Search results for "hydrosilylation"

showing 10 items of 45 documents

First Titanium-Catalyzed anti-1,4-Hydrosilylation of Dienes

2005

1,4-Hydrosilylation of dienes catalyzed by late transition metals constitutes a straightforward access to allylsilanes. However, when unsymmetric dienes are used, it generally leads to a mixture of regioisomers (tail or head products) via Z-specific 1,4-addition. Here we describe the first catalytic anti-1,4-hydrosilylation of dienes using the cheap and stable Cp2TiF2 complex as catalyst. It affords E-allylsilanes in good to excellent yields with an unprecedented regio- and diastereoselectivity. Dehydrogenative double silylation of dienes can be selectively obtained by simply changing the activation protocol of the precatalyst.

Inorganic Chemistrychemistry.chemical_compoundSilylationTransition metalChemistryHydrosilylationOrganic ChemistryStructural isomerchemistry.chemical_elementPhysical and Theoretical ChemistryCombinatorial chemistryCatalysisTitaniumOrganometallics
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[TiPHOS(Rh)]+:  A Fortuitous Coordination Mode and an Effective Hydrosilylation Bimetallic Catalyst

2005

The reaction of the titanocene diphosphine {(η5-C5H5)[η5-C5Me3-1,2-(PPh2)2]TiCl2} (TiPHOS; 1) with [Rh(COD)2](OTf) led to the new early−late heterobimetallic complex [(TiPHOS)Rh(COD)](OTf) (2), who...

Inorganic Chemistrychemistry.chemical_compoundchemistryHydrosilylationOrganic ChemistryPolymer chemistryOrganic chemistryPhysical and Theoretical ChemistryBimetallic stripCatalysisOrganometallics
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Carbene complexes of rhodium and iridium from tripodal N-heterocyclic carbene ligands: synthesis and catalytic properties.

2004

Two tripodal trisimidazolium ligand precursors have been tested in the synthesis of new N-heterocyclic carbene rhodium and iridium complexes. [Tris(3-methylbenzimidazolium-1-yl)]methane sulfate gave products with coordination of the decomposed precursor. [1,1,1-Tris(3-butylimidazolium-1-yl)methyl]ethane trichloride (TIMEH(3)(Bu)) coordinated to the metal in a chelate and bridged-chelate form, depending on the reaction conditions. The crystal structures of two of the products are described. The compounds resulting from the coordination with TIME(Bu) were tested in the catalytic hydrosilylation of terminal alkynes.

LigandHydrosilylationTransition metal carbene complexchemistry.chemical_elementCrystal structureMedicinal chemistryRhodiumCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryOrganic chemistryIridiumPhysical and Theoretical ChemistryCarbeneInorganic chemistry
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C,N-chelated diaminocarbene platinum(II) complexes derived from 3,4-diaryl-1H-pyrrol-2,5-diimines and cis-dichlorobis(isonitrile)platinum(II): Synthe…

2020

The reaction of 3,4-diaryl-1H-pyrrol-2,5-diimines with cis-dichlorobis(isonitrile)platinum(II) affords the C,N-chelated diaminocarbene platinum(II) complexes, which have been fully characterized including molecular spectroscopy, single crystal X-ray diffraction and DFT calculations. The obtained platinum(II) complexes are effective catalysts for the hydrosilylation of alkynes and alkenes. Thus, the reaction of phenylacetylene with triethoxysilane leads to the formation of α- and β-(E)-vinylsilanes, generating TON's in the range of 103 to 104 and TOF's in the range of 102 to 103 h−1. Also, the cross-linked silicones, possessing the luminescence properties, were obtained by the hydrosilylatio…

LuminescenceHydrosilylationchemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundAnti-cancer activityPolymer chemistryluminescenceMaterials ChemistryChelationPhysical and Theoretical Chemistrydiaminocarbene platinum(II) complexescatalysis010405 organic chemistryOrganic Chemistryhydrosilylation0104 chemical scienceschemistryPhenylacetyleneDiaminocarbene platinum(II) complexesHydrosilylationTriethoxysilaneanti-cancer activityLuminescencePlatinumSingle crystalJournal of Organometallic Chemistry
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From Single Molecules to Nanostructured Functional Materials: Formation of a Magnetic Foam Catalyzed by Pd@FexO Heterodimers

2017

Multicomponent nanostructures containing purely organic or inorganic as well as hybrid organic–inorganic components connected through a solid interface are, unlike conventional spherical particles, able to combine different or even incompatible properties within a single entity. They are multifunctional and resemble molecular amphiphiles, like surfactants or block copolymers, which makes them attractive for the self-assembly of complex structures, drug delivery, bioimaging, or catalysis. We have synthesized Pd@FexO heterodimer nanoparticles (NPs) to fabricate a macroporous, hydrophobic, magnetically active, three-dimensional (3D), and template-free hybrid foam capable of repeatedly separati…

NanostructureMaterials scienceHydrosilylationNucleationNanoparticleNanochemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesNanomaterial-based catalyst0104 chemical scienceschemistry.chemical_compoundChemical engineeringchemistryAmphiphileGeneral Materials Science0210 nano-technologyHybrid materialACS Applied Nano Materials
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Connecting Curable Siloxanes to Luminescent Organic Semiconductors - Monomers for Functional Hybrid Materials

2006

ABSTRACTLuminescent stilbenoid chromophores with two alkoxysilane end groups are prepared via hydrosilylation or condensation / reduction of substituted 5-ring OPVs with hydro- and aminopropylsilanes. Chromophore and curable units are connected via flexible spacers. To obtain compounds with a rigid connection between silane and π-system, iodo- or bromo-OPVs were coupled to alkoxysilanes carrying vinyl- or p-vinylphenyl moieties under Heck conditions. This approach allowed a combined connection of the chromophore to the silane moiety with an extension of the π-system. Hydrolysis of the alkoxysilanes yields silanols condensing to curable three-dimensional networks, thus allowing the transform…

Organic semiconductorchemistry.chemical_compoundMonomerMaterials sciencechemistryPolymerizationHydrosilylationPolymer chemistryMoietyChromophoreHybrid materialSilaneMRS Proceedings
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Dimesogenic ferroelectric polysiloxanes

1994

Dimesogenic polysiloxane [Si(Me) 2 O] m [Si(Me)(R)O] n (R= (CH 2 ) 3 CH(COO[CH 2 ] 11 OPhPhOCOPh(NO 2 )OC * H(Me)C 6 H 13 ) 2 are synthesized by hydrosilylation. The phase transition temperaturs are determined and the ferroelectric properties are investigated

Phase transitionMaterials sciencePolymers and PlasticsHydrosilylationTransition temperatureOrganic ChemistryBiphenyl derivativesFerroelectricitychemistry.chemical_compoundchemistryLiquid crystalPolymer chemistryMaterials ChemistrySide chainMacromolecular Rapid Communications
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Amphiphilic Linear-Hyperbranched Block Copolymers with Linear Poly(ethylene oxide) and Hyperbranched Poly(carbosilane) Block

2008

The synthesis of amphiphilic linear-hyperbranched block copolymers with a linear poly(ethylene oxide) (PEO) segment and a hyperbranched poly(carbosilane)s (PCS) block in a rapid three-step strategy is described, combining oxyanionic polymerization with carbosilane chemistry. A linear precursor block copolymer was synthesized via anionic polymerization of allyl glycidyl ether onto a commercial hydroxyl-terminated PEO, using its cesium alkoxide as macro-initiator. The resulting linear AB or ABA-type di- or triblock copolymers serve as polymer cores for the subsequent hydrosilylation polyaddition of an AB2-type carbosilane monomer. Di(allyl)methylsilane or methyldi(undec-10-enylsilane) were em…

Polymers and PlasticsEthylene oxideHydrosilylationAllyl glycidyl etherOrganic ChemistryRing-opening polymerizationInorganic Chemistrychemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryMacromolecules
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Modular Construction of Neutral and Anionic Carboranyl-Containing Carbosilane-Based Dendrimers

2007

A modular construction of new carbosilane dendrimers, which contain four and eight peripheral carborane derivatives and propyl linkages between the C cluster and the Si atoms, has been developed using different methodologies. Regiospecific hydrosilylation of 1-C 6 H 5 -2-(CH 2 CH=CH 2 )-1,2-closo-C 2 B 10 H 10 (1) and 1-CH 3 -2-(CH 2 CH=CH 2 )-1,2-closo-C 2 B 10 H 10 (2) offers an efficient route to molecular precursors and building blocks that can provide both divergent and convergent strategies for dendritic growth. First generations of neutral carboranyl-containing dendrimers were constructed by two approaches: (a) a divergent approach via hydrosilylation of 1 and 2 with the first genera…

Polymers and PlasticsHydrosilylationOrganic ChemistryOligomerInorganic Chemistrychemistry.chemical_compoundEnd-groupchemistryDendrimerYield (chemistry)Polymer chemistryMaterials ChemistryCluster (physics)MoleculeCarboraneMacromolecules
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Pd/C-Catalyzed Hydrosilylation of Enals and Enones with Triethylsilane: Conformer Populations Control the Stereoselectivity

2016

The palladium-on-charcoal-catalyzed chemo-, regio-, and stereoselective 1,4-hydrosilylation and transfer hydrogenation reactions of α,β-unsaturated aldehydes and ketones with triethylsilane have been investigated with a combination of experimental and theoretical methods. The reaction mechanism has been studied experimentally by monitoring the reactions by 1H NMR from aliquots withdrawn from the stirred reaction mixtures, labeling experiments, and control experiments. Our density functional theory results indicate that both aforementioned reactions are initiated with a dissociative adsorption of the triethylsilane on the palladium catalyst. In the hydrosilylation reaction, the α,β-unsaturat…

Reaction mechanismHydrosilylation010402 general chemistryTransfer hydrogenation01 natural sciencesMedicinal chemistryAldehydeDFTCatalysischemistry.chemical_compoundOrganic chemistryheterogeneousta116chemistry.chemical_classificationcatalysisstereoselective010405 organic chemistryChemistryHydridePd/ChydrosilylationGeneral ChemistryEnol0104 chemical scienceskatalyysitransfer hydrogenationreaction mechanismTriethylsilanechemoselective
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