Hydrothermal syntheses and crystal structures of two new phosphomolybdates based on an organoamine template

被引：9

作者：

Yan, Dawei ^{[1
]}

Zheng, Lei ^{[1
]}

Zhang, Zhibin ^{[1
]}

Wang, Congling ^{[1
]}

Yuan, Yan ^{[1
]}

Zhu, Dunru ^{[1
]}

Xu, Yan ^{[1
]}

机构：

[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Coll Chem & Chem Engn, Nanjing 210009, Peoples R China

来源：

JOURNAL OF COORDINATION CHEMISTRY | 2010年 / 63卷 / 24期

基金：

中国国家自然科学基金;

关键词：

Polyoxomolybdate-phosphorus; Hydrothermal synthesis; Crystal structure; INORGANIC HYBRID MATERIALS; STATE COORDINATION CHEMISTRY; MAGNETIC-BEHAVIOR; NETWORK STRUCTURE; BUILDING-BLOCKS; CLUSTERS; COMPLEXES; COMPOUND; POLYOXOMETALATE; COMPONENTS;

D O I：

10.1080/00958972.2010.534783

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Two new compounds of disphosphopentamolybdate (VI), (C6H18N2)2[H2P2Mo5O23] center dot 2(H2O) (1) and (C6H18N2)4.5H3[P2Mo5O23]2 center dot 6(H2O) (2), have been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. Compound 1 crystallizes in the triclinic space group P1 with a = 11.0863(9) angstrom, b = 11.9562(9) angstrom, c = 14.2291(19) angstrom, = 103.0410(10)degrees, = 100.3530(10)degrees, = 103.7390(10)degrees, V = 1729.8(2) angstrom 3, Z = 2; compound 2 crystallizes in the triclinic space group P1 with a = 14.6440(13) angstrom, b = 15.9168(13) angstrom, c = 17.9795(13) angstrom, = 80.4270(10)degrees, = 86.1180(10)degrees, = 64.1890(10)degrees, V = 3720.1(5) angstrom 3, Z = 2. Characterizations by elemental analysis, infrared analysis, and thermal analysis are also given. Formation of 1 and 2 indicates that pH of solution plays an important role during the synthesis.

引用

页码：4215 / 4225

页数：11

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