期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 9, 期 3, 页码 360-368出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b614318k
关键词
-
The C-13 CPMAS spectrum is presented for the polymorph of oxybuprocaine hydrochloride which is stable at room temperature, i.e. Mod. II degrees. It shows crystallographic splittings arising from the fact that there are two molecules, with substantially different conformations, in the asymmetric unit. An INADEQUATE two-dimensional experiment was used to link signals for the same independent molecule. The chemical shifts are discussed in relation to the crystal structure. Of the four ethyl groups attached to NH+ nitrogens, one gives rise to unusually low chemical shifts, very different from those of the other three ethyl groups. This is attributed empirically to gamma-gauche conformational effects, as is confirmed by shielding computations. These considerations allow C-13 signals to be assigned to specific carbons in the two crystallographically inequivalent molecules in the crystal structure. Indeed, information about the conformations is inherent in the NMR spectrum, which thus provides data of crystallographic significance. A C-13/H-1 HETCOR experiment enabled resolution to be obtained in the H-1 dimension and allowed H-1 and C-13 signals for the same independent molecule to be linked.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据