Search results for "double bond"

showing 10 items of 184 documents

Dipeptides of S-Substituted Dehydrocysteine as Artzyme Building Blocks: Synthesis, Complexing Abilities and Antiproliferative Properties †

2021

Background: Dehydropeptides are analogs of peptides containing at least one conjugate double bond between α,β-carbon atoms. Its presence provides unique structural properties and reaction centre for chemical modification. In this study, the series of new class of dipeptides containing S-substituted dehydrocysteine with variety of heterocyclic moieties was prepared. The compounds were designed as the building blocks for the construction of artificial metalloenzymes (artzymes). Therefore, the complexing properties of representative compounds were also evaluated. Furthermore, the acknowledged biological activity of natural dehydropeptides was the reason to extend the study for antiproliferativ…

antiproliferative activityBALB 3T3 CellsDouble bondPotentiometric titrationSulforhodamine BTriazoleAntineoplastic Agents010402 general chemistry01 natural sciencesCatalysisArticlelcsh:ChemistryInorganic ChemistryMiceStructure-Activity Relationshipchemistry.chemical_compoundElimination reactionCell Line TumorAnimalsHumansChelationCysteinePhysical and Theoretical Chemistrydehydrocysteinelcsh:QH301-705.5Molecular BiologySpectroscopyCell Proliferationchemistry.chemical_classification010405 organic chemistryOrganic ChemistryChemical modificationDipeptidesGeneral MedicineHydrogen-Ion ConcentrationCombinatorial chemistryEnzymes0104 chemical sciencesComputer Science Applicationsdehydropeptideslcsh:Biology (General)lcsh:QD1-999chemistrycomplexing agentaddition-elimination reactionDrug Screening Assays AntitumorCopperConjugateInternational Journal of Molecular Sciences
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Mechanism of excited state deactivation of indan-1-ylidene and fluoren-9-ylidene malononitriles.

2016

Herein, we report complementary computational and experimental evidence supporting the existence, for indan-1-ylidene malononitrile and fluoren-9-ylidene malononitrile, of a non-radiative decay channel involving double bond isomerisation motion. The results of UV-Vis transient absorption spectroscopy highlight that the decay takes place within hundreds of picoseconds. In order to understand the related molecular mechanism, photochemical reaction paths were computed by employing multiconfigurational quantum chemistry. The results indicate that the excited state deactivation occurs via concerted double bond twisting of the dicyanovinyl (DCV) unit coupled with a pyramidalisation of its substit…

chemistry.chemical_classification010304 chemical physicsDouble bondGeneral Physics and AstronomyConical intersection010402 general chemistryPhotochemistry01 natural sciencesQuantum chemistry0104 chemical scienceschemistry.chemical_compoundchemistryExcited state0103 physical sciencesUltrafast laser spectroscopyPhysical and Theoretical ChemistrySpectroscopyIsomerizationMalononitrilePhysical chemistry chemical physics : PCCP
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Towards highly luminescent phenylene vinylene films

1996

Abstract Fluorescence and electronic absorption spectra, fluorescence decay curves and fluorescence quantum yields of a series of oligo (p-phenylene vinylenes) are investigated in solution, nanoaggregates and vapour-deposited or cast ultrathin films. The film constituting molecules are varied in chain length and modified by electron donating and withdrawing substituents and bulky alkyl spacers. PPP-MO calculations serve to rationalize the resulting spectral changes. In dilute solutions, fluorescence yields of the short oligomers with alkyl or oxyalkyl substituents approach the region of unity. The yields decrease with chain length, reaching a long-chain limit of ΦF=0.4–0.7. Introduction of …

chemistry.chemical_classificationAbsorption spectroscopyDouble bondMechanical EngineeringMetals and AlloysQuantum yieldCondensed Matter PhysicsInternal conversion (chemistry)PhotochemistryElectronic Optical and Magnetic MaterialschemistryMechanics of MaterialsPhenyleneMaterials ChemistryPolar effectMoleculeAlkylSynthetic Metals
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Novel acrylamido monomers with higher hydrophilicity and improved hydrolytic stability: I. Synthetic route and product characterization.

1996

The novel acrylamido monomer reported by our group (N-acryloylaminoethoxyethanol, AAEE; Chiari et al., Electrophoresis 1994, 15, 177-186), found to combine high hydrophilicity with extraordinary resistance to alkaline hydrolysis, has come under closer scrutiny due to unexpected and random autopolymerization while stored as a 1/1 v/v water solution at 4 degrees C (possibly due to a greater oxidability of the ether group). We have additionally found a unique degradation pathway of the monomer, called "1-6 H-transfer", by which the C1 (on the double bond site), by constantly ramming against the C6, next to the ether oxygen (O7, which in fact favors the transfer of the hydrogen atom by C1), pro…

chemistry.chemical_classificationAcrylamidesMagnetic Resonance SpectroscopyDouble bondEsterificationEthanolMolecular StructureReaction stepChemistryMethanolClinical BiochemistryEtherAcryloyl chlorideBiochemistryAnalytical ChemistrySolventAcetoneDioxanesPropanolamineschemistry.chemical_compoundMonomerEthylaminesOrganic chemistryMethanolTriethylamineElectrophoresis
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A novel phosphorus–carbon bond formation by ring opening with diethyl phosphite of oxazolines derived from serine

2004

Abstract A new reaction of oxazolines derived from serine with diethyl phosphite leading to ring opening products with P–C bond formation is reported. This reaction, which proceeds under neutral conditions and without the use of any halogenated intermediate, results in a mixture of racemic α- and β-phosphono alanines in an approximate 1:2 ratio, with isolated yields up to 77%. The mechanism involves the rearrangement of the oxazoline into the corresponding α-benzamido acrylate, followed by addition of the diethyl phosphite to the double bond. Since no significant transesterification is observed, this method constitutes a simple route for α- and β-phosphono amino acids bearing suitable prote…

chemistry.chemical_classificationAcrylateDouble bondOrganic Chemistrychemistry.chemical_elementOxazolineTransesterificationRing (chemistry)BiochemistryMedicinal chemistryAmino acidSerinechemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryCarbonTetrahedron
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Synthesis of hyperbranched poly(tert-butyl acrylate) by self-condensing atom transfer radical polymerization of a macroinimer

2000

Using 2-hydroxyethyl α-bromoisobuty-rate as initiator, atom transfer radical polymerization (ATRP) of tert-butyl acrylate leads to poly(tert-butyl acrylate) (PtBA) with a hydroxyl group at one and a bromine atom at the other end. Esterification of the hydroxyl group of these heterotelechelic polymers with acryloyl chloride yields PtBA (M n = 3060) with a polymerizable double bond at one end and a bromine atom at the other end which can act as an initiator in ATRP (macroinimer). Self-condensing ATRP of such a macroinimer leads to hyperbranched or highly branched PtBA. The polymer was characterized by GPC viscosity measurements. Even at M w = 78800, a rather low polydispersity index of M w M …

chemistry.chemical_classificationAcrylateTelechelic polymerPolymers and PlasticsDouble bondBulk polymerizationAtom-transfer radical-polymerizationOrganic ChemistryRadical polymerizationAcryloyl chloridechemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistryMacromolecular Rapid Communications
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Endgruppenuntersuchungen an isotaktischen Polystyrolen. VII. Mitt. über die stereospezifische Polymerisation von Styrol mit alkaliorganischen Verbind…

1963

Durch Polymerisation von Styrol mit optisch aktivem 2-Methylbutylnatrium oder -lithium konnen Polystyrole hergestellt werden, welche die Ebene des polarisierten Lichtes drehen; der gemessene Drehwert entspricht bei nicht zu hochmolekularen Polymeren einer 2-Methylbutylgruppe pro Makromolekul. Bei der Suche nach einer ungesattigten Endgruppe konnten weder mit einer infrarotspektroskopischen Kompensationsmethode noch durch eine Anlagerungsreaktion eines Siloxanmonohydrids Doppelbindungen in mit 2-Methylbutylnatrium hergestellten Polystyrolen nachgewiesen werden. Aus der Bestimmung der wachsenden Polystyrolmolekule mit Hilfe von MICHLERS Keton als Abbruchsreagenz ergibt sich, das der groste Te…

chemistry.chemical_classificationAddition reactionEnd-groupchemistry.chemical_compoundKetonePolymerizationDouble bondChemistryPolymer chemistryPolymerPolystyreneStyreneDie Makromolekulare Chemie
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Glycidyl methacrylate derivatization of α,β-poly(N-hydroxyethyl)-dl-aspartamide and α,β-polyasparthydrazide

1997

Abstract α,β-Poly(N-hydroxyethyl)- dl -aspartamide (PHEA) and α,β-polyasparthydrazide (PAHy) are two synthetic macromolecules having many potential applications in the field of biomedical sciences. This paper describes the functionalization of PHEA and PAHy with glycidyl methacrylate (GMA), in order to introduce pendant double bonds in their chains. Derivatized PHEA and PAHy (samples PHG and PAG, respectively) at various GMA content have been obtained and characterized. It has been shown that the derivatization reaction can be controlled by varying some parameters as solvent, catalyst, pH, GMA concentration and reaction time. As expected, PAHy reacted more rapidly and more extensively than …

chemistry.chemical_classificationAddition reactionGlycidyl methacrylatePolymers and PlasticsDouble bondOrganic ChemistryChemical modificationchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerSide chainOrganic chemistryDerivatizationMacromoleculePolymer
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Photochemical Functionalization of Allyl Benzoates by C-H Insertion

2013

The photoreactivity of allyl benzoates, containing an electron-rich double bond, has been explored by irradiation at 305 nm in different solvents. Solvent addition products arising from an insertion of the alpha H–C bonds of THF, dioxane, and i-PrOH to the allylic double bond was realized. The observed reactivity depended on reaction conditions and substitution pattern of the substrate. A DFT study on this unusual reaction was performed allowing the formulation of two mechanistic pathways.

chemistry.chemical_classificationAllylic rearrangementDouble bondChemistryOrganic ChemistryMechanistic organic photochemistrySubstrate (chemistry)Organic photochemistryPhotochemical synthesis THF reactivityBiochemistryMedicinal chemistryC-C bond formationDFTBenzoatesSolventDrug DiscoverySurface modificationReactivity (chemistry)C-H insertion
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Anaerobic Palladium-Catalyzed Chemoselective Oxidation of Allylic and Benzylic Alcohols with α-Bromo Sulfoxide as a Co-Oxidant.

2007

A chemoselective palladium-catalyzed anaerobic oxidation of allylic and benzylic alcohols using an α-bromo sulfoxide as a co-oxidant is described for the first time. The catalyst system is simple and has a long life because of the allowance of phosphane ligands under the non-aerobic conditions. The advantages of the described method include no overoxidation of primary alcohols to carboxylic acids because of the mild conditions applied, the tolerance of oxygen-sensitive functionalities such as a carbon-carbon double bond, an organothio group, or a diorganoamino group and the effective preparation of α,β-unsaturated aldehydes and ketones, resulting from the oxidation of primary and secondary …

chemistry.chemical_classificationAllylic rearrangementPrimary (chemistry)Double bondChemistryorganic chemicalsOrganic Chemistrychemistry.chemical_elementHomogeneous catalysisSulfoxideGeneral MedicineSulfurCatalysisCatalysischemistry.chemical_compoundAlcohol oxidationHeck reactionOrganic chemistryPalladiumChemInform
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