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Light-induced electron transfer occurs in bifunctional compounds consisting of 1,3-diphenylpropanedioato boron oxalate or fluoride electron acceptors and simple aromatic electron-donor groups, linked by a methylene bridge; fluorescence from the highly polar charge-transfer excited state is remarkably efficient and shows an exceptionally large solvatochromicity.

Highly solvatochromic emission of electron donor–acceptor compounds containing propanedioato boron electron acceptors