Published Date
Coordination Chemistry Reviews March–April 2012, Vol.256(5):759–770,doi:10.1016/j.ccr.2011.11.009 Recent Developments in Organometallic Chemistry: 2012 Review Author
Ying-Li Rao
Hazem Amarne
Suning Wang,
Department of Chemistry, Queen's University, Kingston, Ontario K7L 3N6, Canada
Received 14 August 2011. Revised 9 November 2011. Accepted 10 November 2011. Available online 9 December 2011.
Abstract Four-coordinate organoboron compounds with a N,C-chelate backbone have been found recently to display an unusual photoisomerization phenomenon with a distinct change of color. The photoisomerization process is thermally reversible, enabling the potential use of this class of compounds as a new class of photo-responsive materials. This review provides an account of our recent investigation on the effect of substitution, π-conjugation and metal chelation on the photoisomerization process of the N,C-chelate organoboron compounds. The photoisomerization phenomenon of azobenzene-based organoboron compounds will also be presented. Graphical abstract
Highlights
► Photoisomerization of azobenzene organoboron compounds. ► Photochromic phenyl-pyridyl (ppy) chelate boron compounds, the role of the mesityl groups, substitution and π-conjugation effect. ► Alternative photoisomerization pathways in photochromic B-ppy compounds. ► Polyboryl systems and heterocyclic chelate systems. ► Impact of metal chelation on photoisomerization.
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