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Acceleration of carbon-13 spin-lattice relaxation times in amino acids by electrolytes

机译:电解质加速氨基酸中碳13自旋晶格弛豫时间

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Measurements of the enhancement, by various electrolytes, of the spin-lattice relaxation time of carbon-13 at different locations in a number of amino acids are reported. Spin-lattice relaxation times T-1 of all the carbons in amino acids generally tend to decrease with increase in the concentration of electrolytes, the largest effects often being observed for the charged carboxylate groups of the amino acids. Carboxylic carbons in amino acids are the sensitive 'acceptor' of the C-13 spin-lattice relaxation accelerating effects offered by electrolytes, and the C-13 spin-lattice relaxation accelerating ability of electrolytes decreases in the order Mg(ClO4)(2) > MgCl2 > CaCl2 > NaCl > KCl > LiClO4 > NaOH. The mechanisms of the observed phenomena are discussed in terms of intermolecular interaction, paramagnetic impurities in electrolytes and other mechanisms; large contributions of intermolecular interactions with electrolytes are present on complex formation between amino acids and metal ions and the incoming 'unsaturation' of the primary solvation shell of cations with the increase in electrolyte concentration. Copyright (C) 2004 John Wiley Sons, Ltd.
机译:报道了通过各种电解质增强许多氨基酸不同位置的碳13的自旋晶格弛豫时间的测量结果。氨基酸中所有碳的自旋晶格弛豫时间T-1通常会随着电解质浓度的增加而降低,经常观察到最大的影响是氨基酸的带电羧酸盐基团。氨基酸中的羧基碳是电解质提供的C-13自旋晶格弛豫加速作用的敏感“受体”,电解质的C-13自旋晶格弛豫加速能力按Mg(ClO4)的顺序降低(2) > MgCl 2> CaCl 2> NaCl> KCl> LiClO4> NaOH。从分子间相互作用,电解质中的顺磁性杂质和其他机理方面讨论了观察到的现象的机理。氨基酸和金属离子之间的复杂形成以及随着电解质浓度的增加,阳离子的一级溶剂化壳层进入的“不饱和”分子之间存在着与电解质的分子间相互作用的巨大贡献。版权所有(C)2004 John Wiley Sons,Ltd.

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