Abstract: The invention relates to a method of preparing allyl-terminated polyisobutylene (PIB) by allylation with allyltrimethylsilane of tertiary chloro-capped PIB by electrophilic substitution. The synthesis begins with the BCl.sub.3, catalyzed mono- or oligo-tertiary chloride "inifer" initiated polymerization of isobutylene, followed in the same reaction vessel by the addition of hexane, allyltrimethylsilane, and TiCl.sub.4.

Abstract: Macromonomers of polymer-dicyclopentadiene and polymer-ethylidenenorbornene are prepared and then terpolymerized with ethylene and propylene. The terpolymer exhibits compatibilization of ethylene-propylene rubber and butyl rubber, and thus is useful as a sealant, roofing material, caulking agent, and the like.

Abstract: Novel telechelic halogenated polymers of cationically polymerized olefin monomers are formed carrying from 2 to about 6 terminal halogens by a continuous polymerization method. The continuous polymerization method being achieved by feeding to a stirred reactor a first stream composed of a solvent solution of at least one monomer and an inifer and another stream composed of a solvent solution of boron chloride to effect the polymerization of said monomer to a telechelic halogenated polymer product and withdrawing the reaction product from said reactor essentially in amounts equal to that of the sum of the two streams with the feeds to said reactor being simultaneously and continuously fed thereto while maintaining the temperature in the range of minus 10.degree. to minus 80.degree. C.

Abstract: The invention encompasses the synthesis of telechelic, i.e., terminally functional, macromolecular monomers (macromers) and their subsequent homo- and copolymerization. The macromers produced are asymmetric, having dissimilar head and tail groups which provide independent reaction sites. Macromers include .alpha.-phenyl-.omega.-t-chloropolyisobutylene, which can be reacted to form poly(methyl methacrylate-g-isobutylene). The graft copolymers provide novel physical properties which are the product of the respective grafts.

Abstract: A novel terminally functional (i.e., telechelic) polymers having a polyisobutylene are described. The end groups are styryl and can be reacted with conventional monomers to form copolymers having unique physical properties. Copolymerizations with N-vinyl-2-pyrrolidone produce amphiphilic polymers which are useful in the areas of medicine and agricultural chemicals.

Abstract: The method and production of macromolecular monomers from cationically polymerizable monomers and vinyl-substituted hydrocarbon halides is disclosed. These cationically polymerizable monomers may react in the presence of a catalyst with the hydrocarbon halide to produce a macromer retaining a polymerizable headgroup. This compound may be used in a variety of copolymerization processes with a variety of copolymerizable monomers to form graft copolymers.

Abstract: The invention sets forth novel telechelic (terminally functional) prepolymers which may be reacted to form curable epoxides. On account of the incorporation of saturated elastomer chains into the prepolymers improved epoxides arise having increased moisture resistance and less brittleness than conventional epoxides. These prepolymers may be straight chain or three-armed star, emanating from a common phenyl ring nucleus. Molecular weights of the prepolymers range from about 700 to 50,000 (linear) and from about 1000 to about 75,000 (three-arm star). The epoxides are useful as coatings, in adhesives, as additives, and the like.

Abstract: Novel telechelic olefin and hydroxy polymers particularly those of polyisobutylene are prepared according to the process set forth herein. Preparation of a telechelic diolefin polyisobutylene includes the steps of refluxing a solution of telechelic dihalogen polyisobutylene, adding a solution of a strong base such as potassium t-butoxide and stirring to form the telechelic diolefin polyisobutylene. This telechelic diolefin can be converted to the telechelic dihydroxy by refluxing a solution of the former, hydroborating the diolefin to a polymeric borane and oxidizing the polymeric borane to form the telechelic dihydroxy polyisobutylene. The processes are also applicable to the conversion of trihalogenated polyisobutylenes to telechelic triolefin and trihydroxy polyisobutylene tristars.

Abstract: The method and production of macromolecular monomers from cationically polymerizable monomers and vinyl-substituted hydrocarbon halides is disclosed. These cationically polymerizable monomers may react in the presence of a catalyst with the hydrocarbon halide to produce a macromer retaining a polymerizable headgroup. This compound may be used in a variety of copolymerization processes with a variety of copolymerizable monomers to form graft copolymers.

Abstract: Aluminum cyclopentadienyl compounds can be used to synthesize a variety of organic molecules containing the cyclopentadiene group, e.g., substituted cyclopentadiene compounds, polymer molecules with cyclopentadiene pendant groups, and polymer molecules with cyclopentadiene terminal groups.

Abstract: Novel telechelic olefin and hydroxy polymers particularly those of polyisobutylene are prepared according to the process set forth herein. Preparation of a telechelic diolefin polyisobutylene includes the steps of refluxing a solution of telechelic dihalogen polyisobutylene, adding a solution of a strong base such as potassium t-butoxide and stirring to form the telechelic diolefin polyisobutylene. This telechelic diolefin can be converted to the telechelic dihydroxy by refluxing a solution of the former, hydroborating the diolefin to a polymeric borane and oxidizing the polymeric borane to form the telechelic dihydroxy polyisobutylene. The processes are also applicable to the conversion of trihalogenated polyisobutylenes to telechelic triolefin and trihydroxy polyisobutylene tristars.

Abstract: Novel telechelic halogenated polymers of cationically polymerizable olefin monomers are formed carrying from 2 to about 6 terminal halogens. The telechelic halogenated polymers are formed by reacting the monomer with an initiator transfer agent, carrying at least two tertiary halogens, and under cationic polymerization conditions. Additionally, novel thermoplastic elastomer block copolymers are formed from these telechelic halogenated polymers by reacting the latter with vinyl aromatic monomers in the presence of a coinitiator.

Abstract: Aluminum cyclopentadienyl compounds can be used to synthesize a variety of organic molecules containing the cyclopentadiene group, e.g., substituted cyclopentadiene compounds, polymer molecules with cyclopentadiene pendant groups, and polymer molecules with cyclopentadiene terminal groups.

Abstract: Substantially gel free, high molecular weight, high unsaturation copolymers of isobutylene and cyclo-conjugated dienes having a number-average molecular weight of about 30,000 to about 90,000 and a mole % of unsaturation of about 5 to about 45 are prepared by a polymerization in a homogeneous phase, wherein the catalyst which is a hydrocarbyl aluminum dihalide or aluminum halide type catalyst dissolved in an aliphatic type solvent is added to a mixture of the isobutylene, cyclo-conjugated diene, and an aliphatic cosolvent and the polymerization reaction is carried out at a temperature of about -80.degree. to about -110.degree. C.

Abstract: Aluminum cyclopentadienyl compounds can be used to synthesize a variety of organic molecules containing the cyclopentadiene group, e.g., substituted cyclopentadiene compounds, polymer molecules with cyclopentadiene pendant groups, and polymer molecules with cyclopentadiene terminal groups.

Abstract: Substantially gel-free high unsaturation copolymers of isobutylene and methylcyclopentadiene and high unsaturation terpolymers of isobutylene cyclopentadiene and methylcyclopentadiene and terpolymers of isobutylene, isoprene and methylcyclopentadiene having a number average molecular weight of at least about 120,000 and a mole percent of unsaturation of at least 5% and the process for preparing said polymers which comprises carrying out the polymerization in a homogeneous phase, introducing to the system either an aluminum halide in a soluble form or a hydrocarbylaluminum dihalide and carrying the reaction out at a temperature of less than about -100.degree. C.

Abstract: Substantially gel free, high molecular weight, high unsaturation copolymers of isobutylene and cyclo-conjugated dienes having a number-average molecular weight of about 30,000 to about 90,000 and a mole % of unsaturation of about 5 to about 45 are prepared by a polymerization in a homogeneous phase, wherein the catalyst which is a hydrocarbyl aluminum dihalide or aluminum halide type catalyst dissolved in an aliphatic type solvent is added to a mixture of the isobutylene, cyclo-conjugated diene, and an aliphatic cosolvent and the polymerization reaction is carried out at a temperature of about -80.degree. to about -110.degree. C.

Abstract: Substantially gel-free, high unsaturation copolymers of isoolefin and diolefin and high unsaturation terpolymers of isoolefin, acyclic diene and cyclic diene having a number average molecular weight of at least about 90,000 and a mole percent of unsaturation of at least 5% and the process for preparing said polymers which comprises carrying out the polymerization in a homogeneous phase, introducing to the system either an aluminum halide in a soluble form or a hydrocarbylaluminum dihalide and carrying the reaction out at a temperature of less than about -100.degree. C.

Abstract: Substantially gel-free high unsaturation copolymers of isobutylene and methylcyclopentadiene and high unsaturation terpolymers of isobutylene cyclopentadiene and methylcyclopentadiene and terpolymers of isobutylene, isoprene and methylcyclopentadiene having a number average molecular weight of at least about 120,000 and a mole percent of unsaturation of at least 5% and the process for preparing said polymers which comprises carrying out the polymerization in a homogeneous phase, introducing to the system either an aluminum halide in a soluble form or a hydrocarbylaluminum dihalide and carrying the reaction out at a temperature of less than about -100.degree. C.

Abstract: Aluminum cyclopentadienyl compounds can be used to synthesize a variety of organic molecules containing the cyclopentadiene group, e.g., substituted cyclopentadiene compounds, polymer molecules with cyclopentadiene pendant groups, and polymer molecules with cyclopentadiene terminal groups.