Abstract:
An organophosphorus compound useful in a phosphorus containing flame retardant and a flame retardant polyurethane foam, where the organophosphorus compound is shown in Formula (I) where Y is selected from the group consisting of an —OH group, an —NH2 group, an —NHR3 group, and an —SH group, where R3 is a monovalent hydrocarbyl group having 1 to 10 carbon atoms; R is a divalent hydrocarbyl group; X is a heteroatom group; and R1 and R2 are each independently a substituted or unsubstituted hydrocarbyl group, wherein R1 and R2 can be optionally joined to form a ring.
Abstract:
A battery electrolyte solution contains from 0.01 to 80% by weight of an aromatic phosphorus compound. The aromatic phosphorus compound provides increased thermal stability for the electrolyte, helping to reduce thermal degradation, thermal runaway reactions and the possibility of burning. The aromatic phosphorus compound has little adverse impact on the electrical properties of the battery, and in some cases actually improves battery performance.
Abstract:
Supported catalyst compositions use for use in the gas-phase polymerization of one or more α-olefins and methods for making and using the same, the catalyst composition including A) an inert support; B) a Group 4–10 metal complex corresponding to the formula: where M is a metal from one of Groups 4 to 10 of the Periodic Table of the Elements in the +2 or +4 formal oxidation state, Cp is a π-bonded anionic ligand group, Z is divalent moiety bound to Cp and bound to M by either covalent or coordinate/covalent bonds and contains boron or a member of Group 14 of the Periodic Table of the Elements, and also nitrogen, phosphorus, sulfur or oxygen, and X is a neutral conjugated diene ligand group having up to 60 atoms, or a dianionic derivative thereof; and C) an ionic cocatalyst capable of converting the metal complex into an active polymerization catalyst represented by the formula: [L*-H]+[(C6F5)3BC6H4—O—MORCx-1Xay]−, wherein L* is a neutral Lewis base, Mo is a metal or metalloid selected from Groups 1–14 of the Periodic Table of the Elements, RC independently each occurrence is a hydrogen or a hydrocarbyl, hydrocarbylsilyl, or hydrocarbysilylhydrocarbyl group having from 1 to 80 nonhydrogen atoms; Xa is a halo-substituted hydrocarbyl, hydrocarbylamino-substituted hydrocarbyl, hydrocarbyloxy-substituted hydrocarbyl, hydrocarbylamino, di(hydrocarbyl)amino, hydrocarbyloxy or halide noninterfering group having from 1 to 100 nonhydrogen atoms; x is an integer which ranges from 1 to an integer equal to the valence of MO; y is an integer which ranges from 0 to an integer equal to 1 less than the valence of MO; and x+y equals the valence of MO.
Abstract:
Titanium complexes comprising a 3-aryl-substituted cyclopentadienyl ring or substituted derivative thereof and at least one additional aryl substituent on the cyclopentadienyl ring, polymerization catalysts, and olefin polymerization processes using the same are disclosed.
Abstract:
Compounds and metal complexes comprising a polycyclic, fused ring ligand or inertly substituted derivative thereof having up to 60 atoms other than hydrogen, said ligand comprising at least: (1) a cyclopentadienyl ring, (2) a 6, 7, or 8 membered ring other than a 6-carbon aromatic ring, and (3) an aromatic ring, with the proviso that said 6, 7, or 8 membered ring (2), is fused to both the cyclopentadienyl ring (1), and the aromatic ring (3), polymerization catalysts, a process to prepare the novel compounds and complexes, and olefin polymerization processes using the same are disclosed.
Abstract:
Group 4 metal complexes comprising a cyclopentaphenanthreneyl ligand, catalytic derivatives thereof and their use as olefin polymerization catalysts, especially for the copolymerization of ethylene and a vinylaromatic monomer are disclosed. The resulting copolymers are uniform, pseudo-random copolymers of ethylene and a vinylaromatic monomer having a cluster index, CIES less than 1.0 and a polymerized vinylaromatic monomer content less than 50 mole percent.
Abstract:
Disclosed are thiocyanomethyloxy(or thiocyanomethylthio)-1,2,3-benzatriazin-4(3H)-one compounds corresponding to one of the formulae: ##STR1## wherein Z represents oxygen or sulfur; X represents --C1, --F, --I, C.sub.1 -C.sub.7 straight or branched chain alkyl, C.sub.1 -C.sub.7 straight or branched chain alkoxy, --CF.sub.3, --OCF.sub.3, --CN, --COOR wherein R is C.sub.1 -C.sub.7 straight or branched chain alkyl and n is an integer of from 0-4.These compounds have been found to exhibit antimicrobial and marine antifouling activity in industrial and commercial applications and compositions containing these compounds are so employed. e
Abstract:
Disclosed are ((4-phenyl-1,2,5--thiadiazol-3-yl)oxy)methyl ester thiocyanic acid compounds corresponding to the formula: ##STR1## wherein X represents --Br, --Cl, --F, --CF.sub.3, --OCF.sub.3, --CN, C.sub.1 -C.sub.7 straight or branched chain alkyl, C.sub.1 -C.sub.7 straight or branched chain alkoxy or --COOR wherein R is --H or C.sub.1 -C.sub.7 straight or branched chain alkyl and n is an integer of from 0-5.These compounds have been found to exhibit antimicrobial and marine antifouling activity in industrial and commercial applications and compositions containing these compounds are so employed.
Abstract:
Disclosed are substituted-5-thiomethylthiocyanato-1H-tetrazole compounds corresponding to the formula ##STR1## wherein R represents a C.sub.1 -C.sub.6 straight or branched chain alkyl radical, a C.sub.3 -C.sub.6 cycloalkyl or a phenyl radical of the formula ##STR2## wherein each X independently represents hydrogen, halo, a C.sub.1 -C.sub.6 straight or branched chain alkyl radical, a C.sub.3 -C.sub.6 cycloalkyl radical, a C.sub.1 -C.sub.6 straight or branched chain alkoxy radical, a C.sub.3 -C.sub.6 cycloalkoxy radical, cyano or nitro and n is 0-5.These compounds have been found to exhibit antimicrobial and marine antifouling activity in industrial and commercial applications and compositions containing these compounds are so employed.
Abstract:
5,7-Dihydroxy-N-(aryl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides are prepared by the cyclization of N-(3-(((aryl)amino)sulfonyl)-1H-1,2,4-triazol-5-yl)amines with malonyl halides under acidic conditions. With the addition of a phosphorus oxyhalide, malonic acid can be used in place of the malonyl halides and the 5,7-dihydroxy-1,2,4-triazolo[1,5-a]pyrimidine can be directly converted to the corresponding 5,7-dihalo derivative.