Energy-curable cyanate compositions

Claim 2

An energy polymerizable composition consisting essentially of at least one cyanate monomer or oligomer comprising an organic radical bonded through carbon atoms to at lest two --OCN groups and as curing agent a transition-metal containing organometallic compound in which at least one carbon atom of an organic group is bonded to the metal atom.

Claim 3

The composition according to claim 1 wherein said organometallic compound has the formula: [L.sup.2 L.sup.2 L.sup.3 M].sup.+· X.sub.f I L 1 represents none, or 1 to 12 ligands contributing pi-electrons that can be the same or different 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 2 to 24 pi-electrons to the valence shell of M; L 2 represents none, or 1 to 24 ligands that can be the same or different contributing an even number of sigma-electrons selected from mono-, di-, and tri-dentate ligands, each donating 2, 4, or 6 sigma-electrons to the valence shell of M; L 3 represents none, or 1 to 12 ligands that can be the same or different, each contributing no more than one sigma-electron each to the valence shell of each M; M represents 1 to 4 of the same or different metal atoms selected from the elements of Periodic Groups IVB, VB, VIB, VIIB, and VIII (commonly referred to as transition metals); e is an integer having a value of 0, 1 or 2; X is an anion selected from organic sulfonate and halogenated metal or metalloid groups; f is an integer of 0, 1 or 2, the number of anions required to balance the charge e on the organometallic portion; with the proviso that the organometallic compound contains at least one metal-carbon bond; and with the proviso that L 1 , L 2 , L 3 , M, e, X, and f are chosen so as to achieve a stable configuration.

Claim 4

The composition according to claim 2 wherein ligand L 1 is a polymeric compound.

Claim 5

The composition according to claim 2 wherein e of Formula I is equal to zero.

Claim 6

The composition according to claim 2 wherein e of Formula I is equal to 1.

Claim 7

The composition according to claim 2 wherein e of Formula I is equal to 2.

Claim 8

The composition according to claim 2 wherein said organometallic compounds are selected from the group consisting of (eta 5 -methylcyclopentadienyl)manganesetricarbonyl, bis[(eta 5 -cyclopentadienyl)irondicarbonyl], (eta 5 -cyclopentadienyl)iron(triphenyltin)dicarbonyl, (eta 5 -cyclopentadienyl)irondicarbonylchloride, (eta 5 -cyclopentadienyl)(eta 6 -mesitylene)iron(+1)trifluoromethylsulfonate(-1), (eta 5 -cyclopentadienyl)(eta 6 -mesitylene)iron(+1)hexafluorophosphate(-1).

Claim 9

The composition according to claim 1 wherein said cyanate monomer is 2,2-bis(4-cyanatophenyl)propane or oligomers thereof.

Claim 10

The composition according to claim 1 wherein said cyanate monomer has the formula: Q(OCN).sub.p wherein Q comprises at least one 1) a mono-, di-, tri-, or tetravalent aromatic hydrocarbon containing 5 to 30 carbon atoms, 2) 1 to 5 aliphatic or polycyclic aliphatic mono- or divalent hydrocarbons containing 7 to 20 carbon atoms, and 3) a mono- or divalent fluorocarbon group having 3 to 12,500 carbons and 5 to 25,000 fluorine atoms, and p is an integer of 2 to 7.

Claim 11

The composition according to claim 9 wherein Q corresponds to a fluorocarbon group of Formula III or IV: F.sub.3 C(CFX).sub.a A(CFX).sub.b CH.sub.2 -- III wherein A is a carbon-to-carbon bond, in which case a is an integer from 1 to 30 and b is zero, or A is --O--(--CFX--CF 2 --O--) c , in which case a is an integer 1 to 10, b is one, and c is an integer 1 to 100; and X is fluorine or perfluoroalkyl having 1 to 10 carbon atoms; --CH.sub.2 (CFX).sub.a B(CFX).sub.b CH.sub.2 -- IV wherein B is 1) a carbon-to-carbon bond, in which case a is an integer of 1 to 30 and b is zero, or 2) B is [(CFX) d O(CFX) u ] v , in which case a and b are zero, d and u are integers of 1 to 30, and v is an integer of 1 to 20, or 3) B is (OCF 2 --CFX) w O(CFX) h O(CFX--CF 2 O) i , in which case a and b are 1, h is an integer of 1 to 10, and w and i are integers of 1 to 100, or 4) B is [(CF 2 CH 2 ) j (CF 2-CFX ) k ] m , in which case a and b are integers of 1 to 10, j and k are integers whose ratio j/k is 1/1 to 1/10, m is an integer of 1 to 100, and (CF 2 CH 2 ) and (CF 2 --CFX) are randomly distributed units; and where X is fluorine or perfluoroalkyl of 1 to 10 carbon atoms.

Claim 12

The composition according to claim 9 wherein said aromatic hydrocarbon further comprises 1 to 10 hetero atoms selected from the group consisting of non-peroxidic oxygen, sulfur, non-phosphino phosphorus, non-amino nitrogen, halogen, and silicon.

Claim 13

The composition according to claim 9 wherein said aliphatic or polycyclic aliphatic hydrocarbon further comprises 1 to 10 hetero atoms selected from the group consisting of non-peroxidic oxygen, sulfur, non-phosphino phosphorus, non-amino nitrogen, halogen, and silicon.

Claim 14

The composition according to claim 1 which has been cured by at least one of thermal energy, electromagnetic radiation, and accelerated particles.

Claim 15

The composition according to claim 13 which is a shaped article, coating, film , or photoresist.

Claim 16

The composition according to claim 1 which is a film, coating or photoresist.

Claim 17

The composition according to claim 1 wherein said curing agent is present in an amount in the range of 0.01 to 20 weight percent of the total composition.

Claim 18

A method comprising the steps of: a) providing a polymerizable mixture according to claim 1, and b) effecting polymerization of said mixture by at least one of thermal energy, radiation, and accelerated particles.

Claim 19

The method according to claim 17 wherein said polymerization is effected by a two-stage process comprising first activating said polymerizable composition by irradiation to provide activated precursors, and then thermally curing the activated precursors, said irradiation temperature being below the temperature used in the thermal curing.

Claim 20

The method according to claim 18 wherein the temperature of said irradiation step is in the range of 25° to 300° C.

Claim 21

The method according to claim 17 wherein the temperature of said thermal energy is in the range of 80° to 50° C.

Claim 22

The method according to claim 17 wherein the temperature of said irradiation is in the range of 25° to 300° C.

Claim 23

The method according to claim 17 wherein said polymerizable mixture further comprises an effective amount of a solvent.

Claim 24

An article prepared according to the method of claim 17.

Claim 25

The method according to claim 17 wherein said composition is a photoresist.

Claim 26

An energy polymerizable composition consisting essentially of at least one cyanate monomer or oligomer comprising an organic radical bonded to at least two --OCN groups, at least one cyanate monomer or oligomer comprising an organic radical bonded to one --OCN group, and as curing agent a transition-metal containing organometallic compound in which at least one carbon atom of an organic group is bonded to the metal atom.

Claim 27

An energy polymerizable composition consisting essentially of at least one cyanate monomer or oligomer comprising an organic radical bonded to at least two --OCN groups, at least one cyanate monomer or oligomer comprising an organic radical bonded to one --OCN group, and as curing agent a transition-metal containing organometallic compound in which at least one carbon atom of an organic group is bonded to the metal atom.