Aryl‐maleimides undergo a novel [2+4]‐photodimerization instead of the expected [2+2]‐photodimerization under both direct irradiation with visible light and under sensitized energy transfer conditions. This new excited state reactivity in aryl‐maleimides is deciphered through photochemical, photophysical, and spectroscopic studies. The stereochemistry of the photodimer depends on the type of non‐bonding interactions prevalent during photodimerization which is in turn dictated by the substituents on the maleimide ring. More importantly, the stereochemistry of the photodimer formed is complementary to the product observed under thermal conditions.
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Ahuja, Sapna ; Baburaj, Sruthy ; Valloli, Lakshmy Kannadi ; Rakhimov, Sarvar Aminovich ; Manal, Kavyasree ; Kushwaha, Aakrati ; Jockusch, Steffen ; Forbes, Malcolm D. E. ; Sivaguru, Jayaraman ( , Angewandte Chemie International Edition)
Abstract Aryl‐maleimides undergo a novel [2+4]‐photodimerization instead of the expected [2+2]‐photodimerization under both direct irradiation with visible light and under sensitized energy transfer conditions. This new excited state reactivity in aryl‐maleimides is deciphered through photochemical, photophysical, and spectroscopic studies. The stereochemistry of the photodimer depends on the type of non‐bonding interactions prevalent during photodimerization which is in turn dictated by the substituents on the maleimide ring. More importantly, the stereochemistry of the photodimer formed is complementary to the product observed under thermal conditions.
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Brugh, Alexander M. ; Wang, Ruobing ; Therien, Michael J. ; Forbes, Malcolm D. E. ( , ACS Omega)
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Forbes, Malcolm D. E. ( , ChemPhotoChem)