A new class of luminescent dyes incorporates aromatic residues attached by an ethynyl link to the boron center of a subphthalocyanine (SubPc; see picture). Efficient energy transfer from energy-donor subunits to the SubPc produces very large Stokes shifts, while luminescence quantum yields are maintained. An acid-triggered “switching on” of SubPc emission occurs when a dibutylamino fragment is axially coordinated to the SubPc.
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Camerel et al. (2008) studied this question.
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