JP2008518067A5 - - Google Patents
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- Publication number
- JP2008518067A5 JP2008518067A5 JP2007538384A JP2007538384A JP2008518067A5 JP 2008518067 A5 JP2008518067 A5 JP 2008518067A5 JP 2007538384 A JP2007538384 A JP 2007538384A JP 2007538384 A JP2007538384 A JP 2007538384A JP 2008518067 A5 JP2008518067 A5 JP 2008518067A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydrogen
- independently
- phenyl
- oxygen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims description 55
- 229910052739 hydrogen Inorganic materials 0.000 claims description 32
- 239000001257 hydrogen Substances 0.000 claims description 32
- 239000002105 nanoparticle Substances 0.000 claims description 21
- 125000003342 alkenyl group Chemical group 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- -1 amino - Chemical class 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 claims description 5
- 244000028419 Styrax benzoin Species 0.000 claims description 4
- 235000000126 Styrax benzoin Nutrition 0.000 claims description 4
- 235000008411 Sumatra benzointree Nutrition 0.000 claims description 4
- 229960002130 benzoin Drugs 0.000 claims description 4
- 235000019382 gum benzoic Nutrition 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical compound OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 claims description 2
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical compound C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000008062 acetophenones Chemical class 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000012965 benzophenone Substances 0.000 claims description 2
- 239000002530 phenolic antioxidant Substances 0.000 claims description 2
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 2
- 150000003568 thioethers Chemical class 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 22
- 125000003884 phenylalkyl group Chemical group 0.000 claims 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 18
- 229910052760 oxygen Inorganic materials 0.000 claims 18
- 239000001301 oxygen Substances 0.000 claims 18
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 17
- 229910052717 sulfur Inorganic materials 0.000 claims 17
- 239000011593 sulfur Chemical group 0.000 claims 17
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims 4
- 229910004298 SiO 2 Inorganic materials 0.000 claims 4
- 239000002114 nanocomposite Substances 0.000 claims 4
- 230000015556 catabolic process Effects 0.000 claims 3
- 238000006731 degradation reaction Methods 0.000 claims 3
- 239000003063 flame retardant Substances 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 230000003647 oxidation Effects 0.000 claims 3
- 238000007254 oxidation reaction Methods 0.000 claims 3
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 claims 3
- 150000003254 radicals Chemical class 0.000 claims 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 238000011065 in-situ storage Methods 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- 125000002757 morpholinyl group Chemical group 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims 1
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 1
- 239000006096 absorbing agent Substances 0.000 claims 1
- 125000005262 alkoxyamine group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000008199 coating composition Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 239000004611 light stabiliser Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000001038 naphthoyl group Chemical group C1(=CC=CC2=CC=CC=C12)C(=O)* 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 239000011368 organic material Substances 0.000 claims 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000002516 radical scavenger Substances 0.000 claims 1
- 239000012744 reinforcing agent Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 230000000087 stabilizing effect Effects 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- HWRLEEPNFJNTOP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-yl)phenol Chemical class OC1=CC=CC=C1C1=NC=NC=N1 HWRLEEPNFJNTOP-UHFFFAOYSA-N 0.000 description 1
- AVUYXHYHTTVPRX-UHFFFAOYSA-N Tris(2-methyl-1-aziridinyl)phosphine oxide Chemical compound CC1CN1P(=O)(N1C(C1)C)N1C(C)C1 AVUYXHYHTTVPRX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04105278 | 2004-10-25 | ||
| EP04105278.8 | 2004-10-25 | ||
| PCT/EP2005/055287 WO2006045713A1 (en) | 2004-10-25 | 2005-10-17 | Functionalized nanoparticles |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008518067A JP2008518067A (ja) | 2008-05-29 |
| JP2008518067A5 true JP2008518067A5 (enExample) | 2012-06-07 |
| JP5524449B2 JP5524449B2 (ja) | 2014-06-18 |
Family
ID=34929759
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007538384A Expired - Fee Related JP5524449B2 (ja) | 2004-10-25 | 2005-10-17 | 機能性ナノ粒子 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US20090076198A1 (enExample) |
| EP (2) | EP1805255A1 (enExample) |
| JP (1) | JP5524449B2 (enExample) |
| ES (1) | ES2712912T3 (enExample) |
| TW (1) | TW200619298A (enExample) |
| WO (1) | WO2006045713A1 (enExample) |
Families Citing this family (82)
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| US20090291107A1 (en) * | 2005-03-23 | 2009-11-26 | Volker Schehlmann | Chromophore Coated Metal Oxide Particles |
| DE102006012467A1 (de) | 2006-03-17 | 2007-09-20 | Merck Patent Gmbh | Redispergierbare Nanopartikel |
| ES2603838T3 (es) * | 2006-10-24 | 2017-03-01 | Basf Se | Composiciones fotocurables catiónicas térmicamente estables |
| EP2086693A2 (en) * | 2006-12-06 | 2009-08-12 | Ciba Holding Inc. | Changing surface properties by functionalized nanoparticles |
| KR100762298B1 (ko) * | 2006-12-29 | 2007-10-04 | 제일모직주식회사 | 내스크래치성이 향상된 열가소성 나노복합체 수지 조성물 |
| DE102007008663A1 (de) | 2007-02-20 | 2008-08-21 | Merck Patent Gmbh | Bindemittel |
| CN101622315A (zh) * | 2007-03-05 | 2010-01-06 | 巴斯夫欧洲公司 | 用于滤色器中的包含阳离子着色剂的表面-改性的纳米粒子 |
| FR2914631B1 (fr) | 2007-04-06 | 2009-07-03 | Eads Europ Aeronautic Defence | Materiau nanostructure particulier, comme revetement protecteur de surfaces metalliques. |
| EP2144918B1 (en) | 2007-05-11 | 2010-11-17 | Basf Se | Functionalized nanoparticles |
| WO2008138726A2 (en) * | 2007-05-11 | 2008-11-20 | Basf Se | Polymeric dyes |
| JP2009120700A (ja) * | 2007-11-14 | 2009-06-04 | Niigata Univ | 機能性微粒子及びその製造方法、並びにこれを配合してなる被覆性組成物 |
| US20090148653A1 (en) | 2007-12-07 | 2009-06-11 | E.I. Du Pont De Nemours And Company | Fluoropolymer emulsions |
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2005
- 2005-10-17 EP EP05794532A patent/EP1805255A1/en not_active Withdrawn
- 2005-10-17 WO PCT/EP2005/055287 patent/WO2006045713A1/en not_active Ceased
- 2005-10-17 EP EP08168635.4A patent/EP2028228B1/en not_active Expired - Lifetime
- 2005-10-17 JP JP2007538384A patent/JP5524449B2/ja not_active Expired - Fee Related
- 2005-10-17 US US11/665,627 patent/US20090076198A1/en not_active Abandoned
- 2005-10-17 ES ES08168635T patent/ES2712912T3/es not_active Expired - Lifetime
- 2005-10-24 TW TW094137154A patent/TW200619298A/zh unknown
-
2013
- 2013-06-28 US US13/930,848 patent/US8877954B2/en not_active Expired - Lifetime
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