The B. F. Goodrich Company

Promerus, Lcc

Sumitomo Bakelite Company Limited

Dennis A Barnes

Larry Funderburk Rhodes

Brian L Goodall

George M Benedikt

Lester H McIntosh, Iii

Andrew Bell

Xiaoming Wu

John-Henry Lipian

Chun S Chang

Brian K Bennett

Dennis J Janda

John C Fondran

David J Smith

Lindwood P Tenney

Lester H Mclntosh, Iii

Chung Chang

Brian K Bennet

John Henry Lipian

A method of polymerizing poly(cyclic)olefin monomers encompassing (a) combining a monomer composition containing the poly(cyclic)olefin monomers, a non-olefinic chain transfer agent and an activator compound to faun a mixture; (b) heating the mixture; and (c) adding a polymerization catalyst containing Ni and/or Pd. The non-olefinic chain transfer agent includes one or more compounds selected from H, alkylsilanes, alkylalkoxysilanes, alkylgermanes, alkylalkoxygermanes, alkylstannanes, and alkylalkoxystannanes. The activator is characterized as having an active hydrogen with a pKa of at least 5. The resulting poly(cyclic)olefin polymers can be used in photoresist compositions.

Vinyl addition polycyclic olefin polymers prepared with non-olefinic chain transfer agents and uses thereof

A method of polymerizing poly(cyclic)olefin monomers encompassing (a) combining a monomer composition containing the poly(cyclic)olefin monomers, a non-olefinic chain transfer agent and an activator compound to form a mixture; (b) heating the mixture; and (c) adding a polymerization catalyst containing Ni and/or Pd. The non-olefinic chain transfer agent includes one or more compounds selected from H, alkylsilanes, alkylalkoxysilanes, alkylgermanes, alkylalkoxygermanes, alkylstannanes, and alkylalkoxystannanes. The activator is characterized as having an active hydrogen with a pKa of at least 5. The resulting poly(cyclic)olefin polymers can be used in photoresist compositions.

Ni or Pd-catalyzed cationic polymerization of polycyclic olefins with silane chain transfer agents

A catalyst system and a process for the bulk addition polymerization or of polycyclic olefins, such as norbornene, methylnorbornene, ethylnorbornene, butylnorbornene or hexylnorbornene, 1,2,3,4,4,5,8,8-octahydro-1,4:5,8-dimethanonapthalene, 5,5'-(1,2-ethanediyl)bisbicyclo[2.2.1]hept-2-ene, and 1,4,4,4,5,8,8,8-octahydro-1,4:5,8-dimethanobiphenylene are disclosed. The catalyst includes an organonickel or organopalladium transition metal procatalyst and an activator compound. Polymerization can be carried out in a reaction injection molding process to yield thermoplastic and thermoset molded polymeric articles possessing high glass transition temperatures.

Mold addition polymerization of norbornene-type monomers using group 10 metal complexes

Addition polymers derived from norbornene-functional monomers are terminated with an olefinic moiety derived from a chain transfer agent selected from a compound having a terminal olefinic double bond between adjacent carbon atoms, excluding styrenes, vinyl ethers, and conjugated dienes and at least one of said carbon atoms has two hydrogen atoms attached thereto. The addition polymers of this invention are prepared from a single or multicomponent catalyst system including a Group VIII metal ion source. The catalyst systems are unique in that they catalyze the insertion of the chain transfer agent exclusively at a terminal end of the polymer chain.

Addition polymers derived from norbornene-functional monomers and

The invention discloses methods of preparing copolymers from norbornene-type monomers and cationically polymerizable monomers or polymers from catalytically polymerizable monomers by employing Group VIII transition metal ion source in a solvent for said monomers at a temperature in the range from -100.degree. C. to 120.degree. C. Also disclosed are copolymers from norbornene-type monomers and catalytically polymerizable monomers.

Homopolymers and copolymers of cationically polymerizable monomers and

A single component ionic catalyst consists essentially of an organonickel complex cation, and a weakly coordinating neutral counteranion. The cation is a neutral bidentate ligand removably attached to a Group VIII transition metal in an organometal complex. The ligand is easily displaced by a norbornene-type (NB-type) monomer in an insertion reaction which results in an unexpectedly facile addition polymerization. A NB-type monomer includes NB or substituted NB, or a multi-ringed cycloolefin having more than three rings in which one or more of the rings has a structure derived from NB, and a ring may have an alicyclic alkyl, alkylene or alkylidene substituent. The insertion reaction results in the formation of a unique propagating species more soluble in a polar than in a non-polar solvent and devoid of an available .beta.-hydrogen for termination. The ensuing propagation of a polymer chain proceeds without measurable unsaturation. The chain continues to grow until the insertion of a monoolefinic chain transfer reagent results in substantially all chains being terminated with the residue of the chain transfer reagent. This unique chain transfer reaction allows one to control the molecular weight in a relatively narrow range. The reaction mixture for controlling the mol wt of the polymer chains may contain any other catalyst which generates a propagating species by an insertion reaction in an essentially anhydrous solvent. Both, mol wt and glass transition temperature Tg are tailored to provide a weight average mol wt Mw&gt;20,000 but preferably not greater than about 500,000, and a T.sub.g in the range from about 150.degree. C. to about 400.degree. C. or higher, if desired.

Process for making polymers containing a norbornene repeating unit by

Dielectric supports for electronic components, such as circuit boards, are provided which are comprised of two or more bulk polymerized norbornene-type monomers. The monomers may be easily processed into circuit boards, etc. by reaction injection molding. The copolymers obtained exhibit high heat distortion temperatures and good dielectric properties and a balance of properties that make them, for example, well suited for molded wire board materials.

Bulk polymerized cycloolefin circuit boards

Vapor phase chlorosulfonated polyolefins usually contain as much as about 100 to 200 parts of more per million of sulfur dioxide in the chlorosulfonated polyolefin particles, even after degassing, that is released over a period of time. The amount of sulfur dioxide released from vapor phase chlorosulfonated polyolefins can be reduced to an amount of less than 0.5 ppm of sulfur dioxide in air, below the level that it can be detected by odor, when there is mixed with the powdered chlorosulfonated polyolefin, after the chlorosulfonation reaction and purging to reduce the sulfur dioxide content of the powder to less than about 300 ppm, less than about three weight parts per one hundred weight parts of chlorosulfonated powdered polyolefin of an inorganic material, or mixture thereof, selected from the group consisting of aluminum hydroxide, barium carbonate, barium hydroxide, magnesium hydroxide, magnesium oxide, potassium carbonate, dipotassium hydrogen phosphate, tripotassium phosphate, sodium carbonate, disodium hydrogen phosphate and trisodium phosphate.

Growing community of inventors

Medina, OH, United States of America

Dennis A Barnes