- Title
- Photocatalytic oxidation of 1-hexene using GaPc and InPc octasubstituted derivatives
- Creator
- Chauke, Vongani
- Creator
- Nyokong, Tebello
- Subject
- To be catalogued
- Date Issued
- 2008
- Date
- 2008
- Type
- text
- Type
- article
- Identifier
- http://hdl.handle.net/10962/268611
- Identifier
- vital:54214
- Identifier
- xlink:href="https://doi.org/10.1016/j.molcata.2008.04.003"
- Description
- Photocatalytic oxidation of 1-hexene by GaPc (1a–1c) and InPc (2a–2c) derivatives (Pc = phthalocyanine) is hereby presented. The derivatives studied are Pc octasubstituted with phenoxy (a), 4-tert-butylphenoxy (b) or benzyloxyphenoxy (c) at the peripheral positions. The photocatalytic oxidation products for 1-hexene were 1,2-epoxyhexane and 1-hexen-3-ol. The %conversion values of 1-hexene and %selectivity of 1,2-epoxyhexane were generally higher for InPc derivatives. Even though InPc derivatives showed better photocatalytic results than GaPc derivatives, the former were less stable relative to the latter. Both type I and type II mechanism were implicated in the photocatalysis mechanism.
- Format
- computer
- Format
- online resource
- Format
- application/pdf
- Format
- 1 online resource (5 pages)
- Format
- Publisher
- Elsevier
- Language
- English
- Relation
- Journal of Molecular Catalysis A: Chemical
- Relation
- Chauke, V. and Nyokong, T., 2008. Photocatalytic oxidation of 1-hexene using GaPc and InPc octasubstituted derivatives. Journal of Molecular Catalysis A: Chemical, 289(1-2), pp.9-13
- Relation
- Journal of Molecular Catalysis A: Chemical volume 289 number 1 - 2 p. 9 2008 1381-1169
- Rights
- Publisher
- Rights
- Use of this resource is governed by the terms and conditions of the Elsevier Terms and Conditions Statement (https://www.elsevier.com/legal/elsevier-website-terms-and-conditions)
- Rights
- Closed Access
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- Visitors: 433
- Downloads: 48
Collections
Nyokong, Tebello (Distinguished Professor)
RU DST/NRF SARChI for Medicinal Chemistry and Nanotechnology
RU Department of Chemistry
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