首页> 外文期刊>Physical chemistry chemical physics: PCCP >Towards homonuclear J solid-state NMR correlation experiments for half-integer quadrupolar nuclei: experimental and simulated ~(11)B MAS spin-echo dephasing and calculated ~2J_(BB) coupling constants for lithium diborate
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Towards homonuclear J solid-state NMR correlation experiments for half-integer quadrupolar nuclei: experimental and simulated ~(11)B MAS spin-echo dephasing and calculated ~2J_(BB) coupling constants for lithium diborate

机译:走向半整数四极核的同核J固态NMR相关实验:实验和模拟〜(11)B MAS自旋回波移相并计算〜2J_(BB)耦合常数的二硼酸锂

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摘要

Magic-angle spinning (MAS) NMR spin-echo dephasing is systematically investigated for the spin I= 3/2 ~(11)B nucleus in lithium diborate, Li2O·2B2O3. A clear dependence on the quadrupolar frequency (ω_Q~(PAS)/2π = 3C_Q/[4I(2I - 1)]) is observed: the B3 (larger Cq) site dephases more slowly than the B4 site at all investigated MAS frequencies (5 to 20 kHz) at 14.1 T. Increasing the MAS frequency leads to markedly slower dephasing for the B3 site, while there is a much less evident effect for the B4 site. Considering samples at 5, 25, 80 (natural abundance) and 100% ~(11)B isotopic abundance, dephasing becomes faster for both sites as the ~(11)B isotopic abundance increases. The experimental behaviour is rationalised using density matrix simulations for two and three dipolar-coupled ~(11)B nuclei. The experimentally observed slower dephasing for the larger C_Q (B3) site is reproduced in all simulations and is explained by the reintroduction of the dipolar coupling by the so-called "spontaneous quadrupolar-driven recoupling mechanism" having a different dependence on the MAS frequency for different quadrupolar frequencies. Specifically, isolated spin-pair simulations show that the spontaneous quadrupolar-driven recoupling mechanism is most efficient when the quadrupolar frequency is equal to twice the MAS frequency. While for isolated spin-pair simulations, increasing the MAS frequency leads to faster dephasing, agreement with experiment is observed for three-spin simulations which additionally include the homogeneous nature of the homonuclear dipolar coupling network. First-principles calculations, using the GIPAW approach, of the ~2J_(11B-11B) couplings in lithium diborate, metaborate and triborate are presented: a clear trend is revealed whereby the ~2J_(11B-11B) couplings increase with increasing B-O-B bond angle and B-B distance. However, the calculated ~2J_(11B-11B) couplings are small (0.95, 1.20 and 2.65 Hz in lithium diborate), thus explaining why no zero crossing due to /modulation is observed experimentally, even for the sample at 25% ~(11)B where significant spin-echo intensity remains out to durations of ~200 ms.
机译:系统研究了在二硼酸锂Li2O·2B2O3中自旋I = 3/2〜(11)B核的幻角自旋(MAS)NMR自旋回波。观察到明显依赖于四极频率(ω_Q〜(PAS)/2π= 3C_Q / [4I(2I-1)]):在所有研究的MAS频率下,B3(较大Cq)位点的相移速度慢于B4位置( 5至20 kHz)在14.1T。提高MAS频率会导致B3站点的移相明显变慢,而B4站点的影响要小得多。考虑到5、25、80(自然丰度)和100%〜(11)B同位素丰度的样品,随着〜(11)B同位素丰度的增加,两个位点的移相变得更快。实验行为使用两个和三个偶极耦合〜(11)B原子核的密度矩阵模拟来合理化。在所有模拟中均再现了实验观察到的较大C_Q(B3)位置的较慢移相,并通过所谓的“自发四极驱动重耦合机制”重新引入了偶极耦合来解释,该耦合机制对MAS频率的依赖性不同。不同的四极频率。具体而言,隔离的自旋对仿真表明,当四极频率等于MAS频率的两倍时,自发四极驱动的再耦合机制最为有效。虽然对于独立的自旋对模拟,增加MAS频率会导致更快的移相,但对于三自旋模拟(其中还包括同核偶极耦合网络的均匀性质),观察到与实验一致。给出了使用GIPAW方法对二硼酸锂,偏硼酸锂和三硼酸锂中〜2J_(11B-11B)偶联进行的第一性原理计算:揭示了一个清晰的趋势,其中〜2J_(11B-11B)偶联随着BOB键的增加而增加角度和BB距离。但是,计算得出的〜2J_(11B-11B)耦合很小(在二硼酸锂中为0.95、1.20和2.65 Hz),因此可以解释为什么即使在25%〜(11 )B处,自旋回波强度仍然很高,持续时间约200毫秒。

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