Solution photochemistry of azulene - American Chemical Society

Department of Chemistry, University of Alabama in Huntsville, Huntsville, Alabama 35899. Received October 15,1993·. Photochemical reactivity has been...
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J. Org. Chem. 1994,59, 429-433

Solution Photochemistry of Azulene J. I. Selco, T. Brooks, M. Chang, and M. T. Trieu Department of Chemiatry, University of Redlands, P.O. Box 3080, Redlands, California 92373

J. K. McDonald‘ Weapons Sciences Directorate, AMSMI-RD- W S - C M , Research, Development, and Engineering Center, U.S. Army Missile Command, Redstone Arsenal, Alabama 35898-5248

S . P. McManus Department of Chemistry, University of Alabama in Huntsville, Huntsville, Alabama 36899 Received October 15, 1993.

Photochemical reactidty has been observed in solution-phase azulene. Experiments are described which confirm photoinduced deuteration, chlorination, and polymerization. The threshold for the observed chemistry is at the origin of 5 2 which is at 27956 f 8 cm-l(357.7 f 0.1 nm) in chloroform. Only one photon is required to induce the observed chlorine substitution reactions. Although no naphthalene is formed, this chemical channel appears to be the equivalent of a thermal reaction, with the substitutions taking place at the two equivalent positions on the small ring of azulene. The mechanism of these reactions is bimolecular in nature. Chlorination provides a complex mixture of producta in most cases; however, deuteration proceeds cleanly giving only 1,3-&-azulene.

Introduction Azulene 1 is a fused-ring, planar, aromatic isomer of naphthalene 2; both compounds have similar spectra in the ultraviolet which arise from U-T* electronic transitions.’ Naphthalene is not polar, while azulene has a

1

2

permanent dipole moment of 0.80 f 0.02 D, with the smaller of the two rings being the negative end of the molecule.2 As a result of ita permanent dipole and ita asymmetric structure, azulenehas an electronic transition in the visible. It is this trgnsition at 694 nm, resulting from an intramolecularcharge transfer, that is responsible for the blue color of azulene.I Azulene is probably the best known example of a molecule that does not obey Kasha’s Rule.3 The fluorescence quantum yield from the first excited singlet state, SI, is