Search results for "Coupled cluster"

showing 10 items of 175 documents

Coupled-Cluster study of ‘no-pair’ bonding in the tetrahedral Cu4 cluster

2011

Abstract Ab initio Coupled-Cluster calculations with single and double excitations and perturbative correction to the triple, CCSD(T), have been carried out for the high-spin electronic state, ( 5 A 2 ) , of the copper cluster Cu 4 in its tetrahedral arrangement. Like alkali metals clusters, tetrahedral Cu 4 presents a bound quintet state, i.e., a situation where all the valence electrons are unpaired. This rather exotic wavefunction, also known as no-pair bonding state, is examined in detail. The influence of the basis set is also analyzed, as well as the importance of the core correlation and the effect of the basis-set superposition errors.

010304 chemical physicsChemistryAb initioGeneral Physics and Astronomy010402 general chemistryAlkali metal01 natural sciences0104 chemical sciencesCoupled cluster0103 physical sciencesPhysics::Atomic and Molecular ClustersCluster (physics)Tetrahedron[CHIM]Chemical SciencesPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsValence electronWave functionBasis setChemical Physics Letters
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Communication: multireference equation of motion coupled cluster: a transform and diagonalize approach to electronic structure.

2014

The novel multireference equation-of-motion coupled-cluster (MREOM-CC) approaches provide versatile and accurate access to a large number of electronic states. The methods proceed by a sequence of many-body similarity transformations and a subsequent diagonalization of the transformed Hamiltonian over a compact subspace. The transformed Hamiltonian is a connected entity and preserves spin- and spatial symmetry properties of the original Hamiltonian, but is no longer Hermitean. The final diagonalization spaces are defined in terms of a complete active space (CAS) and limited excitations (1h, 1p, 2h, …) out of the CAS. The methods are invariant to rotations of orbitals within their respective…

010304 chemical physicsChemistryGeneral Physics and AstronomyEquations of motionElectronic structure010402 general chemistry7. Clean energy01 natural sciencesLinear subspace0104 chemical sciencessymbols.namesakeCoupled clusterAtomic orbitalQuantum mechanics0103 physical sciencessymbolsComplete active spacePhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Subspace topologyThe Journal of chemical physics
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Spin-orbit ZORA and four-component Dirac-Coulomb estimation of relativistic corrections to isotropic nuclear shieldings and chemical shifts of noble …

2015

Hartree-Fock and density functional theory with the hybrid B3LYP and general gradient KT2 exchange-correlation functionals were used for nonrelativistic and relativistic nuclear magnetic shielding calculations of helium, neon, argon, krypton, and xenon dimers and free atoms. Relativistic corrections were calculated with the scalar and spin-orbit zeroth-order regular approximation Hamiltonian in combination with the large Slater-type basis set QZ4P as well as with the four-component Dirac-Coulomb Hamiltonian using Dyall's acv4z basis sets. The relativistic corrections to the nuclear magnetic shieldings and chemical shifts are combined with nonrelativistic coupled cluster singles and doubles …

010304 chemical physicsElectronic correlationChemical shiftNuclear TheoryKryptonchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesComputational Mathematicssymbols.namesakeNeonCoupled clusterchemistry0103 physical sciencesPhysics::Atomic and Molecular ClusterssymbolsDensity functional theoryAtomic physicsHamiltonian (quantum mechanics)Basis setJournal of Computational Chemistry
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High excitations in coupled-cluster series: vibrational energy levels of ammonia

2004

The ammonia molecule containing large amplitude inversion motion is a revealing system in examining high-order correlation effects on potential energy surfaces. Correlation contributions to the equilibrium and saddle point geometries, inversion barrier height and vibrational energy levels, including inversion splittings, have been investigated. A six-dimensional Taylor-type series expansion of the Born–Oppenheimer potential energy surface, which is scaled to different levels of theory, is used to determine vibrational energy levels and inversion splittings variationally. The electronic energies are calculated by coupled-cluster methods, combining explicitly correlated R12 theory (which incl…

010304 chemical physicsElectronic correlationChemistryBiophysics010402 general chemistryCondensed Matter Physics01 natural sciencesPotential energyFull configuration interaction0104 chemical sciencesCoupled clusterSaddle point0103 physical sciencesPotential energy surfacePhysical and Theoretical ChemistryAtomic physicsWave functionSeries expansionMolecular BiologyMolecular Physics
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Calculation of electronic g-tensors using coupled cluster theory.

2009

A scheme for the calculation of the electronic g-tensor at the coupled cluster (CC) level is presented. The reported implementation employs an effective one-electron spin-orbit operator, allows the inclusion of arbitrary excitations in the cluster operator, and offers various options concerning the treatment of orbital relaxation and choice of reference determinants. In addition, the use of gauge-including atomic orbitals (GIAOs) is possible to overcome the gauge origin problem. Benchmark calculations for the NH ((3)Sigma(-)) radical reveal the importance of electron correlation effects for the accurate prediction of the g-shift as well as the slow basis set convergence of such calculations…

010304 chemical physicsElectronic correlationChemistryOperator (physics)010402 general chemistry01 natural sciences0104 chemical sciencesHybrid functionalCoupled clusterAtomic orbitalQuantum mechanics0103 physical sciencesCluster (physics)Density functional theoryPhysical and Theoretical ChemistryBasis setThe journal of physical chemistry. A
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Bond Dissociation Energies for Diatomic Molecules Containing 3d Transition Metals: Benchmark Scalar-Relativistic Coupled-Cluster Calculations for 20 …

2017

Benchmark scalar-relativistic coupled-cluster calculations for dissociation energies of the 20 diatomic molecules containing 3d transition metals in the 3dMLBE20 database ( J. Chem. Theory Comput. 2015 , 11 , 2036 ) are reported. Electron correlation and basis set effects are systematically studied. The agreement between theory and experiment is in general satisfactory. For a subset of 16 molecules, the standard deviation between computational and experimental values is 9 kJ/mol with the maximum deviation being 15 kJ/mol. The discrepancies between theory and experiment remain substantial (more than 20 kJ/mol) for VH, CrH, CoH, and FeH. To explore the source of the latter discrepancies, the …

010304 chemical physicsElectronic correlationChemistryThermodynamics010402 general chemistry01 natural sciencesDiatomic moleculeHeterolysisBond-dissociation energyDissociation (chemistry)0104 chemical sciencesComputer Science ApplicationsCoupled cluster0103 physical sciencesMoleculePhysical and Theoretical ChemistryAtomic physicsBasis setJournal of Chemical Theory and Computation
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Approximate treatment of higher excitations in coupled-cluster theory. II. Extension to general single-determinant reference functions and improved a…

2008

The theory and implementation of approximate coupled-cluster (CC), in particular approximate CC singles, doubles, triples, and quadruples methods, are discussed for general single-determinant reference functions. While the extension of iterative approximate models to the non-Hartree-Fock case is straightforward, the generalization of perturbative approaches is not trivial. In contrast to the corresponding perturbative triples methods, there are additional terms required for non-Hartree-Fock reference functions, and there are several possibilities to derive approximations to these terms. As it turns out impossible to develop an approach that is consistent with the canonical Hartree-Fock-base…

010304 chemical physicsGeneralizationHartree–Fock methodGeneral Physics and AstronomyContrast (statistics)Extension (predicate logic)010402 general chemistry01 natural sciences0104 chemical sciencesCoupled clusterComputational chemistry0103 physical sciencesApplied mathematicsPerturbation theory (quantum mechanics)Physical and Theoretical ChemistryMathematicsThe Journal of Chemical Physics
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Cycloaddition of Strained Cyclic Alkenes and Ortho-Quinones : A Distortion/Interaction Analysis

2020

The chemistry of strained unsaturated cyclic compounds has experienced remarkable growth in recent years via the development of metal–free click reactions. Among these reactions, the cycloaddition of cyclopropenes and their analogues to ortho-quinones has been established as a highly promising click reaction. The present work investigates the mechanism involved in the cycloaddition of strained dienes to ortho-quinones and structural factors that would influence this reaction. For this purpose, we use B97D density functional theory calculations throughout, and for relevant cases, we use spin component–scaled MP2 calculations and single–point domain-based local pair natural orbital coupled cl…

010405 organic chemistryChemistryOrganic ChemistryInteraction model010402 general chemistry01 natural sciencesOrganische ChemieArticleCycloaddition0104 chemical sciencesCyclic AlkenesCoupled clusterCompostos orgànicsComputational chemistryDistortionClick chemistryLife ScienceDensity functional theorySpin (physics)Química orgànicaVLAG
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Nuclear anapole moment interaction in BaF from relativistic coupled-cluster theory

2018

We present high accuracy relativistic coupled cluster calculations of the P-odd interaction coefficient $W_A$ describing the nuclear anapole moment effect on the molecular electronic structure. The molecule under study, BaF, is considered a promising candidate for the measurement of the nuclear anapole moment, and the preparation for the experiment is now underway [Altunas et al., Phys. Rev. Lett. 120, 142501 (2018)]. Influence of various computational parameters (size of the basis set, treatment of relativistic effects, and treatment of electron correlation) on the calculated $W_A$ coefficient is investigated and a recommended value of 147.7 Hz with an estimated uncertainty of 1.5% is prop…

ATOMIC PARITY NONCONSERVATIONDIATOMIC-MOLECULESP-ODDVIOLATIONAtomic Physics (physics.atom-ph)Nuclear TheoryDENSITY FUNCTIONALSFOS: Physical sciences01 natural sciences010305 fluids & plasmasPhysics - Atomic PhysicsENHANCEMENTMolecular electronic structure0103 physical sciencesIMPLEMENTATIONNuclear Experiment010306 general physicsBasis setPhysicsElectronic correlationELECTRIC-FIELD GRADIENTSDiatomic moleculeWEAK-INTERACTIONSCoupled clusterMoment (physics)Atomic physicsRelativistic quantum chemistryAPPROXIMATIONPhysical Review A
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A Non-antisymmetric Tensor Contraction Engine for the Automated Implementation of Spin-Adapted Coupled Cluster Approaches

2015

We present a symbolic manipulation algorithm for the efficient automated implementation of rigorously spin-free coupled cluster (CC) theories based on a unitary group parametrization. Due to the lack of antisymmetry of the unitary group generators under index permutations, all quantities involved in the equations are expressed in terms of non-antisymmetric tensors. Given two tensors, all possible contractions are first generated by applying Wick's theorem. Each term is then put down in the form of a non-antisymmetric Goldstone diagram by assigning its contraction topology. The subsequent simplification of the equations by summing up equivalent terms and their factorization by identifying co…

AlgebraTheoretical computer scienceCoupled clusterFactorizationAntisymmetric tensorUnitary groupAntisymmetryTensorPhysical and Theoretical ChemistrySymbolic computationNetwork topologyComputer Science ApplicationsMathematicsJournal of Chemical Theory and Computation
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