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聚氨大环-氰基合钴超分子的转动相关时间及59Co核四极耦合常数的测定——动态激光光散射的应用
引用本文:周平,欧阳植勋.聚氨大环-氰基合钴超分子的转动相关时间及59Co核四极耦合常数的测定——动态激光光散射的应用[J].波谱学杂志,2003,20(4):319-328.
作者姓名:周平  欧阳植勋
作者单位:1.聚合物分子工程教育部重点实验室,高分子科学系,复旦大学,上海 200433; 2.香港中文大学化学系,香港
基金项目:国家自然科学基金;20274009,29974004;
摘    要:对于自旋I>1/2的核,其运动的相关时间τc以及核四极耦合常数NQCC是表征分子局部和微观动力学结构的重要参数. 然而,在溶液中,这些参数均难以测定. 该工作以聚氨大环-氰基合钴超分子体系为例,利用在高分子体系中广泛使用的激光光散射技术成功地测量了溶液中超分子络合物[12]aneN4[Co(CN)6], [18]aneN6[Co(CN)6], [24]aneN8[Co(CN)6],[16]aneN4[Co(CN)6], [24]aneN6[Co(CN)6] 和 [32]aneN8[Co(CN)6] 的水合半径,从而根
据Stokes-Einstein-Debye理论计算出了分子转动的相关时间τc. 这些超分子的水合半径在0.4~0.6 nm之间. 对应的转动相关时间τc在3.8~9.5×10-11 s之间. 这一时间范围对于分子量在300~500的分子,有相当的合理性. 进而,通过测量超分子在稀溶液中的纵向弛豫时间T1,结合计算出的相关时间τc,我们得到了该超分子体系中59Co的四极耦合常数,其范围在0.5~2.2 MHz之间. 我们发现,这些超分子在溶液中的四极耦合常数明显小于在固体状态时的值(5~7 MHz). 导致这一现象很可能的原因是在固体状态下59Co核周围的电场梯度是各向异性的,从而有较大的四极耦合常数值. 而在溶液中,由于分子的快速运动,各向异性被平均,因而有较小的四极耦合常数.

关 键 词:59Co  NMR    相关时间    核四极耦合常数    激光光散射    超分子  
收稿时间:2003-04-14

DETERMINATION OF ROTATIONALREORIENTATION CORRELATION TIME AND 59 Co NUCLEAR QUADRUPOLAR COUPLINGCONSTANT OF POLYAMMONIUM MACROCYCLIC COBALTICYANIDE SUPERCOMPLEXES IN DILUTE AQUEOUS SOLUTIONS--An Application of Dynamic Laser Light Scattering Method
Abstract.DETERMINATION OF ROTATIONALREORIENTATION CORRELATION TIME AND 59 Co NUCLEAR QUADRUPOLAR COUPLINGCONSTANT OF POLYAMMONIUM MACROCYCLIC COBALTICYANIDE SUPERCOMPLEXES IN DILUTE AQUEOUS SOLUTIONS--An Application of Dynamic Laser Light Scattering Method[J].Chinese Journal of Magnetic Resonance,2003,20(4):319-328.
Authors:Abstract
Institution:1. The Key Laboratory of Molecular Engineering of Polymers, Ministry of Education. Macromolecular Science Department, Fudan University, Shanghai 200433, China; =; 2. Department of Chemistry, The Chinese University of Hong Kong, Hong Kong, China
Abstract:The correlation time, τc, and the nuclear quadrupolar coupling constant (NQCC) of I>1/2 nuclei are important parameters for characterizing local and microdynamic structures of molecules. However, it is often difficult to determine those constants in solution. In this study,τc and NQCC of the 59Co nuclei were determined for a series of supercomplexes[12]aneN4[Co(CN)6], 18]an eN 6Co(CN) 6],[24]aneN8[Co(CN)6],[16]aneN4[Co(CN)6],[24]aneN6[Co(CN)6]and[32]aneN8[Co(CN)6]in dilute solution. The Dynamic Laser Lig ht Scattering (DLLS) method, which is now widely used in macromolecule research, was first applied to determine the hydrodynamic radii (0.4~0.6 nm) of these molecules. Based on the Stokes Einstein Debye equation and the measured hydrodynamic radii, the rotational reorientation correlation times τc were calculated.τc obtained in this study had a range of 3.8~9.5×10-11s, which are fairly reasonable for molecules with molecular weights of WT]GK2]about 300~500. Finally, NQCC of the59Co nuclei in the supercomplexes were determined by combining the τc values calculated and the experimentally measured longitudinal relaxation times, T1, of the 59Co nuclei. The NQCC values obtained ranged from 0.5 to 2.2 MHz, which are considerably lower than those extracted from solid tatic NMR lineshape (5 to 7 MHz). The difference is probably due to the structural effects originating from the anisotropy of local electric gradient around 59Co nucleus in solid.
Keywords:Co NMR  correlation time  nuclear quadrupolar coupling constant  laser light scattering  supercomplex
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