Peperidine compounds containing silane groups as stabilizers for organic materials

PCT No. PCT/EP95/04546 Sec. 371 Date May 22, 1997 Sec. 102(e) Date May 22, 1997 PCT Filed Nov. 18, 1995 PCT Pub. No. WO96/17002 PCT Pub. Date Jun. 6, 1996Compounds of formula (I) (I) in which m+n is a number from 1 to 100 and n varies from zero to 90% of the sum of m+n; R1 and R3, which may be ident...

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Main Authors CARROZZA; PRIMO, BORZATTA; VALERIO
Format Patent
LanguageEnglish
Published 10.03.1998
Edition6
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Abstract PCT No. PCT/EP95/04546 Sec. 371 Date May 22, 1997 Sec. 102(e) Date May 22, 1997 PCT Filed Nov. 18, 1995 PCT Pub. No. WO96/17002 PCT Pub. Date Jun. 6, 1996Compounds of formula (I) (I) in which m+n is a number from 1 to 100 and n varies from zero to 90% of the sum of m+n; R1 and R3, which may be identical or different, are for example C1-C18alkyl or phenyl; R2 is C2-C12alkylene; G is for example a group of formula (IId) (IId) in which R5 and R6 are for example hydrogen; R4 is for example C1-C18alkyl; L1 has for example any one of the meanings given to R1 or is a group (R28)3SiO- where R28 is C1-C18alkyl; and L2 is for example hydrogen, Na, K, C1-C8alkyl or a group (R28)3Si- with R28 as defined above. The compounds of formula (I) are useful as light, heat and oxidation stabilizers for organic materials.
AbstractList PCT No. PCT/EP95/04546 Sec. 371 Date May 22, 1997 Sec. 102(e) Date May 22, 1997 PCT Filed Nov. 18, 1995 PCT Pub. No. WO96/17002 PCT Pub. Date Jun. 6, 1996Compounds of formula (I) (I) in which m+n is a number from 1 to 100 and n varies from zero to 90% of the sum of m+n; R1 and R3, which may be identical or different, are for example C1-C18alkyl or phenyl; R2 is C2-C12alkylene; G is for example a group of formula (IId) (IId) in which R5 and R6 are for example hydrogen; R4 is for example C1-C18alkyl; L1 has for example any one of the meanings given to R1 or is a group (R28)3SiO- where R28 is C1-C18alkyl; and L2 is for example hydrogen, Na, K, C1-C8alkyl or a group (R28)3Si- with R28 as defined above. The compounds of formula (I) are useful as light, heat and oxidation stabilizers for organic materials.
Author CARROZZA; PRIMO
BORZATTA; VALERIO
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Snippet PCT No. PCT/EP95/04546 Sec. 371 Date May 22, 1997 Sec. 102(e) Date May 22, 1997 PCT Filed Nov. 18, 1995 PCT Pub. No. WO96/17002 PCT Pub. Date Jun. 6,...
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SubjectTerms ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
COMPOSITIONS BASED THEREON
COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
THEIR PREPARATION OR CHEMICAL WORKING-UP
USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS
Title Peperidine compounds containing silane groups as stabilizers for organic materials
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