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Department of Chemistry and Applied Biosciences ETH Zürich, Laboratory of Inorganic Chemistry, Wolfgang Pauli Str. 10, CH-8093 Zürich, Switzerland
E-mail: gruetzmacher@inorg.chem.ethz.ch
Dalton Trans., 2012,41, 14137-14145
DOI:
10.1039/C2DT31691A
Received
26 Jul 2012,
Accepted
13 Sep 2012
First published online
14 Sep 2012
Acids, esters and amides have to date been the only isolated products from the dehydrogenation of primary alcohols with [Rh(trop2N)(L)] (trop = 5-H-dibenzo[a,d]cyclohepten-5yl) type complexes. With the reported method the available product family is finally to aldehydes. Using nitrosobenzene as a hydrogen acceptor the aldehydes could be isolated in up to 96% yield with substrate to catalyst ratios of up to 1000. Nitrosobenzene was found to be reductively coupled to azoxybenzene under the reaction conditions. Several symmetrically substituted azoxybenzene derivatives could be isolated in generally high yields after 2 to 4 h reaction time using a low catalyst loading.
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