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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Format | Patent |
Language | English |
Published |
10.03.1998
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Edition | 6 |
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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. |
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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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