Electron photodetachment photoelectron

Determination of the Singlet-Triplet Gap in TMM by Electron Photodetachment Photoelectron Spectroscopy ... 

Electron photodetachment upon laser excitation of the solvent anion above 1.76 eV was observed (Fig. 2a,c) [18]. The cross section of photodetachment linearly increases between 1.76 and 3 eV (Fig. 2b). Under the same physical conditions, the photodetachment and absorption spectra of the solvent anion are identical (Fig. 2b) [20], suggesting a bound-to-CB transition the quantum yield of the photodetachment is close to unity. The photodetachment spectrum is similar to the photoelectron spectra of (C02) 9 clusters observed by Tsukuda et al. [24] in the gas phase it is distinctly different from the electron photodetachment spectra of CO2 in hydrocarbon liquids [27]. This suggests that a C-C bound, 7)2, symmetric dimer anion constitutes the core of the solvent radical anion [18,19]. 

The electronic structure of several model complexes for mononuclear iron proteins has been evaluated by gas-phase photodetachment photoelectron spectroscopy. Molecules of interest are negatively charged, such as Fe(SCN)3, Fe(SCN)4, and Fe(SCN)4. The anions were transported into the gas phase by electrospray ionization isolated Fe(SCN)4 was not detected in the gas phase, but rather was trapped as the stabilized ion pair Na+ [Fe(SCN)4 ]. 

TABLE 8.2 Atomic Electron Affinities (in eV) Determined by Photodetachment, Photoelectron Spectroscopy and Surface Ionization Techniques [4, 7 12]... 

Photoelectron spectroscopy, the measurement of the intensity and energy of electrons photodetached from an ion by a fixed-energy photon beam. 

Electron detachment from anionic mono-, di-, and trinucleotides was studied experimentally by electrospray photodetachment photoelectron spectroscopy (EPPS) [74]. Substrates did not decompose at the relatively low temperatures of these experiments. 

From a historical perspective, the first unambiguous observation of dipole states came from the group of Kit Bowen (Johns Hopkins) in 1990, who studied the important water dimer dipole anion. The Bowen group has also studied ground state dipole-bound anions produced by electron attachment under high-pressure nozzle-jet expansion condition. They have also used photodetachment photoelectron spectroscopy to determine electron affinities for a number of the molecules shown in Figure 4. 

The electron affinities listed in the table below agree within the error limits given. They were obtained by laser photoelectron spectroscopy (LPES) on the PHg ion [19] and PH2 photodetachment using a tunable laser (LPD) [20, 21] or an Xe arc lamp (with a grating monochromator) [21] and ion cyclotron resonance (ICR) spectrometry [20, 21]. All values are reported in two reviews on electron affinities [22] and electron photodetachment [23], and may be considered as adiabatic (see the remarks below the table) ... 

When treating ion spectroscopy one should not forget anions. Similar spectroscopic techniques may be used as for cation spectroscopy. For instance dissociation spectroscopy is also possible for molecular anions. Since excited anionic electronic states mostly do not exist, one uses infrared multiphoton dissociation to study vibrational levels of the ground state. Another interesting technique is the photoelectron spectroscopy of anions (photodetachment photoelectron spectroscopy), which exhibit a very specific feature. This technique differs from cation <— neutral photoelectron spectroscopy in two respects (i) the final state is a neutral one thus anion photoelectron spectroscopy delivers information about neutrals rather than ionic systems, (ii) The initial state is anionic thus mass selection before spectroscopy is possible. As a result, mass selective spectroscopic information of neutral molecular systems is supplied which otherwise is not accessible. This is of particular interest for neutral systems which are only available in complex mixtures or are short-lived intermediate reaction products or radicals. 

ZEKE (zero kinetic energy) photoelectron spectroscopy has also been applied to negative ions [M]. In ZEKE work, the laser wavelengdi is swept tlirough photodetachment thresholds and only electrons with near-zero kinetic energy are... 

Anion photoelectron spectroscopy [37, 38] amd photodetachment techniques [39] provide accurate information on electron detachment energies of negative ions. Ten closed-shell ainions considered here exhibit sharp peaks, indicative of minor or vanishing final-state nuclear rearrangements, in their photoelectron spectra. Comparisons between theory and experiment are straiightforward, for differences between vertical and adiabatic electron detachment energies (VEDEs and AEDEs, respectively) are small. 

A second role for mass spectrometry in the investigation of reactive intermediates involves the nse of spectroscopy. Althongh an important nse of ion spectroscopy is the determination of thermochemical properties, including ionization energies (addition or removal of an electron), as in photoelectron or photodetachment spectroscopy, and bond dissociation energies in ions, as in photodissociation methods, additional spectroscopic data can also often be obtained, inclnding structural parameters such as frequencies and geometries. 

Sofar the imaging results of Fig. 3.1 were discussed in very classical terms, using the notion of a set of trajectories that take the electron from the atom to the detector. However, this description does not do justice to the fact that atomic photoionization is a quantum mechanical proces. Similar to the interference between light beams that is observed in Young s double slit experiment, we may expect to see the effects of interference if many different quantum paths exist that connect the atom to a particular point on the detector. Indeed this interference was previously observed in photodetachment experiments by Blondel and co-workers, which revealed the interference between two trajectories by means of which a photo-detached electron can be transported between the atom and the detector [33]. The current case of atomic photoionization is more complicated, since classical theory predicts that there are an infinite number of trajectories along which the electron can move from the atom to a particular point on the detector [32,34], Nevertheless, as Fig. 3.2 shows, the interference between trajectories is observable [35] when the resolution of the experiment is improved [36], The number of interference fringes smoothly increases with the photoelectron energy. 

Anion photoelectron spectroscopy is conducted by crossing a mass-selected beam of negative ions with a fixed-frequency photon beam and energy-analyzing the resultant photodetached electrons (Figure 21-8). There are three main regions of such an apparatus the source that generates the anions to be studied, the mass... 

Following the above-mentioned spectroscopic study by Johnson and co-workers [55], Neumark and co-workers [56] explored the ultrafast real-time dynamics that occur after excitation into the CTTS precursor states of I (water) [n — 4-6) by applying a recently developed novel method with ultimate time resolution, i.e., femtosecond photoelectron spectroscopy (FPES). In anion FPES, a size-selected anion is electronically excited with a femtosecond laser pulse (the pump), and a second femtosecond laser pulse (the probe) induces photodetachment of the excess electron, the kinetic energy of which is determined. The time-ordered series of the resultant PE spectra represents the time evolution of the anion excited state projected on to the neutral ground state. In the study of 1 -(water), 263 nm (4.71 eV) and 790 nm (1.57 eV) pulses of 100 fs duration were used as pump and probe pulses, respectively. The pump pulse is resonant with the CTTS bands for all the clusters examined. 

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