1,4-Diphenyl-1-telluro-1,3-butadiene incorporated in a dibenzobarrelene skeleton was synthesized with a good yield by an intramolecular Diels–Alder reaction of the corresponding 1-(9-anthyltelluro)enyne. Oxidation and bromination of the telluride yielded telluroxide and hypervalent Te, Te -dibromide, respectively. Their structures were determined by X-ray crystallography. Unlike its highly fluorescent sulfur and selenium congeners, the telluride is barely fluorescent in solution at room temperature due to the heavy-atom effect of tellurium. The telluride displayed temperature-dependent fluorescence; it is fluorescent with a moderate quantum yield (Φ PL = 0.42) in the glass of 2-methyltetrahydrofuran at 77 K.
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Annaka et al. (2015) studied this question.
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