Über Struktur und Aktivität der den H 2 O 2 ‐Zerfall katalysierenden Cu 2+ ‐Komplexe. V.  Vergleich der katalytischen Aktivität der Cu 2+ ‐Komplexe isomerer β‐Hydroxythiophen‐Derivate. Mettallionen und H 2 O 2 , 9. Mitteilung | Zendy

Petri S. | Zendy; Sigel H. | Zendy; Erlenmeyer H. | Zendy

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Über Struktur und Aktivität der den H 2 O 2 ‐Zerfall katalysierenden Cu 2+ ‐Komplexe. V. Vergleich der katalytischen Aktivität der Cu 2+ ‐Komplexe isomerer β‐Hydroxythiophen‐Derivate. Mettallionen und H 2 O 2 , 9. Mitteilung

Author(s) -

Petri S.,

Sigel H.,

Erlenmeyer H.

Publication year - 1966

Publication title -

helvetica chimica acta

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.74

H-Index - 82

eISSN - 1522-2675

pISSN - 0018-019X

DOI - 10.1002/hlca.19660490611

Subject(s) - chemistry , thiophene , medicinal chemistry , catalysis , chelation , decomposition , ring (chemistry) , stereochemistry , organic chemistry

The catalytic properties in H 2 O 2 decomposition of the Cu 2+ ‐chelates of 2‐ Acetyl‐3‐hydroxy‐thiophene (I) and 3‐Acetyl‐4‐hydroxy‐thiophene (II) have been investigated. Evidence is given that the catalytic activity of the chelates is a function of the respective bond orders of the α, β (I) and β, β′ (II) thiophene bonds of the chelate ring.

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