Search results for "bonding"

showing 10 items of 996 documents

Bis(glycylglycinium) oxalate at 100 K.

2003

The structure of the title compound, 2C(4)H(9)N(2)O(3)(+).C(2)O(4)(2-), which has been determined by X-ray diffraction, contains discrete glycylglycine (HGly-Gly)(+) cations in general positions and oxalate anions which lie across centres of inversion. Although the geometry of the (HGly-Gly)(+) cation is not significantly different compared with other structures containing this residue, a few changes in conformation are observed which indicate the presence of molecular interactions. The molecular network in the crystal consists of one nearly linear O-H...O, five N-H...O and two weak C-H.O hydrogen bonds.

GlycylglycineOxalatesbiologyMolecular StructureHydrogen bondStereochemistryGlycylglycineMolecular ConformationHydrogen BondingGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyOxalateCrystalCold Temperaturechemistry.chemical_compoundCrystallographychemistryCationsbiology.proteinMoleculeCarboxylateOrganic anionActa crystallographica. Section C, Crystal structure communications
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Silicate adsorption by goethite at elevated temperatures

2009

Abstract Batch adsorption experiments with relatively low silica concentrations between 10 µM and 100 µM were conducted at three different ionic strength (0.01  − 0.1 M), and four different temperatures between 10 °C and 75 °C, yielding in a total of 550 experimental data points. The residual concentration of monosilicic acid is controlled by an adsorption equilibrium which is dependent on pH. The % Si adsorbed vs. − log[H + ] curves reveal an upward bend with a maximum at about a pH of 9. With acidification below pH 9 the residual Si concentration in the suspensions steadily increases, as well as in the increasingly alkaline pH range. The slope of the latter is becoming steeper with increa…

GoethiteInorganic chemistryEnthalpyAnalytical chemistryIonic bondingCharge densityGeologySilicatechemistry.chemical_compoundAdsorptionchemistryGeochemistry and PetrologyIonic strengthvisual_artvisual_art.visual_art_mediumSurface chargeChemical Geology
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Probing a Polar Cluster in the Retinal Binding Pocket of Bacteriorhodopsin by a Chemical Design Approach

2012

Bacteriorhodopsin has a polar cluster of amino acids surrounding the retinal molecule, which is responsible for light harvesting to fuel proton pumping. From our previous studies, we have shown that threonine 90 is the pivotal amino acid in this polar cluster, both functionally and structurally. In an attempt to perform a phenotype rescue, we have chemically designed a retinal analogue molecule to compensate the drastic effects of the T90A mutation in bacteriorhodopsin. This analogue substitutes the methyl group at position C(13) of the retinal hydrocarbon chain by and ethyl group (20-methyl retinal). We have analyzed the effect of reconstituting the wild-type and the T90A mutant apoprotein…

Halobacterium salinarumModels MolecularProtein FoldingProtein Denaturation01 natural sciencesBiotecnologiaBiochemistryBiophysics Simulationschemistry.chemical_compoundSensory RhodopsinsHalobacterium salinarum0303 health sciencesMultidisciplinarybiologyProtein StabilityQRTemperatureUltraviolet-visible spectroscopyThermal stabilityBacterial BiochemistryChemistryBiochemistryBacteriorhodopsinsRetinaldehydeMedicineProtonsResearch ArticleSteric effectsHydrogen bondingBioquímicaProtein StructureScienceRetinal bindingBiophysics010402 general chemistryMicrobiologyPhosphates03 medical and health sciencesBiology030304 developmental biologyAspartic AcidBinding SitesAdaptation OcularOrganic ChemistryOrganic SynthesisProteinsChromoproteinsRetinalBacteriorhodopsinBacteriologyBiological TransportChromophorebiology.organism_classification0104 chemical sciencesTransmembrane ProteinschemistryRetinaldehydeBiophysicsbiology.proteinMutant ProteinsPLoS ONE
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Halogen Bonding beyond Crystals in Materials Science

2019

Halogen bonding has recently gained well deserved attention in present-day research for its importance in many fields of supramolecular science and crystal engineering. Although generally overlooked in comprehensive studies in the past, halogen bonding has become an important tool also in the field of materials science. An increased number of scientific reports are published every year where halogen bonding is exploited in soft materials rather than in crystal engineering. Here, we focus on a description of the most exciting contemporary developments in the field of halogen-bonded functional soft materials, assembled using the guiding principles of crystal engineering. We give a particular …

Halogen BondingHalogen bondMaterials science010304 chemical physicsChemieNanotechnology010402 general chemistryCrystal engineering01 natural sciencesSoft materialsSupramolecular Chemistry0104 chemical sciencesSurfaces Coatings and Films0103 physical sciencesMaterials ChemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryLiquid CrystalPolymerCrystals Gel
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Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors

2021

Abstract Neutral halogen‐bonded O−I−N complexes were prepared from in situ formed carbonyl hypoiodites and aromatic organic bases. The carbonyl hypoiodites have a strongly polarized iodine atom with larger σ‐holes than any known uncharged halogen bond donor. Modulating the Lewis basicity of the selected pyridine derivatives and carboxylates leads to halogen‐bonded complexes where the classical O−I⋅⋅⋅N halogen bond transforms more into a halogen‐bonded COO−⋅⋅⋅I−N+ ion‐pair (salt) with an asymmetric O−I−N moiety. X‐ray analyses, NMR studies, and calculations reveal the halogen bonding geometries of the carbonyl hypoiodite‐based O−I−N complexes, confirming that in the solid‐state the iodine at…

Halogen Bondingpyridineinorganic chemicalsHalogen bondOrganic basehalogeenitCommunicationSupramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyGeneral MedicinehypoioditeMedicinal chemistryCatalysisCommunicationssupramolecular chemistrychemistry.chemical_compoundkemialliset sidoksetNMR spectroscopychemistryPyridineTrifluoroacetic acidsupramolekulaarinen kemiaMoietyCarboxylateAngewandte Chemie
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Fine-tuning halogen bonding properties of diiodine through halogen–halogen charge transfer – extended [Ru(2,2′-bipyridine)(CO)2X2]·I2 systems (X = Cl…

2016

The current paper introduces the use of carbonyl containing ruthenium complexes, [Ru(bpy)(CO)2X2] (X = Cl, Br, I), as halogen bond acceptors for a I2 halogen bond donor. In all structures, the metal coordinated halogenido ligand acts as the actual halogen bond acceptor. Diiodine, I2, molecules are connected to the metal complexes through both ends of the molecule forming bridges between the complexes. Due to the charge transfer from Ru–X to I2, formation of the first Ru–X⋯I2 contact tends to generate a negative charge on I2 and redistribute the electron density anisotropically. If the initial Ru–X⋯IA–IB interaction causes a notable change in the electron density of I2, the increased negativ…

Halogen bond010405 organic chemistryChemistryLigandchemistry.chemical_elementCharge densityGeneral Chemistry010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencesAcceptor22'-Bipyridine0104 chemical sciencesRutheniumCrystallographychemistry.chemical_compoundhalogen bondingHalogenruthenium complexesMoleculeGeneral Materials Scienceta116CrystEngComm
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The H2C(X)–X•••X– (X = Cl, Br) Halogen Bonding of Dihalomethanes

2017

The dihalomethane–halide H2C(X)–X···X– (X = Cl, Br) halogen bonding was detected in a series of the cis-[PdX(CNCy){C(NHCy)═NHC6H2Me2NH2}]X•CH2X2 (X = Cl, Br) associates by single-crystal XRD followed by DFT calculations. Although ESP calculations demonstrated that the σ-hole of dichloromethane is the smallest among all halomethane solvents (the maximum electrostatic potential is only 2.6 kcal/mol), the theoretical DFT calculations followed by Bader’s QTAIM analysis (M06/DZP-DKH level of theory) confirmed the H2C(X)–X···X– halogen bond in both the solid-state and gas-phase optimized geometries. The estimated bonding energy in H2C(X)–X···X– is in the 1.9–2.8 kcal/mol range.

Halogen bond010405 organic chemistryHalomethaneGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesdihalomethanes0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryComputational chemistryhalogen bondingGeneral Materials ScienceBond energyta116DichloromethaneCrystal Growth and Design
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The subtle balance of weak supramolecular interactions: The hierarchy of halogen and hydrogen bonds in haloanilinium and halopyridinium salts

2010

The series of haloanilinium and halopyridinium salts: 4-IPhNH3Cl (1), 4-IPhNH3Br (5), 4-IPhNH3H2PO4 (6), 4-ClPhNH3H2PO4 (8), 3-IPyBnCl (9), 3-IPyHCl (10) and 3-IPyH-5NIPA (3-iodopyridinium 5-nitroisophthalate, 13), where hydrogen or/and halogen bonding represents the most relevant non-covalent interactions, has been prepared and characterized by single crystal X-ray diffraction. This series was further complemented by extracting some relevant crystal structures: 4-BrPhNH3Cl (2, CCDC ref. code TAWRAL), 4-ClPhNH3Cl (3, CURGOL), 4-FPhNH3Cl (4, ANLCLA), 4-BrPhNH3H2PO4, (7, UGISEI), 3-BrPyHCl, (11, CIHBAX) and 3-ClPyHCl, (12, VOQMUJ) from Cambridge Structural Database for sake of comparison. Bas…

Halogen bondHydrogenChemistryHydrogen bondOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementCrystal structurehydrogen bondingCrystal engineeringFull Research Papersupramolecular chemistrylcsh:QD241-441ChemistryCrystallographylcsh:Organic chemistrycrystal engineeringhalogen bondingHalogenweak interactionslcsh:Qlcsh:ScienceSingle crystalBeilstein Journal of Organic Chemistry
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NI halogen bonding supported stabilization of a discrete pseudo-linear [I12]2− polyiodide

2015

Two different dicationic N-donors, based on the DABCO diamine, have been studied as templates for polyiodides. The results present a new strategy for polyiodide stabilization, which involves both N⋯I halogen bonding and cation–anion interactions. This is highlighted by the self-assembly of an unprecedented discrete pseudo-linear dodecaiodide species.

Halogen bondInorganic chemistryGeneral ChemistryDABCOCondensed Matter Physicschemistry.chemical_compoundPolyiodideTemplatechemistryhalogen bondingDiaminePolymer chemistryGeneral Materials Scienceta116CrystEngComm
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Synthesis of fluorinated oxadiazoles with gelation and oxygen storage ability

2012

A new family of fluorinated low molecular weight (LMW) gelators has been synthesized through SNAr substitution of 5-polyfluoroaryl-3-perfluoroheptyl-1,2,4-oxadiazoles with glycine ester. The obtained compounds give thermal and pH-sensitive hydrogels or thermo-reversible organogels in DMSO. Oxygen solubility studies showed the ability to maintain high oxygen levels in solution and in gel blend with plate counter agar (PCA).

HalogenationOxygen storageGlycinechemistry.chemical_elementBiochemistryPhase TransitionNucleophilic aromatic substitutionOrganic chemistryDimethyl SulfoxidePhysical and Theoretical ChemistrySolubilityOxadiazolesHydrogen bondChemistryOrganic ChemistryHalogenationEstersHydrogen BondingFluorineSettore CHIM/06 - Chimica OrganicaHydrogen-Ion ConcentrationMolecular WeightOxygenSolubilityGlycineSelf-healing hydrogelsFluorineMicroscopy Electron Scanninglow molecular weight gelators(LMWG) oxadiazoles fluorinated compounds oxgyen carriersThermodynamicsGels
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