Issue 9, 2014

TiO2-photocatalytic acceptorless dehydrogenation coupling of primary alkyl alcohols into acetals

Abstract

Primary alkyl alcohols can be directly converted into acetals and H2via TiO2-photocatalytic dehydrogenation coupling at room temperature, with no need for any hydrogen acceptors. The reaction follows a tandem process integrating photocatalytic alcohol dehydrogenation and H+-catalytic acetalation, in which the H+ ion catalysts are provided by the alcohol dehydrogenation in real time. This approach exhibits a very high reaction rate and product selectivity, and represents a novel green process for the conversion of primary alkyl alcohols, especially for bio-renewable ethanol and 1-butanol.

Graphical abstract: TiO2-photocatalytic acceptorless dehydrogenation coupling of primary alkyl alcohols into acetals

Supplementary files

Article information

Article type
Communication
Submitted
08 Mar 2014
Accepted
13 May 2014
First published
13 May 2014

Green Chem., 2014,16, 4076-4080

Author version available

TiO2-photocatalytic acceptorless dehydrogenation coupling of primary alkyl alcohols into acetals

H. Zhang, Z. Zhu, Y. Wu, T. Zhao and L. Li, Green Chem., 2014, 16, 4076 DOI: 10.1039/C4GC00413B

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