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US3907849A Expired / Lapsed US ⏱️ 0.0 years remaining

Chromium tris-diorgano-orthophosphates and their preparation

Assignee: Anderson Development Co
•
Filing: 1972-12-29
•
Granted: 1975-09-23
•
Expires: 1992-12-29
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Abstract

Abstract This invention comprises novel chromium tris-diorganoorthophosphates, including coordination polymers thereof, and their preparation by the reaction of certain simple salts or esters of trivalent chromium with alkali or alkaline earth metal salts of diorgano orthophosphoric acid and separation of the novel compounds. The simple salts or esters include primarily the halides, nitrates, sulfates and acetates of trivalent chromium. The alkali metal salts or alkaline earth metal salts of diorgano orthophosphoric acids include primarily compounds of the general formula M'' (OP(O)(OR)2)n in which M'' is an alkali metal or an alkaline earth metal, each n is the valence of such metal and each R can be an alkyl, alkoxyalkyl or cycloalkyl group of one to about eight carbon atoms and the chlorinated and brominated derivatives thereof. This invention also comprises the use of these novel compounds in conjunction with alkyl aluminum halides as catalysts for alkylation of benzene and other aromatic compounds and the polymerization of ethylene, propylene and other olefins.

Inventors

  • 👤 Jeffrey G Meyer

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 18:21
CPC Classifications
C; C08; C08F; C08F10/00; B; B01; B01J; B01J31/00; B01J31/02; B01J31/12; B01J31/14; B01J31/143; B01J31/16; B01J31/18; B01J31/1845; B01J31/185; C07; C07C; C07C2/00; C07C2/54; C07C2/64; C07C2/66; C07C2/68; C07F; C07F9/00; C07F9/02; C08F110/00; C08F110/02; B01J2531/00; B01J2531/60; B01J2531/62; C07C2531/00; C07C2531/02; C07C2531/12; C07C2531/14

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 54 words
A COMPOUND SOLUBLE IN HALOGENALKANE SOLVENTS AND HAVING THE FORMULA CR (OP (O) (OR)2)3 IN WHICH EACH R IS SELECTED FROM THE GROUP CONSISTING OF ALKYL CYCLOALKYL, ALKOXYAKYL, CHLORINATED DERIVATES THEREOF AND BROMINATED DERIVATIVES THEREOF, SAID ALKYL AND CYCLOAKYL CONTAINING ONE TO EIGHT CARBON ATOMS AND SAID ALKOXYALKYL CONTAINING THREE TO SIX CARBON ATOMS.
Claim 2
Dependent Claim 54 words
A COMPOUND SOLUBLE IN HALOGENALKANE SOLVENTS AND HAVING THE FORMULA CR (OP (O) (OR)2)3 IN WHICH EACH R IS SELECTED FROM THE GROUP CONSISTING OF ALKYL CYCLOALKYL, ALKOXYAKYL, CHLORINATED DERIVATES THEREOF AND BROMINATED DERIVATIVES THEREOF, SAID ALKYL AND CYCLOAKYL CONTAINING ONE TO EIGHT CARBON ATOMS AND SAID ALKOXYALKYL CONTAINING THREE TO SIX CARBON ATOMS.
Claim 3
Independent Claim 213 words
THE METHOD CONSISTING ESSENTIALLY OF(1) HEATING A COMPOUND OF THE FORMULA M'' (OP (O) (OR)2)N IN WHICH M'' IN AN ALKALI METAL OR ALKALINE EARTH METAL, N IS THE VALENCE OF THAT METAL AND EACH R IS SELECTED FROM THE CLASS CONSISTING OF ALKYL, CYLOAKYL, ALKOXYL, CHLORINATED DERIVATIVES THEREOF AND BROMINATED DERIVATIVES THEREOF, SAID ALKYL AND CYCLOAKYL CONTAINING ONE TO EIGHT CARBON ATOMS AND SAID ALKOXYALKYL CONTAINING THREE TO SIX CARBON ATOMS, WITH A COMPOUND OF THE FORMULA MAZB IN WHICH EACH M IS TRIVALENT CHROMIUM, EACH Z IS A NON-REDUCING SUBSTITUENT SELECTED FROM THE GROUP CONSISTING OF ANIONS OF NON-METALLIC INORGANIC ACIDS, THE HYDROXYL GROUP AND ORGANIC CARBOXYLIC GROUPS OF FROM ONE TO ABOUT 18 CARBON ATOMS, A IS 1 TO 2, B IS 1 OR 3 AND THE VALUES OF A AND B DEPENDEND ON THE VALENCE OF Z, SAID HEATING BEING AT A TEMPERATURE BETWEEN ABOUT 0* AND 150*C. BUT BELOW THE DECOMPOSITITION TEMPERATURES OF THE REACTANTS AND AT A PRESSURE AND FOR A TIME SUFFICIENT TO CAUSE A REACTION, AND (2) SEPARATING FROM THE REACTION MIXTURE A PRODUCT CONSISTING ESSENTIALLY OF A COMPOUND SOLUBLE IN HALOGENO-ALKANE SOLVENTS AND HAVING THE FORMULA CR (OP (O) (OR)2)3 BY EXTRACTION WITH A SOLVENT FOR SAID PRODUCT BUT NOT THE RESULTING M''-CONTAINING BY-PRODUCT
Claim 4
Independent Claim 213 words
THE METHOD CONSISTING ESSENTIALLY OF(1) HEATING A COMPOUND OF THE FORMULA M'' (OP (O) (OR)2)N IN WHICH M'' IN AN ALKALI METAL OR ALKALINE EARTH METAL, N IS THE VALENCE OF THAT METAL AND EACH R IS SELECTED FROM THE CLASS CONSISTING OF ALKYL, CYLOAKYL, ALKOXYL, CHLORINATED DERIVATIVES THEREOF AND BROMINATED DERIVATIVES THEREOF, SAID ALKYL AND CYCLOAKYL CONTAINING ONE TO EIGHT CARBON ATOMS AND SAID ALKOXYALKYL CONTAINING THREE TO SIX CARBON ATOMS, WITH A COMPOUND OF THE FORMULA MAZB IN WHICH EACH M IS TRIVALENT CHROMIUM, EACH Z IS A NON-REDUCING SUBSTITUENT SELECTED FROM THE GROUP CONSISTING OF ANIONS OF NON-METALLIC INORGANIC ACIDS, THE HYDROXYL GROUP AND ORGANIC CARBOXYLIC GROUPS OF FROM ONE TO ABOUT 18 CARBON ATOMS, A IS 1 TO 2, B IS 1 OR 3 AND THE VALUES OF A AND B DEPENDEND ON THE VALENCE OF Z, SAID HEATING BEING AT A TEMPERATURE BETWEEN ABOUT 0* AND 150*C. BUT BELOW THE DECOMPOSITITION TEMPERATURES OF THE REACTANTS AND AT A PRESSURE AND FOR A TIME SUFFICIENT TO CAUSE A REACTION, AND (2) SEPARATING FROM THE REACTION MIXTURE A PRODUCT CONSISTING ESSENTIALLY OF A COMPOUND SOLUBLE IN HALOGENO-ALKANE SOLVENTS AND HAVING THE FORMULA CR (OP (O) (OR)2)3 BY EXTRACTION WITH A SOLVENT FOR SAID PRODUCT BUT NOT THE RESULTING M''-CONTAINING BY-PRODUCT
Claim 5
Dependent Claim 20 words
A composition in accordance with claim 1 wherein each R is an alkyl group of two to four carbon atoms.
Claim 6
Dependent Claim 20 words
A composition in accordance with claim 1 wherein each R is an alkoxyalkyl group containing three to six carbon atoms.
Claim 7
Dependent Claim 20 words
A method in accordance with claim 2 wherein each R is an alkyl group of two to four carbon atoms.
Claim 8
Dependent Claim 20 words
A method in accordance with claim 2 wherein each R is an alkoxyalkyl group containing three to six carbon atoms.
Claim 9
Dependent Claim 15 words
A method in accordance with claim 2 wherein each M'' is an alkaline earth metal.

References Cited (Backward Citations)

US2228659A Cited
US2325597A Cited
US2329707A Cited
US2409774A Cited
US2885417A Cited
US3474080A Cited
US3678086A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1978-09-22 1979-03-24 1979-09-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-09-22 1983-03-24 1983-09-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-09-22 1987-03-24 1987-09-23 $7700.00 Window Closed / Lapsed

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