Breaking the Symmetry of Pyrimidine: Solvent Effects and Core-Excited State Dynamics
journal contributionposted on 02.09.2021, 13:04 by Sebastian Eckert, Vinícius Vaz da Cruz, Miguel Ochmann, Inga von Ahnen, Alexander Föhlisch, Nils Huse
Symmetry and its breaking crucially define the chemical properties of molecules and their functionality. Resonant inelastic X-ray scattering is a local electronic structure probe reporting on molecular symmetry and its dynamical breaking within the femtosecond scattering duration. Here, we study pyrimidine, a system from the C2v point group, in an aqueous solution environment, using scattering though its 2a2 resonance. Despite the absence of clean parity selection rules for decay transitions from in-plane orbitals, scattering channels including decay from the 7b2 and 11a1 orbitals with nitrogen lone pair character are a direct probe for molecular symmetry. Computed spectra of explicitly solvated molecules sampled from a molecular dynamics simulation are combined with the results of a quantum dynamical description of the X-ray scattering process. We observe dominant signatures of core-excited Jahn–Teller induced symmetry breaking for resonant excitation. Solvent contributions are separable by shortening of the effective scattering duration through excitation energy detuning.
Read the peer-reviewed publication
quantum dynamical descriptionobserve dominant signaturesaqueous solution environmentusing scattering thoughfemtosecond scattering durationeffective scattering durationmolecular dynamics simulationexcitation energy detuningdynamical breaking withinbreaking crucially defineray scattering process1 </ subresonant inelastic x2 </ subray scatteringresonant excitationv </c </></ sub>< subsolvent effectssolvent contributionspoint groupmolecular symmetrydirect probedecay transitionscomputed spectrachemical properties