AR065957A1 - Preparacion de ftalocianinas de silicio y germanio; uso como sustancias marcadoras de liquidos, proceso para deteccion de las mismas, liquidos y compuestos - Google Patents
Preparacion de ftalocianinas de silicio y germanio; uso como sustancias marcadoras de liquidos, proceso para deteccion de las mismas, liquidos y compuestosInfo
- Publication number
- AR065957A1 AR065957A1 ARP080101421A ARP080101421A AR065957A1 AR 065957 A1 AR065957 A1 AR 065957A1 AR P080101421 A ARP080101421 A AR P080101421A AR P080101421 A ARP080101421 A AR P080101421A AR 065957 A1 AR065957 A1 AR 065957A1
- Authority
- AR
- Argentina
- Prior art keywords
- same
- independently
- different
- alkyl
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/06—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide
- C09B47/067—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile
- C09B47/0673—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile having alkyl radicals linked directly to the Pc skeleton; having carbocyclic groups linked directly to the skeleton
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/22—Obtaining compounds having nitrogen atoms directly bound to the phthalocyanine skeleton
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/003—Marking, e.g. coloration by addition of pigments
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1608—Well defined compounds, e.g. hexane, benzene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/28—Organic compounds containing silicon
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/301—Organic compounds compounds not mentioned before (complexes) derived from metals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/007—Coloured or dyes-containing lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/09—Complexes with metals
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
Reivindicacion 1: Procedimiento para preparar compuestos de la formula general (1) caracterizado porqeu los símbolos y los índices tienen el siguiente significado; M1, M2, M3 son, de modo independiente entre sí, iguales o diferentes, Si o Ge; A, A',A'' son, de modo independiente entre sí, iguales o diferentes, CH o N; D, D', D'' son, de modo independienteentre sí, iguales o diferentes, CH o N; E, E', E'' son, de modo independiente entre sí, iguales o diferentes, CH o N; G, G', G'' son, de modoindependiente entre sí, iguales o diferentes, CH o N; n, m, p, q son, de modo independiente entre sí, iguales o diferentes, numeros enteros seleccionados del rango de 0 a 2, r numero entero seleccionado del rango de 1 a (4 + n . 2), s numero enteroseleccionado del rango de 1 a (4 + m . 2), u numero entero seleccionado del rango de 1 a (4 + p . 2), v numero entero seleccionado del rango de 1 a (4 + q . 2), W, X, Y, Z son, de modo independiente entre sí, iguales o diferentes, halogeno, nitro,hidroxi, ciano, amino, alquilo C1-20, alquenilo C2-20, alquinilo C2-20, cicloalquilo C3-15, arilo, heterociclos, alcoxi C1-20, ariloxi, dialquil C1-4-amino, cicloalquil C3-6-amino, CO2M, SO3M, dialquil C1-4-sulfamoílo, R1 a R6 son, de modoindependiente entre sí, iguales o diferentes, alquilo C1-20, alquenilo C2-20, alquiniloC2-20, cicloalquilo C3-15, arilo, arilalquilo, alcoxi C1-20, alquil C1-20-tio, ariloxi, trialquilsiloxi, CO2M, SO3M, radicales alquilo C1-20 sustituidos contrialquil C1-4-amonio, M hidrogeno, metal alcalino, en donde los sustituyentes R1 a R6, W, X, Y o Z pueden estar cada uno interrumpidos en cualquier posicion por uno o varios heteroátomos, en donde la cantidad de estos heteroátomos no más de 10, conpreferencia no más de 8, con preferencia muy especial no más de 5 y en especial no más de 3, y/o en cada caso en cualquier posicion, sin embargo pueden estar sustituidos no más de cindo veces, con preferencia no más de cuatro vences y conpreferencia especial no más de tres veces, con alquilo C1-20, alcoxi C1-20, arilo, ariloxi, heterociclos, heteroátomos, NR2 (con R =hidrogeno, alquilo C1-20), SO3M, CO2M o halogeno, en donde pueden estar asimismo sustituidos como máximo dos veces,con preferencia como máximo una vez con los grupos mencionados, con reaccion del compuesto de la formula general (2) en donde L, L' son, de modo independiente entre sí, iguales o diferentes, Cl o OH, en presencia de a. compuestos clorados Cl-M2R1R2R3, Cl-M3R4R5R6, con la condicion de que L y L' no sean ambos al mismo tiempo OH, o b. compuestos hidroxi HO-M2R1R2R3, HO-M3R4R5R6. Reivindicacion 20: Compuesto caracterizado porque tiene la formula (3). Reivindicacion 21: Compuestocaracterizado porque tiene la formula (4). Reivindicacion 22: Compuestos caracterizados porque tienen la formula (5), en donde R1=R2=R4=R5=metilo, iso-propilo. Reivindicacion 23: Compuestos caracterizados porque tienen la formula (6), en donde R'= OH, O-Si(n-butilo)3.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07105776 | 2007-04-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR065957A1 true AR065957A1 (es) | 2009-07-15 |
Family
ID=39769050
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080101421A AR065957A1 (es) | 2007-04-05 | 2008-04-04 | Preparacion de ftalocianinas de silicio y germanio; uso como sustancias marcadoras de liquidos, proceso para deteccion de las mismas, liquidos y compuestos |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20100113767A1 (es) |
| EP (1) | EP2134792A2 (es) |
| JP (1) | JP2010523751A (es) |
| KR (1) | KR20100009566A (es) |
| CN (1) | CN101668818A (es) |
| AR (1) | AR065957A1 (es) |
| BR (1) | BRPI0810076A2 (es) |
| CL (1) | CL2008000992A1 (es) |
| PE (1) | PE20090285A1 (es) |
| RU (1) | RU2009140324A (es) |
| TW (1) | TW200909525A (es) |
| WO (1) | WO2008122531A2 (es) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITFI20110166A1 (it) * | 2011-08-05 | 2013-02-06 | Molteni & C | Nuovi fotosensibilizzanti ad uso terapeutico. |
| WO2014198629A1 (en) | 2013-06-13 | 2014-12-18 | Basf Se | Detector for optically detecting at least one object |
| EP3008421A1 (en) | 2013-06-13 | 2016-04-20 | Basf Se | Detector for optically detecting an orientation of at least one object |
| WO2015170219A1 (en) | 2014-05-07 | 2015-11-12 | Sabic Global Technologies B.V. | Crystallization of additives at p/n junctions of bulk-heterojunction photoactive layers |
| JP6660931B2 (ja) | 2014-07-08 | 2020-03-11 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 少なくとも1つの物体の位置を決定するための検出器 |
| CN107003785B (zh) | 2014-12-09 | 2020-09-22 | 巴斯夫欧洲公司 | 光学检测器 |
| US10775505B2 (en) | 2015-01-30 | 2020-09-15 | Trinamix Gmbh | Detector for an optical detection of at least one object |
| CN108027239B (zh) | 2015-07-17 | 2020-07-24 | 特里纳米克斯股份有限公司 | 用于光学检测至少一个对象的检测器 |
| WO2017027723A1 (en) * | 2015-08-12 | 2017-02-16 | Leishvac Llc | Photosensitized trypanosomatids and vaccine compositions thereof |
| WO2017046121A1 (en) | 2015-09-14 | 2017-03-23 | Trinamix Gmbh | 3d camera |
| CN108292175A (zh) | 2015-11-25 | 2018-07-17 | 特里纳米克斯股份有限公司 | 用于光学检测至少一个对象的检测器 |
| US10070648B2 (en) | 2016-04-15 | 2018-09-11 | Rosalind Franklin University Of Medicine And Science | Photodynamic insecticides |
| EP3491675B1 (en) | 2016-07-29 | 2022-11-16 | trinamiX GmbH | Optical sensor and detector for optical detection |
| US11428787B2 (en) | 2016-10-25 | 2022-08-30 | Trinamix Gmbh | Detector for an optical detection of at least one object |
| US10890491B2 (en) | 2016-10-25 | 2021-01-12 | Trinamix Gmbh | Optical detector for an optical detection |
| CN109964144B (zh) | 2016-11-17 | 2023-07-18 | 特里纳米克斯股份有限公司 | 用于光学探测至少一个对象的检测器 |
| US11860292B2 (en) | 2016-11-17 | 2024-01-02 | Trinamix Gmbh | Detector and methods for authenticating at least one object |
| WO2018096083A1 (en) | 2016-11-25 | 2018-05-31 | Trinamix Gmbh | Optical detector comprising at least one optical waveguide |
| KR102623150B1 (ko) | 2017-04-20 | 2024-01-11 | 트리나미엑스 게엠베하 | 광 검출기 |
| KR102563713B1 (ko) | 2017-04-26 | 2023-08-07 | 오티아이 루미오닉스 인크. | 표면의 코팅을 패턴화하는 방법 및 패턴화된 코팅을 포함하는 장치 |
| EP3645965B1 (en) | 2017-06-26 | 2022-04-27 | trinamiX GmbH | Detector for determining a position of at least one object |
| WO2020225778A1 (en) | 2019-05-08 | 2020-11-12 | Oti Lumionics Inc. | Materials for forming a nucleation-inhibiting coating and devices incorporating same |
| JP2023553379A (ja) | 2020-12-07 | 2023-12-21 | オーティーアイ ルミオニクス インコーポレーテッド | 核形成抑制被膜及び下地金属被膜を用いた導電性堆積層のパターニング |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3094536A (en) * | 1961-01-03 | 1963-06-18 | Malcolm E Kenney | Silicon phthalocyanines |
| US3509146A (en) * | 1967-07-03 | 1970-04-28 | Xerox Corp | Process of preparing phthalocyanine and heterocyclic analogues |
| US4622179A (en) * | 1983-07-19 | 1986-11-11 | Yamamoto Kagaku Gosei Co., Ltd. | Naphthalocyanine compounds |
| GB8415218D0 (en) * | 1984-06-14 | 1984-07-18 | Lucas Ind Plc | Fuel injector |
| DE3783529T2 (de) * | 1986-07-23 | 1993-05-13 | Hitachi Chemical Co Ltd | Optisches aufzeichnungsmedium. |
| DE3810956A1 (de) * | 1988-03-31 | 1989-10-12 | Basf Ag | Neue siliciumnaphthalocyanine sowie duenne strahlungsempfindliche beschichtungsfilme, die diese verbindungen enthalten |
| DE3830041A1 (de) * | 1988-09-03 | 1990-03-08 | Basf Ag | Siliciumnaphthalocyanine mit ungesaettigten liganden sowie duenne strahlungsempfindliche beschichtungsfilme |
| DE4243776A1 (de) * | 1992-12-23 | 1994-06-30 | Basf Ag | Verwendung von im IR-Bereich fluoreszierenden Verbindungen als Markierungsmittel für Flüssigkeiten |
| MX9304188A (es) * | 1992-07-23 | 1994-03-31 | Basf Ag | Uso de compuestos absorbentes y/o fluorescentes enla region infrarroja como marcadores para liquidos. |
| DE4243774A1 (de) * | 1992-12-23 | 1994-06-30 | Basf Ag | Verfahren zur Detektion von Markierstoffen in Flüssigkeiten |
| DE4224301A1 (de) * | 1992-07-23 | 1994-01-27 | Basf Ag | Verwendung von im IR-Bereich absorbierenden Verbindungen als Markierungsmittel für Flüssigkeiten |
| JPH07257037A (ja) * | 1994-03-23 | 1995-10-09 | Hitachi Chem Co Ltd | 高密度光記録媒体 |
| US5576453A (en) * | 1994-07-18 | 1996-11-19 | Es Industries | Stable, sterically-protected, bonded phase silicas prepared from bifunctional silanes |
| US5525516B1 (en) * | 1994-09-30 | 1999-11-09 | Eastman Chem Co | Method for tagging petroleum products |
| US5872248A (en) * | 1997-03-28 | 1999-02-16 | Case Western Reserve University | Methods for inserting silicon into phthalocyanines and naphthalocyanines |
| DE19721399A1 (de) * | 1997-05-22 | 1998-11-26 | Basf Ag | Phthalocyanine und ihre Verwendung als Markierungsmittel |
| JP4796259B2 (ja) * | 2000-05-04 | 2011-10-19 | シーメンス・ヘルスケア・ダイアグノスティックス・プロダクツ・ゲーエムベーハー | 複数のアナライトの検出において使用するための組成物 |
| KR20090101812A (ko) * | 2006-12-20 | 2009-09-29 | 바스프 에스이 | 액체용 마커로서 안트라퀴논 유도체 |
-
2008
- 2008-03-31 US US12/593,097 patent/US20100113767A1/en not_active Abandoned
- 2008-03-31 KR KR1020097023086A patent/KR20100009566A/ko not_active Ceased
- 2008-03-31 JP JP2010501491A patent/JP2010523751A/ja active Pending
- 2008-03-31 RU RU2009140324/05A patent/RU2009140324A/ru unknown
- 2008-03-31 CN CN200880010620A patent/CN101668818A/zh active Pending
- 2008-03-31 WO PCT/EP2008/053779 patent/WO2008122531A2/de not_active Ceased
- 2008-03-31 EP EP08735591A patent/EP2134792A2/de not_active Withdrawn
- 2008-03-31 BR BRPI0810076-4A2A patent/BRPI0810076A2/pt not_active IP Right Cessation
- 2008-04-03 TW TW097112382A patent/TW200909525A/zh unknown
- 2008-04-04 PE PE2008000614A patent/PE20090285A1/es not_active Application Discontinuation
- 2008-04-04 AR ARP080101421A patent/AR065957A1/es not_active Application Discontinuation
- 2008-04-04 CL CL2008000992A patent/CL2008000992A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CL2008000992A1 (es) | 2009-03-27 |
| PE20090285A1 (es) | 2009-03-27 |
| WO2008122531A2 (de) | 2008-10-16 |
| BRPI0810076A2 (pt) | 2014-10-21 |
| WO2008122531A3 (de) | 2009-07-30 |
| US20100113767A1 (en) | 2010-05-06 |
| CN101668818A (zh) | 2010-03-10 |
| JP2010523751A (ja) | 2010-07-15 |
| TW200909525A (en) | 2009-03-01 |
| RU2009140324A (ru) | 2011-05-10 |
| KR20100009566A (ko) | 2010-01-27 |
| EP2134792A2 (de) | 2009-12-23 |
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