Strong Coupling of the Mo Mo Stretching Mode to a Locally Confined Stokes Raman Field in Mo2 Molecular Resonators

Abstract

Confining optical fields to molecular dimensions is a central objective in nanophotonics and molecular quantum optics. Here, we report strong coupling of the Mo Mo stretching vibration to a locally confined Raman scattering field in quadruply bonded dimolybdenum complexes. Under ambient, cavity-free conditions, the dimolybdenum formamidinate complexes Mo2(DAniF)4 and Mo2(DTolF)4 exhibit Rabi-type splitting, Mollow-type sidebands, and higher-order Raman features centered near the Mo Mo stretching frequency of 400 cm-1, indicating formation of dressed vibration field states. The sideband displacements from the resonance follow the photon-number-dependent relation Ωn=Ωνn, consistent with Jaynes Cummings-type coupling, while strongly displaced Raman features are assigned to leapfrog transitions within the same dressed-state ladder. In contrast, the less polarizable Mo2(O2CCH3)4 complex exhibits essentially a single Mo Mo stretching band. Reanalysis of reported resonance Raman spectra of an alkynyl Mo2 complex further supports this coupling framework. These results suggest that the Mo2 unit simultaneously serves as the Raman active oscillator and the molecular resonator that supports, confines, and enhances the locally generated scattering field, providing spectroscopic evidence for vibration field coupling and optical-field confinement within a chemically defined metal metal bond.