The majority of binary chalcogen fluorides are fiercely reactive and extremely difficult to handle. Here, we show that access to crystalline donor-acceptor complexes between chalcogen difluorides (sulfur, selenium) and tetrafluorides (selenium, tellurium) with the N-heterocyclic carbene (NHC) 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr) is possible conveniently and safely without the need to generate the highly unstable EF2 (E=S, Se) or the very toxic and corrosive SeF4 .
Keywords: N-heterocyclic carbine; fluorine; selenium; sulphur; tellurium.
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