ES2386906T3 - Organopolisiloxanos sustituidos y su uso - Google Patents
Organopolisiloxanos sustituidos y su uso Download PDFInfo
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- ES2386906T3 ES2386906T3 ES07703381T ES07703381T ES2386906T3 ES 2386906 T3 ES2386906 T3 ES 2386906T3 ES 07703381 T ES07703381 T ES 07703381T ES 07703381 T ES07703381 T ES 07703381T ES 2386906 T3 ES2386906 T3 ES 2386906T3
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- 229920001296 polysiloxane Polymers 0.000 title description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 83
- 229910052751 metal Inorganic materials 0.000 claims abstract description 29
- 239000002184 metal Substances 0.000 claims abstract description 29
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 22
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 7
- 238000010532 solid phase synthesis reaction Methods 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 90
- 239000000463 material Substances 0.000 claims description 84
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 47
- 239000007787 solid Substances 0.000 claims description 31
- 238000006243 chemical reaction Methods 0.000 claims description 28
- 239000001257 hydrogen Substances 0.000 claims description 27
- 229910052739 hydrogen Inorganic materials 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 229920000642 polymer Polymers 0.000 claims description 22
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 16
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 15
- 150000001412 amines Chemical class 0.000 claims description 15
- 150000001413 amino acids Chemical class 0.000 claims description 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 230000008030 elimination Effects 0.000 claims description 13
- 238000003379 elimination reaction Methods 0.000 claims description 13
- 238000000746 purification Methods 0.000 claims description 13
- 125000003342 alkenyl group Chemical group 0.000 claims description 12
- 150000002500 ions Chemical class 0.000 claims description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 12
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- 239000003352 sequestering agent Substances 0.000 claims description 11
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 9
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 9
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- 239000003446 ligand Substances 0.000 claims description 8
- 238000007254 oxidation reaction Methods 0.000 claims description 8
- 239000004971 Cross linker Substances 0.000 claims description 7
- 150000002739 metals Chemical class 0.000 claims description 7
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- 150000003839 salts Chemical class 0.000 claims description 7
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- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- 239000004599 antimicrobial Substances 0.000 claims description 6
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- 229910052747 lanthanoid Inorganic materials 0.000 claims description 6
- 150000002602 lanthanoids Chemical class 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 229910052697 platinum Inorganic materials 0.000 claims description 6
- 229920005862 polyol Polymers 0.000 claims description 6
- 102000004169 proteins and genes Human genes 0.000 claims description 6
- 108090000623 proteins and genes Proteins 0.000 claims description 6
- 229910052703 rhodium Inorganic materials 0.000 claims description 6
- 239000010948 rhodium Substances 0.000 claims description 6
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 6
- 239000007790 solid phase Substances 0.000 claims description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 5
- 238000007792 addition Methods 0.000 claims description 5
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- 150000004696 coordination complex Chemical class 0.000 claims description 5
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- 229920000768 polyamine Polymers 0.000 claims description 5
- 229910052707 ruthenium Inorganic materials 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 229910052719 titanium Inorganic materials 0.000 claims description 5
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052768 actinide Inorganic materials 0.000 claims description 4
- 150000001255 actinides Chemical class 0.000 claims description 4
- 239000002216 antistatic agent Substances 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 239000003063 flame retardant Substances 0.000 claims description 4
- 239000002638 heterogeneous catalyst Substances 0.000 claims description 4
- 238000005342 ion exchange Methods 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- 102000039446 nucleic acids Human genes 0.000 claims description 4
- 108020004707 nucleic acids Proteins 0.000 claims description 4
- 150000007523 nucleic acids Chemical class 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 3
- 102000004190 Enzymes Human genes 0.000 claims description 3
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- 229910002651 NO3 Inorganic materials 0.000 claims description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 229910003080 TiO4 Inorganic materials 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 230000029936 alkylation Effects 0.000 claims description 3
- 238000005804 alkylation reaction Methods 0.000 claims description 3
- 150000007942 carboxylates Chemical class 0.000 claims description 3
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 229910052737 gold Inorganic materials 0.000 claims description 3
- 239000010931 gold Substances 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- 150000002466 imines Chemical class 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 3
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 3
- 150000003457 sulfones Chemical class 0.000 claims description 3
- 150000003462 sulfoxides Chemical class 0.000 claims description 3
- 230000009466 transformation Effects 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 229910020489 SiO3 Inorganic materials 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- 230000010933 acylation Effects 0.000 claims description 2
- 238000005917 acylation reaction Methods 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 230000000845 anti-microbial effect Effects 0.000 claims description 2
- 238000006254 arylation reaction Methods 0.000 claims description 2
- 230000006315 carbonylation Effects 0.000 claims description 2
- 238000005810 carbonylation reaction Methods 0.000 claims description 2
- 230000021523 carboxylation Effects 0.000 claims description 2
- 238000006473 carboxylation reaction Methods 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 230000032050 esterification Effects 0.000 claims description 2
- 238000005886 esterification reaction Methods 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
- 238000006317 isomerization reaction Methods 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 2
- 125000000101 thioether group Chemical group 0.000 claims description 2
- 238000005809 transesterification reaction Methods 0.000 claims description 2
- 230000007704 transition Effects 0.000 claims description 2
- 230000017105 transposition Effects 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 10
- 239000007788 liquid Substances 0.000 claims 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims 1
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- 238000002523 gelfiltration Methods 0.000 claims 1
- 238000007037 hydroformylation reaction Methods 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract description 12
- 229910010272 inorganic material Inorganic materials 0.000 abstract description 5
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- 238000002414 normal-phase solid-phase extraction Methods 0.000 abstract description 4
- 230000001404 mediated effect Effects 0.000 abstract description 3
- 239000012620 biological material Substances 0.000 abstract 1
- 238000007210 heterogeneous catalysis Methods 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 105
- 239000000047 product Substances 0.000 description 61
- 239000000243 solution Substances 0.000 description 61
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 48
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 37
- -1 arseniates Chemical class 0.000 description 32
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- 125000000524 functional group Chemical group 0.000 description 29
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 18
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- 239000000843 powder Substances 0.000 description 17
- 238000004458 analytical method Methods 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 15
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- 238000012360 testing method Methods 0.000 description 14
- 150000002431 hydrogen Chemical group 0.000 description 13
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
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- 150000001450 anions Chemical class 0.000 description 11
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 10
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- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical group CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 7
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- 239000007858 starting material Substances 0.000 description 7
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 7
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- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 6
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 6
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- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 6
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- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 3
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
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- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
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- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
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- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 2
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- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
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- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
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- QBERHIJABFXGRZ-UHFFFAOYSA-M rhodium;triphenylphosphane;chloride Chemical compound [Cl-].[Rh].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QBERHIJABFXGRZ-UHFFFAOYSA-M 0.000 description 2
- YBCAZPLXEGKKFM-UHFFFAOYSA-K ruthenium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Ru+3] YBCAZPLXEGKKFM-UHFFFAOYSA-K 0.000 description 2
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- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
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- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- PZSJYEAHAINDJI-UHFFFAOYSA-N rhodium(3+) Chemical compound [Rh+3] PZSJYEAHAINDJI-UHFFFAOYSA-N 0.000 description 1
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- 238000001228 spectrum Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 102000055501 telomere Human genes 0.000 description 1
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- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
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- 230000002588 toxic effect Effects 0.000 description 1
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- MYWQGROTKMBNKN-UHFFFAOYSA-N tributoxyalumane Chemical compound [Al+3].CCCC[O-].CCCC[O-].CCCC[O-] MYWQGROTKMBNKN-UHFFFAOYSA-N 0.000 description 1
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- TUQLLQQWSNWKCF-UHFFFAOYSA-N trimethoxymethylsilane Chemical compound COC([SiH3])(OC)OC TUQLLQQWSNWKCF-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/28—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen sulfur-containing groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/50—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Silicon Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0602811 | 2006-02-10 | ||
| GBGB0602811.2A GB0602811D0 (en) | 2006-02-10 | 2006-02-10 | Substituted Organopolysiloxanes And Use Thereof |
| PCT/EP2007/001137 WO2007090676A1 (en) | 2006-02-10 | 2007-02-09 | Subtituted organopolysiloxanes and use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2386906T3 true ES2386906T3 (es) | 2012-09-05 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07703381T Active ES2386906T3 (es) | 2006-02-10 | 2007-02-09 | Organopolisiloxanos sustituidos y su uso |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8343474B2 (enExample) |
| EP (1) | EP1987082B1 (enExample) |
| JP (1) | JP5449782B2 (enExample) |
| CN (1) | CN101405325B (enExample) |
| AT (1) | ATE556105T1 (enExample) |
| ES (1) | ES2386906T3 (enExample) |
| GB (1) | GB0602811D0 (enExample) |
| WO (1) | WO2007090676A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0720579D0 (en) * | 2007-10-20 | 2007-11-28 | Phosphonics Ltd | Functionalised materials and uses thereof |
| GB201006368D0 (en) * | 2010-04-15 | 2010-06-02 | Phosphonics Ltd | Functionalised materials and uses thereof |
| FR2968301B1 (fr) * | 2010-09-23 | 2020-05-01 | Gelest Technologies, Inc. | Derives d'alcoxysilane des acides amines a groupement n-acyle, des dipeptides a groupement n-acyle et des tripeptides a groupement n-acyle, ainsi que les particules et formulations huile dans l'eau stables les utilisant |
| EP2446965A1 (en) * | 2010-11-02 | 2012-05-02 | Evonik Degussa GmbH | Process for preparation of supported catalysts and use of the catalyst for the esterification of free fatty acids in vegetable oil |
| GB201100531D0 (en) * | 2011-01-13 | 2011-03-02 | Phosphonics | Functionalised materials, processes for the production and uses thereof |
| DE102011085492A1 (de) | 2011-10-31 | 2013-05-02 | Evonik Goldschmidt Gmbh | Neue aminogruppenhaltige Siloxane, Verfahren zu deren Herstellung und Anwendung |
| GB2508350A (en) * | 2012-11-28 | 2014-06-04 | Phosphonics Ltd | A process for the selective removal of a catalyst from a liquid phase |
| CN103877952B (zh) * | 2014-03-20 | 2017-01-18 | 江苏大学 | 类软糖状聚硅氧烷吸附材料及其表面改性海绵的制备与应用 |
| GB201505977D0 (en) | 2015-04-08 | 2015-05-20 | Johnson Matthey Davy Technologies Ltd | Catalyst system and process |
| GB201505981D0 (en) | 2015-04-08 | 2015-05-20 | Johnson Matthey Davy Technologies Ltd | Process |
| GB201515414D0 (en) | 2015-08-29 | 2015-10-14 | Advance Performance Materials Ltd | Polyorganic groups modified silica, processes to make and use therof |
| GB201515411D0 (en) * | 2015-08-29 | 2015-10-14 | Advance Performance Materials Ltd | Substituted materials, process for the production and uses thereof |
| CN106397472B (zh) * | 2016-08-06 | 2020-08-11 | 湖北硒诺唯新功能化硅胶材料有限公司 | 功能化材料及其生产工艺与使用 |
| GB201615762D0 (en) | 2016-09-16 | 2016-11-02 | Johnson Matthey Davy Technologies Ltd | Process |
| CN106866975B (zh) * | 2017-02-24 | 2020-10-23 | 苏州硒诺唯新新材料科技有限公司 | 有机聚合官能团改性二氧化硅及其生产工艺和用途 |
| CN107129575B (zh) * | 2017-04-07 | 2020-10-16 | 苏州硒诺唯新新材料科技有限公司 | 功能化材料及其生产工艺与用途 |
| CN107930601B (zh) * | 2017-11-02 | 2020-12-08 | 苏州硒诺唯新新材料科技有限公司 | 新型多聚有机改性硅胶材料的新组分及其使用 |
| CN119056412B (zh) * | 2024-11-05 | 2025-04-25 | 苏州硒诺唯新新材料科技有限公司 | 一种交叉网格结构功能化硅胶材料及其制备方法和应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1527598A (en) * | 1974-11-12 | 1978-10-04 | Dow Corning Ltd | Catalysts and carriers therefor |
| JP3522860B2 (ja) * | 1994-10-31 | 2004-04-26 | 信越化学工業株式会社 | ハイドロシリレーション法 |
| DE19536363A1 (de) * | 1995-09-29 | 1997-04-03 | Degussa | Sulfonat- und mercaptogruppenhaltige Organopolysiloxane, Verfahren zu ihrer Herstellung und Verwendung |
| JPH10101801A (ja) * | 1996-10-02 | 1998-04-21 | Showa Denko Kk | 水酸基含有ポリオルガノシルセスキオキサンおよびその製造方法 |
| US7301042B2 (en) * | 2002-04-23 | 2007-11-27 | Cruse Richard W | Blocked mercaptosilane hydrolyzates as coupling agents for mineral-filled elastomer compositions |
| US9982095B2 (en) | 2004-08-04 | 2018-05-29 | Phosphonics Ltd | Substituted organopolysiloxanes and use thereof |
-
2006
- 2006-02-10 GB GBGB0602811.2A patent/GB0602811D0/en not_active Ceased
-
2007
- 2007-02-09 US US12/278,939 patent/US8343474B2/en not_active Expired - Fee Related
- 2007-02-09 AT AT07703381T patent/ATE556105T1/de active
- 2007-02-09 ES ES07703381T patent/ES2386906T3/es active Active
- 2007-02-09 CN CN2007800100169A patent/CN101405325B/zh not_active Expired - Fee Related
- 2007-02-09 JP JP2008553688A patent/JP5449782B2/ja not_active Expired - Fee Related
- 2007-02-09 EP EP07703381A patent/EP1987082B1/en not_active Not-in-force
- 2007-02-09 WO PCT/EP2007/001137 patent/WO2007090676A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| EP1987082A1 (en) | 2008-11-05 |
| EP1987082B1 (en) | 2012-05-02 |
| CN101405325B (zh) | 2013-11-20 |
| WO2007090676A1 (en) | 2007-08-16 |
| US20090220449A1 (en) | 2009-09-03 |
| ATE556105T1 (de) | 2012-05-15 |
| JP5449782B2 (ja) | 2014-03-19 |
| US8343474B2 (en) | 2013-01-01 |
| GB0602811D0 (en) | 2006-03-22 |
| JP2009526105A (ja) | 2009-07-16 |
| CN101405325A (zh) | 2009-04-08 |
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