Search results for "bond"

showing 10 items of 3527 documents

Multiple cross-linked hydroxypropylcellulose–succinate–salicylate: prodrug design, characterization, stimuli responsive swelling–deswelling and susta…

2015

A hydroxypropylcellulose–succinic anhydride (HPC–SAn) conjugate was synthesized homogeneously at 80 °C for 6 h under N2 in N,N-dimethylacetamide (DMA). The HPC–SAn conjugate was further covalently linked with salicylic acid (SA) drug using the versatile reagent ZrOCl2·8H2O at 80 °C for 6 h. Multiple crosslinking of the benign HPC–SAn–SA conjugate was achieved using oxalyl chloride. The resultant cross-linked prodrug (CL-HPC–SAn–SA conjugate) was characterized using different spectroscopic techniques. UV/Vis analysis of the HPC–SAn–SA conjugate has indicated that it contains 26 mg of SA per 100 mg. CL-HPC–SAn–SA showed reasonably good swelling properties in water and at different physiologic…

General Chemical EngineeringKineticsGeneral ChemistryProdrugchemistry.chemical_compoundchemistryOxalyl chlorideCovalent bondReagentmedicineOrganic chemistrySwellingmedicine.symptomSalicylic acidNuclear chemistryConjugateRSC Advances
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Experimental-Like Affinity Constants and Enantioselectivity Estimates from Flexible Docking

2012

Experimental-like affinity constants and enantioselectivity estimates, not predicted so far computationally, were obtained using a novel flexible modeling/docking combined strategy. The S- and R-warfarin-human serum albumin (HSA, site I) complexes were used as an interaction model. The process for a verified estimation includes the following: (i) ionized open chain forming at physiological pH (a recent focus); (ii) conformational search (molecular mechanics and Monte Carlo methods); (iii) rigid protein-flexible ligand docking (GlideXP) generating low energy paired S- and R-poses; (iv) graphical comparison against the X-ray crystal structure (unsatisfactory verification step); (v) quantum po…

General Chemical EngineeringMonte Carlo methodCrystal structureLibrary and Information SciencesCrystallography X-RayStructure-Activity RelationshipLow energyComputational chemistryHumansSerum AlbuminBinding SitesChemistryHydrogen BondingStereoisomerismInteraction modelGeneral ChemistryHydrogen-Ion ConcentrationComputer Science ApplicationsMolecular Docking SimulationKineticsResearch DesignDocking (molecular)Quantum TheoryThermodynamicsWarfarinMonte Carlo MethodAlgorithmsProtein BindingJournal of Chemical Information and Modeling
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Perfluorocarbons–graphene oxide nanoplatforms as biocompatible oxygen reservoirs

2018

Abstract 3-Pentadecafluoroheptyl,5-perfluorophenyl-1,2,4-oxadiazole (FOX) molecules were attached onto a graphene oxide (GO) via a facile aromatic substitution in alkaline environment. This approach allows achieving high degree of functionalization under mild conditions. The covalent attachment of perfluoromoieties onto GO lamellae was confirmed by spectroscopic analyses. The performance of these nanoplatforms (GOF) as oxygen reservoirs was assessed at different concentrations and temperature. The results revealed that under physiologic conditions GO and FOX synergistically operate for increasing oxygen uptake and release, either from a thermodynamic and a kinetic point of view. Even at low…

General Chemical EngineeringOxidechemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesOxygenIndustrial and Manufacturing Engineeringlaw.inventionchemistry.chemical_compoundTissue engineeringlawXPSEnvironmental ChemistryMoleculeChemical Engineering (all)RamanGraphene oxideGrapheneChemistryChemistry (all)Settore CHIM/06 - Chimica OrganicaGeneral Chemistry021001 nanoscience & nanotechnologyOxygen exchangePerfluorocarbon0104 chemical sciencesSettore BIO/18 - GeneticaSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiChemical engineeringCovalent bondSurface modificationAFM0210 nano-technologySaturation (chemistry)Chemical Engineering Journal
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Synthesis and X-ray Crystal Structure of New Substituted 3-4′-Bipyrazole Derivatives. Hirshfeld Analysis, DFT and NBO Studies

2021

A new compounds named 3-4′-bipyrazoles 2 and 3 were synthesized in high chemical yield from a reaction of pyran-2,4-diketone 1 with aryl hydrazines under thermal conditions in MeOH. Compound 2 was unambiguously confirmed by single-crystal X-ray analysis. It crystalizes in a triclinic crystal system and space group P-1. Its crystal structure was found to be in good agreement with the spectral characterizations. With the aid of Hirshfeld calculations, the H…H (54.8–55.3%) and H…C (28.3–29.2%) intermolecular contacts are the most dominant, while the O…H (5.8–6.5%), N…H (3.8–4.6%) and C…C (3.0–4.9%) are less dominant. The compound has a polar nature with a net dipole moment of 6.388 Debye. The …

General Chemical Engineeringpyran-24-dioneCrystal structureTriclinic crystal systemDFTInorganic Chemistrychemistry.chemical_compoundkemialliset sidoksetNBOGeneral Materials Scienceorgaaniset yhdisteetkemiallinen synteesiCrystallographyArylIntermolecular forcetiheysfunktionaaliteoriaHirshfeld analysisCondensed Matter PhysicskiteetbipyrazoleDipoleCrystallographychemistryQD901-999Intramolecular forceYield (chemistry)röntgenkristallografiaNatural bond orbitalCrystals
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X-ray Single Crystal Structure, Tautomerism Aspect, DFT, NBO, and Hirshfeld Surface Analysis of a New Schiff Bases Based on 4-Amino-5-Indol-2-yl-1,2,…

2021

Four different new Schiff basses tethered indolyl-triazole-3-thione hybrid were designed and synthesized. X-ray single crystal structure, tautomerism, DFT, NBO and Hirshfeld analysis were explored. X-ray crystallographic investigations with the aid of Hirshfeld calculations were used to analyze the molecular packing of the studied systems. The H···H, H···C, S···H, Br···C, O···H, C···C and N···H interactions are the most important in the molecular packing of 3. In case of 4, the S···H, N···H, S···C and C···C contacts are the most significant. The results obtained from the DFT calculations indicated that the thione tautomer is energetically lower than the thiol one by 13.9545 and 13.7464 kcal…

General Chemical Engineeringtautomerism aspectInorganic Chemistrysymbols.namesakeGeneral Materials SciencetyppiyhdisteetDebyechemistry.chemical_classificationkemiallinen synteesiCrystallographyX-rayCondensed Matter Physicsindolyl-triazole-3-thioneTautomerSchiff bases; indolyl-triazole-3-thione; tautomerism aspect; Hirshfeld Surface AnalysisCrystallographyDipolechemistryQD901-999Thiolsymbols1 2 4 triazole 3 thioneSchiff basesHirshfeld Surface AnalysisSingle crystaltautomeriaNatural bond orbitalCrystals; Volume 11; Issue 9; Pages: 1041
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Ab initio simulations on AgCl(111) surface and AgCl(111)/α-Al2O3(0001) interface

2005

The defect chemistry and ionic transport properties of the AgCl(111)/α-Al 2 O 3 (0001) interface were consid by using ab initio slab calculations. These calculations were performed in the framework of plane-wave basis combined with the density functional theory (DFT), as implemented into the VASP computer code, and Gaus basis set combined with the Hartree-Fock method (CRYSTAL-98 code). We analyze the electron density distribu on the interface and the electrostatic potential distribution near the AgCl surface. The size of the silver ion is great to enter the corundum surface layer and to create excess silver ions in this way. This is in agreement the experiments on heterogeneous doping of Ag…

General Computer ScienceChemistryAb initioGeneral Physics and AstronomyIonic bondingGeneral ChemistryMolecular physicsIonComputational MathematicsMechanics of MaterialsAb initio quantum chemistry methodsVacancy defectGeneral Materials ScienceDensity functional theorySurface layerAtomic physicsBasis setComputational Materials Science
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Computer modelling of point defects in ABO3 perovskites and MgO

2004

We present results for basic intrinsic defects: F-type electron centers (O vacancy which trapped one or two electrons) and hole polarons bound to Mg or K vacancy in ionic MgO and partly covalent KNbO3 perovskite, respectively. We demonstrate that a considerable covalency of the perovskite chemical bonding makes the F-type centers therein much more similar to defects in partly-covalent quartz-type oxides rather than the conventional F centers in alkali halides and ionic MgO. Both one-site (atomic) and two-site (molecular) polarons are expected to coexist in KNbO3 characterized by close absorption energies. Our calculations confirm existence of the self-trapped electron polarons in KNbO3, KTa…

General Computer ScienceCondensed matter physicsAbsorption spectroscopyChemistryJahn–Teller effectGeneral Physics and AstronomyIonic bondingGeneral ChemistryPolaronIonComputational MathematicsChemical bondMechanics of MaterialsVacancy defectGeneral Materials SciencePerovskite (structure)Computational Materials Science
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Oxidation of small gas phase Pd clusters: A density functional study

2006

The adsorption sites of O2 on neutral PdN clusters (N = 1–4) were studied using spin density functional theory. Only for Pd1O2 molecular adsorption is found to be favorable. For Pd2–4O2 dissociative adsorption with the oxygen sitting on Pd bridge sites is preferred. Most Pd clusters remain in the same high spin states found for pure gas phase Pd clusters. Only the ground state of Pd4O2 increase its spin from a triplet to a quintet state. For molecular adsorption the O–O bond gets activated to a superoxo-like state.

General Computer ScienceSpin statesChemistryGeneral Physics and Astronomychemistry.chemical_elementGeneral ChemistryOxygenComputational MathematicsAdsorptionTransition metalChemical bondMechanics of MaterialsComputational chemistryChemical physicsGeneral Materials ScienceDensity functional theoryTriplet stateGround stateComputational Materials Science
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A CI study of the CuCO and CuCO+ complexes

1987

MO CI calculations are carried out using an optimal space of valence virtual MOs obtained by means of a projection technique, as a linear combination of the AOs which are more occupied in the molecular Fock space. Localization of the occupied MOs and nonvalence virtual MOs is also achieved. The overall procedure is proven to be quite advantageous and well suited to obtain potential energy curves which keep the same physical meaning along the range of distances studied. Using a slightly better than double‐zeta quality basis set, a valence CAS‐CI, and selected CI wave function by the CIPSI algorithm have revealed a possible weak van der Waals interaction for the 2Σ+ state of CuCO, which remai…

General Physics and AstronomyElectronic structureCopper CompoundsMolecular physicsCopper Complexessymbols.namesake:FÍSICA [UNESCO]CarbonylsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Basis setPi backbondingValence (chemistry)Electronic correlationChemistryUNESCO::FÍSICAConfiguration interactionPotential energyUNESCO::FÍSICA::Química físicaConfiguration InteractionValenceElectronic StructuresymbolsElectron CorrelationConfiguration Interaction ; Electron Correlation ; Copper Compounds ; Carbonyls ; Copper Complexes ; Electronic Structure ; Valencevan der Waals forceAtomic physicsThe Journal of Chemical Physics
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Calcium binding and ionic conduction in single conical nanopores with polyacid chains: model and experiments.

2012

Calcium binding to fixed charge groups confined over nanoscale regions is relevant to ion equilibrium and transport in the ionic channels of the cell membranes and artificial nanopores. We present an experimental and theoretical description of the dissociation equilibrium and transport in a single conical nanopore functionalized with pH-sensitive carboxylic acid groups and phosphonic acid chains. Different phenomena are simultaneously present in this basic problem of physical and biophysical chemistry: (i) the divalent nature of the phosphonic acid groups fixed to the pore walls and the influence of the pH and calcium on the reversible dissociation equilibrium of these groups; (ii) the asym…

General Physics and AstronomyIonic bondingFunctionalizedDissociation (chemistry)Conical nanoporeNanoscale regionschemistry.chemical_compoundNanoporesI - V curveIonic conductivityGeneral Materials ScienceConical nanoporesPhosphonate groupCalcium concentrationChemistryGeneral EngineeringPH effectsPartition functionsIonic channelsIon equilibriumReversible dissociationChemical physicsFunctional groupsThermodynamicsDesalination membranesIon bindingPorosityDissociationBiophysical chemistryDissociation equilibriaInorganic chemistrychemistry.chemical_elementWater filtrationCalciumIonNernst-Planck equationsApplied potentialsIon bindingCarboxylationPhosphonic acidsComputer SimulationCarboxylateParticle SizeControlled drug releaseCurrent voltage curveIonsBinding SitesFixed charge densityPH sensitiveCarboxylic acidsDesalinationPhosphonic acid groupsPoly acidsElectric ConductivityCarboxylic acid groupsFixed ChargesNanostructuresCell membranesCurrent-voltage curvesModels ChemicalQuantum theoryFISICA APLICADACalciumBiological ion channelsCalcium bindingIonic currentCytologyPore wallStatistical mechanicsAcidsACS nano
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