Search results for "INTERACTION"

showing 10 items of 5710 documents

Many-Body Expanded Full Configuration Interaction. II. Strongly Correlated Regime

2019

In this second part of our series on the recently proposed many-body expanded full configuration interaction (MBE-FCI) method, we introduce the concept of multideterminantal expansion references. Through theoretical arguments and numerical validations, the use of this class of starting points is shown to result in a focussed compression of the MBE decomposition of the FCI energy, thus allowing chemical problems dominated by strong correlation to be addressed by the method. The general applicability and performance enhancements of MBE-FCI are verified for standard stress tests such as the bond dissociations in H$_2$O, N$_2$, C$_2$, and a linear H$_{10}$ chain. Furthermore, the benefits of em…

Chemical Physics (physics.chem-ph)010304 chemical physicsThe RenaissanceFOS: Physical sciences010402 general chemistry01 natural sciencesFull configuration interactionMany body0104 chemical sciencesComputer Science ApplicationsFormalism (philosophy of mathematics)Physics - Chemical Physics0103 physical sciencesStatistical physicsPhysical and Theoretical ChemistryGround state
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Virtual Orbital Many-Body Expansions: A Possible Route towards the Full Configuration Interaction Limit

2017

In the present letter, it is demonstrated how full configuration interaction (FCI) results in extended basis sets may be obtained to within sub-kJ/mol accuracy by decomposing the energy in terms of many-body expansions in the virtual orbitals of the molecular system at hand. This extension of the FCI application range lends itself to two unique features of the current approach, namely that the total energy calculation can be performed entirely within considerably reduced orbital subspaces and may be so by means of embarrassingly parallel programming. Facilitated by a rigorous and methodical screening protocol and further aided by expansion points different from the Hartree-Fock solution, al…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsBasis (linear algebra)Embarrassingly parallelFOS: Physical sciences010402 general chemistry01 natural sciencesFull configuration interactionLinear subspace0104 chemical sciencesRange (mathematics)Atomic orbitalComputational chemistryPhysics - Chemical Physics0103 physical sciencesGeneral Materials ScienceLimit (mathematics)Statistical physicsPhysical and Theoretical ChemistryEnergy (signal processing)
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Convergence of coupled cluster perturbation theory.

2016

The convergence of a recently proposed coupled cluster (CC) family of perturbation series [Eriksen, J. J. et al., J. Chem. Phys. 140, 064108 (2014)], in which the energetic difference between two CC models - a low-level parent and a high-level target model - is expanded in orders of the M{\o}ller-Plesset (MP) fluctuation potential, is investigated for four prototypical closed-shell systems (Ne, singlet methylene, distorted HF, and the fluoride anion) in standard and augmented basis sets. In these investigations, energy corrections of the various series have been calculated to high orders and their convergence radii determined by probing for possible front- and back-door intruder states, the…

Chemical Physics (physics.chem-ph)Physics010304 chemical physicsFOS: Physical sciencesGeneral Physics and AstronomyPerturbation (astronomy)010402 general chemistry01 natural sciencesFull configuration interaction0104 chemical sciencesIonCoupled clusterPhysics - Chemical Physics0103 physical sciencesSinglet stateStatistical physicsPhysical and Theoretical ChemistryThe Journal of chemical physics
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HfF+ as a candidate to search for the nuclear weak quadrupole moment

2018

Nuclei with a quadrupole deformation, such as $^{177}\mathrm{Hf}$ have enhanced weak quadrupole moment which induces the tensor weak electron-nucleus interaction in atoms and molecules. Corresponding parity-non-conserving (PNC) effect is strongly enhanced in the ${}^{3}{\mathrm{\ensuremath{\Delta}}}_{1}$ electronic state of the $^{177}\mathrm{HfF}^{+}$ cation which has very close opposite parity levels mixed by this tensor interaction. In the present paper we perform relativistic many-body calculations of this PNC effect. It is shown that the tensor weak interaction induced by the weak quadrupole moment gives the dominating contribution to the PNC effects in $^{177}\mathrm{HfF}^{+}$ which s…

Chemical Physics (physics.chem-ph)PhysicsAtomic Physics (physics.atom-ph)Nuclear TheoryAtoms in moleculesFOS: Physical sciencesParity (physics)Weak interaction01 natural sciencesPhysics - Atomic Physics010305 fluids & plasmasPhysics - Chemical Physics0103 physical sciencesQuadrupoleNeutronPhysics::Atomic PhysicsAtomic physics010306 general physicsPhysical Review A
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Measuring molecular parity nonconservation using nuclear-magnetic-resonance spectroscopy

2017

The weak interaction does not conserve parity and therefore induces energy shifts in chiral enantiomers that should in principle be detectable in molecular spectra. Unfortunately, the magnitude of the expected shifts are small and in spectra of a mixture of enantiomers, the energy shifts are not resolvable. We propose a nuclear magnetic resonance (NMR) experiment in which we titrate the chirality (enantiomeric excess) of a solvent and measure the diasteriomeric splitting in the spectra of a chiral solute in order to search for an anomalous offset due to parity nonconservation (PNC). We present a proof-of-principle experiment in which we search for PNC in the \textsuperscript{13}C resonances…

Chemical Physics (physics.chem-ph)PhysicsGeneral PhysicsChemical shiftphysics.chem-phFOS: Physical sciencesParity (physics)Nuclear magnetic resonance spectroscopyWeak interaction010402 general chemistry01 natural sciencesSpectral lineMathematical Sciences0104 chemical sciences3. Good healthPhysics - Chemical Physics0103 physical sciencesPhysical SciencesChemical SciencesPhysics::Atomic PhysicsAtomic physicsEnantiomer010306 general physicsEnantiomeric excessChirality (chemistry)
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Adversarial reverse mapping of equilibrated condensed-phase molecular structures

2020

A tight and consistent link between resolutions is crucial to further expand the impact of multiscale modeling for complex materials. We herein tackle the generation of condensed molecular structures as a refinement -- backmapping -- of a coarse-grained structure. Traditional schemes start from a rough coarse-to-fine mapping and perform further energy minimization and molecular dynamics simulations to equilibrate the system. In this study we introduce DeepBackmap: A deep neural network based approach to directly predict equilibrated molecular structures for condensed-phase systems. We use generative adversarial networks to learn the Boltzmann distribution from training data and realize reve…

Chemical Physics (physics.chem-ph)Structure (mathematical logic)Artificial neural networkComputer sciencePhase (waves)FOS: Physical sciencesLink (geometry)Condensed Matter - Soft Condensed MatterComputational Physics (physics.comp-ph)Energy minimizationMultiscale modelingBoltzmann distributionHuman-Computer InteractionMolecular dynamicsArtificial IntelligencePhysics - Chemical PhysicsSoft Condensed Matter (cond-mat.soft)Physics - Computational PhysicsAlgorithmSoftwareMachine Learning: Science and Technology
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Incremental Treatments of the Full Configuration Interaction Problem

2020

The recent many-body expanded full configuration interaction (MBE-FCI) method is reviewed by critically assessing its advantages and drawbacks in the context of contemporary near-exact electronic structure theory. Besides providing a succinct summary of the history of MBE-FCI to date within a generalized and unified theoretical setting, its finer algorithmic details are discussed alongside our optimized computational implementation of the theory. A selected few of the most recent applications of MBE-FCI are revisited, before we close by outlining its future research directions as well as its place among modern near-exact wave function-based methods.

Chemical Physics (physics.chem-ph)Theoretical computer science010304 chemical physicsComputer scienceFOS: Physical sciencesContext (language use)010402 general chemistry01 natural sciencesBiochemistryFull configuration interaction0104 chemical sciencesComputer Science ApplicationsComputational MathematicsPhysics - Chemical Physics0103 physical sciencesMaterials ChemistryPhysical and Theoretical Chemistry
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Book Review: Ions in Solution: Basic Principles of Chemical Interactions. By J. Burgess

1989

Chemical engineeringComputational chemistryChemistryMetal ions in aqueous solutionGeneral MedicineGeneral ChemistryChemical interactionCatalysisAngewandte Chemie International Edition in English
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Making Broad Proteome Protein Measurements in 1−5 min Using High-Speed RPLC Separations and High-Accuracy Mass Measurements

2005

The throughput of proteomics measurements that provide broad protein coverage is limited by the quality and speed of both the separations as well as the subsequent mass spectrometric analysis; at present, analysis times can range anywhere from hours (high throughput) to days or longer (low throughput). We have explored the basis for proteomics analyses conducted on the order of minutes using high-speed capillary RPLC combined through on-line electrospray ionization interface with high-accuracy mass spectrometry (MS) measurements. Short 0.8-microm porous C18 particle-packed 50-microm-i.d. capillaries were used to speed the RPLC separations while still providing high-quality separations. Both…

Chemical ionizationElectrosprayTime FactorsChromatographyProteomeChemistryElutionElectrospray ionizationAnalytical chemistryMass spectrometryMass SpectrometryPeptide FragmentsFourier transform ion cyclotron resonanceFourier transform spectroscopyAnalytical ChemistrySpectroscopy Fourier Transform InfraredAnimalsHumansTrypsinHydrophobic and Hydrophilic InteractionsIon cyclotron resonanceChromatography LiquidAnalytical Chemistry
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Visualizing Solubilization by a Realistic Particle Model in Chemistry Education

2019

An application for the visualization of the mixing process of two different types of structureless interacting particles is presented. The application allows to demonstrate on a qualitative basis, as well as by quantitatively monitoring the time evolution of the fractions of aggregates of different sizes, that the formation of a homogeneous mixture is the result of favorable solute-solvent interactions as well as by temperature. It is suggested that, along with the use of suitable macroscopic examples, visualizations by the present application are useful in elucidating concepts related to miscibility/solubility. The application is based on a two-dimensional realistic dynamic model where ato…

Chemistry Education Intermolecular Interaction Mixtures Molecular Dynamics Particle Model Solubility.Settore CHIM/02 - Chimica Fisica
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