Excited states from modified coupled cluster methods: Are they any better than EOM CCSD? - Wikidata - awgldk - TriplyDB

Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

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Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

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Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

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Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

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Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

@en

Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

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Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

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Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

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Journal of Chemical Physics

P1476

Excited states from modified coupled cluster methods: Are they any better than EOM CCSD?

@en

P2093

Ajith Perera

http://www.w3.org/2001/XMLSchema#string

Marcel Nooijen

http://www.w3.org/2001/XMLSchema#string

Rodney J Bartlett

http://www.w3.org/2001/XMLSchema#string

P2860

Coupled-cluster theory in quantum chemistry

Benchmarks for 0-0 transitions of aromatic organic molecules: DFT/B3LYP, ADC(2), CC2, SOS-CC2 and SCS-CC2 compared to high-resolution gas-phase data.

Single-reference ab initio methods for the calculation of excited states of large molecules.

Equation-of-motion coupled-cluster methods for open-shell and electronically excited species: the Hitchhiker's guide to Fock space.

New electron correlation theories for transition metal chemistry.

Progress and challenges in the calculation of electronic excited states.

Semiempirical Quantum-Chemical Orthogonalization-Corrected Methods: Benchmarks of Electronically Excited States.

Benchmark Applications of Variations of Multireference Equation of Motion Coupled-Cluster Theory.

A New Mean-Field Method Suitable for Strongly Correlated Electrons: Computationally Facile Antisymmetric Products of Nonorthogonal Geminals.

A fusion of the closed-shell coupled cluster singles and doubles method and valence-bond theory for bond breaking.

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144104

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scholarly article

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10.1063/1.4979078

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14

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146

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2017-04-01T00:00:00Z

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28411589

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