Instantaneous and Reversible Gelation of Organically Grafted Polyoxometalate Complexes with Dicarboxylic Acids.
			        作者:Zhenfeng He, Huanbing Wang, Yinglin Wang, Haolong Li,* Lihua Bi, Lixin Wu,
关键字:polyoxometalate, supramolecularpolymer gel
论文来源:期刊
具体来源:Soft Matter, 2012, 8, 3315–3321.
发表时间:2012年
	An organically pyridyl-grafted Anderson-type POM complex (TBA–Py–MnMo6) bearing counterions
	of tetrabutylammonium (TBA) was found to form supramolecular gels instantaneously through mixing
	with appropriate dicarboxylic acid additives in acetonitrile. In the gelation process, TBA–Py–MnMo6
	was confirmed to self-assemble into supramolecular polymer chains through unidirectional hydrogen
	bonding between the pyridyl groups of POMs and the carboxylic groups of dicarboxylic acids, which
	drove the complexes into one-dimensional fibers. The fibers were demonstrated to further intertwine
	together through the lateral hydrogen bonding between polymer chains under the support of excess
	acid, forming three-dimensional networks. The distance between TBA–Py–MnMo6 units secluded by
	dicarboxylic acid was proved to be a criterion for the formation of gels, which is related to the TBA
	density along the supramolecular polymer chains and the solvent–fiber interfacial energy. The gelation
	behaviour of the hybrid POM complex can be simply controlled through adjusting the length of
	dicarboxylic acids. More interestingly, the POM hybrid gels exhibited a quick response to organic bases
	and diacids reversibly.