Category: 1271-19-8

Electric Literature of 1271-19-8, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1271-19-8, Name is Titanocenedichloride, molecular formula is C10Cl2Ti. In a Article，once mentioned of 1271-19-8

The standard enthalpies of formation of the title crystalline complexes at 298.15 K have been determined by reaction-solution calorimetry.The results give DeltaHof = -379.2 +/- 8.0, DeltaHfo = -416.7 +/- 8.1 DeltaHof = -393.6 +/- 8.1, DeltaHof = -416.5 +/- 7.8, and DeltaHfo = 407.6 +/- 21.5 kJ mol-1.The metal-oxygen bond strengths have been evaluated as mean bond-disruption enthalpies () and as mean bond-enthalpy terms (E).The method of calculation of these values is analysed and earlier relevant thermochemical data are reviewed.

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 1271-19-8, molcular formula is C10Cl2Ti, introducing its new discovery. SDS of cas: 1271-19-8

Complexes <(C5H5)2MCl2> (M = Ti, Zr) react with the 2-(diphenyl-phosphino)phenol HO(C6H4)PPh2 in the presence of imidazole to give the corresponding complexes , 1 and (2: M = Ti; 3: M = Zr).Under the same experimental conditions, the bulkier ligand 2-(diphenylphosphinomethyl)-4-methylphenol HO(C6H3)(CH3)CH2PPh2 failed to react with (Ti or Zr) but with Cp2Zr(CH3)2 gives the methyl complex >, 4 and 2>, 5.Compounds 1 and 3 crystallize from CH2Cl2 solution, and their structures have been determined.The relatively short Zr-O bond distance of 1.979(7) Angstroem, and the Zr-O-C bond angle of 160.2(5) deg, in one phenoxy ligand of 3 suggest significant double bonding between Zr and O atoms.Chemical reduction of 1 with Na/Hg gives the expected cyclic P-metallated ZrIII species characterized by EPR (g = 1.976; a(31P) = 14.6 G.).Preliminary data indicate that 3 acts as a diphosphine ligand upon reaction with<2>. Keywords: Titanium; Zirconium; X-ray structure; Phenolato complexes; Phosphinophenolato complexes

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Chemistry is an experimental science, Formula: C10Cl2Ti, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1271-19-8, Name is Titanocenedichloride

The ring-opening metathesis polymerization (ROMP) of norbornene (NBE) with 11 substituted titanocene dichlorides and MeLi as catalysts was studied. The substituent effect showed that the catalytic activity was generally decreased as the substituents were introduced into the Cp ring. The more bulky the substituents, the lower the activity and the bis-substituted titanocene appeared to have an even lower catalytic activity. The molecular weight of polynorbornene (PNBE) also decreased as substituents are introduced on the Cp ring. But the molecular weight distribution and cis structure content have no significant differences compared with non-substituted titanocene complex as catalyst.

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 1271-19-8, name is Titanocenedichloride, introducing its new discovery. name: Titanocenedichloride

Binuclear titanocene complexes [Cp2Ti(tcm)]2O (4), [Cp2Ti(dca)]2O (5) and [Cp2Ti(dcnm)]2O (6) (tcm- = tricyanomethanide, dca- = dicyanamide and dcnm- = dicyanonitrosomethanide) were synthesized in moderate yields by the reaction of Cp2TiCl2 (1) with respective alkali metal pseudohalide salts in the aqueous solution. When the reaction was carried out in dry organic solvents, mononuclear compounds Cp2Ti(tcm)2 (2) and Cp2Ti(dca)2 (3) were isolated. Preparation of dipseudohalide complex Cp2Ti(dcnm)2 by this manner was unsuccessful due to decomposition of dcnm ligand resulting in formation of oxygen-bridged compound 6. All prepared compounds were characterized by elemental analysis, NMR, Raman, infrared and UV-Vis spectroscopy. Molecular structures of 2, 4 and 6 (two polymorphs) have been determined by single-crystal X-ray diffraction analysis.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 1271-19-8 is helpful to your research. name: Titanocenedichloride

Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Chemistry is an experimental science, Computed Properties of C10Cl2Ti, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1271-19-8, Name is Titanocenedichloride

An unusual early-late bimetallic complex with direct metal-metal bonding is obtained from a phosphinoenolate ligand-assisted reaction between Ti(IV) and Pt(0) reagents which occurs by formal insertion of the Pt(0) centre into a Ti(IV)-O bond; X-ray data and EHMO calculations indicate the presence of a quasi-covalent Ti(III)-Pt(I) bond (2.721(2) A).

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Application In Synthesis of Titanocenedichloride, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1271-19-8, Name is Titanocenedichloride, molecular formula is C10Cl2Ti. In a Article, authors is Bhagi, Ajay K.，once mentioned of 1271-19-8

The complexes of the types and (where Cp = cyclopentadienyl; M = Ti or Zr; A = monobasic anion of 3-indoleacetic acid, 3-indolepropionic acid, 3-indolebutyric acid or l-tryptophan) have been synthsized by reaction of dichlorobis(cyclopentadienyl)titanium(IV) (Cp2TiCl2) or dichlorobis(cyclopentadienyl)zirconium(IV) (Cp2ZrCl2) with heterocyclic carboxylic acids in 1:1 and 1:2 molar ratios.The new complexes have been characterized by their elemental analyses, conductivity measurements, electronic, IR and 1H NMR spectral studies.

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 1271-19-8, molcular formula is C10Cl2Ti, introducing its new discovery. Computed Properties of C10Cl2Ti

The 4-alkenylbis(eta5-cyclopentadienyl)titanium(IV) chlorides 2 – 4 and 20 – 23 have been prepared from Cp2TiCl2 (1) and the appropriate organomagnesium halides. 1H and 13C NMR investigations indicate that in these compounds as well as in the 1:1 complexes 5 – 7 and 24 formed with ethylaluminium dichloride the C=C-bond of the alkenyl group is not complexed to the Ti. omega-Alkenyl complexes of TiIII of the type Cp2TiCH2nCH=CH2 (n = 0-11) isomerize between 0 and 20 deg C through a betaH-elimination mechanism to give the eta3-allylbis(eta5-cyclopentadienyl)titanium(III ) compounds 9-15.In the titanium(III) complexes 18 and 19 the betaH-elimination process is more difficult.In 18 the C=C valence stretching frequency is shifted to longer wave length to 1510 cm-1.This is interpreted by eta2-interaction of the C=C bond with titanium.

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Synthetic Route of 1271-19-8, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1271-19-8, Name is Titanocenedichloride, molecular formula is C10Cl2Ti. In a Article，once mentioned of 1271-19-8

The titanocene dicarbonyl dication [TiCp2(CO)2][BPh4]2, (1) has been obtained in toluene under carbon monoxide by double protonation of TiCp4 with [NHnBu3][BPh4] or by two-electron oxidation of TiCp2(CO)2 with [FeCp2][BPh4]. Protonation reactions on ZrCp4 and HfCp4 proceed with elimination of 1 mol of cyclopentadiene independently on the ammonium salt/MCp4 molar ratio used. By this route the high electrophilic, solvent-free [ZrCp3]+ cation has been isolated and characterized by IR, 1H-NMR and elemental analysis. In the case of hafnium, the isolation has not been possible; nevertheless, in the presence of CO a rare example of a carbonyl derivative of hafnium(IV), [HfCp3(CO)][BPh4], has been isolated and characterized.

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent， Product Details of 1271-19-8, Which mentioned a new discovery about 1271-19-8

A method for the transformation of o-allyl aryl ketones to gamma- butyrolactones using a catalytic amount of Cp2Ti(PMe3)2 or Cp2Ti(CO)2 iS described. This catalytic ‘hetero Pauson-Khand’-type process proceeds via the carbonylation of an oxatitanacycle followed by thermally-induced reductive elimination to form a gamma-butyrolactone and to regenerate the catalyst. We have investigated the scope and limitations of this catalytic methodology. Our results are consistent with the view that the key step in this catalytic cycle is formation of a charge transfer complex or involves reversible electron transfer between the catalyst and the substrate.

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Related Products of 1271-19-8, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1271-19-8, Name is Titanocenedichloride, molecular formula is C10Cl2Ti. In a article，once mentioned of 1271-19-8

No two ways about it: In the photocatalytic deoxygenation of epoxides, the TiO2 particle concertedly transfers two stored electrons to generate a carbanion intermediate, which dissociates to the alkene product. This pathway ensures the higher alkene and stereoselectivity of the photocatalytic deoxygenation than those involving a single-electron transfer. Copyright

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Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI