IP Library Granted Patent US 8,426,535
Granted Patent B2
US 8,426,535 · App. 12/801,741 · Granted Apr 23, 2013

Chain growth reaction process

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Quick Facts
Patent No.
US 8,426,535
App. No.
12/801,741
Granted
Apr 23, 2013
Kind
B2
Abstract

A process is disclosed for the preparation of zinc alkyl chain growth products via a catalyzed chain growth reaction of an alpha-olefin on a zinc alkyl, wherein the chain growth catalyst system employs a group 3-10 transition metal, or a group 3 main group metal, or a lanthanide or actinide complex, and optionally a suitable activator. The products can be further converted into alpha-olefins by olefin displacement of the grown alkyls as alpha-olefins from the zinc alkyl chain growth product, or into primary alcohols, by oxidation of the resulting zinc alkyl chain growth product to form alkoxide compounds, followed by hydrolysis of the alkoxides.

Claims (20)

1. A composition comprising:

i) a plurality of zinc alkyl compounds; and

ii) one or more chain growth catalysts;

at least one of the chain growth catalysts being selected from the group consisting of:

a) a complex of Formula (IV)

wherein M[T] is Ti[II], Ti[III], Ti[IV], Zr[II], Zr[III], Zr[IV], Hf[II], Hf[III], Hf[IV], V[II], V[III], V[IV], Nb[II], Nb[III], Nb[IV], Nb[V], Ta[II], Ta[III], Ta[IV], Cr[II], Cr[III], Mn[II], Mn[III], Mn[IV], Fe[II], Fe[III], Ru[II], Ru[III], Ru[IV], Co[II], Co[III], Rh[II], Rh[III], Ni[II], or Pd[II]; X represents an atom or group covalently or ionically bonded to the transition metal M; T is the oxidation state of the transition metal M and b is the valency of the atom or group X; Y 1 is C or P(R c ), A 1 to A 3 are each independently N or P or CR, with the proviso that at least one is CR; and R, R c , R 4 , R 5 , R 6 and R 7 are each independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, substituted heterohydrocarbyl or SiR′ 3 where each R′ is independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl;

b) a complex of Formula (III)

wherein M is Cr[II], Cr[III], Mn[II], Mn[III], Mn[IV], Fe[II], Fe[III], Ru[II], Ru[III], Ru[IV], Co[II], Co[III], Rh[II], Rh[III], Pd[II], Cu[I], or Cu[II]; X represents an atom or group covalently or ionically bonded to the transition metal M; R a and R b are each independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, substituted heterohydrocarbyl or SiR′ 3 where each R′ is independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl, and R a and R b may be joined together to form a ring; R 5 and R 7 are each as defined above; and L is a group datively bound to M; n is from 0 to 5; m is 1 to 3 and q is 1 or 2;

c) a complex of Formula (II)

wherein M is Y[II], Y[III], Sc[II], Sc[III], Ti[II], Ti[III], Ti[IV], Zr[II], Zr[III], Zr[IV], Hf[II], Hf[III], Hf[IV], V[II], V[III], V[IV], Nb[II], Nb[III], Nb[IV], Nb[V], Ta[II], Ta[III], Ta[IV], Cr[II], Cr[III], Mn[II], Mn[III], Mn[IV], Fe[II], Fe[III], Ru[II], Ru[III], Ru[IV], Co[II], Co[III], Rh[II], Rh[III], Ni[II], or Pd[II], X represents an atom or group covalently or ionically bonded to the transition metal M; R a , R b , R x , and R 5 are each independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, substituted heterohydrocarbyl or SiR′ 3 where each R′ is independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl, and any adjacent ones may be joined together to form a ring; L is a group datively bound to M; n is from 0 to 5; m is 1 to 3 and q is 1 or 2; and

d) a complex of Formula (I)

wherein M is Y[II], Y[III], Sc[II], Sc[III], Ti[II], Ti[III], Ti[IV], Zr[II], Zr[III], Zr[IV], Hf[II], Hf[III], Hf[IV], V[II], V[III], V[IV], Nb[II], Nb[III], Nb[IV], Nb[V], Ta[II], Ta[III], Ta[IV], Cr[II], Cr[III], Mn[II], Mn[III], Mn[IV], Fe[II], Fe[III], Ru[II], Ru[III], Ru[IV], Co[II], Co[III], Rh[II], Rh[III], Ni[II], or Pd[II], X represents an atom or group covalently or ionically bonded to the transition metal M; Y 1 is C or P(R c ); Y 2 is —O(R 7 ), —O (in which case the bond from O to M is covalent), —C(R b )═O, —C(R b )═N(R 7 ), —P(R b )(R d )═N(R 7 ) or —P(R b )(R d )═O; R a , R b , R c , R d , R 5 and R 7 are each independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, substituted heterohydrocarbyl or SiR′ 3 where each R′ is independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl, and any adjacent ones may be joined together to form a ring; G is either a direct bond between Y 1 and Y 2 , or is a bridging group, which optionally contains a third atom linked to M when q is 1; L is a group datively bound to M; n is from 0 to 5; m is 1 to 3 and q is 1 or 2.

2. The composition of claim 1 wherein the mole ratio of transition metal M to zinc alkyl is between 1×10 −7 and 1×10 −1 .

3. The composition of claim 1 further comprising an activator.

4. The composition of claim 1 wherein the chain growth catalyst system comprises a complex of the Formula (IV):

wherein M[T] is Ti[II], Ti[III], Ti[IV], Zr[II], Zr[III], Zr[IV], Hf[II], Hf[III], Hf[IV], V[II], V[III], V[IV], Nb[II], Nb[III], Nb[IV], Nb[V], Ta[II], Ta[III], Ta[IV], Cr[II], Cr[III], Mn[II], Mn[III], Mn[IV], Fe[II], Fe[III], Ru[II], Ru[III], Ru[IV], Co[II], Co[III], Rh[II], Rh[III], Ni[II], or Pd[II]; X represents an atom or group covalently or ionically bonded to the transition metal M; T is the oxidation state of the transition metal M and b is the valency of the atom or group X; Y 1 is C or P(R c ), A 1 to A 3 are each independently N or P or CR, with the proviso that at least one is CR; and R, R c , R 4 , R 5 , R 6 and R 7 are each independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl, substituted heterohydrocarbyl or SiR′ 3 where each R′ is independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl.

5. The composition according to claim 4 wherein Y 1 is C, and A 1 to A 3 are each independently CR, or A 1 and A 3 are both N and A 2 is CR, or one of A 1 to A 3 is N and the others are independently CR.

6. The composition according to claim 4 wherein Y 1 is C, A 1 to A 3 are each independently CR, and R 5 is represented by the group “P” and R 7 is represented by the group “Q” as follows:

wherein R 19 to R 28 are independently selected from hydrogen, halogen, hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl; when any two or more of R 1 to R 4 , R 6 and R 19 to R 28 are hydrocarbyl, substituted hydrocarbyl, heterohydrocarbyl or substituted heterohydrocarbyl, said two or more can be linked to form one or more cyclic substituents.

7. The composition according to claim 3 wherein the activator for the chain growth catalyst system is selected from organoaluminum compounds or hydrocarbylboron compounds.

Assignments (12)
SECURITY INTEREST Recorded May 4, 2017
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 042400/0019 →
SECURITY INTEREST Recorded May 4, 2017
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 042402/0128 →
SECURITY INTEREST Recorded May 4, 2017
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 042402/0519 →
SECURITY INTEREST Recorded May 4, 2017
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 042402/0758 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2014
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: INEOS SALES (UK) LIMITED
Reel/Frame 032388/0553 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 13, 2014
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 032264/0400 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT SUPPLEMENT Recorded Feb 13, 2014
From: INEOS SALES (UK) LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 032264/0470 →
SECURITY AGREEMENT Recorded Jun 26, 2012
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 028444/0639 →
SECURITY INTEREST Recorded Feb 23, 2012
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 027748/0039 →
SECURITY INTEREST Recorded Nov 28, 2011
From: INEOS COMMERCIAL SERVICES UK LIMITED
To: BARCLAYS BANK PLC
Reel/Frame 027286/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2011
From: INEOS EUROPE LIMITED
To: INEOS COMMERCIAL SERVICES UK LIMITED
Reel/Frame 027060/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2010
From: BRITOVSEK, GEORGE JOHAN PETER; COHEN, STEVEN A.; GIBSON, VERNON CHARLES
To: INEOS EUROPE LIMITED
Reel/Frame 024928/0847 →