Vibrational wave-packet dynamics of the silver pentamer probed by femtosecond NeNePo spectroscopy.

Vibrational wave-packet dynamics on the ground electronic state of the neutral silver pentamer (Ag5) are studied by femtosecond (fs) pump-probe spectroscopy using the 'negative ion - to neutral - to positive ion' (NeNePo) excitation scheme. A vibrational wave packet is prepared on the 2A1 state of Ag5via photodetachment of mass-selected, cryogenically cooled Ag5- anions using a fs pump pulse. The temporal evolution of the vibrational wave packet is then probed by an ultrafast probe pulse via resonant multiphoton ionization to Ag5+. Frequency analysis of the fs NeNePo transients for pump-probe delay times from 0.2 to 8 ps reveals three primary beating frequencies at 157 cm-1, 101 cm-1 and 56 cm-1 as well as four weaker features. A comparison of these experimentally obtained beating frequencies to harmonic normal mode frequencies calculated from electronic structure calculations confirms that Ag5 in the gas phase adopts a planar trapezoidal geometry, similar to that previously observed in solid argon. The dependence of the ionization yield on the laser polarization indicates a s-d wave electron photodetachment from a 'p-type' occupied molecular orbital of Ag5. Franck-Condon analysis shows that both processes, photodetachment and subsequent photoionization determine the beating frequencies probed in the time-dependent cation yield. The present study extends the applicability of fs NeNePo spectroscopy to characterize the vibrational spectra in the far-IR frequency range in the absence of perturbations from a medium or a messenger atom to mass-selected neutral metal clusters with more than three atoms in the ground electronic states.

High-Resolution Photoelectron Spectroscopy of Vibrationally Excited Vinoxide Anions.

High-resolution photoelectron spectra of vibrationally pre-excited vinoxide anions (CH2CHO-) are reported using the recently developed IR-cryo-SEVI technique. This method is combined with a newly developed implementation of vibrational perturbation theory that can readily identify relevant anharmonic couplings among nearly degenerate vibrational states. IR-cryo-SEVI spectra are obtained by resonant infrared excitation of vinoxide anions via the fundamental C-O (ν4, 1566 cm-1) or isolated C-H (ν3, 2540 cm-1) stretching vibrations prior to photodetachment. Excitation of the ν4 mode leads to a well-resolved photoelectron spectrum that is in excellent agreement with a harmonic Franck-Condon simulation. Excitation of the higher-energy ν3 mode results in a more complicated spectrum that requires consideration of the calculated anharmonic resonances in both the anion and the neutral. From this analysis, information about the zeroth-order states that contribute to the nominal ν3 wave function in the anion is obtained. In the neutral, we observe anharmonic splitting of the ν3 fundamental into a polyad feature with peaks at 2737(22), 2 835(18), and 2910(12) cm-1, for which only the center frequency has been previously reported. Overall, 9 of the 12 fundamental frequencies of the vinoxy radical are extracted from the IR-cryo-SEVI and ground-state cryo-SEVI spectra, most of which are consistent with previous measurements. However, we provide a new estimate of the ν5 (CH2 scissoring) fundamental frequency at 1395(11) cm-1 and attribute the discrepancy with previously reported values to a Fermi resonance with the 2ν11 overtone (CH2 wagging).

Photoelectron spectroscopy of cryogenically cooled NiO2-via slow photoelectron velocity-map imaging.

High-resolution anion photoelectron spectra of cryogenically cooled NiO2- anions, obtained using slow photoelectron velocity-map imaging (cryo-SEVI), are presented in tandem with coupled cluster electronic structure calculations including relativistic effects. The experimental spectra encompass the X̃1Σg+ ← X̃2Πg, ã3Πg ← X̃2Πg, and Ã1Πg ← X̃2Πg photodetachment transitions of linear ONiO0/-, revealing previously unobserved vibrational structure in all three electronic bands. The high-resolution afforded by cryo-SEVI allows for the extraction of vibrational frequencies for each state, consistent with those previously measured in the ground state and in good agreement with scalar-relativistic coupled-cluster calculations. Previously unobserved vibrational structure is observed in the ã3Πg and Ã1Πg states and is tentatively assigned. Further, a refined electron affinity of 3.0464(7) eV for NiO2 is obtained as well as precise term energies for the ã and à states of NiO2 of 0.3982(7) and 0.7422(10) eV, respectively. Numerous Franck-Condon forbidden transitions involving the doubly degenerate ν2 bending mode are observed and ascribed to Herzberg-Teller coupling to an excited electronic state.

High Resolution Photoelectron Spectroscopy of the Acetyl Anion.

High-resolution photoelectron spectra of cryogenically cooled acetyl anions (CH3CO-) obtained using slow photoelectron velocity-map imaging are reported. The high resolution of the photoelectron spectrum yields a refined electron affinity of 0.4352 ± 0.0012 eV for the acetyl radical as well as the observation of a new vibronic structure that is assigned based on ab initio calculations. Three vibrational frequencies of the neutral radical are measured to be 1047 ± 3 cm-1 (ν6), 834 ± 2 cm-1 (ν7), and 471 ± 1 cm-1 (ν8). This work represents the first experimental measurement of the ν6 frequency of the neutral. The measured electron affinity is used to calculate a refined value of 1641.35 ± 0.42 kJ mol-1 for the gas-phase acidity of acetaldehyde. Analysis of the photoelectron angular distributions provides insight into the character of the highest occupied molecular orbital of the anion, revealing a molecular orbital with strong d-character. Additionally, details of a new centroiding algorithm based on finite differences, which has the potential to decrease data acquisition times by an order of magnitude at no cost to accuracy, are provided.

High-Resolution Photoelectron Spectroscopy of Vibrationally Excited OH.

The effect of vibrational pre-excitation of anions on their photoelectron spectra is explored, combining slow photoelectron velocity-map imaging of cryogenically cooled anions (cryo-SEVI) with tunable IR radiation to pre-excite the anions. This new IR cryo-SEVI method is applied to OH- as a test system, where the R(0) transition of the hydroxyl anion (3591.53 cm-1) is pumped. Vibrational excitation induces a 30% depletion in photodetachment signal from the v = 0, J = 0 ground state of the anion and the appearance of all five allowed, rotationally resolved photodetachment transitions from the OH- (v = 1, J = 1) level, each with peak widths between 1 and 2 cm-1. By scanning the IR laser, IR cryo-SEVI can also serve as a novel action technique to obtain the vibrational spectrum of OH-, giving an experimental value for the R(0) transition of 3591(1.2) cm-1.

Electronic structure of NdO via slow photoelectron velocity-map imaging spectroscopy of NdO--.

Electronically excited NdO is a possible product of the chemistry associated with the release of Nd into the ionosphere, and emission from these states may contribute to the observations following such experiments. To better characterize the energetics and spectroscopy of NdO, we report a combined experimental and theoretical study using slow photoelectron velocity-map imaging spectroscopy of cryogenically cooled NdO- anions (cryo-SEVI) supplemented by wave function-based quantum-chemical calculations. Using cryo-SEVI, we measure the electron affinity of NdO to be 1.0091(7) eV and resolve numerous transitions to low-lying electronic and vibrational states of NdO that are assigned with the aid of the electronic structure calculations. Additionally, temperature-dependent data suggest contributions from the (2)4.5 state of NdO- residing 2350 cm-1 above the ground anion state. Photodetachment to higher-lying excited states of NdO is also reported, which may help to clarify observations from prior release experiments.

Observation of resonances in the transition state region of the F + NH3 reaction using anion photoelectron spectroscopy.

The transition state of a chemical reaction is a dividing surface on the reaction potential energy surface (PES) between reactants and products and is thus of fundamental interest in understanding chemical reactivity. The transient nature of the transition state presents challenges to its experimental characterization. Transition-state spectroscopy experiments based on negative-ion photodetachment can provide a direct probe of this region of the PES, revealing the detailed vibrational structure associated with the transition state. Here we study the F + NH3 → HF + NH2 reaction using slow photoelectron velocity-map imaging spectroscopy of cryogenically cooled FNH3- anions. Reduced-dimensionality quantum dynamical simulations performed on a global PES show excellent agreement with the experimental results, enabling the assignment of spectral structure. Our combined experimental-theoretical study reveals a manifold of vibrational Feshbach resonances in the product well of the F + NH3 PES. At higher energies, the spectra identify features attributed to resonances localized across the transition state and into the reactant complex that may impact the bimolecular reaction dynamics.

High-Resolution Photoelectron Spectroscopy of Cryogenically Cooled NO3Ì .

High-resolution anion photoelectron spectra of cryogenically cooled NO3̅ anions obtained using slow photoelectron velocity-map imaging are presented and provide new insight into the vibronic structure of the corresponding neutral radical. A combination of improved spectral resolution, measurement of energy-dependent intensity effects, temperature control, and comparison to theory allows for full assignment of the vibronic features observed in this spectrum. We obtain a refined electron affinity of 3.9289(14) eV for NO3. Further, the appearance of Franck-Condon forbidden transitions from vibrationally cold anions to neutral states with excitation along the NO3 ν4 mode confirms that these features arise from vibronic coupling with the B̃2E' excited state of NO3 and are not hot bands, as has been suggested. Together, the suite of experimental and simulated results provides clear evidence that the ν3 fundamental of NO3 resides near 1050 cm-1, addressing a long-standing controversy surrounding this vibrational assignment.