Search results for "Pi interactions"

showing 7 items of 7 documents

Crystallographic and (spectro)electrochemical characterizations of cobalt(II) 10-phenyl-5,15-di-p-tolylporphyrin

2021

International audience; The synthesis, cyclic and rotating disk electrode voltammograms, UV-visible absorption and Xray diffraction analyses of cobalt(II) 10-phenyl-5,15-dip -tolylporphyrin (1-Co) are described. 1-Co was crystallized by slow diffusion of n-hexane into a concentrated CH2Cl2 solution. X-ray diffraction analyses reveals porphyrin aromatic cycle stacking in the crystal, C-H•••π interactions of the CH2Cl2 solvent with the π-system of one tolyl group and Co(II)•••π (porphyrin ring) interactions. The abstraction of 1.0 F/mol during the electrolysis at the first oxidation potential was followed by spectroelectrochemistry. It leads to the Co(II) → Co(III) transformation rather than …

Absorption spectroscopyStackingchemistry.chemical_elementCo(II)•••pi interactions010402 general chemistryElectrochemistryElectrosynthesis01 natural sciencesAnalytical Chemistrylaw.inventionInorganic ChemistryPorphyrinchemistry.chemical_compoundlaw[CHIM.ANAL]Chemical Sciences/Analytical chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryRotating disk electrodeSpectroscopyX-ray crystallographic structureElectrolysis010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryCobalt[CHIM.MATE]Chemical Sciences/Material chemistryPorphyrin0104 chemical sciencesCrystallographychemistrystacked aromatics dimersElectrosynthesisC-H•••pi interactionsCobalt
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Experimental investigation of anion-π interactions : Applications and biochemical relevance

2015

Chemical communications 52(9), 1778 - 1795(2016). doi:10.1039/C5CC09072E

Anionsanion-pi interactionsSolid-stateChemieNanotechnology010402 general chemistry01 natural sciencesCatalysisIonGas phasekemialliset sidoksetTime frameMaterials Chemistrysupramolekulaarinen kemiaanioni-π-vuorovaikutus010405 organic chemistryChemistryIntermolecular forceMetals and AlloysGeneral Chemistry5400104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsintermolecular forcesnon-covalent interactionsChemical physicsddc:540Ceramics and Composites
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Perfluoro-1,1′-biphenyl and perfluoronaphthalene and their derivatives as π-acceptors for anions

2015

Addition of anions to perfluorinated 1,1′-biphenyl 1 or naphthalene 2 results in a shift of the 19F NMR signals. However, any specific interaction cannot be assigned to this effect. In order to study the interaction in more detail, the salt derivatives 3 and 4 were prepared and studied by single crystal X-ray diffraction revealing weak anion–π interactions in the solid state.

Diffractionchemistry.chemical_classificationBiphenylanion-pi interactionsSolid-stateSalt (chemistry)General ChemistryFluorine-19 NMRCatalysisIonCrystallographychemistry.chemical_compoundchemistryMaterials ChemistryOrganic chemistryta116Single crystalNaphthaleneNew Journal of Chemistry
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Genomic determinants of protein folding thermodynamics in prokaryotic organisms.

2004

Here we investigate how thermodynamic properties of orthologous proteins are influenced by the genomic environment in which they evolve. We performed a comparative computational study of 21 protein families in 73 prokaryotic species and obtained the following main results. (i) Protein stability with respect to the unfolded state and with respect to misfolding are anticorrelated. There appears to be a trade-off between these two properties, which cannot be optimized simultaneously. (ii) Folding thermodynamic parameters are strongly correlated with two genomic features, genome size and G+C composition. In particular, the normalized energy gap, an indicator of folding efficiency in statistical…

Models MolecularProtein DenaturationProtein FoldingProtein familyArchaeal ProteinsThermodynamicsdeleterious mutationsthermophilic proteinsBiologymonte-carlo algorithmGenomeNegative selectionBacterial ProteinsStructural BiologyMolecular evolutionGenome ArchaealevolutionbuchneraMolecular BiologyGenome sizeGeneticsPrincipal Component Analysisacid side-chainsBacteriaSequence Homology Amino Acidreplica approachComputational BiologystabilityGenetic codeArchaeaPRI BioscienceFolding (chemistry)endosymbiotic bacteriacation-pi interactionsThermodynamicsProtein foldingHydrophobic and Hydrophilic InteractionsGenome BacterialJournal of molecular biology
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Enhanced electron-transfer properties of cofacial porphyrin dimers through pi-pi interactions

2009

pi-pi assisted: Photoinduced electron transfer from cofacial porphyrin dimers to electron acceptors is prominently accelerated, whereas the back electron transfer is decelerated, relative to the corresponding porphyrin monomer (see figure).The radical cation of zinc tetrapentylporphyrin is dimerized with an excess of the neutral counterpart to form the dimer radical cation in which the unpaired electron is delocalized over both porphyrin rings. The dimeric radical cation exhibits an NIR absorption spectrum characteristic of weak pi-bond formation between the porphyrin rings. When cofacial porphyrin dimers, linked by different spacers, are oxidized such pi-bond formation between the porphyri…

Photosynthetic reaction centrePorphyrinsPhotosynthetic Reaction Center Complex ProteinsElectron donorpi interactionsPhotochemistry010402 general chemistry01 natural sciencesPhotoinduced electron transferCatalysisElectron Transportchemistry.chemical_compoundElectron transferredox chemistrypolycyclic compoundsComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationphotosynthesisphotochemistryMolecular StructureChemistry010405 organic chemistryOrganic ChemistryGeneral ChemistryElectron acceptorelectron transferPorphyrinMarcus theory0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryZincUnpaired electronModels Chemical[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryThermodynamicsOxidation-ReductionAlgorithms
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A Computational Study of Two-State Conformational Changes in 16-Electron [CpW(NO)(L)] Complexes (L=PH3, CO, CH2, HCCH, H2CCH2)

1999

International audience; High-spin and low-spin [CpW(NO) (L)] complexes are calculated to be remarkably close in energy. Several critical conformational changes in the singlet compounds are predicted to proceed more readily by spin crossover to the triplet hypersurface. The relationships between spin state, π bonding, ligand orientation, and geometry at W are explored.

Spin statesChemistryLigandOrganic ChemistryGeneral ChemistryState (functional analysis)ElectronSpin crossoverCatalysisTungstenLigand effects[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyDensity functional calculationsHypersurfaceSpin crossoverComputational chemistryPi interactionsPi interactionCondensed Matter::Strongly Correlated Electrons[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet state
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A Multi-Component Reaction towards the Development of Highly Modular Hydrogelators

2018

Herein we report a multi‐component reaction approach for the development of a new class of hydrogelators based on the OxoTriphenylHexanOate (OTHO) backbone. A focused library of OTHOs has been synthesized and their hydrogelation features evaluated. The two most potent hydrogelators were studied by rheology revealing different stiffness, appearances and thixotropic behavior of the gels. The new gelators showcase the versatility of the OTHO backbone as a platform for the design of functionalized hydrogels with tunable gel properties. peerReviewed

Thixotropymulticomponent reactionNanotechnologypi interactions010402 general chemistry01 natural sciencesCatalysispyridine N-oxideRheologyMulti-component reactionta116geelitkemiallinen synteesi010405 organic chemistryChemistrybusiness.industryOrganic ChemistryGeneral Chemistryself-assemblyModular designgels0104 chemical sciencesSelf-healing hydrogelsSelf-assemblybusiness
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