Direct Measurements of Covalently Bonded Sulfuric Anhydrides from Gas-Phase Reactions of SO3 with Acids under Ambient Conditions.

Sulfur trioxide (SO3) is an important oxide of sulfur and a key intermediate in the formation of sulfuric acid (H2SO4, SA) in the Earth's atmosphere. This conversion to SA occurs rapidly due to the reaction of SO3 with a water dimer. However, gas-phase SO3 has been measured directly at concentrations that are comparable to that of SA under polluted mega-city conditions, indicating gaps in our current understanding of the sources and fates of SO3. Its reaction with atmospheric acids could be one such fate that can have significant implications for atmospheric chemistry. In the present investigation, laboratory experiments were conducted in a flow reactor to generate a range of previously uncharacterized condensable sulfur-containing reaction products by reacting SO3 with a set of atmospherically relevant inorganic and organic acids at room temperature and atmospheric pressure. Specifically, key inorganic acids known to be responsible for most ambient new particle formation events, iodic acid (HIO3, IA) and SA, are observed to react promptly with SO3 to form iodic sulfuric anhydride (IO3SO3H, ISA) and disulfuric acid (H2S2O7, DSA). Carboxylic sulfuric anhydrides (CSAs) were observed to form by the reaction of SO3 with C2 and C3 monocarboxylic (acetic and propanoic acid) and dicarboxylic (oxalic and malonic acid)-carboxylic acids. The formed products were detected by a nitrate-ion-based chemical ionization atmospheric pressure interface time-of-flight mass spectrometer (NO3--CI-APi-TOF; NO3--CIMS). Quantum chemical methods were used to compute the relevant SO3 reaction rate coefficients, probe the reaction mechanisms, and model the ionization chemistry inherent in the detection of the products by NO3--CIMS. Additionally, we use NO3--CIMS ambient data to report that significant concentrations of SO3 and its acid anhydride reaction products are present under polluted, marine and polar, and volcanic plume conditions. Considering that these regions are rich in the acid precursors studied here, the reported reactions need to be accounted for in the modeling of atmospheric new particle formation.

A systematic study on the kinetics of H-shift reactions in pristine acyl peroxy radicals.

A series of acyl peroxy radical H-shifts were systematically studied using computational approaches. Acyl peroxy radicals were categorized into small- (ethanal-pentanal), medium- (hexanal and heptanal) and large-sized (octanal and nonanal) molecules. The H-shifts spanning from 1,4 to 1,9 were inspected for each studied system. For all acyl peroxy radicals, it is the combination of barrier heights and quantum mechanical tunneling that explains the yield of the peracid alkyl radical product. We used the ROHF-ROCCSD(T)-F12a/VDZ-F12//ωB97X-D/aug-cc-pVTZ level of theory to estimate the barrier heights and the subsequent rate coefficients with the exception of the smallest acyl peroxy radical ethanal, for which MN15 density functional was applied. The estimated multiconformer H-shift rate coefficients were found to be in the range of 10-2 s-1 to 10-1 s-1 for the fastest H-migrations. The determined rates imply that these H-shift reactions are often competitive with other RO2 loss processes and should be considered as a path to functionalization in modelling not only rural but also urban air quality.

Molecular rearrangement of bicyclic peroxy radicals is a key route to aerosol from aromatics.

The oxidation of aromatics contributes significantly to the formation of atmospheric aerosol. Using toluene as an example, we demonstrate the existence of a molecular rearrangement channel in the oxidation mechanism. Based on both flow reactor experiments and quantum chemical calculations, we show that the bicyclic peroxy radicals (BPRs) formed in OH-initiated aromatic oxidation are much less stable than previously thought, and in the case of the toluene derived ipso-BPRs, lead to aerosol-forming low-volatility products with up to 9 oxygen atoms on sub-second timescales. Similar results are predicted for ipso-BPRs formed from many other aromatic compounds. This reaction class is likely a key route for atmospheric aerosol formation, and including the molecular rearrangement of BPRs may be vital for accurate chemical modeling of the atmosphere.

Solving the discrepancy between the direct and relative-rate determinations of unimolecular reaction kinetics of dimethyl-substituted Criegee intermediate (CH3)2COO using a new photolytic precursor.

We have performed direct kinetic measurements of the thermal unimolecular reaction of (CH3)2COO in the temperature range 243-340 K and pressure range 5-350 Torr using time-resolved UV-absorption spectroscopy. We have utilized a new photolytic precursor, 2-bromo-2-iodopropane ((CH3)2CIBr), which photolysis at 213 nm in the presence of O2 produces acetone oxide, (CH3)2COO. The results show that the thermal unimolecular reaction is even more important main loss process of (CH3)2COO in the atmosphere than direct kinetic studies have suggested hitherto. The current experiments show that the unimolecular reaction rate of (CH3)2COO at 296 K and atmospheric pressure is 899 ± 42 s-1. Probably more importantly, current measurements bring the direct and relative-rate measurements of thermal unimolecular reaction kinetics of (CH3)2COO into quantitative agreement.

An experimental and master-equation modeling study of the kinetics of the reaction between resonance-stabilized (CH3)2CCHCH2 radical and molecular oxygen.

The kinetics of the reaction between resonance-stabilized (CH3)2CCHCH2 radical (R) and O2 has been investigated using photoionization mass spectrometry, and master equation (ME) simulations were performed to support the experimental results. The kinetic measurements of the (CH3)2CCHCH2 + O2 reaction (1) were carried out at low helium bath-gas pressures (0.2-5.7 Torr) and over a wide temperature range (238-660 K). Under low temperature (238-298 K) conditions, the pressure-dependent bimolecular association reaction R + O2 → ROO determines kinetics, until at an intermediate temperature range (325-373 K) the ROO adduct becomes thermally unstable and increasingly dissociates back to the reactants with increasing temperature. The initial association of O2 with (CH3)2CCHCH2 radical occurs on two distinct sites: terminal 1(t) and non-terminal 1(nt) sites on R, leading to the barrierless formation of ROO(t) and ROO(nt) adducts, respectively. Important for autoignition modelling of olefinic compounds, bimolecular reaction channels appear to open for the R + O2 reaction at high temperatures (T > 500 K) and pressure-independent bimolecular rate coefficients of reaction (1) with a weak positive temperature dependence, (2.8-4.6) × 10-15 cm3 molecule-1 s-1, were measured in the temperature range of 500-660 K. At a temperature of 501 K, a product signal of reaction (1) was observed at m/z = 68, probably originating from isoprene. To explore the reaction mechanism of reaction (1), quantum chemical calculations and ME simulations were performed. According to the ME simulations, without any adjustment to energies, the most important and second most important product channels at the high temperatures are isoprene + HO2 (yield > 91%) and (2R/S)-3-methyl-1,2-epoxybut-3-ene + OH (yield < 8%). After modest adjustments to ROO(t) and ROO(nt) well-depths (∼0.7 kcal mol-1 each) and barrier height for the transition state associated with the kinetically most dominant channel, R + O2 → isoprene + HO2 (∼2.2 kcal mol-1), the ME model was able to reproduce the experimental findings. Modified Arrhenius expressions for the kinetically important reaction channels are enclosed to facilitate the use of current results in combustion models.

Time-resolved, broadband UV-absorption spectrometry measurements of Criegee intermediate kinetics using a new photolytic precursor: unimolecular decomposition of CH2OO and its reaction with formic acid.

We present a time-resolved broadband cavity-enhanced UV-absorption spectrometer apparatus that we have constructed and utilized for temperature- and pressure-dependent kinetic measurements of formaldehyde oxide (CH2OO) reactions. We also introduce and utilize a new photolytic precursor, bromoiodomethane (CH2IBr), which photolysis at 213 nm in presence of O2 produces CH2OO. Importantly, this precursor appears to be free from secondary reactions that may regenerate CH2OO in kinetic experiments. The unimolecular decomposition rate coefficient of CH2OO has been measured over wide pressure (5-400 Torr) and temperature (296-600 K) ranges and master equation simulations of the decomposition kinetics have been performed using MESMER program. The MESMER simulations of the experimental data with the calculated zero-point energy corrected transition state energy 85.9 kJ mol-1 for decomposition required no adjustment and returned 〈ΔE〉down = 123.2 × (T/298 K)0.74 cm-1 for temperature-dependent exponential-down model of the collisional energy transfer in He. A very good agreement between results of simulations and experiments is obtained. The results are compared with the previously reported unimolecular decomposition study by Stone et al. (Phys. Chem. Chem. Phys., 2018, 20, 24940-24954). Current master equation simulations suggest about 61% decomposition yield for the predominant H2 + CO2 channel, whereas the yields of two other channels, H2O + CO, and HCO + OH, are sensitive on the parameters involved in the simulations. The kinetics of CH2OO reaction with formic acid has also been investigated as function of pressure (5-150 Torr) and temperature (296-458 K). The bimolecular rate coefficient for CH2OO + HCOOH reaction shows a negative temperature dependency, decreasing from (1.0 ± 0.03) × 10-10 cm3 molecule-1 s-1 at 296 K to (0.47 ± 0.05) × 10-10 cm3 molecule-1 s-1 at 458 K with an Arrhenius activation energy of -4.9 ± 1.6 kJ mol-1, where statistical uncertainties shown are 2σ. Estimated overall uncertainty in the measured rate coefficients is about ±20%. Current bimolecular rate coefficient at room temperature agrees with the previously reported rate coefficients from the direct kinetic experiments. The reaction is found to be pressure independent over the range between 5 and 150 Torr at 296 K in He.

Binding and Release between Polymeric Carrier and Protein Drug: pH-Mediated Interplay of Coulomb Forces, Hydrogen Bonding, van der Waals Interactions, and Entropy.

The accelerating search for new types of drugs and delivery strategies poses challenge to understanding the mechanism of delivery. To this end, a detailed atomistic picture of binding between the drug and carrier is quintessential. Although many studies focus on the electrostatics of drug-vector interactions, it has also been pointed out that entropic factors relating to water and counterions can play an important role. By carrying out extensive molecular dynamics simulations and subsequently validating with experiments, we shed light herein on the binding in aqueous solution between a protein drug and polymeric carrier. We examined the complexation between the polymer poly(ethylene glycol) methyl ether acrylate-b-poly(carboxyethyl acrylate (PEGMEA-b-PCEA) and the protein egg white lysozyme, a system that acts as a model for polymer-vector/protein-drug delivery systems. The complexation has been visualized and characterized using contact maps and hydrogen bonding analyses for five independent simulations of the complex, each running over 100 ns. Binding at physiological pH is, as expected, mediated by Coulombic attraction between the positively charged protein and negatively charged carboxylate groups on the polymer. However, we find that consideration of electrostatics alone is insufficient to explain the complexation behavior at low pH. Intracomplex hydrogen bonds, van der Waals interactions, as well as water-water interactions dictate that the polymer does not release the protein at pH 4.8 or indeed at pH 3.2 even though the Coulombic attractions are largely removed as carboxylate groups on the polymer become titrated. Experiments in aqueous solution carried out at pH 7.0, 4.5, and 3.0 confirm the veracity of the computed binding behavior. Overall, these combined simulation and experimental results illustrate that coulomb interactions need to be complemented with consideration of other entropic forces, mediated by van der Waals interactions and hydrogen bonding, to search for adequate descriptors to predict binding and release properties of polymer-protein complexes. Advances in computational power over the past decade make atomistic molecular dynamics simulations such as implemented here one of the few avenues currently available to elucidate the complexity of these interactions and provide insights toward finding adequate descriptors. Thus, there remains much room for improvement of design principles for efficient capture and release delivery systems.

Dynamical Interactions of 5-Fluorouracil Drug with Dendritic Peptide Vectors: The Impact of Dendrimer Generation, Charge, Counterions, and Structured Water.

Molecular dynamics simulations are utilized to investigate the interactions between the skin cancer drug 5-fluorouracil (5FU) and peptide-based dendritic carrier systems. We find that these drug-carrier interactions do not conform to the traditional picture of long-time retention of the drug within a hydrophobic core of the dendrimer carrier. Rather, 5FU, which is moderately soluble in its own right, experiences weak, transient chattering interactions all over the dendrimer, mediated through multiple short-lived hydrogen bonding and close contact events. We find that charge on the periphery of the dendrimer actually has a negative effect on the frequency of drug-carrier interactions due to a counterion screening effect that has not previously been observed. However, charge is nevertheless an important feature since neutral dendrimers are shown to have a significant mutual attraction that can lead to clustering or agglomeration. This clustering is prevented due to charge repulsion for the titrated dendrimers, such that they remain independent in solution.

First-Principle Framework for Total Charging Energies in Electrocatalytic Materials and Charge-Responsive Molecular Binding at Gas-Surface Interfaces.

Heterogeneous charge-responsive molecular binding to electrocatalytic materials has been predicted in several recent works. This phenomenon offers the possibility of using voltage to manipulate the strength of the binding interaction with the target gas molecule and thereby circumvent thermochemistry constraints, which inhibit achieving both efficient binding and facile release of important targets such as CO2 and H2. Stability analysis of such charge-induced molecular adsorption has been beyond the reach of existing first-principle approaches. Here, we draw on concepts from semiconductor physics and density functional theory to develop a first principle theoretical approach that allows calculation of the change in total energy of the supercell due to charging. Coupled with the calculated adsorption energy of gas molecules at any given charge, this allows a complete description of the energetics of the charge-induced molecular adsorption process. Using CO2 molecular adsorption onto negatively charged h-BN (wide-gap semiconductor) and g-C4N3 (half metal) as example cases, our analysis reveals that - while adsorption is exothermic after charge is introduced - the overall adsorption processes are not intrinsically spontaneous due to the energetic cost of charging the materials. The energies needed to overcome the barriers of these processes are 2.10 and 0.43 eV for h-BN and g-C4N3, respectively. This first principle approach opens up new pathways for a more complete description of charge-induced and electrocatalytic processes.

Nanodusty plasma chemistry: a mechanistic and variational transition state theory study of the initial steps of silyl anion-silane and silylene anion-silane polymerization reactions.

The growth of nanodusty particles, which is critical in plasma chemistry, physics, and engineering. The aim of the present work is to understand the detailed reaction mechanisms of early steps in this growth. The polymerization of neutral silane with the silylene or silyl anion, which eliminates molecular hydrogen with the formation of their higher homologues, governs the silicon hydride clustering in nanodusty plasma chemistry. The detailed mechanisms of these important polymerization reactions in terms of elementary reactions have not been proposed yet. In the present work, we investigated the initial steps of these polymerization reactions, i.e., the SiH4 + Si2H4(-)/Si2H5(-) reactions, and we propose a three-step mechanism, which is also applicable to the following polymerization steps. CM5 charges of all the silicon-containing species were computed in order to analyze the character of the species in the proposed reaction mechanisms. We also calculated thermal rate constant of each step using multi-structural canonical variational transition state theory (MS-CVT) with the small-curvature tunneling (SCT) approximation, based on the minimum energy path computed using M08-HX/MG3S electronic structure method.

Large entropic effects on the thermochemistry of silicon nanodusty plasma constituents.

Determination of the thermodynamic properties of reactor constituents is the first step in designing control strategies for plasma-mediated deposition processes and is also a key fundamental issue in physical chemistry. In this work, a recently proposed multistructural statistical thermodynamic method is used to show the importance of multiple structures and torsional anharmonicity in determining the thermodynamic properties of silicon hydride clusters, which are important both in plasmas and in thermally driven systems. It includes five different categories of silicon hydride clusters and radicals, including silanes, silyl radicals, and silenes. We employed a statistical mechanical approach, namely the recently developed multistructural (MS) anharmonicity method, in combination with density functional theory to calculate the partition functions, which in turn are used to estimate thermodynamic quantities, namely Gibbs free energy, enthalpy, entropy, and heat capacity, for all of the systems considered. The calculations are performed using all of the conformational structures of each molecule or radical by employing the multistructural quasiharmonic approximation (MS-QH) and also by including torsional potential anharmonicity (MS-T). For those cases where group additivity (GA) results are available, the thermodynamic quantities obtained from our MS-T calculations differ considerably due to the fact that the GA method is based on single-structure data for isomers of each stoichiometry, and hence lack multistructural effects; whereas we find that multistructural effects are very important in silicon hydride systems. Our results also indicate that the entropic effect on the thermochemistry is huge and is dominated by multistructural effects. The entropic effect of multiple structures is also expected to be important for other kinds of chain molecules, and its effect on nucleation kinetics is expected to be large.

Assessment of range-separated time-dependent density-functional theory for calculating C6 dispersion coefficients.

We assess a variant of linear-response range-separated time-dependent density-functional theory (TDDFT), combining a long-range Hartree-Fock (HF) exchange kernel with a short-range adiabatic exchange-correlation kernel in the local-density approximation (LDA) for calculating isotropic C6 dispersion coefficients of homodimers of a number of closed-shell atoms and small molecules. This range-separated TDDFT tends to give underestimated C6 coefficients of small molecules with a mean absolute percentage error of about 5%, a slight improvement over standard TDDFT in the adiabatic LDA which tends to overestimate them with a mean absolute percentage error of 8%, but close to time-dependent Hartree-Fock which has a mean absolute percentage error of about 6%. These results thus show that introduction of long-range HF exchange in TDDFT has a small but beneficial impact on the values of C6 coefficients. It also confirms that the present variant of range-separated TDDFT is a reasonably accurate method even using only a LDA-type density functional and without adding an explicit treatment of long-range correlation.

Kinetics of the hydrogen atom abstraction reactions from 1-butanol by hydroxyl radical: theory matches experiment and more.

In the present work, we study the H atom abstraction reactions by hydroxyl radical at all five sites of 1-butanol. Multistructural variational transition state theory (MS-VTST) was employed to estimate the five thermal rate constants. MS-VTST utilizes a multifaceted dividing surface that accounts for the multiple conformational structures of the transition state, and we also include all the structures of the reactant molecule. The vibrational frequencies and minimum energy paths (MEPs) were computed using the M08-HX/MG3S electronic structure method. The required potential energy surfaces were obtained implicitly by direct dynamics employing interpolated variational transition state theory with mapping (IVTST-M) using a variational reaction path algorithm. The M08-HX/MG3S electronic model chemistry was then used to calculate multistructural torsional anharmonicity factors to complete the MS-VTST rate constant calculations. The results indicate that torsional anharmonicity is very important at higher temperatures, and neglecting it would lead to errors of 26 and 32 at 1000 and 1500 K, respectively. Our results for the sums of the site-specific rate constants agree very well with the experimental values of Hanson and co-workers at 896-1269 K and with the experimental results of Campbell et al. at 292 K, but slightly less well with the experiments of Wallington et al., Nelson et al., and Yujing and Mellouki at 253-372 K; nevertheless, the calculated rates are within a factor of 1.61 of all experimental values at all temperatures. This gives us confidence in the site-specific values, which are currently inaccessible to experiment.

Thermochemistry of radicals formed by hydrogen abstraction from 1-butanol, 2-methyl-1-propanol, and butanal.

We calculate the standard state entropy, heat capacity, enthalpy, and Gibbs free energy for 13 radicals important for the combustion chemistry of biofuels. These thermochemical quantities are calculated from recently proposed methods for calculating partition functions of complex molecules by taking into account their multiple conformational structures and torsional anharmonicity. The radicals considered in this study are those obtained by hydrogen abstraction from 1-butanol, 2-methyl-1-propanol, and butanal. Electronic structure calculations for all conformers of the radicals were carried out using both density functional theory and explicitly correlated coupled cluster theory with quasipertubative inclusion of connected triple excitations. The heat capacity and entropy results are compared with sparsely available group additivity data, and trends in enthalpy and free energy as a function of radical center are discussed for the isomeric radicals.

Statistical thermodynamics of 1-butanol, 2-methyl-1-propanol, and butanal.

The purpose of the present investigation is to calculate partition functions and thermodynamic quantities, viz., entropy, enthalpy, heat capacity, and Gibbs free energies, for 1-butanol, 2-methyl-1-propanol, and butanal in the vapor phase. We employed the multi-structural (MS) anharmonicity method and electronic structure calculations including both explicitly correlated coupled cluster theory and density functional theory. The calculations are performed using all structures for each molecule and employing both the local harmonic approximation (MS-LH) and the inclusion of torsional anharmonicity (MS-T). The results obtained from the MS-T calculations are in excellent agreement with experimental data taken from the Thermodynamics Research Center data series and the CRC Handbook of Chemistry and Physics, where available. They are also compared with Benson's empirical group additivity values, where available; in most cases, the present results are more accurate than the group additivity values. In other cases, where experimental data (but not group additivity values) are available, we also obtain good agreement with experiment. This validates the accuracy of the electronic structure calculations when combined with the MS-T method for estimating the thermodynamic properties of systems with multiple torsions, and it increases our confidence in the predictions made with this method for molecules and temperatures where experimental or empirical data are not available.

Kinetics of the Hydrogen Abstraction from Carbon-3 of 1-Butanol by Hydroperoxyl Radical: Multi-Structural Variational Transition-State Calculations of a Reaction with 262 Conformations of the Transition State.

We estimated rate constants for the hydrogen abstraction from carbon-3 of 1-butanol by hydroperoxyl radical, a critically important reaction in the combustion of biofuel. We employed the recently developed multi-structural variational transition-state theory (MS-VTST), which utilizes a multifaceted dividing surface that allows us to include the contributions of multiple structures for reacting species and transition states. First, multiconfigurational Shepard interpolation-based on molecular-mechanics-guided interpolation of electronic-structure Hessian data obtained by the M08 HX/jun-cc-pVTZ electronic model chemistry-was used to obtain the portion of the potential energy surface needed for single-structure variational transition-state theory rate constants including multidimensional tunneling; then, the M08-HX/MG3S electronic model chemistry was used to calculate multi-structural torsional anharmonicity factors to complete the MS-VTST rate constant calculations. The lowest-energy structures of the transition state have strongly bent hydrogen bonds. Our results indicate that neglect of multi-structural anharmonicity would lead to errors of factors of 0.3, 46, and 171 at 200, 1000, and 2400 K for this reaction.

Carbondioxide rare-gas systems: sensitivity of basis sets and double-hybrid density functionals.

This study emphasizes on the performance of six newly developed double-hybrid density functionals (DHDF) in explaining the potential energy curves of different carbondioxide rare-gas systems. The basis set sensitivity has also been explored with the use of three basis sets. Our results suggest that for lighter He/Ne-CO(2) complexes, proper choice of DHDF and basis set lead to results those matches exactly with earlier calculations and also with the experiment. On the other hand, for heavier Ar/Kr-CO(2) complexes although the equilibrium separation distance matches exactly with earlier observations, the interaction energy values lie far apart. The overall investigation emphasizes on the fact that one has to tune the methods and basis sets properly to achieve good and satisfactory results.

Nonlinear optical switching properties in the furylfulgide aberchrome 540-dihydrobenzofuran derivative pair of photochromic materials.

Time-dependent density functional theoretical investigation has been carried out to justify the switching action of nonlinear optical properties in the furylfulgide Aberchrome 540 (FFA) and dihydrobenzofuran derivative (DHBF) photochromic pair of molecules. The effect of solvents on this switching action has also been addressed. The calculations suggest that DHBF has a higher optical coefficient compared to that of FFA. Notably, a dramatic increase in DHBF is observed in the second harmonic data, particularly in the solvent phase. The ratio of SHG tensor gradually decreases as the polarity of the solvent is decreased using a coulomb-attenuating functional irrespective of the basis sets used. An exploration of the excitation parameters suggests that high excited-state dipole moments are responsible for the observed large beta value in the case of the DHBF system relative to that of the FFA system.

Role of pi-conjugation in influencing the magnetic interactions in dinitrenes: a broken-symmetry approach.

In the present study, we investigated the magnetic interactions of some dinitrenes by employing the broken symmetry-unrestricted density functional theoretical (BS-UDFT) approach along with the use of three basis sets. The magnetic coupling parameter (J) has been calculated, and thereby the magnetic character of the molecule and the strength of magnetic interaction are explored for these molecules. The exchange coupling parameters for the corresponding unconjugated systems are also calculated to see the role of pi-conjugation. Our results suggest that a strong antiferromagnetic interaction exists in conjugated dinitrenes, and the strength of magnetic interaction decreases with increase in spacer length. For the unconjugated dinitrenes, the nature of magnetic interaction reduced appreciably and becomes weakly antiferromagnetic. The singlet-triplet energy gap for each system is also calculated. For the conjugated systems, it is observed that the singlet states are more stable than the triplet states, whereas for the unconjugated systems, the relative stability of the singlet state reduces to a considerable extent. This discrepancy of results for the conjugated and unconjugated dinitrenes can be attributed to the effect of pi-conjugation, and the results can be well explained by this effect.