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Scandium interaction with diantipyrylmethane homologues and 2-(n-sulphophenylazo)-1,8-dihydroxynaphthalene-3,6 sodium disulphonate

Abstract

The reactions of scandium with homologs of diantipyrilmethane (DAM)-propyldiantipyrilmethane (PDAM) and phenyldiantipyrilmethane (PhDAM) - are studied. The relationship of components in the complexes formed is found, and chemism of their formation is established. The complexes Sc-SPADNE (sodium salt 2-(n-sulphophenylazo)-1,8-dioxynaphthalene-3,6-disulphonic acid) are shown to form within a wide pH range. The maximum yield of complexes is observed at 6.0-7.5 pH. By the ion-exchange method the anion character of heteroligand scandium complexes is established. The complex Sc-SPADNE-PDAM is faster as compared with the complexes Sc-SPADNE-DAM and Sc-SPADNE-PhDAM. The decrease in amine excess and increase in the sensitivity of heteroligand formation of the complexes of scandium with SPADNE and PDAM make them better suited for analysis. The technique is developed for the determination of Sc/sub 2/O/sub 3/ in perovskites using the complete differential spectrophotometry method.
Authors:
Ganago, L I; Alinovskaya, L A [1] 
  1. AN Belorusskoj SSR, Minsk. Inst. Fiziki Tverdogo Tela i Poluprovodnikov
Publication Date:
Jan 01, 1979
Product Type:
Journal Article
Reference Number:
AIX-11-520676; EDB-80-078454
Resource Relation:
Journal Name: Zh. Anal. Khim.; (USSR); Journal Volume: 34:1
Subject:
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; SCANDIUM; SPECTROPHOTOMETRY; AZO COMPOUNDS; CHEMICAL REACTION KINETICS; CHEMICAL REACTIONS; COMPLEXES; CONDENSED AROMATICS; HYDROXY COMPOUNDS; PH VALUE; PYRAZOLINES; QUANTITATIVE CHEMICAL ANALYSIS; SCANDIUM COMPLEXES; SCANDIUM OXIDES; SENSITIVITY; SODIUM COMPOUNDS; SULFONIC ACIDS; ALKALI METAL COMPOUNDS; AROMATICS; AZOLES; CHALCOGENIDES; CHEMICAL ANALYSIS; ELEMENTS; HETEROCYCLIC COMPOUNDS; KINETICS; METALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PYRAZOLES; REACTION KINETICS; SCANDIUM COMPOUNDS; TRANSITION ELEMENT COMPLEXES; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS; 400104* - Spectral Procedures- (-1987)
OSTI ID:
5440483
Country of Origin:
USSR
Language:
Russian
Other Identifying Numbers:
Journal ID: CODEN: ZAKHA
Submitting Site:
INIS
Size:
Pages: 111-116
Announcement Date:
Jun 01, 1980

Citation Formats

Ganago, L I, and Alinovskaya, L A. Scandium interaction with diantipyrylmethane homologues and 2-(n-sulphophenylazo)-1,8-dihydroxynaphthalene-3,6 sodium disulphonate. USSR: N. p., 1979. Web.
Ganago, L I, & Alinovskaya, L A. Scandium interaction with diantipyrylmethane homologues and 2-(n-sulphophenylazo)-1,8-dihydroxynaphthalene-3,6 sodium disulphonate. USSR.
Ganago, L I, and Alinovskaya, L A. 1979. "Scandium interaction with diantipyrylmethane homologues and 2-(n-sulphophenylazo)-1,8-dihydroxynaphthalene-3,6 sodium disulphonate." USSR.
@misc{etde_5440483,
title = {Scandium interaction with diantipyrylmethane homologues and 2-(n-sulphophenylazo)-1,8-dihydroxynaphthalene-3,6 sodium disulphonate}
author = {Ganago, L I, and Alinovskaya, L A}
abstractNote = {The reactions of scandium with homologs of diantipyrilmethane (DAM)-propyldiantipyrilmethane (PDAM) and phenyldiantipyrilmethane (PhDAM) - are studied. The relationship of components in the complexes formed is found, and chemism of their formation is established. The complexes Sc-SPADNE (sodium salt 2-(n-sulphophenylazo)-1,8-dioxynaphthalene-3,6-disulphonic acid) are shown to form within a wide pH range. The maximum yield of complexes is observed at 6.0-7.5 pH. By the ion-exchange method the anion character of heteroligand scandium complexes is established. The complex Sc-SPADNE-PDAM is faster as compared with the complexes Sc-SPADNE-DAM and Sc-SPADNE-PhDAM. The decrease in amine excess and increase in the sensitivity of heteroligand formation of the complexes of scandium with SPADNE and PDAM make them better suited for analysis. The technique is developed for the determination of Sc/sub 2/O/sub 3/ in perovskites using the complete differential spectrophotometry method.}
journal = []
volume = {34:1}
journal type = {AC}
place = {USSR}
year = {1979}
month = {Jan}
}