Search results for "non-covalent"

showing 10 items of 83 documents

Synthesis and Characterizations of Novel Isatin-s-Triazine Hydrazone Derivatives : X-ray Structure, Hirshfeld Analysis and DFT Calculations

2023

A novel series of isatin-s-triazine hydrazone derivatives has been synthesized and reported herein. The synthetic methodology involved the reaction of s-triazine hydrazine precursors with isatin derivatives in the presence of CH3COOH as a catalyst and EtOH as solvent to afford the corresponding target products 6a-e in high yields and purities. The characterization data obtained from elemental analysis, FT-IR, NMR (1H- and 13C-) were in full agreement with the expected structures. Furthermore, an X-ray single crystal diffraction study of one of the target s-triazine hydrazone derivatives, 6c confirmed the structure of the desired compounds. It crystallized in the triclinic crystal system and…

Inorganic Chemistryhydrazone derivatives<i>s</i>-triazines-triazinenon-covalent interactionsGeneral Chemical Engineeringorgaaninen kemiaGeneral Materials ScienceCondensed Matter PhysicsisatinDFTorgaaniset yhdisteetHirshfeld
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Mass Spectrometric Investigation of Noncovalent Complexation between a Tetratosylated Resorcarene and Alkyl Ammonium Ions

2004

Noncovalent complexation between tetratosylated tetraethyl resorcarene (1) and primary, secondary, and tertiary alkyl ammonium ions (mMe, dMe, tMe, mEt, dEt, tEt, dBu, and dHex) was studied by electrospray ionization Fourier transform ion cyclotron resonance (ESI-FTICR) mass spectrometry. Interactions of the noncovalent complexes were investigated by means of competition experiments, collision-induced dissociation (CID) experiments, ion-molecule reactions with tripropylamine and gas phase H/D-exchange reactions with deuteroammonia. Gas phase ion-molecule reactions gave especially valuable information about the structure and properties of the complexes. Resorcarene 1 formed relatively stable…

IonsSteric effectschemistry.chemical_classificationSpectrometry Mass Electrospray IonizationMolecular StructureMacromolecular SubstancesChemistryHydrogen bondOrganic ChemistryInorganic chemistryGeneral ChemistryCatalysisDissociation (chemistry)Fourier transform ion cyclotron resonanceQuaternary Ammonium CompoundsTosyl Compoundschemistry.chemical_compoundPolymer chemistryProton affinityNon-covalent interactionsAmmoniumAlkylChemistry - A European Journal
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Bridging rigidity and flexibility : modulation of supramolecular hydrogels by metal complexation

2021

The combination of complementary, noncovalent interactions is a key principle for the design of multistimuli responsive hydrogels. In this work, an amphiphilic peptide, supramacromolecular hydrogelator which combines metal-ligand coordination induced gelation and thermoresponsive toughening is reported. Following a modular approach, the incorporation of the triphenylalanine sequence FFF into a structural (C3EG ) and a terpyridine-functionalized (C3Tpy ) C3 -symmetric monomer enables their statistical copolymerization into self-assembled, 1D nanorods in water, as investigated by circular dichroism (CD) spectroscopy and transmission electron microscopy (TEM). In the presence of a terpyridine …

Ionschemistry.chemical_classificationCircular dichroism540 Chemistry and allied sciencesPolymers and PlasticsOrganic ChemistryHydrogelsPolyethylene glycolPolyethylene Glycolschemistry.chemical_compoundMonomerchemistryChemical engineeringMetals540 ChemieAmphiphileSelf-healing hydrogelsMaterials ChemistryCopolymerNon-covalent interactionsTerpyridinePeptides
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Binding site of different tannins on a human salivary proline-rich protein evidenced by dissociative photoionization tandem mass spectrometry

2015

Abstract The sensation of astringency is thought to originate from the interaction occurring between tannins and the salivary proline-rich proteins (PRPs). Astringency perception can be modified by the structure of tannins. Herein, we study the interactions occurring between the human salivary PRP, IB5, and three model tannins with different structure, epigallocatechin gallate and the procyanidin dimers B2 and B2 3′ O -gallate, using the coupling of mass spectrometry and VUV-synchrotron radiation. The results obtained indicate that the structure of tannins, in particular the degree of polymerization and the galloylation, does not modify the binding site on IB5 involved in the interaction.

Mass spectrometryAstringency[CHIM.ORGA]Chemical Sciences/Organic chemistry[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionOrganic ChemistryGallatePhotoionizationEpigallocatechin gallateDegree of polymerizationMass spectrometryTandem mass spectrometryBiochemistryPro line-rich proteinsBinding sitechemistry.chemical_compoundchemistryProanthocyanidinBiochemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryDrug DiscoveryBinding siteTannins[SDV.AEN]Life Sciences [q-bio]/Food and NutritionNon-covalent interaction
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Hierarchical Self-Assembly of Halogen-Bonded Block Copolymer Complexes into Upright Cylindrical Domains

2017

Summary Self-assembly of block copolymers into well-defined, ordered arrangements of chemically distinct domains is a reliable strategy for preparing tailored nanostructures. Microphase separation results from the system, minimizing repulsive interactions between dissimilar blocks and maximizing attractive interactions between similar blocks. Supramolecular methods have also achieved this separation by introducing small-molecule additives binding specifically to one block by noncovalent interactions. Here, we use halogen bonding as a supramolecular tool that directs the hierarchical self-assembly of low-molecular-weight perfluorinated molecules and diblock copolymers. Microphase separation …

Materials scienceBlock copolymerGeneral Chemical Engineering116 Chemical sciencesSupramolecular chemistryNanotechnologyblock copolymer02 engineering and technologyhierarchical self-assembly010402 general chemistry01 natural sciencesBiochemistryMicelleArticleSDG9: Industry innovation and infrastructuresupramolecular complexesMaterials ChemistryCopolymerEnvironmental ChemistryNon-covalent interactionsMoleculeLamellar structureta116chemistry.chemical_classificationHalogen bondta114Biochemistry (medical)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesblock copolymerschemistryChemical engineeringIndustry innovation and infrastructure [SDG9]nanofabricationhalogen bondSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelf-assembly0210 nano-technology
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Quantum-Chemical Insights into the Self-Assembly of Carbon-Based Supramolecular Complexes

2018

Understanding how molecular systems self-assemble to form well-organized superstructures governed by noncovalent interactions is essential in the field of supramolecular chemistry. In the nanoscience context, the self-assembly of different carbon-based nanoforms (fullerenes, carbon nanotubes and graphene) with, in general, electron-donor molecular systems, has received increasing attention as a means of generating potential candidates for technological applications. In these carbon-based systems, a deep characterization of the supramolecular organization is crucial to establish an intimate relation between supramolecular structure and functionality. Detailed structural information on the se…

Materials scienceFullereneNoncovalent interactionsSurface PropertiesSupramolecular chemistryPharmaceutical Sciencechemistry.chemical_elementNanotechnologyContext (language use)ReviewCarbon nanotube010402 general chemistry01 natural sciencesPolymerizationAnalytical Chemistrylaw.inventionquantum chemistrylcsh:QD241-441noncovalent interactionslcsh:Organic chemistrylawDrug DiscoveryNon-covalent interactionsQuímica FísicaPhysical and Theoretical Chemistrychemistry.chemical_classificationNanotubes Carbon010405 organic chemistryGrapheneOrganic Chemistrycarbon-based supramolecular assemblies0104 chemical sciencesCharacterization (materials science)Models ChemicalchemistryChemistry (miscellaneous)Quantum TheoryMolecular MedicineFullerenesCarbonQuantum chemistryAlgorithmsCarbon-based supramolecular assemblies
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Spectroscopic characterization of non-covalent CuPc-GO system. Experiment and theory

2019

Abstract In this study we report on UV-vis, IR and Raman studies of non-covalent copper phthalocyanine (CuPc) – flake graphene oxide (GO) complex in water and in the solid phase. Experimental results were supported by molecular modeling of structure, electronic and vibrational parameters for free CuPc and its 1 : 1 complexes with water, benzene, phenol, neutral and deprotonated benzoic acid. HOMO-LUMO gaps for these complexes were calculated and compared with data derived from the absorption edge of Q-band in the recorded UV-vis spectra for free CuPc and its adduct with GO in water. Small but non-negligible changes in position of spectral bands observed as result of CuPc interaction with GO…

Materials scienceNon-covalent complexOxidechemistry.chemical_elementMolecular modeling02 engineering and technology010402 general chemistry01 natural sciencesSpectral lineEglaw.inventionchemistry.chemical_compoundsymbols.namesakelawGeneral Materials ScienceBenzeneGrapheneCuPc-GOUV-VIS021001 nanoscience & nanotechnologyCondensed Matter PhysicsCopper0104 chemical scienceschemistryAbsorption edgeRaman spectroscopysymbolsIRPhysical chemistryDensity functional theory0210 nano-technologyRaman spectroscopyMaterials Chemistry and Physics
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Mapping the fluorophilicity of a hydrophobic pocket: synthesis and biological evaluation of tricyclic thrombin inhibitors directing fluorinated alkyl…

2006

In the completion of our fluorine scan of tricyclic inhibitors to map the fluorophilicity/fluorophobicity of the thrombin active site, a series of 11 new ligands featuring alkyl, alkenyl, and fluoroalkyl groups was prepared to explore fluorine effects on binding into the hydrophobic proximal (P) pocket, lined by Tyr 60A and Trp 60D, His 57, and Leu 99. The synthesis of the tricyclic scaffolds was based on the 1,3-dipolar cycloaddition of azomethine ylides, derived from L-proline and 4-bromobenzaldehyde, with N-(4-fluorobenzyl)maleimide. Introduction of alkyl, alkenyl, and partially fluorinated alkyl residues was achieved upon substitution of a sulfonyl group by mixed Mg/Zn organometallics f…

Models MolecularMagnetic Resonance SpectroscopySpectrophotometry InfraredStereochemistrySubstituentCrystallography X-RayBiochemistryAntithrombinschemistry.chemical_compoundDrug DiscoveryNon-covalent interactionsGeneral Pharmacology Toxicology and PharmaceuticsMaleimideAlkylPharmacologychemistry.chemical_classificationSulfonylNucleophilic additionbiologyMolecular StructureOrganic ChemistryActive siteFluorineCycloadditionchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationbiology.proteinMolecular MedicineChemMedChem
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A Fluorine Scan at the Catalytic Center of Thrombin: CF, COH, and COMe Bioisosterism and Fluorine Effects on pKa and logD Values

2006

A series of 16 tricyclic thrombin inhibitors was prepared by using the 1,3-dipolar cycloaddition of azomethine ylides derived from 3- or 4-hydroxyproline and 4-bromobenzaldehyde, with N-(4-fluorobenzyl)maleimide as the key step. The terminal pyrrolidine ring of the inhibitors was systematically substituted to explore the potential bioisosteric behavior of C-F, C-OH, and C-OMe residues pointing into the environment of the catalytic center of a serine protease. X-ray crystal structure analyses revealed a distinct puckering preference of this ring. Substitution by F, HO, and MeO has a strong effect on the basicity of the adjacent pyrrolidine nitrogen center which originates from two sigma-indu…

Models MolecularMagnetic Resonance SpectroscopyTertiary amineStereochemistrychemistry.chemical_elementCrystal structureBiochemistryPyrrolidinechemistry.chemical_compoundCatalytic DomainDrug DiscoveryNon-covalent interactionsGeneral Pharmacology Toxicology and PharmaceuticsMaleimidePharmacologychemistry.chemical_classificationMolecular StructureOrganic ChemistryThrombinFluorineAcceptorCycloadditionchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationFluorineMolecular MedicineChemMedChem
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Accurate Treatment of Large Supramolecular Complexes by Double-Hybrid Density Functionals Coupled with Nonlocal van der Waals Corrections.

2015

In this work, we present a thorough assessment of the performance of some representative double-hybrid density functionals (revPBE0-DH-NL and B2PLYP-NL) as well as their parent hybrid and GGA counterparts, in combination with the most modern version of the nonlocal (NL) van der Waals correction to describe very large weakly interacting molecular systems dominated by noncovalent interactions. Prior to the assessment, an accurate and homogeneous set of reference interaction energies was computed for the supramolecular complexes constituting the L7 and S12L data sets by using the novel, precise, and efficient DLPNO-CCSD(T) method at the complete basis set limit (CBS). The correction of the bas…

Models MolecularWork (thermodynamics)Macromolecular SubstancesAccurate treatmentSupramolecular chemistryVan der Waals surfaceDouble-hybrid density functionalsSet (abstract data type)symbols.namesakeLarge supramolecular complexesQuantum mechanicsNon-covalent interactionsComputer SimulationQuímica FísicaLimit (mathematics)Statistical physicsPhysical and Theoretical ChemistryBasis setNonlocal van der Waals correctionschemistry.chemical_classificationChemistryComputer Science ApplicationsModels ChemicalsymbolsQuantum Theoryvan der Waals forceHydrophobic and Hydrophilic InteractionsJournal of chemical theory and computation
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