Search results for "C C coupling"

showing 10 items of 23 documents

SBA-15/POSS-Imidazolium Hybrid as Catalytic Nanoreactor

2019

Supported imidazolium modified polyhedral oligomeric silsesquioxanes (POSS) on SBA-15 have been used as platform for Pd(II) species. The so-obtained material was firstly characterized by means of TGA, solid state NMR, TEM, XPS, SAXS, porosimetry and ICP-OES and it was successfully tested as pre-catalyst in C−C cross couplings, namely Suzuki-Miyaura and Heck reactions. In both cases, the solid proved to be highly efficient and easily recoverable from the reaction mixture. The recyclability was verified for up to seven cycles without showing any activity decrease. Interestingly, only Pd(II) was detected in the reused catalyst in the Heck reaction. Therefore, the versatility of the material w…

ChemistryC−C couplingchemistry.chemical_elementGeneral ChemistryNanoreactorSettore CHIM/06 - Chimica OrganicaHeterogeneous catalysispalladiumCoupling reactionCatalysisC c couplingHeck reactionheterogeneous catalysisHeck reactionPolymer chemistryheterogeneous catalysiSuzuki-Miyaura reactionPalladiumAdvanced Synthesis and Catalysis
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Developments in the dehydrogenative electrochemical synthesis of 3,3′,5,5′-tetramethyl-2,2′-biphenol

2021

Abstract The symmetric biphenol 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol is a well‐known ligand building block and is used in transition‐metal catalysis. In the literature, there are several synthetic routes for the preparation of this exceptional molecule. Herein, the focus is on the sustainable electrochemical synthesis of 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol. A brief overview of the developmental history of this inconspicuous molecule, which is of great interest for technical applications, but has many challenges for its synthesis, is provided. The electro‐organic method is a powerful, sustainable, and efficient alternative to conventional synthesis to obtain this symmetric biphenol up to the …

Green chemistry540 Chemistry and allied sciencespolycycles010405 organic chemistryChemistryoxidationOrganic ChemistryC−C couplingMinireviewsGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesC c couplingelectrochemistry540 Chemiesustainable chemistryMinireviewC−C Coupling | Reviews Showcase
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Palladium Supported on Cross-Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions

2013

Highly cross-linked imidazolium-based materials, obtained by radical oligomerization of bis-vinylimidazolium salts in the presence of 3-mercaptopropyl-modified silica gel, were used as supports for palladium catalysts. Thanks to the high imidazolium loading these materials were able to support a high amount of the metal (10 wt%). Such materials were characterized by several techniques (13C magic angle spinning nuclear magnetic resonance, the Brunauer-Emmett-Teller technique, X-ray photoelectron spectroscopy, and transmission electron microscopy). The palladium catalysts displayed good activity allowing the synthesis of several biphenyl compounds in high yields working with only 0.1 mol% of …

Green chemistryflow chemistryInorganic chemistrychemistry.chemical_elementCatalysisMetalchemistry.chemical_compoundSuzuki reactionMagic angle spinningsustainable chemistry; catalysis flow chemistrysustainable chemistryC C couplingSuzuki-Miyaura reactioncatalyst recyclingBiphenylcatalysisSilica gelSettore CHIM/06 - Chimica OrganicaGeneral ChemistrypalladiumSuzuki–Miyaura reactionchemistryvisual_artvisual_art.visual_art_mediumC-C couplingPalladiumAdvanced Synthesis & Catalysis
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MoVReagents in Organic Synthesis (Eur. J. Org. Chem. 11/2016)

2016

C c couplingchemistry.chemical_compoundchemistryMolybdenumReagentOrganic Chemistrychemistry.chemical_elementOrganic chemistryOxidative coupling of methaneOrganic synthesisPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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A Decade of Electrochemical Dehydrogenative C,C-Coupling of Aryls.

2019

The importance of sustainable and green synthetic protocols for the synthesis of fine chemicals has rapidly increased during the last decades in an effort to reduce the use of fossil fuels and other finite resources. The replacement of common reagents by electricity provides a cost- and atom-efficient, environmentally friendly, and inherently safe access to novel synthetic routes. The selective formation of carbon-carbon bonds between two distinct substrates is a crucial tool in organic chemistry. This fundamental transformation enables access to a broad variety of complex molecular architectures. In particular, the aryl-aryl bond formation has high significance for the preparation of organ…

010405 organic chemistryChemistrybusiness.industryFossil fuelMolecular ConformationGeneral MedicineGeneral ChemistryElectrochemical Techniques010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryHydrocarbons Aromatic0104 chemical sciencesC c couplingHydrogenationbusinessAccounts of chemical research
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Front Cover Picture: SBA‐15/POSS‐Imidazolium Hybrid as Catalytic Nanoreactor: the role of the Support in the Stabilization of Palladium Species for C…

2019

C c couplingFront coverchemistryHeck reactionPolymer chemistrychemistry.chemical_elementGeneral ChemistryNanoreactorHeterogeneous catalysisCoupling reactionPalladiumCatalysisAdvanced Synthesis & Catalysis
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Inside Cover: Regioselective Metal‐ and Reagent‐Free Arylation of Benzothiophenes by Dehydrogenative Electrosynthesis (Angew. Chem. Int. Ed. 40/2018)

2018

ChemistryINTRegioselectivityGeneral ChemistryElectrosynthesisElectrochemistryCatalysisMetalC c couplingvisual_artReagentPolymer chemistryvisual_art.visual_art_mediumCover (algebra)Angewandte Chemie International Edition
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Templating effect of carbon nanoforms on highly cross-linked imidazolium network: Catalytic activity of the resulting hybrids with Pd nanoparticles

2019

Two different carbon nanoforms (CNFs), namely multi-walled carbon nanotubes (MWCNTs) and carbon nanohorns (CNHs), have been chosen as support for the direct polymerization of a bis-vinylimidazolium salt. Transmission electron microscopy analyses revealed a templating effect of the CNFs on the growth of the polymeric network, which perfectly covers their whole surfaces creating a cylindrical or spherical coating for MWCNTs and CNHs, respectively. Subsequently, the CNFs-polyimidazolium have been used as stabilizers for Pd nanoparticles (Pd NPs), and the obtained materials have been characterized by means of analytical and spectroscopic techniques and then employed as easily recoverable and re…

chemistry.chemical_elementSettore CHIM/06 - Chimica OrganicaGeneral ChemistryHeterogeneous catalysisCatalysisnanotubesInorganic ChemistrySuzuki–Miyaura reactionC c couplingHeck reactionheterogeneous catalysischemistryHeck reactionPd nanoparticlesPolymer chemistrynanotubeheterogeneous catalysiC-C couplingSuzuki-Miyaura reactionCarbon
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Intramolecular coupling of acetylenic groups of bis(alkynyl)phosphanes and silanes mediated by benzynezirconocene: a route to new mono- and tricyclic…

2004

Benzo-zirconacyclohexadiene-phospha or silacyclobutene fused ring systems are easily prepared via a benzynezirconocene intermediate by means of thermolysis of Cp 2 ZrPh 2 in the presence of bis(alkynyl)phosphanes or silanes. These polyunsaturated systems are the source of a variety of new mono- or tricyclic heterocycles incorporating either one or two heteroatoms.

chemistry.chemical_classificationSilanesChemistryOrganic ChemistryHeteroatomThermal decompositionGeneral MedicinePhotochemistryRing (chemistry)BiochemistryMedicinal chemistryCoupling (electronics)chemistry.chemical_compoundC c couplingMain group elementIntramolecular forcePolymer chemistryDrug DiscoveryTricyclicTetrahedron
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Cross-Linked Thiazolidine Network as Support for Palladium: A New Catalyst for Suzuki and Heck Reactions

2015

A thiazolidine-based material was used for the first time as support for palladium. The support was prepared by starting from a highly cross-linked thiazolium-based material, obtained by radical oligomerization of a bisvinylthiazolium dibromide salt in the presence of 3-mercaptopropyl-modified silica SBA-15. Palladium was immobilized by treatment with tetrachloropalladate salt. Reduction with sodium borohydride afforded a thiazolidine-based material that acted as ligands for the Pd species. The thiazolidine-based palladium catalyst was fully characterized and, working in only 0.1 mol% amount, displayed good activity in the Suzuki-Miyaura and in the Heck reactions. Several biphenyl and alken…

metal catalysisThiazolidinechemistry.chemical_elementHeterogeneous catalysisCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundC c couplingN ligandsHeck reactioncross-couplingOrganic chemistryPhysical and Theoretical ChemistryS ligandsgreen chemistryOrganic ChemistrySettore CHIM/06 - Chimica Organicapalladiumheterogeneous catalysischemistryheterogeneous catalysis cross-coupling metal catalysis green chemistryheterogeneous catalysiC-C couplingPalladiumN ligand
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