JP2004500319A5 - - Google Patents
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- JP2004500319A5 JP2004500319A5 JP2000570167A JP2000570167A JP2004500319A5 JP 2004500319 A5 JP2004500319 A5 JP 2004500319A5 JP 2000570167 A JP2000570167 A JP 2000570167A JP 2000570167 A JP2000570167 A JP 2000570167A JP 2004500319 A5 JP2004500319 A5 JP 2004500319A5
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- 125000004432 carbon atom Chemical group C* 0.000 description 24
- 150000001875 compounds Chemical class 0.000 description 23
- 125000000217 alkyl group Chemical group 0.000 description 20
- 125000003118 aryl group Chemical group 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 125000001072 heteroaryl group Chemical group 0.000 description 12
- 125000003545 alkoxy group Chemical group 0.000 description 10
- 125000001424 substituent group Chemical group 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- -1 naphthoxy group Chemical group 0.000 description 7
- 229910052757 nitrogen Chemical group 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 125000000753 cycloalkyl group Chemical group 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000001301 oxygen Chemical group 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 125000005842 heteroatom Chemical group 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 125000006574 non-aromatic ring group Chemical group 0.000 description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VCMLCMCXCRBSQO-UHFFFAOYSA-N 3h-benzo[f]chromene Chemical group C1=CC=CC2=C(C=CCO3)C3=CC=C21 VCMLCMCXCRBSQO-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 150000001412 amines Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 125000004438 haloalkoxy group Chemical group 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000004475 heteroaralkyl group Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000007333 cyanation reaction Methods 0.000 description 1
- 125000004987 dibenzofuryl group Chemical group C1(=CC=CC=2OC3=C(C21)C=CC=C3)* 0.000 description 1
- 125000004988 dibenzothienyl group Chemical group C1(=CC=CC=2SC3=C(C21)C=CC=C3)* 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- LJJQENSFXLXPIV-UHFFFAOYSA-N fluorenylidene Chemical group C1=CC=C2[C]C3=CC=CC=C3C2=C1 LJJQENSFXLXPIV-UHFFFAOYSA-N 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 125000005347 halocycloalkyl group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002578 polythiourethane polymer Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical class OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9811519A FR2783248A1 (fr) | 1998-09-11 | 1998-09-11 | Naphtopyranes anneles en c5-c6, leur preparation, et les compositions et matrices (co)polymeres les renfermant |
| FR98/11519 | 1998-09-11 | ||
| FR9900162A FR2783249B1 (fr) | 1998-09-11 | 1999-01-06 | Naphtopyranes anneles en c5-c6, leur preparation et les compositions et matrices (co)polymeres les renfermant |
| FR99/00162 | 1999-01-06 | ||
| PCT/US1999/020471 WO2000015628A1 (en) | 1998-09-11 | 1999-09-07 | Naphthopyrans annelated in c5-c6, their preparation and compositions and (co) polymer matrices containing them |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011028893A Division JP5325243B2 (ja) | 1998-09-11 | 2011-02-14 | Ｃ５−ｃ６においてアネル化されたナフトピラン、その調製並びにそれらを含有する組成物および（コ）ポリマーマトリクス |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004500319A JP2004500319A (ja) | 2004-01-08 |
| JP2004500319A5 true JP2004500319A5 (https=) | 2007-01-11 |
| JP4737830B2 JP4737830B2 (ja) | 2011-08-03 |
Family
ID=26234545
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000570167A Expired - Lifetime JP4737830B2 (ja) | 1998-09-11 | 1999-09-07 | Ｃ５−ｃ６においてアネル化されたナフトピラン、その調製並びにそれらを含有する組成物および（コ）ポリマーマトリクス |
| JP2011028893A Expired - Lifetime JP5325243B2 (ja) | 1998-09-11 | 2011-02-14 | Ｃ５−ｃ６においてアネル化されたナフトピラン、その調製並びにそれらを含有する組成物および（コ）ポリマーマトリクス |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011028893A Expired - Lifetime JP5325243B2 (ja) | 1998-09-11 | 2011-02-14 | Ｃ５−ｃ６においてアネル化されたナフトピラン、その調製並びにそれらを含有する組成物および（コ）ポリマーマトリクス |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US6506538B1 (https=) |
| EP (1) | EP1119560B1 (https=) |
| JP (2) | JP4737830B2 (https=) |
| CN (1) | CN1315948A (https=) |
| AR (1) | AR021799A1 (https=) |
| AT (1) | ATE233749T1 (https=) |
| AU (1) | AU747191B2 (https=) |
| BR (1) | BR9912649A (https=) |
| CA (1) | CA2342338A1 (https=) |
| DE (1) | DE69905739T2 (https=) |
| ES (1) | ES2195659T3 (https=) |
| FR (1) | FR2783249B1 (https=) |
| WO (1) | WO2000015628A1 (https=) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2783249B1 (fr) * | 1998-09-11 | 2001-06-22 | Flamel Tech Sa | Naphtopyranes anneles en c5-c6, leur preparation et les compositions et matrices (co)polymeres les renfermant |
| US6686468B2 (en) * | 2000-09-14 | 2004-02-03 | Optische Werke G. Rodenstock | H-annellated benzo[f]chromenes |
| FR2815034B1 (fr) * | 2000-10-11 | 2003-02-07 | Corning Sa | Naphtopyranes anneles en c5-c6 par un carbocycle de type dihydrobenzocycloheptatriene et les compositions et matrices les refermant |
| US6736998B2 (en) * | 2000-12-29 | 2004-05-18 | Transitions Optical, Inc. | Indeno-fused photochromic naphthopyrans |
| US7048876B2 (en) * | 2001-05-02 | 2006-05-23 | Tokuyama Corporation | Chromene compound |
| US6608215B2 (en) | 2001-09-20 | 2003-08-19 | Vision-Ease Lens, Inc. | Oxygen-containing heterocyclic fused naphthopyrans |
| TW200302828A (en) * | 2001-11-16 | 2003-08-16 | Tokuyama Corp | Chromene compound |
| AU2003286709B8 (en) * | 2002-10-28 | 2009-11-19 | Insight Equity A.P.X., Lp | Oxygen-containing heterocyclic fused naphthopyrans |
| FR2854631B1 (fr) * | 2003-05-05 | 2007-12-21 | Corning Inc | Benzo-, naphto- et phenantrochromenes substitues en position 2 par un groupe arylamine et les compositions les renfermant |
| JP2007505842A (ja) | 2003-09-18 | 2007-03-15 | ローデンストック．ゲゼルシャフト．ミット．ベシュレンクテル．ハフツング | 置換されたフェナントロピラン |
| ES2326215T3 (es) * | 2003-11-05 | 2009-10-05 | Corning Incorporated | Piranos condensados fotocromicos sustituidos con fenilo que porta un grupo carbamilo o urea. |
| WO2005047277A1 (en) * | 2003-11-05 | 2005-05-26 | Corning Incorporated | Photochromic fused pyrans substituted with phenyl carrying a carbamyl or urea group |
| TW200530373A (en) * | 2003-12-12 | 2005-09-16 | Sumitomo Chemical Co | Polymer and light-emitting element using said polymer |
| EP1945625B1 (de) * | 2005-11-10 | 2010-03-03 | Rodenstock GmbH | Photochrome spirodihydrophenanthropyrane |
| KR20080091349A (ko) | 2006-01-25 | 2008-10-10 | 가부시끼가이샤 도꾸야마 | 크로멘 화합물 |
| JP2008074832A (ja) | 2006-08-24 | 2008-04-03 | Tokuyama Corp | クロメン化合物 |
| JP2009014689A (ja) * | 2007-07-09 | 2009-01-22 | Saitama Univ | フォトクロミック化合物を利用した紫外線強度測定装置 |
| US20090122261A1 (en) * | 2007-11-09 | 2009-05-14 | Insight Equity A.P.X., L.P. | Reflective Polarized Lenses With High Transmission |
| WO2009068247A1 (de) * | 2007-11-26 | 2009-06-04 | Rodenstock Gmbh | Photochrome benzopyrane |
| DE102008060096A1 (de) | 2007-12-20 | 2009-06-25 | Rodenstock Gmbh | Photochrome Spirobenzopyranobenzopyrane |
| WO2009132842A1 (de) | 2008-04-30 | 2009-11-05 | Rodenstock Gmbh | Photochrome naphthopyrane mit doppelt verbrückter terphenyl-untereinheit |
| US8217188B2 (en) * | 2008-08-27 | 2012-07-10 | Corning Incorporated | 2H-chromenes annelated at C5-C6 and methods of making and using thereof |
| DE102009058906A1 (de) | 2008-12-18 | 2010-06-24 | Rodenstock Gmbh | Photochrome Naphthopyrane mit Verbrückung zweier aromatischer Teilsysteme |
| US7829745B1 (en) | 2009-08-18 | 2010-11-09 | Corning Incorporated | Methods for selectively synthesizing 1-aryl-2-tetralones |
| US8188181B2 (en) * | 2009-09-22 | 2012-05-29 | Corning Incorporated | Photochromic compositions, resins and articles obtained therefrom |
| WO2013045086A1 (de) | 2011-09-26 | 2013-04-04 | Rodenstock Gmbh | Photochrome zweifach-annellierte naphthopyrane |
| ES2563502T3 (es) | 2011-12-09 | 2016-03-15 | Rodenstock Gmbh | Naftopiranos fotocromáticos doblemente indenoanillados |
| KR101610574B1 (ko) | 2012-06-26 | 2016-04-07 | 미쓰이 가가쿠 가부시키가이샤 | 광학재료용 중합성 조성물, 해당 조성물로부터 얻어지는 광학재료 및 플라스틱렌즈 |
| ES2578007T3 (es) | 2012-07-12 | 2016-07-20 | Rodenstock Gmbh | Fluorenopiranos fotocrómicos con anillación Dibenzo[b,d]-pirano |
| CN102976911A (zh) * | 2012-07-16 | 2013-03-20 | 上海甘田光学材料有限公司 | 萘酚酮衍生物及其制备方法和应用 |
| US9529118B2 (en) | 2012-11-30 | 2016-12-27 | Mitsui Chemicals, Inc. | Composition for optical material and use of same |
| JP6328751B2 (ja) * | 2013-06-17 | 2018-05-23 | ローデンシュトック ゲーエムベーハー | Ｕｖ硬化適合性フォトクロミック縮合ナフトピラン |
| KR101776540B1 (ko) | 2013-08-02 | 2017-09-07 | 미쯔이가가꾸가부시끼가이샤 | 포토크로믹 광학 재료의 제조 방법 |
| KR101821078B1 (ko) | 2014-02-03 | 2018-01-22 | 미쯔이가가꾸가부시끼가이샤 | 광학 재료용 중합성 조성물, 당해 조성물로부터 얻어지는 광학 재료 및 플라스틱 렌즈 |
| WO2017047745A1 (ja) | 2015-09-16 | 2017-03-23 | 三井化学株式会社 | 光学材料用重合性組成物、該組成物から得られる光学材料およびプラスチックレンズ |
| EP3351573B1 (en) * | 2015-09-16 | 2020-06-17 | Mitsui Chemicals, Inc. | Molded body and polymerizable composition for optical materials |
| US10921489B2 (en) | 2015-09-16 | 2021-02-16 | Mitsui Chemicals, Inc. | Polymerizable composition for optical material, optical material obtained from the composition, and plastic lens |
| JP6949946B2 (ja) | 2016-09-26 | 2021-10-13 | ローデンシュトック ゲーエムベーハー | 可視波長帯に向けて遠くから伸びる超長波長吸収を有する、フォトクロミック多環縮合ナフトピラン |
| MX2019003634A (es) | 2016-09-30 | 2019-06-17 | Mitsui Chemicals Inc | Composicion polimerizable para material optico y producto moldeado. |
| EP3650480A4 (en) | 2017-07-03 | 2021-03-24 | Mitsui Chemicals, Inc. | POLYMERIZABLE COMPOSITION FOR OPTICAL MATERIALS AND SHAPED BODIES |
| JP7123082B2 (ja) | 2018-02-09 | 2022-08-22 | 三井化学株式会社 | レンズおよびレンズの製造方法 |
| DE102018004790A1 (de) | 2018-06-14 | 2019-12-19 | Rodenstock Gmbh | Photochrome annellierte Naphthopyran-Systeme mit speziellen Substituenten zur Realisierung sehr schneller Aufhellgeschwindigkeiten |
| CN113135883B (zh) * | 2021-04-16 | 2023-04-07 | 天津孚信阳光科技有限公司 | 䓛并[1,2,f]吡喃光致变色化合物及其制备方法和应用 |
| EP4240797B1 (de) * | 2022-01-17 | 2024-08-28 | Rodenstock GmbH | Kombination spezifischer annellierter naphthopyran-isomere |
| DE102023109737A1 (de) | 2023-04-18 | 2024-10-24 | Rodenstock Gmbh | Höhermolekulare photochrome Farbstoffe mit mindestens einer und höchstens vier Naphthopyran-Untereinheiten sowie mehreren Polyether-Ketten |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5066818A (en) * | 1990-03-07 | 1991-11-19 | Ppg Industries, Inc. | Photochromic naphthopyran compounds |
| US5384077A (en) * | 1993-06-21 | 1995-01-24 | Transitions Optical, Inc. | Photochromic naphthopyran compounds |
| US5451344A (en) | 1994-04-08 | 1995-09-19 | Transitions Optical, Inc. | Photochromic naphthopyran compounds |
| US5514817A (en) | 1994-08-04 | 1996-05-07 | Ppg Industries, Inc. | Substituted phenanthropyrans |
| IL115803A (en) * | 1994-11-03 | 2000-02-17 | Ppg Industries Inc | Indeno-naphthopyran derivatives useful for photochromic articles |
| US5645767A (en) | 1994-11-03 | 1997-07-08 | Transitions Optical, Inc. | Photochromic indeno-fused naphthopyrans |
| US5723072A (en) * | 1996-06-17 | 1998-03-03 | Ppg Industries, Inc. | Photochromic heterocyclic fused indenonaphthopyrans |
| US5955520A (en) | 1996-06-17 | 1999-09-21 | Ppg Industries, Inc. | Photochromic indeno-fused naphthopyrans |
| US5698141A (en) * | 1996-06-17 | 1997-12-16 | Ppg Industries, Inc. | Photochromic heterocyclic fused indenonaphthopyrans |
| CN1220734A (zh) * | 1996-07-25 | 1999-06-23 | 康宁股份有限公司 | 萘并吡喃、包含萘并吡喃的组合物和制品 |
| DE19741705A1 (de) | 1997-09-22 | 1999-04-01 | Rodenstock Optik G | Naphtopyrane |
| WO1999015518A1 (de) | 1997-09-22 | 1999-04-01 | Optische Werke G. Rodenstock | Photochrome naphthopyran-farbstoffe, verfahren zu ihrer herstellung, ihre verwendung sowie ein photochromer gegenstand |
| US5783116A (en) * | 1997-10-16 | 1998-07-21 | Ppg Industries, Inc. | Derivatives of carbocyclic fused naphthopyrans |
| US5869658A (en) | 1997-12-15 | 1999-02-09 | Ppg Industries, Inc. | Photochromic indeno-fused naptho 2,1-b!pyrans |
| WO1999067234A1 (de) * | 1998-06-19 | 1999-12-29 | Optische Werke G. Rodenstock | Photochrome naphthopyrane |
| US6022497A (en) | 1998-07-10 | 2000-02-08 | Ppg Industries Ohio, Inc. | Photochromic six-membered heterocyclic-fused naphthopyrans |
| US6022495A (en) | 1998-07-10 | 2000-02-08 | Transitions Optical, Inc. | Photochromic benzopyrano-fused naphthopyrans |
| FR2783249B1 (fr) * | 1998-09-11 | 2001-06-22 | Flamel Tech Sa | Naphtopyranes anneles en c5-c6, leur preparation et les compositions et matrices (co)polymeres les renfermant |
| US5961892A (en) | 1998-09-11 | 1999-10-05 | Ppg Industries Ohio, Inc. | Polyalkoxylated naphthopyrans |
| FR2789680B1 (fr) * | 1999-02-17 | 2002-05-17 | Corning Sa | Naphtopyranes et phenanthropyranes anneles en c5-c6 avec un groupe bicyclique et les compositions et matrices (co)polymeres les renfermant |
| US6296785B1 (en) * | 1999-09-17 | 2001-10-02 | Ppg Industries Ohio, Inc. | Indeno-fused photochromic naphthopyrans |
| FR2800739B1 (fr) * | 1999-11-04 | 2002-10-11 | Corning Sa | Naphtopyranes avec un heterocycle en position 5,6, preparation et compositions et matrices (co) polymeres les renfermant |
| FR2801052B1 (fr) * | 1999-11-17 | 2004-04-02 | Corning Sa | Naphtopyranes anneles en c5-c6 par un carbocycle de type indene ou dihydronaphtalene et les compositions et matrices (co) polymeres les renfermant |
| FR2815034B1 (fr) * | 2000-10-11 | 2003-02-07 | Corning Sa | Naphtopyranes anneles en c5-c6 par un carbocycle de type dihydrobenzocycloheptatriene et les compositions et matrices les refermant |
| ES2326215T3 (es) * | 2003-11-05 | 2009-10-05 | Corning Incorporated | Piranos condensados fotocromicos sustituidos con fenilo que porta un grupo carbamilo o urea. |
-
1999
- 1999-01-06 FR FR9900162A patent/FR2783249B1/fr not_active Expired - Fee Related
- 1999-09-07 CN CN99810262.8A patent/CN1315948A/zh active Pending
- 1999-09-07 BR BR9912649-4A patent/BR9912649A/pt not_active IP Right Cessation
- 1999-09-07 AT AT99969091T patent/ATE233749T1/de not_active IP Right Cessation
- 1999-09-07 WO PCT/US1999/020471 patent/WO2000015628A1/en not_active Ceased
- 1999-09-07 JP JP2000570167A patent/JP4737830B2/ja not_active Expired - Lifetime
- 1999-09-07 DE DE69905739T patent/DE69905739T2/de not_active Expired - Lifetime
- 1999-09-07 CA CA002342338A patent/CA2342338A1/en not_active Abandoned
- 1999-09-07 AU AU60284/99A patent/AU747191B2/en not_active Ceased
- 1999-09-07 ES ES99969091T patent/ES2195659T3/es not_active Expired - Lifetime
- 1999-09-07 EP EP99969091A patent/EP1119560B1/en not_active Expired - Lifetime
- 1999-09-09 US US09/393,213 patent/US6506538B1/en not_active Expired - Lifetime
- 1999-09-10 AR ARP990104548A patent/AR021799A1/es unknown
-
2002
- 2002-07-16 US US10/196,114 patent/US7332260B2/en not_active Expired - Lifetime
-
2011
- 2011-02-14 JP JP2011028893A patent/JP5325243B2/ja not_active Expired - Lifetime
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