Search results for "Dendrimers"

showing 8 items of 38 documents

Divergent route to the preparation of hybrid Pt–Fe 2,4,6-Tris(4-ethynyl)phenyl-1,3,5-triazine metallodendrimers for nonlinear optics

2013

Abstract: The synthesis strategy for the preparation of novel platinum acetylide homometallic and heterobimetallic dendrimers (containing Fe as the other metal fragment) based on a 2,4,6-tris(4-ethynyl)phenyl-1,3,5-triazine core (3) is reported. All the dendrimer generations (G0G2) were synthesized under copper-free conditions following a divergent route. The G0-Pt dendrimer (4) was synthesized using the 1,3,5-triazine core (3) and cis-[Pt(PEt3)2Cl2] with a molar ratio of 1/4. The advantage of the current method is that different dendrimers can be prepared by following the same procedure with only changes in the molar ratios of the reactants involved. For instance, when 3 reacts with 4 in a…

TrisMolarPreparation of hybrid Pt−Fe 246-Tris(4ethynyl)phenyl-135-triazinePhysicsAcetylideOrganic Chemistrychemistry.chemical_element.Inorganic ChemistryMetalChemistrychemistry.chemical_compoundMetallodendrimers for nonlinear opticsFaculdade de Ciências Exatas e da Engenhariachemistry135-Triazinevisual_artDendrimerPolymer chemistryvisual_art.visual_art_mediumMoietyPhysical and Theoretical ChemistryPlatinumta116
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An Atom-Economical Approach to Functionalized Single-Walled Carbon Nanotubes: Reaction with Disulfides

2013

Owing to their unique structure, thermal stability, and mechanical and electronic properties, single-walled carbon nanotubes (SWCNTs) have been a subject of continuous and intense interest. However, various applications in many fields, such as molecular electronics, solar cells, and nanomedicine, often require the development of reproducible protocols for the chemical modification of SWCNTs. In fact, one of the main drawbacks of the use of SWCNTs is their tendency to aggregate and intrinsic poor solubility, which prevent their manipulation and limit their potential. To date, several methods have been described for the chemical functionalization of SWCNTs; however, new versatile and reliable…

atom economydisulfidesCarbon NanotubeInorganic chemistryOrganic Functionalization02 engineering and technologyCarbon nanotubedendrimer010402 general chemistry01 natural sciencesCatalysisdendrimerslaw.inventionchemistry.chemical_compoundlawAtom economyDendrimerThermal stabilitycarbon nanotubeCarbon Nanotubes; Organic FunctionalizationDiphenyl disulfidecarbon nanotubesMolecular electronicsGeneral MedicineSettore CHIM/06 - Chimica OrganicaGeneral Chemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryfunctionalizationSurface modification0210 nano-technologydisulfideCarbon monoxide
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Cyclotriveratrylene-Containing Porphyrins

2016

International audience; The C-3-symmetric cyclotriveratrylene (CTV) was covalently bonded via click chemistry to 1, 2, 3, and 6 zinc(II) porphyrin units to various host for C-60. The binding constants, Ka, were measured from the quenching of the porphyrin fluorescence by C-60. These constants vary between 400 and 4000 M-1 and are considered weak. Computer modeling demonstrated that the zinc(II) porphyrin units, [Zn], exhibit a strong tendency to occupy the CTV cavity, hence blocking the access for C-60 to land on this site. Instead, the pincer of the type [Zn]-[Zn] and in one case [Zn]-CTV, were found to be the most probable geometry to promote host-guest associations in these systems.

cagesStereochemistrychemistry.chemical_elementCyclotriveratryleneZinc010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencessupramolecular chemistrydendrimersInorganic Chemistrychemistry.chemical_compoundc-60[CHIM]Chemical SciencesmoleculesctvPhysical and Theoretical Chemistryinclusion complexesQuenching (fluorescence)010405 organic chemistryfullereneFluorescencePorphyrin0104 chemical sciencesPincer movementCrystallographychemistryCovalent bondClick chemistryderivativeshosts
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Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics

2012

The preparation of low-generation dendrimers based on a simple calix[4]arene scaffold by insertion of the iminosugar-analogue C2-symmetric 3,4-dihydroxypyrrolidine is described. This methodology allows a rapid incorporation of a considerable number of iminosugar-like moieties in a reduced volume and in a well-defined geometry. The inclusion of alkali-metal ions (sodium and potassium) in the polar cavity defined by the acetamide moieties at the lower rim of the calixarene was demonstrated, which allows also the rigidification of the dendrimer structure and the iminosugar presentation in the clusters. The combination of the supramolecular properties of calixarenes with the advantage of a dend…

calixarenesLetterOrganic ChemistrySupramolecular chemistryIminosugarmultivalencyCombinatorial chemistryPyrrolidinedendrimerslcsh:QD241-441Chemistrychemistry.chemical_compoundlcsh:Organic chemistrychemistryDendrimerCalixareneiminosugarslcsh:Qlcsh:ScienceAcetamidecation-responsive systemBeilstein Journal of Organic Chemistry
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Synthesis and Photoluminescent Properties of 1,1‘-Binaphthyl-Based Chiral Phenylenevinylene Dendrimers

2003

New chiral, soluble binaphthyl derivatives that incorporate stilbenoid dendrons at the 6,6′-positions have been prepared. The synthesis of the new enantiopure dendrimers was performed in a convergent manner by Horner-Wadsworth-Emmons (HWE) reaction of the appropriately functionalized 1,1′-binaphthyl derivative (R)-1 and the appropriate dendrons (R)2nGn-CHO. Different electroactive units were incorporated in the peripheral positions of the dendrons in order to tune both the optical and electrochemical behavior of these systems. Fluorescence measurements on the chiral dendrimers reveal a strong emission with maxima between 409 and 508 nm depending upon the substitution pattern. Finally, t…

chemistry.chemical_classificationCatenaneOrganic ChemistrySettore CHIM/06 - Chimica OrganicaGeneral MedicineElectrochemistryPhotochemistryAldehydeCombinatorial chemistryChemical synthesisFluorescenceRedoxEnantiopure drugchemistryDendrimerCalixareneCyclic voltammetryConjugated DendrimersThe Journal of Organic Chemistry
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Supramolecular organic-inorganic hybrid assemblies with tunable particle size: interplay of three noncovalent interactions.

2013

chemistry.chemical_classificationDendrimersMaterials scienceSupramolecular chemistryNanoparticleMetal NanoparticlesNanotechnologyGeneral ChemistrySulfidesCatalysisPolyelectrolyteColloidchemistryMicroscopy Electron TransmissionOrganic inorganicCadmium CompoundsNon-covalent interactionsSelf-assemblyParticle sizeGoldParticle SizeColoring AgentsAngewandte Chemie (International ed. in English)
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Inorganic Mercury Sequestration by a Poly(ethylene imine) Dendrimer in Aqueous Solution

2015

The interaction of the G-2 poly(ethylene imine) dendrimer L, derived from ammonia as initiating core, with Hg(II) and HgCl4 2− was studied in aqueous solution by means of potentiometric (pH-metric) measurements. Speciation of these complex systems showed that L is able to form a wide variety of complexes including 1:1, 2:1, 3:1 and 3:2 metal-to-ligand species, of different protonation states, as well as the anion complexes ((H7L)HgCl4) 5+ and ((H8L)HgCl4) 6+ . The stability of the metal complexes is very high, making L an excellent sequestering agent for Hg(II), over a large pH range, and a promising ligand for the preparation of functionalized activated carbons to be employed in the remedi…

mercuryImineInorganic chemistryPotentiometric titrationPharmaceutical Sciencechemistry.chemical_elementProtonationmercury dendrimers sequestration water contamination environmentArticleAnalytical Chemistrydendrimerspoly(ethylene imine)Metallcsh:QD241-441chemistry.chemical_compoundAmmoniacontaminationlcsh:Organic chemistryDendrimerDrug DiscoveryremediationPhysical and Theoretical ChemistryAqueous solutionMolecular StructureOrganic ChemistryMercury (element)chemistryChemistry (miscellaneous)visual_artPotentiometryvisual_art.visual_art_mediumMolecular MedicineEnvironmental PollutantsIminesPolyethylenesMolecules
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1,1prime-Binaphthyl-2-methylpyridinium-based peroxophosphotungstate salts: synthesis, characterization, and their use as oxidation catalysts

2009

A series of 1,1′-binaphthyl-2-methylammonium and pyridinium salts 6, 7, and 8 was synthesized through the coupling reaction of 2-(bromomethyl)-1,1′-binaphthalene (5) with the dendritic tetraallyl pyridinedicarbinol dendron 2 as well as triethylamine and 4-tert-butylpyridine. Tetraallyl pyridinedicarbinol dendron 2 was prepared by allylation of commercially available diethyl pyridine-3,5-dicarboxylate (1). The allylation of 2 with allyltrimethylsilane in the presence of boron trifluoride was unsuccessful, as tetraallyl pyridinedicarbinol trifluoroboron adduct 3 was obtained instead of expected hexaallylpyridine compound 4. The catalytic hydrogenation of allyl groups of the ammonium salt of 2…

oxidationCyclohexanolSalt (chemistry)010402 general chemistry01 natural sciencesCoupling reactionCatalysisdendrimersInorganic Chemistrychemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysis[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistrypolyoxometalatesTriethylamineBoron trifluorideComputingMilieux_MISCELLANEOUSchemistry.chemical_classification[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryThioanisole[CHIM.CATA]Chemical Sciences/Catalysishomogeneous catalysis0104 chemical scienceschemistryPyridinium
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