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9-Anthroylacetone and its photodimer

Academic Article
Publication Date:
2004
abstract:
9-Anthroylacetone undergoes a head-to-tail [4pC4p] photo-dimerisation reaction that leads to the formation of 5,11-bis(1,3- diketobutyl)-5,6,11,12-tetrahydro-5,12,6,11-di-o-benzeno-dibenzo[a,e]cyclooctene both in solution and in the solid state when irradiated with different sources (sunlight, tungsten lamp, xenon lamp, UV laser beam 351-364 nm), the reaction being accompanied by a colour variation from bright yellow to colourless. Quantum yieldsO0.023 mol/Einstein are evaluated for the solid state reaction. Interestingly, the dimer dissociates to give 9-anthroylacetone, both thermally (TO130 8C) and photochemically, by short UV wavelength irradiation. The single-crystal X-ray structure of 9-anthroylacetone and its dimer are reported. q 2004 Elsevier Ltd. All rights reserved.
Iris type:
01.01 Articolo in rivista
Keywords:
Anthracene derivatives; Anthracene photo-dimerisation; Photochromism.
List of contributors:
Cicogna, Francesca
Authors of the University:
CICOGNA FRANCESCA
Handle:
https://iris.cnr.it/handle/20.500.14243/226844
Published in:
TETRAHEDRON (OXF., ONLINE)
Journal
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