Some scientific research about 3153-26-2

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Effects of Fe, Ti, and v doping on the microstructure and electrical properties of grain and grain boundary of giant dielectric NiO-based ceramics

We report the giant dielectric response and electrical properties of Li0.05 B0.02 Ni0.93 O (B=Fe, Ti, and V) ceramics prepared by a polymer pyrolysis route. The giant dielectric response in these materials can be ascribed based on the Maxwell-Wagner polarization and thermally activated mechanisms. It is found that Fe, Ti, and V doping has a strong effect on the microstructure and the conduction of grains and grain boundaries of these NiO-based ceramic systems, which make large contribution to their dielectric properties.

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

More research is needed about 27012-25-5

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Chemistry is traditionally divided into organic and inorganic chemistry. SDS of cas: 27012-25-5. The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent,Which mentioned a new discovery about 27012-25-5

ORGANOMETALLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING SAME

The present specification provides an organic metal compound represented 1 by chemical formula (I) and an organic light-emitting device including the same. (by machine translation)

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

The important role of 68737-65-5

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Synthetic Route of 68737-65-5, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 68737-65-5, Name is (1R,2R)-N,N’-Dimethyl-1,2-cyclohexanediamine,introducing its new discovery.

An efficient synthesis of enantiomerically pure trans-N1,N 2-dimethylcyclohexane-1,2-diamine

A new pathway is described to produce a highly optically pure isomer of trans-N1,N2-dimethylcyclohexane-1,2-diamine through four simple steps. Reaction of cyclohexene oxide with aqueous methylamine, followed by cyclisation with Mitsunobu reagent and ring-opening reactions gave rac-trans-N1,N2-dimethylcyclohexane-1,2-diamine, and the enantiomers were obtained via a kinetic resolution using tartaric acid.

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

Extended knowledge of 1941-30-6

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Application of 1941-30-6, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 1941-30-6, Name is Tetrapropylammonium bromide, molecular formula is C12H28BrN. In a Article,once mentioned of 1941-30-6

Hydrogen peroxide oxidation of D-glucose with titanium-containing zeolites as catalysts

The oxidation of D-glucose with hydrogen peroxide as oxidant over several titanium-containing zeolites and titania as catalysts was studied. TS-1 and Ti-MCM-41 were synthesized directly while titanium-containing zeolites Y, L and mordenite were obtained through post-synthesis treatment using ammonium hexafluorotitanate. The oxidation of D-glucose occured mainly to gluconic acid, glucuronic acid, tartaric acid, glycolic acid and glyceric acid. (C) 2000 Elsevier Science B.V.

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

Extended knowledge of Vanadyl acetylacetonate

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Application of 3153-26-2, 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. 3153-26-2, Name is Vanadyl acetylacetonate, molecular formula is C10H14O5V. In a Article,once mentioned of 3153-26-2

The Preparation and Structure of *CH2Cl2 and of Some Homologues of Related Schiff Bases

The elusive < salen = N,N'-ethylenebis(salicylideneiminate)(2-)> and some of its homologues have been successfully prepared.The structure of *CH2Cl2 has been determined by X-ray crystallography, and the conformation is trans-octahedral, as expected, with long V-I separations.The complex is air-stable in the solid state, but appears to be moisture-sensitive in solution, and undergoes autoredox reactions (V(IV) –> V(III), I(-) –> I2) in ionising solvents.

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

Awesome Chemistry Experiments For 1271-19-8

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Synthetic Route of 1271-19-8, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 1271-19-8, Name is Titanocenedichloride, molecular formula is C10Cl2Ti. In a Article,once mentioned of 1271-19-8

Syntheses and characterization of titanium(IV) and titanium(III) complexes with (2-dimethylphosphino)ethane-1-thiolate and (3-dimethylphosphino)propane-1-thiolate as ligands

Reactions of Cp2TiCl2 (Cp = eta 5-cyclopentadienide) with 2 or 1 equiv of hybrid P-S ligands (L), (CH3)2P(CH2)nS- n = 2, dmpet; n = 3, dmppt), produced new dicyclopentadienyltitanium(IV) complexes with L, Cp2Ti(L-kappaS)2 (1, L = dmpet; 2, L = dmppt) and [Cp2Ti(L-kappa2S,P)]BPh4 (3, L = dmpet; 4, L = dmppt). The Ti(III) complexes, Cp2Ti(L-kappa2S,P) (5, L = dmpet; 6, L = dmppt), were prepared by the reaction of Cp 2Ti(eta3-C3H5) with 1 equiv of L. The structures of complexes 1-6 were confirmed by X-ray diffraction analyses. It was found that complexes 3 and 5 were isostructural around Ti(IV) and Ti(III) centers: the Ti(IV)-S bond length in 3 (2.3498(9) A) is shorter by 0.14 A than Ti(III)-S in 5 (2.4877(7) A), while Ti(IV)-P (2.534(1) A) was merely 0.05 A shorter than Ti(III)-P (2.5844(7) A). The redox potential between 3 and 5 in acetonitrile was -1.14 V vs the ferricinium/ferrocene couple. A heterobimetallic complex that has the frame of complex 1, [Cp2Ti(dmpet)2Cu]PF6 (7), was also isolated and structurally characterized: the Ti-Cu distance (2.95(1) A) was shorter than that in [Cp2Ti(SC2H4PPh 2)2Cu]BF4, previously reported by White and Stephan. Structural characterization was also carried out for Cp*Ti(dmpet-kappaS)2(dmpet-kappa2S,P) (8) and CpTiCl2(dmppt-kappa2S,P) (9), which were obtained by the reactions of Cp*(or Cp)TiCl3 (Cp* = eta 5-C5Me5-) with n equiv (n = 1-3) of L. The mutual site-exchange reaction between phosphorus atoms on a coordinated dmpet in the kappa2S,P mode and on two other coordinated dmpet’s in the kappaS mode within complex 8 was analyzed by the variable-temperature 31P{1H} dynamic NMR method. The kinetic parameters for this process, kex298 = 1.9 × 105 s -1, DeltaH? = 48 kJ mol-1, and DeltaS? = 17 J mol-1 K-1, as well as the rather long Ti(IV)-P distance (2.652(1) A), indicate the fluxional nature of the coordination geometry in complex 8.

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

Brief introduction of 4411-80-7

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Synthetic Route of 4411-80-7, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4411-80-7, Name is 6,6′-Dimethyl-2,2′-bipyridine, molecular formula is C12H12N2. In a Article,once mentioned of 4411-80-7

Rock ‘n’ roll with gold: Synthesis, structure, and dynamics of a (bipyridine)AuCl3 complex

Our previously reported microwave synthesis of (N-N)AuCl2 + complexes (where N-N = 2,2?-bipyridine (bpy) and sterically unencumbered bpy derivatives) was used to prepare derivatives where the bpy moiety was substituted in the 6,6?-positions. Instead of the square-planar complexes, these reactions produced neutral (N-N)AuCl3 complexes. In these, the tethered N-N ligand is bonded such that one N occupies a regular position in the square coordination plane of the Au(III) center and the other N occupies a pseudoaxial position, interacting with Au through an elongated Au-N bond, as determined by X-ray crystallography of two complexes. Variable-temperature 1H NMR spectroscopy reveals that the two sites of the N-N ligand undergo exchange on the NMR time scale. For N-N = 6,6?-Me2bpy the activation parameters were determined to be DeltaH? = 8.5 ± 0.4 kcal mol-1 and DeltaS? = 0.7 ± 2.0 cal K-1 mol -1. The dynamic behavior of (6,6?-Me2bpy)AuCl 3 was investigated by a DFT computational study, which detailed the in-plane rocking motion seen by NMR as well as decoordination of the axially bonded N with concomitant rolling of half of the bpy moiety by rotation around the central C-C bond of the bidentate ligand.

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

Top Picks: new discover of 4730-54-5

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Application of 4730-54-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4730-54-5, Name is 1,4,7-Triazacyclononane, molecular formula is C6H15N3. In a Article,once mentioned of 4730-54-5

Filariasis in the new millennium

The Indonesian national fdariasis eradication program in its pursuit in obtaining microfilarial rates below 1% in filariasis endemic locations was on its right track until the monetary crisis started 3 years ago. This crisis which is not over yet at present is complicated by unstable public safety causing population shifts where people from filaria endemic locations seek refuge in non-endemic areas. This updated review will hopefully serve as a timely reminder to our physicians and health workers especially on the mode of filarial transmission as well as on its clinical presentations and presently accepted ways of management. This paper also will serve as an introduction into the present breakthroughs in this new millenium as noted in the field of diagnostics and simplified mass treatment schedules making it possible for the elimination of lymphatic filariasis as a public health problem. A global alliance under the guidance of the World Health Organization with support of the multinational pharmaceutical companies for providing free expensive medication as needed. The WHO also cooperates closely with the Tropical Diseases Research task forces of Filariasis Intervention Research and of Product Development, that in the end will provide the means to eradicate this disease for once and forever from the face of the earth.

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

Archives for Chemistry Experiments of Titanocenedichloride

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ESTIMATION OF STEPWISE M-L BOND DISSOCIATION ENTHALPIES IN M(eta-C5H5)2L2 COMPLEXES

Stepwise bond dissociation enthalpies D1(M-L) and D2(M-L) in M(eta-C5H5)2L2 complexes (M = Ti, Mo; L = H, Cl, CO, CH3, SCH3) have been estimated from using thermochemical data and extended Hueclel MO calculations.It is concluded that for the systems studied ligand to metal ?-donation results in larger differences D2-D1 than ?-donation.

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

Final Thoughts on Chemistry for 295-64-7

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Synthesis and anthelmintic activity of indazoles and nitroindazoles

The synthesis and anthelmintic evaluation of indazole aminomethylated compounds and ureas were performed. The anthelmintic activity of ureas against Syphacia obvelata was pointed out.

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