Holland G P, Cherry B R, Alam T M
Department of Organic Materials, Sandia National Laboratories, Albuquerque, NM 87185, USA.
J Magn Reson. 2004 Mar;167(1):161-7. doi: 10.1016/j.jmr.2003.12.008.
The effect of a distribution in the (1)H-(1)H dipolar coupling on (1)H double-quantum (DQ) magic angle spinning (MAS) nuclear magnetic resonance (NMR) spinning sideband patterns is considered. In disordered or amorphous materials a distribution in the magnitude of the (1)H-(1)H dipolar coupling is a realistic possibility. Simulations of the (1)H DQ MAS NMR spinning sideband spectra were performed with the two-spin approximation. These simulations reveal that a dipolar coupling distribution can greatly affect the DQ spectral shape and behavior of the DQ build-up. The spectral line shapes are quantified by measurement of the relative intensities of the DQ sidebands. These variations in the (1)H DQ NMR spectra are evaluated as a function of the width of the dipolar coupling distribution. As an example, the experimental DQ spinning sideband spectrum for a hydrated polyoxoniobate containing 15 H(2)O molecules per hexaniobate cluster, are better simulated with a distribution of dipolar couplings opposed to a single coupling constant.
考虑了¹H-¹H偶极耦合分布对¹H双量子(DQ)魔角旋转(MAS)核磁共振(NMR)旋转边带模式的影响。在无序或无定形材料中,¹H-¹H偶极耦合大小的分布是一种现实的可能性。使用双自旋近似对¹H DQ MAS NMR旋转边带光谱进行了模拟。这些模拟表明,偶极耦合分布会极大地影响DQ光谱形状和DQ积累行为。通过测量DQ边带的相对强度来量化光谱线形状。将¹H DQ NMR光谱中的这些变化作为偶极耦合分布宽度的函数进行评估。例如,对于每个六铌酸盐簇含有15个H₂O分子的水合聚氧铌酸盐,其实验DQ旋转边带光谱用偶极耦合分布比用单个耦合常数能得到更好的模拟。