Lee Young Hoon, Clegg Jack K, Lindoy Leonard F, Lu G Q Max, Park Yu-Chul, Kim Yang
Acta Crystallogr Sect E Struct Rep Online. 2008 Sep 13;64(Pt 10):i69-i70. doi: 10.1107/S1600536808028365.
Single crystals of Co(3)(PO(4))(2)·H(2)O, tricobalt(II) bis-[ortho-phosphate(V)] monohydrate, were obtained under hydro-thermal conditions. The compound is the second polymorph of this composition and is isotypic with its zinc analogue, Zn(3)(PO(4))(2)·H(2)O. Three independent Co(2+) cations are bridged by two independent orthophosphate anions. Two of the metal cations exhibit a distorted tetra-hedral coordination while the third exhibits a considerably distorted [5 + 1] octa-hedral coordination environment with one very long Co-O distance of 2.416 (3) Å. The former cations are bonded to four different phosphate anions, and the latter cation is bonded to four anions (one of which is bidentate) and one water mol-ecule, leading to a framework structure. Additional hydrogen bonds of the type O-H⋯O stabilize this arrangement.
在水热条件下获得了三水合二价钴双(正磷酸根(Ⅴ))(Co(3)(PO(4))(2)·H(2)O)的单晶。该化合物是此组成的第二种多晶型物,且与其锌类似物Zn(3)(PO(4))(2)·H(2)O同型。三个独立的Co(2+)阳离子由两个独立的正磷酸根阴离子桥连。其中两个金属阳离子呈现扭曲的四面体配位,而第三个呈现明显扭曲的[5 + 1]八面体配位环境,有一个非常长的Co - O距离为2.416(3) Å。前两个阳离子与四个不同的磷酸根阴离子键合,后一个阳离子与四个阴离子(其中一个是双齿的)和一个水分子键合,形成一种骨架结构。O - H⋯O型的额外氢键稳定了这种排列。