Single-molecule spectroscopic study demonstrates direct tracking of transient Pd-PEPPSI intermediates at micromolar concentrations, revealing reactant-driven changes to catalytic mechanisms.
Single-molecule measurements on molecular catalysts are uniquely poised to allow observation of unsynchronized chemical dynamics and transient intermediates that are not observable using traditional bulk techniques. However, single-molecule fluorescence spectroscopy is typically performed at nanomolar concentrations, far lower than typical synthetic conditions. Here, we use nanophotonic zero-mode waveguides (ZMWs) to enable observation of the dynamics of a single catalyst under synthetically relevant (micromolar) reaction concentrations. We deploy ZMWs to perform the direct observation of a previously hypothesized intermediate of Pd-PEPPSI (Pyridine-Enhanced Precatalyst Preparation, Stabilization, and Initiation), a well-known molecular C–C cross-coupling catalyst, by using a fluorescently labeled ligand to report on ligand binding and dissociation. Kinetic analysis of single-catalyst ligand dynamics reveals how the presence of cross-coupling reactants influences the underlying mechanism. This paradigm for single-molecule investigation of molecular catalysts at synthetically relevant concentrations is general for investigation of a wide variety of ligand and reactant dynamics.
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Smith et al. (2026) studied this question.
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