首页> 外文期刊>Journal of the American Chemical Society >Oxidative Reactivity Difference Among The Metal Oxo And Metal Hydroxo Moieties: Ph Dependent Hydrogen Abstraction By A Manganese(iv) Complex Having Two Hydroxide Ligands
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Oxidative Reactivity Difference Among The Metal Oxo And Metal Hydroxo Moieties: Ph Dependent Hydrogen Abstraction By A Manganese(iv) Complex Having Two Hydroxide Ligands

机译:金属氧和金属氧部分之间的氧化反应性差异:具有两个氢氧化物配体的锰(iv)配合物的PH依赖性氢提取

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Clarifying the difference in redox reactivity between the metal oxo and metal hydroxo moieties for the same redox active metal ion in identical structures and oxidation states, that is, M~(n+)=O and M~(n+)-OH, contributes to the understanding of nature's choice between them (M~(n+)=O or M~(n+)-OH) as key active intermediates in redox enzymes and electron transfer enzymes, and provides a basis for the design of synthetic oxidation catalysts. The newly synthesized manganese(IV) complex having two hydroxide ligands, [Mn(Me_2EBC)_2(OH)_2](PF_6)_2, serves as the prototypic example to address this issue, by investigating the difference in the hydrogen abstracting abilities of the Mn~(IV)=O and Mn~(IV)-OH functional groups. Independent thermodynamic evaluations of the O-H bond dissociation energies (BDEoh) for the corresponding reduction products, Mn~(III)-OH and Mn~(III)-OH_2, reveal very similar oxidizing power for Mn~(IV)=O and Mn~(IV)-OH (83 vs 84.3 kcal/mol). Experimental tests showed that hydrogen abstraction proceeds at reasonable rates for substrates having BDE_(CH) values less than 82 kcal/mol. That is, no detectable reaction occurred with diphenyl methane (BDE_(CH) = 82 kcal/mol) for both manganese(IV) species. However, kinetic measurements for hydrogen abstraction showed that at pH 13.4, the dominant species Mn(Me_2EBC)_2(O)_2, having only Mn~(IV)=O groups, reacts more than 40 times faster than the Mn~(IV)-OH unit in Mn(Me_2EBC)_2(OH)_2~(2+), the dominant reactant at pH 4.0. The activation parameters for hydrogen abstraction from 9,10-dihydroanthracene were determined for both manganese(IV) moieties: over the temperature range 288-318 K for Mn~(IV)(OH)_2~(2+), ΔH~(++) = 13.1 ± 0.7 kcal/mol, and ΔS~(++) = -35.0 ± 2.2 cal K~(-1) mol~(-1); and the temperature range 288-308 K for for Mn~(IV)(O))2, ΔH~(++) = 12.1 ± 1.8 kcal/mol, and ΔS~(++) = -30.3 ± 5.9 cal K~(-1) mol~(-1).
机译:澄清在相同结构和氧化态下相同氧化还原活性金属离子的金属氧代和金属羟基部分之间的氧化还原反应性差异,即M〜(n +)= O和M〜(n +)-OH,有助于理解大自然之间的选择(M〜(n +)= O或M〜(n +)-OH)作为氧化还原酶和电子转移酶中的关键活性中间体,为合成氧化催化剂的设计提供了基础。新合成的具有两个氢氧化物配体[Mn(Me_2EBC)_2(OH)_2](PF_6)_2的锰(IV)络合物是通过研究该化合物氢提取能力的差异来解决此问题的原型实例。 Mn〜(IV)= O和Mn〜(IV)-OH官能团。对相应的还原产物Mn〜(III)-OH和Mn〜(III)-OH_2的OH键解离能(BDEoh)的独立热力学评估表明,Mn〜(IV)= O和Mn〜 (IV)-OH(83对84.3 kcal / mol)。实验测试表明,对于BDE_(CH)值小于82 kcal / mol的底物,吸氢以合理的速率进行。即,对于两种锰(IV)物种,都没有与二苯甲烷(BDE_(CH)= 82 kcal / mol)发生可检测到的反应。然而,动力学分析表明,在pH为13.4时,仅具有Mn〜(IV)= O基团的优势物种Mn(Me_2EBC)_2(O)_2的反应速率比Mn〜(IV)高40倍以上Mn(Me_2EBC)_2(OH)_2〜(2+)中的-OH单元,pH为4.0的主要反应物。确定了两个锰(IV)部分从9,10-二氢蒽中提取氢的活化参数:在Mn〜(IV)(OH)_2〜(2+)的288-318 K温度范围内,ΔH〜(+ +)= 13.1±0.7 kcal / mol,ΔS〜(++)= -35.0±2.2 cal K〜(-1)mol〜(-1); Mn〜(IV)(O))2的温度范围为288-308 K,ΔH〜(++)= 12.1±1.8 kcal / mol,ΔS〜(++)= -30.3±5.9 cal K〜 (-1)摩尔〜(-1)。

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