Search results for "OXY"

showing 10 items of 11443 documents

A synergic nanoantioxidant based on covalently modified halloysite–trolox nanotubes with intra-lumen loaded quercetin

2016

We describe the preparation and properties of the first example of a synergic nanoantioxidant, obtained by different functionalizations of the external surface and the inner lumen of halloysite nanotubes (HNTs). Trolox, a mimic of natural α-tocopherol, was selectively grafted on the HNT external surface; while quercetin, a natural polyphenolic antioxidant, was loaded into the inner lumen to afford a bi-functional nanoantioxidant, HNT–Trolox/Que, which was investigated for its reactivity with transient peroxyl radicals and a persistent 1,1-diphenyl-2-picrylhydrazyl (DPPH˙) radical in comparison with the corresponding mono-functional analogues HNT–Trolox and HNT/Que. Both HNT–Trolox and HNT/Q…

halloysite nanotubes antioxidants peroxyl radicals quercetin Trolox synergismAntioxidantRadicalmedicine.medical_treatmentBiomedical Engineering02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundReaction rate constantmedicinehalloysite trolox release quercetin antioxidantOrganic chemistryGeneral Materials ScienceAcetonitrileSettore CHIM/02 - Chimica FisicaAutoxidationChemistryGeneral ChemistryGeneral MedicineSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesChlorobenzeneTrolox0210 nano-technologyQuercetinNuclear chemistry
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Very strong −N–X+⋯−O–N+ halogen bonds

2016

A new (-)N-X(+)(-)O-N(+) paradigm for halogen bonding is established by using an oxygen atom as an unusual halogen bond acceptor. The strategy yielded extremely strong halogen bonded complexes with very high association constants characterized in either CDCl3 or acetone-d6 solution by (1)H NMR titrations and in the solid-state by single crystal X-ray analysis. The obtained halogen bond interactions, RXB, in the solid-state are found to be in the order of strong hydrogen bonds, viz. RXB ≈ RHB.

halogen bondsNanotechnologychemistry010402 general chemistry01 natural sciencesCatalysisoxygen atomMaterials Chemistryta116Halogen bond010405 organic chemistryChemistryHydrogen bondMetals and AlloysGeneral ChemistryAcceptor0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyOxygen atomHalogenCeramics and CompositesProton NMRTitrationSingle crystalChemical Communications
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Reduction-oxidation dynamics of oxidized graphene: Functional group composition dependent path to reduction

2018

Micrometer-sized oxidation patterns containing varying composition of functional groups including epoxy, ether, hydroxyl, carbonyl, carboxyl, were created in chemical vapor deposition grown graphene through scanning probe lithography and pulsed laser two-photon oxidation. The oxidized graphene films were then reduced by a focused x-ray beam. Through in-situ x-ray photoelectron spectroscopy measurement, we found that the path to complete reduction depends critically on the total oxygen coverage and concentration of epoxy and ether groups. Over the threshold concentrations, a complex reduction-oxidation process involving conversion of functional groups of lower binding energy to higher bindin…

hapetusMaterials sciencekemiax-ray examinationBinding energyOxideEther02 engineering and technologyChemical vapor depositionchemistry010402 general chemistryPhotochemistry01 natural sciencesRedoxepoxylaw.inventionchemistry.chemical_compoundX-ray photoelectron spectroscopylawgrafeeniGeneral Materials Sciencefysiikkata116ta114GraphenegrapheneepoksiGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesröntgenkuvausoxidation (active)chemistryreduction-oxidation processes0210 nano-technologyphysicsScanning probe lithographyCarbon
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From the forest to the plate – Hemicelluloses, galactoglucomannan, glucuronoxylan, and phenolic-rich extracts from unconventional sources as function…

2021

This study aimed to characterise pressurised hot water (PHW) extracts from nonconventional sources of functional carbohydrates and phenolic compounds in terms of antioxidant capacity, antiviral activity, toxicity, and human erythrocytes’ protection antidiabetic potential. PHW extracts of Norway spruce bark (E1 + E2) and Birch sawdust (E3 + E4) contained mostly galactoglucomannan and glucuronoxylan. In contrast, samples E5 to E9 PHW extracted from Norway spruce, and Scots pine bark are rich sources of phenolic compounds. Overall, phenolic-rich extracts presented the highest inhibition of α-amylase and α-glucosidase and protection against stable non-enveloped enteroviruses. Additionally, all …

hemiselluloosagalactoglucomannanssolumallitForestsAntioxidantsAnalytical ChemistryMannansforest byproductshappiradikaalitPolysaccharidestanninsterveysvaikutuksetHumanscell-based modelsmetsäteollisuuden sivuvirratreactive oxygen speciestanniinitPlant ExtractsFood IngredientsGeneral Medicinefenoliset yhdisteetsivutuotteetXylansgalaktoglukomannaanithiilihydraatitFood Sciencephenolic composition
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Advanced biorefinery concepts related to non-wood feedstocks

2018

Agricultural residues, such as wheat straw (Triticum aestivum), okra stalk (Abelmoschus esculentus), and giant miscanthus (Miscanthus × giganteus, a hybrid of M. sinensis and M. sacchariflorus) were investigated to assess their possible consumption for integrated lignocellulosic biorefining. The efficient fractionation and recovery of all important chemical components (cellulose, hemicelluloses, and lignin) of such feedstocks are a prerequisite for realistic biorefinery concepts. Water is one of the most eco-friendly solvents with the highest potential for industrial use, and it is also suitable for full-scale biorefinery purposes. For example, under pressure at elevated temperatures over 1…

hemiselluloosakarboksyylihapotbiomassaaliphatic carboxylic acidsselluloosafood and beveragesalkaline pulpingligninligniinihot-water extractionesikäsittelynon-wood feedstockkasvimateriaalitbiojalostamotuuttomassanvalmistusbiorefining
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The Role Played by Ionic Liquids in Carbohydrates Conversion into 5-Hydroxymethylfurfural: A Recent Overview

2022

Obtaining industrially relevant products from abundant, cheap, renewable, and low-impacting sources such as lignocellulosic biomass, is a key step in reducing consumption of raw fossil materials and, consequently, the environmental footprint of such processes. In this regard, a molecule that is similar to 5-hydroxymethylfurfural (5-HMF) plays a pivotal role, since it can be produced from lignocellulosic biomass and gives synthetic access to a broad range of industrially important products and polymers. Recently, ionic liquids (ILs) have emerged as suitable solvents for the conversion of biomass and carbohydrates into 5-HMF. Herein, we provide a bird’s-eye view on recent achievements about t…

heterogenous catalysisOrganic ChemistryCarbohydratesIonic LiquidsPharmaceutical ScienceSettore CHIM/06 - Chimica OrganicaCatalysisAnalytical Chemistryhomogenous catalysiscarbohydrates conversionChemistry (miscellaneous)Drug DiscoverySolventsMolecular Medicine5-hydrodroxymethylfurfuralFuraldehydePhysical and Theoretical ChemistryHexosesMolecules
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CCDC 1508045: Experimental Crystal Structure Determination

2021

Related Article: Raminder S. Mulla, Javier Pitarch-Jarque, Enrique García-España, Tanya Desa, Elena Lurie-Luke, J. A. Gareth Williams|2017|Chem. Sel.|2|5045|doi:10.1002/slct.201700995

hexa-sodium bis(mu-22'-({2-[(carboxylatomethyl){2-[(carboxylatomethyl)amino]-2-oxoethyl}amino]ethyl}azanediyl)diacetato)-diaqua-di-calcium(ii) bis(chloride) hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 732637: Experimental Crystal Structure Determination

2010

Related Article: E.Colacio, H.Aouryaghal, A.J.Mota, J.Cano, R.Sillanpaa, A.Rodriguez-Dieguez|2009|CrystEngComm|11|2054|doi:10.1039/b906382j

hexakis((mu~2~-Pyrimidine-2-carboxylato)-(NNN'N'-tetramethyl-ethylene-12-diamine))-hexa-cobalt hexaperchlorate tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 725441: Experimental Crystal Structure Determination

2010

Related Article: E.Colacio, H.Aouryaghal, A.J.Mota, J.Cano, R.Sillanpaa, A.Rodriguez-Dieguez|2009|CrystEngComm|11|2054|doi:10.1039/b906382j

hexakis((mu~2~-Pyrimidine-2-carboxylato)-(NNN'N'-tetramethyl-ethylene-12-diamine))-hexa-nickel hexakis(tetrafluoroborate) tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 725440: Experimental Crystal Structure Determination

2010

Related Article: E.Colacio, H.Aouryaghal, A.J.Mota, J.Cano, R.Sillanpaa, A.Rodriguez-Dieguez|2009|CrystEngComm|11|2054|doi:10.1039/b906382j

hexakis((mu~2~-Pyrimidine-2-carboxylato)-(NNN'N'-tetramethyl-ethylene-12-diamine))-hexa-nickel hexaperchlorate tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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