Search results for "polymer chemistry"

showing 10 items of 3410 documents

Regioselective Bromination and Functionalization of Dibenzo[hi,st]ovalene as Highly Luminescent Nanographene with Zigzag Edges.

2019

Dibenzo[hi,st]ovalene (DBOV) is a nanographene with a combination of zigzag and armchair edges, consisting of 38 sp2 carbons. Excellent optical properties with strong red emission have been demonstrated. Here we report the regioselective bromination of DBOV bearing two mesityl groups (DBOV-Mes) by treatment with N-bromosuccinimide (NBS) under mild conditions. The dibrominated DBOV was further subjected to transition-metal-catalyzed cross-coupling reactions, that is, Suzuki and Sonogashira coupling, demonstrating the edge-decoration of DBOV with different functional groups. Notably, DBOVs arylated at the bay regions showed intense red emission and enhanced fluorescence quantum yields of up t…

010405 organic chemistryChemistryOrganic ChemistrySonogashira couplingRegioselectivityHalogenationGeneral ChemistryOvalene010402 general chemistry01 natural sciencesBiochemistryRedox0104 chemical scienceschemistry.chemical_compoundRadical ionPolymer chemistryCyclic voltammetryLuminescenceChemistry, an Asian journal
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Interactions of a Diplumbyne with Dinuclear Transition Metal Carbonyls to Afford Metalloplumbylenes

2020

The metathesis reactions of the diplumbyne AriPr6PbPbAriPr6 (AriPr6 = −C6H3–2,6-(C6H2–2,4,6-iPr3)2) with the dinuclear metal carbonyls Mn2(CO)10, Fe2(CO)9, and Co2(CO)8 under mild conditions afforded the complexes Mn(CO)5(PbAriPr6) (1), Fe(CO)4(PbAriPr6)2 (2), and Co4(CO)9(PbAriPr6)2 (3), respectively. Complexes 1–3 were structurally characterized by single-crystal X-ray diffraction and spectroscopically characterized by 1H, 13C{1H}, 59Co{1H}, and 207Pb{1H} NMR; UV–vis; and IR methods. They are rare examples of species formed by the direct reaction of a group 14 dimetallyne with transition metal carbonyls. Complexes 1 and 2 feature Mn–Pb or Fe–Pb single bonds, whereas in 3 a Co–Pb cluster i…

010405 organic chemistryChemistryOrganic ChemistrycarbonylsmetalsMetal carbonylkompleksiyhdisteetorganometalliyhdisteet010402 general chemistry01 natural sciencescobalttransition metals0104 chemical sciencesInorganic ChemistryTransition metalPolymer chemistrySalt metathesis reactionPhysical and Theoretical Chemistrykarbonyylitnuclear magnetic resonance spectroscopy
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Vinyl Fluorides: Competent Olefinic Counterparts in the Intramolecular Pauson–Khand Reaction

2019

Despite the great advances achieved in the Pauson-Khand reaction and the ever-increasing demand for fluorinated compounds, the use of vinyl fluorides as olefinic counterparts in the above-mentioned transformation had been completely overlooked. Herein, we describe, for the first time, the intramolecular Pauson-Khand reaction of enynes containing a vinyl fluoride moiety.

010405 organic chemistryChemistryPauson–Khand reactionOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundIntramolecular forcePolymer chemistryMoietyPhysical and Theoretical ChemistryVinyl fluorideOrganic Letters
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Formation of dibutyl carbonate and butylcarbamate via CO2 insertion in titanium(IV) butoxide and reaction with n-butylamine

2016

Abstract The species resulting from insertion of 12CO2 and 13CO2 into titanium(IV) butoxide is for the first time fully characterized by means of infrared and nuclear magnetic resonance spectroscopy. Results show formation of Ti-monobutylcarbonate, that easily undergoes nucleophilic attack by an aliphatic amine. The hydrolysis of the resulting species produces butylcarbamate and dibutylcarbonate as the only main products. Characterization results of the carbonate-like adduct, along with its reactivity with amine molecules open the route to new ways of CO2 utilization as building block for valuable organic compounds.

010405 organic chemistryChemistryProcess Chemistry and Technologyn-Butylaminechemistry.chemical_elementNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesAdductHydrolysischemistry.chemical_compoundNucleophilePolymer chemistryChemical Engineering (miscellaneous)Organic chemistryReactivity (chemistry)Amine gas treatingSettore CHIM/07 - Fondamenti Chimici Delle TecnologieWaste Management and DisposalTitaniumDibutyl carbonate CO2 insertion Titanium alkoxides Carbamate
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Towards the synthesis of substituted porphyrins by a pyridyl group bearing a reactive functionality

2010

Pyridyl-substituted porphyrins bearing a reactive functionality were prepared via Suzuki cross-coupling reactions and resulted in very good yields. These compounds are precursors of new porphyrin architectures able to coordinate two metals: one in the porphyrin core and the second around the pyridyl moiety. During the coupling reactions, a higher reactivity of a chloro picolyl group was evidenced compared to a bromo function on the same reacting molecule.

010405 organic chemistryChemistryStereochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry010402 general chemistry01 natural sciencesPorphyrinCoupling reaction0104 chemical sciencesA3B-porphyrinschemistry.chemical_compoundSuzuki reactionGroup (periodic table)[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPolymer chemistrypolycyclic compoundsMoietyMoleculeheterocyclic compoundsReactivity (chemistry)meso-functionalizationSuzuki couplingpyridyl substituted porphyrinsComputingMilieux_MISCELLANEOUS
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Versatile behavior of conjugated diynes with zirconocene reactive species

2008

Thermal decomposition of Cp2ZrPh2 in the presence of the buta-1,3-diynes RC≡CC≡CR (R = Ph, SiMe3) can lead to seven- or five-membered metallacycles. In both cases a stable benzo-fused seven-membered zirconacyclocumulene arising from a 2-fold insertion of the triple bonds of the dialkyne in the in situ generated zirconocene benzyne is formed. In the case of Me3SiC≡CC≡CSiMe3 a second minor complex is isolated: a 3-alkynyl-substituted zirconaindene arising from a β monoinsertion of one acetylenic function of the conjugated diyne in the zirconocene benzyne. No stable 2-alkynyl-substituted zirconacycle was isolated. This α monoinsertion complex is an intermediate in the exchange of the metalated…

010405 organic chemistryChemistrycycloaddition reactionOrganic ChemistryThermal decomposition[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementmetalationConjugated system010402 general chemistryTriple bond01 natural sciencesAryne0104 chemical sciencesInorganic ChemistrycyclometalationAntimonyReagentAtomPolymer chemistryMoiety[CHIM.COOR]Chemical Sciences/Coordination chemistryzirconocene- benzyn intermediatePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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Vinyl sulfone building blocks in covalently reversible reactions with thiols

2015

In the present study we use quantum-chemical calculations to investigate how the reactivity of vinyl sulfone-based compounds can be modified from an irreversible to a reversible reaction with thiols. Based on the predictions from theory, an array of nine different vinyl sulfones with systematically varying substitution pattern was synthesized and their crystal structures were determined. Subsequent Hirshfeld surface analyses employing the principle of electrostatic complementarity aid the understanding of the crystal packing of the synthesized compounds. Reactivity studies against the nucleophile 2-phenylethanethiol mirror the properties predicted by the quantum-chemical computations in sol…

010405 organic chemistryChemistrytechnology industry and agricultureGeneral ChemistryCrystal structureVinyl sulfone010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisReversible reaction0104 chemical sciencesCrystalNucleophileCovalent bondPolymer chemistryMaterials ChemistryReactivity (chemistry)New Journal of Chemistry
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Insight into the Mechanism of Water Adsorption/Desorption in Hydrophilic Viologen-Carboxylate Based PCP

2017

A water stable and highly hydrophilic porous coordination polymer based on viologen-carboxylate type ligand, the 4,4′-bipyridinium,1,1-bis(3-carboxyphenyl) (pc2), is obtained by the solvothermal method: [Cd3(pc2) (BTC)2(H2O)2]·6H2O ([1(H2O)2]·6H2O; BTC3– = 1,3,5-carboxybenzene). Its crystal structure and the ones of two partially dehydrated phases have been determined, allowing insight into the mechanism of water adsorption/desorption of this PCP material. It is shown that the dehydrated compound [1] first adsorbs two water molecules which fill the pores, leading to [1]·2H2O. On the other hand, the partial dehydration of the as-synthesized compound leads to the intermediate phase [1(H2O)]·3…

010405 organic chemistryCoordination polymerLigandInorganic chemistryGeneral ChemistryCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundAdsorptionchemistryDesorptionPolymer chemistryMoleculeGeneral Materials ScienceCarboxylatePyridiniumComputingMilieux_MISCELLANEOUSCrystal Growth & Design
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Functionalised diimidazolium salts: the anion effect on the catalytic ability

2016

The catalytic ability of some functionalised diimidazolium ionic liquids was tested using the Michael addition of malononitrile to t-chalcone as probe reaction. Diimidazolium salts characterized by the presence of 1-(1-imidazolylmethyl)-3,5-di-[1-(3-octylimidazolylmethyl)]benzene cation and differing in the anion structure were used. Both mono- and dianions were employed and among these some chiral anions generally used as organocatalysts were taken into account. Data collected were analysed both as function of ionic liquids structure and basicity, evaluated using the Hammett basicity function. Although the use of chiral anions did not allow performing a stereochemical control of the reacti…

010405 organic chemistryGeneral Chemical EngineeringSettore CHIM/06 - Chimica OrganicaGeneral Chemistry010402 general chemistry01 natural sciencesIonic Liquids Michael Reaction Base catalysis0104 chemical sciencesCatalysisIonchemistry.chemical_compoundchemistryIonic liquidPolymer chemistryMichael reactionOrganic chemistryBenzeneMalononitrileRSC Advances
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Hydrogen-Bonded Open-Framework with Pyridyl-Decorated Channels: Straightforward Preparation and Insight into Its Affinity for Acidic Molecules in Sol…

2017

International audience; An hydrogen-bonded open framework with pores decorated by pyridyl groups has been constructed following an off-charge-stoichiometry assemblage of protonated tetrakis(4-pyridyl-oxymethyl)methane and [Al(oxalate)3]3-, respectively the H-bond donor and acceptor of the ionic H-bond interactions. This supramolecular porous architecture (SPA-2) possesses 1 nm-large pores interconnected in 3D with high solvent accessible void (53%). It demonstrated remarkable affinity for acidic organic molecules in solution, which was investigated by the means of various carboxylic acids including larger drug molecules. Noteworthy, competing sorption between acetic acid and its halogenated…

010405 organic chemistryHydrogen bondChemistryOrganic ChemistrySupramolecular chemistryIonic bondingProtonationSorptionGeneral ChemistryHydrogen-Bonding010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencessupramolecular chemistryCatalysis0104 chemical sciencesSolventPolymer chemistryhost-guest chemistry[CHIM]Chemical SciencesMoleculeOrganic chemistryoxalate complexporous materialHost–guest chemistryChemistry (Weinheim an der Bergstrasse, Germany)
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