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Calculations at the theoretical gold standard generally yield accurate results for a variety of energy-transfer processes in molecular collisions. Using anti-seeding methods in a crossed-beam inelastic scattering experiment, a resonance structure is clearly resolved for NO–H₂ collisions, pushing the required accuracy for theoretical potentials beyond the gold standard.

When molecules collide with atoms or other molecules their quantum mechanical character can lead to the diffraction of matter waves. Making use of advances in molecular beam technology, such diffraction oscillations have now been observed with unprecedented sharpness and angular resolution in the benchmark NO + He, Ne, or Ar systems.

Long-lived molecular collision complexes — or ‘resonances’ — are difficult to identify experimentally. Now crossed-beam experiments and quantum calculations are reported for rotationally inelastic CO−He collisions at energies corresponding to temperatures as low as 4 K. Quantum dynamical resonances that are predicted by theory were detected and fully characterized.

Stereodynamics describes how the vector properties of molecules affect the probabilities of specific processes in molecular collisions. Measurements of irregular diffraction patterns for NO radicals colliding with rare-gas atoms reveal a previously unrecognized type of quantum stereodynamics and a ‘propensity rule’ for the magnetic quantum number (m) of the molecules.

Experimentally following the ultrafast dynamics of microsolvated molecules is challenging due to the inherently produced soup mix of various gas-phase aggregates. Here, the authors exploit neutral-species selection to reveal intimate details of the UV-induced ultrafast dynamics in the prototypical indole-water system.

Field-free 3D alignment of complex molecules is an important step toward the imaging of molecular dynamics. Here, the authors demonstrate pulse-shaping of long picosecond pulses for the 3D field-free alignment of the prototypical non-rotation-symmetric molecule indole.

Interaction of strong laser fields with matter provides powerful tools to image transient dynamics with high spatiotemporal resolution. The authors investigate strong-field ionisation of laser-aligned molecules showing the effect of molecular alignment on the photoelectron dynamics and the resulting influence of the molecular frame in imaging experiments.