Search results for "BIF"

showing 10 items of 539 documents

Bifunctional coordination polymers as efficient catalysts for carbon dioxide conversion

2019

chemistry.chemical_classification010405 organic chemistryGeneral ChemistryPolymerActivation energy010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisInorganic ChemistryChemical kineticschemistry.chemical_compoundChemical engineeringchemistryCarbon dioxideBifunctionalApplied Organometallic Chemistry
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Extraction of dansylated amino acids using the supported liquid membrane technique

1997

Extraction using the supported liquid membrane (SLM) technique demands conditions where the extracted compounds can be made uncharged allowing them to pass through the membrane. For amino acids, being bifunctional, such conditions can not be obtained directly. One way to overcome this problem is to block one of the functionalities by derivatization, utilising the other group for the transport. The SLM extraction of dansylated amino acids was investigated and optimized. It was possible to obtain high extraction efficiencies (>90%) for most amino acids. For amino acids with polar side chains, such high extraction efficiencies were only obtained at low analyte concentrations ( 10 nmol 1-l). Fo…

chemistry.chemical_classificationAnalyteamino acidsChromatographyLysineExtraction (chemistry)BiochemistrydansylationAnalytical ChemistryAmino acidchemistry.chemical_compoundMembranechemistrysupported liquid membrane extractionSide chainEnvironmental ChemistryBifunctionalDerivatizationSpectroscopyAnalytica Chimica Acta
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Reductive transformations - 11. stereoselective cycloannelation and bridging of the cyclooctatetraene dianionMakromol. Chem., Rapid. Commun. 1988, 9,…

1988

Abstract Bifunctional electrophiles with C4-, C6-, and C8-chains are reacted with the cyclooctatetraene dianion to selectively give novel cycloannelation and bridging products which possess a surprising stereochemistry and are useful starting compounds for further syntheses.

chemistry.chemical_classificationAnnulationStereochemistryOrganic ChemistryHalocarbonBiochemistrychemistry.chemical_compoundCyclooctatetraenePolycyclic compoundchemistryDrug DiscoveryElectrophileStereoselectivityBifunctionalAliphatic compoundTetrahedron Letters
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3'-Arylazido-beta-alanyl-2-azido ATP, a cross-linking photoaffinity label for F1ATPases.

1989

Abstract The synthesis of the 3′-arylazido-2-azido ATP derivative 3′-O-{3-[N-(4-azido-2-nitrophenyl)-amino]propionyl}2-azido-adenosine 5′-triphosphate (2,3′-DiN3ATP) is described. The bifunc­ tional photoreactive ATP analog is characterized spectroscopically. Photoaffinity labeling of F, ATPase from Micrococcus luteus by this analog results in the inactivation of the enzyme and in the formation of higher molecular weight cross-links,

chemistry.chemical_classificationAzidesPhotoaffinity labelingbiologyLightStereochemistryAffinity Labelsbiology.organism_classificationGeneral Biochemistry Genetics and Molecular BiologyMicrococcuschemistry.chemical_compoundKineticsProton-Translocating ATPasesEnzymeAdenosine TriphosphatechemistryIndicators and ReagentsBifunctionalBeta (finance)Micrococcus luteusDerivative (chemistry)Zeitschrift fur Naturforschung. C, Journal of biosciences
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Effect of chelatants on gellan gel rheological properties and setting temperature for immobilization of living bifidobacteria.

1993

The effect of various concentrations of sequestrants (sodium citrate, sodium metaphosphate, and EDTA) was studied on gellan gel (1.5-2.5% (w/v)) setting temperature and rheological properties. Addition of EDTA between 0 and 0.8% (w/v) led to a progressive decrease of setting temperature. Citrate and metaphosphate decreased this parameter when added up to 0.4 or 0.6%, depending on gellan gum concentration, eventually resulting in the absence of gel formation at room temperature for the 1.5% gellan solution containing 0.4% citrate. This effect was accompanied by a significant decrease of gel strength and stiffness and might be attributed to the binding of the divalent cations required for cha…

chemistry.chemical_classificationBifidobacterium longumChromatographybiologyMetaphosphatePolysaccharides BacterialTemperatureConcentration effectHydrogen-Ion ConcentrationPolysaccharidebiology.organism_classificationGellan gumLactic acidCulture Mediachemistry.chemical_compoundchemistryCell MovementSodium citrateFermentationBifidobacteriumRheologyGelsBiotechnologyChelating AgentsBiotechnology progress
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Catalytic Diastereo- and Enantioselective Synthesis of 2-Imidazolinones.

2019

Chiral cyclic ureas (2-imidazolinones) were prepared by the reaction of nitrones and isocyanoacetate esters using a multicatalytic system that combines a bifunctional Brønsted base-squaramide organocatalyst and Ag+ as a Lewis acid. The reaction could be achieved with a range of nitrones derived from aryl- and cycloalkylaldehydes with moderate diastereo- and good enantioselectivity. A plausible mechanism involving an initial formal [3 + 3] cycloaddition of the nitrone and isocyanoacetate ester, followed by rearrangement to an aminoisocyanate and cyclization to the imidazolinone, is proposed.

chemistry.chemical_classificationChemistryArylOrganic ChemistryEnantioselective synthesisBiochemistryCombinatorial chemistryCycloadditionCatalysisNitronechemistry.chemical_compoundCatàlisiLewis acids and basesPhysical and Theoretical ChemistryBifunctionalQuímica orgànicaOrganic letters
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Relationship between conformation and physicochemical properties of polypeptides. I. Synthesis of homo- and co-oligopeptides by the liquid-phase meth…

1980

The synthesis of the following oligo- and co-oligopeptides by the liquid-phase method is described: (L-Met)15 (I), [L-Glu(OBzl)]20 (II), (L-Val)8-Gly (IV), (L-Ile)8-Gly (V), (L-Ile)4-Gly-(L-Ile)4 (VI), (L-Ile)4-Pro-(L-Ile)4 (VII), (L-Met)5-L-Pro-(L-Met)5 (VIII), [L-Glu(OBzl)]7-L-Pro-[L-Glu(OBzl)]7 (IX). The oligomers are covalently bound to bifunctional polyethylene glycol (PEG) and monofunctional PEG-M of Mr 5 × 103−2 × 104. Analytical controls were carried out after each step of synthesis in order to ensure quantitative coupling yields. All products could be obtained in high purity as indicated by amino acid analysis, thin-layer chromatography and chiroptical methods. The solubility of th…

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryBiophysicsPeptideGeneral MedicinePolyethylene glycolBiochemistryBiomaterialschemistry.chemical_compoundCovalent bondPEG ratioPeptide synthesisReactivity (chemistry)SolubilityBifunctionalBiopolymers
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2,2′:6′,2″-Terpyridine Trimethylplatinum(IV) Iodide Complexes as Bifunctional Halogen Bond Acceptors

2016

Three new organometallic trimethylplatinum(IV) iodide complexes of 2,2′:6′,2″-terpyridines have been synthesized and characterized by 1H NMR spectroscopy, mass spectrometry, elemental analysis, and single crystal X-ray diffraction analysis. The X-ray crystal structures of PtMe3I(L) complexes 1–3 {L for 1 = 4′-chloro-2,2′:6′,2″-terpyridine, 2 = 4′-(4-cyanophenyl)-2,2′:6′,2″-terpyridine, and 3 = 4′-(4-tolyl)-2,2′:6′,2″-terpyridine} reveal distorted octahedral coordination geometry of the platinum(IV) metal centers with bidentate coordination of the terpyridine ligands. Complexation of 1–3 with iodopentafluorobenzene (IPFB) afforded single-crystal structures of halogen bond (XB) complexes 1a–3…

chemistry.chemical_classificationDenticityHalogen bond010405 organic chemistryhalogen bondsIodideGeneral ChemistryCrystal structurehalogen bond acceptors010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencestransition metal complexes0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryPyridineGeneral Materials ScienceTerpyridineBifunctionalta116Coordination geometryCrystal Growth & Design
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Supramolecular Assembly of Metal Complexes by (Aryl)I⋅⋅⋅d[PtII] Halogen Bonds

2020

The theoretical data for the half-lantern complexes [{Pt( CN^ )(μ- SN^ )}2 ] [1-3; CN^ is cyclometalated 2-Ph-benzothiazole; SN^ is 2-SH-pyridine (1), 2-SH-benzoxazole (2), 2-SH-tetrafluorobenzothiazole (3)] indicate that the Pt⋅⋅⋅Pt orbital interaction increases the nucleophilicity of the outer d z2 orbitals to provide assembly with electrophilic species. Complexes 1-3 were co-crystallized with bifunctional halogen bonding (XB) donors to give adducts (1-3)2 ⋅(1,4-diiodotetrafluorobenzene) and infinite polymeric [1⋅1,1'-diiodoperfluorodiphenyl]n . X-ray crystallography revealed that the supramolecular assembly is achieved through (Aryl)I⋅⋅⋅d z2 [PtII ] XBs between iodine σ-holes and lone pa…

chemistry.chemical_classificationHalogen bond010405 organic chemistryArylOrganic ChemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSupramolecular assemblychemistry.chemical_compoundCrystallographychemistryElectrophileNon-covalent interactionsBifunctionalLone pairChemistry – A European Journal
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First Evidence of Proline Acting as a Bifunctional Catalyst in the Baylis–Hillman Reaction Between Alkyl Vinyl Ketones and Aryl Aldehydes

2008

Proline in the presence of sodium hydrogen carbonate has been found to be an effective catalyst for the Baylis–Hillman reaction between methyl or ethyl vinyl ketone and aryl aldehydes. Screening of several amine catalysts showed that an ionizable carboxylic function directly linked to the secondary amine catalyst plays an important role in the synthesis of the desired product in good yield. The data obtained has allowed us to suggest, for the first time, that proline, sarcosine, pipecolinic acid and homoproline may act as bifunctional catalysts via a bicyclic enaminolactone species as intermediate. Quantum-mechanical calculations (PM3/COSMO and ab initio 3-21G/COSMO) support this mechanism …

chemistry.chemical_classificationKetoneProlineAldehydeArylOrganic ChemistrySemi-empiricalcalculationSettore CHIM/06 - Chimica OrganicaBifunctional catalystCatalysisOrganocatalysichemistry.chemical_compoundchemistryOrganocatalysisOrganic chemistryAmine gas treatingBaylis–Hillman reactionPhysical and Theoretical ChemistryBaylis–Hillman reactionBifunctionalReaction mechanismEuropean Journal of Organic Chemistry
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