Abstract:
The present invention relates to a process for the preparation of metal phthalocyanine sulphonamide [MPc(SO2NHR)x] catalyst useful for sweetening of LPG and light petroleum distillates which comprises reacting a metal phthalocyanine with chlorosulphonic acid at 90-150° C. for 1-5 hrs. cooling the reaction mixture adding 1-7 parts of a chloride reagent heating the said mixture at 60-80° C. from 0.5-3 hrs. to obtain the metal phthalocyanine sulphonyl chloride, isolating it by adding the reaction mixture in ice cold water, reacting the isolated metal phthalocyanine sulphonyl chloride with an amine of general formula H2NR where R is selected from hydrogen, aryl, alkyl and cycloalkyl in an aqueous or non-aqueous medium or a mixture thereof at a temperature in the range −4 to 15° C. and at a pH ranging between 7-9 in the presence of an acid binding agent to obtain the described metal phthalocyanine sulphonamide catalyst wherein the chloride reagent used is selected from the group consisting of thionyl chloride, phosphorus trichloride and phosphorus pentachloride, the binding agent used is selected from the group consisting of sodium bicarbonate, sodium carbonate, sodium hydroxide and tertiary organic bases selected from pyridine triethyl amine and piperidine and the catalyst metal phthalocyanine sulphonamide is selected from the group consisting of cobalt, manganese, nickel, iron vanadium phthalocyanine sulfonamide most preferably cobalt phthalocyanine sulphonamide.
Abstract:
The invention provides a process for an improved oxirane hydroformylation catalyst, the improved oxirane hydroformylation catalyst, and a one step process for preparing a 1,3-diol in the presence of such a catalyst. One process for preparing the hydroformylation catalyst involves: a) forming a complex (A) by contacting a ruthenium(0) compound with a ditertiary phosphine ligand; and b) forming a complex (B) by subjecting complex (A) to a redox reaction with a cobalt(0) carbonyl compound. This catalyst is used in a one step hydroformylation process for preparing a 1,3-diol, comprising the reaction of an oxirane with syngas at hydroformylation conditions in an inert solvent in the presence of the above hydroformylation catalyst where recovery of product is preferably accomplished via phase separation of a diol rich phase from the bulk reaction liquor.
Abstract:
The present invention relates to MgCl2.mROH.nH2O adducts, where R is a C1-C10 alkyl, 2≦m≦4.2, 0≦n≦0.7, characterized by an X-ray diffraction spectrum in which, in the range of 2&thgr; diffraction angles between 5° and 15°, the three main diffraction lines are present at diffraction angles 2&thgr; of 8.8±0.2°, 9.4±0.2° and 9.8±0.2°, the most intense diffraction lines being the one at 2&thgr;=8.8±0.2°, the intensity of the other two diffraction lines being at least 0.2 times the intensity of the most intense diffraction line. Catalyst components obtained from the adducts of the present invention are capable to give catalysts for the polymerization of olefins characterized by enhanced activity and stereospecificity with respect to the catalysts prepared from the adducts of the prior art.
Abstract translation:本发明涉及MgCl 2·mROH·nH 2 O加合物,其中R是C 1 -C 10烷基,2 <= m <= 4.2,0 <= n <0.7,其特征在于X射线衍射光谱,其中在 2θ衍射角在5°和15°之间的范围内,三条主要的衍射线分别以8.8±0.2°,9.4±0.2°和9.8±0.2°的衍射角2θ处存在,最强的衍射线为2θ= 8.8±0.2°,其他两条衍射线的强度是最强衍射线强度的0.2倍。由本发明的加合物得到的催化剂成分能够提供用于烯烃聚合的催化剂,其特征在于增强的 相对于由现有技术的加合物制备的催化剂的活性和立体定向性。
Abstract:
Disclosed are new catalysts for electroless metallization deposition, particularly catalysts that can be selectively activated and may be free of palladium and/or tin. Catalysts of the invention are preferably employed for electroless copper deposition.
Abstract:
A composition comprising a boron or aluminum containing neutral Lewis acid and a compound of formula I or Ia: wherein R1 and R2 are each independently hydrocarbyl, substituted hydrocarbyl, or silyl; Q is (i) C—R4, where R4 is hydrocarbyl, substituted hydrocarbyl, heteroatom connected hydrocarbyl, or heteroatom connected substituted hydrocarbyl, (ii) P(NH2)2, or (iii) S(NH)(NH2) or S(O)(OH); L is a monoolefin or a neutral Lewis base that can be displaced by a monoolefin; T is hydrogen, hydrocarbyl or substituted hydrocarbyl, or with L forms a &pgr;-allyl group; and M is Ni(II), Pd(II), Co(II) or Fe(II). The composition is useful as an olefin polymerization catalyst. Also described is a process for preparing a supported catalyst.
Abstract:
The invention provides new polymerization catalyst activator compositions including a non-coordinating or ionizing activator having a siloxane moiety. The invention also provides a new supported catalyst activator composition and method of making the composition. In one embodiment, the activator composition having a siloxane moiety represented by the formulae: [L—H]+[MQn]−O(SiR2O)x[MQn]−[L—H]+ or [L—H]+[MQn]−O(SiR2O)xR wherein L is an neutral Lewis base; [L—H]+ is a Bronsted acid or Lewis acid; n is 3 or 4; x is a positive integer; [MQn]− is a non-coordinating anion, wherein Q is independently selected from the group consisting of a hydride, a dialkylamido, a halide, an alkoxide, an aryloxide, a hydrocarbyl, a substituted hydrocarbyl, a halocarbyl, a substituted halocarbyl, a halosubstituted-hydrocarbyl radical and combinations thereof, M is an element selected from Group 13 of the Periodic Table of the Elements; and each R is independently selected from the group consisting of a hydrogen, a hydroxyl group, an alkyl, and combinations thereof.
Abstract:
The invention provides for compositions that are useful for polymerizing at least one monomer to produce a polymer, wherein the composition comprises a post-contacted organometal compound, a post-contacted organoaluminum compound, and a post-contacted solid oxide compound treated with boron and fluoride.
Abstract:
The invention provides a process for the in-situ generation of a metathesis active catalyst of the formula: comprising contacting an NHC carbene with a dimer of the formula [(arene)MX1X]2 and an alkyne of the formula RC≡CR1 or wherein M is ruthenium or osmium; X and X1 are the same or different and are each independently an anionic ligand; NHC is any N-heterocyclic carbene ligand; R, R1 and R2 are each independently hydrogen or a substituted or unsubstituted substituent selected from the group consisting of C1-C20 alkyl, C2-C20 alkenyl, C2-C20 alkynyl, aryl, C1-C20 carboxylate, C1-C20 alkoxy, C2-C20 alkenyloxy, C2-C20 alkynyloxy, aryloxy, C2-C20 alkoxycarbonyl, C1-C20 alkylthio, C1-C20 alkylsulfonyl and C1-C20 alkylsulfinyl; and R3 is OH. Preferably, the NHC is an s-IMES or IMES carbene ligand; the arene is preferably p-cymene and the alkyne is preferably acetylene. The invention further provides a process for ROMP and RCM reactions using the metathesis active catalysts.
Abstract:
The invention generally relates to a metallocene-based, olefin polymerization catalyst system. The easily processible polymer product has a broad molecular weight distribution, a high molecular weight, and a narrow composition distribution. The catalyst system comprises a first component with a Group-4-6 metal bonded to cyclopentadienyl-containing rings having at least two substituents bonded to the rings in the same position; a second component comprising a Group-4-6 metal bonded to cyclopentadienyl-containing rings having at least two substituents bonded to the rings; and a third component comprising a Group-4-6 metal bonded to cyclopentadienyl-containing rings where one of the rings is substituted identically to the first component and another is substituted identically to the second component. When the substituents of the first and second components are the same, they are bonded to the first component rings at positions different from the bonding positions of the second component rings.
Abstract:
A method and catalyst system for economically producing aromatic carbonates from aromatic hydroxy compounds is disclosed. In one embodiment, the present invention provides a method of carbonylating aromatic hydroxy compounds by contacting at least one aromatic hydroxy compound with oxygen and carbon monoxide in the presence of a carbonylation catalyst system that includes an effective amount of at least one Group 8, 9, or 10 metal source; an effective amount of at least one bromide composition; an effective amount of at least one activating organic solvent; an effective amount of a combination of inorganic co-catalysts comprising at least one titanium source and at least one copper source; and an effective amount of at least one base.