Biomedical subjects

Jeffrey M Headrick

Publications and source records attributed to Jeffrey M Headrick.

8 recordsLinked to original sources

PubMed2006

Determination of the CO3- bond strength via the resonant two-photon photodissociation threshold: Electronic and vibrational spectroscopy of CO3-.Ar(n).

We use a two-laser pump-probe technique coupled with messenger atom tagging to determine the bond energy of O(-) to CO(2) in the CO(3) (-) ion, a prevalent species in the upper atmosphere. In this technique, the argon-tagged ion is first electronically excited using a visible laser, then irradiated with a tunable near-infrared beam across the CO(2)...O(-) dissociation threshold while O(-) products are monitored. This method yields a bond energy of 2.79+/-0.05 eV, which is about 0.5 eV higher than previously reported. Combining this with the well-known heats of formation of O(-) and CO(2), 105.6 and -393.1 kJmol, respectively [Thermodynamic Properties of Individual Substances, edited by L. V. Gurvich, I. V. Veyts, and C. B. Alcock (Hemisphere, New York, 1989), Vol. 1 and CODATA Thermodynamic Tables, edited by O. Garvin, V. B. Parker, and J. H. J. White (Hemisphere, New York, 1987)], yields the CO(3) (-) heat of formation: DeltaH(0) (0)=-556.7+/-4.8 kJmol. The one-photon (i.e., linear) infrared and electronic spectra of CO(3) (-) are also presented and compared to those obtained previously. The one-photon electronic spectrum is nearly identical to two-photon spectra, implying that argon does not significantly perturb the ion or its symmetry. The infrared spectrum is drastically different than that obtained in an argon matrix, however, indicating that the ion is likely distorted in the matrix environment.

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PubMed2005

Vibrational predissociation spectroscopy of the (H2O)(6-21)- clusters in the OH stretching region: evolution of the excess electron-binding signature into the intermediate cluster size regime.

We report vibrational predissociation spectra of the (H2O)n- cluster ions in the OH stretching region to determine whether the spectral signature of the electron-binding motif identified in the smaller clusters [Hammer et al. Science 306, 675 (2004)] continues to be important in the intermediate size regime (n = 7-21). This signature consists of a redshifted doublet that dominates the OH stretching region, and has been traced primarily to the excitation of a single water molecule residing in a double H-bond acceptor (AA) binding site, oriented with both of its H atoms pointing toward the excess electron cloud. Strong absorption near the characteristic AA doublet is found to persist in the spectra of the larger clusters, but the pattern evolves into a broadened triplet around n = 11. A single free OH feature associated with dangling hydrogen atoms on the cluster surface is observed to emerge for n > or = 15, in sharp contrast to the multiplet pattern of unbonded OH stretches displayed by the H+(H2O)n clusters throughout the n = 2-29 range. We also explore the vibration-electronic coupling associated with normal-mode displacements of the AA molecule that most strongly interact with the excess electron. Specifically, electronic structure calculations on the hexamer anion indicate that displacement along the -OH2 symmetric stretching mode dramatically distorts the excess electron cloud, thus accounting for the anomalously large oscillator strength of the AA water stretching vibrations. We also discuss these vibronic interactions in the context of a possible relaxation mechanism for the excited electronic states involving the excess electron.

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PubMed2005

Spectral signatures of hydrated proton vibrations in water clusters.

The ease with which the pH of water is measured obscures the fact that there is presently no clear molecular description for the hydrated proton. The mid-infrared spectrum of bulk aqueous acid, for example, is too diffuse to establish the roles of the putative Eigen (H3O+) and Zundel (H5O2+) ion cores. To expose the local environment of the excess charge, we report how the vibrational spectrum of protonated water clusters evolves in the size range from 2 to 11 water molecules. Signature bands indicating embedded Eigen or Zundel limiting forms are observed in all of the spectra with the exception of the three- and five-membered clusters. These unique species display bands appearing at intermediate energies, reflecting asymmetric solvation of the core ion. Taken together, the data reveal the pronounced spectral impact of subtle changes in the hydration environment.

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PubMed2005

Photoelectron spectroscopy of the [glycine x (H2O)(1,2)]- clusters: sequential hydration shifts and observation of isomers.

The electron binding energies of the small hydrated amino acid anions, [glycine x (H2O)(1,2)]-, are determined using photoelectron spectroscopy. The vertical electron detachment energies (VDEs) are found to increase by approximately 0.12 eV with each additional water molecule such that the higher electron binding isomer of the dihydrate is rather robust, with a VDE value of 0.33 eV. A weak binding isomer of the dihydrate is also recovered, however, with a VDE value (0.14 eV) lower than that of the monohydrate. Unlike the situation in the smaller (n < or = 13) water cluster anions, the [Gly x (H2O)(n > or = 6)]- clusters are observed to photodissociate via water monomer evaporation upon photoexcitation in the O-H stretching region. We discuss this observation in the context of the mechanism responsible for the previously observed [S. Xu, M. Nilles, and K. H. Bowen, Jr., J. Chem. Phys. 119, 10696 (2003)] sudden onset in the cluster formation at [Gly x (H2O)5]-.

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PubMed2005

Fundamental excitations of the shared proton in the H3O2- and H5O2+ complexes.

We exploit recent advances in argon predissociation spectroscopy to record the spectroscopic signature of the shared proton oscillations in the H3O2- system and compare the resulting spectrum with that of the H5O2+ ion taken under similar conditions. Very intense 1 <-- 0 transitions are observed below 1100 cm(-1) in both cases and are surprisingly sharp, with the 697 cm(-1) transition in H3O2- being among the lowest in energy of any shared proton system measured to date. The assignments of the three fundamental transitions associated with the three-dimensional confinement of the shared proton in H3O2- are carried out with full-dimensional (DMC) calculations to treat this strongly anharmonic vibrational problem.

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PubMed2005

Argon predissociation spectroscopy of the OH-.H2O and Cl-.H2O complexes in the 1000-1900 cm(-1) region: intramolecular bending transitions and the search for the shared-proton fundamental in the hydroxide monohydrate.

We present argon predissociation vibrational spectra of the OH(-).H(2)O and Cl(-).H(2)O complexes in the 1000-1900 cm(-1) energy range, far below the OH stretching region reported in previous studies. This extension allows us to explore the fundamental transitions of the intramolecular bending vibrations associated with the water molecule, as well as that of the shared proton inferred from previous assignments of overtones in the higher energy region. Although the water bending fundamental in the Cl(-).H(2)O spectrum is in very good agreement with expectations, the OH(-).H(2)O spectrum is quite different than anticipated, being dominated by a strong feature at 1090 cm(-1). New full-dimensionality calculations of the OH(-).H(2)O vibrational level structure using diffusion Monte Carlo and the VSCF/CI methods indicate this band arises from excitation of the shared proton.

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PubMed2004

Predissociation spectroscopy of the argon-solvated H5O2+ "zundel" cation in the 1000-1900 cm(-1) region.

Predissociation spectra of the H5O2+.Ar(1,2) cluster ions are reported in the 1000-1900 cm(-1) region. The weakly bound argon atoms enable investigation of the complex in a linear action mode, and the resulting spectra are much simpler than those reported previously in this region [Asmis et al., Science 299, 1375 (2003) and Fridgen et al., J. Phys. Chem. A 108, 9008 (2004)], which were obtained using infrared multiphoton dissociation of the bare complex. The observed spectrum consists of two relatively narrow bands at 1080 and 1770 cm(-1) that are likely due to excitation of the shared proton and intramolecular bending vibrations of the two water molecules, respectively. The narrow linewidths and relatively small (60 cm(-1)) perturbation introduced by the addition of a second argon atom indicate that the basic "zundel" character of the H5O2+ ion survives upon complexation.

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PubMed2004

How do small water clusters bind an excess electron?

The arrangement of water molecules around a hydrated electron has eluded explanation for more than 40 years. Here we report sharp vibrational bands for small gas-phase water cluster anions, (H2O)(4-6)- and (D2O)(4-6)-. Analysis of these bands reveals a detailed picture of the diffuse electron-binding site. The electron is closely associated with a single water molecule attached to the supporting network through a double H-bond acceptor motif. The local OH stretching bands of this molecule are dramatically distorted in the pentamer and smaller clusters because the excited vibrational levels are strongly coupled to the electron continuum. The vibration-to-electronic energy transfer rates, as revealed by line shape analysis, are mode-specific and remarkably fast, with the symmetric stretching mode surviving for less than 10 vibrational periods [50 fs in (H2O)4-].

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