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Dive into the research topics where Daniel P. Gerrity is active.

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Featured researches published by Daniel P. Gerrity.


Chemical Physics Letters | 1980

Multiphoton ionization of metal atoms produced in the photodissociation of group VI hexacarbonyls

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

Electronic spectra of butadiene and its methyl derivatives: A multiphoton ionization study

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

Electronic spectrum of furan from 2200 to 1950 Å

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

Gas phase multiphoton photodissociation of Mn2(CO)10: The effect of collisions on photofragmentation

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

Evidence of a state dependent depletion process in the two‐photon fluorescence excitation spectra of saturated amines

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

Effects of nonresonant ionization on multiphoton ionization line shapes

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

Role of the divalent metal ion in sugar binding, ring opening, and isomerization by D-xylose isomerase: replacement of a catalytic metal by an amino acid.

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

Ultraviolet-visible multiphoton dissociation of hexacarbonylchromium: experimental evidence for statistical fragmentation

Daniel P. Gerrity; L. J. Rothberg; Veronica Vaida


The Journal of Physical Chemistry | 1990

UV resonance Raman studies of Group 6 transition-metal carbonyls: evidence of Jahn-Teller distortion in the excited states of the lowest allowed charge-transfer transitions

David. Adelman; Daniel P. Gerrity


ChemInform | 1977

Structural studies of precursor and partially oxidized conducting complexes. 9. The new one-dimensional tetracyanoplatinates, M2[Pt(CN)4](FHF)0.39.xH2O (M = rubidium, cesium), and a new lower limit for the platinum-platinum separation (2.80 .ANG.)

Jack M. Williams; Daniel P. Gerrity; Arthur J. Schultz

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Veronica Vaida

University of Colorado Boulder

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Arnon Lavie

University of Illinois at Chicago

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Arthur J. Schultz

Argonne National Laboratory

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