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铑催化剂的结构探索及其通过侧链氢化实现高效仲氢诱导极化的动力学研究。

Structural exploration of rhodium catalysts and their kinetic studies for efficient parahydrogen-induced polarization by side arm hydrogenation.

作者信息

Itoda Marino, Naganawa Yuki, Ito Makoto, Nonaka Hiroshi, Sando Shinsuke

机构信息

Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo 7-3-1 Hongo Bunkyo-ku Tokyo 113-8656 Japan

Interdisciplinary Research Center for Catalytic Chemistry, National Institute of Advanced Industrial Science and Technology (AIST) 1-1-1 Higashi Tsukuba Ibaraki 305-8565 Japan

出版信息

RSC Adv. 2019 Jun 10;9(32):18183-18190. doi: 10.1039/c9ra02580d.

Abstract

Parahydrogen-induced polarization (PHIP) is a rapid and cost-effective hyperpolarization technique using transition metal-catalysed hydrogenation with parahydrogen. We examined rhodium catalysts and their kinetic studies, rarely considered in the research of current PHIP. It emerged that rhodium complexes with electron-donating bisphosphine ligands, with a dicyclohexylphosphino group, appear to be more effective than conventional rhodium catalysts.

摘要

仲氢诱导极化(PHIP)是一种快速且经济高效的超极化技术,它利用过渡金属催化仲氢进行氢化反应。我们研究了铑催化剂及其动力学,这在当前PHIP研究中很少被考虑。结果表明,带有给电子双膦配体且含有二环己基膦基的铑配合物似乎比传统铑催化剂更有效。

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