Selective oxidation of benzyl alcohol over copper phthalocyanine immobilized on MCM-41

Hamza, A. and Srinivas, D. (2009) Selective oxidation of benzyl alcohol over copper phthalocyanine immobilized on MCM-41. Catalysis Letters, 128 (2). pp. 434-442. ISSN 1011-372X

Full text not available from this repository.

Abstract

Copper phthalocyanine (CuPc) complexes immobilized on “neat” and Ti4+ and Al3+ containing MCM-41 mimic the functionality of metalloenzymes. These novel materials catalyze the oxidation of benzyl alcohol to selectively benzaldehyde at moderate temperatures using peroxides and molecular oxygen as oxidant. Electron paramagnetic resonance and X-ray photoelectron spectroscopic studies revealed that the acidity of the support (MCM-41) influences the electronic structure of the immobilized CuPc. On acidic supports a part of copper in CuPc got reduced from a “formal” +2 to +1 oxidation state. This reduction of copper in its oxidation state on different supports decreased in the order: Al-MCM-41 (Brönsted and strong Lewis acid sites) > MCM-41 (silanol sites) > Ti-MCM-41 (weak Lewis acid sites). A linear variation in catalytic activity with the concentration of Cu1+ ions in different catalyst samples was observed. The study reveals that by suitably modifying the acidic properties of the support one can, in principle, fine-tune the electronic and catalytic properties of the active oxidation sites.

Item Type:
Journal Article
Journal or Publication Title:
Catalysis Letters
Uncontrolled Keywords:
/dk/atira/pure/subjectarea/asjc/1600/1600
Subjects:
?? general chemistrycatalysischemistry(all) ??
ID Code:
171773
Deposited By:
Deposited On:
15 Jun 2022 14:20
Refereed?:
Yes
Published?:
Published
Last Modified:
16 Jul 2024 11:51