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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Organo-f-element catalysts for efficient and highly selective hydroalkoxylation and hydrothiolation
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Organo-f-element catalysts for efficient and highly selective hydroalkoxylation and hydrothiolation

机译:用于高效且高度选择性的加氢烷氧基化和加氢硫醇化反应的有机元素催化剂

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摘要

Lanthanide and actinide catalysts have made significant contributions to many areas of homogeneous catalysis with hydroelementation of C-C unsaturation being a notable area of success. In this Perspective, we review recent advances in f-element hydroelementation for highly selective hydroalkoxylation and hydrothiolation processes. As will be discussed, f-element hydroalkoxylation and hydrothiolation catalysts exhibit selectivities unobtainable by many late transition metal complexes. First, we review lanthanide-mediated hydroalkoxylation processes with mechanistic, thermodynamic, and kinetic considerations discussed, and then compare/contrast them with analogous C-N and C-P bond-forming transformations. In addition, computational studies are discussed which provide further insight into this transformation and the observed selectivities. Next, actinide-mediated alkyne hydrothiolation is reviewed with a similar discussion of reactivity, mechanism, and thermodynamics.
机译:镧系元素和act系元素催化剂在均相催化的许多领域做出了重要贡献,其中C-C不饱和键的加氢元素化是一个成功的领域。在此观点中,我们回顾了用于高选择性加氢烷氧基化和加氢硫醇化工艺的f元素加氢元素的最新进展。如将要讨论的,f-元素加氢烷氧基化和加氢硫醇化催化剂显示出许多后期过渡金属配合物无法获得的选择性。首先,我们以讨论的机理,热力学和动力学方面的考虑来审查镧系元素介导的加氢烷氧基化过程,然后将其与类似的C-N和C-P键形成转化进行比较/对比。另外,讨论了计算研究,这些研究为这种转变和观察到的选择性提供了进一步的见识。接下来,用对反应性,机理和热力学的类似讨论来综述act系元素介导的炔烃氢硫醇化反应。

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