Search results for "Linear Algebra."

showing 10 items of 552 documents

Pilot applications of internally contracted multireference coupled cluster theory, and how to choose the cluster operator properly.

2011

The internally contracted multireference coupled cluster (icMRCC) method allows a highly accurate description of both static and dynamic correlation with a computational scaling similar to single reference coupled cluster theory. The authors show that the method can lose its orbital invariance and size consistency when no special care is taken in the elimination of redundant excitations. Using the BeH(2) model system, four schemes are compared which differ in their treatment of linear dependencies between excitations of different rank (such as between singles and doubles). While the energy curves agree within tens of μE(h) when truncating the cluster operator at double excitations (icMRCCSD…

Coupled clusterRank (linear algebra)ChemistryOperator (physics)Cluster (physics)General Physics and AstronomySpecial careStatistical physicsPhysical and Theoretical ChemistryAtomic physicsSize consistency and size extensivityLinear combinationEnergy (signal processing)The Journal of chemical physics
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Importance of Triples Contributions to NMR Spin–Spin Coupling Constants Computed at the CC3 and CCSDT Levels

2016

We present the first analytical implementation of CC3 second derivatives using the spin-unrestricted approach. This allows, for the first time, the calculation of nuclear spin–spin coupling constants (SSCC) relevant to NMR spectroscopy at the CC3 level of theory in a fully analytical manner. CC3 results for the SSCCs of a number of small molecules and their fluorine substituted derivatives are compared with the corresponding coupled cluster singles and doubles (CCSD) results obtained using specialized basis sets. For one-bond couplings the change when going from CCSD to CC3 is typically 1–3%, but much higher corrections were found for 1JCN in FCN, 15.7%, and 1JOF in OF2, 6.4%. The changes v…

Coupling constant010304 chemical physicsBasis (linear algebra)ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesComputer Science ApplicationsCoupled cluster0103 physical sciencesPhysical and Theoretical ChemistryAtomic physicsSpin-½Second derivativeJournal of Chemical Theory and Computation
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H2 O, H2 , HF, F2 and F2 O nuclear magnetic shielding constants and indirect nuclear spin-spin coupling constants (SSCCs) in the BHandH/pcJ-n and BHa…

2009

Good performance of segmented contracted basis sets XZP, where X = D, T, Q and 5, for obtaining H(2)O, H(2), HF, F(2) and F(2)O nuclear isotropic shielding constants in the BHandH Kohn-Sham basis set limit was shown. The results of two- and three-parameter complete basis set limit extrapolation schemes were compared with experimental results, earlier literature data and benchmark ab initio results. Similar convergence patterns of shieldings obtained from calculations using general purpose XZP basis sets and from polarization-consistent basis sets pcS-n and pcJ-n, where n = 0, 1, 2, 3 and 4, designed to accurately predict magnetic properties were observed. On the contrary, the SSCCs were mor…

Coupling constantBasis (linear algebra)ChemistryComputational chemistryAtomAb initioExtrapolationKohn–Sham equationsGeneral Materials ScienceGeneral ChemistryAtomic physicsSpin (physics)Basis setMagnetic Resonance in Chemistry
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Basis Set Convergence of Indirect Spin-Spin Coupling Constants in the Kohn-Sham Limit for Several Small Molecules

2012

The performance of more than 40 density functionals in predicting indirect spin-spin coupling constants (SSCCs) in the Kohn-Sham basis set limit was tested. For comparison, similar calculations were performed using the RHF, SOPPA, SOPPA(CC2), and SOPPA(CCSD) methods, and the results were estimated toward the complete basis set (CBS) limit. The SSCCs of nine small molecules (N(2), CO, CO(2), NH(3), CH(4), C(2)H(2), C(2)H(4), C(2)H(6), and C(6)H(6)) were calculated using the dedicated Jensen pcJ-n polarization-consistent basis sets and used for the CBS limit estimations within the Kohn-Sham limit. These CBS results were compared with calculations using the aug-cc-pVTZ-J basis set. Among the 4…

Coupling constantBasis (linear algebra)Computational chemistryChemistryConvergence (routing)Kohn–Sham equationsLimit (mathematics)Physical and Theoretical ChemistryMolecular physicsSmall moleculeBasis setSpin-½
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Relative Transition Probability Measurements for Prominent Infrared Spectral Lines of NI

2002

Applying a high-current wall-stabilized arc operated either in helium or in argon always with some admixtures of nitrogen, relative transition probabilities for more than 100 individual spectral lines (fine structure components) have been measured. The studied lines belong mainly to the 3p–3d and 3p–4s transition arrays. Ten lines of the measured set are intersystem transitions. Our data are compared with other experimental results (for about one half of the studied set there are available), with evaluated on the basis of the LS coupling scheme, with semiempirical data, and with recent CIV3 calculations. Some of our results are compared also with experimental data for the next member of the…

CouplingPhysicsArgonBasis (linear algebra)Infraredchemistry.chemical_elementCondensed Matter PhysicsAtomic and Molecular Physics and OpticsAstronomical spectroscopySpectral linechemistryAtomic physicsMathematical PhysicsHeliumLine (formation)Physica Scripta
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Ab-initio crystal structure analysis and refinement approaches of oligo p-benzamides based on electron diffraction data.

2012

Ab-initio crystal structure analysis of organic materials from electron diffraction data is presented. The data were collected using the automated electron diffraction tomography (ADT) technique. The structure solution and refinement route is first validated on the basis of the known crystal structure of tri-p-benzamide. The same procedure is then applied to solve the previously unknown crystal structure of tetra-p-benzamide. In the crystal structure of tetra-p-benzamide, an unusual hydrogen-bonding scheme is realised; the hydrogen-bonding scheme is, however, in perfect agreement with solid-state NMR data.

CrystallographyElectron diffractionBasis (linear algebra)ChemistryAb initioGeneral MedicineCrystal structureNmr dataGeneral Biochemistry Genetics and Molecular BiologyElectron backscatter diffractionActa crystallographica. Section B, Structural science
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Response properties with explicitly correlated coupled-cluster methods using a Slater-type correlation factor and cusp conditions

2009

The recently proposed extension of the explicitly correlated coupled-cluster ansatz using cusp conditions [A. Kohn, J. Chem. Phys. 130, 104104 (2009)] is tested for suitability in the calculation of response properties. For this purpose, static and dynamic electrical properties up to ESHG hyperpolarizabilities as well as optical rotations have been computed within the CCSD(F12) model. It is shown that effectively converged correlation contributions can reliably be obtained using augmented quadruple zeta basis sets already. The ansatz is optionally equipped with an extension capable of reducing the one-electron basis set error. A further simplification of the method specific Lagrangian aimed…

Cusp (singularity)Coupled clusterBasis (linear algebra)ChemistryQuantum mechanicsGeneral Physics and AstronomyStatistical physicsExtension (predicate logic)Physical and Theoretical ChemistryOptical rotationType (model theory)Basis setAnsatzThe Journal of Chemical Physics
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Criminal networks analysis in missing data scenarios through graph distances.

2021

Data collected in criminal investigations may suffer from: (i) incompleteness, due to the covert nature of criminal organisations; (ii) incorrectness, caused by either unintentional data collection errors and intentional deception by criminals; (iii) inconsistency, when the same information is collected into law enforcement databases multiple times, or in different formats. In this paper we analyse nine real criminal networks of different nature (i.e., Mafia networks, criminal street gangs and terrorist organizations) in order to quantify the impact of incomplete data and to determine which network type is most affected by it. The networks are firstly pruned following two specific methods: …

Data AnalysisFOS: Computer and information sciencesComputer and Information SciencesScienceIntelligenceSocial SciencesTransportationCriminologyCivil EngineeringSocial NetworkingComputer Science - Computers and SocietyLaw EnforcementSociologyComputers and Society (cs.CY)PsychologyHumansComputer NetworksSocial and Information Networks (cs.SI)Algorithms; Humans; Terrorism; Criminals; Data Analysis; Social NetworkingSettore INF/01 - InformaticaQCognitive PsychologyRBiology and Life SciencesEigenvaluesComputer Science - Social and Information NetworksCriminalsTransportation InfrastructurePoliceRoadsProfessionsAlgebraLinear AlgebraPeople and PlacesPhysical SciencesEngineering and TechnologyCognitive ScienceMedicineLaw and Legal SciencesPopulation GroupingsTerrorismCrimeCriminal Justice SystemMathematicsNetwork AnalysisAlgorithmsResearch ArticleNeurosciencePLoS ONE
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NMR chemical shift calculations within local correlation methods: the GIAO-LMP2 approach

2000

A scheme for the calculation of NMR chemical shifts using local second-order Moller–Plesset (LMP2) perturbation theory together with gauge-including atomic orbitals (GIAOs) is presented. Test calculations on the basis of a preliminary implementation within a conventional GIAO-MP2 code show that the deviations between GIAO-LMP2 and GIAO-MP2 are small, e.g., for 13C typically less than 1 ppm, and that the GIAO-LMP2 approach holds great promise for application to larger molecules.

Density matrixAtomic orbitalBasis (linear algebra)ChemistryComputational chemistryChemical shiftGeneral Physics and AstronomyMoleculeCorrelation methodPhysical and Theoretical ChemistryPerturbation theoryMolecular physicsPhysical Chemistry Chemical Physics
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Fast noniterative orbital localization for large molecules

2006

We use Cholesky decomposition of the density matrix in atomic orbital basis to define a new set of occupied molecular orbital coefficients. Analysis of the resulting orbitals ("Cholesky molecular orbitals") demonstrates their localized character inherited from the sparsity of the density matrix. Comparison with the results of traditional iterative localization schemes shows minor differences with respect to a number of suitable measures of locality, particularly the scaling with system size of orbital pair domains used in local correlation methods. The Cholesky procedure for generating orthonormal localized orbitals is noniterative and may be made linear scaling. Although our present implem…

Density matrixPhysicsBasis (linear algebra)Minor (linear algebra)General Physics and AstronomySTO-nG basis setsOrbital calculationsUNESCO::FÍSICA::Química físicaHF calculations ; Orbital calculationsPhysics and Astronomy (all)Atomic orbitalComputational chemistryMolecular orbitalOrthonormal basisStatistical physicsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]HF calculationsCholesky decompositionThe Journal of Chemical Physics
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