Self-assembly morphology and packing structures depend on the "head' of organic cations anchored on polyoxometalate anions in hybrids

被引:8
|
作者
Tan, Chunxia [1 ]
Feng, Ruofei [2 ]
机构
[1] Gansu Univ Chinese Med, Key Lab Traditioanal Chinese Med Qual & Standard, Lanzhou, Peoples R China
[2] Northwest Univ Nationalities, Key Bioengn & Technol Lab SEAC, Lanzhou, Peoples R China
关键词
Organic-polyoxometalates; self-assembly; morphology; layered structure; hexagonal structure; LANGMUIR-BLODGETT-FILMS; CHARGE-TRANSFER SALTS; MOLECULAR MATERIALS; ELECTRON-TRANSFER; MULTILAYER FILMS; ION-PAIRS; ENERGY; SIZE; NANOSTRUCTURES; LUMINESCENT;
D O I
10.1080/10610278.2017.1301451
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two organic-polyoxometalates (organic-POMs) hybrids were constructed by fan-shaped 1-methyl-3-[3, 4, 5-tris(octadecyloxy) benzyl]imidazolium salts (labelled as I-Cl) and triethyl-[3, 4, 5-tris (octadecyloxy) benzyl] ammonium salts (labelled as Q-Cl) and Keggin anions [SiW12O40](4-) by electrostatic interaction. Self-assembled behaviours of two aggregates in organic solvent and solid state were investigated in detail by scanning electron microscopy, transmission electron microscopy and X-ray analysis. The mixed solution of chloroform-methanol or chloroform-acetone provided the stable environment for aggregates and aggregates showed a uniform micron size. X-ray analysis results showed that flower-like aggregates morphology of I-4[SiW12O40] based on imidazole ring as head' in organic cations was formed by the stacking of multilamellar discs and kept the lamellar structure in solid state. Bulk thorn spheres appeared in Q(4)[SiW12O40] aggregates, which were formed by closely interspersed of lots flatted blocks with hexagonal structure characteristics in solid state. The comprehension for the self-assembly morphology and solid structure of organic-polyoxometalate hybrids would help us to use easily modified organic moiety and functional inorganic polyoxoanions as blocks to build novel and giant supramolecular architecture. [GRAPHICS] .
引用
收藏
页码:634 / 642
页数:9
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