Search results for "BOND"

showing 10 items of 3527 documents

Speciation of trialkyltin(IV) cations in natural fluids

2004

The hydrolysis of (CH(3))(3)Sn(+), (C(2)H(5))(3)Sn(+) and (C(3)H(7))(3)Sn(+) has been studied in a Synthetic Seawater (SSW) ionic medium simulating the major composition of natural seawater, at different salinities (5 less than or equal to S less than or equal to 45), and at t = 25 degreesC. Interactions with anionic components of SSW, considered as single sea salt, are determined by means of a complex formation model. By potentiometric measurements (ISE-H(+) and ISE-F(-) electrodes), the model has been extended to also consider interactions of organotins with carbonate and fluoride ions, which are other important components of seawater. Literature and new values of hydrolysis constants in …

chemistry.chemical_classificationfood.ingredientChemistryHydrolysisSea saltmedia_common.quotation_subjectInorganic chemistryIonic bondingArtificial seawaterSalt (chemistry)General ChemistryOceanographytrialkyltin(IV)SpeciationHydrolysisfoodIonic strengthEnvironmental ChemistrySeawaterIonic strength Protonation protonation constantsHydrolysis; trialkyltin(IV); Natural FluidsNatural FluidsWater Science and Technologymedia_commonMarine Chemistry
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Structural Investigation of Water/Lecithin/Cyclohexane Microemulsions by FT-IR Spectroscopy

1995

Abstract FT-IR spectra of water/lecithin/deuterated cyclohexane microemulsions as a function of water/lecithin molar ratio R ( R = [water]/[lecithin]) at various volume fractions ( O ) of the micellar phase have been recorded at 25°C. After elimination of the small spectral contributions due to deuterated cyclohexane and normalization, the shape of the C–H stretching band due to lecithin has been found dependent upon R and O whereas that of the O–H stretching band has been found dependent only upon R . The change in shape of the C–H band was interpreted in terms of a modification of the lecithin alkyl chain packing order. The analysis of the O–H band provides evidence that the hydroxylic gr…

chemistry.chemical_classificationfood.ingredientCyclohexaneHydrogen bondChemistryLecithinSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryfoodDeuteriumPhase (matter)Organic chemistryPhysical chemistryMicroemulsionAlkylJournal of Colloid and Interface Science
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Photocrosslinkable dextran hydrogel films as substrates for osteoblast and endothelial cell growth

2012

Functional hydrogel films on solid supports are versatile materials with large potential for cell growth and tissue engineering. Here, we report on a modular approach to generate functional hydrogel composite films for endothelial and osteoblast cell co-culture. The polymer network of the parent hydrogel was formed by a dextran derivative (BP-CMD), which contained carboxymethyl (CM) groups for further chemical functionalization and benzophenone (BP) moieties as a photocrosslinkable unit. BP-CMD could be synthesized by three different routes, first with the benzophenone unit attached via an amide bond, or second by an ether bond, or third as an ion pair between the benzophenone ammonium salt…

chemistry.chemical_classificationfood.ingredientMaterials scienceComposite numberGeneral ChemistryPolymerGelatinchemistry.chemical_compoundDextranfoodchemistryTissue engineeringCovalent bondPolymer chemistryMaterials ChemistryBenzophenoneSurface plasmon resonanceJournal of Materials Chemistry
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An Insight into Substrate-Dependent Fluorination of some Highly Substituted Alicyclic Scaffolds

2017

The substrate-dependent fluorination of some highly-functionalized cyclopentane derivatives with multiple chiral centers has been investigated. The key steps of the stereocontrolled syntheses are the oxidative cleavage of the ring carbon–carbon double bond of readily available diexo or diendo norbornene β-amino acid derivatives followed by transformation of the resulted dialdehyde stereoisomers by reduction. Finally, substrate-directable chemodifferentiation of different types of hydroxy groups under fluorination procedures gave various densely functionalized alicyclic derivatives or heterocycles.

chemistry.chemical_classificationheterocyclescyclizationDouble bond010405 organic chemistrySubstrate (chemistry)chemistry.chemical_elementGeneral Chemistryaminohapot010402 general chemistryRing (chemistry)01 natural scienceslactones0104 chemical sciencesAmino acidchemistry.chemical_compoundAlicyclic compoundchemistryfluorineamiamino acidsFluorineOrganic chemistryCyclopentaneta116NorborneneChemistrySelect
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Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

2018

Abstract Molecular recognition of aromatic hydrocarbons by four endo -functionalized molecular tubes has been studied by 1 H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅ π interactions.

chemistry.chemical_classificationhydrogen bond010405 organic chemistryHydrogen bondStereochemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesmolecular dynamics0104 chemical sciencesMolecular recognitionmacrocycleschemistryhydrogenProton NMRhost-guest chemistryaromatic hydrocarbonhydrocarbonsmolecular recognitionAromatic hydrocarbonSpectroscopyHost–guest chemistryta116Binding selectivityChinese Chemical Letters
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Cu(II), Ni(II) and Zn(II) mononuclear building blocks based on new polynucleating azomethine ligand : Synthesis and characterization

2017

Five new mononuclear complexes formed by the polynucleating ligand 2-[1-(3,5-dimethyl)pyrazolyl]-2-hydroxyimino-N′-[1-(2-pyridyl)ethylidene]acetohydrazide (HL): [Ni(L)(HL)]ClO4·2CH3OH (1), [Ni(L)2]·CH3OH (2), [Zn(L)(HL)]ClO4·2CH3OH (3), [Zn(L)2]·CH3OH (4) and [Cu(L)2]·CH3OH (5) were synthesized and characterized by elemental analysis, mass-spectrometry, IR-spectroscopy and X-ray analysis. The complexes reveal distorted octahedral N4O2 coordination arrangement formed by both protonated and deprotonated (1, 3) or two deprotonated ligand molecules (2, 4, 5). The presence of non-coordinated oxime and pyrazole groups resulted in the formation of extensive systems of hydrogen bonds in the crystal…

chemistry.chemical_classificationkemia010405 organic chemistryStereochemistryLigandHydrogen bondligandsProtonationliganditPyrazole010402 general chemistryOximechemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCoordination complexInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryMaterials ChemistryMoleculePhysical and Theoretical Chemistryta116
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The Influence of the Amide Linkage in the FeIII-Binding Properties of Catechol-Modified Rosamine Derivatives

2015

The two new fluorescent ligands RosCat1 and RosCat2 contain catechol receptors connected to rosamine platforms through an amide linkage and were synthesized by using microwave-assisted coupling reactions of carboxyl- or amine-substituted rosamines with the corresponding catechol units and subsequent deprotection. RosCat1 possesses a reverse amide, whereas RosCat2 has the usual oriented amide bond (HNCO vs. CONH, respectively). The ligands were characterized by means of NMR spectroscopy, mass-spectrometry, and DFT calculations and X-ray crystallography studies for RosCat1. The influence of the amide linkage on the photophysical properties of the fluorescent ligands was assessed in different …

chemistry.chemical_classificationligand designCatecholChemistryStereochemistryOrganic ChemistryChemistry (all)Quantum yieldGeneral ChemistryNuclear magnetic resonance spectroscopyamideCatalysisCoupling reactionCoordination complexCrystallographychemistry.chemical_compoundironSettore CHIM/03 - Chimica Generale E InorganicaAmidePeptide bondChelationcoordination modemass spectrometry
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Crystal structure of C-2-benzo-thia-zole-N-methyl-nitrone.

2015

The molecule of the title compound {systematic name:N-[(benzothiazol-2-yl)methylidene]methylamineN-oxide}, C9H8N2OS, is close to planar [maximum deviation from the mean plane = 0.081 (2) Å], its conformation being stabilized by a strong intramolecular attractive S...O interaction [2.6977 (16) Å]. In the crystal, molecules are linked into centrosymmetric dimers by pairs of weak C—H...O hydrogen bonds.

chemistry.chemical_classificationnitronecrystal structureCrystallographyHydrogen bondS...O attractive interactionMaximum deviationbenzo­thia­zolebenzothiazoleGeneral ChemistryCrystal structureCondensed Matter PhysicsBioinformaticsData ReportsS⋯O attractive inter­actionNitroneCrystalchemistry.chemical_compoundCrystallographychemistryBenzothiazoleQD901-999General Materials ScienceActa crystallographica. Section E, Crystallographic communications
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Michael additions to double bonds of esters of N-protected (s)-phenylalanyldehydroalanine (X-(s)-Phe-ΔAla-OMe) and its phosphonic acid counterpart (X…

2017

Electrophilic addition of amines, thiols and bromide to the double bonds of model dehydrodipeptides and dehydrophosphonodipeptide was studied. The double bond in these two classes of peptides reacted similarly and gave the same products. These results indicate that dehydropeptides are very good candidates as substrates for modifications of peptide side-chains.

chemistry.chemical_classificationphosphonopeptidesdehydrodipeptidesDouble bond010405 organic chemistryElectrophilic additionOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryBromideMichael additionMichael reactiondehydrophosphonodipeptides
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Studies of Nature of Uncommon Bifurcated I–I···(I–M) Metal-Involving Noncovalent Interaction in Palladium(II) and Platinum(II) Isocyanide Cocrystals

2021

Two isostructural trans-[MI2(CNXyl)2]·I2 (M = Pd or Pt; CNXyl = 2,6-dimethylphenyl isocyanide) metallopolymeric cocrystals containing uncommon bifurcated iodine···(metal–iodide) contact were obtained. In addition to classical halogen bonding, single-crystal X-ray diffraction analysis revealed a rare type of metal-involved stabilizing contact in both cocrystals. The nature of the noncovalent contact was studied computationally (via DFT, electrostatic surface potential, electron localization function, quantum theory of atoms in molecules, and noncovalent interactions plot methods). Studies confirmed that the I···I halogen bond is the strongest noncovalent interaction in the systems, followed …

chemistry.chemical_classificationplatinaHalogen bondhalogeenit010405 organic chemistryChemistryIsocyanideAtoms in moleculeskompleksiyhdisteet010402 general chemistrypalladium01 natural sciencesCocrystalElectron localization function0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographykemialliset sidoksetNucleophileNon-covalent interactionsPhysical and Theoretical ChemistryIsostructuralmetallit
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