Search results for "Ferrocene"

showing 10 items of 306 documents

Conformational stability of oligoferrocene oligoamide foldamers

2016

Abstract Organometallic oligoamides built from three to four ferrocene amino acid units ( H-Fca-OH , 1-amino-1′-ferrocene carboxylic acid) fold into hydrogen bonded secondary structures featuring eight-membered rings by cooperative hydrogen bonds. NMR studies and DFT calculations (CAM-B3LYP, LANL2DZ, IEFPCM (THF)) reveal that the organometallic zigzag foldamer structures are highly resistant toward denaturation by hydrogen bond acceptors such as dimethyl sulfoxide and 2,4-lutidine. Replacing one ferrocene amino acid unit by the organic α -amino acid glycine at the C -terminal end (Fca → Gly) significantly destabilizes the secondary zigzag structure facilitating denaturation by DMSO. Highly …

chemistry.chemical_classificationHydrogen010405 organic chemistryDimethyl sulfoxideStereochemistryHydrogen bondCarboxylic acidOrganic ChemistryFoldamerchemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesAmino acidInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryFerroceneMaterials ChemistryPhysical and Theoretical ChemistryProtein secondary structureJournal of Organometallic Chemistry
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Electroactive linear-hyperbranched block copolymers based on linear poly(ferrocenylsilane)s and hyperbranched poly(carbosilane)s.

2009

A convenient two-step protocol is presented for synthesis of linear-hyperbranched diblock copolymers consisting of a linear, organometallic poly(ferrocenylsilane) (PFS) block and hyperbranched poly(carbosilane) (hbPCS) segments. Linear PFS diblock copolymers were synthesized through photolytic ring-opening polymerization of dimethyl[1]silaferrocenophane as the first block and methylvinyl[1]sila-ferrocenophane as the second. These block copolymers served as polyfunctional cores in a subsequent hydrosilylation polyaddition of different silane-based AB 2 monomers. Three AB 2 monomers (methyldiallylsilane; methyldiundecenylsilane, and ferrocenyldiallylsilane) were investigated; they introduced …

chemistry.chemical_classificationHydrosilylationOrganic ChemistryDispersityGeneral ChemistryPolymerCatalysischemistry.chemical_compoundMonomerchemistryFerrocenePolymerizationPolymer chemistryCopolymerReactivity (chemistry)Chemistry (Weinheim an der Bergstrasse, Germany)
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Inside Front Cover: Redox-Tunable Defects in Colloidal Photonic Crystals (Adv. Mater. 20/2005)

2005

The inside front cover illustrates reversible tuning of an intragap transmitting state induced by redox cycling, accomplished using a redox-active polyferrocenylsilane polyelectrolyte multilayer planar defect embedded in a colloidal photonic crystal (CPC) synthesized by a bottom–up method combining colloidal self-assembly and microcontact printing. In work reported on p. 2455 by Manners, Ozin, and co-workers, the wavelength position of the defect state can be changed by changing the oxidation state of the ferrocene moieties in the polymer backbone. This could find applications in electrochemically tunable microcavities, and—if light emitters are incorporated—electrochemically tunable CPC-ba…

chemistry.chemical_classificationMaterials scienceMechanical EngineeringNanotechnologyPolymerLaserPolyelectrolytelaw.inventionchemistry.chemical_compoundWavelengthColloidPlanarFerrocenechemistryMechanics of MaterialslawMicrocontact printingGeneral Materials ScienceAdvanced Materials
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Blends from redox active liquid crystal ionomers and amorphous ionomers

1994

Abstract Biphasic blends (mixtures) of liquid crystal ionomers (prepared from ferrocene containing liquid crystal polymers by a redox reaction) and partially sulfonated polystyrene combine the constituent properties in a way, which is dependent on the measuring method. Polarizing microscopy shows homogenous textures similar to the pure liquid crystal polymer. Mechanical measurements show however the elastomeric behaviour of sulfonated polystyrene. The phase separated structure of these blends is proved by differential scanning calorimetry measurements.

chemistry.chemical_classificationMaterials sciencePolymerGeneral ChemistryElastomerCondensed Matter PhysicsAmorphous solidchemistry.chemical_compoundDifferential scanning calorimetryFerrocenechemistryChemical engineeringLiquid crystalPhase (matter)Organic chemistryGeneral Materials SciencePolystyreneLiquid Crystals
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Cellulose-click-ferrocenes as docking spots for cyclodextrin

2012

A novel synthesis of ferrocene-modified cellulose, prepared from 6-azido-6-deoxy-cellulose and ethynylferrocene, is presented. The two components were coupled via copper-catalyzed click-type cycloaddition under microwave-assisted conditions. The surface structure of the cellulose derivative was investigated in comparison with that of pure, microcrystalline cellulose using electron microscopy (scanning, transmission and scanning transmission), showing iron atoms of ferrocene as homogeneously distributed particles. They are detectable as clear signals in the energy-dispersive X-ray profile. In addition, Rame-β-cyclodextrin was supramolecularly attached to cellulose and the complex formed was …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsCyclodextrinOrganic ChemistryCycloadditionlaw.inventionMicrocrystalline cellulosechemistry.chemical_compoundFerrocenechemistryDynamic light scatteringlawPolymer chemistryMaterials ChemistryClick chemistryElectron microscopeCellulosePolymer International
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Group 4 and Group 8 unbridged metallocene derivatives with a pendant fluorenyl group. X-ray structure of 1,1′-bis[2-(2-fluorenyl)propyl]ferrocene

1999

Abstract The action of one equivalent of BuLi on 2-cyclopentadienyl-2-fluorenylpropane (C5H5CMe2C13H9) led to the monoanionic salt LiC5H4CMe2C13H9. This anion was reacted with Fe2Cl4(THF)3, TiCl3(THF)3, ZrCl4, HfCl4 or CpZrCl3, DME and, in a mixture with CpLi, with Fe2Cl4(THF)3 affording the corresponding metallocenes and metallocene dichlorides. The X-ray structure of Fe(η5-C5H4CMe2C13H9)2 is described. The first results about the reactivity of the fluorenyl group are reported together with the synthesis of Zr(η5-C5H5)[η5-C5H4CMe2-η5-C13H8Rh(cod)]Cl2, which has been tested using hydroformylation and cyclotrimerisation catalysis.

chemistry.chemical_classificationOrganic ChemistryX-raySalt (chemistry)BiochemistryMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundFerrocenechemistryGroup (periodic table)Materials ChemistryOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryMetalloceneHydroformylationJournal of Organometallic Chemistry
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Ferrocene-Containing Multifunctional Polyethers: Monomer Sequence Monitoring via Quantitative 13C NMR Spectroscopy in Bulk

2014

Ferrocenyl glycidyl ether (fcGE) and allyl glycidyl ether (AGE) are copolymerized via living anionic ring-opening polymerization to generate polyfunctional copolymers with molecular weights up to 40 300 g/mol and low molecular weight dispersities (Mw/Mn < 1.18). Copolymerizations were carried out in bulk at 100 °C and unexpectedly found to proceed without any isomerization of the allyl double bonds. The copolymerization behavior of fcGE and AGE was monitored by in situ quantitative 13C NMR kinetic measurements in bulk, evidencing the formation of random copolymers under these conditions, showing no gradient of comonomer incorporation. The redox-active behavior of the copolymers and homopoly…

chemistry.chemical_classificationPolymers and PlasticsAllyl glycidyl etherComonomerOrganic ChemistryPolymerCarbon-13 NMRInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationFerrocenePolymer chemistryMaterials ChemistryCopolymerMacromolecules
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Supramolecular Nanocycles Comprisingβ-Cyclodextrin-click-Ferrocene Units: Rings of Rings of Rings

2010

We applied 1,3-dipolar cycloaddition to bind ethynylferrocene onto 6I-azido-6I-deoxycyclomaltoheptaose under microwave assisted conditions. The process was investigated by (1) H NMR, FT-IR spectroscopy, and MALDI-TOF mass spectrometry. The ability of the synthesized compound to self-organize to cyclic supramolecular structures was investigated by dynamic light scattering measurements and cryo-transmission electron microscopy.

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinOrganic ChemistrySupramolecular chemistrymacromolecular substancesCycloadditionInclusion compoundchemistry.chemical_compoundchemistryFerrocenePolymer chemistry13-Dipolar cycloadditionMaterials ChemistryProton NMROrganic chemistryMetalloceneMacromolecular Rapid Communications
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Ferrocenyl Glycidyl Ether: A Versatile Ferrocene Monomer for Copolymerization with Ethylene Oxide to Water-Soluble, Thermoresponsive Copolymers

2013

The first ferrocene-containing epoxide monomer, ferrocenyl glycidyl ether (fcGE), is introduced. The monomer has been copolymerized with ethylene oxide (EO). This leads to electroactive, water-soluble, and thermoresponsive poly(ethylene glycol) (PEG) derived copolyethers. Anionic homo- and copolymerization of fcGE with EO was possible. Molecular weights could be varied from 2000 to 10 000 g mol–1, resulting in polymers with narrow molecular weight distribution (Mw/Mn = 1.07–1.20). The ferrocene (fc) content was varied from 3 to 30 mol %, obtaining water-soluble materials up to 10 mol % incorporation of the apolar ferrocenyl comonomer. Despite the steric bulk of fcGE, random copolymers were …

chemistry.chemical_classificationPolymers and PlasticsEthylene oxideComonomerOrganic ChemistryEpoxidePolymerInorganic Chemistrychemistry.chemical_compoundMonomerchemistryFerrocenePolymer chemistryMaterials ChemistryCopolymerOrganic chemistryEthylene glycolMacromolecules
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Zum Ligandenaustausch des Ferrocens mit Methyl- und Ethyl-substituierten Naphthalinen

1988

Abstract The replacement of a Cp ligand of ferrocene by each of ten unsymmetrically substituted naphthalenes yields pairs of complex ions [arene-FeCp] + , which have been identified from their 1 H NMR spectra. The influence of the substituent on the ratio of the two isomers, and its temperature dependence implies a complex reaction mechanism involving an η 2 -bound intermediate of the associated naphthalene. The proton resonances of the alkyl groups of the naphthalenes are shifted to lowfield by complexation; this effect decreases with increasing distance from the iron. The resonance shift of the arene protons has a different sign for the complexed (highfield) and the uncomplexed part (lowf…

chemistry.chemical_classificationReaction mechanismStereochemistryLigandOrganic ChemistrySubstituentNuclear magnetic resonance spectroscopyBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryFerroceneMaterials ChemistryProton NMRPhysical and Theoretical ChemistryMetalloceneAlkylJournal of Organometallic Chemistry
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