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Articles 241 - 270 of 384
Full-Text Articles in Chemistry
Time-Dependent Density-Functional-Theory Calculation Of High-Order-Harmonic Generation Of H-2, Xi Chu, Gerrit C. Groenenboom
Time-Dependent Density-Functional-Theory Calculation Of High-Order-Harmonic Generation Of H-2, Xi Chu, Gerrit C. Groenenboom
Chemistry and Biochemistry Faculty Publications
The observation of the isotope effect in the high-order-harmonic generation (HHG) of H-2 presents a challenge for time-dependent density-functional-theory (TDDFT) methods, since this effect is related to the dynamics of the ion created in the tunneling ionization step of HHG and it depends on the harmonic order. As an initial step toward describing this effect within current computational capacity, we benchmark a method in which the nuclear and electronic degrees of freedom are separated and both treated quantum mechanically. For the electrons two TDDFT formalisms are adopted. Although the ion-dynamics effect is not described in our method, it reproduces the …
Dimensionality Selection In A Molecule-Based Magnet, Paul A. Goddard, Jamie L. Manson, John Singleton, Isabel Franke, Tom Lancaster, Andrew J. Steele, Stephen J. Blundell, Christopher Baines, Francis L. Pratt, Ross D. Mcdonald, Oscar E. Ayala-Valenzuela, Jordan F. Corbey, Heather I. Southerland, Pinaki Sengupta, John A. Schlueter
Dimensionality Selection In A Molecule-Based Magnet, Paul A. Goddard, Jamie L. Manson, John Singleton, Isabel Franke, Tom Lancaster, Andrew J. Steele, Stephen J. Blundell, Christopher Baines, Francis L. Pratt, Ross D. Mcdonald, Oscar E. Ayala-Valenzuela, Jordan F. Corbey, Heather I. Southerland, Pinaki Sengupta, John A. Schlueter
Chemistry and Biochemistry Faculty Publications
Gaining control of the building blocks of magnetic materials and thereby achieving particular characteristics will make possible the design and growth of bespoke magnetic devices. While progress in the synthesis of molecular materials, and especially coordination polymers, represents a significant step towards this goal, the ability to tune the magnetic interactions within a particular framework remains in its infancy. Here we demonstrate a chemical method which achieves dimensionality selection via preferential inhibition of the magnetic exchange in an S = 1/2 antiferromagnet along one crystal direction, switching the system from being quasi-two-to quasi-one-dimensional while effectively maintaining the nearest-neighbor coupling strength.
Van Der Waals Density Functional Study Of Co2 Binding In Zeolitic Imidazolate Frameworks, Keith G. Ray, David Olmsted, Ning He, Yao Houndonougbo, Brian B. Laird, Mark Asta
Van Der Waals Density Functional Study Of Co2 Binding In Zeolitic Imidazolate Frameworks, Keith G. Ray, David Olmsted, Ning He, Yao Houndonougbo, Brian B. Laird, Mark Asta
Chemistry and Biochemistry Faculty Publications
The van der Waals density functional (vdW-DF) formalism is employed in a study of the binding energetics for CO2 in a set of five zeolitic imidazolate framework (ZIF) compounds. The ZIF structures investigated share the same RHO-type zeolite topology and metal atoms, but feature imidazolate linkers with different chemical functionalization. Three distinct binding sites are identified, for which the binding energies are found to show different dependencies on the functionalization of the linker molecules. The origin of the variations in the binding energies across the ZIF compounds is discussed through analyses of the binding geometries and charge-density distributions. A comparison …
Detailed Comparison Of The Pnicogen Bond With Chalcogen, Halogen And Hydrogen Bonds, Steve Scheiner
Detailed Comparison Of The Pnicogen Bond With Chalcogen, Halogen And Hydrogen Bonds, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
The characteristics of the pnicogen bond are explored using a variety of quantum chemical techniques. In particular, this interaction is compared with its halogen and chalcogen bond cousins, as well as with the more common H-bond. In general, these bonds are all of comparable strength. More specifically, they are strengthened by the presence of an electronegative substituent on the electron-acceptor atom, and each gains strength as one moves down the appropriate column of the periodic table, for example, from N to P to As. These noncovalent bonds owe their stability to a mixture in nearly equal parts of electrostatic attraction …
First Steps In Growth Of A Polypeptide Toward Β-Sheet Structure, U. Adhikari, Steve Scheiner
First Steps In Growth Of A Polypeptide Toward Β-Sheet Structure, U. Adhikari, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
The full conformational energy surface is examined for a molecule in which a dipeptide is attached to the same spacer group as another peptide chain, so as to model the seminal steps of β-sheet formation. This surface is compared with the geometrical preferences of the isolated dipeptide to extract the perturbations induced by interactions with the second peptide strand. These interpeptide interactions remove any tendency of the dipeptide to form a C5 ring structure, one of its two normally stable geometries. A C7 structure, the preferred conformation of the isolated dipeptide, remains as the global minimum in the full molecule. …
Extrapolation To The Complete Basis Set Limit For Binding Energies Of Noncovalent Interactions, Steve Scheiner
Extrapolation To The Complete Basis Set Limit For Binding Energies Of Noncovalent Interactions, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
A means of extrapolating from double and triple-valence basis sets to a complete basis set is examined in the context of the pnicogen bonds in the BH2P⋯NH3 complexes, with B = CH3, H, NH2, CF3, OH, Cl, F, and NO2. Binding energies converge smoothly, and the trends for the various substituents B are unaffected by the basis set size, extrapolation, or level of inclusion of electron correlation, including MP2 and CCSD(T). The approach appears to be successful also for H-bonded systems, in particular the water dimer. In the event that full extrapolation within the context of CCSD(T) is not feasible, …
Sensitivity Of Noncovalent Bonds To Intermolecular Separation: Hydrogen, Halogen, Chalcogen, And Pnicogen Bonds, Steve Scheiner
Sensitivity Of Noncovalent Bonds To Intermolecular Separation: Hydrogen, Halogen, Chalcogen, And Pnicogen Bonds, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
It is well known that noncovalent bonds are weakened when stretched from their equilibrium intermolecular separation. Quantum chemical calculations are used to examine and compare the sensitivity to stretches of hydrogen, halogen, chalcogen, and pnicogen bonds. NH3 was taken as the universal electron donor, paired with HOH and FH in H-bonds, as well as with FPH2, FSH, and FCl. Even though the binding energies span a wide range, stretching the intermolecular separation by 1 Å cuts this quantity by the same proportion, roughly in half, for each system. Taking the sum of van der Waals radii as an arbitrary cutoff, …
Preferred Configurations Of Peptide-Peptide Interactions, U. Adhikari, Steve Scheiner
Preferred Configurations Of Peptide-Peptide Interactions, U. Adhikari, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
The natural and fundamental proclivities of interaction between a pair of peptide units are examined using high-level ab initio calculations. The NH···O H-bonded structure is found to be the most stable configuration of the N-methylacetamide (NMA) model dimer, but only slightly more so than a stacked arrangement. The H-bonded geometry is destabilized by only a small amount if the NH group is lifted out of the plane of the proton-accepting amide. This out-of-plane motion is facilitated by a stabilizing charge transfer from the CO π bond to the NH σ* antibonding orbital. The parallel and antiparallel stacked dimers are nearly …
Evaluation Of Dft Methods To Study Reactions Of Benzene With Oh Radical, Steve Scheiner
Evaluation Of Dft Methods To Study Reactions Of Benzene With Oh Radical, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
Several density functional theory” (DFT) methods are applied to two different reaction channels involving OH• + C6H6, and the results compared with high-level ab initio calculations. The OH• adds directly to one C atom in the first channel, first forming an encounter complex with the OH• poised above the aromatic plane. B3LYP, BH&HLYP, and MPW1K compute an accurate estimate of the overall exothermicity, whereas M05-2X, PBE0, and PBEPBE overestimate this quantity to some degree. With the exceptions of PBEPBE and PBE0, the other methods produce an acceptable barrier to addition. All approaches except BH&HLYP correctly predict an exothermic H• abstraction, …
Contributions Of Various Noncovalent Bonds To The Interaction Between An Amide And S-Containing Molecules, U. Adhikari, Steve Scheiner
Contributions Of Various Noncovalent Bonds To The Interaction Between An Amide And S-Containing Molecules, U. Adhikari, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
N-Methylacetamide, a model of the peptide unit in proteins, is allowed to interact with CH3SH, CH3SCH3, and CH3SSCH3 as models of S-containing amino acid residues. All of the minima are located on the ab initio potential energy surface of each heterodimer. Analysis of the forces holding each complex together identifies a variety of different attractive forces, including SH⋅⋅⋅O, NH⋅⋅⋅S, CH⋅⋅⋅O, CH⋅⋅⋅S, SH⋅⋅⋅π, and CH⋅⋅⋅π H-bonds. Other contributing noncovalent bonds involve charge transfer into σ* and π* antibonds. Whereas some of the H-bonds are strong enough that they represent the sole attractive force in several dimers, albeit not usually in the …
Botppi, A New Wittig Salt Used In The Synthesis Of 12-(S)-Hydroxy-Eicosatetraenoic Acid [12-(S)-Hete], Michael A. Christiansen, Merritt B. Andrus
Botppi, A New Wittig Salt Used In The Synthesis Of 12-(S)-Hydroxy-Eicosatetraenoic Acid [12-(S)-Hete], Michael A. Christiansen, Merritt B. Andrus
Chemistry and Biochemistry Faculty Publications
An efficient route to (Z)-(8-benzyloxy-8-oxooct-3-en-1-yl)triphenylphosphonium iodide, or BOTPPI, is disclosed, complete with full experimental details, NMR spectra, and HRMS data. BOTPPI serves as a surrogate for (Z)-(8-methoxy-8-oxooct-3-en-1-yl)triphenylphosphonium iodide, or MOTPPI, a Wittig salt previously used in two 12-HETE syntheses. BOTPPI has the advantage over MOTPPI of being derived from a sequence for which every intermediate is UV-active and amenable to large-scale chromatographic purification. A formal asymmetric total synthesis of 12-(S)-HETE is also reported, involving a stereoselective phase-transfer catalyzed (PTC) alkylation in its key step.
Effects Of Carbon Chain Substituent On The P∙∙∙N Noncovalent Bond, U. Adhikari, Steve Scheiner
Effects Of Carbon Chain Substituent On The P∙∙∙N Noncovalent Bond, U. Adhikari, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
The effects of carbon chains placed on the electron-accepting P atom of a P⋯N bond are examined via ab initio calculations. Saturated alkyl groups have a mild weakening effect, regardless of chain length. In contrast, incorporation of double bonds into the chain strengthens the interaction, Ctriple bond; length of mdashC triple bonds even more so. These effects are only slightly enhanced by additional conjugated double bonds or an aromatic ring. Placing F atoms onto the carbon chains strengthens the P⋯N bond, but only by a small amount, which wanes as the F atom is displaced further from the P along …
Organ-Distribution Of The Metabolite 2-Aminothiazoline-4-Carboxylic Acid In A Rat Model Following Cyanide Exposure, Ilona Petrikovics, David E. Thompson, Gary A. Rockwood, Brian A. Logue
Organ-Distribution Of The Metabolite 2-Aminothiazoline-4-Carboxylic Acid In A Rat Model Following Cyanide Exposure, Ilona Petrikovics, David E. Thompson, Gary A. Rockwood, Brian A. Logue
Chemistry and Biochemistry Faculty Publications
The reaction of cyanide (CN−) with cystine to produce 2-aminothiazoline-4-carboxylic acid (ATCA) is one of the independent detoxification pathways of cyanide in biological systems. In this report, in vivo production of ATCA and its distributions in plasma and organs were studied after a subcutaneous sublethal dose of 4 mg/kg body weight potassium cyanide (KCN) administration to rats. At this sublethal dose of KCN, ATCA concentration was not significantly increased in the plasma samples, however, it was found significantly increased in liver samples. These results suggested that ATCA might not be a good diagnostic biomarker in plasma for sublethal …
Field-Induced Xy And Ising Ground States In A Quasi-Two-Dimensional S=1/2 Heisenberg Antiferromagnet, Yoshimitsu Kohama, Marcelo Jaime, Oscar E. Ayala-Valenzuela, Ross D. Mcdonald, Eun Deok Mun, Jordan F. Corbey, Jamie L. Manson
Field-Induced Xy And Ising Ground States In A Quasi-Two-Dimensional S=1/2 Heisenberg Antiferromagnet, Yoshimitsu Kohama, Marcelo Jaime, Oscar E. Ayala-Valenzuela, Ross D. Mcdonald, Eun Deok Mun, Jordan F. Corbey, Jamie L. Manson
Chemistry and Biochemistry Faculty Publications
High field specific heat up to 35 T, C-p, and magnetic susceptibility, chi, measurements were performed on the quasi-two-dimensional (2D) Heisenberg antiferromagnet [Cu(pyz)(2)(pyO)(2)](PF6)(2). While no C-p anomaly is observed down to 0.5 K in zero magnetic field, the application of field parallel to the crystallographic ab-plane induces a lambda-like anomaly in C-p, suggesting Ising-type magnetic order. On the other hand when the field is parallel to the c-axis, C-p and chi show evidence of XY-type antiferromagnetism. This dependence upon the field orientation occurs because the extreme two-dimensionality allows the intrinsic (zero field) spin anisotropy to dominate the interlayer coupling, which …
Measurement Of Magnetic Susceptibility In Pulsed Magnetic Fields Using A Proximity Detector Oscillator, S Ghannadzadeh, M Coak, I Franke, P A. Goddard, J Singleton, Jamie L. Manson
Measurement Of Magnetic Susceptibility In Pulsed Magnetic Fields Using A Proximity Detector Oscillator, S Ghannadzadeh, M Coak, I Franke, P A. Goddard, J Singleton, Jamie L. Manson
Chemistry and Biochemistry Faculty Publications
We present a novel susceptometer with a particularly small spatial footprint and no moving parts. The susceptometer is suitable for use in systems with limited space where magnetic measurements may not have been previously possible, such as in pressure cells and rotators, as well as in extremely high pulsed fields. The susceptometer is based on the proximity detector oscillator, which has a broad dynamic resonant frequency range and has so far been used predominantly for transport measurements. We show that for insulating samples, the resonance frequency behavior as a function of field consists of a magnetoresistive and an inductive component, …
Magnetic Order In Quasi-Two-Dimensional Molecular Magnets Investigated With Muon-Spin Relaxation, A J. Steele, T Lancaster, S J. Blundell, P J. Baker, F L. Pratt, C Baines, M M. Conner, H I. Southerland, Jamie L. Manson, J A. Schlueter
Magnetic Order In Quasi-Two-Dimensional Molecular Magnets Investigated With Muon-Spin Relaxation, A J. Steele, T Lancaster, S J. Blundell, P J. Baker, F L. Pratt, C Baines, M M. Conner, H I. Southerland, Jamie L. Manson, J A. Schlueter
Chemistry and Biochemistry Faculty Publications
We present the results of a muon-spin relaxation (mu+SR) investigation into magnetic ordering in several families of layered quasi-two-dimensional molecular antiferromagnets based on transition-metal ions such as S = 1/2 Cu2+ bridged with organic ligands such as pyrazine. In many of these materials magnetic ordering is difficult to detect with conventional magnetic probes. In contrast, mu+SR allows us to identify ordering temperatures and study the critical behavior close to T-N. Combining this with measurements of in-plane magnetic exchange J and predictions from quantum Monte Carlo simulations we may assess the degree of isolation of the 2D layers through estimates of …
The Nucleotide Exchange Factor Ric-8a Is A Chaperone For The Conformationally Dynamic Nucleotide-Free State Of G Alpha I1, Celestine J. Thomas, Klara Briknarova, Jonathan K. Hilmer, Navid Movahed, Brian Bothner, John P. Sumida, Gregory G. Tall, Stephen R. Sprang
The Nucleotide Exchange Factor Ric-8a Is A Chaperone For The Conformationally Dynamic Nucleotide-Free State Of G Alpha I1, Celestine J. Thomas, Klara Briknarova, Jonathan K. Hilmer, Navid Movahed, Brian Bothner, John P. Sumida, Gregory G. Tall, Stephen R. Sprang
Chemistry and Biochemistry Faculty Publications
Heterotrimeric G protein alpha subunits are activated upon exchange of GDP for GTP at the nucleotide binding site of G alpha, catalyzed by guanine nucleotide exchange factors (GEFs). In addition to transmembrane G protein-coupled receptors (GPCRs), which act on G protein heterotrimers, members of the family cytosolic proteins typified by mammalian Ric-8A are GEFs for Gi/q/12/13-class G alpha subunits. Ric-8A binds to G alpha.GDP, resulting in the release of GDP. The Ric-8A complex with nucleotide-free G alpha i1 is stable, but dissociates upon binding of GTP to G alpha i1. To gain insight into the mechanism of Ric-8A-catalyzed GDP release …
Quantifying The Flux Of Caco3 And Organic Carbon From The Surface Ocean Using In Situ Measurements Of O-2, N-2, Pco(2), And Ph, Steven Emerson, Christopher Sabine, Meghan F. Cronin, Richard Feely, Sarah E. Cullison Gray, Michael Degrandpre
Quantifying The Flux Of Caco3 And Organic Carbon From The Surface Ocean Using In Situ Measurements Of O-2, N-2, Pco(2), And Ph, Steven Emerson, Christopher Sabine, Meghan F. Cronin, Richard Feely, Sarah E. Cullison Gray, Michael Degrandpre
Chemistry and Biochemistry Faculty Publications
Ocean acidification from anthropogenic CO2 has focused our attention on the importance of understanding the rates and mechanisms of CaCO3 formation so that changes can be monitored and feedbacks predicted. We present a method for determining the rate of CaCO3 production using in situ measureme nts of fCO(2) and pH in surface waters of the eastern subarctic Pacific Ocean. These quantities were determined on a surface mooring every 3 h for a period of about 9 months in 2007 at Ocean Station Papa (50 degrees N, 145 degrees W). We use the data in a simple surface ocean, mass balance …
A New Noncovalent Force: Comparison Of P∙∙∙N Interaction With Hydrogen And Halogen Bonds, Steve Scheiner
A New Noncovalent Force: Comparison Of P∙∙∙N Interaction With Hydrogen And Halogen Bonds, Steve Scheiner
Chemistry and Biochemistry Faculty Publications
When PH(3) is paired with NH(3), the two molecules are oriented such that the P and N atoms face one another directly, without the intermediacy of a H atom. Quantum calculations indicate that this attraction is due in part to the transfer of electron density from the lone pair of the N atom to the σ(∗) antibond of a P-H covalent bond. Unlike a H-bond, the pertinent hydrogen is oriented about 180° away from, instead of toward, the N, and the N lone pair overlaps with the lobe of the P-H σ(∗) orbital that is closest to the P. In …
The Fire Inventory From Ncar (Finn): A High Resolution Global Model To Estimate The Emissions From Open Burning, C. Wiedinmyer, S. K. Akagi, Robert J. Yokelson, L. K. Emmons, J. A. Al-Saadi, J. J. Orlando, A. J. Soja
The Fire Inventory From Ncar (Finn): A High Resolution Global Model To Estimate The Emissions From Open Burning, C. Wiedinmyer, S. K. Akagi, Robert J. Yokelson, L. K. Emmons, J. A. Al-Saadi, J. J. Orlando, A. J. Soja
Chemistry and Biochemistry Faculty Publications
The Fire INventory from NCAR version 1.0 (FINNv1) provides daily, 1 km resolution, global estimates of the trace gas and particle emissions from open burning of biomass, which includes wildfire, agricultural fires, and prescribed burning and does not include biofuel use and trash burning. Emission factors used in the calculations have been updated with recent data, particularly for the non-methane organic compounds (NMOC). The resulting global annual NMOC emission estimates are as much as a factor of 5 greater than some prior estimates. Chemical speciation profiles, necessary to allocate the total NMOC emission estimates to lumped species for use by …
Emission Factors For Open And Domestic Biomass Burning For Use In Atmospheric Models, S. K. Akagi, Robert J. Yokelson, C. Wiedinmyer, M. Alvarado, J. S. Reid, T. Karl, J. D. Crounse, P. O. Wennberg
Emission Factors For Open And Domestic Biomass Burning For Use In Atmospheric Models, S. K. Akagi, Robert J. Yokelson, C. Wiedinmyer, M. Alvarado, J. S. Reid, T. Karl, J. D. Crounse, P. O. Wennberg
Chemistry and Biochemistry Faculty Publications
Biomass burning (BB) is the second largest source of trace gases and the largest source of primary fine carbonaceous particles in the global troposphere. Many recent BB studies have provided new emission factor (EF) measurements. This is especially true for non-methane organic compounds (NMOC), which influence secondary organic aerosol (SOA) and ozone formation. New EF should improve regional to global BB emissions estimates and therefore, the input for atmospheric models. In this work we present an up-to-date, comprehensive tabulation of EF for known pyrogenic species based on measurements made in smoke that has cooled to ambient temperature, but not yet …
Airborne And Ground-Based Measurements Of The Trace Gases And Particles Emitted By Prescribed Fires In The United States, I. R. Burling, Robert J. Yokelson, S. K. Akagi, S. P. Urbanski, C. E. Wold, David W. T. Griffith, T. J. Johnson, J. Reardon, D. R. Weise
Airborne And Ground-Based Measurements Of The Trace Gases And Particles Emitted By Prescribed Fires In The United States, I. R. Burling, Robert J. Yokelson, S. K. Akagi, S. P. Urbanski, C. E. Wold, David W. T. Griffith, T. J. Johnson, J. Reardon, D. R. Weise
Chemistry and Biochemistry Faculty Publications
We have measured emission factors for 19 trace gas species and particulate matter (PM2.5) from 14 prescribed fires in chaparral and oak savanna in the southwestern US, as well as conifer forest understory in the southeastern US and Sierra Nevada mountains of California. These are likely the most extensive emission factor field measurements for temperate biomass burning to date and the only published emission factors for temperate oak savanna fuels. This study helps to close the gap in emissions data available for temperate zone fires relative to tropical biomass burning. We present the first field measurements of the biomass burning …
Trace Gas And Particle Emissions From Open Biomass Burning In Mexico, Robert J. Yokelson, I. R. Burling, S. P. Urbanski, E. Atlas, K. Adachi, P. R. Buseck, C. Wiedinmyer, S. K. Akagi, D. W. Toohey, C. E. Wold
Trace Gas And Particle Emissions From Open Biomass Burning In Mexico, Robert J. Yokelson, I. R. Burling, S. P. Urbanski, E. Atlas, K. Adachi, P. R. Buseck, C. Wiedinmyer, S. K. Akagi, D. W. Toohey, C. E. Wold
Chemistry and Biochemistry Faculty Publications
We report airborne measurements of emission factors (EF) for trace gases and PM(2.5) made in southern Mexico in March of 2006 on 6 crop residue fires, 3 tropical dry forest fires, 8 savanna fires, 1 garbage fire, and 7 mountain pine-oak forest fires. The savanna fire EF were measured early in the local dry season and when compared to EF measured late in the African dry season they were at least 1.7 times larger for NO(x), NH(3), H(2), and most non-methane organic compounds. Our measurements suggest that urban deposition and high windspeed may also be associated with significantly elevated NOx …
Boreal Forest Fire Emissions In Fresh Canadian Smoke Plumes: C-1-C-10 Volatile Organic Compounds (Vocs), Co2, Co, No2, No, Hcn And Ch3cn, Isobel J. Simpson, S. K. Akagi, B. Barletta, N. J. Blake, Y. Choi, G. S. Diskin, A. Fried, H. E. Fuelberg, S. Meinardi, F. S. Rowland, S. A. Vay, A. J. Weinheimer, P. O. Wennberg, P. Wiebring, A. Wisthaler, M. Yang, Robert J. Yokelson, Donald R. Blake
Boreal Forest Fire Emissions In Fresh Canadian Smoke Plumes: C-1-C-10 Volatile Organic Compounds (Vocs), Co2, Co, No2, No, Hcn And Ch3cn, Isobel J. Simpson, S. K. Akagi, B. Barletta, N. J. Blake, Y. Choi, G. S. Diskin, A. Fried, H. E. Fuelberg, S. Meinardi, F. S. Rowland, S. A. Vay, A. J. Weinheimer, P. O. Wennberg, P. Wiebring, A. Wisthaler, M. Yang, Robert J. Yokelson, Donald R. Blake
Chemistry and Biochemistry Faculty Publications
Boreal regions comprise about 17% of the global land area, and they both affect and are influenced by climate change. To better understand boreal forest fire emissions and plume evolution, 947 whole air samples were collected aboard the NASA DC-8 research aircraft in summer 2008 as part of the ARCTAS-B field mission, and analyzed for 79 non-methane volatile organic compounds (NMVOCs) using gas chromatography. Together with simultaneous measurements of CO2, CO, CH4, CH2O, NO2, NO, HCN and CH3CN, these measurements represent the most comprehensive assessment of trace gas emissions from boreal forest fires to date. Based on 105 air samples …
Measurements Of Gas‐Phase Inorganic And Organic Acids From Biomass Fires By Negative‐Ion Proton‐Transfer Chemical‐Ionization Mass Spectrometry, P. Veres, James M. Roberts, I. R. Burling, C. Warneke, Joost De Gouw, Robert J. Yokelson
Measurements Of Gas‐Phase Inorganic And Organic Acids From Biomass Fires By Negative‐Ion Proton‐Transfer Chemical‐Ionization Mass Spectrometry, P. Veres, James M. Roberts, I. R. Burling, C. Warneke, Joost De Gouw, Robert J. Yokelson
Chemistry and Biochemistry Faculty Publications
[1] Emissions from 34 laboratory biomass fires were investigated at the combustion facility of the U.S. Department of Agriculture Fire Sciences Laboratory in Missoula, Montana. Gas-phase organic and inorganic acids were quantified using negative-ion proton-transfer chemical-ionization mass spectrometry (NI-PT-CIMS), open-path Fourier transform infrared spectroscopy (OP-FTIR), and proton-transfer-reaction mass spectrometry (PTR-MS). NI-PT-CIMS is a novel technique that measures the mass-to-charge ratio (m/z) of ions generated from reactions of acetate (CH3C(O)O−) ions with inorganic and organic acids. The emission ratios for various important reactive acids with respect to CO were determined. Emission ratios for isocyanic acid (HNCO), 1,2 …
Determination Of Cyanide Exposure By Gas Chromatography–Mass Spectrometry Analysis Of Cyanide-Exposed Plasma Proteins, Stephanie L. Youso, Gary A. Rockwood, John A. Lee, Brian A. Logue
Determination Of Cyanide Exposure By Gas Chromatography–Mass Spectrometry Analysis Of Cyanide-Exposed Plasma Proteins, Stephanie L. Youso, Gary A. Rockwood, John A. Lee, Brian A. Logue
Chemistry and Biochemistry Faculty Publications
Exposure to cyanide can occur in a variety of ways, including exposure to smoke from cigarettes or fires, accidental exposure during industrial processes, and exposure from the use of cyanide as a poison or chemical warfare agent. Confirmation of cyanide exposure is difficult because, in vivo, cyanide quickly breaks down by a number of pathways, including the formation of both free and protein-bound thiocyanate. A simple method was developed to confirm cyanide exposure by extraction of protein-bound thiocyanate moieties from cyanide-exposed plasma proteins. Thiocyanate was successfully extracted and subsequently derivatized with pentafluorobenzyl bromide for GC–MS analysis. Thiocyanate levels as low …
Measurement Of Hono, Hnco, And Other Inorganic Acids By Negative-Ion Proton-Transfer Chemical-Ionization Mass Spectrometry (Ni-Pt-Cims): Application To Biomass Burning Emissions, J. M. Roberts, P. Veres, C. Warneke, J. A. Neuman, R. A. Washenfelder, S. S. Brown, M. Baasandorj, J. B. Burkholder, I. R. Burling, T. J. Johnson, Robert J. Yokelson, J. De Gouw
Measurement Of Hono, Hnco, And Other Inorganic Acids By Negative-Ion Proton-Transfer Chemical-Ionization Mass Spectrometry (Ni-Pt-Cims): Application To Biomass Burning Emissions, J. M. Roberts, P. Veres, C. Warneke, J. A. Neuman, R. A. Washenfelder, S. S. Brown, M. Baasandorj, J. B. Burkholder, I. R. Burling, T. J. Johnson, Robert J. Yokelson, J. De Gouw
Chemistry and Biochemistry Faculty Publications
A negative-ion proton-transfer chemical ionization mass spectrometric technique (NI-PT-CIMS), using acetate as the reagent ion, was applied to the measurement of volatile inorganic acids of atmospheric interest: hydrochloric (HCl), nitrous (HONO), nitric (HNO(3)), and isocyanic (HNCO) acids. Gas phase calibrations through the sampling inlet showed the method to be intrinsically sensitive (6-16 cts/pptv), but prone to inlet effects for HNO(3) and HCl. The ion chemistry was found to be insensitive to water vapor concentrations, in agreement with previous studies of carboxylic acids. The inlet equilibration times for HNCO and HONO were 2 to 4s, allowing for measurement in biomass burning …
Magnetic Properties Of The Quasi-Two-Dimensional S=1/2 Heisenberg Antiferromagnet [Cu(Pyz)(2)(Hf2)]Pf6, E Cizmar, S A. Zvyagin, R Beyer, M Uhlarz, M Ozerov, Y Skourski, Jamie L. Manson, J A. Schlueter, J Wosnitza
Magnetic Properties Of The Quasi-Two-Dimensional S=1/2 Heisenberg Antiferromagnet [Cu(Pyz)(2)(Hf2)]Pf6, E Cizmar, S A. Zvyagin, R Beyer, M Uhlarz, M Ozerov, Y Skourski, Jamie L. Manson, J A. Schlueter, J Wosnitza
Chemistry and Biochemistry Faculty Publications
We report on high-field magnetization, specific heat, and electron-spin-resonance (ESR) studies of the quasi-two-dimensional spin-1/2 Heisenberg antiferromagnet [Cu(pyz)(2)(HF2)]PF6. The frequency-field diagram of ESR modes below T-N=4.38 K is described in the frame of the mean-field theory, confirming a collinear magnetic structure with an easy-plane anisotropy. The obtained results allowed us to determine the anisotropy/exchange interaction ratio, A/J=0.003, and the upper limit for the interplane/intraplane exchange interaction ratio, J'/J=1/16. It is argued that despite the onset of three-dimensional long-range magnetic ordering the magnetic properties of this material (including high-magnetic-field magnetization and nonmonotonic field dependence of the Neel temperature) are strongly affected …
The Analysis Of Cyanide And Its Breakdown Products In Biological Samples, Brian A. Logue, Diane M. Hinkens, Steven I. Baskin, Gary A. Rockwood
The Analysis Of Cyanide And Its Breakdown Products In Biological Samples, Brian A. Logue, Diane M. Hinkens, Steven I. Baskin, Gary A. Rockwood
Chemistry and Biochemistry Faculty Publications
Cyanide is a toxic chemical that may be introduced into living organisms as a result of natural processes and/or anthropogenic uses (legal or illicit). Exposure to cyanide can be verified by analysis of cyanide or one of its breakdown products from biological samples. This verification may be important for medical, law-enforcement, military, forensic, research, or veterinary purposes. This review will discuss current bioanalytical techniques used for the verification of cyanide exposure, identify common problems associated with the analysis of cyanide and its biological breakdown products, and briefly address the metabolism and toxicokinetics of cyanide and its breakdown products in biological …
Trace Gas And Particle Emissions From Domestic And Industrial Biofuel Use And Garbage Burning In Central Mexico, Ted J. Christian, Robert Yokelson, B. Cardenas, L. T. Molina, G. Engling, S. C. Hsu
Trace Gas And Particle Emissions From Domestic And Industrial Biofuel Use And Garbage Burning In Central Mexico, Ted J. Christian, Robert Yokelson, B. Cardenas, L. T. Molina, G. Engling, S. C. Hsu
Chemistry and Biochemistry Faculty Publications
In central Mexico during the spring of 2007 we measured the initial emissions of 12 gases and the aerosol speciation for elemental and organic carbon (EC, OC), anhydrosugars, Cl(-), NO(3)(-), and 20 metals from 10 cooking fires, four garbage fires, three brick making kilns, three charcoal making kilns, and two crop residue fires. Global biofuel use has been estimated at over 2600 Tg/y. With several simple case studies we show that cooking fires can be a major, or the major, source of several gases and fine particles in developing countries. Insulated cook stoves with chimneys were earlier shown to reduce …