Search results for "Resorcinol"

showing 10 items of 32 documents

Alkoxy-, Acyloxy-, and Bromomethylation of Resorcinarenes

2004

Reaction of resorcinarene octols with tris-hydroxymethylmethylamine (TRIS), formaldehyde, and alcohols results in tetraalkoxymethylation of the resorcinol rings. Harsh acylation of aminomethylated resorcinarenes with acid anhydrides leads to the complete acylation of eight hydroxyls and substitution of the amino versus acyloxy groups. Acyloxymethylated resorcinarene 6b can be transformed into a tetrabromomethylated derivative 7 through the reaction with HBr in acetic acid.

TrisOrganic ChemistryFormaldehydeResorcinolResorcinareneBiochemistryMedicinal chemistryAcylationchemistry.chemical_compoundAcetic acidchemistryAlkoxy groupOrganic chemistryPhysical and Theoretical ChemistryDerivative (chemistry)Organic Letters
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Bis-, Tris-, and Tetrakis(squaraines) Linked by Stilbenoid Scaffolds

2001

The oligosquaraines 1−5, with stilbenoid scaffolds, were prepared by multistep syntheses in which the final steps consisted of condensation reactions between the semisquaric acid 21 and multiple resorcinols 12b−15b and 17b. The target compounds exhibit intense (ϵ > 250000 L·mol−1·cm−1) and sharp absorption bands with maxima between 687 to 778 nm, depending on the conjugation in the stilbenoid scaffold. Comparison with the monosquaraine 6 as a model compound reveals intramolecular interactions between different donor−acceptor−donor moieties, which give rise to increased absorption intensities.

Trischemistry.chemical_compoundUltraviolet visible spectroscopychemistryIntramolecular forceOrganic ChemistryPolymer chemistryResorcinolPhysical and Theoretical ChemistryAbsorption (chemistry)StilbenoidCondensation reactionPhotochemistryEuropean Journal of Organic Chemistry
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ChemInform Abstract: Bis-, Tris-, and Tetrakis(squaraines) Linked by Stilbenoid Scaffolds.

2010

The oligosquaraines 1−5, with stilbenoid scaffolds, were prepared by multistep syntheses in which the final steps consisted of condensation reactions between the semisquaric acid 21 and multiple resorcinols 12b−15b and 17b. The target compounds exhibit intense (ϵ > 250000 L·mol−1·cm−1) and sharp absorption bands with maxima between 687 to 778 nm, depending on the conjugation in the stilbenoid scaffold. Comparison with the monosquaraine 6 as a model compound reveals intramolecular interactions between different donor−acceptor−donor moieties, which give rise to increased absorption intensities.

Trischemistry.chemical_compoundchemistryIntramolecular forceGeneral MedicineResorcinolAbsorption (chemistry)StilbenoidCondensation reactionPhotochemistryChemInform
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Fast blue B functionalized silica-polymer composite to evaluate 3,5-dihy-droxyhydrocinnamic acid as biomarker of gluten intake

2021

Celiac disease is an immune-mediated systemic disorder elicited by gluten and related prolamines in genetically susceptible individuals. The current treatment is a strict and lifelong gluten-free diet. However, compliance with the gluten-free diet is not always adequate and many food products contain low concentrations of gluten. The determination of dietary transgressions is a challenge for patients, physicians and dietitians. Alkylresorcinols (AR) have been proposed as sensitive and specific biomarkers of gluten consumption. In this work silica-polymer composites doped with fast blue B reagent (FB) have been used to estimate alkylresorcinols in biological samples. The proposed colorimetri…

alkylresorcinols02 engineering and technology010402 general chemistry01 natural sciencesfast blue BMaterials ChemistryElectrical and Electronic EngineeringInstrumentationFast blueVolume concentrationchemistry.chemical_classificationChromatographyMetals and AlloysbiomarkersGluten intake021001 nanoscience & nanotechnologyCondensed Matter PhysicsGlutencapillary liquid chromatography0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryReagentFood productsPDMS compositesPolymer compositesBiomarker (medicine)0210 nano-technologyceliac disease
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Calix[4]arenes with resorcinol units incorporated in 2,6-position

1990

Abstract Calix[4]arenes containing one or two resorcinol units incorporated via their 2,6-positions were prepared by fragment condensation. Due to the cyclic array of intramolecular hydrogen bonds these molecules assume the cone-conformation.

chemistry.chemical_classificationHydrogen bondChemistryOrganic ChemistryResorcinolCondensation reactionBiochemistryAldehydechemistry.chemical_compoundIntramolecular forceDrug DiscoveryPolymer chemistryCalixareneOrganic chemistryMoleculeCyclophaneTetrahedron Letters
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Die zweifache unterdrückung der polymerisation einiger bis(methacrylsäureester) mittels radikalischer additionsreaktionen

1973

Aus Hydrochinon, Resorcin, Dihydroxydiphenylen und Dihydroxynaphthalinen wurden mit Methacrylsaurechlorid Bis(methacrylsaureester) hergestellt. Setzte man diese in siedendem Benzol mit groser Verdunnung gelosten Ester dem Angriff von Radikalen aus α.α′-Azoisobuttersauredinitril (Primarradikale) aus, dessen Uberschus in Beziehung zum Ester mindestens zwanzigfach molar war, so erhielt man mittels saulenchromatographischer Trennung Verbindungen, bei denen je olefinische Doppelbindung zwei Primarradikale addiert waren (unterdruckte Polymerisation). Die Struktur dieser Produkte wurde mittels Elementaranalyse, Molekulargewichtsbestimmung, IR- und 1H-NMR-Spektren bewiesen. Demnach kann die Polymer…

chemistry.chemical_classificationchemistry.chemical_compoundMolar concentrationColumn chromatographychemistryHydroquinoneMethacrylic acidDouble bondPolymerizationRadicalPolymer chemistryResorcinolDie Makromolekulare Chemie
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A resorcinol derived calix[5]arene with C5-symmetry

1994

Abstract Condensation of 2,4-dihydroxy-3-hydroxymethyl benzophenone (4) in dioxane/H2SO4 gave the cyclic pentamer 5, a calix[5]arene with regular incorporation of the resorcinol units via their 2- and 6-positions. The structure follows from the 1H NMR and mass spectra and was further confirmed by single crystal X-ray analysis. Dynamic NMR in C2D2Cl4 gave a surprisingly high barrier of ΔG‡ = 17.3 kcal/mol for the cone-to-cone ring inversion.

chemistry.chemical_compoundCrystallographychemistryRing flipStereochemistryPentamerCondensationBenzophenoneProton NMRMass spectrumGeneral ChemistryResorcinolSingle crystalSupramolecular Chemistry
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Resorcinol. Its Uses and Derivatives (Topics in Applied Chemistry). VonH. Dressler. Plenum Press, New York, 1994. 500 S., geb., 115.00 $ - ISBN 0-306…

1995

chemistry.chemical_compoundPolymer scienceChemistryGeneral MedicineResorcinolPlenum spaceAngewandte Chemie
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ChemInform Abstract: Calix(4)arenes with Resorcinol Units Incorporated in 2,6-Position.

2010

chemistry.chemical_compoundPosition (vector)ChemistryPolymer chemistryGeneral MedicineResorcinolChemInform
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Partial aminomethylation of resorcarenes.

2002

Aminomethylation of resorcarenes at the wider rim with bulky diisopropylamine and formaline leads to trisubstituted derivatives. Analogous reaction with C(2v)-symmetrical resorcarene tetratosylate gives the monoaminomethylated compound. Further reactions of remaining unsubstituted resorcinol rings result in new resorcarene derivatives. [reaction: see text]

chemistry.chemical_compoundchemistryOrganic ChemistryOrganic chemistryDiisopropylamineResorcinolPhysical and Theoretical ChemistryResorcinareneBiochemistryOrganic letters
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