Ligand components, associated reaction products, activated reaction products, hydrosilylation catalysts and hydrosilylation curable compositions including the ligand components, and associated methods for preparing same

Patent metadata

Field	Value
Publication number	US-10046318-B2
Application number	US-201515537630-A
Country	US
Kind code	B2
Filing date	Nov 13, 2015
Priority date	Dec 19, 2014
Publication date	Aug 14, 2018
Grant date	Aug 14, 2018

Abstract

A ligand component is formed according to formula (1):R 1 2 P—X—N═C(R 2 )—Y, wherein R 1 is Ph or Cyc or a C 1 -C 20 substituted or unsubstituted ailkyl group; each Ph is a substituted or unsubstituted phenyl group; each Cyc is a substituted or unsubstituted cycloalkyl group; X is an unsubstituted arylene or a C 2 -C 3 substituted or unsubstituted alkylene; R 2 is H, methyl or Ph; and Y N is pyridyl, 6-phenylpyridyl or 6-methylpyridyl; with the proviso that when X is a C 2 substituted or unsubstituted alkylene and Y is pyridyl, R 2 is methyl or Ph. A reaction product including the ligand component and a metal precursor is prepared by combining the ligand component with the metal precursor. An activated reaction product is formed by activating the reaction product as a hydrosilylation catalyst.

First claim

What is claimed is:

1. A reaction product comprising a ligand component according to formula (1):
R 1 2 P—X—N═C(R 2 )—Y  (1),

wherein:
R 1 is Ph or Cyc or a C 1 -C 20 substituted or unsubstituted alkyl group;
each Ph is a substituted or unsubstituted phenyl group;
each Cyc is a substituted or unsubstituted cycloalkyl group;
X is an unsubstituted arylene or a C 2 -C 3 substituted or unsubstituted alkylene;
R 2 is H, methyl or Ph; and
Y is pyridyl or 6-phenylpyridyl or 6-methylpyridyl;
with the proviso that when X is a C 2 substituted or unsubstituted alkylene and Y is pyridyl, R 2 is methyl or Ph; and
a metal precursor according to formula (2):
[M-A x ] n   (2),

wherein:
M is a metal selected from iron, cobalt, manganese, and ruthenium;
each A is independently a displaceable substituent;
subscript x is an integer with a value ranging from 1 to a maximum valence number of M; and
n is 1 or 2,
wherein the reaction product comprises a single phosphorus atom.

2. The reaction product of claim 1 , wherein the metal precursor is selected from iron (II) bromide, cobalt (II) chloride, cobalt (I) chloride, Co (I) Me, and any combination thereof.

3. The reaction product according to claim 1 , wherein the reaction product is further defined according to any one of formulas (2A), (2B), (2C), (2D), (2F), and (2G) as:

wherein each Ph is an unsubstituted phenyl group.

4. An activated reaction product comprising the reaction product of claim 1 and an ionic activator or a reducing agent.

5. The activated reaction product of claim 4 , wherein the ionic activator is LiCH 2 SiMe 3 .

6. A composition comprising:
(A) the activated reaction product according to claim 4 ;
(B) a compound having an average, per molecule, of one or more aliphatically unsaturated organic groups; and
optionally (C) an Si—H functional compound having an average, per molecule, of at least one silicon-bonded hydrogen atom, wherein component (C) is present when the compound of component (B) does not contain a silicon-bonded hydrogen atom.

7. The composition of claim 6 , where:
compound (B) is a polyorganosiloxane having an average, per molecule, of one or more aliphatically unsaturated organic groups capable of undergoing hydrosilylation reaction;
compound (C) a silane according to formula (5):
R 4 e SiH f   (5),

wherein:
subscript e is 0, 1, 2, or 3; subscript f is 1, 2, 3, or 4, with the proviso that a sum of (e+f) is 4, and
each R 4 is independently a halogen atom or a monovalent organic group.

8. A method comprising:
(1) combining components comprising a metal precursor and a ligand component, thereby preparing a reaction product, where:
the metal precursor has formula (2): [M-A x ] n , wherein M is a metal selected from iron, cobalt, manganese, and ruthenium; each A is independently a displaceable substituent; subscript x is an integer with a value ranging from 1 to a maximum valence number of M; and n is 1 or 2; and
the ligand component has general formula (1): R 1 2 P—X—N═C(R 2 )—Y, wherein R 1 is Ph or Cyc or a C 1 -C 20 substituted or unsubstituted alkyl group; each Ph is a substituted or unsubstituted phenyl group; each Cyc is a substituted or unsubstituted cycloalkyl group; X is an unsubstituted arylene or a C 2 -C 3 substituted or unsubstituted alkylene; R 2 is H, methyl or Ph; and Y is pyridyl or 6-phenylpyridyl or 6-methylpyridyl; with the proviso that when X is a C 2 substituted or unsubstituted alkylene and Y is pyridyl, R 2 is methyl or Ph,
wherein the reaction product comprises a single phosphorus atom.

9. The method according to claim 8 , wherein the reaction product is further defined according to any one of formulas (2A), (2B), (2C), (2D), (2F), and (2G) as:

wherein each Ph is an unsubstituted phenyl group.

10. The method according to claim 8 , wherein formula (1) is further defined according to any one of formulas (1A)-(1I) as:

wherein each Ph is an unsubstituted phenyl group, wherein Cy is an unsubstituted cyclohexyl group and iPr is an isopropyl group.

11. The method according to claim 8 , wherein the metal precursor is selected from iron (II) bromide, iron (II) chloride, cobalt (II) chloride, cobalt (I) chloride, Co (I) Me, and any combination thereof.

12. The method according to claim 8 further comprising (2) combining the reaction product with an ionic activator or a reducing agent to form an activated reaction product.

13. The method of claim 12 , wherein the ionic activator is LiCH 2 SiMe 3 or LiCH 3 .

14. The composition of claim 6 , where the composition further comprises one or more additional components, which are distinct from components (A), (B), and (C), and which are selected from the group consisting of (D) a spacer; (E) an extender, a plasticizer, or a combination thereof; (F) a filler; (G) a filler treating agent; (H) a biocide; (I) a stabilizer, (J) a flame retardant; (K) a surface modifier; (L) a chain lengthener; (M) an endblocker; (N) a flux agent; (O) an anti-aging additive; (P) a pigment; (Q) an acid acceptor; (R) a rheological additive; (S) a vehicle; (T) a surfactant; (U) a corrosion inhibitor; and a combination thereof.

15. A reaction product of the composition of claim 6 .

16. A method comprising:
(1) combining components comprising a metal precursor and a ligand component, thereby preparing a reaction product (A), where:
the metal precursor has formula (2): [M-A x ] n , wherein M is a metal selected from iron, cobalt, manganese, and ruthenium; each A is independently a displaceable substituent; subscript x is an integer with a value ranging from 1 to a maximum valence number of M; and n is 1 or 2; and
the ligand component has general formula (1): R 1 2 P—X—N═C(R 2 )—Y, wherein R 1 is Ph or Cyc or a C 1 -C 20 substituted or unsubstituted alkyl group; each Ph is a substituted or unsubstituted phenyl group; each Cyc is a substituted or unsubstituted cycloalkyl group; X is an unsubstituted arylene or a C 2 -C 3 substituted or unsubstituted alkylene; R 2 is H, methyl or Ph; and Y is pyridyl or 6-phenylpyridyl or 6-methylpyridyl; with the proviso that when X is a C 2 substituted or unsubstituted alkylene and Y is pyridyl, R 2 is methyl or Ph;

(2) combining the prepared reaction product (A) with a composition comprising:
(B) a compound having an average, per molecule, of one or more aliphatically unsaturated organic groups; and
optionally (C) an Si—H functional compound having an average, per molecule, of at least one silicon-bonded hydrogen atom, wherein component (C) is present when the compound of component (B) does not contain a silicon-bonded hydrogen atom;

(3) combining the reaction product with an ionic activator or a reducing agent to form an activated reaction product; and
(4) reacting component (B) and optionally component (C) in the presence of the activated reaction product via a hydrosilylation reaction to form a reaction product of component (B) and optionally component (C).

17. The method of claim 16 , the activated reaction product is formed in situ with component (B) and optional component (C).

18. The reaction product according to claim 2 , wherein the reaction product is further defined according to any one of f

Assignees

• Dow Corning
• Univ Illinois
• Dow Silicones Corp

Inventors

• Dash Aswini
• Rauchfuss Thomas B
• Chu wan-yi
• Gilbert-Wilson Ryan J

Classifications

• B01J2531/845

  Cobalt · CPC title

• C07F15/06

  Cobalt compounds · CPC title

• C07F7/1876

  by reactions involving the formation of Si-C linkages · CPC title

• C07F9/582

  Chemistry & Metallurgy · mapped topic

• C07F15/065

  without a metal-carbon linkage · CPC title