Journal of Photosciences

TiO2-Mediated Photoreactions of Cinnamic Acid and Related Compounds in Methanol

Volume 10(2003), 181-184 page

ÀúÀÚ: Sung Sik Kim, Hyun Jin Kim, Hye Jong Lee, and Sang Kyu Park

   10-2-181.pdf (83.2K)

Keywords: titanium dioxide  trans-cinnamic acid  trans-cinnamamide  trans-cinnamaldehyde  1-naphthaldehyde  2-naphthaldehyde  9-anthraldehyde


Photochemical reactions of some organic molecules on titanium dioxide were investigated in methanol. A methanolic solution of trans-cinnamic acid and titanium dioxide was irradiated with 300 nm UV lamps for 24 h to afford methyl cinnamate. In the case of trans-cinnamamide, the major product was found to be 3-phenylpropionamide, i.e., a saturation product of ethylenic double bond. However, irradiation of urocanic acid, caffeic acid, ethyl cinnamate, trans-chalcone, trans-cinnamonitrile, trans-stilbene or trans,trans-1,4-diphenyl-1,3-butadiene on titanium dioxide under the same conditions did not give any noticeable products. Meanwhile, when irradiated some aromatic aldehydes, such as trans-cinnamaldehyde, 1-naphthaldehyde, and 2-naphthaldehyde in methanol, vicinal diols and alcohols derived from the diols were produced. On the other hand, irradiation of 9-anthraldehyde and titanium dioxide in methanol afforded only alcohols, in which diol was not observed.