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Building up 3-D framework structure from interlinking layered cobalt phosphates and organic pillars

机译:由层状磷酸钴和有机支柱相互连接构建3-D框架结构

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A new cobalt phosphates (trans-1,4-dach)(0.5)Co-3(H(2)o)(OH)(PO4)(HPO4)center dot (3 + x)H2O (1), has been synthesized under a hydrothermal condition and structurally characterized by single-crystal X-ray diffraction. It consists of cobalt phosphates layers and coordinated bis-N-clonor ligands, trans-1,4-diaminocycloltexane, which are interlinked to form a 3-D framework structure with I-D tunnel occupied by water molecules. When its channel water is fully removed at a relatively low temperature, the pillars fold up, and no porosity can be detected by sorption. However, the structural integrity of the compound is retained, and the pillar can still rise to its original upright position after contact with water vapor. This implies that some channel water molecules play a wedge function to control the up and down positions of the organic bis-N-donor ligands. When 1 is partially dehydrated, it revealed adsorption of various linear organic molecules, although the fully dehydrated one did not adsorb any organic molecules. Magnetic susceptibility measurements showed that I is,in antiferromagnet with a canted interaction at a transition temperature of about 10 K. Crystal data: monoclinic, C21e, a=28.653(10)angstrom, b=12.874(4)angstrom, c=8.266(3)angstrom, beta=97.257(7), V=3025(2)angstrom 3, Z=8. (c) 2007 Elsevier Inc. All rights reserved.
机译:合成了一种新的磷酸钴(trans-1,4-dach)(0.5)Co-3(H(2)o)(OH)(PO4)(HPO4)中心点(3 + x)H2O(1)在水热条件下,在结构上通过单晶X射线衍射表征。它由磷酸钴层和配位的双-N-克隆配体trans-1,4-diaminocycloltexane组成,它们相互连接形成3-D骨架结构,I-D通道被水分子占据。当其通道中的水在较低的温度下被完全除去时,柱子会折叠,并且无法通过吸附检测到孔隙。但是,保留了化合物的结构完整性,并且在与水蒸气接触后,立柱仍可以升至其原始的直立位置。这意味着某些通道水分子起楔形作用,以控制有机双-N-供体配体的上下位置。当1部分脱水时,尽管完全脱水的一个分子不吸附任何有机分子,但它显示出各种线性有机分子的吸附。磁化率测量表明,I在反铁磁体中具有约10 K的转变温度下的倾斜相互作用。晶体数据:单斜晶系C21e,a = 28.653(10)埃,b = 12.874(4)埃,c = 8.266( 3)埃,β= 97.257(7),V = 3025(2)埃3,Z = 8。 (c)2007 Elsevier Inc.保留所有权利。

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