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非均相催化过程中的仲氢诱导极化

Parahydrogen-induced polarization in heterogeneous catalytic processes.

作者信息

Kovtunov Kirill V, Zhivonitko Vladimir V, Skovpin Ivan V, Barskiy Danila A, Koptyug Igor V

机构信息

International Tomography Center, SB RAS, 3A Institutskaya St, Novosibirsk, 630090, Russian Federation.

出版信息

Top Curr Chem. 2013;338:123-80. doi: 10.1007/128_2012_371.

DOI:10.1007/128_2012_371
PMID:23097028
Abstract

Parahydrogen-induced polarization of nuclear spins provides enhancements of NMR signals for various nuclei of up to four to five orders of magnitude in magnetic fields of modern NMR spectrometers and even higher enhancements in low and ultra-low magnetic fields. It is based on the use of parahydrogen in catalytic hydrogenation reactions which, upon pairwise addition of the two H atoms of parahydrogen, can strongly enhance the NMR signals of reaction intermediates and products in solution. A recent advance in this field is the demonstration that PHIP can be observed not only in homogeneous hydrogenations but also in heterogeneous catalytic reactions. The use of heterogeneous catalysts for generating PHIP provides a number of significant advantages over the homogeneous processes, including the possibility to produce hyperpolarized gases, better control over the hydrogenation process, and the ease of separation of hyperpolarized fluids from the catalyst. The latter advantage is of paramount importance in light of the recent tendency toward utilization of hyperpolarized substances in in vivo spectroscopic and imaging applications of NMR. In addition, PHIP demonstrates the potential to become a useful tool for studying mechanisms of heterogeneous catalytic processes and for in situ studies of operating catalytic reactors. Here, the known examples of PHIP observations in heterogeneous reactions over immobilized transition metal complexes, supported metals, and some other types of heterogeneous catalysts are discussed and the applications of the technique for hypersensitive NMR imaging studies are presented.

摘要

仲氢诱导的核自旋极化可增强各种原子核的核磁共振信号,在现代核磁共振光谱仪的磁场中,信号增强可达四到五个数量级,在低磁场和超低温磁场中增强效果甚至更高。它基于在催化氢化反应中使用仲氢,仲氢的两个氢原子成对加成时,可强烈增强溶液中反应中间体和产物的核磁共振信号。该领域最近的一项进展是证明不仅在均相氢化反应中,而且在多相催化反应中也能观察到PHIP。与均相过程相比,使用多相催化剂产生PHIP具有许多显著优势,包括生产超极化气体的可能性、对氢化过程更好的控制以及超极化流体与催化剂分离的简便性。鉴于最近在核磁共振的体内光谱和成像应用中使用超极化物质的趋势,后一个优势至关重要。此外,PHIP显示出成为研究多相催化过程机理和原位研究运行中的催化反应器的有用工具的潜力。在此,讨论了在固定化过渡金属配合物、负载型金属和其他一些类型的多相催化剂上的多相反应中观察到PHIP的已知实例,并介绍了该技术在超灵敏核磁共振成像研究中的应用。

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