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Visualizing molecular transformations in real-time requires a structural retrieval method with {AA}ngstrom spatial and femtosecond temporal atomic resolution. Imaging of hydrogen-containing molecules additionally requires an imaging method that is sensitive to the atomic positions of hydrogen nuclei, with most methods possessing relatively low sensitivity to hydrogen scattering. Laser-induced electron diffraction (LIED) is a table top technique that can image ultrafast structural changes of gas-phase polyatomic molecules with sub-{AA}ngstrom and femtosecond spatiotemporal resolution together with relatively high sensitivity to hydrogen scattering. Here, we image the umbrella motion of an isolated ammonia molecule (NH$_3$) following its strong field ionization. Upon ionization of a neutral ammonia molecule, the ammonia cation (NH$_3^+$) undergoes an ultrafast geometrical transformation from a pyramidal ($Phi_{HNH} = 107 ^circ$) to planar ($Phi_{HNH}=120^circ$) structure in approximately 8 femtoseconds. Using LIED, we retrieve a near-planar ($Phi_{HNH}=117 pm 5^circ$) field-dressed NH$_3^+$ molecular structure $7.8-9.8$ femtoseconds after ionization. Our measured field-dressed NH$_3^+$ structure is in excellent agreement with our calculated equilibrium field dressed structure using quantum chemical ab initio calculations.
We address the feasibility of imaging geometric and orbital structure of a polyatomic molecule on an attosecond time-scale using the laser induced electron diffraction (LIED) technique. We present numerical results for the highest molecular orbitals
Structural information on electronically excited neutral molecules can be indirectly retrieved, largely through pump-probe and rotational spectroscopy measurements with the aid of calculations. Here, we demonstrate the direct structural retrieval of
Photoelectron Angular Distributions (PADs) resulting from 800 nm and 1300 nm strong field ionization of impulsively aligned CF$_3$I molecules were analyzed using time-dependent density functional theory (TDDFT). The normalized difference between the
Knowledge of molecular structure is paramount in understanding, and ultimately influencing, chemical reactivity. For nearly a century, diffractive imaging has been used to identify the structures of many biologically-relevant gas-phase molecules with
The ultrafast photoinduced ring-opening of 1,3-cyclohexadiene constitutes a textbook example of electrocyclic reactions in organic chemistry and a model for photobiological reactions in vitamin D synthesis. Here, we present direct and unambiguous obs