## A B S r n C T 1,8-anthraquinono-l8-crown-6 and 10-[(2,4-dinitrophenyl)azol-9-liydroxy-l,&anthraceno-18-crown-6 were prepared from 1, 8-dichloroanthraquinone and used in the development of ion-selective electrodes. The electrodes based on 10-[(2,4-dinitrophenyl)azo]-~-hydroxy-1,8-anthraceno-18-c
โฆ LIBER โฆ
Comparative evaluation of neutral, and proton-ionizable crown ether compounds as lithium ionophores in ion-selective electrodes and in solvent extraction
โ Scribed by Attiyat, Abdulrahman S.; Christian, Gary D.; Xie, Robert Y.; Wen, Xiaowen.; Bartsch, Richard A.
- Book ID
- 125511751
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 506 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0003-2700
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Crown ether derivatives of anthraquinone
โ
John R. Allen; Tadeusz Cynkowski; Jayant Desai; Leonidas G. Bachas
๐
Article
๐
1992
๐
John Wiley and Sons
๐
English
โ 451 KB
๐ 1 views
Comparison of dibenzo-16-crown-5 compoun
โ
Akira Ohki; Kaoru Iwaki; Kensuke Naka; Shigeru Maeda; James J. Collier; Youngcha
๐
Article
๐
1996
๐
John Wiley and Sons
๐
English
โ 497 KB
๐ 2 views
Potentiometric selectivities for alkali metal, alkaline earth metal and ammonium ions for a series of N,N-dialkyl .qwz-( R)dibenro-16-crown-5-oxyacetamides in solvent polymeric membrane electrodes are determined. For N,N-dipentyl sym-(R)dibenzo-16-crown-5-oxyacetdmides, the Na+/K ' selectivity incre