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首页> 外文期刊>Chemical engineering journal >Hydrogen transfer from cyclohexanol to aromatic aldehydes catalyzed by heterogenized ruthenium(II)complexes bound to swellable polymer matrices
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Hydrogen transfer from cyclohexanol to aromatic aldehydes catalyzed by heterogenized ruthenium(II)complexes bound to swellable polymer matrices

机译:氢键合到可溶胀聚合物基质上的异质钌(II)络合物催化氢从环己醇转移到芳族醛

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Aromatic aldehydes can be reduced to corresponding alcohols by hydrogen transfer from cyclohexanol in the presence of Ru(II)complexes bound to swellable polymer matrices.The kinetics of the reaction has been measured between 100 and 140 °C.The process was shown to depend on the structure of aromatic aldehydes,on the concentrations of aldehyde and hydrogen donor,and on the amount of catalyst.The reaction proceeded efficiently in halogenated hydrocarbon solvents.The metal leaching and deactivation of the catalyst was studied.The metal leaching was different for subsequent catalytic runs and it is most pronounced in the first catalytic run.The IR spectra study for the catalyst deactivation showed that catalyst deactivation may be ascribed to the formation of metallic units bound to two carboxylate groups.This problem can be prevented by esterifying the groups.An apparent activation energy,Ea = 22 ± 1 kcal/mol was obtained,which suggests that the catalytic process involves predominantly a chemically controlled reaction.A general reaction mechanism and rate equation have been proposed.
机译:在与可溶胀的聚合物基体结合的Ru(II)配合物存在下,可通过环己醇的氢转移将芳香醛还原为相应的醇。反应动力学已在100至140°C的温度范围内进行了测量。芳香醛的结构,醛和氢供体的浓度以及催化剂的用量。在卤代烃溶剂中反应有效进行。研究了催化剂的金属浸出和失活。红外光谱研究表明,催化剂的失活可能归因于与两个羧酸盐基团结合的金属单元的形成,可以通过酯化这些基团来避免这一问题。表观活化能Ea = 22±1 kcal / mol,表明催化过程主要涉及提出了一般的反应机理和速率方程。

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