Godino Salido M Luz, Arranz Mascarós Paloma, López Garzón Rafaél, Gutiérrez Valero M Dolores, Low John N, Gallagher John F, Glidewell Christopher
Departamento de Química Inorgánica y Orgánica, Universidad de Jaén, 23071 Jaén, Spain.
Acta Crystallogr B. 2004 Feb;60(Pt 1):46-64. doi: 10.1107/S0108768103029136. Epub 2004 Jan 21.
Nine hydrated complexes of Group 2 (alkaline earth) cations with organic ligands which are N-substituted amino acids containing the 6-amino-3,4-dihydro-3-methyl-5-nitroso-4-oxopyrimidin-2-yl group have been structurally characterized. The octahydrated calcium glycinate complex, where the six-coordinate Ca cation lies on an inversion centre in the space group P(-)1, forms a finite (zero-dimensional) complex. The hexahydrated barium glycinate complex contains eight-coordinate Ba and it is isostructural with the known Sr analogue, and its one-dimensional coordination polymer takes the form of a simple chain. The octahydrated calcium and strontium threonine complexes are isostructural, with eight-coordinate cations lying on twofold rotation axes in the space group C2: the one-dimensional coordination polymers take the form of a chain of spiro-fused rings and a similar chain of spiro-fused rings is found in the heptahydrated barium serine complex, although here the ten-coordinate cation lies in a general position. In the tetrahydrated strontium and barium glycylglycinate complexes, the eight-coordinate cations lie on twofold rotation axes in the space group C2/c, but in the Sr complex the coordination polymer is a chain of spiro-fused rings, while in the Ba complex the coordination polymer forms deeply puckered sheets. There are two types of Ca site in the hexahydrated calcium valine complex: one is eight coordinate and gives rise to a two-dimensional coordination polymer, while the other is seven coordinate forming a finite, zero-dimensional coordination complex. In the heptahydrated barium methionine complex, the coordination polymer is three dimensional. In all of the complexes, the coordination aggregates are further linked by an extensive series of hydrogen bonds.
已对第2族(碱土)阳离子与有机配体形成的9种水合配合物进行了结构表征,这些有机配体是含有6-氨基-3,4-二氢-3-甲基-5-亚硝基-4-氧代嘧啶-2-基的N-取代氨基酸。八水合甘氨酸钙配合物中,六配位的Ca阳离子位于空间群P(-)1的对称中心上,形成有限(零维)配合物。六水合甘氨酸钡配合物含有八配位的Ba,它与已知的Sr类似物同构,其一维配位聚合物呈简单链状。八水合钙和苏氨酸锶配合物同构,八配位阳离子位于空间群C2的二重旋转轴上:一维配位聚合物呈螺稠环链状,在七水合丝氨酸钡配合物中也发现了类似的螺稠环链,不过这里十配位的阳离子位于一般位置。在四水合甘氨酰甘氨酸锶和钡配合物中,八配位阳离子位于空间群C2/c的二重旋转轴上,但在Sr配合物中,配位聚合物是螺稠环链,而在Ba配合物中,配位聚合物形成深度褶皱的片层。六水合缬氨酸钙配合物中有两种类型的Ca位点:一种是八配位,产生二维配位聚合物,另一种是七配位,形成有限的零维配位配合物。在七水合蛋氨酸钡配合物中,配位聚合物是三维的。在所有配合物中,配位聚集体通过一系列广泛的氢键进一步连接。