Simultaneous determination of the lithium-6 nuclear quadrupolar coupling constant and chemical shift anisotropy in monomeric tri(isopropyl)phenyllithium
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Cited by (8)
Practical considerations for the acquisition of ultra-wideline <sup>14</sup>N NMR spectra
2017, Solid State Nuclear Magnetic ResonanceCitation Excerpt :NMR powder patterns of integer spin nuclides like 2H and 6Li are normally easy to acquire in comparison to those of 14N, since the breadths of the former are comparatively smaller. However, due to their smaller breadths, the effects of the CSA can alter the positions of key discontinuities (i.e., they are not symmetric about the Larmor frequency), making simulations more challenging [60–63]. By comparison, since most 14N powder patterns are dominated by the contributions of the FOQI, the positions of the discontinuities on either side of the Larmor frequency are approximately the same (detection of slight differences is limited by the relatively low resolution of 14N NMR patterns, vide infra).
NMR studies of alkali metal ions in organic and biological solids
2012, Progress in Nuclear Magnetic Resonance SpectroscopyCarbanion Chemistry
2007, eMagResLinear Ni(I) complex in cis-[Ni(CN)<inf>4</inf>Cl<inf>2</inf>]<sup>5-</sup> cluster
2002, Journal of Physical Chemistry APulsed EPR and ab initio calculation on [Ni(CN)<inf>4</inf>]<sup>3-</sup> in NaCl and KCl host lattices
2001, Journal of Physical Chemistry A
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