Day: March 18, 2021

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Titanocene and zirconocene complexes containing dendrimer-substituted cyclopentadienyl ligands – Synthesis and ethylene polymerization

This paper describes the synthesis of a series of titanium and zirconium metallocenes bearing one or two first-generation silane dendritic wedges as bulky substituents at their cyclopentadienyl rings. Wedges (R2R?SiCH2CH2)3SiCl [R = R? = Et (1); R = Ph, R? = Me (2)] were prepared by hydrosilylation of chlorotrivinylsilane with R2R?SiH. They were reacted with K(C5H5 and, subsequently, with KH to give K[(R2R?SiCH2 CH2)3Si(C5H4)] [R = R? = Et (3); R = Ph, R? = Me (4)]. The dendronized cyclopentadienides 3 and 4 were the starting materials for preparation of the mixed-ring titanocenes [{(R2R?SiCH2 CH2)3SiC5H4} (C5R?5)TiCl2] [R = R? = Et, R? = H (5), R? = Me (6); R = Ph, R? = Me, R? = H (7), R? = Me (8)] or the symmetrically substituted metallocenes [{(Ph2MeSiCH2 CH2)3SiC5 H4}2MCl2] [M = Ti (9), Zr (10)]. Cyclic voltammograms and catalytic behavior of all the new metallocenes in ethylene polymerization, using MAO as a co-catalyst, have been studied and compared to that of related non-dendritic complexes. Polyethylene polydispersities increase with the number of dendritic wedges in the catalyst, while activities decrease. Bimodal molecular weight distributions were clearly observed for the bis-dendritic titanocene 9. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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

Related Products of 344-25-2, 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.344-25-2, Name is H-D-Pro-OH, molecular formula is C5H9NO2. In a article£¬once mentioned of 344-25-2

Enantioselective approach to 13a-methylphenanthroindolizidine alkaloids

The first enantioselective approach to 13a-methylphenanthroindolizidine alkaloids is reported, featuring an efficient stereoselective Seebach’s alkylation and Pictet-Spengler cyclization. The proposed and other three most probable structures were ruled out, indicating hypoestestatin 1 needs further assignment.

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

Electric Literature of 4408-64-4, In heterogeneous catalysis, the catalyst is in a different phase from the reactants. At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 4408-64-4, name is 2,2′-(Methylazanediyl)diacetic acid. In an article£¬Which mentioned a new discovery about 4408-64-4

A general method for interconversion of boronic acid protecting groups: Trifluoroborates as common intermediates

We have developed a general protocol for the interconversion of diverse protected boronic acids, via intermediate organotrifluoroborates. N-Methyliminodiacetyl boronates, which have been hitherto resistant to direct conversion to trifluoroborates, have been shown to undergo fluorolysis at elevated temperatures. Subsequent solvolysis of organotrifluoroborates in the presence of trimethylsilyl chloride and a wide range of bis-nucleophiles enables the generation of a variety of protected boronic acids.

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

Synthetic Route of 1941-30-6, 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. 1941-30-6, Name is Tetrapropylammonium bromide, molecular formula is C12H28BrN. In a Article£¬once mentioned of 1941-30-6

Synthesis and modification of ZSM-5 with manganese and lanthanum and their effects on decolorization of indigo carmine dye

Hydrothermally synthesized ZSM-5 zeolite modified by manganese (Mn/ZSM-5) or lanthanum (La/ZSM-5) or mixture of both (Mn-La/ZSM-5) using impregnation technique was characterized by powder XRD, FTIR and N2 adsorption measurements. These materials were tested for discoloration (adsorption) and mineralization (in the presence of UV irradiation) of indigo carmine (IC) dye. The results indicate that MnOx incorporated ZSM-5 that showed the highest lattice volume and pore radius between all samples presented the highest photocatalytic activity, comparatively. However, the Mn-La/ZSM-5 catalyst exhibited the lowest activity even when compared with the parent ZSM-5 sample. This was in part due to evoking of Mn3O4 species at the expense of Mn2O3 ones, which were proposed to be the active sites of the reaction. This reaction was found to be acidity dependent since Mn/ZSM-5 showed significant bands at 3650 and 3619 cm -1 those in contrast appeared shapely in La/ZSM-5, whereas for Mn-La/ZSM-5 only a band at 3619 cm-1 was obtained. On the other hand, the decolorization activity showed comparable high rates for Mn/ZSM-5 and Mn-La/ZSM-5 samples (100% removal) implying that the adsorption process is more referred to acid-base site pairs where the photocatalytic activity seems to be more restricted to acidic sites. The influence of pH, catalyst amount and time on the decolorization rate of IC on Mn/ZSM-5 was thoroughly investigated and correlated with ZPC of MnOx species, various exposed species of MnOx and surface properties.

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

Synthetic Route of 29841-69-8, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.29841-69-8, Name is (1S,2S)-(-)-1,2-Diphenylethylenediamine, molecular formula is C14H16N2. In a Article£¬once mentioned of 29841-69-8

Chiral diphenylselenophosphoramides: A new class of chiral ligands for the titanium(IV) alkoxide-promoted addition of diethylzinc to aldehydes

Chiral C2-symmetric diphenylselenophosphoramides 1 and 2 were prepared from the reaction of diphenylselenophosphinic chloride with (1R,2R)-(-)-1,2-diaminocyclohexane and (1R,2R)-(+)-1,2-diphenylethylenediamine, respectively, in high yields. Another novel chiral ligand 3 was prepared from the reaction of diphenylselenophosphinic chloride with (R)-(+)-1,1′-binaphthyl-2,2′-diamine using butyllithium as the base. The ligands were used as catalytic chiral ligands in the titanium(IV) alkoxide-promoted enantioselective addition reaction of diethylzinc to aldehydes. Copyright (C) 2000 Elsevier Science Ltd.

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

Chemistry is an experimental science, Safety of 6,6′-Dimethyl-2,2′-bipyridine, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 4411-80-7, Name is 6,6′-Dimethyl-2,2′-bipyridine

Reactions of 6,6?-dimethyl-2,2?-bipyridyl with iron(II) in aqueous and non-aqueous media

Reaction of anhydrous FeCl2 with 6,6?-dimethyl- 2,2?-bipyridyl (dmby) in non-aqueous media gives the yellow, high spin, tetrahedral complex FeCl2(dmby), which is characterized crystallographically, magnetically and by 1H NMR spectroscopy. In contrast, reaction of FeCl2¡¤4H2O with dmby in 0.1 M hydrochloric acid, the method of choice for preparing 3:1 and 2:1 iron(II) complexes of 2,2?-bipyridyl, gives [H2dmby] [FeCl4] and [Hdmby][FeCl4], in which the dmby has been protonated. These complexes are also characterized crystallographically.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of 6,6′-Dimethyl-2,2′-bipyridine, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 4411-80-7, in my other articles.

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

Related Products of 153-94-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153-94-6, Name is H-D-Trp-OH, molecular formula is C11H12N2O2. In a Review£¬once mentioned of 153-94-6

Molecularly imprinted polymers for biomedical and biotechnological applications

This survey covers main advances in the preparation and application of molecularly imprinted polymers which are capable of specific recognition of biologically active compounds. The principles underlying the production of highly efficient and template-specific molecularly imprinted polymers are discussed. The focus is on the imprinting of highly structured macromolecular and supramolecular templates. The existing and potential applications of molecularly imprinted polymers in various fields of chemistry and molecular biology are considered.

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

Reference of 29841-69-8, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.29841-69-8, Name is (1S,2S)-(-)-1,2-Diphenylethylenediamine, molecular formula is C14H16N2. In a Article£¬once mentioned of 29841-69-8

Dielectric anisotropy of a homochiral rare-earth metal complex

A homochiral rare-earth metal Tb complex that exhibited a very large dielectric anisotropic property with a temperature-independent feature is obtained. Our findings on high-dielectric anisotropy will provide a new impetus in this field of materials science. The Royal Society of Chemistry.

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Reference£º
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, SDS of cas: 2177-47-1, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 2177-47-1, Name is 2-Methyl-1H-indene, molecular formula is C10H10. In a Article, authors is Goodell, John R.£¬once mentioned of 2177-47-1

Development of an automated microfluidic reaction platform for multidimensional screening: Reaction discovery employing bicyclo[3.2.1]octanoid scaffolds

(Chemical Equation Presented) An automated, silicon-based microreactor system has been developed for rapid, low-volume, multidimensional reaction screening. Use of the microfluidic platform to identify transformations of densely functionalized bicyclo[3.2.1]octanoid scaffolds will be described.

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Reference£º
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, 131833-93-7, molcular formula is C17H30N2O2, introducing its new discovery. Formula: C17H30N2O2

Chiral bis(oxazoline)copper(II) complexes as lewis acid catalysts for the enantioselective Diels-Alder reaction

Bis(oxazoline)copper(II) complexes are highly enantioselective catalysts in Diels-Alder reactions involving bidentate dienophiles. Cationic [Cu((S,S)- t-Bu-box)]X2 complexes with different counterions have been used as catalysts, revealing a profound influence of the counterion on the rate and stereoselectivity of the catalyst. A square-planar catalyst-substrate complex is proposed to account for the high diastereo- and enantioselectivities observed. Three bis(oxazoline)-Cu(II) X-ray structures have been obtained that support this model. Double-stereodifferentiating experiments, performed employing chiral dienophiles, afforded results that are fully consistent with the proposed square-planar transition-state assemblage. In addition to imide- based substrates, alpha,beta-unsaturated thiazolidine-2-thiones have been introduced as a new class of dienophiles with enhanced reactivity. Kinetics experiments were performed to quantify the role that product inhibition plays in the course of the reaction. Rate and equilibrium binding constants of various catalyst inhibitors were also derived from the kinetic analysis. A comparative study was undertaken to elucidate the differences between the bis(oxazoline)-Cu(II) catalyst and the bis(oxazoline) catalysts derived from Fe(III), Mg(II), and Zn(II). Catalyst performance was found to be a function of a subtle relationship between bis(oxazoline) structure and transition metal.

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