Tag: M.W:500-600

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.166330-10-5, Name is (Oxybis(2,1-phenylene))bis(diphenylphosphine), molecular formula is C36H28OP2. In a Article，once mentioned of 166330-10-5, Recommanded Product: 166330-10-5

Synthesis, characterization, and photophysical properties of heteroleptic copper(I) complexes with functionalized 3-(2′-pyridyl)-1,2,4-triazole chelating ligands

A new series of mononuclear copper(I) complexes (1-9) with functionalized 3-(2′-pyridyl)-1,2,4-triazole chelating ligands, as well as the halide and/or phosphine ancillary ligands, have been synthesized. Complexes 1-9 were fully characterized by elemental analysis, NMR spectroscopy, mass spectroscopy, electronic absorption spectroscopy, fluorescence spectroscopy, cyclic voltammetry, and X-ray crystallography (1-8). They adopt a distorted tetrahedral configuration, and are considerably air-stable in solid state and in solution. All these Cu(I) complexes display a comparatively weak low-energy absorption in CH2Cl2 solution, assigned to charge-transfer transitions with appreciable MLCT character, as supported by TD-DFT studies. Cu(I) halide complexes 1-4 each shows bright solid-state emission at room temperature, although they are nonemissive in fluid solutions, in which the emission markedly depends on the halide and the substituent on the 2-pyridyl ring. Complexes 5-9 bearing 2-pyridyl functionalized 1,2,4-triazole and phosphine exhibit good photoluminescence properties in solution and solid states at ambient temperature, which are well-modulated via the alteration of the auxiliary phosphine ligand and the structural modification of 3-(2′-pyridyl)-1,2,4- triazole. Interestingly, cationic complex 6 and neutral derivative 7 can readily be interconverted through the ring inversion of the 1,2,4-triazolyl regulated by the NH a?” N- transformation.

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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

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.161265-03-8, Name is (9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine), molecular formula is C39H32OP2. In a Article，once mentioned of 161265-03-8, HPLC of Formula: C39H32OP2

Organosilane-Patterned Paper-based Colorimetric Sensors for High-Throughput Screening of Cross-Coupling Reactions with Aryl Bromides

An organosilane-patterned paper-based colorimetric sensor for bromides was developed using the 4-(2-pyridylazo)resorcinol (PAR)-Hg2+ complex and patterned hydrophobic paper. The red color of the (PAR)-Hg2+ spot was converted to yellow by ligand exchange between PAR and added bromide ions. This paper-based sensor was applied to detect the extent of conversion of aryl bromides in palladium-catalyzed coupling reactions such as Stille, Suzuki, Heck, direct arylation and decarboxylative coupling. A good correlation was demonstrated between the conversion of paper-based sensor and conversion of gas chromatography. (Figure presented.).

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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

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 161265-03-8, C39H32OP2. A document type is Patent, introducing its new discovery., Computed Properties of C39H32OP2

PYRAZINE DERIVATIVES AS FGFR INHIBITORS

The present invention relates to pyrazine derivatives of formula I, and pharmaceutical compositions including the same, that are inhibitors of one or more FGFR enzymes and are useful in the treatment of FGFR-associated diseases such as cancer. Wherein ring A is selected from

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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 12150-46-8, Name is 1,1-Bis(diphenylphosphino)ferrocene,molecular formula is C34H28FeP2, is a conventional compound. this article was the specific content is as follows.Safety of 1,1-Bis(diphenylphosphino)ferrocene

Microwave-assisted organometallic syntheses: Formation of dinuclear [(Arene)Ru(mu-Cl)3RuCl(L-L’)] complexes (L-L’ : Chelate ligands with P-,N-, or S-donor atoms) by displacement of Arene pi ligands

Microwave heating was employed to promote arene displacement in reactions of [{(p-cymene)RuCl2}2] or [{(1,3,5- C6H 3iPr3)RuCl2}2] with neutral chelate ligands L-L’ [L-L’: 1,1 ?-bis(diphenylphosphanyl)methane, 1,1?-bis(diphenylphosphanyl)ferrocene, S)-BINAP, (S.S)-DIOP, N,N?-bis(2,4,6-t:rimethylphenyl)-1,2-ethanediylidenediamine], R)-Ph-PHOX, and 3 (phenylsulfanylpropyl)diphenylphosphane. The reactions gave complexes of the general formula [(arene)Ru(mu Cl)3-RuCl(L-L’)l in good yield. The synthesis of [(p cymene)Ru(muCl)3RuCl{PPh2(CH 2)3NH2}] 22) was accomplished in two steps via the intermediate [{(p-cymene)RuCl2}2{mu PPh 2(CH2)3-NH2}] (21). The structures of [ l,3,5 C6H3iPr3)Ru(u-Cl) 3RuCl-(dppf)] (16), [(l,3,5 C6H3iPr 3)Ru(mu-Cl)3RuCl{(S)-BINAP}] (17),and [(p cymene)Ru((mu-Cl)3RuCl(MesNCHCHNMes)] (18) were determined by single-crystal X-ray diffraction. Wiley-VCH Verlag GmbH &Co, KGaA.

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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

Electric Literature of 161265-03-8, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 161265-03-8, Name is (9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine), molecular formula is C39H32OP2. In a Patent，once mentioned of 161265-03-8

COMPOSITION HAVING A MUGUET ODOR

The present invention relates to a composition of matter comprising a) at least one compound of formula (I) in the form of any one of its isomers or a mixture thereof; wherein R1 represents a hydrogen atom or a C1-2 alkyl group; and R represents a group of formula ? CH2C(Me)2OH; said R being, relative to position 1, a meta, a para substituent of the aromatic ring or a mixture thereof; and b) at least one compound of formula (II) in the form of any one of its isomers or a mixture thereof; wherein R1 and R have the same meaning as defined in formula (I); said R being, relative to position 1, an ortho, a meta, a para substituent of the aromatic ring or a mixture thereof; their uses as perfuming ingredients as well as the composition and consumer product including such a composition of matter and the process to prepare it.

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 161265-03-8 is helpful to your research., Electric Literature of 161265-03-8

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

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 12150-46-8, Name is 1,1-Bis(diphenylphosphino)ferrocene, Product Details of 12150-46-8.

Novel solvates in AgX:dpex (n:1) systems (n = 1 or 2); X = oxyanion; dppx = Ph2P(Y)PPh2, Y = (CH2)3, Fc

Novel solvated forms are spectroscopically (1H, 13C, 31P, IR and conductivity studies) and structurally described for diverse silver oxyanion salt:bis(diphenylphosphino)-ligand adducts of 2:1:n (AgX:dppx:S) stoichiometry. AgClO4:dppf:MeCN (2:1:4) (‘dppf’ = bis(diphenylphosphino)ferrocene) is a binuclear centrosymmetric species: [(O3ClO)(MeCN)2Ag(P-dppf-P?)Ag(NCMe)2(OClO3)], Ag-P short at 2.368(1) A. Two MeOH/H2O solvates are described, of AgX:dppp (2:1) stoichiometry, both single stranded polymers (X = carboxylate: ‘ac’ = acetate, ‘tfa’ = trifluoroacetate; ‘dppp’ = Ph2P(CH2)xPPh2; x = 3), with silver atoms spanned alternately by: (i) a P-dppp-P? bridge, supported by tenuously bridging water or methanol, and (ii) O-ac, tfa-O? bridge(s), being assigned stoichiometries Agtfa:dppp:H2O (2:1:1) · MeOH and Agac : dppp : MeOH ( 2 : 1 : 0.5 ) · 3 frac(1, 2) H2 O. The structure of AgClO4:dppe:MeCN (1:1:1) (‘dppe’, x = 2), also a one-dimensional polymer, but with all Ag…Ag sequences bridged by the P,P? ligand, and with unidentate MeCN and OClO3 coordinated to the silver, is also recorded.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Product Details of 12150-46-8. In my other articles, you can also check out more blogs about 12150-46-8

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.12150-46-8, Name is 1,1-Bis(diphenylphosphino)ferrocene, molecular formula is C34H28FeP2. In a Article，once mentioned of 12150-46-8, Product Details of 12150-46-8

Ni-catalyzed carboxylation of C(sp2)- and C(sp3)-O bonds with CO2

In recent years a significant progress has been made for the carboxylation of aryl and benzyl halides with CO2, becoming convenient alternatives to the use of stoichiometric amounts of well-defined metal species. Still, however, most of these processes require the use of pyrophoric and air-sensitive reagents and the current methods are mostly restricted to organic halides. Therefore, the discovery of a mild, operationally simple alternate carboxylation that occurs with a wide substrate scope employing readily available coupling partners will be highly desirable. Herein, we report a new protocol that deals with the development of a synergistic activation of CO2 and a rather challenging activation of inert C(sp2)-O and C(sp3)-O bonds derived from simple and cheap alcohols, a previously unrecognized opportunity in this field. This unprecedented carboxylation event is characterized by its simplicity, mild reaction conditions, remarkable selectivity pattern and an excellent chemoselectivity profile using air-, moisture-insensitive and easy-to-handle nickel precatalysts. Our results render our method a powerful alternative, practicality and novelty aside, to commonly used organic halides as counterparts in carboxylation protocols. Furthermore, this study shows, for the first time, that traceless directing groups allow for the reductive coupling of substrates without extended pi-systems, a typical requisite in many C-O bond-cleavage reactions. Taking into consideration the limited knowledge in catalytic carboxylative reductive events, and the prospective impact of providing a new tool for accessing valuable carboxylic acids, we believe this work opens up new vistas and allows new tactics in reductive coupling events.

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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

Synthetic Route of 161265-03-8. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 161265-03-8, Name is (9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine)

Synthesis and characterisation of 2,2-bis(hydroxymethyl)-1,3-diselenolato metal(II) complexes bearing various phosphanes

An improved synthesis of 4,4-bis(hydroxymethyl)-1,2-diselenolane and the complexation properties of the corresponding diselenolato dianion to group-10 metals are reported. We describe an efficient and straightforward procedure that bypasses the isolation of the malodorous and airsensitive diselenol and starts with the diselenide appropriate group-10 metal complex bearing phosphane and chlorido ligands. A series of complexes with various monoand bidentate phosphanes is prepared and characterised by multinuclear NMR spectroscopy, mass spectrometry, and elemental analysis. Furthermore, the structure of most complexes is studied by single-crystal X-ray diffraction to establish their supramolecular arrangement in the solid state. Consequently, several group-10 metal complexes with P-M-P angles (bite angles) in the range from 71-108 are investigated. The use of the sterically demanding bridging phosphane 4,5-bis(diphenylphosphanyl)-9,9-dimethylxanthene, which exhibits a large bite angle yields a mixture of a di- and trinuclear complex. While the platinum-containing complexes are proven to be rather stable, the palladium and nickel analogues tend to decompose. Especially, the nickel complexes were found to be sensitive against: oxidation. This circumstance leads to the formation of the so far unknown 1,8-bis(diphenylphosphanyl)naphthalene monooxide, the formation and structure of which could be confirmed from NMR spectroscopic data and single-crystal X-ray diffraction.

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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

Electric Literature of 161265-03-8, An article , which mentions 161265-03-8, molecular formula is C39H32OP2. The compound – (9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) played an important role in people’s production and life.

Synthesis of Adipic Aldehyde by n-Selective Hydroformylation of 4-Pentenal

Several phosphine and phosphite ligands were tested in the hydroformylation of 4-pentenal to adipic aldehyde, a versatile starting material for industrially very relevant compounds. By varying the ligand structure we were able to increase the selectivity toward adipic aldehyde to >95%. Additionally, two molecular structures of important catalytic intermediates [(bisphosphite)RhH(CO)2] and one structure of a previously unknown catalyst decomposition product were obtained. (Chemical Equation Presented).

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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

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.12150-46-8, Name is 1,1-Bis(diphenylphosphino)ferrocene, molecular formula is C34H28FeP2. In a Article，once mentioned of 12150-46-8, name: 1,1-Bis(diphenylphosphino)ferrocene

Carbon-nitrogen-bond-forming reductive elimination of arylamines from palladium(II) phosphine complexes

A series of monomeric palladium amido complexes of the form trans-(PPh3)2Pd(Ar)(NAr’2) and (DPPF)Pd(Ar)NAr’2) (DPPF = 1,1′-bis(diphenylphosphino)ferrocene) and dimeric palladium amido complexes of the form {(PPH3)Pd(Ar)mu-NHR)}2 (R = Ph, t-Bu) have been prepared by the reaction of lithium and potassium amides with palladium aryl halide complexes. An X-ray crystal structure of (DPPF)Pd(p-NMe2C6H4)[N(p-CH3C6H4)2] was obtained. Upon thermolysis in the presence of PPh3, serving as a trapping agent, both the monomeric and dimeric palladium amido complexes underwent C-N-bond-forming reductive elimination to form arylamines in high yields along with a Pd(0) species. Reductive elimination was also observed from azametallacycle (PPh3)Pd(eta2-C6H4C6H4-NH), to form carbazole and Pd(PPh3)4 at room temperature. Mechanistic studies on the reductive elimination reactions of the monomeric PPh3-ligated amido complexes indicated the presence of two competing pathways for the formation of amine. At low [PPh3], reductive elimination occurs via phosphine dissociation to form a three-coordinate intermediate; however, as [PPh3] is increased, a pathway of reductive elimination from a four-coordinate complex becomes dominant. The DPPF-ligated palladium amido complexes directly eliminated amine from the four-coordinate complex. The mechanism of the reductive elimination from dimeric palladium amido complexes was also studied. These complexes undergo reductive elimination of amine via dimer dissociation to generate a three-coordinate intermediate analogous to those formed by the PPh3-ligated monomeric amido complexes. The C-N-bond forming reductive elimination reactions were accelerated by electron-withdrawing groups on the Pd bound aryl group and by electron-donating groups on the amido ligand, suggesting that the aryl group acts as an electrophile and the amido ligand acts as a nucleophile.

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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