Search results for " interaction"

showing 10 items of 5187 documents

Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n(n=1–4;m=3–7)

2020

The Te⋅⋅⋅Te secondary bonding interactions (SBIs) in solid cyclic telluroethers were explored by preparing and structurally characterizing a series of [Te(CH2 )m ]n (n=1-4; m=3-7) species. The SBIs in 1,7-Te2 (CH2 )10 , 1,8-Te2 (CH2 )12 , 1,5,9-Te3 (CH2 )9 , 1,8,15-Te3 (CH2 )18 , 1,7,13,19-Te4 (CH2 )20 , 1,8,15,22-Te4 (CH2 )24 and 1,9,17,25-Te4 (CH2 )28 lead to tubular packing of the molecules, as has been observed previously for related thio- and selenoether rings. The nature of the intermolecular interactions was explored by solid-state PBE0-D3/pob-TZVP calculations involving periodic boundary conditions. The molecular packing in 1,7,13,19-Te4 (CH2 )20 , 1,8,15,22-Te4 (CH2 )24 and 1,9,17,…

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryIntermolecular forcechemistry.chemical_elementThio-General ChemistryOrbital overlap010402 general chemistry01 natural sciencesBond orderCatalysis0104 chemical sciencesChalcogenCrystallographychemistryMoleculeNon-covalent interactionsTelluriumChemistry – A European Journal
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Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three-Component Complexes

2020

Cethyl-2-methylresorcinarene (A), pyridine (B), and a set of 10 carboxylic acids (Cn) associate to form A·B·Cn ternary assemblies with 1:1:1 stoichiometry, representing a useful class of ternary systems where the guest mediates complex formation between the host and a third component. Although individually weak in solution, the combined strength of the multiple noncovalent interactions organizes the complexes even in a highly hydrogen-bond competing methanol solution, as explored by both experimental and computational methods. The interactions between A·B and Cn are dependent on the pKa values of carboxylic acids. The weak interactions between A and C further reinforce the interactions betw…

chemistry.chemical_classification010405 organic chemistryStereochemistryComponent (thermodynamics)Organic ChemistryComplex formationCarboxylic AcidsCooperative bindingHydrogen Bonding010402 general chemistry01 natural sciences0104 chemical sciencesChemistrychemistry.chemical_compoundMolecular recognitionchemistryPyridineNon-covalent interactionsTernary operationBiochemistry Biophysics and Structural BiologyStoichiometryThe Journal of Organic Chemistry
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Characterization of β-B-Agostic Isomers in Zirconocene Amidoborane Complexes

2009

The reaction of Cp(x)(2)ZrCl(2) (Cp(x) = Cp, Cp*) with ammonia borane in presence of n-butyllithium yielded Cp(2)Zr(Cl)NH(2)BH(3) and Cp(x)(2)Zr(H)NH(2)BH(3). These derivatives are isoelectronic with the ethyl zirconocene chloride and hydride, respectively, and feature a chelating amidoborane ligand coordinating through a Zr-N bond and a Zr-H-B bridge. In solution, each of the complexes consists of an equilibrium mixture of two isomers differing in the orientation of the amidoborane ligand with respect to the Zr-X bond (X = H, Cl), while in the solid state, only one isomer was observed. Such isomers have not been characterized for any metal complexes containing the isoelectronic beta-agosti…

chemistry.chemical_classificationAgostic interactionLigandHydrideStereochemistryAmmonia boraneGeneral ChemistryBiochemistryChlorideMedicinal chemistryCatalysisMetalchemistry.chemical_compoundColloid and Surface Chemistrychemistryvisual_artvisual_art.visual_art_mediummedicineChelationAlkylmedicine.drugJournal of the American Chemical Society
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2,4,5-Trimethylimidazolium Scaffold for Anion Recognition Receptors Acting Through Charge-Assisted Aliphatic and Aromatic C–H Interactions

2016

A series of two-armed 2,4,5-trimethylimidazolium-based oxoanion receptors, which incorporate two end-capped photoactive anthracene rings, being the central core an aromatic or heteroaromatic ring, has been designed. In the presence of HP2O7(3-), H2PO4(-), and SO4(2-) anions, (1)H- and (31)P NMR spectroscopical data clearly indicate the simultaneous occurrence of several charge-assisted aliphatic and aromatic C-H noncovalent interactions, i.e., significant downfield shifts were observed for the imidazolium C(2)-CH3 protons, the methylene N-CH2 protons, and the inner aromatic proton or the outer heteroaromatic protons. Density functional theory calculations confirm the occurrence of these non…

chemistry.chemical_classificationAnthraceneProton010405 organic chemistryStereochemistryOrganic ChemistryNuclear magnetic resonance spectroscopy010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciences3. Good healthIonCrystallographychemistry.chemical_compoundchemistryNon-covalent interactionsDensity functional theoryMethyleneThe Journal of Organic Chemistry
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Adsorption of triblock copolymers and their homopolymers at laponite clay/solution interface. Role played by the copolymer nature

2009

The adsorption thermodynamics of copolymers, based on ethylene oxide (EO) and propylene oxide ( PO) units, at the laponite (RD) clay/liquid interface was determined at 298 K. The copolymer nature was tuned at molecular level by changing the hydrophilicity, the architecture and the molecular weight (Mw) keeping constant the EO/PO ratio. Polyethylene (PEGs) and polypropylene (PPGs) glycols with varying Mw and their mixture were also investigated to discriminate the role of the EO and the PO segments in the adsorption process. Enthalpies of transfer of RD, at fixed concentration, from water to the aqueous macromolecule solutions as functions of the macromolecule molality were determined. They …

chemistry.chemical_classificationAqueous solutionEthylene oxideGeneral Physics and AstronomyPolymerSURFACTANT INTERACTIONSANGLE NEUTRON-SCATTERINGCLAY PARTICLESHEAT-CAPACITIESBLOCK-COPOLYMERSchemistry.chemical_compoundAdsorptionchemistryChemical engineeringCONCENTRATION RANGEAQUEOUS-SOLUTIONSPolymer chemistryCopolymerPOLY(ETHYLENE OXIDE)Propylene oxideOXIDE)(13)-(PROPYLENE OXIDE)(30)-(ETHYLENE OXIDE)(13)SODIUM DODECYL-SULFATEPhysical and Theoretical ChemistryEquilibrium constantMacromoleculePhysical Chemistry Chemical Physics
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Sponge aggregation factor: identification of the specific collagen-binding site by means of a monoclonal antibody.

1988

The aggregation factor (AF) from the sponge Geodia cydonium is known to be a complex proteinaceous particle, composed of a series of different (glyco)proteins (Mr lower than 150,000) around a 90S sunburst-like core structure. One of the low-Mr proteins is the 47-KD cell binding fragment. We describe a new monoclonal antibody (mAb), III1E6, raised against purified AF particles, which recognizes in tissue slices structures present both on the plasma membrane and in a network-like manner in the extracellular space. By applying immunoelectron microscopical, immunoblotting, and immunoaffinity chromatographical techniques, the mAb III1E6 was shown to recognize the core structure of the AF partic…

chemistry.chemical_classificationBinding SitesHistologyCell adhesion moleculeImmunoelectron microscopyAntibodies MonoclonalProteinsCell CommunicationAdhesionBiologyMolecular biologyPoriferachemistryCell–cell interactionCell surface receptorBiophysicsAnimalsCollagenAnatomyBinding siteCell adhesionGlycoproteinCell Adhesion MoleculesCell AggregationJournal of Histochemistry & Cytochemistry
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Biophysical approaches for the study of metal-protein interactions

2019

Protein-protein interactions play important roles for a variety of cell functions, often involving metal ions; in fact, metal-ion binding mediates and regulates the activity of a wide range of biomolecules. Enlightening all of the specific features of metal-protein and metal-mediated protein-protein interactions can be a very challenging task; a detailed knowledge of the thermodynamic and spectroscopic parameters and the structural changes of the protein is normally required. For this purpose, many experimental techniques are employed, embracing all fields of Analytical and Bioinorganic Chemistry. In addition, the use of peptide models, reproducing the primary sequence of the metal-binding …

chemistry.chemical_classificationBiophysical methodsBinding Sites010405 organic chemistryChemistryBiomoleculeMetal-protein interactionsStructural and kinetic toolsProteinsComputational biologyAnalytical techniques010402 general chemistry01 natural sciencesBiochemistryCell function0104 chemical sciencesProtein–protein interactionInorganic ChemistryKineticsMetalsPeptidesPrimary sequenceProtein BindingJournal of Inorganic Biochemistry
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Synthesis, characterization, and complexation of tetraarylborates with aromatic cations and their use in chemical sensors.

2005

Five aromatic borate anions, namely tetrakis(4-phenoxyphenyl)borate (1), tetrakis(biphenyl)borate (2), tetrakis(2-naphthyl)borate (3), tetrakis(4-phenylphenol)borate (4), and tetrakis(4-phenoxy)borate (5), have been prepared and tested as ion-recognition sites in chemical sensors for certain aromatic cations and metal ions. To gain further insight into the complexation of the cations, some complexes have been prepared and structurally characterized. The complexation behavior of 1 and 2 towards N-methylpyridinium (6), 1-ethyl-4-(methoxycarbonyl)pyridinium (7), tropylium (8), imidazolium (9), and 1-methylimidazolium (10) cations has been studied, and the stability constants of the complexes o…

chemistry.chemical_classificationBiphenylModels MolecularTetraphenylborateMolecular StructureMetal ions in aqueous solutionOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureCrystallography X-RayMedicinal chemistryHydrocarbons AromaticCatalysisIon selective electrodechemistry.chemical_compoundchemistryCationsBoratesNon-covalent interactionsPyridiniumBoronElectrodesChemistry (Weinheim an der Bergstrasse, Germany)
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Synthesis and structural studies on Ni(II) dithiocarbamates : Exploring intramolecular Ni···H-C interactions

2017

Abstract Five new Ni(II) dithiocarbamates with NiS4, NiS2PN and NiS2PCl coordination spheres, viz. [Ni(bupmbzdtc)2] (1), [Ni(bupmbzdtc)(PPh3)(NCS)] (2), [Ni(bupmbzdtc)(PPh3)Cl] (3), [Ni(4-dpmpzdtc)(PPh3)Cl] (4) and [Ni(pbbzbudtc)(PPh3)(NCS)] (5), where bupmbzdtc = N-butyl(p-methylbenzyl)dithiocarbamato anion, 4-dpmpzdtc = 4-(diphenylmethyl)piperazinecarbodithioato anion, pbbzbudtc = N-(p-bromobenzyl)butyl-dithiocarbamato anion and PPh3 = triphenylphosphine, were synthesized and characterized by UV, IR, NMR and single crystal X-ray diffraction methods. Spectral results suggest a square planar geometry around the Ni(II) metal center for all the synthesized complexes. Single crystal X-ray stru…

chemistry.chemical_classificationC-H···Ni interaction010405 organic chemistryChemistryInorganic chemistrySolid-state010402 general chemistry01 natural sciencesNMR0104 chemical sciencesIonInorganic ChemistryMetalCrystallographydithiocarbamateIntramolecular forcevisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryDithiocarbamateX-ray structural analysisSingle crystalta116Polyhedron
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Carbamate Linker Strategy in Solid-Phase Synthesis of Amino-Functionalized Glycoconjugates for Attachment to Solid Surfaces and Investigation of Prot…

2009

Amino-functionalized serine-based galactose and glucose neoglycolipids were prepared by solid-phase synthesis using a carbamate strategy for anchoring amino functionalities to a (2-fluoro-4-hydroxy ...

chemistry.chemical_classificationCarbamateGlycoconjugateSolid surfacemedicine.medical_treatmentOrganic ChemistrySerinechemistry.chemical_compoundSolid-phase synthesischemistryGalactosemedicineProtein–carbohydrate interactionsOrganic chemistryPhysical and Theoretical ChemistryLinkerEuropean Journal of Organic Chemistry
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