AU2011235140B2 - Adjustable chromophore compounds and materials incorporating such compounds - Google Patents
Adjustable chromophore compounds and materials incorporating such compounds Download PDFInfo
- Publication number
- AU2011235140B2 AU2011235140B2 AU2011235140A AU2011235140A AU2011235140B2 AU 2011235140 B2 AU2011235140 B2 AU 2011235140B2 AU 2011235140 A AU2011235140 A AU 2011235140A AU 2011235140 A AU2011235140 A AU 2011235140A AU 2011235140 B2 AU2011235140 B2 AU 2011235140B2
- Authority
- AU
- Australia
- Prior art keywords
- compound
- chromophore
- chemical moiety
- adjustable
- lens
- 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.)
- Active
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 161
- 239000000463 material Substances 0.000 title claims abstract description 34
- 239000000126 substance Substances 0.000 claims abstract description 58
- 230000005670 electromagnetic radiation Effects 0.000 claims abstract description 25
- 230000031700 light absorption Effects 0.000 claims description 23
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical group C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 8
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 7
- 239000012964 benzotriazole Substances 0.000 claims description 7
- 150000001565 benzotriazoles Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 230000010287 polarization Effects 0.000 claims description 6
- 239000012965 benzophenone Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 239000000987 azo dye Substances 0.000 claims description 4
- 150000008366 benzophenones Chemical class 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 238000002513 implantation Methods 0.000 claims description 4
- 238000000338 in vitro Methods 0.000 claims description 4
- 238000001727 in vivo Methods 0.000 claims description 4
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical class [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 claims 1
- 230000005855 radiation Effects 0.000 abstract description 17
- 238000010521 absorption reaction Methods 0.000 description 23
- 230000002401 inhibitory effect Effects 0.000 description 10
- 239000011159 matrix material Substances 0.000 description 9
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 230000002093 peripheral effect Effects 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 5
- 150000001335 aliphatic alkanes Chemical group 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 125000006575 electron-withdrawing group Chemical group 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 210000001747 pupil Anatomy 0.000 description 2
- 238000011002 quantification Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 1
- ILZXXGLGJZQLTR-UHFFFAOYSA-N 2-phenylethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC1=CC=CC=C1 ILZXXGLGJZQLTR-UHFFFAOYSA-N 0.000 description 1
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000005829 chemical entities Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229940125758 compound 15 Drugs 0.000 description 1
- 229940125846 compound 25 Drugs 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- -1 dicyclohexadiene Chemical compound 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
- B01J19/122—Incoherent waves
- B01J19/123—Ultraviolet light
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
- B01J19/122—Incoherent waves
- B01J19/127—Sunlight; Visible light
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D11/00—Producing optical elements, e.g. lenses or prisms
- B29D11/00009—Production of simple or compound lenses
- B29D11/00432—Auxiliary operations, e.g. machines for filling the moulds
- B29D11/00461—Adjusting the refractive index, e.g. after implanting
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
- C07D249/20—Benzotriazoles with aryl radicals directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
- G02B1/043—Contact lenses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2430/00—Materials or treatment for tissue regeneration
- A61L2430/16—Materials or treatment for tissue regeneration for reconstruction of eye parts, e.g. intraocular lens, cornea
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Toxicology (AREA)
- Electromagnetism (AREA)
- Polymers & Plastics (AREA)
- Optics & Photonics (AREA)
- General Physics & Mathematics (AREA)
- Transplantation (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Dermatology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Mechanical Engineering (AREA)
- Ophthalmology & Optometry (AREA)
- Manufacturing & Machinery (AREA)
- Eyeglasses (AREA)
- Materials For Medical Uses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Prostheses (AREA)
- Optical Filters (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32044210P | 2010-04-02 | 2010-04-02 | |
| US61/320,442 | 2010-04-02 | ||
| PCT/US2011/030634 WO2011123587A1 (en) | 2010-04-02 | 2011-03-31 | Adjustable chromophore compounds and materials incorporating such compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2011235140A1 AU2011235140A1 (en) | 2012-09-27 |
| AU2011235140B2 true AU2011235140B2 (en) | 2015-01-15 |
Family
ID=44148789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2011235140A Active AU2011235140B2 (en) | 2010-04-02 | 2011-03-31 | Adjustable chromophore compounds and materials incorporating such compounds |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | US20110245818A1 (enExample) |
| EP (1) | EP2553501B1 (enExample) |
| JP (3) | JP2013523961A (enExample) |
| CN (1) | CN102844683B (enExample) |
| AR (1) | AR080739A1 (enExample) |
| AU (1) | AU2011235140B2 (enExample) |
| BR (1) | BR112012024962A2 (enExample) |
| CA (1) | CA2794284C (enExample) |
| ES (1) | ES2474094T3 (enExample) |
| RU (1) | RU2563640C2 (enExample) |
| TW (1) | TWI583673B (enExample) |
| WO (1) | WO2011123587A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI583673B (zh) * | 2010-04-02 | 2017-05-21 | 艾爾康股份有限公司 | 可調整之發色團化合物及併合該化合物之材料 |
| TW201311621A (zh) | 2011-08-15 | 2013-03-16 | Novartis Ag | 眼用鏡片材料之紫外光吸收劑 |
| US9204962B2 (en) | 2013-03-13 | 2015-12-08 | Acufocus, Inc. | In situ adjustable optical mask |
| EP3363794A1 (en) * | 2017-02-15 | 2018-08-22 | Merck Patent GmbH | Bis-compounds for optically active devices |
| US12486403B2 (en) | 2018-03-02 | 2025-12-02 | Johnson & Johnson Vision Care, Inc. | Polymerizable absorbers of UV and high energy visible light |
| US10935695B2 (en) | 2018-03-02 | 2021-03-02 | Johnson & Johnson Vision Care, Inc. | Polymerizable absorbers of UV and high energy visible light |
| US11543683B2 (en) | 2019-08-30 | 2023-01-03 | Johnson & Johnson Vision Care, Inc. | Multifocal contact lens displaying improved vision attributes |
| US12486348B2 (en) | 2019-08-30 | 2025-12-02 | Johnson & Johnson Vision Care, Inc. | Contact lens displaying improved vision attributes |
| US11993037B1 (en) | 2018-03-02 | 2024-05-28 | Johnson & Johnson Vision Care, Inc. | Contact lens displaying improved vision attributes |
| US11958824B2 (en) | 2019-06-28 | 2024-04-16 | Johnson & Johnson Vision Care, Inc. | Photostable mimics of macular pigment |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6864325B2 (en) * | 2000-02-22 | 2005-03-08 | Ciba Specialty Chemicals Corporation | Romp with oligomeric UV-absorbers |
| US7459106B2 (en) * | 2001-03-30 | 2008-12-02 | The Arizona Board Of Regents On Behalf Of The University Of Arizona | Materials, methods, and uses for photochemical generation of acids and/or radical species |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5112623B2 (enExample) | 1972-10-12 | 1976-04-21 | ||
| US4528311A (en) | 1983-07-11 | 1985-07-09 | Iolab Corporation | Ultraviolet absorbing polymers comprising 2-hydroxy-5-acrylyloxyphenyl-2H-benzotriazoles |
| GB2237567A (en) * | 1989-10-24 | 1991-05-08 | Kuwait Inst Scient Res | Naphthylbenzotriazoles |
| US7511630B2 (en) * | 1999-05-04 | 2009-03-31 | Intellimat, Inc. | Dynamic electronic display system with brightness control |
| AU2001264162A1 (en) | 2000-06-16 | 2001-12-24 | Optilink Ab | Optical storage using materials comprising chromophore oligomers which can undergo cycloaddition |
| CN1317535A (zh) | 2001-02-23 | 2001-10-17 | 秦皇岛耀华玻璃股份有限公司 | 光致变色萘并吡喃化合物，制备方法及含此化合物的制品 |
| GB0119137D0 (en) * | 2001-08-06 | 2001-09-26 | Clariant Int Ltd | Property enhancement of polyamides by co-condensation with lightstabilizers |
| ATE329629T1 (de) | 2003-01-09 | 2006-07-15 | Alcon Inc | Doppelfunktions-uv-absorbierer materialien für ophthalmische linsen |
| US20040186241A1 (en) * | 2003-03-20 | 2004-09-23 | Gemert Barry Van | Photochromic ocular devices |
| DE602006016943D1 (de) * | 2005-06-13 | 2010-10-28 | Alcon Inc | Materialien für ophthalmische und otorhinolaryngologische geräte |
| DE102005045540A1 (de) * | 2005-09-23 | 2007-03-29 | Hampp, Norbert, Prof. Dr. | Intraokularlinse |
| US7727514B2 (en) | 2005-10-03 | 2010-06-01 | Biotechnology Research & Development Corporation | Compositions comprising a UV-absorbing chromophore |
| US20070140058A1 (en) * | 2005-11-21 | 2007-06-21 | Motorola, Inc. | Method and system for correcting transducer non-linearities |
| JP4961142B2 (ja) | 2006-01-30 | 2012-06-27 | 株式会社リコー | 画像形成装置 |
| US7481955B2 (en) * | 2006-05-31 | 2009-01-27 | Transitions Optical, Inc. | Photochromic materials comprising metallocenyl groups |
| KR20090012353A (ko) * | 2006-06-08 | 2009-02-03 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 편광 광학 요소 및 폴리우레탄-함유 필름의 제조방법 |
| MX2009003813A (es) * | 2006-10-13 | 2009-05-12 | Alcon Inc | Lentes intraoculares con caracteristicas unicas para bloquear el paso de luz azul-violeta y para transmitir luz azul. |
| WO2008109624A2 (en) | 2007-03-05 | 2008-09-12 | Benz Research And Development Corp. | Light filters comprising a naturally occurring chromophore and derivatives thereof |
| EP2177524A4 (en) * | 2007-08-16 | 2011-12-14 | Fujifilm Corp | HETEROCYCLIC COMPOUND, ULTRAVIOLET RADIATION ABSORBER, AND COMPOSITION COMPRISING THE ULTRAVIOLET RADIATION ABSORBER |
| US8043607B2 (en) | 2008-07-15 | 2011-10-25 | Novartis Ag | UV-absorbers for ophthalmic lens materials |
| TWI583673B (zh) * | 2010-04-02 | 2017-05-21 | 艾爾康股份有限公司 | 可調整之發色團化合物及併合該化合物之材料 |
-
2011
- 2011-03-18 TW TW100109328A patent/TWI583673B/zh not_active IP Right Cessation
- 2011-03-30 AR ARP110101042 patent/AR080739A1/es unknown
- 2011-03-31 BR BR112012024962A patent/BR112012024962A2/pt not_active Application Discontinuation
- 2011-03-31 WO PCT/US2011/030634 patent/WO2011123587A1/en not_active Ceased
- 2011-03-31 CN CN201180017513.8A patent/CN102844683B/zh active Active
- 2011-03-31 US US13/076,665 patent/US20110245818A1/en not_active Abandoned
- 2011-03-31 AU AU2011235140A patent/AU2011235140B2/en active Active
- 2011-03-31 JP JP2013502825A patent/JP2013523961A/ja not_active Withdrawn
- 2011-03-31 ES ES11715630.7T patent/ES2474094T3/es active Active
- 2011-03-31 EP EP20110715630 patent/EP2553501B1/en active Active
- 2011-03-31 RU RU2012146774/04A patent/RU2563640C2/ru not_active IP Right Cessation
- 2011-03-31 CA CA2794284A patent/CA2794284C/en active Active
-
2015
- 2015-07-07 US US14/792,877 patent/US10029229B2/en active Active
- 2015-11-09 JP JP2015219150A patent/JP6254135B2/ja active Active
-
2017
- 2017-02-01 JP JP2017016554A patent/JP2017128728A/ja not_active Withdrawn
-
2018
- 2018-06-21 US US16/014,639 patent/US10434489B2/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6864325B2 (en) * | 2000-02-22 | 2005-03-08 | Ciba Specialty Chemicals Corporation | Romp with oligomeric UV-absorbers |
| US7459106B2 (en) * | 2001-03-30 | 2008-12-02 | The Arizona Board Of Regents On Behalf Of The University Of Arizona | Materials, methods, and uses for photochemical generation of acids and/or radical species |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102844683A (zh) | 2012-12-26 |
| JP2017128728A (ja) | 2017-07-27 |
| WO2011123587A1 (en) | 2011-10-06 |
| EP2553501A1 (en) | 2013-02-06 |
| JP6254135B2 (ja) | 2017-12-27 |
| US10029229B2 (en) | 2018-07-24 |
| JP2016094602A (ja) | 2016-05-26 |
| US20180297003A1 (en) | 2018-10-18 |
| AR080739A1 (es) | 2012-05-02 |
| ES2474094T3 (es) | 2014-07-08 |
| TW201202207A (en) | 2012-01-16 |
| CA2794284A1 (en) | 2011-10-06 |
| US10434489B2 (en) | 2019-10-08 |
| JP2013523961A (ja) | 2013-06-17 |
| RU2563640C2 (ru) | 2015-09-20 |
| US20150306562A1 (en) | 2015-10-29 |
| TWI583673B (zh) | 2017-05-21 |
| EP2553501B1 (en) | 2014-05-14 |
| CA2794284C (en) | 2018-02-13 |
| BR112012024962A2 (pt) | 2016-07-12 |
| AU2011235140A1 (en) | 2012-09-27 |
| US20110245818A1 (en) | 2011-10-06 |
| CN102844683B (zh) | 2014-11-26 |
| RU2012146774A (ru) | 2014-05-10 |
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