JP2007523973A5 - - Google Patents
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- JP2007523973A5 JP2007523973A5 JP2006548291A JP2006548291A JP2007523973A5 JP 2007523973 A5 JP2007523973 A5 JP 2007523973A5 JP 2006548291 A JP2006548291 A JP 2006548291A JP 2006548291 A JP2006548291 A JP 2006548291A JP 2007523973 A5 JP2007523973 A5 JP 2007523973A5
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- Prior art keywords
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- carbon atoms
- substituted
- unsubstituted
- alkyl group
- Prior art date
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- 239000000203 mixture Substances 0.000 claims description 5
- 239000003446 ligand Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 43
- 125000000217 alkyl group Chemical group 0.000 claims 33
- 229910052757 nitrogen Inorganic materials 0.000 claims 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 16
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 16
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 14
- 125000002947 alkylene group Chemical group 0.000 claims 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 13
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 12
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 12
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 9
- 239000002243 precursor Substances 0.000 claims 7
- 125000000547 substituted alkyl group Chemical group 0.000 claims 7
- 125000003107 substituted aryl group Chemical group 0.000 claims 7
- -1 N-phenylamino group Chemical group 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000003725 azepanyl group Chemical group 0.000 claims 6
- 125000003277 amino group Chemical group 0.000 claims 5
- 150000001721 carbon Chemical group 0.000 claims 5
- 150000004967 organic peroxy acids Chemical class 0.000 claims 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 4
- 125000003282 alkyl amino group Chemical group 0.000 claims 4
- 150000004965 peroxy acids Chemical class 0.000 claims 4
- 125000004193 piperazinyl group Chemical group 0.000 claims 4
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 3
- 238000004140 cleaning Methods 0.000 claims 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 150000001768 cations Chemical class 0.000 claims 2
- 230000000249 desinfective effect Effects 0.000 claims 2
- 238000009472 formulation Methods 0.000 claims 2
- 125000005186 naphthyloxy group Chemical group C1(=CC=CC2=CC=CC=C12)O* 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000003386 piperidinyl group Chemical group 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 claims 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims 1
- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 claims 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 150000001447 alkali salts Chemical class 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical group C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims 1
- 150000001537 azepanes Chemical group 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 238000004061 bleaching Methods 0.000 claims 1
- 239000007844 bleaching agent Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000012459 cleaning agent Substances 0.000 claims 1
- 239000010941 cobalt Substances 0.000 claims 1
- 229910017052 cobalt Inorganic materials 0.000 claims 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 1
- 150000004696 coordination complex Chemical class 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 239000000645 desinfectant Substances 0.000 claims 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 claims 1
- 239000008393 encapsulating agent Substances 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 229910052748 manganese Inorganic materials 0.000 claims 1
- 239000011572 manganese Substances 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims 1
- 125000005544 phthalimido group Chemical group 0.000 claims 1
- 229960001922 sodium perborate Drugs 0.000 claims 1
- 229940045872 sodium percarbonate Drugs 0.000 claims 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000010936 titanium Substances 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- WYJIQGIMJMPVFP-UHFFFAOYSA-N 2,6-bis[4-(4-methylpiperazin-1-yl)pyridin-2-yl]-1h-pyrimidin-4-one Chemical compound C1CN(C)CCN1C1=CC=NC(C=2N=C(N=C(O)C=2)C=2N=CC=C(C=2)N2CCN(C)CC2)=C1 WYJIQGIMJMPVFP-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- JUIYRRWOPHCMQM-UHFFFAOYSA-N 2,6-bis(4-chloropyridin-2-yl)-1h-pyrimidin-4-one Chemical compound N=1C(O)=CC(C=2N=CC=C(Cl)C=2)=NC=1C1=CC(Cl)=CC=N1 JUIYRRWOPHCMQM-UHFFFAOYSA-N 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04100078 | 2004-01-12 | ||
| PCT/EP2005/050000 WO2005068074A2 (en) | 2004-01-12 | 2005-01-03 | Use of metal complex compounds comprising pyridine pryimidine or s-triazne derived ligands as catalysts for oxidations with organic peroxy acids and/or precursors of organic peroxy acid and h2o2 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007523973A JP2007523973A (ja) | 2007-08-23 |
| JP2007523973A5 true JP2007523973A5 (enExample) | 2008-02-14 |
Family
ID=34778211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006548291A Withdrawn JP2007523973A (ja) | 2004-01-12 | 2005-01-03 | 有機ペルオキシ酸及び/又は有機ペルオキシ酸の前駆体並びにH2O2との酸化のための触媒としてのピリジンピリミジン又はs−トリアジンに由来した配位子を含む金属錯体化合物の使用 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20090189119A1 (enExample) |
| EP (1) | EP1703976A2 (enExample) |
| JP (1) | JP2007523973A (enExample) |
| KR (1) | KR20060126531A (enExample) |
| CN (1) | CN1929920A (enExample) |
| AU (1) | AU2005205064A1 (enExample) |
| BR (1) | BRPI0506799A (enExample) |
| MX (1) | MXPA06007817A (enExample) |
| WO (1) | WO2005068074A2 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1740306A1 (en) * | 2004-04-29 | 2007-01-10 | CIBA SPECIALTY CHEMICALS HOLDING INC. Patent Departement | Use of metal complexes having bispyridylpyrimidine or bispyridyltriazine ligands as catalysts for reactions with peroxy compounds for bleaching coloured stains on hard surfaces |
| WO2007090461A1 (en) * | 2006-02-06 | 2007-08-16 | Ciba Holding Inc. | Use of metal complex compounds as oxidation catalysts |
| EP1878733A1 (en) * | 2006-07-14 | 2008-01-16 | Novartis AG | Pyrimidine derivatives as ALK-5 inhibitors |
| WO2009000685A1 (en) * | 2007-06-25 | 2008-12-31 | Basf Se | Use of metal complex oxidation catalysts together with zinc compounds in laundry compositions |
| DE102007034725A1 (de) | 2007-07-23 | 2009-01-29 | Henkel Kgaa | TOC-Abbau in Abwässern durch Übergangsmetallkatalysatoren |
| CN101808742B (zh) * | 2007-07-23 | 2013-04-03 | 巴斯夫欧洲公司 | 金属络合物作为氧化催化剂的用途 |
| DE102007042615A1 (de) | 2007-09-07 | 2009-03-12 | Bk Giulini Gmbh | Erhöhung der bioziden Wirkung von Wasserstoffperoxid in Abwässern durch Übergangsmetallkatalysatoren |
| US20090325841A1 (en) * | 2008-02-11 | 2009-12-31 | Ecolab Inc. | Use of activator complexes to enhance lower temperature cleaning in alkaline peroxide cleaning systems |
| EP2252683B1 (en) * | 2008-02-11 | 2015-07-15 | Ecolab Inc. | Use of activator complexes to enhance lower temperature cleaning in alkaline peroxide cleaning systems |
| EP2103735A1 (en) | 2008-03-18 | 2009-09-23 | Unilever PLC | Catalytic bleaching of substrates |
| CN101503242B (zh) * | 2009-03-13 | 2011-04-20 | 哈尔滨工业大学 | 利用中间态锰强化高锰酸钾除污染的水处理药剂 |
| AU2010253926B2 (en) | 2009-05-28 | 2016-02-18 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
| US9512237B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Method for inhibiting the growth of microbes with a modified cellulose fiber |
| US9511167B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
| US9512563B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Surface treated modified cellulose from chemical kraft fiber and methods of making and using same |
| CN102612378B (zh) * | 2009-11-17 | 2014-11-26 | 诺华股份有限公司 | 用于接触透镜清毒的过氧化氢溶液和套件 |
| JP2013512978A (ja) * | 2009-12-02 | 2013-04-18 | ビーエーエスエフ ソシエタス・ヨーロピア | 包装適用のための酸素吸収/捕捉要素としての金属錯体の使用 |
| TWI558439B (zh) * | 2010-04-26 | 2016-11-21 | 三菱瓦斯化學股份有限公司 | 含過硫酸鹽及銀錯合物之化學物質分解用處理劑及使用該處理劑之化學物質分解方法 |
| US8877353B2 (en) * | 2010-07-21 | 2014-11-04 | Versitech Limited | Platinum (II) tetradentate ONCN complexes for organic light-emitting diode applications |
| RU2608686C2 (ru) | 2011-05-23 | 2017-01-23 | ДжиПи СЕЛЛЬЮЛОУС ГМБХ | Крафт-волокно древесины хвойных пород с улучшенной белизной и яркостью и способы его производства и применения |
| US10144005B2 (en) * | 2011-09-08 | 2018-12-04 | Richard William Kemp | Catalysts |
| CN103174006A (zh) * | 2011-11-24 | 2013-06-26 | 东华大学 | 双吡啶嘧啶金属配合物在纺织品低温练漂助剂中的应用 |
| CN103194896A (zh) * | 2011-11-24 | 2013-07-10 | 东华大学 | 三联吡啶金属配合物在纺织品低温练漂助剂中的应用 |
| CA2860609C (en) | 2012-01-12 | 2021-02-16 | Gp Cellulose Gmbh | A low viscosity kraft fiber having reduced yellowing properties and methods of making and using the same |
| PL2839071T3 (pl) | 2012-04-18 | 2019-05-31 | Gp Cellulose Gmbh | Zastosowanie środka powierzchniowo czynnego do obróbki masy celulozowej i poprawa przyłączania masy celulozowej siarczanowej do włókna w celu produkcji wiskozy i innych drugorzędnych produktów włóknistych |
| MX365675B (es) | 2013-02-08 | 2019-06-10 | Gp Cellulose Gmbh | Fibra kraft de madera blanda que tiene un contenido mejorado de a-celulosa, y su uso en la produccion de productos de celulosa quimica. |
| JP6379116B2 (ja) | 2013-03-14 | 2018-08-22 | ゲーペー ツェルローゼ ゲーエムベーハー | 酸性漂白シーケンスを使用する、高機能、低粘度クラフト繊維の作製方法およびそのプロセスによって作製される繊維 |
| BR112015020000A2 (pt) | 2013-03-15 | 2017-07-18 | Gp Cellulose Gmbh | fibra kraft quimicamente modificada e métodos de fabricação da mesma |
| EP3033409B1 (en) | 2013-08-16 | 2021-09-22 | Catexel Technologies Limited | Composition |
| WO2016052196A1 (ja) * | 2014-09-29 | 2016-04-07 | 富士フイルム株式会社 | 光電変換素子、色素増感太陽電池、金属錯体色素、色素溶液、およびターピリジン化合物またはそのエステル化物 |
| WO2016052193A1 (ja) * | 2014-09-29 | 2016-04-07 | 富士フイルム株式会社 | 光電変換素子、色素増感太陽電池、金属錯体色素、色素溶液、およびターピリジン化合物またはそのエステル化物 |
| CN105369581A (zh) * | 2015-11-04 | 2016-03-02 | 泉州市新宏化工贸易有限公司 | 一种棉织物练漂后除氧工艺及棉洁爽 |
| CN106478745B (zh) * | 2016-10-14 | 2019-02-05 | 高介平 | 一种无甲醛水性交联剂及其制备方法和对织物的整理工艺 |
| US10865519B2 (en) | 2016-11-16 | 2020-12-15 | Gp Cellulose Gmbh | Modified cellulose from chemical fiber and methods of making and using the same |
| EP3967742A1 (en) | 2020-09-15 | 2022-03-16 | WeylChem Performance Products GmbH | Compositions comprising bleaching catalyst, manufacturing process thereof, and bleaching and cleaning agent comprising same |
| CN114887663B (zh) * | 2022-05-03 | 2023-05-12 | 东华大学 | 一种产生单线态氧的催化系统及其应用 |
| CN115634716A (zh) * | 2022-10-20 | 2023-01-24 | 金宏气体股份有限公司 | 光催化剂、其制备方法、光催化体系及应用 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3912648A (en) * | 1973-03-21 | 1975-10-14 | American Cyanamid Co | Ring halogen-free substituted triazine compounds as bleach activators |
| US5268477A (en) * | 1985-09-12 | 1993-12-07 | The Upjohn Company | Triazinylpiperazinyl amine intermediates |
| WO1997048786A1 (de) * | 1996-06-19 | 1997-12-24 | Call Hans Peter | Mehrkomponentensystem zur verwendung mit waschaktiven substanzen |
| DE19726241A1 (de) * | 1997-06-20 | 1998-12-24 | Call Krimhild | Erweitertes enzymatisches Multikomponentensystem zur Behandlung von Abwässern, zur Herstellung von Holzverbundstoffen, zum Deinken von Altpapier, Colour stripping von Altpapier, zum Einsatz als Oxidationssystem bei der organischen Synthese und zum Einsatz bei der Kohleverflüssigung |
| JPH1150096A (ja) * | 1997-08-01 | 1999-02-23 | Lion Corp | 自動食器洗浄機用粒状洗浄剤組成物 |
| DE60025492T2 (de) * | 1999-07-14 | 2006-07-27 | Ciba Speciality Chemicals Holding Inc. | Metallkomplexe von tripodalen liganden |
| AU2001256155A1 (en) * | 2000-02-29 | 2001-09-12 | Unilever Plc | Composition and method for bleaching a substrate |
| JP3605012B2 (ja) * | 2000-08-11 | 2004-12-22 | 独立行政法人科学技術振興機構 | オレフィンの酸化的分解によるケトンの製造法 |
| WO2002088289A2 (en) * | 2001-04-30 | 2002-11-07 | Ciba Specialty Chemicals Holding Inc. | Use of metal complex compounds as oxidation catalysts |
| KR101004084B1 (ko) * | 2002-10-30 | 2010-12-27 | 시바 홀딩 인코포레이티드 | 산화 촉매로서 유용한 금속 착화합물 |
| US20070072787A1 (en) * | 2003-05-21 | 2007-03-29 | Menno Hazenkamp | Stable particulate composition comprising bleach catalysts |
-
2005
- 2005-01-03 KR KR1020067013458A patent/KR20060126531A/ko not_active Withdrawn
- 2005-01-03 BR BRPI0506799-5A patent/BRPI0506799A/pt not_active IP Right Cessation
- 2005-01-03 MX MXPA06007817A patent/MXPA06007817A/es unknown
- 2005-01-03 EP EP05701417A patent/EP1703976A2/en not_active Withdrawn
- 2005-01-03 WO PCT/EP2005/050000 patent/WO2005068074A2/en not_active Ceased
- 2005-01-03 AU AU2005205064A patent/AU2005205064A1/en not_active Abandoned
- 2005-01-03 US US10/585,543 patent/US20090189119A1/en not_active Abandoned
- 2005-01-03 JP JP2006548291A patent/JP2007523973A/ja not_active Withdrawn
- 2005-01-03 CN CNA2005800074023A patent/CN1929920A/zh active Pending
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