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Sequence-independent activation of photocycloadditions using two colours of light
Authors:Philipp W Kamm  Leona L Rodrigues  Sarah L Walden  James P Blinco  Andreas-Neil Unterreiner  Christopher Barner-Kowollik
Institution:Centre for Materials Science, Queensland University of Technology (QUT), 2 George Street, Brisbane QLD 4000 Australia.; School of Chemistry and Physics, Queensland University of Technology (QUT), 2 George Street, Brisbane QLD 4000 Australia ; Molecular Physical Chemistry Group, Institute of Physical Chemistry, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 2, Geb. 30.44, Karlsruhe 76131 Germany,
Abstract:We exploit two reactive chromophores to establish sequence-independent photochemical activation, employing ortho-methyl benzaldehyde (oMBA) and N,N-(dimethylamino)pyrene aryl tetrazole (APAT) with N-(2-hydroxy)ethyl maleimide (NHEM), without any additives. Critically, the order of the irradiation sequence is irrelevant, as the shorter wavelength does not activate the higher wavelength activated species. Therefore, full sequence-independent λ-orthogonality is achieved through differences in both the reaction quantum yields (Φr,oMBA and Φr,APAT) and wavelength-dependent reactivity profiles of the employed chromophores.

We exploit two reactive chromophores to establish sequence-independent photochemical activation without any additives.
Keywords:
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