Search results for "010402 general chemistry"

showing 10 items of 6896 documents

[60]Fullerene l -Amino Acids and Peptides: Synthesis under Phase-Transfer Catalysis Using a Phosphine–Borane Linker. Electrochemical Behavior

2017

International audience; A new method to link amino acid and peptide derivatives to [60]fullerene is described. It uses hydrophosphination with a secondary phosphine borane. First, the stereoselective synthesis of secondary phosphine borane amino acid derivatives was achieved by alkylation of phenylphosphine borane with gamma-iodo-alpha-amino ester reagents under phase transfer catalysis (PTC). Second, a sec-phosphine borane amino ester was saponified and coupled with alpha,gamma-diamino esters to afford the corresponding dipeptide derivatives in good yields. Finally, the hydrophosphination reaction of [60]fullerene by the sec-phosphine borane compounds was performed under PTC to obtain C-60…

p-chiral phosphiniteshiv-1 proteaseBoraneAlkylation010402 general chemistrychemistry01 natural scienceschemistry.chemical_compoundc60[ CHIM.ORGA ] Chemical Sciences/Organic chemistryredox propertiesOrganic chemistrytertiary phosphinesRacemizationchemistry.chemical_classificationAddition reactionbond activationDipeptide010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistrybuckminsterfullereneCombinatorial chemistryfullerene c-600104 chemical sciencesAmino acidchemistryPhenylphosphinederivativesPhosphine
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Feedback and Communication in Active Hydrogel Spheres with pH Fronts: Facile Approaches to Grow Soft Hydrogel Structures

2021

Abstract Compartmentalized reaction networks regulating signal processing, communication and pattern formation are central to living systems. Towards achieving life‐like materials, we compartmentalized urea‐urease and more complex urea‐urease/ester‐esterase pH‐feedback reaction networks into hydrogel spheres and investigate how fuel‐driven pH fronts can be sent out from these spheres and regulated by internal reaction networks. Membrane characteristics are installed by covering urease spheres with responsive hydrogel shells. We then encapsulate the two networks (urea‐urease and ester‐esterase) separately into different hydrogel spheres to devise communication, pattern formation and attracti…

pH feedback system540 Chemistry and allied sciencesSystems ChemistrySupramolecular chemistry3D printingPattern formationlife-like systemsNanotechnology010402 general chemistry01 natural sciencessupramolecular chemistryCatalysisResearch Articleshydrogels010405 organic chemistrybusiness.industrychemical reaction networksGeneral MedicineGeneral ChemistrySoft materials0104 chemical sciencesLiving systems540 ChemieSelf-healing hydrogelsSPHERESAlginate hydrogelbusinessResearch ArticleAngewandte Chemie International Edition
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Synthesis, NMR spectral and structural studies on mixed ligand complexes of Pd(II) dithiocarbamates: First structural report on palladium(II) dithioc…

2016

Abstract Three new mixed ligand complexes of palladium(II) dithiocarbamates; [Pd(4-dpmpzdtc)(PPh3)(SCN)] (1), [Pd(4-dpmpzdtc)(PPh3)Cl] (2) and [Pd(bzbudtc)(PPh3)Cl] (3), (where, 4-dpmpzdtc = 4-(diphenylmethyl)piperazinecarbodithioato anion, bzbudtc = N-benzyl-N-butyldithiocarbamato anion and PPh3 = triphenylphosphine) have been synthesized from their respective parent dithiocarbamates by ligand exchange reactions and characterized by IR and NMR (1H, 13C and 31P) spectroscopy. IR and NMR spectral data support the isobidentate coordination of the dithiocarbamate ligands in all complexes (1–3) in solid and in solution, respectively. Single crystal diffraction analysis of complexes 1–3 evidence…

palladium(II)synthesisStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesSingle Crystal DiffractionAnalytical ChemistryIonInorganic Chemistryligand exchange reactionsDithiocarbamateSpectral dataSpectroscopyta116Spectroscopysingle crystal X-ray diffractionchemistry.chemical_classification010405 organic chemistryChemistryLigandOrganic ChemistryMixed ligandNMR0104 chemical sciencesCrystallographyPalladiumJournal of Molecular Structure
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Reproducibility in Electroorganic Synthesis—Myths and Misunderstandings

2021

Abstract The use of electric current as a traceless activator and reagent is experiencing a renaissance. This sustainable synthetic method is evolving into a hot topic in contemporary organic chemistry. Since researchers with various scientific backgrounds are entering this interdisciplinary field, different parameters and methods are reported to describe the experiments. The variation in the reported parameters can lead to problems with the reproducibility of the reported electroorganic syntheses. As an example, parameters such as current density or electrode distance are in some cases more significant than often anticipated. This Minireview provides guidelines on reporting electrosyntheti…

parameterscathodeReproducibilityanodesynthesisElectroorganic Chemistry010405 organic chemistryComputer scienceThe RenaissanceMinireviewsGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceselectrochemistryMinireviewBiochemical engineeringAngewandte Chemie International Edition
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Hexagonal Microparticles from Hierarchical Self-Organization of Chiral Trigonal Pd3L6 Macrotetracycles

2021

Construction of structurally complex architectures using inherently chiral, asymmetric, or multi-heterotopic ligands is a major challenge in metallosupramolecular chemistry. Moreover, the hierarchical self-organization of such complexes is unique. Here, we introduce a water-soluble, facially amphiphilic, amphoteric, chiral, asymmetric, and hetero-tritopic ligand derived from natural bile acid, ursodeoxycholic acid. We show that via the supramolecular transmetalation reaction, using nitrates of Cu(II) or Fe(III), and subsequently Pd(II), a superchiral Pd3L6 complex can be obtained. Even though several possible constitutional isomers of Pd3L6 could be formed, because of the ligand asymmetry a…

particlesurfactantSupramolecular chemistryGeneral Physics and Astronomychemistry.chemical_elementchirality02 engineering and technology010402 general chemistry01 natural sciences114 Physical sciencessupramolecular chemistryTransmetalationPhysico-chimie généraleChimie des colloïdesAmphiphileStructural isomersupramolekulaarinen kemiaChimiebile acidGeneral Materials ScienceLigandChemistryGeneral Engineeringheterotopic ligandChimie des surfaces et des interfacesGeneral Chemistrykompleksiyhdisteetself-assembly021001 nanoscience & nanotechnologypalladiumself-organization0104 chemical sciences3. Good healthmikrorakenteetCrystallographyChimie organiqueGeneral EnergytransmetalationSelf-assembly0210 nano-technologyChirality (chemistry)Palladium
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Effect of Gold(I) on the Room-Temperature Phosphorescence of Ethynylphenanthrene.

2020

The synthesis of two series of gold(I) complexes containing the general formulae PR 3 ‐Au‐C≡C‐phenanthrene (PR 3 = PPh 3 ( 1a / 2a ), PMe 3 ( 1b / 2b ), PNaph 3 ( 1c / 2c )) or (diphos)(Au‐C≡C‐phenanthrene) 2 (diphos = 1,1‐ bis (diphenylphosphino)methane, dppm ( 1d / 2d ); 1,4‐ bis (diphenylphosphino)butane, dppb ( 1e / 2e )) have been synthesized. The two series differ on the position of the alkynyl substituent on the phenanthrene chromophore, being at the 9‐position (9‐ethynylphenanthrene) for the L1 ‐series and at the 2‐position (2‐ethynylphenanthrene) for the L2 ‐series. The compounds have been fully characterized by 1 H and 31 P NMR and IR spectroscopy, mass spectrometry and single cry…

phenanthreneorganic matrixesSubstituentInfrared spectroscopyOr010402 general chemistryMass spectrometry01 natural scienceskultaCatalysischemistry.chemical_compoundheavy atom effectroom temperature phosphorescence (RTP)010405 organic chemistryChemistryPhosphorescenceluminesenssiOrganic ChemistryButanekompleksiyhdisteetGeneral ChemistryChromophoreFluorescence0104 chemical sciencesPhysical chemistryFosforescènciaGoldPhosphorescenceLuminescenceChemistry (Weinheim an der Bergstrasse, Germany)
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Designing P-Chirogenic 1,2-Diphosphinobenzenes at Both P-Centers Using P(III)-Phosphinites

2016

International audience; A new enantiodivergent synthesis of P-chirogenic 1,2-diphosphinobenzenes (DP*B) bearing the chirality on one or both phosphorus centers is reported using aryne chemistry. The principle is based on successive reactions of 1,2-dibromobenzene with sec-phosphide boranes, then DABCO to remove the borane, and finally with chlorophosphines or P(III)-chirogenic phosphinites. The efficiency of this synthesis was demonstrated by the stereoselective preparation of (S,S)-1,2-bis(o-anisylphenylphosphino)benzene. A comparison of DIPAMP and homochiral DP*B ligands in asymmetric Rh- or Pd-catalyzed reactions was reported.

phosphine-ligandsDIPAMPketonesStereochemistryBoranesDABCOBorane010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryArynecatalyzed asymmetric hydrogenationchemistry.chemical_compoundfunctionalized alkenes[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesorganocatalysisPhysical and Theoretical Chemistryhydroformylation010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycarbon-monoxide0104 chemical scienceshighly enantioselective hydrogenationOrganocatalysisderivativesStereoselectivityChirality (chemistry)phospholane ligands
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Surfactant-Mediated Morphology and Photocatalytic Activity of α‑Ag2WO4 Material

2018

In the present work, the morphology (hexagonal rod-like vs cuboid-like) of an α-Ag2WO4 solid-state material is manipulated by a simple controlled-precipitation method, with and without the presence of the anionic surfactant sodium dodecyl sulfate (SDS), respectively, over short reaction times. Characterization techniques, such as X-ray diffraction analysis, Rietveld refinement analysis, Fourier-transform (FT) infrared spectroscopy, FT Raman spectroscopy, UV–vis spectroscopy, transmission electron microscopy (TEM), high-resolution TEM, selected area electron diffraction, energy-dispersive X-ray spectroscopy, field emission-scanning electron microscopy (FE-SEM), and photoluminescence emission…

photocatalytic activityMaterials scienceAnalytical chemistryInfrared spectroscopy02 engineering and technology010402 general chemistry01 natural sciencesdyeslaw.inventionchemistry.chemical_compoundlawmorphologyPhysical and Theoretical ChemistrySodium dodecyl sulfateSpectroscopyinfrared spectroscopyRietveld refinementenamels021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergychemistryTransmission electron microscopyelectron diffractionSelected area diffractionElectron microscopeWulff construction0210 nano-technology
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Unravelling the Photocatalytic Behavior of All-Inorganic Mixed Halide Perovskites: The Role of Surface Chemical States

2019

Within the most mesmerizing materials in the world of optoelectronics, mixed halide perovskites (MHPs) have been distinguished because of the tunability of their optoelectronic properties, balancing both the light-harvesting efficiency and the charge extraction into highly efficient solar devices. This feature has drawn the attention of analogous hot topics as photocatalysis for carrying out more efficiently the degradation of organic compounds. However, the photo-oxidation ability of perovskite depends not only on its excellent light-harvesting properties but also on the surface chemical environment provided during its synthesis. Accordingly, we studied the role of surface chemical states …

photocatalytic activityMaterials scienceIodideHalide02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyiodide vacanciesSurface chemicalGeneral Materials Sciencehot-injectionPerovskite (structure)chemistry.chemical_classificationanion-exchangedegradation pathwaysIon exchangesurface chemical states021001 nanoscience & nanotechnology0104 chemical sciencesNanocrystalChemical engineeringchemistryPhotocatalysisDegradation (geology)0210 nano-technologysuperoxide ions
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Room-Temperature Autoconversion of Free-Base Corrole into Free-Base Porphyrin

2006

International audience

photochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryoxidation010405 organic chemistryFree baseporphyrinoidsGeneral ChemistryGeneral MedicinePhotochemistry010402 general chemistryPorphyrin01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistrycorrole[ CHIM.ORGA ] Chemical Sciences/Organic chemistrynitrogen heterocyclesCorroleComputingMilieux_MISCELLANEOUSAngewandte Chemie
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