Olefin metathesis catalysts
US-2021053043-A1 · Feb 25, 2021 · US
US9815765B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9815765-B2 |
| Application number | US-201214348407-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 28, 2012 |
| Priority date | Sep 28, 2011 |
| Publication date | Nov 14, 2017 |
| Grant date | Nov 14, 2017 |
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Cis and trans ruthenium complexes that can be used as catalysts for ring opening metathesis polymerization (ROMP) are described. The complexes are generally square pyramidal in nature, having two anionic ligands X. Corresponding cationic complexes where one or both of the anionic ligands X are replaced by a non-co-ordinating anionic ligand are also described. Polymers such as polydicyclopentadiene (PDCPD) can be prepared using the catalysts.
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The invention claimed is: 1. A method of catalyzing a ring-opening metathesis polymerization (ROMP) reaction comprising: providing a reactant having at least two olefin and/or alkyne functional groups; providing a cis ruthenium complex according to formula I: wherein for each occurrence the groups X are the same or different and are anionic ligands or are fused to form a bidentate ligand; the groups R 1 and R 2 are fused together to form an indenylidene ring that may be substituted or unsubstituted; and the group Z is selected from the group consisting of: wherein the groups R 3 , R 4 and R 5 are each independently for each occurrence selected from the group consisting of substituted or unsubstituted primary, secondary or tertiary alkyl, that may be cyclic and may be unsaturated; substituted or unsubstituted aryl or heteroaryl; and optionally two or more of the groups R 3 , R 4 and R 5 are fused to form a ring; the group A is selected from the group consisting of a N-heterocyclic carbine (NHC) and contacting the reactant with the cis ruthenium complex according to formula I for a time and at a temperature capable of causing ring-opening metathesis polymerization (ROMP). 2. The method according to claim 1 wherein the group Z is a phosphite: 3. The method according to claim 1 wherein the anionic ligands X are independently selected from the group consisting of halogen, benzoate, and C 1 -C 5 carboxylates. 4. The method according to claim 1 wherein the group A is an N-heterocyclic carbene selected from the group consisting of: 5. The method according to claim 1 wherein the ruthenium complex is: 6. The method according to claim 1 wherein the ruthenium complex is according to formula XI: wherein the substituent Rs is selected from the group consisting of: OMe, CF 3 , Cl, NO 2 and SF 5 . 7. A ruthenium complex of the formula: 8. A ruthenium complex of the formula XI: wherein the substituent Rs is selected from the group consisting of: OMe, CF 3 , Cl, NO 2 and SF 5 . 9. A ruthenium complex of the formula: 10. A ruthenium complex of the formula: 11. The method according to claim 1 wherein the anionic ligands X are independently selected from the group consisting pivalate, trifluoroacetate, C 1 -C 5 alkoxy, phenoxy, C 1 -C 5 alkyl thio, tosylate, mesylate, brosylate, trifluoromethane sulfonate, phenylacetate, and pseudo-halogen. 12. A method of catalyzing a metathesis reaction comprising: introducing at least one olefin and/or alkyne functional group; providing a cis ruthenium complex according to formula I: wherein for each occurrence the groups X are the same or different and are anionic ligands or are fused to form a bidentate ligand; the groups R 1 and R 2 are fused together to form a substituted or unsubstituted indenylidene moiety that may be fused to a further ring; and the group Z is selected from the group consisting of: wherein the groups R 3 , R 4 and R 5 are each independently for each occurrence selected from the group consisting of substituted or unsubstituted primary, secondary or tertiary alkyl, that may be cyclic and may be unsaturated; substituted or unsubstituted aryl or heteroaryl; and optionally, two or more of the groups R 3 , R 4 and R 5 are fused to form a ring; the group A is a N-heterocyclic carbene; and contacting the reactant with the cis ruthenium complex according to formula I, for a time and at a temperature capable of causing metathesis polymerization. 13. A method of catalyzing a ring-opening metathesis polymerization (ROMP) reaction comprising: providing a reactant having at least two olefin and/or alkyne functional groups; providing a ruthenium complex according to the formula: and contacting the reactant with the ruthenium complex for a time and at a temperature capable of causing ring-opening metathesis polymerization (ROMP).
the ring being unsaturated · CPC title
Metathesis reactions at an unsaturated carbon-to-carbon bond · CPC title
Organic complexes · CPC title
with only hydrogen atoms, halogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms · CPC title
by reactions not involving the formation of cyano groups · CPC title
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