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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Iron(II), manganese(II) and cobalt(II) complexes containing tetradentate biphenyl-bridged ligands and their application in alkane oxidation catalysis
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Iron(II), manganese(II) and cobalt(II) complexes containing tetradentate biphenyl-bridged ligands and their application in alkane oxidation catalysis

机译:含四齿联苯桥联配体的铁(II),锰(II)和钴(II)配合物及其在烷烃氧化催化中的应用

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摘要

A series of manganese(n), iron(II) and cobalt(II) bis(triflate) complexes containing linear tetradentate bis(imine) and bis(amine) ligands with a biphenyl bridge have been synthesized. The twist in the ligand backbone due to the biphenyl unit leads in the case of the bis(imine) ligands (1 and 2) containing sp(2) hybridised N donors, to a distorted cis-alpha coordination geometry, whereas in the case of the biphenyland biphenylether-bridged bis(amine) ligands (7-9 and 12), a trans coordination geometry is observed. The catalytic properties of the complexes for the oxidation of cyclohexane, using H2O2 as the oxidant, have been evaluated. Only the iron complexes show any catalytic activity under the conditions used, but the low conversions and selectivies observed indicate that these catalysts lead predominantly to free radical auto-oxidation.
机译:合成了一系列锰(n),铁(II)和钴(II)双(三氟甲磺酸酯)配合物,它们含有带有联苯桥的线性四齿双(亚胺)和双(胺)配体。在双(亚胺)配体(1和2)包含sp(2)杂化的N供体的双(亚胺)配体的情况下,配体主链的扭曲导致扭曲的顺式-α配位几何,而在在联苯和联苯醚桥联的双(胺)配体(7-9和12)上,观察到反式配位几何。已经评价了使用H 2 O 2作为氧化剂的配合物对环己烷氧化的催化性能。在使用的条件下,只有铁配合物显示出任何催化活性,但是观察到的低转化率和选择性表明这些催化剂主要导致自由基自氧化。

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