Doyle Robert P, Julve Miguel, Lloret Francesc, Nieuwenhuyzen Mark, Kruger Paul E
School of Chemistry, University of Dublin, Trinity College, Dublin 2, Ireland.
Dalton Trans. 2006 May 7(17):2081-8. doi: 10.1039/b515889c. Epub 2006 Feb 2.
The reaction of copper(II) hydroxide with 2,2'-bipyridine (bipy) (1 : 1) in alkaline aqueous solution (pH 14) at room temperature affords the alternating carbonate/hydroxo-bridged copper(II) polymeric chain compound {[Cu3(bipy)3(mu-OH)2(mu-CO3)2].11H2O}n, 1, as determined by single-crystal X-ray diffraction. The structure of 1 is built up from two similar centro-symmetric dinuclear [(bipy)Cu(mu-OH)]2 cores which link together via bridging carbonate groups to mononuclear [(bipy)Cu] fragments to form the chain. Interdigitation of adjacent chains through pi-pi interactions, which involve each bipy ligand, forms sheets that are separated by the water molecules of crystallisation. Variable-temperature magnetic susceptibility measurements have shown that 1 behaves as an isolated spin doublet with two non-interacting spin triplets with the magnetic coupling through the bis-mu-hydroxo bridges being strongly ferromagnetic in nature. The hydrothermal reaction of copper(II) hydroxide, bipy and ammonium hydrogenphosphate (pH 8) yields a dinuclear copper(II) complex of formula {[Cu2(bipy)2(mu-OH)2(HPO4)(H2O)].4H2O}, 2, as determined by single-crystal X-ray diffraction. The structure of consists of an asymmetric dinuclear bis-mu-hydroxo copper(II) core with a monodentate hydrogenphosphate dianion coordinating to one copper(II) atom (above) and a water molecule to the other (below). Intra- and inter-molecular hydrogen bond interactions involving the hydrogenphosphate, water molecules and bis-mu-hydroxo groups link adjacent dinuclear fragments into chains, which interdigitate to form sheets that are separated by the water molecules of crystallisation. The investigation of the magnetic properties of 2 showed that the strength of the ferromagnetic interaction through the bis-mu-hydroxo bridges is influenced by the significant out-of-plane displacement of the hydrogen atom of the hydroxo groups, brought about through hydrogen bonding to the hydrogenphosphate ligand, and yielded the strongest ferromagnetic coupling yet reported for the bis-mu-hydroxo copper(II) core.
通过单晶X射线衍射测定,室温下,在碱性水溶液(pH = 14)中,氢氧化铜与2,2'-联吡啶(bipy)(1 : 1)反应生成交替的碳酸根/羟基桥联的铜(II)聚合物链状化合物{[Cu₃(bipy)₃(μ-OH)₂(μ-CO₃)₂]·11H₂O}ₙ,即化合物1。化合物1的结构由两个相似的中心对称双核[(bipy)Cu(μ-OH)]₂核组成,它们通过桥连碳酸根基团连接到单核[(bipy)Cu]片段上形成链。相邻链通过涉及每个联吡啶配体的π-π相互作用相互交错,形成由结晶水分子隔开的片层。变温磁化率测量表明,化合物1表现为一个孤立的自旋二重态,带有两个非相互作用的自旋三重态,通过双μ-羟基桥的磁耦合本质上是强铁磁性的。通过单晶X射线衍射测定,氢氧化铜、联吡啶和磷酸氢铵在水热反应(pH = 8)中生成式为{[Cu₂(bipy)₂(μ-OH)₂(HPO₄)(H₂O)]·4H₂O}的双核铜(II)配合物,即化合物2。其结构由一个不对称的双核双μ-羟基铜(II)核组成,一个单齿磷酸氢根二价阴离子与一个铜(II)原子(上方)配位,一个水分子与另一个铜(II)原子(下方)配位。涉及磷酸氢根、水分子和双μ-羟基基团的分子内和分子间氢键相互作用将相邻的双核片段连接成链,这些链相互交错形成由结晶水分子隔开的片层。对化合物2磁性的研究表明,通过双μ-羟基桥的铁磁相互作用强度受羟基氢原子显著的面外位移影响,这种位移是通过与磷酸氢根配体形成氢键产生的,并且产生了迄今为止报道的双μ-羟基铜(II)核中最强的铁磁耦合。