Search results for "Bond Analysis"

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Unveiling the Sulfur–Sulfur Bridge: Accurate Structural and Energetic Characterization of a Homochalcogen Intermolecular Bond

2018

open 12 si MIUR “PRIN 2015” funds (Grant Number 2015F59J3R) By combining rotational spectroscopy in supersonic expansion with the capability of state-of-the-art quantum-chemical computations in accurately determining structural and energetic properties, the genuine nature of a sulfur–sulfur chalcogen bond between dimethyl sulfide and sulfur dioxide has been unveiled in a gas-jet environment free from collision, solvent and matrix perturbations. A SAPT analysis pointed out that electrostatic S⋅⋅⋅S interactions play the dominant role in determining the stability of the complex, largely overcoming dispersion and C−H⋅⋅⋅O hydrogen-bond contributions. Indeed, in agreement with the analysis of the…

Materials sciencechemistry.chemical_element02 engineering and technologybond analysi010402 general chemistry01 natural sciencesQuantum chemistryCatalysisCatalysibond analysisquantum chemistrysymbols.namesakeChalcogenrotational spectroscopyVan der Waals radiusPhysics::Chemical PhysicsAstrophysics::Galaxy Astrophysicsbond analysis; energy and charge decomposition models; quantum chemistry; rotational spectroscopy; semi-experimental equilibrium structure; Catalysis; Chemistry (all)energy and charge decomposition model010405 organic chemistryIntermolecular forceChemistry (all)General MedicineGeneral Chemistryenergy and charge decomposition modelssemi-experimental equilibrium structure021001 nanoscience & nanotechnologySulfur0104 chemical scienceschemistryChemical physicssymbolsRotational spectroscopy0210 nano-technologyDispersion (chemistry)Natural bond orbital
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Donation and back-donation in cis- and trans-[(η5-C5H5)Fe(η1-CO)(μ-CO)]2 tautomers: Which relative is more generous? An ETS-NOCV bond analysis

2022

The ETS-NOCV bond analysis has been exploited to quantitatively estimate donation and back-donation properties of [(η5-C5H5)]−, CO, and FeI in the cis-/trans-[(η5-C5H5)Fe(η1-CO)(μ-CO)]2 (cis-I/trans-I) tautomers. Theoretical outcomes indicate that the Fe-CO bond, regardless to the CO monoapto (η1-) or bridging (μ-) coordination, has a sizeable π Fe → CO back-bonding contribution, which is stronger in trans-I than in cis-I. Moreover, [(η5-C5H5)]− has the weakest back-donation acceptor capability. The back-bonding behaviour of the Fe → η1-CO interaction well agrees with the experimental symmetric/antisymmetric infrared νCO (sνηjavax.xml.bind.JAXBElement@fc12185-CO/aνηjavax.xml.bind.JAXBElemen…

Bond Analysis cis-/trans-[(η5-C5H5)Fe(η1-CO)(μ-CO)]2 Charge Displacement analysis DFT.Inorganic ChemistrySettore CHIM/03 - Chimica Generale E InorganicaMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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