Category: 13406-29-6

In an article, published in an article, once mentioned the application of 13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine,molecular formula is C21H12F9P, is a conventional compound. this article was the specific content is as follows.name: Tris(4-(trifluoromethyl)phenyl)phosphine

New phenoxybenzylidene ruthenium chelates were synthesised from the second generation Grubbs catalysts bearing a triphenylphosphine ligand (or its para-substituted analogues) by metathesis exchange with substituted 2-vinylphenols. The complexes behave like a latent catalyst and are characterized by an improved catalytic behaviour as compared to that of the known analogues, i.e., they exhibit high catalytic inactivity in their dormant forms and a profound increase in activity after activation with HCl. The strong electronic influence of substituents in the chelating ligand on the catalytic activity was demonstrated. The catalytic properties were tested in ROMP of cyclooctadien (COD) and a single selected norbornene derivative.

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Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

Related Products of 13406-29-6, An article , which mentions 13406-29-6, molecular formula is C21H12F9P. The compound – Tris(4-(trifluoromethyl)phenyl)phosphine played an important role in people’s production and life.

An NCN pincer palladium complex was developed as a probe molecule to index the coordination ability of various monodentate ligands. Coordination constants of 27 monodentate ligands (L) with a pincer palladium complex to form complexes of the type ArPd(L)2Cl were determined by 1H NMR spectroscopy. This allowed the coordination ability of a wide variety of ligands, including P-coordinating ligands (phosphane, phosphite), as well as As-coordinating AsPh3, and N-coordinating pyridine, to be indexed. The differential between the highest/lowest coordination constants was 10 12. The relative coordination ability is described in a logarithmic manner, log(Keq(L)/Keq(PPh3)), with respect to the value of PPh3 to exhibit high linearity in the Hammett plot. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

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Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

Application of 13406-29-6, Chemistry can be defined as the study of matter and the changes it undergoes. You’ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine, molecular formula is C21H12F9P. In a patent, introducing its new discovery.

We report here on the syntheses of rhodium(I) complexes bearing a phosphine-quinolinolate ligand and the isolation of two classes of important intermediates in the anti-Markovnikov hydroamination of terminal alkynes with secondary amines: vinylidene-bridged dirhodium complexes and (amino)carbene complexes. We first prepared various rhodium(I) complexes bearing a phosphine-quinolinolate ligand and found that some of these complexes had catalytic activity for the anti-Markovnikov hydroamination of terminal alkynes with secondary amines. The reaction of stoichiometric amounts of a (PNO)Rh complex with terminal alkynes provided vinylidene-bridged dirhodium complexes. When the resulting vinylidene complexes were reacted with secondary amines, (amino)carbene complexes were generated, which gave the hydroamination product upon heating with an additive. These results suggest that this anti-Markovnikov hydroamination catalyzed by (PNO)Rh complexes proceeds via vinylidene and (amino)carbene complexes.

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Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

In an article, published in an article, once mentioned the application of 13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine,molecular formula is C21H12F9P, is a conventional compound. this article was the specific content is as follows.Quality Control of: Tris(4-(trifluoromethyl)phenyl)phosphine

An unprecedented Rh(I)-catalyzed, amino-group-assisted C-H carboxylation of 2-arylanilines with CO2 under redox-neutral conditions has been developed. This reaction was promoted by a phosphine ligand with t-BuOK as the base and did not require the use of additional strong organometallic reagent. It enabled an efficient direct conversion of a broad range of 2-(hetero)arylanilines including electron-deficient heteroarenes to various phenanthridinones. Possible intermediates of the reaction were also evaluated in the preliminary mechanistic studies.

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Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

In an article, published in an article, once mentioned the application of 13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine,molecular formula is C21H12F9P, is a conventional compound. this article was the specific content is as follows.Quality Control of: Tris(4-(trifluoromethyl)phenyl)phosphine

The Pt(ii) coordination chemistry of oligocationic ammoniomethyl- and neutral aminomethyl-substituted triarylphosphines (L) is described. Complexes of the type PtX2(L)2 (X = Cl, I) have been isolated and characterized. For the hexa-meta-ammoniomethyl-substituted ligands [1] 6+ and [2]6+, two ligands always occupy a trans-configuration with respect to each other in complexes of the type PtX 2(L)2, while for the tri-para-ammoniomethyl-substituted ligand [7]3+, the trans/cis ratio is dependent on the ionic strength of the solution. This behaviour was not observed for the neutral aminomethyl-substituted ligands. In the crystal structure of trans-[PtI 2(1)2]I12, the geometrical parameters of the phosphine ligand [1]6+ are very similar to those found in the analogous complex of the benchmark ligand PPh3, i.e. trans-PtI 2(PPh3)2, indicating that no significant increase in the steric congestion is present in the complex. Instead, the coordination chemistry of this class of phosphine ligands is dominated by repulsive Coulombic inter-ligand interactions.

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Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

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. 13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine, molecular formula is C21H12F9P. In a Article，once mentioned of 13406-29-6, SDS of cas: 13406-29-6

Convenient synthesis of four new distorted octahedral ruthenium(II) complexes (1, 2, 3, 4) having general molecular formula [RuCl2LPAr3] (L = pyridine-based tridentate ligands not containing N-H bonds) is described. Their composition and structure were determined by elemental analysis and NMR spectra, and complexes 2 and 4 were also identified by X-ray single-crystal diffraction. All ruthenium(II) complexes exhibited good to excellent catalytic activity in the transfer hydrogenation of ketones. Among them, complex 4 achieved the highest final TOF value of 51600 h-1 for a high molar ratio of substrate to catalyst (2000:1).

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.SDS of cas: 13406-29-6. In my other articles, you can also check out more blogs about 13406-29-6

Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

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. 13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine, molecular formula is C21H12F9P. In a Article，once mentioned of 13406-29-6, Application In Synthesis of Tris(4-(trifluoromethyl)phenyl)phosphine

The di-reduced state of the naphthalene moiety and its congeners have long captivated chemists as it is elusive to stabilize these intrinsically reactive electron-rich pi-systems and for their emergent multifaceted properties. Herein we report the synthesis and isolation of two-electron (2e-) reduced, highly electron-rich naphthalenediimides (NDIs). A doubly zwitterionic structure is observed for the first time in a naphthalene moiety and validated by single crystal X-ray crystallography and spectroscopic methods. The synthesis avoids hazardous reducing agents and offers an easy, high-yielding route to bench-stable di-reduced NDIs. Notably, we realized high negative first oxidation potentials of up to -0.730 V vs. Fc/Fc+ in these systems, which establish these systems to be one of the strongest ambient stable electron donors. The study also provides the first insights into the NMR spectra of the di-reduced systems revealing a large decrease in diatropicity of the naphthalene ring compared to its 2e- oxidized form. The NICS, NICS-XY global ring current, gauge-including magnetically induced current (GIMIC) and AICD ring current density calculations revealed switching of the antiaromatic and aromatic states at the naphthalene and the imide rings, respectively, in the di-reduced system compared to the 2e- oxidized form. Notably, the substituents at the phosphonium groups significantly tune the antiaromatic-aromatic states and donor ability, and bestow an array of colors to the di-reduced systems by virtue of intramolecular through-space communication with the NDI scaffold. Computational studies showed intramolecular noncovalent interactions to provide additional stability to these unprecedented doubly zwitterionic systems.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.Application In Synthesis of Tris(4-(trifluoromethyl)phenyl)phosphine, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 13406-29-6, in my other articles.

Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine, molecular formula is C21H12F9P, belongs to chiral-phosphine-ligands compound, is a common compound. In a patnet, once mentioned the new application about 13406-29-6, category: chiral-phosphine-ligands

PROBLEM TO BE SOLVED: the present invention, perfluorolefin alkylphosphines compound, and a metal complex and perfluorolefin alkylphosphines and provide. SOLUTION: the present invention, the general formula R f-PR 1 R 2 organophosphine compound represented by, in the formula, R 1 and R 2 comprises, independently of each other or non-substituted hydrocarbon substituents, R f comprises, a hydrocarbon group perfluorocyclic, perfluorolefin alkylphosphines compound, and a metal complex and alkylphosphines perfluorocyclic organophosphine ligand. Selected drawing: no (by machine translation)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.category: chiral-phosphine-ligands. In my other articles, you can also check out more blogs about 13406-29-6

Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine, molecular formula is C21H12F9P. In a Review，once mentioned of 13406-29-6, Quality Control of: Tris(4-(trifluoromethyl)phenyl)phosphine

In situ, high-pressure NMR was used to investigate the hydroformylation reaction of ethylene in liquid CO2 using Rh(CO)2acac as the catalyst precursor and (p-CF3C6H4)3P, tris(p-trifluoromethylphenyl)phosphine, as the ligand under different thermodynamic conditions (T = 10-23 C, PCO = PH2 = 10-15 bar, PC2H4 = 10-15 bar, PCO2 = 207 bar). 1H-NMR was used to monitor the reaction progress of the hydroformylation of ethylene with a rhodium catalyst under select conditions of temperature and CO2 solvent pressure. Potential resting states of the rhodium catalyst were investigated by 31P(1H)-NMR. This is the first description of a rhodium catalyzed hydroformylation reaction in liquid CO2 monitored in situ by high pressure NMR.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of: Tris(4-(trifluoromethyl)phenyl)phosphine, you can also check out more blogs about13406-29-6

Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

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. 13406-29-6, Name is Tris(4-(trifluoromethyl)phenyl)phosphine, molecular formula is C21H12F9P. In a Article，once mentioned of 13406-29-6, name: Tris(4-(trifluoromethyl)phenyl)phosphine

The alpha-amidoalkylating properties of 1-(N-acylamino)alkyltriarylphosphonium salts with weakened Calpha-P+ bond strength are discussed and examined. It is demonstrated that such type of phosphonium salts reacts smoothly with a diverse array of carbon- and heteroatom-based nucleophiles, including 1-morpholinocyclohexene, 1,3-dicarbonyl compounds, benzotriazole sodium salt, p-toluenesulfinate sodium salt, benzylamine, triarylphosphines, and other P-nucleophiles. Reactions are conducted at room temperature, in a short time (5?15 min) and mostly without catalysts. Simple work-up procedures result in good or very good yields of products. The structures of known compounds were established by spectroscopic methods and all new compounds have been fully characterized using 1H-, 13C-, 31P-NMR, IR spectroscopy, and high-resolution mass spectrometry. Mechanistic aspects of described transformations are also performed and discussed. It was demonstrated that unique properties make 1-(N-acylamino)alkyl-triarylphosphonium salts with weakened Calpha-P+ bond strength interesting building blocks with great potential, especially in alpha-amidoalkylation reactions.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.name: Tris(4-(trifluoromethyl)phenyl)phosphine, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 13406-29-6, in my other articles.

Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate