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首页> 外文期刊>Progress in Nuclear Magnetic Resonance Spectroscopy: An International Review Journal >Lanthanide paramagnetic probes for NMR spectroscopic studies of molecular conformational dynamics in solution: Applications to macrocyclic molecules
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Lanthanide paramagnetic probes for NMR spectroscopic studies of molecular conformational dynamics in solution: Applications to macrocyclic molecules

机译:镧系顺磁性探针,用于NMR光谱研究溶液中的分子构象动力学:在大环分子中的应用

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摘要

In 1969 it was reported [1] that the 1H NMR chemical shifts of organic compounds containing donor-active heteroatoms with lone electron pairs (O, N, S, etc.) change dramatically when so-called lanthanide (Ln) shift reagents (LSR) are added to solutions of these compounds in relatively inert nonaqueous solvents. Since that time, many original papers and reviews have been published on various aspects of using the properties of LSR, on interactions of LSR with various types of organic compounds [1–23], on nuclear spin interactions with the paramagnetic metal center [27–51], and on the lanthanide-induced shifts (LIS) and relaxation rate enhancement both in aqueous [13,14,24,25,35,36,46] and nonaqueous solvents [2,5,9,31].
机译:1969年有报道[1],当所谓的镧系元素(Ln)位移试剂(LSR)发生变化时,含有供体活性杂原子和单电子对(O,N,S等)的有机化合物的1H NMR化学位移发生巨大变化。 )加入到这些化合物在相对惰性的非水溶剂中的溶液中。自那时以来,关于使用LSR的特性的各个方面,关于LSR与各种类型的有机化合物的相互作用[1-23],关于与自磁金属中心的核自旋相互作用[27-]的许多原始论文和评论已经发表。 51],以及在水[13,14,24,25,35,36,46]和非水溶剂[2,5,9,31]中镧系元素引起的位移(LIS)和弛豫速率增强。

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