, a strong coordinative interaction is introduced as indicated by the structure of 2a. One dianion coordinates to two dications through two trans-cyano groups. The resulting trinuclear dications {[Ni(tmc)][Co(mnt)_2][Ni(tmc)]}~(2+) from segregated columns separated by the non-interacting, remaining dianion. Crystallisation in the presence of a coordinating solvent like dimethyl sulfoxide (dmso) leads to the ion pairs {[Ni(cyclam)(dmso)_2]~(2+) [M(mnt)_2]~(2-)} containing hexacoordinated dications. Magnetic susceptibility measurements at room temperature are in accord with the observed structures. While 1b is diamagnetic, 1a, 2a, 2b, and the two solvent complexes exhibit values characteristic of the isolated ions, in agreement with the absence of any electronic interaction between dication and dianion within the ion pair. Temperature-dependent measurements down to 1.7 K indicate that a weak antiferromagnetic interaction is present in 2a.
机译:离子对{[Ni(Cyclam)]〜(2+)[M(MNT)_2]〜(2-)}(m = Co,Ni:1a,b),{[ni(tmc)]〜(2 +)[m(mnt)_2]〜(2-)}(m = co,ni:2a,b)和溶剂络合物{[ni(kycsam)(dmso)_2]〜(2 +)[m(mnt )_2]〜(2-)}(m = Co,Ni,MnT〜(2-)=马来腈硅酸盐=(Z)1,2-二氰基-1,2-乙二醇,CyclaM = 1,4,8,11-四氮杂环丁二原烷,TMC = 1,4,8,11-四甲基-1,4,8,11-11-11-11-11-11-11-11-11-四氮杂环丁二烷)分离和结构表征。大环配体的性质和配位溶剂的存在确定了该溶剂是否存在为四,五戊基或六氧化络合物。在1A中,四元化的Diantimate和Dianions布置在混合堆叠结构中;任何短触点和相互离子对电荷传递带的缺点都表明缺乏电荷转移相互作用。高褶皱的锡甘圈配体将防止平面BIS(马来氮硅酸盐)钴酸盐(II)的密切接近。当循环氨酸被其四甲基衍生物TMC取代时,如图2A的结构所示​​,引入强协调相互作用。一位冒光通过两个跨越氰基坐标坐落在两个染色体中。由此产生的三核浸渍{[Ni(TMC)] [CO(MNT)] [Ni(TMC)]}〜(2+)由由非交互,剩余的Dianion分开的隔离列。含有环化的离子对(DMSO)的邻离亚甲醚(DMSO)存在下的结晶,导致离子对([Ni(环)(DMSO)_2]〜(2 +)[M(MNT)_2]〜(2-)} Datage。室温下的磁化率测量符合观察到的结构。虽然1B是二磁,1A,2A,2B,以及两种溶剂络合物表现出隔离离子的值特征,同时不存在离子对内的DIANION之间的任何电子相互作用。将温度依赖的测量降至1.7 k表明2A中存在弱的反铁磁相互作用。

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    Institute of Inorganic Chemistry University of Erlangen-Nurnberg Egerlandstr. 1 91058 Erlangen Germany;

    Institute of Inorganic Chemistry University of Erlangen-Nurnberg Egerlandstr. 1 91058 Erlangen Germany;

    Institute of Inorganic Chemistry University of Erlangen-Nurnberg Egerlandstr. 1 91058 Erlangen Germany;

    The Institute of Physical and Chemical Research (RIKEN) Wako Saitama 351-0198;

    The Institute of Physical and Chemical Research (RIKEN) Wako Saitama 351-0198;

    The Institute of Physical and Chemical Research (RIKEN) Wako Saitama 351-0198;

    The Institute of Physical and Chemical Research (RIKEN) Wako Saitama 351-0198;

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  • 正文语种 eng
  • 中图分类 化学 ; 化学工业 ;
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