IP Library › Granted Patent US 11,104,751
Granted Patent B2
US 11,104,751 · App. 16/624,564 · Granted Aug 31, 2021

Biaryl phenoxy group iv transition metal catalysts for olefin polymerization

Inventors: Andrew M. Camelio (Midland, MI); Endre Szuromi (Lake Jackson, TX); David D. Devore (Midland, MI); Robert D. J. Froese (Midland, MI)
Assignee: Dow Global Technologies LLC
C08F210/16C07F7/28C08F4/64058C08F4/65908C08F4/65912C08F2420/05
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Quick Facts
Patent No.
US 11,104,751
App. No.
16/624,564
Granted
Aug 31, 2021
Kind
B2
Abstract

Embodiments are directed to catalyst systems comprising at least one metal ligand complex and to processes for polyolefin polymerization incorporating the catalyst systems. The metal ligand complexes have the following structures: (I)

Claims (42)

1. A catalyst system comprising a metal-ligand complex according to formula (I):

where

M is a metal chosen from titanium, zirconium, or hafnium, the metal having a formal oxidation state of +2, +3, or +4;

each X is a monodentate or bidentate ligand independently chosen from unsaturated (C 2 -C 50 )hydrocarbon, unsaturated (C 2 -C 50 )heterohydrocarbon, (C 1 -C 50 )hydrocarbyl, (C 6 -C 50 )aryl, (C 4 -C 50 )heteroaryl, cyclopentadienyl, substituted cyclopentadienyl, (C 4 -C 12 )diene, halogen, —N(R N ) 2 , or —NCOR C ;

n is 1, 2, or 3;

m is 1 or 2;

the metal-ligand complex has 6 or fewer metal-ligand bonds;

each Y is independently selected from oxygen or sulfur;

each R 1 is independently selected from the group consisting of (C 1 -C 50 )hydrocarbyl, (C 1 -C 50 )heterohydrocarbyl, (C 6 -C 50 )aryl, (C 4 -C 50 )heteroaryl, —Si(R C ) 3 , —Ge(R C ) 3 , —P(R P ) 2 , —N(R N ) 2 , —OR C , —SR C , —NO 2 , —CN, —CF 3 , R C S(O)—, —P(O)(R P ) 2 , R C S(O) 2 —, (R C ) 2 C═N—, R C C(O)O—, R C OC(O)—, R C C(O)N(R)—, (R C ) 2 NC(O)—, halogen, and —H;

each R 2 is independently chosen from (C 1 -C 50 )hydrocarbyl, (C 1 -C 50 )heterohydrocarbyl, (C 6 -C 50 )aryl, (C 4 -C 50 )heteroaryl, —Si(R C ) 3 , and or —Ge(R C ) 3 ;

for each individual ring containing groups z 1 and z 2 , each of z 1 and z 2 is independently selected from the group consisting of sulfur, oxygen, —N(R R )—, ═N—, and —C(R R )—, provided that at least one of z 1 or z 2 is —C(R R )—;

each A is independently chosen from -z 3 -z 4 -z 5 - or —C(R 3 )C(R 4 )C(R 5 )C(R 6 )—, where:

each of z 3 , z 4 , and z 5 is selected from the group consisting of sulfur, oxygen, —N(R R )—, and —C(R R )—, provided that exactly one of z 3 , z 4 , or z 5 is —C(R R )— or that exactly two of z 3 , z 4 , or z 5 are —C(R R )—; and

each R 3 , R 4 , R 5 , and R 6 is independently chosen from (C 1 -C 50 )hydrocarbyl, (C 1 -C 50 )heterohydrocarbyl, (C 6 -C 50 )aryl, (C 4 -C 50 )heteroaryl, —Si(R C ) 3 , —Ge(R C ) 3 , —P(R P ) 2 , —N(R N ) 2 , —OR C , —SR C , —NO 2 , —CN, —CF 3 , R C S(O)—, R C S(O) 2 —, (R C ) 2 C═N—, R C C(O)O—, R C OC(O)—, R C C(O)N(R)—, (R C ) 2 NC(O)—, halogen, or —H;

each R C , R N , and R P in formula (I) is independently a (C 1 -C 50 )hydrocarbyl; and

each R R is independently chosen from (C 1 -C 50 )hydrocarbyl, (C 1 -C 50 )heterohydrocarbyl, (C 6 -C 50 )aryl, (C 4 -C 50 )heteroaryl, —Si(R C ) 3 , —Ge(R C ) 3 , —P(R P ) 2 , —N(R N ) 2 , —OR C , —SR C , —NO 2 , —CN, —CF 3 , R C S(O)—, R C S(O) 2 —, (R C ) 2 C═N—, R C C(O)O—, R C OC(O)—, R C C(O)N(R)—, (R C ) 2 NC(O)—, halogen, or —H, wherein any two R R groups bonded to neighboring atoms are optionally linked.

2. The catalyst system according to claim 1 , wherein:

M is zirconium or hafnium;

each X is independently chosen from (C 6 -C 20 )aryl, (C 4 -C 20 )heteroaryl, (C 4 -C 12 )diene, or a halogen;

each Y is oxygen; and

each R 1 is independently chosen from (C 6 -C 50 )aryl or (C 4 -C 50 )heteroaryl.

3. The catalyst system according to claim 1 , wherein for each individual ring containing groups z 1 and z 2 , one of z 1 and z 2 is sulfur, and the other is C(H).

4. The catalyst system according to claim 1 , wherein each A is —C(R 3 )C(R 4 )C(R 5 )C(R 6 )— each R 3 , R 4 , R 5 , and R 6 is —H.

5. The catalyst system according to claim 1 , wherein each R 1 is carbazolyl and each R 2 is methyl.

6. The catalyst system according to claim 1 , wherein each R 1 is phenyl or a substituted phenyl.

7. The catalyst system according to claim 1 , wherein m is 2 and the metal-ligand complex has a structure according to formula (II):

where R 1 , R 2 , z 1 , z 2 , A, Y, and X are as defined in formula (I); and n is 1 or 2.

8. The catalyst system according to claim 7 , wherein:

M is zirconium or hafnium;

each X is independently chosen from (C 6 -C 50 )aryl, (C 6 -C 50 )heteroaryl, (C 4 -C 12 )diene, or halogen;

each Y is oxygen;

each R 1 and R 2 is independently chosen from (C 1 -C 50 )hydrocarbyl, (C 1 -C 50 )heterohydrocarbyl, (C 6 -C 50 )aryl, (C 4 -C 50 )heteroaryl, halogen, and hydrogen.

9. The catalyst system according to claim 7 , wherein for each individual ring containing groups z 1 and z 2 , one of z 1 and z 2 is sulfur, and the other is —C(H)—.

10. The catalyst system according to claim 7 , wherein each R 1 is carbazolyl and each R 2 is methyl.

11. The catalyst system according to claim 7 , wherein each R 1 is independently 3,6-di-tert-butylcarbazol-9-yl or 2,7-di-tert-butylcarbazol-9-yl.

12. The catalyst system according to claim 7 , wherein each R 1 is 3,5-di-tert-butylphenyl.

13. The catalyst system according to claim 7 , wherein each R 1 is 2,4,6-trimethylphenyl.

14. A polymerization process for producing an ethylene-based polymer, the polymerization process comprising:

polymerizing ethylene and at least one additional α-olefin in the presence of a catalyst system according to claim 1 and at least one activator to form a polymer.

15. A polymerization process for producing a propylene-based polymer, the polymerization process comprising:

polymerizing propylene with or without an additional α-olefin in the presence of a catalyst system according to claim 1 and at least one activator to form a polymer.

16. The polymerization process according claim 15 , wherein the activator comprises MMAO, bis(hydrogenated tallow alkyl)methylammonium, tetrakis(pentafluorophenyl)borate, or tris(pentafluorophenyl)borane.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 19, 2019
From: CAMELIO, ANDREW M.; SZUROMI, ENDRE; DEVORE, DAVID D.; FROESE, ROBERT D.J.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 051333/0599 →
Continuity (2)
Provisional Application 62522213 · Jun 20, 2017
Related Publication 20200131289A1 · Apr 30, 2020
Cited By (2)
US 12,221,508 US 12,552,879