IP Library Granted Patent US 7,169,863
Granted Patent B2
US 7,169,863 · App. 10/762,619 · Granted Jan 30, 2007

Salts of lewis acid/acid adducts and catalyst activators therefrom

Assignee: Dow Global Technologies Inc.
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Quick Facts
Patent No.
US 7,169,863
App. No.
10/762,619
Granted
Jan 30, 2007
Kind
B2
Abstract

A compound useful as a cocatalyst or cocatalyst component, especially for use as an addition polymerization catalyst compound, corresponding to the formula: (A* +a ) b (Z*J* j ) −c d , wherein: A* is a proton or a cation of from 1 to 80 atoms, preferably 1 to 60 atoms, not counting hydrogen atoms, said A* having a charge +a; Z* is an anion group of from 1 to 50 atoms, preferably 1 to 30 atoms, not counting hydrogen atoms, further containing two or more Lewis base sites, said Z* being the conjugate base of an inorganic Bronsted acid or a carbonyl- or non-cyclic, imino-group containing organic Bronsted acid; J* independently each occurrence is a Lewis acid of from 1 to 80 atoms, preferably 1 to 60 atoms, not counting hydrogen atoms, coordinated to at least one Lewis base site of Z*, and optionally two or more such J* groups may be joined together in a moiety having multiple Lewis acidic functionality; j is a number from 1 to 12; and a, b, c, and d are integers from 1 to 3, with the proviso that a×b is equal to c×d.

Claims (19)

1. A compound corresponding to the formula: (A* +a ) b (Z*J* j ) −c d , wherein:

A* is a proton or a cation of from 1 to 80 atoms not counting hydrogen atoms, said A* having a charge +a;

Z* is an anion group of from 1 to 50 atoms not counting hydrogen atoms, further containing two or more Lewis base sites, said Z* being the conjugate base of an inorganic Bronsted acid or a carbonyl- or non-cyclic, imino-group containing organic Bronsted acid;

J* independently each occurrence is a Lewis acid of from 1 to 80 atoms not counting hydrogen atoms, coordinated to at least one Lewis base site of Z*, and optionally two or more such J* groups may be joined together in a moiety having multiple Lewis acidic functionality;

j is a number from 1to 12; and

a, b, c, and d are integers from 1 to 3, with the proviso that a×b is equal to c×d.

2. A compound according to claim 1 wherein Z* is selected from the group consisting of: NO 3 − , PO 4 3 − ′, SO 4 2 − , RSO 3 − , CO 3 2− , [RC(O)O] − , [RC(NR)NR] − , [R′C(O)CR′C(O)R′] − , [(R′C(O)) 3 C] − , [RC(NR)CRC(NR)R] − , and [(RC(NR)) 3 C] − ,

wherein each R is independently a hydrogen-; hydrocarbyl-; or halocarbyl- group; a hydrocarbyl group further substituted with one or more carbonyl-, halo-, hydroxy-, dialkylamino-, dialkylaluminumoxy-, trihydrocarbylsilyl-, trihydrocarbylsiloxy-, or hydrocarbyloxy- groups; or a halocarbyl group further substituted with one or more carbonyl-, hydroxy-, dialkylamino-, dialkylaluminumoxy-, trihydrocarbylsilyl-, trihydrocarbylsiloxy-, or hydrocarbyloxy- groups; and

each R′ is independently R or two R′ groups may be joined together thereby forming a divalent group.

3. A compound according to claim 1 wherein Z* is an acetylacetonate, cyclohexa-1,3-dionate, [RC(O)O] − or NO 3 −2 , wherein R is a C 6-24 hydrocarbyl group, or an indane-1,3-dione anion or methyl triacetyl anion of the following structure:

4. A compound according to claim 1 wherein A* +a is a proton or is selected from the group consisting of ammonium, sulfonium, phosphonium, oxonium, carbonium, silylium, ferrocenium, Ag + , and Pb +2 cations.

5. A compound according to claim 1 wherein A* +a is a trimethylammonium-, triethylammonium-, tripropylammonium-, tri(n-butyl)ammonium-, methyldi(C 14-18 alkyl)ammonium-, dimethyl(C 14-18 alkyl)ammonium-, N,N-dimethylanilinium-, N,N-diethylanilinium-, N,N-dimethyl(2,4,6-trimethylanilinium)-, N,N-di(tetradecyl)lanilinium-, N,N-di(tetradecyl)-2,4,6-trimethylanilinium)-, N,N-di(octadecyl)lanilinium-, N,N-di(octadecyl)-2,4,6-trimethylanilinium)-, or methyldicyclohexylammonium- cation.

6. A compound according to claim 1 wherein J* ′ is tris(pentafluorophenyl)borane or tris(pentafluorophenyl)alumane.

7. A compound according to claim 1 that is a bis(tris(pentafluorophenyl)borane)- coordinated derivative of a trihydrocarbylammonium stearate or a mono(tris(pentafluorophenyl)-borane)- coordinated derivative of a trihydrocarbylammonium stearate.

8. A composition of matter comprising a compound according to any one of claims 1 – 7 and an organoaluminum compound.

9. A composition of matter comprising the admixture or reaction product, optionally in an inert diluent, of an inorganic Bronsted acid or a carbonyl- or non-cyclic, imino-group-containing organic Bronsted acid; from one to twelve moles per mole of Bronsted acid of a Lewis acid of from 1 to 80 atoms, not counting hydrogen atoms; optionally an amine or phosphine containing Lewis base of from 1 to 80 atoms, not counting hydrogen atoms; and further optionally an organoaluminum compound.

10. A catalyst composition for polymerization of addition polymerizable monomers comprising the combination or reaction product resulting from combining: 1) a Group 3–10 or Lanthanide metal complex, 2) a compound according to any one of claims 1 – 7 , 3 ) optionally an organoaluminum compound, and further optionally 4) a solid, particulated support.

11. The catalyst composition of claim 10 wherein the organoaluminum compound is an alumoxane.

12. A catalyst composition for polymerization of addition polymerizable monomers comprising the combination or reaction product resulting from combining: 1) a Group 3–10 or Lanthanide metal complex, 2) a compound according to claim 8 , and optionally 3) a solid, particulated support.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2017
From: VOGEL, ALEXANDER
To: THE DOW CHEMICAL COMPANY
Reel/Frame 043126/0687 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2017
From: THE DOW CHEMICAL COMPANY
To: DOW GLOBAL TECHNOLOGIES INC.
Reel/Frame 043126/0732 →
CHANGE OF NAME Recorded Jul 28, 2017
From: DOW GLOBAL TECHNOLOGIES INC.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 043368/0501 →
Continuity (3)
Division 1016409900 · Jun 4, 2002
Provisional Application 6030724900 · Jul 23, 2001
Related Publication 20040162215A1 · Aug 19, 2004