Search results for "Open shell"

showing 10 items of 48 documents

Vertical spectrum of the C2H 2+ system. An open shell (SC)2-CAS-SDCI study

2003

The open shell (SC)(2)-CAS-SDCI method along with a basis set of atomic natural orbitals (ANO) has been applied for calculating the main ionization potentials of acetylene, as well as the manifold of excited states of the different symmetries up to 32 eV. In this method, the single and double excitations of a CAS space are generated and the corresponding CI matrix is corrected by means of the (SC)(2) procedure that cancels the size-extensivity error and adds some high order contributions. The mean absolute error for the outer-valence X (2)Pi(u)(1pi(u) (-1)), A (2)Sigma(g) (+)(3sigma(g) (-1)), and B (2)Sigma(u) (+)(2sigma(u) (-1)) states, and the inner-valence C (2)Sigma(g) (+)(2sigma(g) (-1…

Computational MathematicsChemistryExcited stateSigmaGeneral ChemistryState (functional analysis)Complete active spaceAtomic physicsConfiguration interactionWave functionOpen shellBasis setJournal of Computational Chemistry
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Communication: spin-orbit splittings in degenerate open-shell states via Mukherjee's multireference coupled-cluster theory: a measure for the couplin…

2012

We propose a generally applicable scheme for the computation of spin-orbit (SO) splittings in degenerate open-shell systems using multireference coupled-cluster (MRCC) theory. As a specific method, Mukherjee's version of MRCC (Mk-MRCC) in conjunction with an effective mean-field SO operator is adapted for this purpose. An expression for the SO splittings is derived and implemented using Mk-MRCC analytic derivative techniques. The computed SO splittings are found to be in satisfactory agreement with experimental data. Due to the symmetry properties of the SO operator, SO splittings can be considered a quality measure for the coupling between reference determinants in Jeziorski-Monkhorst base…

CouplingPhysicsCoupled clusterOperator (physics)Quantum mechanicsDegenerate energy levelsGeneral Physics and AstronomyQuantum TheoryPhysical and Theoretical ChemistryOrbit (control theory)Spin (physics)Measure (mathematics)Open shellThe Journal of chemical physics
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An Open-Shell Coronoid with Hybrid Chichibabin-Schlenk Conjugation.

2021

A hexaradicaloid molecule with alternating Kekule and non-Kekule connectivities between adjacent spin centers was obtained by fusing two conjugation motifs in Chichibabin and Schlenk hydrocarbons into a coronoid structure. 1 H NMR, ESR, and SQUID experiments and computational analyses show that the system has a singlet ground state with a significant hexaradicaloid character (γ0 =0.826, γ1 =γ2 =0.773). It has multiple thermally accessible high-spin states (up to the septet), with uniform energy gaps of ca 1.0 kcal mol-1 between consecutive multiplicities. In line with its open-shell character, the coronoid has a small electronic band gap (ca. 0.8 eV) and undergoes two consecutive one-electr…

CrystallographyMaterials scienceΠ conjugationCationic polymerizationMoleculeAromaticityGeneral MedicineGeneral ChemistryAbsorption (chemistry)Spin (physics)SpectroscopyOpen shellCatalysisAngewandte Chemie (International ed. in English)
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Molecular and supramolecular structures of self-assembled Cu(II) and Co(II) complexes with 4,4’-[6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazine-2,4-…

2020

Abstract The molecular and supramolecular structures of [Cu(PTM)Cl2]∗0.75MeOH (1), [Co(PTM)Cl2]; (2A) and [Co(PTM)Cl2(EtOH)]; (2B) complexes, where PTM is 4,4’-[6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazine-2,4-diyl]dimorpholine, were presented. In complexes 1 and 2A, the Cu(II) and Co(II) are tetra-coordinated with a distorted tetrahedral coordination environment. In case of complex 2B, an additional ethanol molecule is found coordinated with Co(II) leading to a highly distorted penta-coordinated Co(II) complex. In all cases, the PTM ligand is acting as a bidentate NN-chelate. Hirshfeld surface analysis indicated the importance of H⋯H (49.0–55.1%), Cl⋯H (18.8–20.5%) and O⋯H (8.3–9.9%) co…

Denticity010405 organic chemistryLigandChemistryOrganic ChemistryAtoms in moleculesSupramolecular chemistry010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystallographyCovalent bondMoleculeOpen shellSpectroscopyNatural bond orbitalJournal of Molecular Structure
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Molybdenum Open-Shell Organometallics. Spin State Changes and Pairing Energy Effects

1997

International audience

EnergySpin states010405 organic chemistrychemistry.chemical_elementGroup 15 compoundsGeneral MedicineGeneral ChemistryLigands010402 general chemistryQuantum mechanics01 natural sciencesMolecular physicsStabilization0104 chemical scienceschemistryMolybdenumPairing[CHIM.COOR]Chemical Sciences/Coordination chemistryOpen shellComputingMilieux_MISCELLANEOUSEnergy (signal processing)Accounts of Chemical Research
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Interstitial defects in diamond: A quantum mechanical simulation of their EPR constants and vibrational spectra

2020

The local geometry, electronic structure, and vibrational features of three vicinal double interstitial defects in diamond, ICIC, ICIN, and ININ, are investigated and compared with those of three "simple" ⟨100⟩ interstitial defects, ICC, ICN, and INN, previously reported by Salustro et al. [Phys. Chem. Chem. Phys. 20, 16615 (2018)], using a similar quantum mechanical approach based on the B3LYP functional constructed from Gaussian-type basis sets, within a supercell scheme, as implemented in the CRYSTAL code. For the first time, the Fermi contact term and hyperfine coupling tensor B of the four open shell structures, ICIC, ICIN, ICC, and ICN, are evaluated and compared with the available ex…

Fermi contact interactionMaterials science010304 chemical physicsGeneral Physics and AstronomyDiamondElectronic structureengineering.material010402 general chemistry01 natural sciencesMolecular physics0104 chemical scienceslaw.inventionCrystallaw0103 physical sciencesSupercell (crystal)engineeringPhysical and Theoretical ChemistryElectron paramagnetic resonanceOpen shellVicinalThe Journal of Chemical Physics
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The study of neutron-rich nuclei production in the region of the closed shell N=126 in the multi-nucleon transfer reaction 136Xe+208Pb

2015

Expérience LNL/PRISMA; International audience; The unexplored area of heavy neutron rich nuclei is extremely important for nuclearastrophysics investigations and, in particular, for the understanding of the r-process ofastrophysical nucleogenesis. For the production of heavy neutron rich nuclei located along theneutron closed shell N=126 (probably the last "waiting point" in the r-process of nucleosynthesis)the low-energy multi-nucleon transfer reaction 136Xe+208Pb at Elab=870MeV was explored.Due to the stabilizing eect of the closed neutron shells in both nuclei, N=82 and N=126, andthe rather favorable proton transfer from lead to xenon, the light fragments formed in this processare well b…

Historynuclear astro-physicsProtonNuclear Theoryspektrometritchemistry.chemical_element[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]01 natural sciences7. Clean energyEducationNuclear physicsXenonNucleosynthesisneutron-rich nuclei0103 physical sciencesNuclear astrophysicschemical elementsNeutron010306 general physicsNuclear ExperimentOpen shellheavy neutron rich nuclei PRISMA spectrometerPhysicsneutron shellsSpectrometer010308 nuclear & particles physicsbeam linesclosed shellsComputer Science Applicationsneutron beamschemistrytime of flightAtomic physicsNucleon
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The Al 50 Cp* 12 Cluster – A 138‐Electron Closed Shell ( L = 6) Superatom

2011

Metal clusters stabilized by a surface ligand shell represent an interesting intermediate state of matter between molecular metal-ligand complexes and bulk metal. Such "metalloid" clusters are characterized by the balance between metal-metal bonds in the core and metal-ligand bonds at the exterior of the cluster. In previous studies, the electronic stability for the Al50Cp*(12) cluster was not fully understood. We show here that the known cluster Al50Cp*(12) can be considered as an analogue to a giant atom ("superatom") with 138 sp electrons organized in concentric angular momentum shells up to L = 6 symmetry.

Inorganic ChemistryAngular momentumAb initio quantum chemistry methodsChemical physicsComputational chemistryChemistrySuperatomAtomShell (structure)Cluster (physics)Condensed Matter::Strongly Correlated ElectronsElectronic structureOpen shellEuropean Journal of Inorganic Chemistry
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Nature of Bonding in Group 13 Dimetallenes: a Delicate Balance between Singlet Diradical Character and Closed Shell Interactions

2010

The nature of metal-metal bonding in group 13 dimetallenes REER (E = Al, Ga, In, Tl; R = H, Me, (t)Bu, Ph) was investigated by use of quantum chemical methods that include HF, second order Møller-Plesset perturbation theory (MP2), coupled cluster (CCSD(T)), complete active space with (CASPT2) and without (CAS) second order perturbation theory, and two density functionals, namely, B3LYP and M06-2X. The results show that the metal-metal interaction in group 13 dimetallenes stems almost exclusively from static and dynamic electron correlation effects: both dialuminenes and digallenes have an important singlet diradical component in their wave function, whereas the bonding in the heavier diinde…

Inorganic ChemistryCoupled clusterElectronic correlationDiradicalChemical physicsChemistrySinglet stateComplete active spacePhysical and Theoretical ChemistryPerturbation theoryAtomic physicsWave functionOpen shellInorganic Chemistry
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Quaternary Heusler Compounds without Inversion Symmetry: CoFe 1+ x Ti 1– x Al and CoMn 1+ x V 1– x Al

2011

We report the quaternary Heusler compound derivatives CoFe1+xTi1–xAl and CoMn1+xV1–xAl, which do not have centers of inversion. Classical T2T′M (T, T′ = transition metal, M = main group element) Heusler compounds (prototype: Cu2MnAl) crystallize in the L21 structure, space group Fmm (225) that exhibits a center of inversion. Replacing one of the T2 atoms by another transition element (T″) results in a quaternary TT′T″M compound with F3m symmetry (Y; structure type LiMgPdSn) without center of inversion. In the case of “quasi closed shell” compounds with 24 valence electrons in the primitive cell, one expects the absence of ferromagnetism according to the Slater–Pauling rule. Increasing the n…

Inorganic ChemistryCrystallographyFerromagnetismChemistryengineeringPrimitive cellElectronic structureCrystal structureengineering.materialGround stateHeusler compoundValence electronOpen shellEuropean Journal of Inorganic Chemistry
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