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Title: US5780701: Process for alkane group dehydrogenation with organometallic catalyst
[ Derwent Title ]


Country: US United States of America

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10 pages

 
Inventor: Kaska, William C.; Goleta, CA
Jensen, Craig M.; Kailua, HI

Assignee: The Regents of the University of California, Oakland, CA
University of Hawaii, Honolulu, HI
other patents from UNIVERSITY OF CALIFORNIA, THE REGENTS OF (599425) (approx. 4,840)
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Published / Filed: 1998-07-14 / 1996-07-26

Application Number: US1996000687717

IPC Code: Advanced: B01J 31/18; B01J 31/24; C07B 35/04; C07C 5/333; C07F 15/00;
Core: B01J 31/16; C07B 35/00; C07C 5/00; more...
IPC-7: C07C 5/327; C07C 5/333; C07C 5/373; C07F 15/02;

ECLA Code: B01J31/18; B01J31/24; C07B35/04; C07C5/333; C07F15/00N3; C07F15/00N6; M07C531/22; L01J531/02F2B; L01J531/82B; L01J531/82D; L01J531/82F; L01J531/82H; L01J531/82J; L01J531/82L;

U.S. Class: Current: 585/654; 556/013; 556/014; 556/021; 556/022; 556/023; 556/136; 556/137; 556/138; 556/140; 585/660;
Original: 585/654; 585/660; 556/013; 556/014; 556/021; 556/022; 556/023; 556/136; 556/137; 556/138; 556/140;

Field of Search: 585/659,660 556/014,23,138,140,13,21,22,136,137

Government Interest:

ORIGIN OF THE INVENTION
    This invention was completed with funding in part from the U.S. Department of Energy (Hydrogen Program), Contract No. DE-FC36-94AL85804. The U.S. Government has certain rights in this invention.

Priority Number:
1996-07-26  US1996000687717

Abstract:     An improved process is described for the catalytic dehydrogenation of organic molecules having a <IMAGE> group to produce a <IMAGE> group. The organic molecules are: <IMAGE> I <IMAGE> II <IMAGE> III <IMAGE> IV wherein: A1, A2, A3, and A4 are each independently P, As or N: E2 is independently C or N; E3 is independently C, Si or Ge; E4 is independently C, Si, or Ge; and E5 is independently C, Si or Ge; M1, M2, M3, and M4 each is a metal atom independently selected from the group consisting of ruthenium, rhodium, palladium, osmium, iridium and platinum; Q1, Q2, Q3, and Q4 are each independently a direct bond, -CH2-, -CH2CH2-, or CH=CH-; in structure I, structure II or structure IV, R1, R2, R3, and R4 are each independently selected from alkyl, alkenyl, cycloalkyl, and aryl, or R1 and R2 together and R3 and R4 together form a ring structure having from 4 to 10 carbon atoms, or in structure III, R5, R6, R7, and R8 are each independently selected from alkyl, alkenyl, cycloalkyl, and aryl, or R5 and R6 together and R7 and R8 together form a ring structure having from 4 to 10 carbon atoms, at a temperature of between about 100 DEG and 250 DEG C. for between about 1 hr and 300 days in the absence of N2. The surprisingly stable catalyst is a complex of an organic ligand comprising H, C, Si, N, P atoms, and a platinum group metal. The dehydrogenation is performed between about 100 to 200 DEG C., and has increased turnover.

Attorney, Agent or Firm: Peters, Verny, Jones & Biksa L.L.P. ;

Primary / Asst. Examiners: Caldarola, Glenn; Pasterczyk, J.

Maintenance Status: E2 Expired  Check current status

INPADOC Legal Status: Show legal status actions

Family: None

First Claim:
Show all 20 claims
We claim:     1. An improved process to remove hydrogen from an allyl-containing organic compound having at least one [Figure] group to produce an alkene compound having at least one [Figure] group, and hydrogen which process comprises: (a) contacting the alkyl-containing compound with a soluble complex of structure A, which structure is selected from structure I: [Figure] wherein: A1, A2, A3, and A4 are each independently P, As or N;
    • E2 is independently C or N;
    • E3 is independently C, Si, or Ge;
    • E4 is independently C, Si, or Ge;
    • and E5 is independently C, Si or Ge,
    • M1, M2, M3, and M4 each is a metal atom independently selected from the group consisting of ruthenium, rhodium, palladium, osmium, iridium and platinum;
    • Q1, Q2, Q3, and Q4 are each independently a direct bond, --CH2 --, --CH2 CH2--,--CH=CH--;
    • in structure I, structure II or structure IV, R1, R2, R3, and R4 are each independently selected from alkyl, alkenyl, cycloalkyl, and aryl, or R1 and R2 together and R3 and R4 together form a ring structure having from 4 to 10 carbon atoms, or
    • in structure III, R5, R6, R7, and R8 are each independently selected from alkyl, alkenyl, cycloalkyl, and aryl, or R5 and R6 together and R7 and R8 together form a ring structure having from 4 to 10 carbon atoms;
    • at a temperature of between about 100° and 250° C. for between about 1 hr and 300 days in the absence of N2.


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Forward References: Show 8 U.S. patent(s) that reference this one

       
U.S. References: Go to Result Set: All U.S. references   |  Forward references (8)   |   Backward references (10)   |   Citation Link

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Patent  Pub.Date  Inventor Assignee   Title
Buy PDF- 11pp US4447665  1984-05 Wennerberg  Standard Oil Company (Indiana) Dehydrogenation reactions
Buy PDF- 4pp US4472517  1984-09 Tsao et al.  Mobil Oil Corporation Preparation of metal-containing zeolite catalysts of increased stability and activity
Buy PDF- 18pp US4473505  1984-09 Mitchell, III  Exxon Research and Engineering Co. Phosphine and phosphonium compounds and catalysts
Buy PDF- 18pp US4522932  1985-06 Mitchell, III  Exxon Research & Engineering Co. Phosphine and phosphonium compounds and catalysts
Buy PDF- 25pp US4950798  1990-08 Stobart et al.  University of Victoria Process for catalytic hydroformylation
Buy PDF- 6pp US4962265  1990-10 De Clippeleir et al.  Labofina, S.A. Process and catalyst for the catalytic dehydrogenation of hydrocarbons
Buy PDF- 15pp US5554778  1996-09 Beatty et al.  E. I. Du Pont de Nemours and Company Ruthenium hydrogenation catalysts
Buy PDF- 11pp US5559262  1996-09 Beatty et al.  E. I. Du Pont de Nemours and Company Process for the preparation of ruthenium complexes and their in situ use as hydrogenation catalysts
Buy PDF- 19pp US5599962  1997-02 Beatty et al.  E. I. Du Pont de Nemours and Company Process for the preparation of ruthenium hydrogenation catalysts and products thereof
Buy PDF- 16pp US5689003  1997-11 Beatty et al.  E. I. Du Pont de Nemours and Company Ruthenium hydrogenation catalysts
       
Foreign References: None

Other Abstract Info: CHEMABS 129(11)136616V CHEMABS 129(11)136616V DERABS C1998-413172 DERABS C1998-413172

Other References:
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