Search results for "Cyanate"

showing 10 items of 210 documents

Synthesis of plagiochiline N from santonin.

2001

This article reports the transformation of O-acetylisophotosantonin, obtained by photochemical rearrangement of santonin, into plagiochiline N, an ent-2,3-secoaromadendrane isolated from Plagiochila ovalifolia. The synthesis was carried out in a sequence involving as the key steps (a) the substitution of the lactone moiety by a gem-dimethylcyclopropane ring through a synthetic intermediate having a C(6)-C(7) double bond and (b) the ozonolysis of the C(2)-C(3) bond followed by cyclization to the dihydropyran ring characteristic of plagiochiline N. Spectroscopic data of the synthetic product fully coincided with the reported data for the natural product.

chemistry.chemical_classificationNatural productOzonolysisPlants MedicinalDouble bondDihydropyranStereochemistryAntinematodal AgentsOrganic ChemistryAlkenesRing (chemistry)chemistry.chemical_compoundchemistryMoietySantoninLactoneThiocyanatesSantoninThe Journal of organic chemistry
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Synthesis and Physicochemical Characterization ofmeso-Functionalized Corroles: Precursors of Organic-Inorganic Hybrid Materials

2005

Cobalt(III) corroles exhibit an infinite selectivity for the coordination of carbon monoxide towards dioxygen and dinitrogen. This peculiar property thus allows their use as sensing devices for CO detection. Here are described the syntheses and physico-chemical characterization of meso mono-, bis- and tris(triethoxysilyl)-functionalized corroles, precursors of organic–inorganic materials. The corrole ring formation was achieved in every case using the “2+1” method involving the reaction of two equivalents of an encumbered dipyrromethane with one equivalent of an aromatic aldehyde in the presence of a catalytic amount of trifluoroacetic acid. The functionalization of the corrole by triethoxy…

chemistry.chemical_classificationOrganic ChemistryCondensation reactionIsocyanateAldehydeCatalysischemistry.chemical_compoundchemistryTrifluoroacetic acidOrganic chemistryPhysical and Theoretical ChemistryCorroleHybrid materialSelectivityEuropean Journal of Organic Chemistry
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Study by FT-IR spectroscopy of ageing of adhesives used in restoration of archaeological glass objects

1999

Abstract A study by FT-IR spectroscopy which aims to compare the stability of five polymers, Araldit XW396/XW 397, Vitralit 7256, Loctite 350, Desmodur N 75/Viacryl SM 564/65 and Krafft silicone commonly used in the restoration of archaeological glass objects when subjected to thermal ageing, UV light ageing and cyclic ageing in SO 2 pollutant chamber has been carried out. Two series of test specimens were prepared in order to reproduce the two methods of application of polymers commonly used in restoration treatments as adhesive and consolidant or coating of glass fragments. Modifications in the chain or side chain structure of polymers, alterations of carbonyl groups in Araldit and isocya…

chemistry.chemical_classificationOrganic ChemistryPolymerengineering.materialArchaeologyIsocyanateAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundSiliconechemistryCoatingAgeingSide chainengineeringAdhesiveSpectroscopySpectroscopyJournal of Molecular Structure
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Lineare polyester mit carboxylendgruppen und deren bestimmung

1955

Durch Umsetzung von „alkoholischen” Bernsteinsaure-1,6-Hexandiol-Polyestern mit Bernsteinsaureanhydrid in Benzol werden kettenanaloge Polyester mit endstandigen Carboxylgruppen hergestellt. Die Titration dieser Carboxylgruppen ergibt Molgewichte bis ∼ 7 · 103. Mit Phenylisocyanat in indifferenten Losungsmitteln reagieren Polyesterdicarbonsauren unter Kettenverlangerung und Bildung von kettenstandigen Carbonsaureanhydridgruppen. Die Umsetzung der Polyester-dicarbonsauren in Phenylisocyanat ohne Verdunnungsmittel erfolgt kettenanalog unter Bildung von Carboxanilidendgruppen. Durch photometrische Anilinbestimmung nach der Hydrolyse konnen diese Endgruppen quantitativ bestimmt und Molgewichte b…

chemistry.chemical_classificationPolyesterchemistry.chemical_compoundHydrolysisAnilinechemistryCarboxylic acidPolymer chemistrySuccinic anhydrideTitrationBenzenePhenylisocyanateDie Makromolekulare Chemie
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Multilayer build-up of a reactive polymer with α,ω-functionalized chromophores

1997

Alternating multilayers with up to ten layers have been prepared by sequential reaction of a reactive polymer (poly[(1-methylvinyl isocyanate)-alt-(maleic anhydride)]) with α,ω-functionalized chromophores. For this purpose new chromophores were synthesized varying the length of the hydrophobic spacer. The analysis of the multilayer build-up shows that physisorption is more important than chemisorption for fixation of new polymer layers. Thus, a multilayer build-up is only possible with the shorter, more hydrophilic chromophore and not with the long hydrophobic spacer.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryChemical modificationMaleic anhydridePolymerChromophoreCondensed Matter PhysicsIsocyanatechemistry.chemical_compoundchemistryPhysisorptionChemisorptionMonolayerPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Ferrochirality: A simple theoretical model of interacting dynamically invertible helical polymers, 1. The basic effects

1994

The effect of interaction between reversible helical polymers of the poly(hexyl isocyanate) type is investigated by using a molecular field model. It is shown that for interacting helices a critical temperature exists below which they must adopt a common helix-sense spontaneously, even in the absence of any external or intrinsic chiral force

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsField (physics)ChemistryOrganic ChemistryPolymerType (model theory)Isocyanatelaw.inventionchemistry.chemical_compoundInvertible matrixlawChemical physicsSimple (abstract algebra)Materials ChemistryPhysical chemistryChemical solutionChirality (chemistry)Macromolecular Rapid Communications
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A novel ?-N-cyanate-bridged nickel dinier exhibiting ferromagnetic coupling: Di-?-cyanate-bis(aqua-2,2?:6?,2?-terpyridine)dinickel(II) hexafluorophos…

1986

chemistry.chemical_classificationStereochemistryMetals and Alloyschemistry.chemical_elementCrystal structureCyanateInorganic Chemistrychemistry.chemical_compoundNickelchemistryHexafluorophosphatePolymer chemistryMaterials ChemistryMoleculeTerpyridineInorganic compoundOrganometallic chemistryTransition Metal Chemistry
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ChemInform Abstract: Glycoside Synthesis via Electrophile-Induced Activation of N-Allyl Carbamates.

2010

Abstract O-Benzyl-, O-acyl-, N-acyl- and isopropylidene-protected glycosyl N-allylcarbamates, obtained from anomerically unprotected monosaccharides and allyl isocyanate, are activated by an electrophile-induced cyclisation and react with hydroxyl compounds to form the corresponding glycosides.

chemistry.chemical_classificationStereochemistryorganic chemicalsGlycosideGeneral MedicineGlycoside synthesischemistry.chemical_compoundchemistryElectrophileMonosaccharideOrganic chemistrylipids (amino acids peptides and proteins)GlycosylAllyl isocyanateChemInform
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Thermal degradation of highly crosslinked rigid PU-PIR foams based on high functionality tall oil polyol

2019

Abstract This study presents the development and analysis of rigid polyurethane-polyisocyanurate (PU-PIR) foam synthesized from high functionality tall oil (TO) based polyols. Three PU-PIR formulations with varied high functionality TO based polyol content (45, 75 and 95 pbw) and a different tier of isocyanate (NCO) indexes (110, 150, 200, 300 and 400) for each formulation were compared to a formulation developed using conventional raw materials, mainly obtained from petrochemicals. Using the Fourier transform infrared spectral analysis (FTIR), the chemical structure of the foams was evaluated with emphasis on the characteristic PU-PIR signal ratio and isocyanurate signal peaks. The thermal…

chemistry.chemical_classificationThermogravimetric analysisMaterials scienceChemical substancePolymers and PlasticsTall oil02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesIsocyanate0104 chemical scienceschemistry.chemical_compoundPetrochemicalchemistryPolyolChemical engineeringMechanics of MaterialsMaterials ChemistryFourier transform infrared spectroscopy0210 nano-technologyPolymer Degradation and Stability
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Synthesis, structure, physicochemical characterization and theoretical evaluation of non-covalent interaction energy of a polymeric copper(II)-hydraz…

2019

Abstract One dimensional polymeric copper-hydrazone complex {[Cu(H0.5L)(µ1,3-SCN)]0.5ClO4·0.5MeOH}n (1) has been synthesized with Cu(ClO4)2·xH2O and N'-(1-(pyridin-2-yl)ethylidene)acetohydrazide (HL) in presence of NaSCN. The ligand and the complex have been characterized by several spectroscopic techniques (IR, UV–Vis and EPR), cyclic voltammetry and the structure of 1 has been determined by single crystal X-ray diffraction. The complex is an infinite one dimensional polymer bridged by thiocyanate. The magneto-structural correlation has been determined and the non-covalent interactions present in the molecule have been energetically evaluated by means of DFT calculations.

chemistry.chemical_classificationThiocyanateChemistryLigandHydrazoneInteraction energylaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographylawMaterials ChemistryMoleculePhysical and Theoretical ChemistryCyclic voltammetryElectron paramagnetic resonanceSingle crystalInorganica Chimica Acta
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