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Accessing metal-specific orbital interactions in C–H activation with resonant inelastic X-ray scattering† Photochemically prepared transition-metal complexes are known to be effective at cleaving the strong C–H bonds of organic molecules in room temperature solutions.
The degree of electron itinerancy and shell closing in the core-ionized state of transition metals probed by Auger-photoelectron coincidence spectroscopy† Artur Born,‡abc Fredrik O. L.
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