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filingDate 1994-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44887913f18049de97465fc956b1c902
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publicationDate 1995-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0632085-A1
titleOfInvention Silicone polymers having olefinic functional groups, process for their preparation, and curable compositions comprising them
abstract R est un groupe alkyle, vinyle, aryle ou aralkyle, au moins 80% desdits radicaux R étant un groupe méthyle ; X est H ou une fonction polaire réactive exempte des hétéroéléments azote et soufre Y est un reste alcényle ou alcényloxy au moins en C₄ présentant au moins une insaturation éthylénique en extrêmité de chaîne et/ou dans la chaîne ; a , b et c sont égaux à 0, 1, 2, ou 3; - a + b + c = 0, 1, 2, ou 3 ; n le taux de motifs SiO 4/2 étant inférieur à 30% en mole. nIls sont obtenus par réactions d'addition simultanées ou successives ou par réactions de déshydrogénocondensation et d'addition simultanées ou par réactions de déshydrogénocondensation puis d'addition successives, ce à partir des organohydrogénopolysiloxanes correspondants exempts des fonctions X et restes Y, du ou des alcène(s) dont dérivent le ou les reste(s) alcényle(s) ou alcényloxy Y et du ou des composé(s) organique(s) éthyléniquement insaturé(s) ou hydroxylé(s) dont dérive(nt) la ou les fonction(s) X. nIls peuvent être utilisés pour la réalisation de compositions durcissables anti-adhérentes, pour papier notamment.Mixed polyorganosiloxanes containing similar or different units of formula (I) R a Y b X c Si O (4-abc) / 2 in which : R is an alkyl, vinyl, aryl or aralkyl group, at least 80% of said radicals R being a methyl group; X is H or a reactive polar function free of nitrogen and sulfur heteroelements Y is an alkenyl or alkenyloxy residue at least in C₄ having at least one ethylenic unsaturation at the chain end and / or in the chain; a , b and c are 0, 1, 2, or 3; - a + b + c = 0, 1, 2, or 3; the rate of SiO 4/2 units being less than 30% by mole. They are obtained by simultaneous or successive addition reactions or by simultaneous dehydrogenocondensation and addition reactions or by successive dehydrogenocondensation and then addition reactions, this from the corresponding organohydrogenopolysiloxanes free of the X functions and Y residues, of the alkene (s) (s) from which the alkenyl (s) or alkenyloxy Y residue (s) are derived and from the ethylenically unsaturated or hydroxylated organic compound (s) from which the function (s) are derived (s) X. They can be used for the production of non-stick curable compositions, for paper in particular.
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