Zakaria Choudhury M, Ferguson George, Lough Alan J, Glidewell Christopher
School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST, Scotland.
Acta Crystallogr B. 2002 Feb;58(Pt 1):78-93. doi: 10.1107/s010876810101850x. Epub 2001 Jan 24.
In the complexes [Ni(cyclam)(OCOR)2] (cyclam = 1,4,8,11-tetraazacyclotetradecane), where (RCOO)- is 2-naphthoate [bis-(2-naphthoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (I), monoclinic P2(1)/c, Z' = 0.5], 3,5-dinitrobenzoate [bis-(3,5-dinitrobenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (II), triclinic P1, Z' = 0.5], 4-nitrobenzoate [bis-(4-nitrobenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (III), monoclinic P2(1)/n, Z' = 0.5], 3-hydroxybenzoate [bis-(3-hydroxybenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (IV), monoclinic P2(1)/c, Z' = 0.5] and 4-aminobenzoate [bis-(4-aminobenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (V), monoclinic C2/c, Z' = 0.5], the Ni lies on a centre of inversion with monodentate carboxylato ligands occupying trans sites. Compound (I) consists of isolated molecules. In (II) and (III), N-H...O hydrogen bonds link the complexes into chains. Compounds (IV) and (III) form two- and three-dimensional structures generated entirely by hard hydrogen bonds. The 5-hydroxyisophthalate(2-) anion forms a hydrated complex, [Ni(cyclam)(5-hydroxyisophthalate)(H2O)]4H2O [[aqua-(5-hydroxyisophthalato)-1,4,8,11-tetraazacyclotetradecanenickel(II)] tetrahydrate, (VI), monoclinic Cc, Z' = 1], in which the monodentate carboxylato ligand and a water molecule occupy trans sites at Ni: extensive hydrogen bonding links the molecular aggregates into a three-dimensional framework. The terephthalate(2-) anion forms a hydrated linear coordination polymer [catena-poly[terephthalato-1,4,8,11-tetraazacyclotetradecanenickel(II)] monohydrate, (VII), monoclinic C2/c, Z' = 0.5]. In 1,2,4,5-benzenecarboxylate tris[1,4,8,11-tetraazacyclotetradecanenickel(II)] diperchlorate hydrate (VIII), [Ni(cyclam)]3[1,2,4,5-benzenetetracarboxylate(4-)][ClO4]2[H2O]3, there are two distinct Ni sites: [Ni(cyclam)]2+ and centrosymmetric [C10H2O8]4- units form a two-dimensional coordination polymer, whose sheets are linked by centrosymmetric [Ni(cyclam)(H2O)2]2+ cations.
在配合物[Ni(环胺)(OCOR)₂](环胺 = 1,4,8,11 - 四氮杂环十四烷)中,其中(RCOO)⁻为2 - 萘甲酸根[双(2 - 萘甲酸根)-1,4,8,11 - 四氮杂环十四烷镍(II),(I),单斜晶系P2(1)/c,Z' = 0.5]、3,5 - 二硝基苯甲酸根[双(3,5 - 二硝基苯甲酸根)-1,4,8,11 - 四氮杂环十四烷镍(II),(II),三斜晶系P1,Z' = 0.5]、4 - 硝基苯甲酸根[双(4 - 硝基苯甲酸根)-1,4,8,11 - 四氮杂环十四烷镍(II),(III),单斜晶系P2(1)/n,Z' = 0.5]、3 - 羟基苯甲酸根[双(3 - 羟基苯甲酸根)-1,4,8,11 - 四氮杂环十四烷镍(II),(IV),单斜晶系P2(1)/c,Z' = 0.5]和4 - 氨基苯甲酸根[双(4 - 氨基苯甲酸根)-1,4,8,11 - 四氮杂环十四烷镍(II),(V),单斜晶系C2/c,Z' = 0.5]中,Ni位于对称中心,单齿羧基配体占据反位。化合物(I)由孤立分子组成。在(II)和(III)中,N - H...O氢键将配合物连接成链。化合物(IV)和(III)形成完全由强氢键产生的二维和三维结构。5 - 羟基间苯二甲酸根(2 - )阴离子形成水合配合物,[Ni(环胺)(5 - 羟基间苯二甲酸根)(H₂O)]·4H₂O [[水合(5 - 羟基间苯二甲酸根)-1,4,8,11 - 四氮杂环十四烷镍(II)]四水合物,(VI),单斜晶系Cc,Z' = 1],其中单齿羧基配体和一个水分子在Ni处占据反位:广泛的氢键将分子聚集体连接成三维框架。对苯二甲酸根(2 - )阴离子形成水合线性配位聚合物[链状聚[对苯二甲酸根 - 1,4,8,11 - 四氮杂环十四烷镍(II)]一水合物,(VII),单斜晶系C2/c,Z' = 0.5]。在1,2,4,5 - 苯四羧酸三[1,4,8,11 - 四氮杂环十四烷镍(II)]二高氯酸盐一水合物(VIII),[Ni(环胺)]₃·[1,2,4,5 - 苯四羧酸根(4 - )]·[ClO₄]₂·[H₂O]₃中,有两个不同的Ni位点:[Ni(环胺)]²⁺和中心对称的[C₁₀H₂O₈]⁴⁻单元形成二维配位聚合物,其片层由中心对称的[Ni(环胺)(H₂O)₂]²⁺阳离子连接。