http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2417480-T3

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a2435874dc6f5eba095414e0fc683316
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-5465
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G77-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L83-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09J183-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08L83-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-5465
filingDate 2007-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d88cff3569ae42e03bad6c362e3893ce
publicationDate 2013-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2417480-T3
titleOfInvention Additive containing an azometin compound
abstract Fluid additive comprising an azomethinasilane component A), activatable by Si and an azomethine component B) in a molar ratio of 100: 0.1 to 1: 1, with a fraction that totals > 5% by weight, being able to prepare the azomethine component azomethinasilane A), activatable by Si by reacting an aminosilane c) of the general formula (I) R1R2Si-(CH2)n-(CR4R5)-(CH2)n-NH-R6 where n >= 0 or 1; R4 and R5 each independent of the other >= H or C1-C4 n-alkyl; R1 and R2 each independently of the other >= Cl, OR7, C1-C18 n-alkyl, C5-C8 cycloalkyl or C1-C18 branched alkyl; R3 >= Cl or OR7; R7 >= C1-C6 n-alkyl, C1-C6 branched alkyl or phenyl; R6 >= H, CH2-CH2-NH2 or CH2-CH2-NH-CH2-CH2-NH2, With formation of water and an oligomeric azomethinasilane activatable by Si as intermediates with a carbonyl compound d) of the general formula (II) R11 -CO-R12 where R11 >= C1-C30 n-alkyl, C1-C30 branched alkyl, C5-C8 cycloalkyl, C6-C18 aryl, C1-C30 alkylaryl or H; R12 >= C1-C30 n-alkyl, C1-C30 branched alkyl, C5-C8 cycloalkyl, C6-C18 aryl, or C1-C30 alkylaryl; or a C5-C8 cyclic alkyl group formed jointly by R11 and R12 together with the C atom connecting R11 and R12, with the proviso that per mole of aminosilane c) used there are 0.6 to 1.2 moles of the intermediate water formed available for the oligomerization –which consumes water as a reaction component- of the Si-activatable oligomeric azomethinasilane component produced as an intermediate, and the azomethine component B) is described by the general formula (III) XN>=CR21R22 where R21 >= C1-C30 n -alkyl, C1-C30 branched alkyl, C5-C8 cycloalkyl, C6-C18 aryl, C1-C30 alkylaryl or H; R22 >= C1-C30 n-alkyl, C1-C30 branched alkyl, C5-C8 cycloalkyl, C6-C18 aryl, or C1-C30 alkylaryl; or a cyclic C5-C8 alkyl group formed jointly by R21 and R22 together with the C atom connecting R21 and R22; X >= C1-C18 n-alkyl, C5-C8 cycloalkyl or C1-C18 branched alkyl group, C1-C18 n-alkyl group containing O and/or N heteroatoms, C5-C8 cycloalkyl group containing O and/or heteroatoms N or C1-C18 branched alkyl group containing O and/or N heteroatoms, in each case having 0 to 3 identical or different -N>=CR21R22 substituents.
priorityDate 2006-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 44.