The subject matter described herein relates to methods for polymer xanthylation and the xanthylated polymers produced by such methods. Subsequent replacement of the xanthylate moiety allows facile entry into functionalized polymers.

The subject matter described herein relates to methods for polymer xanthylation and the xanthylated polymers produced by such methods. Subsequent replacement of the xanthylate moiety allows facile entry into functionalized polymers.

It is an object of the present invention to provide a novel organic sulfur material which is capable of improving a charge/discharge capacity and cycle characteristics, an electrode comprising the organic sulfur material, that is, a positive electrode or a negative electrode, and a lithium-ion secondary battery comprising the electrode. Provided is an organic sulfur material comprising a sulfur-modified acrylic resin, wherein an acrylic resin has peaks around 756 cm.sup.−1, around 1066 cm.sup.−1, around 1150 cm.sup.−1, around 1245 cm.sup.−1, around 1270 cm.sup.−1, around 1453 cm.sup.−1, and around 1732 cm.sup.−1 in an FT-IR spectrum.

It is an object of the present invention to provide a novel organic sulfur material which is capable of improving a charge/discharge capacity and cycle characteristics, an electrode comprising the organic sulfur material, that is, a positive electrode or a negative electrode, and a lithium-ion secondary battery comprising the electrode. Provided is an organic sulfur material comprising a sulfur-modified acrylic resin, wherein an acrylic resin has peaks around 756 cm.sup.−1, around 1066 cm.sup.−1, around 1150 cm.sup.−1, around 1245 cm.sup.−1, around 1270 cm.sup.−1, around 1453 cm.sup.−1, and around 1732 cm.sup.−1 in an FT-IR spectrum.

A polyisobutylene-based polymer network comprising the thiol-ene reaction product of at least two thiol-terminated polyisobutylene precursor polymers and at least one multi-functional allyl-containing precursor moiety or polymer in the presence of light or heat. The at least two thiol-terminated polyisobutylene precursor polymers have at least two thiol end groups. When each polyisobutylene precursor polymer has only two thiol end groups then the allyl-containing precursor moiety or polymer has at least three functional groups, and wherein when the allyl-containing precursor moiety or polymer has two functional groups then each polyisobutylene precursor polymer has at least three thiol end groups.

A polyisobutylene-based polymer network comprising the thiol-ene reaction product of at least two thiol-terminated polyisobutylene precursor polymers and at least one multi-functional allyl-containing precursor moiety or polymer in the presence of light or heat. The at least two thiol-terminated polyisobutylene precursor polymers have at least two thiol end groups. When each polyisobutylene precursor polymer has only two thiol end groups then the allyl-containing precursor moiety or polymer has at least three functional groups, and wherein when the allyl-containing precursor moiety or polymer has two functional groups then each polyisobutylene precursor polymer has at least three thiol end groups.

A method of making a polymer having the structure (I): ##STR00001##
wherein L is a linking group, R is a hydrocarbon group or a substituted-hydrocarbon group, and x is 2 or more, preferably from 2 to 100, more preferably from 2 to 50; and wherein each {Q} is an identical polymer block or contains a plurality of polymer blocks. The method comprises reacting a di-halo initiator with a selected monomer one or more times and then reacting the resulting moiety with a dithiol compound of the structure HS—R—SH.

A method of making a polymer having the structure (I): ##STR00001##
wherein L is a linking group, R is a hydrocarbon group or a substituted-hydrocarbon group, and x is 2 or more, preferably from 2 to 100, more preferably from 2 to 50; and wherein each {Q} is an identical polymer block or contains a plurality of polymer blocks. The method comprises reacting a di-halo initiator with a selected monomer one or more times and then reacting the resulting moiety with a dithiol compound of the structure HS—R—SH.

A self-healing polymer material that includes a multiphase copolymer, and a method of making the copolymer, are provided. The multiphase copolymer includes one or more hydrogen bond-forming copolymer segments, each segment including a polymerized acrylamide monomer and a polymerized acrylic monomer. The polymerized acrylamide monomer includes functional groups that form hydrogen bonds in the multiphase copolymer, and is present in the one or more copolymer segments in an amount sufficient for self-healing of the multiphase copolymer.

A self-healing polymer material that includes a multiphase copolymer, and a method of making the copolymer, are provided. The multiphase copolymer includes one or more hydrogen bond-forming copolymer segments, each segment including a polymerized acrylamide monomer and a polymerized acrylic monomer. The polymerized acrylamide monomer includes functional groups that form hydrogen bonds in the multiphase copolymer, and is present in the one or more copolymer segments in an amount sufficient for self-healing of the multiphase copolymer.