Search results for "zirconocene"

showing 10 items of 11 documents

Versatile behavior of conjugated diynes with zirconocene reactive species

2008

Thermal decomposition of Cp2ZrPh2 in the presence of the buta-1,3-diynes RC≡CC≡CR (R = Ph, SiMe3) can lead to seven- or five-membered metallacycles. In both cases a stable benzo-fused seven-membered zirconacyclocumulene arising from a 2-fold insertion of the triple bonds of the dialkyne in the in situ generated zirconocene benzyne is formed. In the case of Me3SiC≡CC≡CSiMe3 a second minor complex is isolated: a 3-alkynyl-substituted zirconaindene arising from a β monoinsertion of one acetylenic function of the conjugated diyne in the zirconocene benzyne. No stable 2-alkynyl-substituted zirconacycle was isolated. This α monoinsertion complex is an intermediate in the exchange of the metalated…

010405 organic chemistryChemistrycycloaddition reactionOrganic ChemistryThermal decomposition[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementmetalationConjugated system010402 general chemistryTriple bond01 natural sciencesAryne0104 chemical sciencesInorganic ChemistrycyclometalationAntimonyReagentAtomPolymer chemistryMoiety[CHIM.COOR]Chemical Sciences/Coordination chemistryzirconocene- benzyn intermediatePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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Reactivity of di-n-butyl-dicyclopentadienylzirconium towards amido stabilized stannylenes

2009

Abstract Reaction of Sn[(N(C 6 H 3 i Pr 2 -2,6)(SiMe 3 )] 2 and [{Sn(N(C 6 H 3 i Pr 2 -2,6)(SiMe 3 )(μ-Cl) 2 ] with di- n -butyl-dicyclopentadienylzirconium yielded the trimetallic a carbene-like complex {[(N(C 6 H 3 i Pr 2 -2,6)(SiMe 3 )]( n -Bu)Sn} 2 Cp 2 Zr. The oxidation of {[(N(C 6 H 3 i Pr 2 -2,6)(SiMe 3 )]( n -Bu)Sn} 2 Cp 2 Zr by oxygen gives the five-membered dioxadistannazirconacyclic complex {[(N(C 6 H 3 i Pr 2 -2,6)(SiMe 3 )]( n -Bu)Sn} 2 O 2 Cp 2 Zr.

010405 organic chemistryoxidationOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryOxygenMedicinal chemistryNMR0104 chemical sciences3. Good healthInorganic ChemistrychemistryzirconoceneMaterials ChemistryReactivity (chemistry)stannylene[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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A Comprehensive Experimental and Theoretical Study on the [{(η5-C5H5)2Zr[P(µ-PNEt2)2P(NEt2)2P]}]2O Crystalline System

2021

The structure of tetraphosphetane zirconium complex C52H100N8OP10Zr21 was determined by single crystal X-ray diffraction analysis. The crystal belongs to the monoclinic system, space group P21/c, with a = 19.6452(14), b = 17.8701(12), c = 20.7963(14)Å, α = γ = 90°, β = 112.953(7)°, V = 6722.7(8)Å3, Z = 4. The electronic structure of the organometallic complex has been characterized within the framework of Quantum Chemical Topology. The topology of the Electron Localization Function (ELF) and the electron density according to the Quantum Theory of Atoms in Molecules (QTAIM) show no covalent bonds involving the Zr atom, but rather dative, coordinate interactions between the metal and the liga…

Organic ChemistryPharmaceutical SciencephosphetaneX-ray crystal structureArticleAnalytical ChemistryQD241-441ELFQTAIMChemistry (miscellaneous)zirconoceneX-ray crystal structure; zirconocene; phosphetane; ELF; QTAIMDrug DiscoveryMolecular MedicinePhysical and Theoretical ChemistryMolecules
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Copolymerization of ethylene with 1‐hexene over metallocene catalyst supported on complex of magnesium chloride with tetrahydrofuran

2004

The study of ethylene/1-hexene copolymerization with the zirconocene catalyst, bis(cyclopentadienyl)zirconium dichloride (Cp 2 ZrCl 2 )/methylaluminoxane (MAO), anchored on a MgCl 2 (THF) 2 support was carried out. The influence of 1-hexene concentration in the feed on catalyst productivity and comonomer reactivity as well as other properties was investigated. Additionally, the effect of support modification by the organoaluminum compounds [(MAO, trimethylaluminum (AlMe 3 ), or diethylaluminum chloride (Et 2 AlCl)] on the behavior of the MgCl 2 (THF) 2 /Cp 2 ZrCl/MAO catalyst in the copolymerization process and on the properties of the copolymers was explored. Immobilization of the Cp 2 ZrC…

Polymers and PlasticssupportsOrganic Chemistrymetallocene catalystsMethylaluminoxaneHomogeneous catalysisethylene/1‐hexene copolymersmagnesium supportPost-metallocene catalystzirconocene catalystCatalysischemistry.chemical_compoundcopolymerizationchemistryCyclopentadienyl complexHexenePolymer chemistryMaterials ChemistryMetalloceneTetrahydrofuranJournal of Polymer Science. Part A : Polymer Chemistry
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CCDC 215636: Experimental Crystal Structure Determination

2004

Related Article: E.Ortega, N.Pirio, P.Meunier, B.Donnadieu|2004|Chem.Commun.||678|doi:10.1039/b312954c

Space GroupCrystallographyCrystal SystemCrystal Structuremeso-bis((mu~2~-1-Diphenylphosphino-3-phenyl-3-thiolato-propenyl-CS)-zirconocene)Cell ParametersExperimental 3D Coordinates
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Insertion Reactions of Neutral Phosphidozirconocene Complexes as a Convenient Entry into Frustrated Lewis Pair Territory

2016

International audience; Neutral phosphidozirconocene complexes [Cp2Zr(PR2)Me] (Cp=cyclopentadienyl; 1a: R=cyclohexyl (Cy); 1b: R=mesityl (Mes); 1c: R=tBu) undergo insertion into the Zr-P bond by non-enolisable carbonyl building blocks (O=CRR), such as benzophenone, aldehydes, paraformaldehyde or CO2, to give [Cp2Zr(OCRRPR2)Me] (3-7). Depending on the steric bulk around P, complexes 3-7 react with B(C6F5)(3) to give O-bridged cationic zirconocene dimers that display typical frustrated Lewis pair (FLP)/ambiphilic ligand behaviour. Thus, the reaction of {[Cp2Zr(-OCHPhPCy2)][MeB(C6F5)(3)]}(2) (10a) with chalcone results in 1,4 addition of the Zr+/P FLP, whereas the reaction of {[Cp2Zr(-OCHFcPCy…

Steric effectsChalconeStereochemistryzirconiumc-h activation010402 general chemistry01 natural sciencesMedicinal chemistry[ CHIM ] Chemical SciencesCatalysisFrustrated Lewis pairinsertionchemistry.chemical_compoundCyclopentadienyl complexx-ray structuresphosphinidene complexesBenzophenone[CHIM]Chemical SciencesParaformaldehydezr-p bondzirconocene-phosphido complexesmolecular-structure010405 organic chemistryLigandphosphidesOrganic ChemistryCationic polymerizationcrystal-structureGeneral Chemistry0104 chemical sciencesfunctionalized ligandsbis(trimethylsilyl)phosphido complexeschemistryfrustrated Lewis pairsphosphinoaryloxide complexesambiphilic ligands
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Exploring reactivity of a bis-sulfonium zirconocene-ate dimer: synthesis of various zwitterionic phosphonium anionic zirconocene complexes

2007

Abstract Formal [3+2] cycloaddition reactions between the bis-sulfonium zirconocene-ate dimer 1a and methylpropiolate, benzaldehyde and carbon disulfide afforded stable zwitterionic phosphonium zirconocene-ate complexes 2–4, respectively, with two orthocondensed five-membered heterocycles. X-ray crystal structure of 4 has been determined. Elemental chalcogens (S, Se, Te) gave rise also to a new variety of five-coordinate zirconium(IV) complexes (5–7) by a formal [3+1] cycloaddition reaction. In these bicyclic zirconates, sulfur is included in a five-membered ring while the second chalcogen is in a four-membered one.

SulfoniumDimer010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryInorganic ChemistryBenzaldehydechemistry.chemical_compoundChalcogenanionic zirconoceneMaterials ChemistryOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)PhosphoniumPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSBicyclic molecule010405 organic chemistrysulfoniumOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryzirconocene-atephosphoniumCycloaddition3. Good health0104 chemical scienceschemistrychalcogenszwitterionic complexes
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Studies on ethylene/1-hexene copolymerization over the zirconocene catalyst supported on MAO-modified MgCl2(THF)2. The effect of copolymerization con…

2002

Badania dotyczą układu katalitycznego MgCl2(THF)2/MAO/Cp2ZrCl2/MAO (MAO — metyloaluminoksan). Stwierdzono, że zarówno aktywność tego układu katalitycznego, jak i właściwości kopolimerów w znacznym stopniu zależą od stosunku molowego Al:Zr (zmienianego w przedziae 1500—7000) i od temperatury kopolimeryzacji (tabele 1 i 2), natomiast wpływ czasu kopolimeryzacji jest mniejszy (tabela 3). Aktywność katalizatora oraz zawartość 1-heksenu wbudowanego do kopolimeru zwiększają się ze wzrostem temperatury i stosunku Al:Zr, a jednocześnie maleje ciężar cząsteczkowy i temperatura topnienia produktów. Ustalono także, że osadzenie katalizatora cyrkonocenowego na stosowanym nośniku powoduje zwiększenie je…

aktywność katalizatoracopolymer propertieskopolimeryzacja etylenu z 1-heksenemnośnikowy katalizator cyrkonocenowycopolymerization of ethylene with 1-hexenewłaściwości kopolimerówcatalyst activitywarunki kopolimeryzacjicopolymerization conditionssupported zirconocene catalystPolimery
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Zirconocene-Based Methods for the Preparation of BN-Indenes : Application to the Synthesis of 1,5-Dibora-4a,8a-diaza-1,2,3,5,6,7-hexaaryl-4,8-dimethy…

2017

A method for the preparation of 3-bora-9aza-indene heterocycles based on zirconocene mediated functionalization of the ortho-CH bonds of pyridines has been developed and used to make two such compounds. Unlike other methods, the boron center in these heterocycles remains functionalized with a chloride ligand and so the compounds can be further elaborated through halide abstraction and reduction. The utility of the method was further demonstrated by applying it towards the preparation of 1,5- dibora-4a,8a-diaza BN analogues of the intriguing hydrocarbon s-indacene starting from 2,5-dimethylpyrazine. Gram quantities of one such compound was prepared and fully characterized, and both experimen…

chemistry.chemical_classification010405 organic chemistryLigandOrganic ChemistryHalidechemistry.chemical_elementAromaticity010402 general chemistry01 natural sciencesChloride0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundHydrocarbonchemistryBN-indenesmedicineOrganic chemistrySurface modificationzirconocene-based methodsPhysical and Theoretical ChemistryBoronta116Derivative (chemistry)medicine.drug
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Studies of ethylene/1-hexene copolymerization over zirconocene catalyst supported on MAO-modified MgCl2(THF)2. The effect of copolymerization conditi…

2003

Composition of catalytic system and copolymerization reaction conditions influence on heterogeneity of ethylene/1-hexene copolymers obtained over MgCI2(THF)2/MAO/Cp2ZrCl2/MAO catalyst was studied. One of the DSC techniques, i.e. successive self-nucleation/annealing (SSA) method allowing separation of the polymer into fractions with differing chemical composition in result of alternating crystallization and melting cycles was applied. It was found that the intermolecular heterogeneity exists inside all studied samples irrespective of the reaction conditions (temperature and time) and the catalyst composition (Al/Zr molar ratio). It was also confirmed that catalyst composition has a considera…

lamella thicknessintermolecular heterogeneityethylene/1-hexene copolymerszirconocene catalystSSA methodPolimery
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