Daniel P. Gerrity
Harvard University
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Featured researches published by Daniel P. Gerrity.
Chemical Physics Letters | 1980
Daniel P. Gerrity; L. J. Rothberg; Veronica Vaida
Abstract The photodissociation of M(CO) 6 , M = Cr or W, and the multiphoton ionization spectra of the resulting atoms M(I) have been studied using a tunable visible dye laser M(I) fragments are produced throughout the range between 363 and 585 nm, and multiphoton absorption allows all of the states formed to be probed.
Journal of Chemical Physics | 1980
L. J. Rothberg; Daniel P. Gerrity; Veronica Vaida
The multiphoton ionization (MPI) spectra of trans‐1,3‐butadiene and three of its methyl substituted derivatives have been recorded using a tunable visible dye laser. The effect of methyl substitution on the electronic structure of butadiene is investigated, resulting in a reassignment of the spectra of these molecules. Quantum defects are found to be independent of principal quantum number, indicating little mixing between Rydberg and core orbitals. The validity of retaining conventional s, p, d, and f descriptions of Rydberg orbitals in these quasilinear molecules is demonstrated. Two electronic states of butadiene, assigned to the 3d and 4s Rydberg states, are observed for the first time in optical spectroscopy. No evidence for an excited 1Ag valence state is found in the MPI spectra.
Chemical Physics Letters | 1980
J.L. Roebber; Daniel P. Gerrity; R. J. Hemley; Veronica Vaida
Abstract The electronic spectrum of furan is re-examined from 2200 to 1950 A via multiphoton ionization of the vapor and onephoton UV absorption of a supersonic jet. A new state found at 47700 cm −1 is assigned to the 1a 2 → 3s Rydberg. The vibratioral progression beginning at 45960 cm −1 on the low energy side of the N → V 1 band is tentatively assigned to that of the N → V 2 (π → π * ) transition.
Journal of Chemical Physics | 1981
L. J. Rothberg; Daniel P. Gerrity; Veronica Vaida
Multiphoton dissociation of Mn2(CO)10 followed by multiphoton ionization of the generated fragments is accomplished with a single tunable pulsed dye laser. Efficient dissociation to bare Mn atoms occurs over a broad range of wavelengths via a sequential photodissociation mechanism. Spectral changes upon addition of buffer gases are shown to reflect collisional effects on intermediates in the dissociation process.
Journal of Chemical Physics | 1982
Arthur M. Halpern; Daniel P. Gerrity; L. J. Rothberg; Veronica Vaida
The two‐photon fluorescence excitation (TPFE) spectra of regions of the ? states of two saturated amines 1‐azabicyclo [2.2.2]octane (ABCO) and trimethylamine (TMA) are reported. These spectra are compared with the respective one‐photon absorption (OPA), one‐photon fluorescence excitation (OPFE), and multiphoton ionization (MPI) spectra for both molecules. For ABCO, this comparison clearly indicates major differences in both the vibronic band intensities and the amount of sequence structure present in the TPFE spectrum relative to the MPI, OPA, and OPFE spectra, which are all comparable. The ’’distortions’’ of the TPFE spectrum are interpreted in terms of a laser‐induced ? state‐dependent depletion process from ? which results in ionization. Pressure effects on the TPFE spectrum imply that the rate of this up‐pumping process depends strongly upon the particular vibrational modes excited in the two‐photon‐induced ?←? transition. A further implication of this interpretation is that the intramolecular vibrati...
Journal of Chemical Physics | 1981
L. J. Rothberg; Daniel P. Gerrity; Veronica Vaida
A kinetics model of multiphoton ionization (MPI) is developed to account for nonresonant ionization and collisional rethermalization effects on MPI. Simple quantitative criteria to describe MPI line shapes are derived. In cases where resonantly enhanced MPI (REMPI) is not an effective spectroscopic tool, it is demonstrated that absorption can deplete ground state levels which would otherwise have contributed to nonresonant ionization. The resulting structured valleys in the ionization current contain spectroscopic and dynamical information which may otherwise be unattainable. The feasibility of depletion of nonresonant ionization (DNRI) as a general technique is investigated and the first experimental observations of DNRI are reported and analyzed.
Biochemistry | 1994
Karen N. Allen; Arnon Lavie; Arthur Glasfeld; Timothy N. Tanada; Daniel P. Gerrity; Steven C. Carlson; Gregory K. Farber; Gregory A. Petsko; Dagmar Ringe
The Journal of Physical Chemistry | 1983
Daniel P. Gerrity; L. J. Rothberg; Veronica Vaida
The Journal of Physical Chemistry | 1990
David. Adelman; Daniel P. Gerrity
ChemInform | 1977
Jack M. Williams; Daniel P. Gerrity; Arthur J. Schultz