Patent classifications
B01J31/223
Diruthenium Catalyst Compositions and Synthetic Processes Related Thereto
This disclosure relates to compositions comprising diruthenium catalysts and uses related thereto. In certain embodiments, the diruthenium catalyst comprises a cyclopropyl ring substituted with a carboxylic acid ligand. In certain embodiments, the diruthenium catalyst comprises an N-(sulfonyl)pyrrolidine ring substituted with a carboxylic acid ligand. In certain embodiments, the diruthenium catalyst comprises a 2-(1,3-dioxoisoindolin-2-yl)acetic acid ligand. In certain embodiments, this disclosure relates to methods of using catalysts in chemical transformations disclosed herein.
Five-coordinate bis-phenylphenoxy catalysts for the preparation of ethylene-based polymers
The invention provides a molecular transition metal complex selected from Formula 1, as described herein; an ethylene-based polymer; and a process to form the ethylene-based polymer, said process comprising polymerizing ethylene in the presence of at least one molecular transition metal complex selected from Formula 1, as described herein, and wherein either Z.sub.1 or Z.sub.2 is dative covalent (coordinate) to the metal (M). ##STR00001##
HAFNIUM-BASED METAL-ORGANIC FRAMEWORKS AS EPOXIDE RING-OPENING CATALYSTS
Metal-organic frameworks (MOFs) having inorganic nodes that comprise an octahedral Hf.sub.6 cluster capped by eight .sub.3-ligands and having twelve octahedral edges, wherein the .sub.3-ligands are hydroxo ligands, oxo ligands or aquo ligands; and organic linkers connecting the organic nodes, the organic linkers comprising 1,3,6,8-tetrakis(p-benzoic acid)pyrene units; wherein eight of the twelve octahedral edges of the inorganic nodes are connected to the 1,3,6,8-tetrakis(p-benzoic acid)pyrene units are provided.
Catalyst compositions and use thereof
This invention relates to novel transition metal catalyst compounds comprising four oxygen atoms bonded to a transition metal where two of the oxygen groups are bonded to the metal by dative bonds and a silyl or germyl bridge, catalyst systems comprising such, and polymerization processes using such.
PROCESS FOR THE PREPARATION OF LIGHTLY-BRANCHED HYDROPHOBES AND THE CORRESPONDING SURFACTANTS AND APPLICATIONS THEREOF
Processes to prepare lightly branched surfactant products comprise combining at least one olefin and a coordination-insertion catalyst under conditions such that at least one oligomer product is formed. The surfactant products comprise a main carbon chain containing an average of between 0.5 and 2.5 branches, wherein more than 50% of the branches are ethyl branches, wherein the branches are located more than one carbon away from each end of the main carbon chain in more than 20% of surfactant product molecules
Bridged bi-aromatic ligands and transition metal compounds prepared therefrom
Disclosed are novel bridged bi-aromatic phenol ligands and transition metal compounds derived therefrom. Also disclosed are methods of making the ligands and transition metal compounds.
Zirconium- and hafnium-based metal-organic frameworks as epoxide ring-opening catalysts
Metal-organic frameworks (MOFs) and method of using the MOFs to catalyze reactions involving epoxide ring-opening mechanisms are provided. The structure of the MOFs can be represented by the formula: M.sub.6(.sub.3-ligand).sub.8(OH.sub.x).sub.8(TBAPy).sub.2, where M is Zr or Hf, the ligands are selected from hydroxo-, oxo- and aquo-ligands, and x is independently selected from 1 or 2.
Homogenous catalytic composition for improving LPG combustion
The present invention discloses a homogenous cerium (Ce) catalyst composition comprising Ce(IV) complex alone, or Ce(IV) complex in a mixture with Ce(III) complex, that can significantly improve both LPG and soot combustion, resulting in higher flame temperatures, faster heating, reduced cooking time and reduced fuel consumption. The cerium(III) complex is cerium(III) 2-ethylhexanoate and the cerium(IV) complex is aqua(2-N-(2-hydroxyethylimino)-4-pentanoate) dinitrocerium(IV) [Ce(L1)(H.sub.2O)(NO.sub.3).sub.2], wherein L1 is 2-N-(2-hydroxyethylimino)-4-pentanone.
THERMOLATENT CATALYST AND ITS USE IN CURABLE COMPOSITIONS
Tin-containing catalysts are provided comprising a compound of formula I.
I:
##STR00001##
L1, L2, L3, and L4 are each independently selected from O, S, OC(?O), OC(?S), SC(?O), SC(?S), OS(?O).sub.2O, OS(?O).sub.2 N(R6)-, and OP(?O)(R6)-, wherein R6 represents hydrogen or a monovalent aliphatic, araliphatic, cycloaliphatic or aromatic group having up to 20 carbon atoms. R1, R2, R3, R1, R2, and R3 each independently represent a divalent aliphatic, araliphatic, cycloaliphatic or aromatic group having up to 20 carbon atoms; and R4, R5, R4, and R5 each independently represent hydrogen or a monovalent residue derived from reaction of a respective NH group with an isocyanate, an ethylenically unsaturated compound, a lactone, a dilactone, a thiolactone, a lactam, a thiolactam, a carboxylic acid or derivative thereof, or an epoxide. Also provided are curable compositions containing these catalysts and methods of controlling the rate of cure of curable compositions.
Metal complex and supported metal complex having disiloxane as ligand, method for production therefor, and supported metal catalyst prepared by using the same
A metal complex represented by the following Formula (1): ##STR00001##
(wherein M represents palladium or platinum; L represents a ligand selected from carbon monoxide, an olefin compound, an amine compound, a phosphine compound, an N-heterocyclic carbene compound, a nitrile compound and an isocyanide compound; n represents an integer of 0 to 2 showing the number of the ligand; and each of R.sup.1 to R.sup.4 represents an organic group). The metal complex described above can be fixed on an inorganic oxide while maintaining a skeletal structure thereof to obtain a supported metal complex, and this makes it possible to allow the supported metal complex to maintain the same catalytic activity as that of the original metal complex. Also, calcining the supported metal complex obtained in the manner described above makes it possible to obtain a supported metal catalyst which is improved in catalytic activity to a greater extent than conventional supported metal catalysts.