化学
硼
化学位移
电场梯度
核磁共振波谱
部分
结晶学
固态核磁共振
计算化学
核磁共振
立体化学
物理化学
电场
有机化学
物理
量子力学
作者
Amanda E. Alain,Yoshiaki Shoji,Takanori Fukushima,David L. Bryce
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2015-12-01
卷期号:54 (24): 11889-11896
被引量:14
标识
DOI:10.1021/acs.inorgchem.5b02161
摘要
Borinium cations (R2B(+)) are of particular fundamental and applied interest in part due to their pronounced Lewis acidity which enables unique chemical transformations. Solid-state NMR spectroscopy of magic-angle spinning and stationary powdered samples of the dicoordinate boron cation in the recently reported dimesitylborinium tetrakis(pentafluorophenyl)borate compound (Shoji et al. Nature Chem. 2014, 6, 498) is applied to characterize the (11)B electric field gradient (EFG) and chemical shift (CS) tensors. The experimental data are consistent with linear C-B(+)-C geometry. The (11)B quadrupolar coupling constant, 5.44 ± 0.08 MHz, and the span of the CS tensor, 130 ± 1 ppm, are both particularly large relative to literature data for a variety of boron functional groups, and represent the first such data for the linear C-B(+)-C borinium moiety. The NMR data are similar to those for the neutral tricoordinate analogue, trimesitylborane, but contrast with those of the Cp*2B(+) cation. Quantum chemical calculations are applied to provide additional insights into the relationship between the NMR observables and the molecular and electronic structure of the dimesitylborinium cation.
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