利用阴离子交换层状无机氢氧化物制备“插层催化剂”

Takayoshi Hara
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摘要

利用层状Ni-Zn羟基双盐(NiZn)的阴离子交换能力,可以在温和的反应条件下将[Pd(OH) 4] 2−、[(D-val)Pd(OH) 2]−或[Rh(OH) 6] 3−等不稳定的阴离子过渡金属配合物插入到NiZn中间层中。中间层中的催化活性物质通过NiZn主阴离子和客体阴离子之间的强静电相互作用而稳定。此外,Brønsted碱性阴离子(如PO 43−或OH−)也能够集成到NiZn中间层中。这些“插层催化剂”更有效地促进了各种液相反应。用Cu-Al层状氢氧化物(CuAl LDH)高温煅烧(1073 K)合成的CuO-CuAl 2 O 4纳米复合材料作为一种有效的非均相催化剂,以甲酸为氢供体进行羰基化合物的选择性加氢和各种醇的无受体脱氢。通过原位还原形成具有催化活性的Cu 0。制备过程中铜铝比对催化活性的影响很大。
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Creation of “Intercalation Catalysts” by Use of Anion Exchangeable Layered Inorganic Hydroxides
By use of anion-exchangeable ability of layered Ni-Zn hydroxy double salt (NiZn), unstable anionic transition metal complexes such as [Pd(OH) 4 ] 2− , [(D-val)Pd(OH) 2 ] − , or [Rh(OH) 6 ] 3− are able to be intercalated into NiZn interlayer under mild reaction conditions. Catalytically active species in interlayer are stabilized by the strong electrostatic interaction between the NiZn host and the guest anion. Furthermore, Brønsted basic anions such as PO 43− or OH − were also able to be integrated into NiZn interlayer. These “intercalation catalysts” promote various liquid phase reactions more effectively. The CuO-CuAl 2 O 4 nanocomposite synthesized by high temperature calcination (1073 K) of Cu-Al layered double hydroxide (CuAl LDH) acted as an effective heterogeneous catalyst for selective hydrogenation of carbonyl compounds with formic acid as a hydrogen donor and acceptorless dehydrogenation of various alcohols. The catalytically active Cu 0 species was formed by in situ reduction. The catalytic activity strongly depended on the Cu/Al ratio in preparation.
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