1) Hydrocarbon copolymer P comprising 2 alkoxysilane end groups F.sup.1 and F.sup.2 of formulae: F.sup.1: (RO).sub.3-tR.sub.tSi(CH.sub.2).sub.g1- and F.sup.2: (CH.sub.2).sub.d1SiR.sub.t(OR).sub.3-t; or F.sup.1: (RO).sub.3-tR.sub.tSiRO(O)C(CH.sub.2).sub.g2 and F.sup.2: (CH.sub.2).sub.d2C(O)ORSiR.sub.t(OR).sub.3-t; wherein t is 0, 1 or 2; g1 and d1 are 1, 2 or 3; g2 and d2 are 0, 1, 2 or 3; R et R represent a C.sub.1-C.sub.4 alkyl; R is a C.sub.1-C.sub.4 alkylene radical; the main chain comprising motifs (I) and (II) in which R.sup.0 is in particular the methyl radical; and the number average molecular mass Mn thereof being between 400 and 100,000 g/mol. 2) Method for producing said copolymer, comprising: (i) a step of heating a statistical bipolymer A selected from a poly(butadiene-isoprene), a poly(butadiene-myrcene) and a poly(butadiene-farnesene); and subsequently (ii) a step of heating the formed product, in the presence of a chain transfer agent of formula (C). 3) Adhesive composition comprising said copolymer.

A method for producing conjugated diene rubber is provided, including: a first step of obtaining a conjugated diene polymer chain having an active end by polymerizing a monomer comprising a conjugated diene compound and a vinyl compound having a functional group interactive with silica using a polymerization initiator in an inert solvent; a second step of reacting a siloxane compound with the active end of the conjugated diene polymer chain having the active end; and a third step of reacting a hydrocarbyloxysilane compound with the conjugated diene polymer chain with which the siloxane compound has been reacted that is obtained in the second step.

A method for producing conjugated diene rubber is provided, including: a first step of obtaining a conjugated diene polymer chain having an active end by polymerizing a monomer comprising a conjugated diene compound and a vinyl compound having a functional group interactive with silica using a polymerization initiator in an inert solvent; a second step of reacting a siloxane compound with the active end of the conjugated diene polymer chain having the active end; and a third step of reacting a hydrocarbyloxysilane compound with the conjugated diene polymer chain with which the siloxane compound has been reacted that is obtained in the second step.

The present invention relates to articles comprising crosslinked polymer network comprising thioether crosslinks and process of making and using same. Such thiol-ene crosslinking reactions not only make the isocyanate crosslinking reaction unnecessary, but they also improve the article's strength due to chemical crosslinking between the article's resin layers, and reduce or eliminate post curing. Thus resulting in a sufficiently cured article in a much shorter time.

The present invention relates to articles comprising crosslinked polymer network comprising thioether crosslinks and process of making and using same. Such thiol-ene crosslinking reactions not only make the isocyanate crosslinking reaction unnecessary, but they also improve the article's strength due to chemical crosslinking between the article's resin layers, and reduce or eliminate post curing. Thus resulting in a sufficiently cured article in a much shorter time.

In one or more embodiments, the present invention provides an way to modify the isoprene unit using an alder-ene reaction to form thermoset compounds comprising the resultant electron-deficient, readily crosslinkable polyisobutylene-based rubber that avoids the use of corrosive bromine or chlorine to make the activated butyl rubber, is easier to crosslink than the halobutyls, allows crosslinking with a simple organic base or a peroxide, and has mechanical properties as good as or better than sulfur crosslinked butyl rubbers.

In one or more embodiments, the present invention provides an way to modify the isoprene unit using an alder-ene reaction to form thermoset compounds comprising the resultant electron-deficient, readily crosslinkable polyisobutylene-based rubber that avoids the use of corrosive bromine or chlorine to make the activated butyl rubber, is easier to crosslink than the halobutyls, allows crosslinking with a simple organic base or a peroxide, and has mechanical properties as good as or better than sulfur crosslinked butyl rubbers.

Provided are a modified hydrocarbon resin that can provide a hot-melt adhesive composition with low odor, low Gardner color and high peel adhesion, a method for producing the resin, and the hot-melt adhesive composition. A modified hydrocarbon resin comprising a 1,3-pentadiene monomer unit, a C4-C6 alicyclic monoolefin monomer unit, a C4-C8 acyclic monoolefin monomer unit, an alicyclic diolefin monomer unit, and an aromatic monoolefin monomer unit, and containing a carboxyl group or acid anhydride group, wherein a weight average molecular weight (Mw), a Z average molecular weight (Mz), a ratio (Mz/Mw), a Gardner color scale of a 50 mass % toluene solution, a softening point, and an acid value are in specific ranges.

Provided are a modified hydrocarbon resin that can provide a hot-melt adhesive composition with low odor, low Gardner color and high peel adhesion, a method for producing the resin, and the hot-melt adhesive composition. A modified hydrocarbon resin comprising a 1,3-pentadiene monomer unit, a C4-C6 alicyclic monoolefin monomer unit, a C4-C8 acyclic monoolefin monomer unit, an alicyclic diolefin monomer unit, and an aromatic monoolefin monomer unit, and containing a carboxyl group or acid anhydride group, wherein a weight average molecular weight (Mw), a Z average molecular weight (Mz), a ratio (Mz/Mw), a Gardner color scale of a 50 mass % toluene solution, a softening point, and an acid value are in specific ranges.

The present invention relates to articles comprising crosslinked polymer network comprising thioether crosslinks and process of making and using same. Such thiol-ene crosslinking reactions not only make the isocyanate crosslinking reaction unnecessary, but they also improve the article's strength due to chemical crosslinking between the article's resin layers, and reduce or eliminate post curing. Thus resulting in a sufficiently cured article in a much shorter time.