Search results for "Conjugated system"

showing 10 items of 225 documents

A Short Synthesis of Polysubstituted Pyrrolidines via α-(Alkylidene­amino)nitriles

2004

α-(Alkylideneamino)nitriles can be deprotonated under mild conditions. Their conjugated anions react with enones in a 1,4-addition to yield δ-keto-α-(alkylideneamino)nitriles which in turn can be reduced to form pyrrolidines in a one-pot reaction sequence.

Turn (biochemistry)DeprotonationReaction sequenceChemistryYield (chemistry)Organic ChemistryOrganic chemistryAmino nitrilesGeneral MedicineConjugated systemMedicinal chemistryPyrrole derivativesSynlett
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Thermal Induction of 9t12t Linoleic Acid: a New Pathway for the Formation of Conjugated Linoleic Acids

2009

Accepted version of an article published in the journal: International Journal of Engineering and Technology Published version available at: http://www.ijetch.org/papers/066.pdf Thermal induction of 9t12t fatty acid leading to the formation of Conjugated Linoleic Acids (CLA) has been demonstrated by subjecting glyceride, and methyl ester of the acid to heat treatment. Fifteen micro liter portions of the glyceride sample containing 9t12t fatty acid (trilinoelaidin) were placed in micro glass ampoules and sealed under nitrogen and then subjected to thermal treatment at 250oC. The glass ampoules were taken out at regular time intervals, and the contents were subjected to composition analysis b…

VDP::Mathematics and natural science: 400::Basic biosciences: 470::Biochemistry: 476chemistry.chemical_compoundChemistryLinoleic acidOrganic chemistryConjugated systemGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)International Journal of Engineering and Technology
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MRI-visible nanoparticles from hydrophobic gadolinium poly(ε-caprolactone) conjugates

2015

International audience; In this work we report on the synthesis of two hydrophobic and degradable gadolinium poly(ε-caprolactone) conjugates and their use for the preparation of MRI-visible nanoparticles intended for diagnosis applications. Advantage has been taken from functional poly(ε-caprolactone)s (PCL) bearing propargyl (PCL-yne) or amine groups (P(CL-co-NH2VL)) to yield conjugates by following two strategies. In a first approach, an azido-chelate of gadolinium (Gd(III)) has been conjugated by CuAAC to PCL-yne to yield a polymeric chelate containing 2.6 wt% of Gd(III). In a second approach, a dianhydride Gd(III)-ligand was reacted with P(CL-co-NH2VL) to yield, after complexation with …

[CHIM.POLY] Chemical Sciences/PolymersMaterials sciencePolymers and PlasticsBiocompatibility[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingGadoliniumchemistry.chemical_elementNanoparticle02 engineering and technologyConjugated system010402 general chemistry01 natural scienceschemistry.chemical_compoundNanoparticlePolymer chemistryMaterials ChemistrypolyesterChelationOrganic Chemistry021001 nanoscience & nanotechnology0104 chemical sciences[CHIM.POLY]Chemical Sciences/Polymers[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingchemistryPropargylnanoparticlesAmine gas treating0210 nano-technologyCaprolactoneMRIPolymer
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Electrochemistry of Bis(pyridine)cobalt (Nitrophenyl)corroles in Nonaqueous Media

2018

International audience; A series of bis(pyridine)cobalt corroles with one or three nitrophenyl groups on the meso positions of the corrole macrocycle were synthesized and characterized as to their electrochemical and spectroscopic properties in dichloromethane, benzonitrile, and pyridine. The potentials for each electrode reaction were measured by cyclic voltammetry and the electron-transfer mechanisms evaluated by analysis of the electrochemical data combined with UV-visible spectra of the neutral, electroreduced, and electroxidized forms of the corroles. The proposed electronic configurations of the initial compounds and the prevailing redox reactions involving the electroactive central c…

[SPI.OTHER]Engineering Sciences [physics]/Otherelectronic-structuremanganese corroleschemistry.chemical_element[CHIM.INOR]Chemical Sciences/Inorganic chemistryConjugated system010402 general chemistryElectrochemistry01 natural sciencesInorganic Chemistryporphyrin-corrole dyadschemistry.chemical_compoundcopper corroleswater-oxidationPyridinePolymer chemistryacid-media[CHIM]Chemical Sciencesaryl-substituted corrolesredox potentialsPhysical and Theoretical ChemistryCorrole010405 organic chemistry0104 chemical sciencesSolventBenzonitrilechemistrystructural-characterizationefficient synthesisCyclic voltammetryCobaltInorganic Chemistry
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Nonlinear optical properties of diaromatic stilbene, butadiene and thiophene derivatives

2021

Series of highly polar stilbene (1a–e), diphenylbutadiene (2a–c) and phenylethenylthiophene (3a–c) derivatives were prepared via Horner–Wadsworth–Emmons method with a view to produce new and efficient materials for second harmonic generation (SHG) in the solid-state. The single-crystal X-ray structures of compounds 1–3 reveal extensive polymorphism and a peculiar photodimerization of the 2-chloro-3,4-dimethoxy-4′-nitrostilbene derivative 1a to afford two polymorphs of tetra-aryl cyclobutane 4. The stilbene congeners 2-chloro-3,4-dimethoxy-4′-nitrostilbene (1a·non-centro), 5-bromo-2-hydroxy-3-nitro-4′-nitrostilbene (1b) and 4-dimethylamino-4′-nitrostilbene (1e), as well as 4′-fluoro-4′′-nitr…

aromaattiset yhdisteet010405 organic chemistrySecond-harmonic generationbutadieeniGeneral ChemistryConjugated systemChromophoreoptiset ominaisuudetkiteet010402 general chemistry01 natural sciencesFluorescenceCatalysis0104 chemical sciencesCyclobutaneCrystallographychemistry.chemical_compoundNonlinear opticalPolymorphism (materials science)chemistrystilbeenitMaterials ChemistryUreaorgaaniset yhdisteetNew Journal of Chemistry
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Metallomacrocycles with metalmetal bonds: synthesis, characterization and electrochemistry of [(P)SnRe(CO)5]BF4 and [{(P)Sn}2Re(CO)4]BF4 derivatives…

1996

Abstract The synthesis and characterization of bimetallic and trimetallic porphyrins of the type [(P)SnRe(CO) 5 ]BF 4 and [{(P)Sn} 2 Re(CO) 4 ]BF 4 are reported where P is the dianion of tetra- p -tolyporphyrin (TpTP) or tetra- m -tolyporphyrin (TmTP). These metal-metal bonded complexes were synthesized by reaction of Re 2 (CO) 10 with the corresponding (P)SnCl 2 derivatives in 1,2-dichlorobenzene followed by a reaction with NaBF 4 or TBABF 4 in toluene to give the BF − 4 salt. Each compound was characterized by a variety of spectroscopic and electrochemical techniques while the structures were assigned on the basis of FAB mass spectral data and by comparison of their physicochemical proper…

biologyInorganic chemistryConjugated systembiology.organism_classificationElectrochemistryCleavage (embryo)PorphyrinMedicinal chemistryTolueneRedoxInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryTetraPhysical and Theoretical ChemistryBimetallic stripInorganica Chimica Acta
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The Structural Diversity of Benzofuran Resorcinarene Leads to Enhanced Fluorescence

2014

An unexpected and previously unknown resorcinarene mono-crown with a fused benzofuran moiety in its macrocyclic core was obtained as a byproduct from a bridging reaction of tetramethoxy resorcinarene with tetraethylene glycol ditosylate. The formation of the fused benzofuran moiety in the resorcinarene macrocycle resulted in a unique rigid and puckered boat conformation, as shown by XRD studies in the solid state. Modification of the macrocycle was also observed to affect the photophysical properties in solution by enhancing the fluorescence brightness compared with a conventional resorcinarene macrocycle. The fluorescent properties enabled unique detection of structural features, that is, …

calixarenesStereochemistryPhenylalanineCyclohexane conformationMolecular ConformationSupramolecular chemistryChemistry Techniques SyntheticConjugated systemCrystallography X-RayBiochemistrysupramolecular chemistryStructure-Activity Relationshipchemistry.chemical_compoundCalixarenePolymer chemistrysupramolekulaarinen kemiaresorcinarenesMoietyBenzofuranX-ray diffractta116BenzofuransMolecular StructureOrganic Chemistryfluoresenssita1182benzofuranGeneral ChemistryResorcinareneFluorescenceX-ray diffractionSpectrometry FluorescencechemistryfluorescenceChemistry - An Asian Journal
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Copper-Catalyzed One-Pot Synthesis of 3-(N -Heteroarenyl)acrylonitriles through Radical Conjugated Addition of β-Nitrostyrene to Methylazaarenes

2020

chemistryOrganic ChemistryOne-pot synthesisPolymer chemistryCopper catalyzedchemistry.chemical_elementPhysical and Theoretical ChemistryConjugated systemCopperEuropean Journal of Organic Chemistry
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Cycloalkin-vinylidencycloalkan-umlagerungen

1989

Abstract Flash pyrolysis of the strained cyclic alkynes 1 leads to ring systems 2 with an exocyclic allene group and in a further isomerization step to the conjugated vinyl compounds 3 .

chemistry.chemical_classificationAlleneOrganic ChemistryConjugated systemRing (chemistry)PhotochemistryBiochemistryMedicinal chemistrychemistry.chemical_compoundHydrocarbonchemistryDrug DiscoveryIsomerizationPyrolysisTetrahedron Letters
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Anthracene Based Conjugated Polymers: Correlation between π−π-Stacking Ability, Photophysical Properties, Charge Carrier Mobility, and Photovoltaic P…

2010

This article reports on the synthesis, characterization and properties of a series of anthracene−containing poly(p-phenylene-ethynylene)-alt-poly(p-phenylene-vinylene)s (PPE−PPV) copolymers with general constitutional unit (Ph−C≡C−Anthr−C≡C−Ph−CH═CH−Ph−CH═CH−)n denoted AnE-PV. Solely linear (AnE-PVaa, -ad, -ae) and solely branched (AnE-PVbb) as well as mixed linear and branched (AnE-PVab, -ac, -ba, -cc) alkoxy side chains were grafted to the backbone in order to tune the π−π-stacking ability of the materials. It has been possible to establish a correlation between π−π-stacking ability, absorptive behavior, charge carrier mobility, solar cell active layer nanoscale morphology and resulting p…

chemistry.chemical_classificationAnthraceneMaterials sciencePolymers and PlasticsOpen-circuit voltageOrganic ChemistryStackingPolymerConjugated systemlaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawSolar cellPolymer chemistryMaterials ChemistrySide chainAlkoxy groupMacromolecules
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