D˙–A radicals fabricated from polychlorinated trityl and pyridinium featuring a SOMO–LUMO electronic transition
Abstract
D˙–A radicals 2a–2c were developed by combining polychlorinated trityl as a donor with pyridinium as an acceptor. The electron-deficient nature of the pyridinium unit significantly lowers the LUMO energy, thereby enabling SOMO–LUMO (α-type) electronic transitions, in contrast to conventional luminescent radicals that predominantly exhibit HOMO–SUMO (β-type) transitions.

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