PROCEDE DE FABRICATION DE TELOMERES PHOTORETICULABLES

PCT No. PCT/FR82/00122 Sec. 371 Date Mar. 7, 1983 Sec. 102(e) Date Mar. 7, 1983 PCT Filed Jul. 20, 1982 PCT Pub. No. WO83/00336 PCT Pub. Date Feb. 3, 1983.Telomers and cotelomers with at least one sequence which can be cross-linked by light, and a method of preparing them. They are of the general fo...

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Hauptverfasser: MARC MALISZEWICZ, YVES PIETRASANTA, BERNARD BOUTEVIN, WILLY-JEAN DEISS
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creator MARC MALISZEWICZ
YVES PIETRASANTA
BERNARD BOUTEVIN
WILLY-JEAN DEISS
description PCT No. PCT/FR82/00122 Sec. 371 Date Mar. 7, 1983 Sec. 102(e) Date Mar. 7, 1983 PCT Filed Jul. 20, 1982 PCT Pub. No. WO83/00336 PCT Pub. Date Feb. 3, 1983.Telomers and cotelomers with at least one sequence which can be cross-linked by light, and a method of preparing them. They are of the general formula wherein the taxogen links -(Xi)- belong to the group made up of 2-hydroxy ethyl acrylate and methacrylate, acrylic or methacrylic acid, vinyl alcohol and allyl alcohol; the links emanate from the same taxogen Xi, esterified by means of a group with at least one photo-crosslinkable double bond in its molecule; and where 1
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No. WO83/00336 PCT Pub. Date Feb. 3, 1983.Telomers and cotelomers with at least one sequence which can be cross-linked by light, and a method of preparing them. They are of the general formula wherein the taxogen links -(Xi)- belong to the group made up of 2-hydroxy ethyl acrylate and methacrylate, acrylic or methacrylic acid, vinyl alcohol and allyl alcohol; the links emanate from the same taxogen Xi, esterified by means of a group with at least one photo-crosslinkable double bond in its molecule; and where 1&lt;x+y&lt;/=1000, Z being chosen form the group -H, -Cl, -Br; and where R may be a simple or macromolecular radical, in the latter case leading to the formation of dual sequence cotelomers. The manufacturing process comprises telomerization by redox or radical catalysis, followed by grafting on the photo-crosslinkable group, the first phase of telomerization being duplicated in the case of a cotelomer. 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No. WO83/00336 PCT Pub. Date Feb. 3, 1983.Telomers and cotelomers with at least one sequence which can be cross-linked by light, and a method of preparing them. They are of the general formula wherein the taxogen links -(Xi)- belong to the group made up of 2-hydroxy ethyl acrylate and methacrylate, acrylic or methacrylic acid, vinyl alcohol and allyl alcohol; the links emanate from the same taxogen Xi, esterified by means of a group with at least one photo-crosslinkable double bond in its molecule; and where 1&lt;x+y&lt;/=1000, Z being chosen form the group -H, -Cl, -Br; and where R may be a simple or macromolecular radical, in the latter case leading to the formation of dual sequence cotelomers. The manufacturing process comprises telomerization by redox or radical catalysis, followed by grafting on the photo-crosslinkable group, the first phase of telomerization being duplicated in the case of a cotelomer. 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No. WO83/00336 PCT Pub. Date Feb. 3, 1983.Telomers and cotelomers with at least one sequence which can be cross-linked by light, and a method of preparing them. They are of the general formula wherein the taxogen links -(Xi)- belong to the group made up of 2-hydroxy ethyl acrylate and methacrylate, acrylic or methacrylic acid, vinyl alcohol and allyl alcohol; the links emanate from the same taxogen Xi, esterified by means of a group with at least one photo-crosslinkable double bond in its molecule; and where 1&lt;x+y&lt;/=1000, Z being chosen form the group -H, -Cl, -Br; and where R may be a simple or macromolecular radical, in the latter case leading to the formation of dual sequence cotelomers. The manufacturing process comprises telomerization by redox or radical catalysis, followed by grafting on the photo-crosslinkable group, the first phase of telomerization being duplicated in the case of a cotelomer. The main application for the products is in coating metals.</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
APPARATUS SPECIALLY ADAPTED THEREFOR
CHEMISTRY
CINEMATOGRAPHY
COMPOSITIONS BASED THEREON
ELECTROGRAPHY
HOLOGRAPHY
MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVINGCARBON-TO-CARBON UNSATURATED BONDS
MATERIALS THEREFOR
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
ORIGINALS THEREFOR
PHOTOGRAPHY
PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES,e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTORDEVICES
PHYSICS
THEIR PREPARATION OR CHEMICAL WORKING-UP
title PROCEDE DE FABRICATION DE TELOMERES PHOTORETICULABLES
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