## Abstract The mechanism of metal ion incorporation into phthalocyanine tetrasulfonic acid has been investigated. The rate determining step of these reactions is the pyrrole‐NH‐dissociation of the ligand, which is catalysed by particles like MeOH^+^.
Phtalocyanine in wässeriger Lösung III. Säuredissoziation der Pyrrol-NH-Gruppe in Phtalocyanintetrasulfonsäure
✍ Scribed by Klaus Bernauer; S. Fallab
- Publisher
- John Wiley and Sons
- Year
- 1962
- Tongue
- German
- Weight
- 490 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The acid NH‐dissociation of Pthalocyanintetrasulfonate has been investigated. We found, that the monomer H~2~PTS behaves as a moderately weak acid. The p__K__~a~‐value has been determined to 9,6. Due to steric and electrostatic hindrance of attack by hydroxide ion the reaction is surprisingly slow. The bimolecular rate constant is of the order of 3·10^2^ l mol^−1^ s^−1^.
📜 SIMILAR VOLUMES
## Abstract Die Decarboxylierung von 2‐Hydroxynaphtoesäure‐(1) in wässeriger Lösung verläuft nach der Reaktionsgeschwindigkeitsgleichung __v__ = __k__ [HA] = __k__ [A^−^] [H~3~O^+^]. Die ARRHENIUS‐Parameter liegen in der gleichen Grössenordnung wie bei den 4‐substituierten Salicylsäuren. In Acetatp