Energy curable compositions: two component curing agents

Claim 3

The method according to claim 1 wherein said energy is at least one of electromagnetic radiation, accelerated particles, or thermal energy.

Claim 4

The method according to claim 1 wherein said polymerization is effected in two stages, the first stage involving radiation and the second step involving thermal cure.

Claim 5

The method composition according to claim 1 wherein said organometallic salt has the formula: [((L.sup.1)(L.sup.2)M).sub.b (L.sup.3)(L.sup.4)].sup.+e X.sub.f I wherein M represents the same or different metals selected from the elements of Periodic Groups IVB, VB, VIB, VIIB, and VIIIB; with the proviso that Formula I can represent an organometallic salt having a mono- or bimetallic cation; L 1 represents none, 1, 2, or 3 ligands contributing pi-electrons that can be the same or different ligand selected from substituted and unsubstituted acyclic and cyclic unsaturated compounds and groups and substituted and unsubstituted carbocyclic aromatic and heterocyclic aromatic compounds, each capable of contributing two to twelve pi-electrons to the valence shell of M; L 2 represent none or 1 to 6 ligands contributing an even number of sigma-electrons that can be the same or different selected from mono-, di-, and tri-dentate ligands, each contributing 2, 4, or 6 sigma-electrons to the valence shell of M; L 3 represents none, 1 or 2 bridging ligands pi-electrons that can be the same or different ligand selected from substituted and unsubstituted acyclic and cyclic unsaturated compounds and groups and substituted and unsubstituted carbocyclic aromatic and heterocyclic aromatic compounds, each capable of acting as a bridging ligand contributing 2 to 24 pi-electrons to the valence shells of two metal atoms simultaneously; L 4 represents none, 1, 2 or 3 bridging ligands contributing an even number of sigma-electrons that can be the same or different selected from mono, di, and tri-dentate ligands, each donating 2, 4, or 6 sigma-electrons to the valence shells of two M simultaneously; with the proviso that the total electronic charge contributed to M by the ligands L 1 , L 2 , L 3 and L 4 plus the product of ionic charge on M with b results in a residual net positive charge of e to the cation; b is an integer having a value of 1 or 2; e is an integer having a value of 1 or 2, the residual electrical charge of the cation; X is an anion selected from organic sulfonate anions and halogen-containing complex anions of a metal or metalloid; f is an integer of 1 or 2, the number of anions required to neutralize the charge e on the cation.

Claim 6

The method according to claim 4 wherein (a) the ligand L 1 is provided by a monomeric or polymeric compound having an accessible unsaturated group, and contains less than 100 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-peroxidic oxygen, phosphorus, arsenic, selenium, antimony, tellurium, silicon, germanium, tin, and boron, (b) the ligand L 2 is selected from: (1) monodentate ligands having up to 30 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-peroxidic oxygen, phosphorus, arsenic, selenium, antimony, tellurium, and (2)/ polydentate ligands capable of forming with metal M a 4-, 5-, or 6-membered saturated or unsaturated ring containing up to 30 carbon atoms and up to /10 hetero atoms selected from the group consisting of nitrogen sulfur, non-peroxidic oxygen, phosphorus, arsenic, selenium, antimony, tellurium, in addition to the metal atom; (c) the ligand L 3 of the ionic salt each is provided by a monomeric or polymeric compound, has an accessible unsaturated group and has up to 30 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-peroxidic oxygen, phosphorus, arsenic, selenium, antimony, tellurium, silicon, germanium, tin, and boron; and (d) the bridging ligand L 4 of the ionic salt is provided by monodentate and polydentate compound which contains less than 100 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-peroxidic oxygen, nitrogen, phosphorus, arsenic, selenium, antimony and tellurium.

Claim 7

The method according to claim 5 wherein the ligand L 1 is substituted by a group selected from the group consisting of hydrocarbyl, hydrocarbyloxy, hydrocarbylmercapto, hydrocarbylcarbonyloxy, hydrocarbylcarbonyl, hydrocarbylcarbonamido, azo, boryl, halo, hydroxy, cyano, nitro, nitroso, oxo, dimethylamino, diphenylphosphino, diphenylarsino, diphenylstibine, tributyltin, methylseleno, ethyltelluro, trimethylsiloxy, and condensed rings, said group containing up to 30 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-periodic oxygen, nitrogen, sulfur, oxygen, phosphorous, arsenic, selenium, antimony, tellurium, silicon, germanium, tin, and boron.

Claim 8

The method according to claim 1 wherein said salt has the formula: [(L.sup.5)(L.sup.6)M].sup.+e X.sub.f II wherein M represents a metal selected from the group consisting of elements of the Periodic Groups IVB, VB, VIB, VIIB, and VIIIB; L 5 represents none, one, or two pi-electron contributing ligands that can be the same or different ligand selected from the same groups of ligands as L 1 of formula I; L 6 represents none or 1 to 6 ligands that can be the same or different ligand, contributing an even number of sigma-electrons selected from the same groups of ligands as L 2 of formula I; with the proviso that the total electronic charge contributed to M by L 5 and L 6 plus the ionic charge on M results in a residual net positive charge of e to the complex; and e, f, and X have the same definition as defined in claim 3.

Claim 9

The method according to claim 7 wherein ligand L 5 of the ionic salt contains less than 100 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-peroxidic oxygen, phosphorus, arsenic, selenium, antimony, tellurium, silicon, germanium, tin, and boron; and ligand L 6 of the ionic salt is selected from: (a) monodentate ligands having up to 30 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, oxygen, phosphorus, arsenic, selenium, antimony, and tellurium, and (b) polydentate ligands capable of forming with metal M a 4-, 5-, or 6-membered saturated or unsaturated ring containing up to 30 carbon atoms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-peroxidic oxygen, phosphorus, arsenic, selenium, antimony, and tellurium.

Claim 10

The method according to claim 8 wherein ligand L 5 is substituted by a group selected from hydrocarbyl, hydrocarbyloxy, hydrocarbylmercapto, hydrocarbyloxycarbonyl, hydrocarbylcarbonyl, hydrocarbylcarbonamido, phenyl, azo, boryl, halo, hydroxy, cyano, nitro, nitroso, oxo, dimethylamino, diphenylphosphino, diphenylarsino, diphenylstibine, tributyltin, methylseleno, ethylselluro, trimethylsiloxy, and condensed rings, said group containing up to 30 carbon toms and up to 10 hetero atoms selected from the group consisting of nitrogen, sulfur, non-peroxidic oxygen, phosphorus, arsenic, selenium, antimony, tellurium, silicon, germanium, tin, and boron.

Claim 11

The method according to claim 1, wherein said bicomponent curing agent is present in an amount sufficient to effect polymerization.

Claim 12

The method according to claim 1 wherein said onium salt has the formula III AY III wherein A is an iodonium, sulfonium, or diazonium cation, and Y is an organic sulfonate counterion, or a halogen-containing metal or metalloid counterion.

Claim 13

The method according to claim 1 wherein said two-component curing agent is present in the range of 0.01 to 20 weight percent of the total composition.

Claim 14

The method according to claim 12 wherein said two-component curing agent is present in the range of 0.1 to 10 weight percent of said total composition.

Claim 15

The method according to claim 1 wherein the ratio of organometallic compound to onium salt of said curing agent is in the range of 10:1 to 1:10 by weight.

Claim 16

The method according to claim 1 wherein the ratio of organometallic salt to onium salt is in the range of 5:1 to 1:5 by weight.

Claim 17

The method according to claim 1, wherein said ethylenically-unsaturated monomer is selected from the group consisting of acrylates, acrylamides, vinyl compounds, and bireactive monomers.

Claim 18

The method according to claim 16 wherein said ethylenically-unsaturated monomer is an acrylate or methacrylate.

Claim 19

The method according to claim 1 wherein said polymeric precursor is at least one ethylenically-unsaturated compound, at least one isocyanate selected from di- and polyisocyanates, and at least one compound bearing at least two isocyanate-reactive hydrogen atoms, the isocyanate and reactive hydrogen-containing compound constituting polyurethane precursors.

Claim 21

The method according to claim 1 wherein said organometallic compound is selected from the group consisting of (eta 6 -mesitylene)(eta 5 -cyclopentadienyl)iron(1+) hexafluoroantimonate, (eta 6 -mesitylene)(eta 5 -cyclopentadienyl)iron(1+) hexafluorophosphate, (eta 6 -naphthalene)(eta 5 -cyclopentadienyl)iron(1+), hexafluoroantimonate, (eta 6 -naphthalene)(eta 5 -cyclopentadienyl)iron(1+)hexafluoro phosphate, (eta 5 -cyclopentadienyl)dicarbonyltriphenylphosphineiron(1+) hexafluorophosphate, and (eta 5 -cyclopentadienyl)dicarbonyl-triphenylphosphineiron (1+) hexafluoroantimonate.

Claim 22

The method according to claim 1 wherein said onium salt is at least one of Ph 2 I + PF 6 - , Ph 3 I + SbF 6 - , Ph 2 I + AsF 6 - , Ph 2 I + SbF 5 (OH) - , Ph 3 S + PF 6 - , Ph 2 S + SbF 6 - , Ph 3 S + AsF 6 - , PhSC 6 H 4 SPh 2 +SbF 6 - , and Ph 3 S + SbF 5 (OH) - , wherein Ph is phenyl.

Claim 23

The method according to claim 1 wherein said polymerizable mixture further comprises up to 90 weight percent of a solvent based on the total mixture.

Claim 24

A polymerizable composition comprising a polymeric precursor selected from one of the groups consisting of (1) at least one isocyanate selected from di- and polyisocyanates, and at least one compound bearing at least two isocyanate-reactive hydrogen atoms, the isocyanate and reactive hydrogen-containing compound constituting polyurethane precursors, and (2) at least one ethylenically-unsaturated monomer, at least one isocyanate selected from di- and polyisocyanates, and at least one compound bearing at least two isocyanate-reactive hydrogen atoms, the isocyanate and reactive hydrogen-containing compound constituting polyurethane precursors, and a two-component curing agent for (1) and (2) comprising an organometallic salt and an onium salt.

Claim 25

A polymerizable composition comprising a polymeric precursor selected from one of the groups consisting of (1) at least one isocyanate selected from di- and polyisocyanates, and at least one compound bearing at least two isocyanate-reactive hydrogen atoms, the isocyanate and reactive hydrogen-containing compound constituting polyurethane precursors, and (2) at least one ethylenically-unsaturated monomer, at least one isocyanate selected from di- and polyisocyanates, and at least one compound bearing at least two isocyanate-reactive hydrogen atoms, the isocyanate and reactive hydrogen-containing compound constituting polyurethane precursors, and a two-component curing agent for (1) and (2) comprising an organometallic salt and an onium salt.

Claim 26

The composition according to claim 23 which is at least on of photopolymerizable, accelerated particle polymerizable, and thermally polymerizable.

Claim 27

The composition according to claim 23 wherein said polymeric precursors are selected from the group consisting of said polyurethane precursors.

Claim 28

The composition according to claim 23 wherein said organometallic salt is an organometallic iron salt.

Claim 29

The composition according to claim 23 wherein said salt is present in an amount in the range of 0.01 to 20 weight percent of said polymerizable composition.

Claim 30

The composition according to claim 23 wherein said salt is present in an amount in the range of 0.1 to 10 weight percent of said polymerizable composition.

Claim 31

The composition according to claim 23 which has been subjected to sufficient energy to effect polymerization and provide a cured composition.

Claim 32

The composition according to claim 23 wherein said polyisocyanate is an aliphatic, cycloaliphatic, araliphatic, aromatic, or heterocyclic polyisocyanate, or any combination thereof.

Claim 33

The composition according to claim 23 wherein said polyurethane precursor is at least one polyisocyanate and at least one polyol or other isocyanate-reactive group bearing at least two isocyanate-reactive groups.

Claim 34

The composition according to claim 23 wherein said polyisocyanate has the formula Q(NCO)n wherein n=an integer 2 to 4 and Q=represents an aliphatic hydrocarbon radical containing from 2 to 100 carbon atoms, and zero to 50 heteroatoms, a cycloaliphatic hydrocarbon radical containing from 4 to 100 carbon atoms and zero to 50 heteroatoms, an aromatic hydrocarbon radical or heterocyclic aromatic radical containing from 6 to 15 carbon atoms and zero to 10 heteroatoms, or an araliphatic hydrocarbon radical containing from 8 to 100 carbon atoms and zero to 50 heteroatoms, wherein the heteroatoms in all of the radicals are selected from the group consisting of non-peroxidic oxygen, sulfur, non-amino nitrogen, halogen, silicon, and non-phosphine phosphorus.

Claim 35

A cured composition prepared according to the method of claim 1 wherein said di- and polysiocyanates have reactive functionality consisting essentially of socyanate groups, and said at least one other polyurethane precursor has reactive functionality consisting essentially of at least two isocyanate-reactive hydrogen atoms.

Claim 36

A shaped article according to claim 33.

Claim 37

A layered structure comprising a substrate having coated on at least one surface thereof the polymerizable composition according to claim 23.

Claim 38

The cured structure according to claim 35 wherein said di- and polyisocyanates have reactive functionality consisting essentially of isocyanate groups, and said at least one other polyurethane precursor has reactive functionality consisting essentially of at least two isocyanate-reactive hydrogen atoms.

Claim 39

The layered structure according to claim 35 which is an imageable structure.

Claim 40

The composition according to claim 23 further comprising an effective amount of a photosensitizer.

Claim 41

The method according to claim 1 wherein said at least one ethylenically-unsaturated monomer as disclosed in (a) (2) comprises at least one ethylenically-unsaturated monomer and at least one bireactive monomer different from said ethylenically-unsaturated monomer.

Claim 42

The composition according to claim 23 wherein said ethylenically-unsaturated monomer is selected from the group consisting of acrylates, acrylamides, vinyl compounds, and bireactive monomers.

Claim 43

The composition according to claim 23 wherein said at least one ethylenically-unsaturated monomer as disclosed in (2) comprises at least one ethylenically-unsaturated monomer and at least one bireactive monomer different from said ethylenically-unsaturated monomer.

Claim 44

The composition according to claim 23 wherein said polymeric precursor comprises at least one ethylenically-unsaturated compound, at least one isocyanate selected from di- and polyisocyanates, and at least one compound bearing at least two isocyanate-reactive hydrogen atoms, the isocyanate and reactive hydrogen-containing compound constituting polyurethane precursors.