z-logo
Premium
Quaternary salts from 2‐(methylpyridyl or quinolyl)benzimidazoles and related polymethine dyes
Author(s) -
Barni Ermanno,
Savarino Piero
Publication year - 1979
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570160814
Subject(s) - cyanine , chemistry , iodide , medicinal chemistry , organic chemistry , physics , quantum mechanics , fluorescence
The quaternisation of 2‐(methylpyridyl or quinolyl)benzimidazoles with methyl iodide leads to a variety of salts depending on the relative position of the nuclei and on the experimental conditions: N ‐methylpyridinium, N ‐methylquinolinium, methyl and 1,3‐dimethylbenzimidazolium iodides, and hydroiodides were isolated. Cyanine dyes were prepared from N ‐methylpyridinium and N ‐methylquinolinium methiodides. The main spectrospcopic features of these compounds are briefly discussed.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom