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Full-Text Articles in Social and Behavioral Sciences
Photoelectron-Photofragment Coincidence Studies Of No-_X Clusters (X = H2o, Cd4), Berwyck Poad, Christopher Johnson, Robert Continetti
Photoelectron-Photofragment Coincidence Studies Of No-_X Clusters (X = H2o, Cd4), Berwyck Poad, Christopher Johnson, Robert Continetti
Berwyck L. J. Poad
The dissociative photodetachment of NO -(H2O)and NO -(CD4) anion clusters was studied at 775 nm (1.60 eV) using photoelectron-photofragment coincidence spectroscopy. The correlation between the photoelectron and photodetached neutral spectra indicates vibrational excitation in the recoiling NO neutral fragments from NO-(H2O), with a progression consistent with vibrational excitation up to v(NO) = 3 in the products. The correlation remains when D2O is substituted for H2O, implying the NO vibrational mode plays a role in the dissociation coordinate of the complex. In contrast, no correlation was observed between photoelectron kinetic …
Ozone-Induced Dissociation On A Modified Tandem Linear Ion-Trap: Observations Of Different Reactivity For Isomeric Lipids, Berwyck Poad, Huong Pham, Michael Thomas, Jessica Hughes, J Campbell, Todd Mitchell, Stephen Blanksby
Ozone-Induced Dissociation On A Modified Tandem Linear Ion-Trap: Observations Of Different Reactivity For Isomeric Lipids, Berwyck Poad, Huong Pham, Michael Thomas, Jessica Hughes, J Campbell, Todd Mitchell, Stephen Blanksby
Berwyck L. J. Poad
Ozone-induced dissociation (OzID) exploits the gas-phase reaction between mass-selected lipid ions and ozone vapor to determine the position(s) of unsaturation. In this contribution, we describe the modification of a tandem linear ion-trap mass spectrometer specifically for OzID analyses wherein ozone vapor is supplied to the collision cell. This instrumental configuration provides spatial separation between mass-selection, the ozonolysis reaction, and mass-analysis steps in the OzID process and thus delivers significant enhancements in speed and sensitivity (ca. 30-fold). These improvements allow spectra revealing the double-bond position(s) within unsaturated lipids to be acquired within 1 s: significantly enhancing the utility of OzID in …
Communication: New Insight Into The Barrier Governing Co2 Formation From Oh + Co, Christopher Johnson, Berwyck Poad, Ben Shen, Robert Continetti
Communication: New Insight Into The Barrier Governing Co2 Formation From Oh + Co, Christopher Johnson, Berwyck Poad, Ben Shen, Robert Continetti
Berwyck L. J. Poad
Despite its relative simplicity, the role of tunneling in the reaction OH + CO → H + CO(2) has eluded the quantitative predictive powers of theoretical reaction dynamics. In this study a one-dimensional effective barrier to the formation of H + CO(2) from the HOCO intermediate is directly extracted from dissociative photodetachment experiments on HOCO and DOCO. Comparison of this barrier to a computed minimum-energy barrier shows that tunneling deviates significantly from the calculated minimum-energy pathway, predicting product internal energy distributions that match those found in the experiment and tunneling lifetimes short enough to contribute significantly to the overall reaction. …
Attachment Of Molecular Hydrogen To An Isolated Boron Cation: An Infrared And Ab Initio Study, Viktoras Dryza, Berwyck L. J Poad, Evan J. Bieske
Attachment Of Molecular Hydrogen To An Isolated Boron Cation: An Infrared And Ab Initio Study, Viktoras Dryza, Berwyck L. J Poad, Evan J. Bieske
Berwyck L. J. Poad
Structural properties of the B+−H2 electrostatic complex are investigated through its rotationally resolved infrared spectrum in the H−H stretch region (3905−3975 cm−1). The spectrum, which was obtained by monitoring B+ photofragments while the IR wavelength was scanned, is consistent with the complex having a T-shaped structure and a vibrationally averaged intermolecular separation of 2.26 Å, which decreases by 0.04 Å when the H2 subunit is vibrationally excited. The H−H stretch transition of B+−H2 is red-shifted by 220.6 ± 1.5 cm−1 from that of the free H2 molecule, much more than for other dihydrogen complexes with comparable binding energies. Properties of …
Interactions Between The Chloride Anion And Aromatic Molecules: Infrared Spectra Of The Cl-_C6h5ch3, Cl-_C6h5nh2 And Cl-_C6h5oh Complexes, Corinna Emmeluth, Berwyck L. J Poad, Christopher D. Thompson, Evan J. Bieske
Interactions Between The Chloride Anion And Aromatic Molecules: Infrared Spectra Of The Cl-_C6h5ch3, Cl-_C6h5nh2 And Cl-_C6h5oh Complexes, Corinna Emmeluth, Berwyck L. J Poad, Christopher D. Thompson, Evan J. Bieske
Berwyck L. J. Poad
The Cl-−C6H5CH3·Ar, Cl-−C6H5NH2·Ar, and Cl-−C6H5OH·Ar anion complexes are investigated using infrared photodissociation spectroscopy and ab initio calculations at the MP2/aug-cc-pVDZ level. The results indicate that for Cl-−C6H5NH2 and Cl-−C6H5OH, the Cl- anion is attached to the substituent group by a single near-linear hydrogen bond. For Cl-−C6H5CH3, the Cl- is attached to an ortho-hydrogen atom on the aromatic ring and to a hydrogen atom on the methyl group by a weaker hydrogen bond. The principal spectroscopic consequence of the hydrogen-bonding interaction in the three complexes is a red-shift and intensity increase for the CH, NH, and OH stretching modes. Complexities in …
Mixing Laser Spectroscopy And Mass Spectrometry- Infrared Spectra Of Metal Cation- Hydrogen Complexes, Vikoras Dryza, Berwyck Poad, Evan Bieske
Mixing Laser Spectroscopy And Mass Spectrometry- Infrared Spectra Of Metal Cation- Hydrogen Complexes, Vikoras Dryza, Berwyck Poad, Evan Bieske
Berwyck L. J. Poad
We describe recent experiments in which mass spectrometry and laser spectroscopy are combined to characterize Li(+)-H(2), Na(+)-H(2), B(+)-H(2), and Al(+)-H(2) complexes in the gas-phase. The infrared spectra, which feature full resolution of rotational sub-structure, are recorded by monitoring M(+) photo fragments as the infrared wavelength is scanned. The spectra deliver detailed information on the way in which a hydrogen molecule is attached to a metal cation including the intermolecular separation, the force constant for the intermolecular bond and the H-H stretching frequency. The complexes all possess T-shaped equilibrium geometries and display a clear correlation between the length and force constant …
Attaching Molecular Hydrogen To Metal Cations: Perspectives From Gas-Phase Infrared Spectroscopy, Viktoras Dryza, Berwyck Poad, Evan Bieske
Attaching Molecular Hydrogen To Metal Cations: Perspectives From Gas-Phase Infrared Spectroscopy, Viktoras Dryza, Berwyck Poad, Evan Bieske
Berwyck L. J. Poad
In this perspective article we describe recent infrared spectroscopic investigations of mass-selected M+–H2 and M+–D2 complexes in the gas-phase, with targets that include Li+–H2, B+–H2, Na+–H2, Mg+–H2, Al+–H2, Cr+–D2, Mn+–H2, Zn+–D2 and Ag+–H2. Interactions between molecular hydrogen and metal cations play a key role in several contexts, including in the storage of molecular hydrogen in zeolites, metal–organic frameworks, and …
Electron Affinities, Well Depths, And Vibrational Spectroscopy Of Cis- And Trans-Hoco, Christopher J. Johnson, Michael E. Harding, Berwyck L. J Poad, John F. Stanton, Robert E. Continetti
Electron Affinities, Well Depths, And Vibrational Spectroscopy Of Cis- And Trans-Hoco, Christopher J. Johnson, Michael E. Harding, Berwyck L. J Poad, John F. Stanton, Robert E. Continetti
Berwyck L. J. Poad
We report vibrationally resolved photoelectron spectra of internally cold HOCO– and DOCO– anions at wavelengths near and well above the detachment threshold. These spectra are dominated by a strong Franck–Condon progression of three low-energy modes of the cis isomer, the first gas-phase measurement of these vibrations. Using highly resolved, near-threshold spectra we are able to reassign the electron affinities (EAs) of cis- and trans-HOCO to 1.51 ± 0.01 and 1.37 ± 0.01 eV, respectively. Using these EAs, well depths with respect to OH + CO are determined to be 1.07 ± 0.02 eV for trans-HOCO and 0.99 ± 0.02 eV …
Rotationally Resolved Infrared Spectrum Of The Na+-D2 Complex: An Experimental And Theoretical Study, Berwyck L. Poad, V Dryza, J Klos, A A. Buchachenko, E J. Bieske
Rotationally Resolved Infrared Spectrum Of The Na+-D2 Complex: An Experimental And Theoretical Study, Berwyck L. Poad, V Dryza, J Klos, A A. Buchachenko, E J. Bieske
Berwyck L. J. Poad
The infrared spectrum of mass-selected Na+-D2 complexes is recorded in the D-D stretch vibration region (2915-2972 cm−1) by detecting Na+ photofragments resulting from photo-excitation of the complexes. Analysis of the rotationally resolved spectrum confirms a T-shaped equilibrium geometry for the complex and a vibrationally averaged intermolecular bond length of 2.461 Å. The D-D stretch band centre occurs at 2944.04 cm−1, representing a −49.6 cm−1 shift from the Q1(0) transition of the free D2 molecule. Variational rovibrational energy level calculations are performed for Na+-D2 utilising an ab initio potential energy surface developed previously for investigating the Na+-H2 complex [B. L. J. …
Photoelectron-Photofragment Coincidence Spectroscopy In A Cryogenically Cooled Linear Electrostatic Ion Beam Trap, Christopher J. Johnson, Ben B. Shen, Berwyck L. J Poad, Robert E. Continetti
Photoelectron-Photofragment Coincidence Spectroscopy In A Cryogenically Cooled Linear Electrostatic Ion Beam Trap, Christopher J. Johnson, Ben B. Shen, Berwyck L. J Poad, Robert E. Continetti
Berwyck L. J. Poad
A cryogenically cooled linear electrostatic ion beam trap for use in photoelectron-photofragment coincidence (PPC) spectroscopy is described. Using this instrument, anions created in cold, low-dutycycle sources can be stored for many seconds in a ∼20 K environment to cool radiatively, removing energetic uncertainties due to vibrationally excited precursor anions. This apparatus maintains a well-collimated beam necessary for high-resolution fragment imaging and the high experimental duty cycle needed for coincidence experiments. Ion oscillation is bunched and phase-locked to a modelocked laser, ensuring temporal overlap between ion bunches and laser pulses and that ions are intersected by the laser only when travelling …
Infrared Spectra Of Cl-_(C6h6)Mm=1, 2, Christopher Thompson, Berwyck Poad, Corinna Emmeluth, Evan Bieske
Infrared Spectra Of Cl-_(C6h6)Mm=1, 2, Christopher Thompson, Berwyck Poad, Corinna Emmeluth, Evan Bieske
Berwyck L. J. Poad
The Cl--(C6H6)Arn n = 0,1,2 and Cl--(C6H6)2 complexes are investigated using photodissociation infrared spectroscopy in the CH stretch region and through ab initio calculations at the MP2/aug-cc-pVDZ level. The results indicate that Cl--C6H6 possesses a planar structure in which the benzene molecule is attached to the Cl- anion by a double hydrogen bond. The calculations predict that Cl (C6H6)2 has a C2 symmetry structure in which the two face-to-face benzene molecules are attached to …
Infrared Spectra Of Mass-Selected Mg+-H2 And Mg +-D2 Complexes, Viktoras Dryza, Berwyck L. Poad, Evan J. Bieske
Infrared Spectra Of Mass-Selected Mg+-H2 And Mg +-D2 Complexes, Viktoras Dryza, Berwyck L. Poad, Evan J. Bieske
Berwyck L. J. Poad
Rotationally resolved infrared spectra of Mg(+)-H(2) and Mg(+)-D(2) are recorded in the H-H (4025-4080 cm(-1)) and D-D (2895-2945 cm(-1)) stretch regions by monitoring Mg(+) photofragments. The nu(HH) and nu(DD) transitions of Mg(+)-H(2) and Mg(+)-D(2) are red-shifted by 106.2 +/- 1.5 and 76.0 +/- 0.1 cm(-1) respectively from the fundamental vibrational transitions of the free H(2) and D(2) molecules. The spectra are consistent with a T-shaped equilibrium structure in which the Mg(+) ion interacts with a slightly perturbed H(2) or D(2) molecule. From the spectroscopic constants, a vibrationally averaged intermolecular separation of 2.716 A (2.687 A) is deduced for the ground …
Reactions Of Simple And Peptidic Alpha-Carboxylate Radical Anions With Dioxygen In The Gas Phase, Tony Ly, Benjamin B. Kirk, Pramesh I. Hettiarachchi, Berwyck L. Poad, Adam J. Trevitt, Gabriel Da Silva, Stephen J. Blanksby
Reactions Of Simple And Peptidic Alpha-Carboxylate Radical Anions With Dioxygen In The Gas Phase, Tony Ly, Benjamin B. Kirk, Pramesh I. Hettiarachchi, Berwyck L. Poad, Adam J. Trevitt, Gabriel Da Silva, Stephen J. Blanksby
Berwyck L. J. Poad
α-Carboxylate radical anions are potential reactive intermediates in the free radical oxidation of biological molecules (e.g., fatty acids, peptides and proteins). We have synthesised well-defined α-carboxylate radical anions in the gas phase by UV laser photolysis of halogenated precursors in an ion-trap mass spectrometer. Reactions of isolated acetate (CH2CO 2-) and 1-carboxylatobutyl (CH3CH 2CH2CHCO2-) radical anions with dioxygen yield carbonate (CO3-) radical anions and this chemistry is shown to be a hallmark of oxidation in simple and alkyl-substituted cross-conjugated species. Previous solution phase studies have shown that Cα-radicals in peptides, formed from free radical damage, combine with dioxygen to form …
Spectroscopic Study Of The Benchmark Mn+-H2 Complex, Viktoras Dryza, Berwyck L. J Poad, Evan J. Bieske
Spectroscopic Study Of The Benchmark Mn+-H2 Complex, Viktoras Dryza, Berwyck L. J Poad, Evan J. Bieske
Berwyck L. J. Poad
We have recorded the rotationally resolved infrared spectrum of the weakly bound Mn+-H2 complex in the H-H stretch region (4022-4078 cm(-1)) by monitoring Mn+ photodissociation products. The band center of Mn+-H2, the H-H stretch transition, is shifted by -111.8 cm(-1) from the transition of the free H2 molecule. The spectroscopic data suggest that the Mn+-H2 complex consists of a slightly perturbed H2 molecule attached to the Mn+ ion in a T-shaped configuration with a vibrationally averaged intermolecular separation of 2.73 A. Together with the measured Mn+...H2 binding energy of 7.9 kJ/mol (Weis, P.; et al. J. Phys. Chem. A 1997, …