Electronic structure with spin-orbit coupling effect of HfH molecule for laser cooling investigations.

The electronic structure, including the spin-orbit coupling effect of the HfH molecule, has been studied to determine if it can be cooled through Doppler and Sysphus laser cooling techniques. The multi-reference configuration interaction plus Davidson correction (MRCI + Q) method has been used to calculate its potential energy curves (P.E.C.s) in the Ω(±) and 2s+1Ʌ(+/-) representation. The spectroscopic constants Te, Re, ωe, Be, αe, the dipole moment µe, and the dissociation energies De agree very well with previously published work. In addition, we present in this work twenty new doublet and quartet states in the Ω(±) representation. The electronic transition dipole moment curves (TDMCs) between the lowest-lying electronic states have been investigated for the Δ - Π, Π - ∑+ and Δ - Φ transitions among specific Ω(±) states. The Franck-Condon factors (FCFs), the Einstein coefficient of spontaneous emission [Formula: see text] , and the radiative lifetime τ have been computed for the investigated transitions. In addition, properties of the molecules' electronic and vibrational states, such as the static dipole moment curves (D.M.C.s), the ionic character fionic, and the rovibrational constants are calculated. We deduce from our results that the HfH molecule is indeed a laser-cooling candidate that can reach a temperature as low as the nK regime. We present a complementary scheme with suitable experimental parameters. These results can be of great interest to experimental spectroscopists interested in ultracold diatomic molecules and their applications.

Theoretical insights into the HO●-induced oxidation of chlorpyrifos pesticide: Mechanism, kinetics, ecotoxicity, and cholinesterase inhibition of degradants.

The oxidation of the common pesticide chlorpyrifos (CPF) initiated by HO● radical and the risks of its degradation products were studied in the gaseous and aqueous phases via computational approaches. Oxidation mechanisms were investigated, including H-, Cl-, CH3- abstraction, HO●-addition, and single electron transfer. In both phases, HO●-addition at the C of the pyridyl ring is the most energetically favorable and spontaneous reaction, followed by H-abstraction reactions at methylene groups (i.e., at H19/H21 in the gas phase and H22/H28 in water). In contrast, other abstractions and electron transfer reactions are unfavorable. However, regarding the kinetics, the significant contribution to the oxidation of CPF is made from H-abstraction channels, mostly at the hydrogens of the methylene groups. CPF can be decomposed in a short time (5-8 h) in the gas phase, and it is more persistent in natural water with a lifetime between 24 days and 66 years, depending on the temperature and HO● concentration. Subsequent oxidation of the essential radical products with other oxidizing reagents, i.e., HO●, NO2●, NO●, and 3O2, gave primary neutral products P1-P15. Acute and chronic toxicity calculations estimate very toxic levels for CPF and two degradation products, P7w and P12w, in aquatic systems. The neurotoxicity of these products was investigated by docking and molecular dynamics. P7w and P12w show the most significant binding scores with acetylcholinesterases, while P8w and P13w are with butyrylcholinesterase enzyme. Finally, molecular dynamics illustrate stable interactions between CPF degradants and cholinesterase enzyme over a 100 ns time frame and determine P7w as the riskiest degradant to the neural developmental system.

Cyclo[n]carbons and catenanes from different perspectives: disentangling the molecular thread.

All-carbon atomic rings, cyclo[n]carbons, have recently attracted vivid attention of experimentalists and theoreticians. Among them, cyclo[18]carbon is the most studied system. In this paper, we summarize and review various properties of cyclo[n]carbons, emphasising the aspects of their aromaticity/antiaromaticity. In the first part, the trends in bonding patterns and selected aromaticity indices with the increasing size of the rings are discussed. In the second part we explore the properties of catenane models based on interlocked cyclo[18]carbon rings from different perspectives and investigate their behaviour under the action of external force using computational experiments.

Potential Energy Surface and Bound States of Ne-Li2+(X2Σg+) van der Waals Complex Based on Ab Initio Calculations.

Theoretical studies of the potential energy surface and vibrational bound states calculations were performed for the ground state of the Ne-Li2+(X2Σg+) van der Waals (vdW) complex. The intermolecular interactions were investigated by using an accurate monoconfigurational RCCSD(T) method and large basis sets (aug-cc-pVnZ, n = T, Q, 5), extrapolated to the complete basis set (CBS) limit. In turn, the obtained raw data from RCCSD(T)/CBS(Q5) calculations were numerically interpolated using the Morse + vdW model and the Reproducing Kernel Hilbert Space (RKHS) polynomial method to generate analytic expressions for the 2D-PES. The RKHS interpolated PES was then used to assess the bound states of the Ne-Li2+(X2Σg+) system through nuclear quantum calculations. By studying the aspect of the potential energy surface, the analysis sheds light on the behavior of the Ne-Li2+(X2Σg+) complex and its interactions between repulsive and attractive forces with other particles. By examining the vibrational states and wave functions of the system, the researchers were able to gain a better understanding of the behavior of the Ne-Li2+(X2Σg+) complex. The calculated radial and angular distributions for all even and odd symmetries are discussed in detail. We observe that the radial distributions exhibit a more complicated nodal structure, representing stretching vibrational behavior in the neon atom along its radial coordinate. For the highest bound states, the situation is very different, and the energies surpass the angular barrier.

Modelling interactions of cationic dimers in He droplets: microsolvation trends in HenK2+ clusters.

We report the results of a detailed theoretical investigation of small K2+-doped He clusters. The structural characteristics and stabilities of such cations are determined from ab initio electronic structure calculations at the MRCI+Q level of theory. The underlying interactions show a multireference character and such effects are analyzed. The interaction potentials are constructed employing an interpolation technique within the inverse problem theory method, while the nuclear quantum effects are computed for the trimers, their spatial arrangements are discussed, and information was extracted on the orientational anisotropy of the forces. We found that energetically the most stable conformer corresponds to linear arrangements that are taking place under large amplitude vibrations, with high zero-point energy. We have further looked into the behavior of higher-order species with various He atoms surrounding the cationic dopant. By using a sum of potentials approach and an evolutionary programming method, we analyzed the structural stability of clusters with up to six He atoms in comparison with interactions energies obtained from MRCI+Q quantum chemistry computations. Structures containing Hen motifs that characterize pure rare gas clusters, appear for the larger K2+-doped He clusters, showing selective growth during the microsolvation process of the alkali-dimer cation surrounded by He atoms. Such results indicate the existence of local solvation microstructures in these aggregates, where the cationic impurity could get trapped for a short time, contributing to the slow ionic mobility observed experimentally in ultra-cold He-droplets.

Theoretical Study of Cationic Alkali Dimers Interacting with He: Li2+-He and Na2+-He van der Waals Complexes.

We present a theoretical study on the potential energy surface and bound states of He-A2+ complexes, where A is one of the alkali Li or Na atoms. The intermolecular interactions were systematically investigated by high-level ab initio electronic structure computations, and the corresponding raw data were then employed to reproduce accurate analytical expressions of the potential surfaces. In turn, we used these potentials to evaluate bound configurations of the trimers from nuclear quantum calculations and to extract information on the effect of orientational anisotropy of the forces and the interplay between repulsive and attractive interaction within the potential surfaces. The spatial features of the bound states are analyzed and discussed in detail. We found that both systems are going under large amplitude stretching and bending motions with high zero-point energies. Despite the large differences in the potential well-depths, the correct treatment of nuclear quantum effects provides insights on the effect of different strength of the ionic interaction on the spectral structure of such cationic alkali van der Waals complexes, related to the mobility of ions and the formation of cold-molecules in He-controlled environments.