Search results for "oxetane"

showing 10 items of 17 documents

Frontispiece: Recent Advances in Enantioselective Desymmetrizations of Prochiral Oxetanes

2021

chemistry.chemical_compoundChemistryOrganic ChemistryEnantioselective synthesisOrganic chemistryGeneral ChemistryOxetaneDesymmetrizationCatalysisChemistry – A European Journal
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Kristallisations- und schmelzverhalten von copolymeren aus 3,3-bis(chlormethyl)oxetan und ß-propiolacton

1974

Einkristalle von Copolymeren aus 3,3-Bis(chlormethyl)oxetan und s-Propiolacton wurden bezuglich Schmelzverhalten, Schmelzenthalpie, Dichte und Langperiode untersucht. Aus der Messung der Schmelzenthalpie und der Dichte berechnen sich Kristallisationsgrade von 50—60% in guter Ubereinstimmung mit einem Modell, welches den Ausschlus der aus s-Propiolacton (PL) entstandenen Grundbausteine von dem aus Sequenzen der 3,3-Bis(chlormethyl)oxetan (BCMO-)Einheiten aufgebauten Gitter verlangt. Im Vergleich zu reinem Poly-BCMO wird die Dicke der Copolymereinkristalle nur wenig durch Anderung der Kristallisationstemperatur beEinflust. Wegen des blockartigen Aufbaus der Copolymeren bestimmt die mittlere S…

Crystalchemistry.chemical_compoundlawChemistryEnthalpy of fusionPolymer chemistryCopolymerMelting pointCrystallizationEntropy of mixingSequence structureOxetanelaw.inventionDie Makromolekulare Chemie
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Recent Advances in Enantioselective Desymmetrizations of Prochiral Oxetanes

2021

Abstract Strain relief of oxetanes offers a plethora of opportunities for the synthesis of chiral alcohols and ethers. In this context, enantioselective desymmetrization has been identified as a powerful tool to construct molecular complexity and this has led to the development of elegant strategies on the basis of transition metal, Lewis acid, and Brønsted acid catalysis. This review highlights recent examples that harness the inherent reactivity of prochiral oxetanes and offers an outlook on the immense possibilities for synthetic application.

Molecular complexity010405 organic chemistryChemistryOrganic Chemistryoxetaneoxygen heterocyclesEnantioselective synthesisMinireviewsContext (language use)General ChemistryStrain relief010402 general chemistry01 natural sciencesCombinatorial chemistryDesymmetrizationCatalysis0104 chemical sciencesdesymmetrizationstrained moleculesMinireviewLewis acids and basesAsymmetric SynthesisChemistry – A European Journal
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Theoretical study of the dark photochemistry of 1,3-butadiene via the chemiexcitation of Dewar dioxetane.

2015

Excited-state chemistry is usually ascribed to photo-induced processes, such as fluorescence, phosphorescence, and photochemistry, or to bio-and chemiluminescence, in which light emission originates from a chemical reaction. A third class of excited-state chemistry is, however, possible. It corresponds to the photochemical phenomena produced by chemienergizing certain chemical groups without light - chemiexcitation. By studying Dewar dioxetane, which can be viewed as the combination of 1,2-dioxetane and 1,3-butadiene, we show here how the photo-isomerization channel of 1,3-butadiene can be reached at a later stage after the thermal decomposition of the dioxetane moiety. Multi-reference mult…

General Physics and AstronomyPhotochemistryChemical reactionQuantum chemistryDioxetaneReaction coordinatechemistry.chemical_compoundchemistryExcited stateTeoretisk kemiMoietyLight emissionPhysical and Theoretical ChemistryPhosphorescenceTheoretical ChemistryPhysical chemistry chemical physics : PCCP
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Intramolecular Interactions in the Triplet Excited States of Benzophenone–Thymine Dyads

2005

Time-resolved and product studies on the synthesized dyads 1 and 2 have provided evidence that the benzophenone-to-thymine orientation strongly influences intramolecular photophysical and photochemical processes. The prevailing reaction mechanism has been established as a Paterno-Büchi cycloaddition to give oxetanes 3-6; however, the ability of benzophenone to achieve a formal hydrogen abstraction from the methyl group of thymidine has also been evidenced by the formation of photoproducts 7 and 8. These processes have been observed only in the case of the cisoid dyad 1. Adiabatic photochemical cycloreversion of the oxetane ring is achieved upon direct photolysis to give the starting dyad 1 …

PhotochemistryOrganic ChemistryGeneral ChemistryOxetaneHydrogen atom abstractionPhotochemistryCatalysisCycloadditionBenzophenoneschemistry.chemical_compoundchemistryEthers CyclicExcited stateIntramolecular forceBenzophenoneTriplet stateThymineThymidineMethyl groupChemistry - A European Journal
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Theoretical Study on the Photo-Oxidation and Photoreduction of an Azetidine Derivative as a Model of DNA Repair

2021

Photocycloreversion plays a central role in the study of the repair of DNA lesions, reverting them into the original pyrimidine nucleobases. Particularly, among the proposed mechanisms for the repair of DNA (6-4) photoproducts by photolyases, it has been suggested that it takes place through an intermediate characterized by a four-membered heterocyclic oxetane or azetidine ring, whose opening requires the reduction of the fused nucleobases. The specific role of this electron transfer step and its impact on the ring opening energetics remain to be understood. These processes are studied herein by means of quantum-chemical calculations on the two azetidine stereoisomers obtained from photocyc…

AnionsAcetonitrilesPyrimidineLightPhotochemistryAzetidinePharmaceutical ScienceOrganic chemistryDNA repair010402 general chemistryRing (chemistry)PhotochemistryOxetane01 natural sciencesArticleAnalytical ChemistryNucleobaseElectron transferchemistry.chemical_compoundElectron transferQUIMICA ORGANICAQD241-441AzetidineCationsredox propertiesDrug DiscoveryPhotosensitizerPhysical and Theoretical ChemistryPhotolyasering openingdensity functional theoryphotochemistry010405 organic chemistryRing openingModels Theoreticalelectron transfer0104 chemical scienceschemistryChemistry (miscellaneous)Density functional theoryMolecular MedicineAzetidinesThermodynamicsGasesazetidineOxidation-ReductionRedox propertiesMolecules
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Hydroxyfunctional oxetane-inimers with varied polarity for the synthesis of hyperbranched polyether polyols via cationic ROP

2014

Polymers and PlasticsChemistryOrganic ChemistryCationic polymerizationChain transferOxetaneRing-opening polymerizationchemistry.chemical_compoundChain-growth polymerizationPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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Cationic Copolymerization of 3,3-Bis(hydroxymethyl)oxetane and Glycidol: Biocompatible Hyperbranched Polyether Polyols with High Content of Primary H…

2015

The cationic ring-opening copolymerization of 3,3-bis(hydroxymethyl)oxetane (BHMO) with glycidol using different comonomer ratios (BHMO content from 25 to 90%) and BF3OEt2 as an initiator has been studied. Apparent molecular weights of the resulting hyperbranched polyether copolymers ranged from 1400 to 3300 g mol(-1) (PDI: 1.21-1.48; method: SEC, linear PEG standards). Incorporation of both comonomers is evidenced by MALDI-TOF mass spectroscopy. All hyperbranched polyether polyols with high content of primary hydroxyl groups portray good solubility in water, which correlates with an increasing content of glycerol units. Detailed NMR characterization was employed to elucidate the copolymer …

Polymers and PlasticsPropanolsProton Magnetic Resonance SpectroscopyComonomerGlycidolCationic polymerizationBiocompatible MaterialsBioengineeringOxetanePolymerizationBiomaterialschemistry.chemical_compoundchemistryPolymerizationEthers CyclicCationsSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationPolymer chemistryMaterials ChemistryCopolymerEpoxy CompoundsOrganic chemistryHydroxymethylCarbon-13 Magnetic Resonance SpectroscopySolubilityBiomacromolecules
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Aliphatic Polyethers: Classical Polymers for the 21st Century.

2015

Polyethers-polymers with the structural element (R'-O-R)n in their backbone--are an old class of polymers which were already used at the time of the ancient Egyptians. However, still today these materials are highly important with applications in all areas of our life, reaching from the automotive and paper industry to cosmetics and biomedical applications. In this Review, different aliphatic polyethers like poly(epoxide)s, poly(oxetane)s, and poly(tetrahydrofuran) are discussed. Special emphasis is placed on the history, the polymerization techniques (industrially and in academia), the properties, the applications as well as recent developments of these materials.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymer sciencePolymersOrganic ChemistryPolymerOxetanechemistry.chemical_compoundchemistryPolymerizationPropylene GlycolsMaterials ChemistryOrganic chemistryButylene GlycolsTetrahydrofuranMacromolecular rapid communications
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Chemische charakterisierung des kettenaufbaus und kristallisationsverhaltens von copolymeren aus 3,3-bis(chlormethyl)oxetan und β-propiolacton

1974

Aus 3,3-Bis(chlormethyl)oxetan (1) und β-Propiolacton (2) wurden durch kationische Polymerisation Copolymere hergestellt, in denen Propiolactoneinheiten bis zu einem Molenbruch von 0,16 eingebaut sind. Das Copolymerisationsverhalten wurde untersucht, und die Copolymerisationsparameter wurden bestimmt. Die Copolymeren wurden kristallisiert und die Einkristalle hinsichtlich ihrer Zusammensetzung und Morphologie charakterisiert. Durch selektive Umesterung in den amorphen Bereichen der suspendierten Einkristalle wurde die Verteilung der aus β-Propiolacton gebildeten Einheiten (PL) uber den Kristall untersucht, und die Ergebnisse mit Abbauversuchen an den gelosten Copolymeren wurden verglichen. …

chemistry.chemical_compoundPolymerizationChemistryHomogeneousPolymer chemistryCationic polymerizationCopolymerLamellar structureOxetaneAmorphous phaseDie Makromolekulare Chemie
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