Structural Study of Nicotine Salts

Structural Study of Nicotine Salts
复制标题

尼古丁盐的结构研究

DOI:
--
复制
发表时间:
1983
期刊:
影响因子:
--
通讯作者:
T.A. Perfetti
T.A. Perfetti
中科院分区:
--
文献类型:
--
作者:
T.A. Perfetti

文献摘要

被引文献

相似文献

测定了三种烟碱盐的结构。这些盐具有1:1、2:1或3:1的酸碱比。有机酸和尼古丁之间的成盐取决于酸的结构(脂肪族或芳香族)及其功能。尼古丁的1:1盐具有与尼古丁的N-甲基吡咯烷氮结合的氨基酸或苯甲酸型酸。发现2:1盐与1:1盐中的一个酸基结合,第二个酸基与吡啶环的氮结合。尼古丁的2:1盐与甲酸、脂族二羧酸和/或硝基芳族酸形成。尼古丁与脂肪族一元羧酸形成3:1的盐,起始于乙酸。这里,一种酸如在1:1盐中那样结合,而另外两种酸二聚化并结合到吡啶基团的氮上。采用红外光谱、紫外光谱、质子核磁共振、碳核磁共振以及场解吸-质谱等方法对烟碱盐的结构进行了研究。
Abstract The structures of three types of nicotine salts have been determined. These salts have acid to base ratios of either 1 : 1, 2 : 1, or 3 : 1. Salt formation between organic acids and nicotine is dependent upon the structure of the acids (aliphatic or aromatic) and their functionality. The 1 : 1 salts of nicotine have amino acids or benzoic-type acids bound to the N-methylpyrrolidine nitrogen of nicotine. The 2 : 1 salts are found to bind to one acid group as in the 1 : 1 salts and a second to the nitrogen of the pyridine ring. The 2 : 1 salts of nicotine are formed with formic acid, aliphatic dicarboxylic acids, and/or nitroaromatic acids. Nicotine forms 3 : 1 salts with aliphatic monocarboxylic acids starting with acetic acid. Here one acid is bound as in the 1 : 1 salts while the other two acids dimerize and bind to the nitrogen of the pyridine group. Infra-red (IR), ultra-violet (UV), proton nuclear magnetic resonance (PMR), and carbon nuclear magnetic resonance (CMR) spectroscopy as well as field desorption - mass spectroscopy (FD-MS) were used in this investigation of the structure of nicotine salts.