4.8 Article

Exclusive production of chloroaniline from chloronitrobenzene over Au/TiO2 and Au/Al2O3

Journal

CHEMSUSCHEM
Volume 1, Issue 3, Pages 215-221

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.200700105

Keywords

gold; heterogeneous catalysis; hydrogenation; supported catalysts

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The gas-phase continuous hydrogenation of p-chloronitrobenzene (p-CNB) over 1 mol% Au/TiO2 and Au/Al2O3 was compared for the first time. Both catalysts exhibit 700916 selectivity in terms of -NO2 group reduction, resulting in the sole formation of p-chloroaniline (p-CAN). Au/TiO2 exhibited a narrower particle size (1-10 nm) distribution than Au/Al2O3 (1-20nm) and a smaller surface-area-weighted mean Au size (6 nm versus 9 nm). Au/TiO2 delivered a higher specific hydrogenation rate (by a factor of up to four), a response that is discussed in terms of Au particle size and a possible contribution of the support to p-CNB activation. A CNB isomer reactivity sequence was established, that is, o > p > m, which is attributed to resonance stabilisation effects. The results presented establish a basis for the development of a sustainable alternative route for the production of haloamines.

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