3.9 Article

Product Selectivity in Solar Photocatalytic Dehydrazonation of Aromatic Hydrazones by TiO2-Based Catalysts

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15533174.2013.768650

Keywords

azine; dehydrazonation; product selectivity; solar light

Funding

  1. CSIR, New Delhi [21(0799)/10/EMR-II]

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Product selectivity of ketone and azine in the photocatalytic dehydrazonation of aromatic hydrazones with TiO2-based photocatalysts has been investigated using solar light. Product selectivity is dependent on the nature of the photocatalysts, substituents and the solvents. Loading of metals on TiO2-P25 selectively enhances the formation of azine from benzophenone hydrazone. Solvents such as dichloromethane, chloroform, ethanol, and 2-propanol enhance the formation of azine under solar irradiation. Structures of products have been established by FT-IR, H-1-NMR, C-13-NMR, and GC-MS spectrometry. Supplementary materials are available for this article. Go to the publisher's online edition of Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry to view the supplemental file.

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