Search results for "Interaction"

showing 10 items of 5710 documents

Noncovalent Saccharide Recognition by Means of a Tetrakis(bile acid)-Porphyrin Conjugate: Selectivity, Cooperation, and Stability

2010

Molecular recognition of Glu, Glc 2 -Glc 6 and Mal 3 by a tetrakis(bile acid)―porphyrin conjugate has been studied by using ESI-FTICR mass spectrometry. The bile acid conjugate was observed to form 1:1 noncovalent complexes with saccharides. The conjugate was found to have size-selectivity towards saccharides with three or more glucose residues. The Glc 3 and Glc 4 also formed kinetically the most stable complexes. The electron capture dissociation (ECD) experiments revealed that in complexation of an oligosaccharide three glucose residues interact with the bile acid conjugate, whereas additional glucose residues are susceptible to fragmentation. The ECD results also showed the significance…

chemistry.chemical_classificationElectron-capture dissociationBile acidmedicine.drug_classStereochemistryOrganic ChemistryOligosaccharidePorphyrinchemistry.chemical_compoundMolecular recognitionchemistryAldosemedicineNon-covalent interactionsPhysical and Theoretical ChemistryConjugateEuropean Journal of Organic Chemistry
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Binding and isomerization energies for the Cu/CN and Cu(I)CN interactions

1993

Abstract Binding and isomerization energies of the CuCN, CuNC, CuCN+, and CuNC+ systems were investigated by means of a multireference CI perturbatively selected, MRCI-PS approach. The inclusion of the main dynamical correlation effects are evaluated. The binding energies for CuCN and CuNC are 4.37 and 4.03 eV, respectively, and those for CuCN+ and CuNC+ are 0.08 and 1.61 eV. Calculated isomerization energies are 7.86 and 35.98 kcal/mol for CuCN and Cu(I)CN isomerizations, respectively.

chemistry.chemical_classificationElectronic correlationBinding energyGaussian orbitalGeneral Physics and AstronomyConfiguration interactionBond-dissociation energyCrystallographychemistryComputational chemistryElectron affinityPhysical and Theoretical ChemistryInorganic compoundIsomerizationChemical Physics
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Dissociation energies within selected configuration interaction and perturbation theory

1993

Abstract Selected configuration interaction (CI) calculations and second-order perturbational theory are used to truncate systematically multireference single and double excitation CI (MRCI) expansions in the calculation of the bond dissociation energies of several systems like the single-bonded LiF molecule or the multiple-bonded N2, NO and O2 diatomic systems. The method is extended to compute the CH bond dissociation energy ofethene C2H4. It is shown how the proposed scheme (perturbation-selected MRCI (MRCI-PS)) is able to reproduce the accuracy of complete MRCI expansions with only a small number of configurations variationally evaluated.

chemistry.chemical_classificationElectronic correlationConfiguration interactionCondensed Matter PhysicsBiochemistryBond-dissociation energyDiatomic moleculeMolecular physicsDissociation (chemistry)chemistryComputational chemistryMoleculePhysical and Theoretical ChemistryInorganic compoundExcitationJournal of Molecular Structure: THEOCHEM
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Thermodynamics of the interaction between the spike protein of severe acute respiratory syndrome- coronavirus-2 and the receptor of human angiotensin…

2020

Since the end of 2019, the coronavirus SARS-CoV-2 has caused more than 180,000 deaths all over the world, still lacking a medical treatment despite the concerns of the whole scientific community. Human Angiotensin-Converting Enzyme 2 (ACE2) was recently recognized as the transmembrane protein serving as SARS-CoV-2 entry point into cells, thus constituting the first biomolecular event leading to COVID-19 disease. Here, by means of a state-of-the-art computational approach, we propose a rational evaluation of the molecular mechanisms behind the formation of the complex and of the effects of possible ligands. Moreover, binding free energy between ACE2 and the active Receptor Binding Domain (RB…

chemistry.chemical_classificationEnzymechemistrySevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Angiotensin-converting enzyme 2medicineSpike ProteinComputational biologymedicine.disease_causeReceptorTransmembrane proteinCoronavirusProtein–protein interaction
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Peptide–Membrane Interactions Monitored by Fluorescence Lifetime Imaging: A Study Case of Transportan 10

2021

The interest on detailed analysis of peptide-membrane interactions is of great interest in both fundamental and applied sciences as these may relate to both functional and pathogenic events. Such interactions are highly dynamic and spatially heterogeneous, making the investigation of the associated phenomena highly complex. The specific properties of membranes and peptide structural details, together with environmental conditions, may determine different events at the membrane interface, which will drive the fate of the peptide-membrane system. Here, we use an experimental approach based on the combination of spectroscopy and fluorescence microscopy methods to characterize the interactions …

chemistry.chemical_classificationFluorescence-lifetime imaging microscopyChemistryRecombinant Fusion ProteinsSpectrum AnalysisGalaninWasp VenomsPeptideSurfaces and InterfacesCondensed Matter PhysicsFluorescenceArticleMembraneMicroscopy FluorescenceAmphiphileElectrochemistryFluorescence microscopeHigh spatial resolutionBiophysicsPeptide−Membrane Interactions FLIM Transportan 10 PhasorGeneral Materials SciencePeptidesSpectroscopySpectroscopyLangmuir
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DLPNO-CCSD(T) scaled methods for the accurate treatment of large supramolecular complexes

2017

In this work, we present scaled variants of the DLPNO-CCSD(T) method, dubbed as (LS)DLPNO-CCSD(T) and (NS)DLPNO-CCSD(T), to obtain accurate interaction energies in supramolecular complexes governed by noncovalent interactions. The novel scaled schemes are based on the linear combination of the DLPNO-CCSD(T) correlation energies calculated with the standard (LoosePNO and NormalPNO) and modified (Loose2PNO and Normal2PNO) DLPNO-CCSD(T) accuracy levels. The scaled DLPNO-CCSD(T) variants provide nearly TightPNO accuracy, which is essential for the quantification of weak noncovalent interactions, with a noticeable saving in computational cost. Importantly, the accuracy of the proposed schemes is…

chemistry.chemical_classificationFullerene010304 chemical physicsDispersion forcesNoncovalent interactionsSupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesLondon dispersion force0104 chemical sciencesComputational MathematicsCrystallographychemistryComputational chemistryAb initio quantum chemistry methods0103 physical sciencesNon-covalent interactionsDLPNO-CCSD(T) scaled methodsDonor–acceptor supramolecular complexesAb initio calculationsQuímica FísicaLinear combination
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Understanding the affinity of bis-exTTF macrocyclic receptors towards fullerene recognition

2019

A new series of fullerene receptors based on exTTF macrocycles with alkyl ether chains of increasing length is reported. The novel macrocyclic receptors are able to favourably interact with fullerene C60 through a synergistic combination of π–π, CH⋯π and n⋯π noncovalent interactions. We identify that the highest affinity towards C60 recognition is achieved for the host with the tightest fit; that is, the smallest receptor with a cavity large enough to host the buckyball inside (log Ka = 5.2 in chlorobenzene at 298 K). However, besides this expected observation, theoretical calculations evidence that the most stable self-assembling configuration corresponds for all the receptors to an outsid…

chemistry.chemical_classificationFullereneGeneral Physics and Astronomy02 engineering and technologySynergistic combination010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences3. Good health0104 chemical sciencesAlkyl etherchemistry.chemical_compoundCrystallographychemistryChlorobenzeneNon-covalent interactionsPhysical and Theoretical Chemistry0210 nano-technologyReceptorPhysical Chemistry Chemical Physics
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(1-Adamantyl)methyl glycidyl ether: a versatile building block for living polymerization.

2014

(1-Adamantyl)methyl glycidyl ether (AdaGE) is introduced as a versatile monomer for oxyanionic polymerization, enabling controlled incorporation of adamantyl moieties in aliphatic polyethers. Via copolymerization with ethoxyethyl glycidyl ether (EEGE) and subsequent cleavage of the acetal protection groups of EEGE, hydrophilic linear polyglycerols with an adjustable amount of pendant adamantyl moieties are obtained. The adamantyl unit permits control over thermal properties and solubility profile of these polymers (LCST). Additionally, AdaGE is utilized as a termination agent in carbanionic polymerization, affording adamantyl-terminated polymers. Using these structures as macroinitiators fo…

chemistry.chemical_classificationGlycerolMaterials sciencePolymers and PlasticsEthylene oxidePolymersOrganic ChemistryAcetalAdamantanePolymerPolymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryAmphiphileMaterials ChemistryCopolymerLiving polymerizationOrganic chemistryEpoxy CompoundsHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Supramolecular Assembly of Metal Complexes by (Aryl)I⋅⋅⋅d[PtII] Halogen Bonds

2020

The theoretical data for the half-lantern complexes [{Pt( CN^ )(μ- SN^ )}2 ] [1-3; CN^ is cyclometalated 2-Ph-benzothiazole; SN^ is 2-SH-pyridine (1), 2-SH-benzoxazole (2), 2-SH-tetrafluorobenzothiazole (3)] indicate that the Pt⋅⋅⋅Pt orbital interaction increases the nucleophilicity of the outer d z2 orbitals to provide assembly with electrophilic species. Complexes 1-3 were co-crystallized with bifunctional halogen bonding (XB) donors to give adducts (1-3)2 ⋅(1,4-diiodotetrafluorobenzene) and infinite polymeric [1⋅1,1'-diiodoperfluorodiphenyl]n . X-ray crystallography revealed that the supramolecular assembly is achieved through (Aryl)I⋅⋅⋅d z2 [PtII ] XBs between iodine σ-holes and lone pa…

chemistry.chemical_classificationHalogen bond010405 organic chemistryArylOrganic ChemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSupramolecular assemblychemistry.chemical_compoundCrystallographychemistryElectrophileNon-covalent interactionsBifunctionalLone pairChemistry – A European Journal
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Host–Guest Chemistry: Oxoanion Recognition Based on Combined Charge‐Assisted C−H or Halogen‐Bonding Interactions and Anion⋅⋅⋅Anion Interactions Media…

2016

Several bis-triazolium-based receptors have been synthesized and their anion-recognition capabilities have been studied. The central chiral 1,1'-bi-2-naphthol (BINOL) core features either two aryl or ferrocenyl end-capped side arms with central halogen- or hydrogen-bonding triazolium receptors. NMR spectroscopic data indicate the simultaneous occurrence of several charge-assisted aliphatic and heteroaromatic C-H noncovalent interactions and combinations of C-H hydrogen and halogen bonding. The receptors are able to selectively interact with HP2 O7 (3-) , H2 PO4 (-) , and SO4 (2-) anions, and the value of the association constant follows the sequence: HP2 O7 (3-) >SO4 (2-) >H2 PO4 (-) . The …

chemistry.chemical_classificationHalogen bond010405 organic chemistryChemistryHydrogen bondStereochemistryArylOrganic ChemistryGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCatalysis0104 chemical sciencesIonCrystallographychemistry.chemical_compoundHalogenNon-covalent interactionsHost–guest chemistryChemistry – A European Journal
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