Evidence for Triplet Sensitization in the Visible-Light-Induced [2+2] Photocycloaddition of Eniminium Ions

Angew Chem Int Ed Engl. 2018 Jan 15;57(3):827-831. doi: 10.1002/anie.201710441. Epub 2017 Dec 13.

Abstract

Εniminium ions were prepared from the corresponding α,β-unsaturated carbonyl compounds (enones and enals), and were found to be promoted to their respective triplet states by energy transfer. The photoexcited intermediates underwent intra- or intermolecular [2+2] photocycloaddition in good yields (50-78 %) upon irradiation at λ=433 nm or λ=457 nm. Iridium or ruthenium complexes with a sufficiently high triplet energy were identified as efficient catalysts (2.5 mol % catalyst loading) for the reaction. The intermolecular [2+2] photocycloaddition of an eniminium ion derived from a chiral secondary amine proceeded with high enantioselectivity (88 % ee).

Keywords: cycloaddition; enantioselectivity; enones; homogenous catalysis; photochemistry.

Publication types

  • Research Support, Non-U.S. Gov't