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F-19/Na-23 multiple quantum cross polarization NMR in solids

机译:固体中的F-19 / Na-23多量子交叉极化NMR

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F-19 -->Na-23 triple quantum (TQ) cross polarization (TQCP) experiments and numerical simulations have been performed on the oxyfluoride NaMoO3F. Due to the orientation dependence of the quadrupolar tensor and thus the TQ nutation frequency (omega(s,nut)), only a fraction of the spins in the powder can match the Hartmann-Hahn condition at the same time, for a fixed F-19 rf field strength (omega(1I)). Numerical simulations of the static TQCP process, for different single crystallite orientations, demonstrate that the most efficient TQCP occurs for parts of the powder where the quadrupolar splitting, Q', is largest, and where the TQ coherences are pure eigenstates of the system, even though omega(s,nut) is smallest for these orientations. Under magic angle spinning (MAS) conditions, omega(s,nut) becomes time dependent and again, efficient TQCP is observed at times during the rotor period where Q' is largest. TQCP intensities for different crystallites were calculated as a function of omega(1I), for fixed Na-23 rf field strengths, to obtain TQCP matching profiles and to determine optimum Hartmann-Hahn conditions. The TQCP matching profiles vary significantly with crystallite orientation and with spinning speed, due to the different time dependences of the quadrupolar interaction for the different orientations. Centerband matching conditions are observed at F-19 rf fields, close to the minimum values of omega(s,nut) observed during the rotor period. Two different centerbands are observed for crystallite orientations where there are two different local minima for omega(s,nut). The time dependence of omega(s,nut) results in higher-order (> 2) sideband matching conditions. The experimentally observed static and MAS TQCP NMR matching profiles, and changes in the Na-23 static and MAS second-order quadrupolar NMR lineshapes, could be rationalized on the basis of the calculated distributions of omega(S,nut) that occur within the powder. Optimum TQCP intensities were obtained with high Na-23 rf power, to maximize omega(s,nut), and slow MAS, to ensure efficient spin-locking; a further increase in intensity could be achieved by ramping the F-19 rf field during the contact time. The efficiencies of the single quantum cross polarization (SQCP) multiple quantum (MQ) MAS and TQCP-MQMAS experiments were compared and were found to be very similar for NaMoO3F. Finally, the two-dimensional TQCP-MQMAS experiment was illustrated. (C) 2000 American Institute of Physics. [S0021-9606(00)00617-6]. [References: 35]
机译:F-19-> Na-23三重量子(TQ)交叉极化(TQCP)实验和数值模拟已在氟氧化物NaMoO3F上进行。由于四极张量的取向相关性以及TQ章动频率(omega(s,nut)),对于固定的F-,粉末中只有一部分自旋可以同时匹配Hartmann-Hahn条件19 rf场强(omega(1I))。静态TQCP过程针对不同单晶取向的数值模拟表明,最有效的TQCP发生在四极劈裂Q'最大,且TQ相干为系统纯本征态的粉末部分中,即使尽管在这些方向上,Ω是最小的。在魔角旋转(MAS)条件下,ω(s,nut)随时间而变,并且再次在Q'最大的转子周期中观察到有效的TQCP。对于固定的Na-23 rf场强,计算不同微晶的TQCP强度作为omega(1I)的函数,以获得TQCP匹配曲线并确定最佳的Hartmann-Hahn条件。由于不同取向的四极相互作用的时间依赖性不同,TQCP匹配曲线随微晶取向和旋转速度而显着变化。在F-19 rf磁场中观察到了中心带匹配条件,接近转子期间观测到的Ω的最小值。对于微晶取向,观察到两个不同的中心带,其中ω(螺母)有两个不同的局部最小值。 ω(s,nut)的时间依赖性导致更高阶(> 2)边带匹配条件。实验观察到的静态和MAS TQCP NMR匹配曲线,以及Na-23静态和MAS二阶四极NMR线形的变化,可以根据粉末中omega(S,nut)的计算分布合理化。在高Na-23 rf功率下可获得最佳的TQCP强度,以使ω最大化,而MAS缓慢,以确保有效的自旋锁定。通过在接触时间内倾斜F-19 rf磁场,可以进一步提高强度。比较了单量子交叉极化(SQCP)多量子(MQ)MAS和TQCP-MQMAS实验的效率,发现它们与NaMoO3F非常相似。最后,对二维TQCP-MQMAS实验进行了说明。 (C)2000美国物理研究所。 [S0021-9606(00)00617-6]。 [参考:35]

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