The Effect of β-Hydrogens on the Tropospheric Photochemistry of Aldehydes: Norrish Type 1, Triple Fragmentation, and Methylketene Formation from Propanal.

Wavelength and pressure dependent quantum yields (ϕ, QYs) of propanal photolysis have been measured for photolysis wavelengths, λ = 300-330 nm, and buffer gases of 3-10 Torr propanal and 0-757 Torr N. Following laser photolysis, three photochemical pathways were established, using Fourier transform infrared spectroscopy of the stable end-products. Photolysis is dominated by the Norrish Type 1 reaction, which has been reported previously, but with inconsistent quantum yields.

Photophysical oxidation of HCHO produces HO radicals.

Formaldehyde, HCHO, is the highest-volume carbonyl in the atmosphere. It absorbs sunlight at wavelengths shorter than 330 nm and photolyses to form H and HCO radicals, which then react with O to form HO. Here we show HCHO has an additional HO formation pathway.

Rotational resonances in the HCO roaming reaction are revealed by detailed correlations.

Since its discovery 16 years ago, roaming has become a ubiquitous mechanism in molecular photochemistry. Its general features are now understood, but little detail is known about how the potential energy surface (PES) determines reaction outcomes. We performed detailed experiments on formaldehyde (HCO) photodissociation and determined fully correlated quantum state distributions of the molecular hydrogen and carbon monoxide products.

Structural Effects on the Norrish Type I α-Bond Cleavage of Tropospherically Important Carbonyls.

Norrish Type I (NTI) α-bond cleavage is the dominant photolysis mechanism in small carbonyls and is an important source of radicals in the troposphere. In nonsymmetric species two cleavages are possible, NTI and NTI, forming larger and smaller alkyl radicals, respectively. For a data set of 20 small, atmospherically relevant carbonyls we predict NTI and NTI thresholds on the , , and electronic states.

Nutrients mediate the effects of temperature on methylmercury concentrations in freshwater zooplankton.

Methylmercury (MeHg) bioaccumulation in freshwater aquatic systems is impacted by anthropogenic stressors, including climate change and nutrient enrichment. The goal of this study was to determine how warmer water temperatures and excess nutrients would alter zooplankton communities and phytoplankton concentrations, and whether those changes would in turn increase or decrease MeHg concentrations in freshwater zooplankton. To test this, we employed a 2 × 2 factorial experimental design with nutrient and temperature treatments.

Dynamics and quantum yields of H + CHCO as a primary photolysis channel in CHCHO.

The first experimental observation of the primary photochemical channel of acetaldehyde leading to the formation of ketene (CHCO) and hydrogen (H) molecular products is reported. Acetaldehyde (CHCHO) was photolysed in a molecular beam at 305.6 nm and the resulting H product characterized using velocity-map ion (VMI) imaging.

Zero-point energy conservation in classical trajectory simulations: Application to HCO.

A new approach for preventing zero-point energy (ZPE) violation in quasi-classical trajectory (QCT) simulations is presented and applied to HCO "roaming" reactions. Zero-point energy may be problematic in roaming reactions because they occur at or near bond dissociation thresholds and these channels may be incorrectly open or closed depending on if, or how, ZPE has been treated. Here we run QCT simulations on a "ZPE-corrected" potential energy surface defined as the sum of the molecular potential energy surface (PES) and the global harmonic ZPE surface.

Photo-tautomerization of acetaldehyde as a photochemical source of formic acid in the troposphere.

Organic acids play a key role in the troposphere, contributing to atmospheric aqueous-phase chemistry, aerosol formation, and precipitation acidity. Atmospheric models currently account for less than half the observed, globally averaged formic acid loading. Here we report that acetaldehyde photo-tautomerizes to vinyl alcohol under atmospherically relevant pressures of nitrogen, in the actinic wavelength range, λ = 300-330 nm, with measured quantum yields of 2-25%.

Path integrals with higher order actions: Application to realistic chemical systems.

Quantum thermodynamic parameters can be determined using path integral Monte Carlo (PIMC) simulations. These simulations, however, become computationally demanding as the quantum nature of the system increases, although their efficiency can be improved by using higher order approximations to the thermal density matrix, specifically the action. Here we compare the standard, primitive approximation to the action (PA) and three higher order approximations, the Takahashi-Imada action (TIA), the Suzuki-Chin action (SCA) and the Chin action (CA).

The energy dependence of CO(v,J) produced from HCO via the transition state, roaming, and triple fragmentation channels.

The dynamics of CO production from photolysis of HCO have been explored over a 8000 cm energy range (345 nm-266 nm). Two-dimensional ion imaging, which simultaneously measures the speed and angular momentum distribution of a photofragment, was used to characterise the distribution of rotational and translational energy and to quantify the branching fraction of roaming, transition state (TS), and triple fragmentation (3F) pathways. The rotational distribution for the TS channel broadens significantly with increasing energy, while the distribution is relatively constant for the roaming channel.

Infrared Spectra of Gas-Phase 1- and 2-Propenol Isomers.

Fourier transform infrared spectra of isolated 1-propenol and 2-propenol in the gas-phase have been collected in the range of 900-3800 cm, and the absolute infrared absorption cross sections reported for the first time. Both cis and trans isomers of 1-propenol were observed with the trans isomer in greater abundance. Syn and anti conformers of both 1- and 2-propenol were also observed, with abundance consistent with thermal population.

Assessment of Adults Experiencing Chronic Non-Cancer Pain: A Randomized Trial of Group Versus Individual Format at an Australian Tertiary Pain Service.

Objective: To compare the outcomes of a new group assessment format with conventional individual assessment.

Design: A randomized controlled trial.

Setting: An Australian tertiary hospital multidisciplinary pain service.

Path integral Monte Carlo simulations of H2 adsorbed to lithium-doped benzene: A model for hydrogen storage materials.

Finite temperature quantum and anharmonic effects are studied in H2-Li(+)-benzene, a model hydrogen storage material, using path integral Monte Carlo (PIMC) simulations on an interpolated potential energy surface refined over the eight intermolecular degrees of freedom based upon M05-2X/6-311+G(2df,p) density functional theory calculations. Rigid-body PIMC simulations are performed at temperatures ranging from 77 K to 150 K, producing both quantum and classical probability density histograms describing the adsorbed H2. Quantum effects broaden the histograms with respect to their classical analogues and increase the expectation values of the radial and angular polar coordinates describing the location of the center-of-mass of the H2 molecule.

H2 Adsorption in a Porous Crystal: Accurate First-Principles Quantum Simulation.

A general method is presented for constructing, from ab initio quantum chemistry calculations, the potential energy surface (PES) for H2 absorbed in a porous crystalline material. The method is illustrated for the metal-organic framework material MOF-5. Rigid body quantum diffusion Monte Carlo simulations are used in the construction of the PES and to evaluate the quantum ground state of H2 in MOF-5, the zero-point energy, and the enthalpy of adsorption at 0 K.

"Plug-and-Play" potentials: Investigating quantum effects in (H2)2-Li(+)-benzene.

Quantum and anharmonic effects are investigated in (H2)2-Li(+)-benzene, a model for hydrogen adsorption in metal-organic frameworks and carbon-based materials, using rigid-body diffusion Monte Carlo (RBDMC) simulations. The potential-energy surface (PES) is calculated as a modified Shepard interpolation of M05-2X/6-311+G(2df,p) electronic structure data. The RBDMC simulations yield zero-point energies (ZPE) and probability density histograms that describe the ground-state nuclear wavefunction.

A multi-agent quantum Monte Carlo model for charge transport: Application to organic field-effect transistors.

We have developed a multi-agent quantum Monte Carlo model to describe the spatial dynamics of multiple majority charge carriers during conduction of electric current in the channel of organic field-effect transistors. The charge carriers are treated by a neglect of diatomic differential overlap Hamiltonian using a lattice of hydrogen-like basis functions. The local ionization energy and local electron affinity defined previously map the bulk structure of the transistor channel to external potentials for the simulations of electron- and hole-conduction, respectively.

What is Novel About Novel Ecosystems: Managing Change in an Ever-Changing World.

Influenced by natural climatic, geological, and evolutionary changes, landscapes and the ecosystems within are continuously changing. In addition to these natural pressures, anthropogenic drivers have increasingly influenced ecosystems. Whether affected by natural or anthropogenic processes, ecosystems, ecological communities, and ecosystem functioning are dynamic and can lead to "novel" or "emerging" ecosystems.

Generating accurate dipole moment surfaces using modified Shepard interpolation.

We outline an approach for building molecular dipole moment surfaces using modified Shepard interpolation. Our approach is highly automated, requires minimal parameterization, and is iteratively improvable. Using the water molecule as a test case, we investigate how different aspects of the interpolation scheme affect the rate of convergence of calculated IR spectral line intensities.

Quantum effects and anharmonicity in the H2-Li(+)-benzene complex: a model for hydrogen storage materials.

Quantum and anharmonic effects are investigated in H2-Li(+)-benzene, a model for hydrogen adsorption in metal-organic frameworks and carbon-based materials. Three- and 8-dimensional quantum diffusion Monte Carlo (QDMC) and rigid-body diffusion Monte Carlo (RBDMC) simulations are performed on potential energy surfaces interpolated from electronic structure calculations at the M05-2X/6-31+G(d,p) and M05-2X/6-311+G(2df,p) levels of theory using a three-dimensional spline or a modified Shepard interpolation. These calculations investigate the intermolecular interactions in this system, with three- and 8-dimensional 0 K H2 binding enthalpy estimates, ΔH(bind) (0 K), being 16.

Experimental and theoretical investigation of triple fragmentation in the photodissociation dynamics of H2CO.

The photodissociation dynamics of H2CO molecules at energies bracketing the triple fragmentation threshold were investigated using velocity map ion imaging of the H-atom fragments. An algorithm was developed to model the experimental results as a two-step process: initially barrierless C-H bond fission on the S0 potential energy surface to form H + HCO, followed by secondary fragmentation of those HCO radicals with sufficient internal energy to overcome the small exit channel barrier on the HCO surface to form H + CO. Our model treats the first step using phase space theory (PST) and the second using a combined PST-impulsive model, with a tunneling correction.

A phase space theory for roaming reactions.

We describe a new, simple theory for predicting the branching fraction of products in roaming reactions, compared to the analogous barrierless bond dissociation products. The theory uses a phase space theory (PST) formalism to divide reactive states in the bond dissociation channel into states with enough translational energy to dissociate and states that may roam. Two parameters are required, ΔEroam, the energy difference between the bond dissociation threshold and the roaming threshold, and the roaming probability, Proam, the probability that states that may roam do roam rather than recombine to form reactants.

Modeling molecular response in uniform and non-uniform electric fields.

The response of a molecule to an electric field E, often a model of environment, can be expressed in terms of a sum of power series expansions. We investigate the accuracy and limits of applicability of this expression using one-, two-, and three-dimensional models of the hydrogen-bonded complex, ClH:NH(3). Energetic, structural, and vibrational spectroscopic characteristics are determined at first- and second-order in E and [nabla]E and compared with ab initio values for a range of uniform and non-uniform electric fields chosen to simulate molecular environments.

Phototautomerization of Acetaldehyde to Vinyl Alcohol: A Primary Process in UV-Irradiated Acetaldehyde from 295 to 335 nm.

The concentrations of organic acids, key species in the formation of secondary organic aerosols, are underestimated by atmospheric chemistry models by a factor of ∼2. Vinyl alcohol (VA, CH2═CHOH, ethenol) has been suggested as a precursor to formic acid, but sufficient tropospheric sources of VA have not been identified. Here, we show that VA is formed upon irradiation of neat acetaldehyde (CH3CHO) in the actinic ultraviolet region, between 295 and 330 nm.

Ceasing intrathecal therapy in chronic non-cancer pain: an invitation to shift from biomedical focus to active management.

Objective: To report long term experience (1997-2009) of intrathecal (IT) therapy for chronic non-cancer pain in the context of our team's increasing emphasis on active management.

Design: Descriptive case series.

Setting: Australian tertiary multidisciplinary pain center, Hunter Integrated Pain Service (HIPS).