Chemically reversible binding of H 2 S to a zinc porphyrin complex: towards implementation of a reversible sensor via a "coordinative-based approach".

Binding of hydrogen sulfide (H2 S) to a zinc porphyrin complex and the stabilization of the related zinc hydrosulfido adduct are explored. High-resolution MALDI Fourier transform ion cyclotron resonance mass spectrometry (HR MALDI-FT-ICR) and1 H NMR experiments provide evidence that HS- coordination occurs at the zinc centre. The coordination of HS- occurs in a reversible manner and modulates fluorescence emission of a tetra(N-methylpyridyl)porphine zinc complex (TMPyPZn). The results highlight the potential of TMPyPZn and related systems for the implementation of fast and simple H2 S sensors via a coordinative-based approach.