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Hydrothermal synthesis, crystal structure and heterogeneous catalytic activity of a novel inorganic-organic hybrid complex, possessing infinite La-O-La linkages

机译:具有无限La-O-La键的新型无机-有机杂化复合物的水热合成,晶体结构和非均相催化活性

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摘要

In this paper, a novel lanthanum coordination polymer formulated as {[La2(Hpdc)3(H2O)4]·2H 2O}n (1, H3pdc = 3,5-pyrazoledicarboxylic acid) has been synthesized by the reaction of H3pdc with chloride salt of La(III) under hydrothermal conditions and characterized by elemental analysis, FT-IR, TGA and single-crystal X-ray diffraction. The complex crystallized in the monoclinic system Cc space group. The single-crystal X-ray structural analysis revealed that central metal La atoms are nine-coordinate and linked by bridging μ2-OCOO - groups to form [La(1)- (μ2-OCOO -)2-La(2)]n inorganic-organic chains that produce a supramolecular polymeric framework structure. The three-dimensional structure of 1 is accompanied by non-coordinating water molecules. Thermal behavior and catalytic performance of 1 have also been studied. The complex 1 showed 100% selectivity and a conversion rate of 24% on the oxidation of thymol (T) to thymoquinone (TQ).
机译:本文通过H3pdc与氯化物的反应合成了一种新型的镧配位聚合物{[La2(Hpdc)3(H2O)4]·2H 2O} n(1,H3pdc = 3,5-吡唑二甲酸)。在水热条件下的La(III)盐,并通过元素分析,FT-IR,TGA和单晶X射线衍射进行表征。复合物在单斜晶系Cc空间群中结晶。单晶X射线结构分析表明,中心金属La原子为9坐标,并通过桥接μ2-OCOO-形成基团以形成[La(1)-(μ2-OCOO-)2-La(2)] n产生超分子聚合框架结构的无机有机链。 1的三维结构伴随着非配位水分子。还研究了1的热行为和催化性能。在将百里香酚(T)氧化成胸腺醌(TQ)时,配合物1表现出100%的选择性和24%的转化率。

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