Abstract:
The present disclosure is directed to a catalyst composition used in the production of aromatic carbonates, and in particular to a catalyst composition which comprises an activating solvent. In one embodiment the disclosure relates to a catalyst composition which comprises to a combination of two activating solvents, a first activating solvent chosen for its coordinative properties, and a second activating solvent chosen for its dielectric constant properties. In alternative embodiments, the present disclosure also pertains to a method for producing aromatic carbonates using the catalyst compositions disclosed herein.
Abstract:
A process for solubilizing an organometallic compound in a fluorinated solvent to form an organometallic solution by adding and reacting a co-solubilizer having a partly fluorinated polymer, an organometallic compound, and a fluorinated solvent, and the co-solubilizer has the ability to cause the organometallic compound to become miscible in a fluorinated solvent, and further, the co-solubilizer is not a catalyst and is present in the final organometallic solution.
Abstract:
The object of the present invention is to provide 3-hydroxy-3-(2-thienyl)propionamides useful as synthesis intermediates of pharmaceutical preparations and the like and a method for obtaining optically active 3-amino-1-(2-thienyl)-1-propanols using the same with high reaction yield, high optical yield and industrially low cost. According to the present invention, 3-amino-1-(2-thienyl)-1-propanols are obtained by carrying out asymmetric reduction of a β-ketocarbonyl compound having thiophene ring in the presence of a catalyst constituted from a compound of a group VIII or IX metal in the periodic table (e.g., a ruthenium compound) and an asymmetric ligand represented by a specified optically active diamine derivative (e.g., a diphenylethylenediamine derivative), or using a cell, a treated product of said cell or the like of a microorganism, and as occasion demands, carrying out amidation of the ester group and then carrying out reduction of the amido group. (each of the substituents is as described in claim 1).
Abstract:
The invention relates to novel diphosphines, in optically pure or racemic form, of formula (I): in which: R1 and R2 are a (C5-C7)cycloalkyl group, an optionally substituted phenyl group or a 5-membered heteroaryl group; and A is (CH2—CH2) or CF2. The invention further relates to the use of a compound of formula (I) as a ligand for the preparation of a metal complex useful as a chiral catalyst in asymmetric catalysis, and to the chiral metal catalysts comprising at least one ligand of formula (I).
Abstract:
A process for producing organic substituted aromatic or heteroaromatic compounds including biaryl and biheteroaryl compounds in a two-step reaction. In the first step, the aromatic or heteroaromatic compound is borylated in a reaction comprising a borane or diborane reagent (any boron reagent where the boron reagent contains a B—H, B—B or B—Si bond) and an iridium or rhodium catalytic complex. In the second step, a metal catalyst catalyzes the formation of the organic substituted aromatic or heteroaromatic compound from the borylated compound and an electrophile such as an aryl or organic halide, triflate (OSO2CF3), or nonaflate (OSO2C4F9). The steps in the process can be performed in a single reaction vessel or in separate reaction vessels. The present invention also provides a process for synthesis of complex polyphenylenes starting from halogenated aromatic compounds.
Abstract translation:一种在两步反应中制备包括联芳基和双杂芳基化合物的有机取代的芳族或杂芳族化合物的方法。 在第一步中,在包含硼烷或乙硼烷试剂(硼试剂含有B-H,B-B或B-Si键的任何硼试剂)和铱或铑催化络合物的反应中,芳族或杂芳族化合物被硼酸化。 在第二步中,金属催化剂催化从硼化化合物和亲电体如芳基或有机卤化物,三氟甲磺酸酯(OSO 2 CF 3)或非卤化物(OSO 2 C 4 F 9)形成有机取代的芳香族或杂芳族化合物。 该方法中的步骤可以在单个反应容器中或在单独的反应容器中进行。 本发明还提供从卤代芳族化合物开始合成络合聚苯的方法。
Abstract:
An amino acid complex of the formula I, where M is selected from among Fe, Co, Ni, Pd, Pt and Ir, preferably Ni, can be used for the polymerization of olefins.
Abstract:
A process that can be used as catalyst in esterification, transesterification or polycondensation is disclosed, which comprises a stable solution comprising (a) titanium in the form of a titanium α-hydroxycarboxylic acid or its salt, (b) a C1-C6 carboxylic acid, and (c) zinc in the form of a water-soluble zinc salt, and (d) water. Also disclosed is an esterification, transesterification or polycondensation process, which comprises contacting, in the presence of the solution process, an organic acid or its ester or its salt with an alcohol, optionally in the presence of a phosphorus compound, an organic or inorganic toning agent such as cobalt acetate, or combinations thereof. The process can also comprise combining aqueous solutions of a titanium α-hydroxycarboxylic acid or its salt and a zinc salt in an alcohol to produce an alcohol solution contacting the alcohol solution with a mixture comprising organic acid or its ester or its salt and a second alcohol, or comprise combining an aqueous solutions of a titanium α-hydroxycarboxylic acid or its salt and aqueous solution of a zinc salt with the mixture.
Abstract:
There is provided processes for metal mediated reactions, particularly cross coupling and carbometallation reactions, wherein the metal is present as a catalyst system comprising a catalyst microencapsulated within a permeable polymer microcapsule shell and the reaction is carried out under super-critical or near super-critical conditions. Preferred metal-mediated cross coupling reactions include Heck, Suzuki, Sonogashira and Stille reactions. Preferred carbometallation reactions include hydroformylations.
Abstract:
Titanium alkoxide catalysts for polymerization of cyclic esters such as LA and CL and methods of polymerization are disclosed. Titanium is known to be non-toxic and the various compounds described herein can catalyze cyclic esters to produce polyesters with controlled molecular weights and relatively narrow molecular weight distributions. In one embodiment, caged titanium alkoxides catalysts are used. The caged titanium alkoxides can be atranes or non-atranes.
Abstract:
Novel catalyst systems which comprise diimine nickel complexes comprising additional ligands selected from the group consisting of acetylacetonate, hexaflourylacetylacetonate, halogens and mixtures thereof can be used with methylaluminoxane in slurry polymerization processes to polymerize mono-1-olefins and, optionally one or more higher mono-1-olefin comonomer(s), to produce high molecular weight polymers.