Search results for "PALLADIUM"

showing 10 items of 956 documents

CCDC 849920: Experimental Crystal Structure Determination

2011

Related Article: Francisco Estevan, Pipsa Hirva, Mercedes Sanaú, MaAngeles Úbeda|2018|Organometallics|37|2980|doi:10.1021/acs.organomet.8b00342

bis(mu~2~-2-(diphenylphosphanyl)phenyl)-bis(mu~2~-(4-methylphenyl)([(4-methylphenyl)imino]methyl)aminato)-di-palladium dichloromethane solvate monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 616084: Experimental Crystal Structure Determination

2007

Related Article: S.Chikkali, D.Gudat, M.Niemeyer|2007|Chem.Commun.||981|doi:10.1039/b616102b

bis(mu~2~-3-(Diphenylphosphinoylmethyl)benzene-12-diolato)-dichloro-palladium(ii)-tin(iv) dichloromethane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1541823: Experimental Crystal Structure Determination

2017

Related Article: Svetlana A. Katkova, Mikhail A. Kinzhalov, Peter M. Tolstoy, Alexander S. Novikov, Vadim P. Boyarskiy, Anastasiia Yu. Ananyan, Pavel V. Gushchin, Matti Haukka, Andrey A. Zolotarev, Alexander Yu. Ivanov, Semen S. Zlotsky, Vadim Yu. Kukushkin|2017|Organometallics|36|4145|doi:10.1021/acs.organomet.7b00569

bis{(t-butylamino)[(NN'-diphenylcarbamimidoyl)imino]methyl}-palladium(ii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Palladium-catalyzed heteroaryl thioethers synthesis overcoming palladium dithiolate resting states inertness: Practical road to sulfones and NH-sulfo…

2018

International audience; We provide efficient synthetic access to heteroaryl sulfones in two-steps using a simple palladium-1,1'-bis [(diphenyl)phosphanyl]ferrocene catalyst to form in high yields variously functionalized heteroaromatic thioethers. Pyridinyl-containing substrates can be subsequently selectively oxidized into sulfones and NH-sulfoximines by using very mild oxidation conditions with a high functional group tolerance. In the palladium catalyzed C-S coupling of heteroaromatic thiols, reactivity limitation is attached with electron-deficient thiols. We show that this limitation can be resolved by the successful use of 2-bromoheteroarenes in the C-S coupling. We established herein…

bond formationarenessulfideschemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisefficientCatalysischemistry.chemical_compounds-arylation[CHIM]Chemical SciencesReactivity (chemistry)SulfonesResting statethiols[PHYS]Physics [physics]010405 organic chemistryProcess Chemistry and TechnologyGeneral Chemistryindolesacid saltsCombinatorial chemistry0104 chemical sciencesThiolatesC-S couplingchemistryFerroceneNH-sulfoximinesReagentElectrophileFunctional groupH functionalizationdirecting groupPalladiumStoichiometryPalladiumCatalysis Communications
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Materiali catalitici a base di nanoparticelle di palladio immobilizzate su nanoforme di carbonio

2019

carbon nanostructurecarbon nanohornpalladium catalysihybrid materialcarbon nanotubeC-C cross-couplingimidazolium salt
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Hydrogenation of but-2-yne-1,4-diol on a palladium cluster: a computational study

2013

catalysisDFT calculationpalladium cluster
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Density Functional Theory Investigation on the Nucleation and Growth of Small Palladium Clusters on a Hyper-Cross-Linked Polystyrene Matrix

2014

Density functional theory calculations were employed to investigate the nucleation and growth of small palladium clusters, up to Pd9, into a microcavity of the porous hyper-cross-linked polystyrene (HPS). The geometries and the electronic structures of the palladium clusters inside the HPS cavity, following the one-by-one atom addition, are affected by a counterbalance between the Pd–phenyl (Pd−Φ) and Pd–Pd interactions. The analysis performed on energetics, cavity distortions, and cluster geometries indeed suggest that the cluster growth is dominated by the Pd−Φ interactions up to the formation of Pd4 aggregates, whereas the metal–metal interactions actually rule the growth of the larger c…

catalysispolymeric supportNucleationchemistry.chemical_elementSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (mathematics)chemistry.chemical_compoundGeneral EnergychemistryChemical physicsComputational chemistryAtomCluster (physics)Density functional theoryPolystyrenePhysical and Theoretical ChemistryElasticity (economics)Metal nanoparticlemetal-phenyl interactionPalladiumThe Journal of Physical Chemistry C
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Multi-layered, covalently supported ionic liquid phase (mlc-SILP) as highly cross-linked support for recyclable palladium catalysts for the suzuki re…

2011

The reaction between an excess of 1,4-bis(3-vinylimidazolium-1-yl) bromide and a mercaptopropyl-modified amorphous silica gel or ordered mesoporous silica SBA-15 in the presence of azobisisobutyronitrile (AIBN) afforded new materials, which have a high loading of imidazolium moieties. These materials, which contain a highly cross-linked polymeric network, have been denoted as multi-layered, covalently supported ionic liquid phase (mlc-SILP) and have been used as support for palladium catalysts containing a high loading of the metal (10 wt%). Such materials were characterized by several techniques (13C magic angle spinning nuclear magnetic resonance, the Brunauer–Emmett–Teller technique, sma…

catalyst recyclingInorganic chemistryAzobisisobutyronitrilechemistry.chemical_elementGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMesoporous silicapalladiumCatalysisBiphenyl compoundchemistry.chemical_compoundSuzuki reactionchemistryIonic liquidMagic angle spinningPalladiumionic liquidAdvanced Synthesis and Catalysis
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A general diastereoselective synthesis of highly functionalized ferrocenyl ambiphiles enabled on a large scale by electrochemical purification

2017

International audience; A general synthesis of highly functionalized ferrocenes, which include (P,B)- and (N,B)-ambiphiles, has been developed at a multigram scale. Diastereoselective stepwise modification of di-tert-butylated ferrocenes included the unprecedented separation of electroactive species. Bulky alkyl groups on ferrocenes ensure planar chirality of ambiphiles and enforce closer proximity of antagonist Lewis functions.

catalytic applicationsPlanar chirality010402 general chemistryElectrochemistrycarbon-dioxide01 natural sciences[ CHIM ] Chemical SciencesCatalysisMaterials ChemistryOrganic chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryfree hydrogen activationaryl bromidesAlkylchemistry.chemical_classificationcomplexes010405 organic chemistryChemistryligandsdirect arylationMetals and AlloysGeneral ChemistrypalladiumCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsfrustrated lewis pairsCeramics and Compositescoordination chemistry
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CCDC 266218: Experimental Crystal Structure Determination

2005

Related Article: F.Bonadio, M.-C.Senna, J.Ensling, A.Sieber, A.Neels, H.Stoeckli-Evans, S.Decurtins|2005|Inorg.Chem.|44|969|doi:10.1021/ic049209u

catena-(bis(mu~2~-Cyano)-dicyano-(213-dimethyl-312-diaza-69-dioxa-1(26)-pyridinacyclotridecaphane-212-diene)-manganese(ii)-palladium(ii))Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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