Search results for "site"

showing 10 items of 8388 documents

Exploratory Synthesis of Low-Silica Nanozeolites through Geopolymer Chemistry

2019

Nanozeolites are of great interest with the premise of their efficiency in traditional applications such as catalysis and separation, as well as their emerging applications including chemical sensors, medicine, and food industry. We report a new geopolymerization route for the synthesis of nanozeolites with different crystal structures by exploring the Na–Al–Si–H2O quaternary phase space under a mild hydrothermal condition. Nanostructured faujasite (FAU), cancrinite (CAN), and sodalite (SOD) zeolites with a crystallite size smaller than 40 nm were successfully produced from our exploration, as well as a submicron-sized Linde-Type A (LTA) zeolite. The transmission electron microscopy and nit…

010405 organic chemistryGeneral ChemistryFaujasiteengineering.material010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesCancriniteCatalysisGeopolymerchemistry.chemical_compoundChemical engineeringchemistryengineeringSodaliteGeneral Materials ScienceCrystalliteMesoporous materialZeoliteCrystal Growth & Design
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Higher MLCT lifetime of carbene iron(ii) complexes by chelate ring expansion

2021

Combining strong σ-donating N-heterocyclic carbene ligands and π-accepting pyridine ligands with a high octahedricity in rigid iron(ii) complexes increases the 3MLCT lifetime from 0.15 ps in the prototypical [Fe(tpy)2]2+ complex to 9.2 ps in [Fe(dpmi)2]2+12+. The tripodal CNN ligand dpmi (di(pyridine-2-yl)(3-methylimidazol-2-yl)methane) forms six-membered chelate rings with the iron(ii) centre leading to close to 90° bite angles and enhanced iron-ligand orbital overlap.

010405 organic chemistryLigandMetals and AlloysGeneral ChemistryOrbital overlap010402 general chemistryRing (chemistry)01 natural sciencesCatalysisPyridine ligand0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryMaterials ChemistryCeramics and CompositesChelationCarbeneChemical Communications
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Macrocyclic complexes based on [N⋯I⋯N]+ halogen bonds

2021

New 1–2 nm macrocyclic iodine(I) complexes prepared VIA a simple ligand exchange reaction manifest rigid 0.5–1 nm cavities that bind the hexafluorophosphate anion in the gas phase. The size of the cavities and the electrostatic interactions with the iodine(I) cations influence the anion binding properties of these macrocyclic complexes.

010405 organic chemistryLigandMetals and Alloyschemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrostaticsIodine01 natural sciencesCatalysis0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonGas phasechemistry.chemical_compoundchemistryHexafluorophosphatePolymer chemistryHalogenMaterials ChemistryCeramics and CompositesAnion bindingChemical Communications
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Triazole vs. triazolium carbene ligands in the site-selective cyclometallation of o-carboranes by M(iii) (M = Ir, Rh) complexes

2018

Ir(iii) and Rh(iii)-mediated site-selective cage B-H and C-H bond activation in o-carboranylmethyl derivatives has been achieved. The selectivity of the reaction is related to the electron donating properties of the ligand. 1,2,3-Triazole-derivatives use the N2 position of the triazole ring to direct the selective o-carborane B-H bond activation, whereas the corresponding triazolylidene derivatives lead to the cage C-H bond activation with complete site-selectivity.

010405 organic chemistryLigandTriazole010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistrySite selectiveSelectivityCarbeneDalton Transactions
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Electrochemical meso-functionalization of magnesium(II) porphine

2010

International audience; Regioselective meso-functionalization of the totally unsubstituted magnesium(II) porphine was performed by controlled potential electrolysis with pyridine and triphenylphosphine as nucleophiles leading to the original pyridinium and phosphonium substituted derivatives, respectively. The crystallographic structure of the latter is described as the only meso-phosphonium porphyrin reported to date.

010405 organic chemistryMagnesiumMetals and AlloysRegioselectivitychemistry.chemical_elementGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesPorphyrinCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundNucleophilechemistryPolymer chemistryPyridineMaterials ChemistryCeramics and Composites[CHIM.COOR]Chemical Sciences/Coordination chemistryPhosphoniumPyridiniumTriphenylphosphine
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Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis

2018

[EN] A multicatalytic approach that combines a bifunctional Brønsted base¿squaramide organocatalyst and Ag+ as Lewis acid has been applied in the reaction of unactivated ketones with tert-butyl isocyanoacetate to give chiral oxazolines bearing a quaternary stereocenter. The formal [3+2] cycloaddition provided high yields of the corresponding cis-oxazolines with good diastereoselectivity and excellent enantioselectivity, being applied to aryl¿alkyl and alkyl¿alkyl ketones.

010405 organic chemistryMetals and AlloysEnantioselective synthesisGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCycloaddition0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundchemistryCatàlisiFISICA APLICADAOrganocatalysisMaterials ChemistryCeramics and CompositesLewis acids and basesBifunctionalQuímica orgànica
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Formation and trapping of the thermodynamically unfavoured inverted-hemicucurbit[6]uril

2019

Amplification of a thermodynamically unfavoured macrocyclic product through the directed shift of the equilibrium between dynamic covalent chemistry library members is difficult to achieve. We show for the first time that during condensation of formaldehyde and cis-N,N'-cyclohexa-1,2-diylurea formation of inverted-cis-cyclohexanohemicucurbit[6]uril (i-cis-cycHC[6]) can be induced at the expense of thermodynamically favoured cis-cyclohexanohemicucurbit[6]uril (cis-cycHC[6]). The formation of i-cis-cycHC[6] is enhanced in low concentration of the templating chloride anion and suppressed in excess of this template. We found that reaction selectivity is governed by the solution-based template-a…

010405 organic chemistryPrecipitation (chemistry)Metals and AlloysDiastereomerGeneral ChemistryTrapping010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryComputational chemistryYield (chemistry)Materials ChemistryCeramics and CompositesTrifluoroacetic acidDynamic combinatorial chemistrySelectivityBinding affinitiesChemical Communications
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Metal Complexes of Two Specific Regions of ZnuA, a Periplasmic Zinc(II) Transporter from Escherichia coli

2020

The crystal structure of ZnZnuA from Escherichia coli reveals two metal binding sites. (i) The primary binding site, His143, is located close the His-rich loop (residues 116-138) and plays a significant role in Zn(II) acquisition. (ii) The secondary binding site involves His224. In this work, we focus on understanding the interactions of two metal ions, Zn(II) and Cu(II), with two regions of ZnuA, which are possible anchoring sites for Zn(II): Ac-115MKSIHGDDDDHDHAEKSDEDHHHGDFNMHLW145-NH2 (primary metal binding site) and Ac-223GHFTVNPEIQPGAQRLHE240-NH2 (secondary metal binding site). The histidine-rich loop (residues 116-138) has a role in the capture of zinc(II), which is then further deliv…

010405 organic chemistryStereochemistryChemistrychemistry.chemical_elementMetal Binding SitePeriplasmic spaceZinc010402 general chemistryLigand (biochemistry)01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundvisual_artvisual_art.visual_art_mediumImidazolePhysical and Theoretical ChemistryBinding siteHistidine
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Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness.

2016

The cooperative supramolecular polymerization of 1 and 2 yields P- or M-type helical aggregates depending on the absolute configuration (S or R) of the stereogenic centres attached to the side chains. The connectivity of the amide group does not affect the handedness of the helical aggregates, but determines a larger cooperativity for retroamides 1.

010405 organic chemistryStereochemistryMetals and AlloysSupramolecular chemistryAbsolute configurationCooperativityGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundCrystallographychemistryPolymerizationAmideMaterials ChemistryCeramics and CompositesSide chainChemical communications (Cambridge, England)
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Research Regarding the Physical-Mechanical Properties of Knits for Garments – Abrasion Resistance

2017

Abstract During wear, the fabric is subjected to a complex combination of forces acting at various rates, in various intensities, in various directions and for various periods. This is one of the main causes of a fabric and garment becoming unacceptable for further wear. The main goal of this research paper is to improve the physical-mechanical properties of knits for garments by choosing the right fabric structure and raw material. The abrasion resistance is a mechanical deterioration and progressive loss of substance from a fabric, resulting from the fabric rubbing against itself or another surface. Tests was done on weft knitted fabric for garments using cotton, wool and mixed yarns, thr…

010407 polymersEngineeringbusiness.industry02 engineering and technologyGeneral MedicineRaw material021001 nanoscience & nanotechnologyClothing01 natural sciencesFabric structure0104 chemical sciencesRubbingWoolComposite material0210 nano-technologybusinessProcedia Engineering
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