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.
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CITATION STYLE
Kamm, P. W., Rodrigues, L. L., Walden, S. L., Blinco, J. P., Unterreiner, A. N., & Barner-Kowollik, C. (2022). Sequence-independent activation of photocycloadditions using two colours of light. Chemical Science, 13(2), 531–535. https://doi.org/10.1039/d1sc06154b
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