JP2015501292A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015501292A5 JP2015501292A5 JP2014532194A JP2014532194A JP2015501292A5 JP 2015501292 A5 JP2015501292 A5 JP 2015501292A5 JP 2014532194 A JP2014532194 A JP 2014532194A JP 2014532194 A JP2014532194 A JP 2014532194A JP 2015501292 A5 JP2015501292 A5 JP 2015501292A5
- Authority
- JP
- Japan
- Prior art keywords
- butyl
- group
- och
- compound
- substituted
- 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
- 0 Cc1c(*)c(*)c(*)c(*)c1* Chemical compound Cc1c(*)c(*)c(*)c(*)c1* 0.000 description 20
- GDZAVHGIQPTDDN-UHFFFAOYSA-N CC1(CO2)COC2(C)OC1 Chemical compound CC1(CO2)COC2(C)OC1 GDZAVHGIQPTDDN-UHFFFAOYSA-N 0.000 description 3
- ZGZDOKSRWQEKAE-UHFFFAOYSA-N CCC1(C=N)OCCO1 Chemical compound CCC1(C=N)OCCO1 ZGZDOKSRWQEKAE-UHFFFAOYSA-N 0.000 description 2
- NTBYFTIXJORAAQ-UHFFFAOYSA-N CN(c(cc1)ccc1C1=CC1)c(cc1)ccc1Cl Chemical compound CN(c(cc1)ccc1C1=CC1)c(cc1)ccc1Cl NTBYFTIXJORAAQ-UHFFFAOYSA-N 0.000 description 2
- STTBJVFWVJBKHU-UHFFFAOYSA-N CC(C)(C)C1C=CC(C(c([o]c2c3)c(C(C(C4(F)F)(F)F)=C5C4(F)F)c2ccc3OCCOC)(c2c5c(ccc(OCCOC)c3)c3[o]2)c2ccc(C(C)(C)C)cc2)=CC1 Chemical compound CC(C)(C)C1C=CC(C(c([o]c2c3)c(C(C(C4(F)F)(F)F)=C5C4(F)F)c2ccc3OCCOC)(c2c5c(ccc(OCCOC)c3)c3[o]2)c2ccc(C(C)(C)C)cc2)=CC1 STTBJVFWVJBKHU-UHFFFAOYSA-N 0.000 description 1
- DTYWVUXQHQQMOR-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c3ccc(C(C)(C)C)cc3)[o]c3c2ccc(OC)c3)c(ccc(OC)c2)c2[o]1 Chemical compound CC(C)(C)c(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c3ccc(C(C)(C)C)cc3)[o]c3c2ccc(OC)c3)c(ccc(OC)c2)c2[o]1 DTYWVUXQHQQMOR-UHFFFAOYSA-N 0.000 description 1
- PHJQTDHOVKWCEQ-UHFFFAOYSA-L CC(C)(C)c(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c3ccc(C(C)(C)C)cc3)[o]c3c2ccc([O-])c3)c(ccc([O-])c2)c2[o]1 Chemical compound CC(C)(C)c(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c3ccc(C(C)(C)C)cc3)[o]c3c2ccc([O-])c3)c(ccc([O-])c2)c2[o]1 PHJQTDHOVKWCEQ-UHFFFAOYSA-L 0.000 description 1
- PHJQTDHOVKWCEQ-UHFFFAOYSA-N CC(C)(C)c(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c3ccc(C(C)(C)C)cc3)[o]c3cc(O)ccc23)c(ccc(O)c2)c2[o]1 Chemical compound CC(C)(C)c(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c3ccc(C(C)(C)C)cc3)[o]c3cc(O)ccc23)c(ccc(O)c2)c2[o]1 PHJQTDHOVKWCEQ-UHFFFAOYSA-N 0.000 description 1
- VJWHMDDNUBLGLU-UHFFFAOYSA-N CC(C)(C)c1ccc(-c([o]c2c3)c(C(C(C(C4(F)F)(F)F)(F)F)=C4c4c(-c5ccc(C(C)(C)C)[s]5)[o]c5cc(OC)ccc45)c2ccc3OC)[s]1 Chemical compound CC(C)(C)c1ccc(-c([o]c2c3)c(C(C(C(C4(F)F)(F)F)(F)F)=C4c4c(-c5ccc(C(C)(C)C)[s]5)[o]c5cc(OC)ccc45)c2ccc3OC)[s]1 VJWHMDDNUBLGLU-UHFFFAOYSA-N 0.000 description 1
- BRETWPYFDNANSC-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c(cc4)ccc4O)[s]c(-c4ccc(C(C)(C)C)[s]4)c3)c(-c(cc3)ccc3O)[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c(cc4)ccc4O)[s]c(-c4ccc(C(C)(C)C)[s]4)c3)c(-c(cc3)ccc3O)[s]2)[s]1 BRETWPYFDNANSC-UHFFFAOYSA-N 0.000 description 1
- AWXUABDQOLDRFJ-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c(cc4)ccc4OC)[s]c(-c4ccc(C(C)(C)C)[s]4)c3)c(-c(cc3)ccc3OC)[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c(cc4)ccc4OC)[s]c(-c4ccc(C(C)(C)C)[s]4)c3)c(-c(cc3)ccc3OC)[s]2)[s]1 AWXUABDQOLDRFJ-UHFFFAOYSA-N 0.000 description 1
- GZTNDMGDAVDPLS-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c(cc5)ccc5N5CCOCC5)c(cc5)ccc5N5CCOCC5)[s]c(-c5ccc(C(C)(C)C)[s]5)c3)c4[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c(cc5)ccc5N5CCOCC5)c(cc5)ccc5N5CCOCC5)[s]c(-c5ccc(C(C)(C)C)[s]5)c3)c4[s]2)[s]1 GZTNDMGDAVDPLS-UHFFFAOYSA-N 0.000 description 1
- RDVJICWIZLWWHA-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c(cc5)ccc5OCCCCC#N)c(cc5)ccc5OCCCCC#N)[s]c(-c5ccc(C(C)(C)C)[s]5)c3)c4[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c(cc5)ccc5OCCCCC#N)c(cc5)ccc5OCCCCC#N)[s]c(-c5ccc(C(C)(C)C)[s]5)c3)c4[s]2)[s]1 RDVJICWIZLWWHA-UHFFFAOYSA-N 0.000 description 1
- AQWNDOUNYWXKSP-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c(cc5)ccc5OCCCO)c(cc5)ccc5OCCCO)[s]c(-c5ccc(C(C)(C)C)[s]5)c3)c4[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c(cc5)ccc5OCCCO)c(cc5)ccc5OCCCO)[s]c(-c5ccc(C(C)(C)C)[s]5)c3)c4[s]2)[s]1 AQWNDOUNYWXKSP-UHFFFAOYSA-N 0.000 description 1
- KVXLUEMIGRIYGN-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c5ccc(C(O)=O)[s]5)c5ccc(C(O)=O)[s]5)[s]c(-c([s]c(C(C)(C)C)c5)c5C(O)=O)c3)c4[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(C4(c5ccc(C(O)=O)[s]5)c5ccc(C(O)=O)[s]5)[s]c(-c([s]c(C(C)(C)C)c5)c5C(O)=O)c3)c4[s]2)[s]1 KVXLUEMIGRIYGN-UHFFFAOYSA-N 0.000 description 1
- YXEDDIJYFAIGMT-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2cc(C(C(C3(F)F)(F)F)=C(C4C=C(c5ccc(C(C)(C)C)[s]5)SC4C4(c(cc5)ccc5O[Si+](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si+](C)(C)C)c(cc5)ccc5[O](C[Si](C)(C)C)[S+]([OH2+])O[Si](C)(C)C)C3(F)F)c4[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2cc(C(C(C3(F)F)(F)F)=C(C4C=C(c5ccc(C(C)(C)C)[s]5)SC4C4(c(cc5)ccc5O[Si+](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si+](C)(C)C)c(cc5)ccc5[O](C[Si](C)(C)C)[S+]([OH2+])O[Si](C)(C)C)C3(F)F)c4[s]2)[s]1 YXEDDIJYFAIGMT-UHFFFAOYSA-N 0.000 description 1
- AYKCVCAIAXNSBV-UHFFFAOYSA-N CC(C)(C)c1ccc(-c2ccc(-c3c(C(C(C(C4(F)F)(F)F)(F)F)=C4c4c(-c5ccc(-c6ccc(C(C)(C)C)[s]6)[s]5)[o]c5cc(OC)ccc45)c(ccc(OC)c4)c4[o]3)[s]2)[s]1 Chemical compound CC(C)(C)c1ccc(-c2ccc(-c3c(C(C(C(C4(F)F)(F)F)(F)F)=C4c4c(-c5ccc(-c6ccc(C(C)(C)C)[s]6)[s]5)[o]c5cc(OC)ccc45)c(ccc(OC)c4)c4[o]3)[s]2)[s]1 AYKCVCAIAXNSBV-UHFFFAOYSA-N 0.000 description 1
- XRBOKXBLZKFKED-UHFFFAOYSA-N CC(C)(C)c1ccc(C(c([o]c2c3)c(C(C(C4(F)F)(F)F)=C5C4(F)F)c2cc(OC)c3OC)(c2c5c(c(OC)cc(OC)c3)c3[o]2)c2ccc(C(C)(C)C)cc2)cc1 Chemical compound CC(C)(C)c1ccc(C(c([o]c2c3)c(C(C(C4(F)F)(F)F)=C5C4(F)F)c2cc(OC)c3OC)(c2c5c(c(OC)cc(OC)c3)c3[o]2)c2ccc(C(C)(C)C)cc2)cc1 XRBOKXBLZKFKED-UHFFFAOYSA-N 0.000 description 1
- PGGFLBRZIUXZOX-UHFFFAOYSA-N CC(C)(C)c1ccc(C(c2c(C(C(C3(F)F)(F)F)=C4C3(F)F)c(cc(c(OC)c3)OC)c3[o]2)(c([o]c2c3)c4c2cc(OC)c3OC)c2ccc(C(C)(C)C)cc2)cc1 Chemical compound CC(C)(C)c1ccc(C(c2c(C(C(C3(F)F)(F)F)=C4C3(F)F)c(cc(c(OC)c3)OC)c3[o]2)(c([o]c2c3)c4c2cc(OC)c3OC)c2ccc(C(C)(C)C)cc2)cc1 PGGFLBRZIUXZOX-UHFFFAOYSA-N 0.000 description 1
- BWECUNHBTZUZCS-UHFFFAOYSA-N CC(C)c(cc1)ccc1-c([o]c1c2)c(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c4ccc(C(C)(C)C)cc4)[o]c4c3cc3OCOc3c4)c1cc1c2OCO1 Chemical compound CC(C)c(cc1)ccc1-c([o]c1c2)c(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c4ccc(C(C)(C)C)cc4)[o]c4c3cc3OCOc3c4)c1cc1c2OCO1 BWECUNHBTZUZCS-UHFFFAOYSA-N 0.000 description 1
- LSJQQQGAVZPYDL-UHFFFAOYSA-N CCC(CC)(c1ccc(C2(c3ccc(C(CC)(CC)OCCOCCOCCOCC)[s]3)c([s]c(-c3ccc(C(C)(C)C)[s]3)c3)c3C(C(C(C3(F)F)(F)F)(F)F)=C3c3c2[s]c(-c2ccc(C(C)(C)C)[s]2)c3)[s]1)OCCOCCOCCOCC Chemical compound CCC(CC)(c1ccc(C2(c3ccc(C(CC)(CC)OCCOCCOCCOCC)[s]3)c([s]c(-c3ccc(C(C)(C)C)[s]3)c3)c3C(C(C(C3(F)F)(F)F)(F)F)=C3c3c2[s]c(-c2ccc(C(C)(C)C)[s]2)c3)[s]1)OCCOCCOCCOCC LSJQQQGAVZPYDL-UHFFFAOYSA-N 0.000 description 1
- YXQMMTJKVQLCLN-UHFFFAOYSA-N CCOCCOCCOCCOc1ccc(C2(c([s]c(-c3ccc(C(C)(C)C)[s]3)c3)c3C(C(C(C3(F)F)(F)F)(F)F)=C3c3c2[s]c(-c2ccc(C(C)(C)C)[s]2)c3)c(cc2)ccc2OCCOCCOCCOCC)cc1 Chemical compound CCOCCOCCOCCOc1ccc(C2(c([s]c(-c3ccc(C(C)(C)C)[s]3)c3)c3C(C(C(C3(F)F)(F)F)(F)F)=C3c3c2[s]c(-c2ccc(C(C)(C)C)[s]2)c3)c(cc2)ccc2OCCOCCOCCOCC)cc1 YXQMMTJKVQLCLN-UHFFFAOYSA-N 0.000 description 1
- YLECFQSZLORXHD-UHFFFAOYSA-N CCc1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c(cc4)ccc4OCCOC)[s]c(-c4ccc(C(C)(C)C)[s]4)c3)c(-c(cc3)ccc3OCCOC)[s]2)[s]1 Chemical compound CCc1ccc(-c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c(cc4)ccc4OCCOC)[s]c(-c4ccc(C(C)(C)C)[s]4)c3)c(-c(cc3)ccc3OCCOC)[s]2)[s]1 YLECFQSZLORXHD-UHFFFAOYSA-N 0.000 description 1
- JBIHBBAASGBBLX-UHFFFAOYSA-N CN(c(cc1)ccc1Cl)c(cc1)ccc1Cl Chemical compound CN(c(cc1)ccc1Cl)c(cc1)ccc1Cl JBIHBBAASGBBLX-UHFFFAOYSA-N 0.000 description 1
- YNSQDHOYMARFRI-UHFFFAOYSA-N COCCC[Si](CCCOC)(CCCOC)C1SC(c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c4ccc([Si](CCCOC)(CCCOC)CCCOC)[s]4)[s]c(-c4ccc([Si](CCCOC)(CCCOC)CCCOC)[s]4)c3)c(-c3ccc([Si](CCCOC)(CCCOC)CCCOC)[s]3)[s]2)=CC1 Chemical compound COCCC[Si](CCCOC)(CCCOC)C1SC(c2cc(C(C(C(C3(F)F)(F)F)(F)F)=C3c3c(-c4ccc([Si](CCCOC)(CCCOC)CCCOC)[s]4)[s]c(-c4ccc([Si](CCCOC)(CCCOC)CCCOC)[s]4)c3)c(-c3ccc([Si](CCCOC)(CCCOC)CCCOC)[s]3)[s]2)=CC1 YNSQDHOYMARFRI-UHFFFAOYSA-N 0.000 description 1
- JPPWJPOSJBENFT-UHFFFAOYSA-N COc(cc1)cc2c1c(C(C(C(C1(F)F)(F)F)(F)F)=C1c1c(-c(cc3OC)ccc3OC)[o]c3c1ccc(OC)c3)c(-c(cc1OC)ccc1OC)[o]2 Chemical compound COc(cc1)cc2c1c(C(C(C(C1(F)F)(F)F)(F)F)=C1c1c(-c(cc3OC)ccc3OC)[o]c3c1ccc(OC)c3)c(-c(cc1OC)ccc1OC)[o]2 JPPWJPOSJBENFT-UHFFFAOYSA-N 0.000 description 1
- QNJKIIDNZIUIBF-UHFFFAOYSA-N COc(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c(cc3)ccc3OC)[o]c(cc3)c2cc3OC)c2cc(OC)ccc2[o]1 Chemical compound COc(cc1)ccc1-c1c(C(C(C(C2(F)F)(F)F)(F)F)=C2c2c(-c(cc3)ccc3OC)[o]c(cc3)c2cc3OC)c2cc(OC)ccc2[o]1 QNJKIIDNZIUIBF-UHFFFAOYSA-N 0.000 description 1
- JHRTXUKYYQWPNK-UHFFFAOYSA-N COc1ccc(C(c([o]c2c3)c(C(C(C4(F)F)(F)F)=C5C4(F)F)c2ccc3OC)(c([o]c2c3)c5c2ccc3OC)c(cc2)ccc2OC)cc1 Chemical compound COc1ccc(C(c([o]c2c3)c(C(C(C4(F)F)(F)F)=C5C4(F)F)c2ccc3OC)(c([o]c2c3)c5c2ccc3OC)c(cc2)ccc2OC)cc1 JHRTXUKYYQWPNK-UHFFFAOYSA-N 0.000 description 1
- RJQZITCFESTYHA-UHFFFAOYSA-N Cc1ccc(-c([o]c2c3)c(C(C(C(C4(F)F)(F)F)(F)F)=C4c4c(-c5ccc(C)[s]5)[o]c5cc(OC)ccc45)c2ccc3OC)[s]1 Chemical compound Cc1ccc(-c([o]c2c3)c(C(C(C(C4(F)F)(F)F)(F)F)=C4c4c(-c5ccc(C)[s]5)[o]c5cc(OC)ccc45)c2ccc3OC)[s]1 RJQZITCFESTYHA-UHFFFAOYSA-N 0.000 description 1
- HOKBEUJEVJTDCI-UHFFFAOYSA-N FC(C(C(c1c(C2(c([s]3)ccc3Cl)c([s]3)ccc3Cl)[s]c(-c([s]3)ccc3Cl)c1)=C1c3c2[s]c(-c([s]2)ccc2Cl)c3)(F)F)(C1(F)F)F Chemical compound FC(C(C(c1c(C2(c([s]3)ccc3Cl)c([s]3)ccc3Cl)[s]c(-c([s]3)ccc3Cl)c1)=C1c3c2[s]c(-c([s]2)ccc2Cl)c3)(F)F)(C1(F)F)F HOKBEUJEVJTDCI-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161541841P | 2011-09-30 | 2011-09-30 | |
| US61/541,841 | 2011-09-30 | ||
| US201261675460P | 2012-07-25 | 2012-07-25 | |
| US61/675,460 | 2012-07-25 | ||
| PCT/CA2012/000910 WO2013044371A1 (en) | 2011-09-30 | 2012-09-28 | Photochromic and electrochromic diarylcyclopentene derivatives as optical filters |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017171192A Division JP6480997B2 (ja) | 2011-09-30 | 2017-09-06 | ジアリールエテン化合物およびそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015501292A JP2015501292A (ja) | 2015-01-15 |
| JP2015501292A5 true JP2015501292A5 (https=) | 2015-11-19 |
| JP6208137B2 JP6208137B2 (ja) | 2017-10-04 |
Family
ID=47994069
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014532194A Expired - Fee Related JP6208137B2 (ja) | 2011-09-30 | 2012-09-28 | ジアリールエテン化合物およびそれらの使用 |
| JP2017171192A Expired - Fee Related JP6480997B2 (ja) | 2011-09-30 | 2017-09-06 | ジアリールエテン化合物およびそれらの使用 |
| JP2019021745A Pending JP2019123713A (ja) | 2011-09-30 | 2019-02-08 | ジアリールエテン化合物およびそれらの使用 |
| JP2020185146A Pending JP2021042212A (ja) | 2011-09-30 | 2020-11-05 | ジアリールエテン化合物およびそれらの使用 |
| JP2022077367A Pending JP2022110051A (ja) | 2011-09-30 | 2022-05-10 | ジアリールエテン化合物およびそれらの使用 |
Family Applications After (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017171192A Expired - Fee Related JP6480997B2 (ja) | 2011-09-30 | 2017-09-06 | ジアリールエテン化合物およびそれらの使用 |
| JP2019021745A Pending JP2019123713A (ja) | 2011-09-30 | 2019-02-08 | ジアリールエテン化合物およびそれらの使用 |
| JP2020185146A Pending JP2021042212A (ja) | 2011-09-30 | 2020-11-05 | ジアリールエテン化合物およびそれらの使用 |
| JP2022077367A Pending JP2022110051A (ja) | 2011-09-30 | 2022-05-10 | ジアリールエテン化合物およびそれらの使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (4) | US9227986B2 (https=) |
| EP (2) | EP2760969B1 (https=) |
| JP (5) | JP6208137B2 (https=) |
| KR (2) | KR102038447B1 (https=) |
| CN (2) | CN103890133A (https=) |
| CA (1) | CA2832149C (https=) |
| WO (1) | WO2013044371A1 (https=) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9176357B2 (en) | 2010-12-15 | 2015-11-03 | Switch Materials, Inc. | Variable transmittance optical devices |
| EP2652547B1 (en) | 2010-12-15 | 2019-10-23 | Switch Materials, Inc. | Variable transmittance optical filter with substantially co- planar electrode system |
| KR102038447B1 (ko) | 2011-09-30 | 2019-11-29 | 스위치 머티리얼즈 인코퍼레이티드 | 디아릴에텐 화합물 및 그것의 이용 |
| US9910301B2 (en) | 2012-02-23 | 2018-03-06 | Switch Materials, Inc. | Switchable optical filter apparatus with light |
| US10054835B2 (en) | 2012-04-09 | 2018-08-21 | Switch Materials, Inc. | Switching materials, and compositions and methods for making same |
| EP4600727A3 (en) | 2012-05-29 | 2025-10-22 | Solutia Canada Inc. | Optical filter comprising a variable transmittance layer |
| CN110515251A (zh) | 2013-03-07 | 2019-11-29 | 思维奇材料公司 | 包封的可转换膜、密封的膜和形成其的方法 |
| WO2015089663A1 (en) | 2013-12-19 | 2015-06-25 | Switch Materials Inc. | Switchable objects and methods of manufacture |
| WO2015135867A1 (de) * | 2014-03-12 | 2015-09-17 | Ludwig-Maximilians-Universität München | Terminal substituierte oligothiophene und ihre verwendung in optischen signalübertragungssystemen und/oder als farbpigmente |
| US9708528B2 (en) | 2014-06-13 | 2017-07-18 | The University Of Hong Kong | Robust photochromic compounds with silicon- or phosphorus-containing heterocyclic ring and the production thereof |
| US10647913B2 (en) | 2014-11-17 | 2020-05-12 | Switch Materials Inc. | Photochromic-electrochromic compositions |
| US20180231887A1 (en) * | 2015-08-24 | 2018-08-16 | Toyo Gosei Co., Ltd. | Method for manufacturing device, and composition |
| CN107011317B (zh) * | 2016-05-24 | 2020-03-20 | 北京大学 | 光致异构化合物及包含其的器件 |
| EP3284764A1 (en) | 2016-08-18 | 2018-02-21 | Basf Se | Composition especially for printing or coating comprising polyurethane polymers |
| WO2018033620A1 (en) | 2016-08-18 | 2018-02-22 | Basf Se | Composition especially for printing or coating comprising polyurethane polymers |
| EP3284800A1 (en) | 2016-08-18 | 2018-02-21 | Basf Se | Composition for preparing an electrochromic layer |
| EP3284799A1 (en) | 2016-08-18 | 2018-02-21 | Basf Se | Composition especially for printing or coating comprising (meth)acrylate polymers |
| WO2018033621A1 (en) | 2016-08-18 | 2018-02-22 | Basf Se | Composition for preparing an electrochromic layer |
| CN106371258B (zh) * | 2016-10-21 | 2019-08-06 | 北京华逸高科科技有限公司 | 电致变色薄膜的制备方法及电致变色器件 |
| CN107118757A (zh) * | 2017-04-24 | 2017-09-01 | 上海电力学院 | 一种基于呋喃的二芳基乙烯有机光致变色材料及其制备方法和应用 |
| CN108359439B (zh) * | 2018-02-06 | 2019-07-26 | 厦门大学 | 光致变色化合物及其制备方法和光致变色制品 |
| DE102018004790A1 (de) * | 2018-06-14 | 2019-12-19 | Rodenstock Gmbh | Photochrome annellierte Naphthopyran-Systeme mit speziellen Substituenten zur Realisierung sehr schneller Aufhellgeschwindigkeiten |
| KR101989876B1 (ko) * | 2019-04-02 | 2019-06-17 | 주식회사 제이텍 | 표면 보호 테이프용 점착제 조성물 및 이의 제조방법 |
| US20220220100A1 (en) * | 2019-04-03 | 2022-07-14 | Switch Materials Inc. | Photochromic and electrochromic diarylethene compounds with improved photostability and solubility |
| US20230341276A1 (en) * | 2020-02-07 | 2023-10-26 | Chromatic Technologies, Inc. | Roofing Membrane Bond Indicator |
| CN111430564B (zh) | 2020-03-19 | 2022-06-03 | 武汉天马微电子有限公司 | 一种显示面板以及显示装置 |
| KR102693003B1 (ko) * | 2020-04-29 | 2024-08-09 | 삼성디스플레이 주식회사 | 표시 패널 |
| DE102021110210A1 (de) | 2021-04-22 | 2022-10-27 | Delo Industrie Klebstoffe Gmbh & Co. Kgaa | Verfahren zum Herstellen eines optischen Moduls und optisches Modul |
| JP7770645B2 (ja) * | 2021-08-30 | 2025-11-17 | 日産自動車株式会社 | フォトクロミック化合物 |
| CN116789661B (zh) * | 2022-11-23 | 2025-12-30 | 河南农业大学 | 一种光致变色分子、可见光调节的固态复合膜及其制备方法和应用 |
| CN116397242B (zh) * | 2023-03-31 | 2025-06-20 | 平湖市浙江工业大学新材料研究院 | 一种基于萘二并噻二唑受体结构的薄膜材料的制备方法及其应用 |
| CN119060013A (zh) * | 2024-08-26 | 2024-12-03 | 华中科技大学 | 一种烷氧基三苯胺修饰的二噻吩基乙烯衍生物及其及应用 |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3635544A (en) | 1963-12-23 | 1972-01-18 | American Cyanamid Co | Photochromic polymer matrix |
| JPS6422872A (en) | 1987-07-16 | 1989-01-25 | Yamaha Corp | Photochromic compound |
| GB8916860D0 (en) | 1989-07-24 | 1989-09-06 | Traqson Ltd | Novel photoactive compounds |
| JP3067031B2 (ja) | 1992-04-03 | 2000-07-17 | カリフォルニア インスティチュート オブ テクノロジー | オレフィンメタセシス重合方法 |
| US5312940A (en) | 1992-04-03 | 1994-05-17 | California Institute Of Technology | Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization |
| JPH06240242A (ja) | 1993-02-15 | 1994-08-30 | Nippon Telegr & Teleph Corp <Ntt> | 重合体フォトクロミック組成物 |
| JP3264573B2 (ja) | 1994-01-14 | 2002-03-11 | 株式会社三協精機製作所 | 小型モータ |
| JP3395854B2 (ja) | 1994-02-02 | 2003-04-14 | 日立化成工業株式会社 | 酸化銅の化学還元液およびこれを用いた多層プリント配線板の製造方法 |
| JPH07311979A (ja) | 1994-03-24 | 1995-11-28 | Sanyo Electric Co Ltd | 光記録媒体及びその再生方法 |
| JP3132630B2 (ja) | 1994-08-25 | 2001-02-05 | 科学技術振興事業団 | チオフェン誘導体の重合体とその製造法 |
| JP3491704B2 (ja) | 1994-10-21 | 2004-01-26 | 入江 正浩 | ジチエニルエテン系化合物及び該化合物からなるフォトクロミック材料 |
| JPH10152679A (ja) | 1996-11-22 | 1998-06-09 | Mita Ind Co Ltd | 光メモリ素子と、それを用いた電子写真感光体、エレクトロルミネッセンス素子、液晶表示素子、および空間光変調素子 |
| FR2772266B1 (fr) | 1997-12-12 | 2000-02-04 | Oreal | Utilisation d'agent de coloration photochrome dans une composition cosmetique, et composition cosmetique le comprenant |
| EP0933375A1 (en) | 1997-12-17 | 1999-08-04 | Amersham Life Science Ltd | Photochromic compounds |
| JP3538019B2 (ja) * | 1998-03-11 | 2004-06-14 | 独立行政法人 科学技術振興機構 | フォトクロミック結晶材料 |
| JPH11256147A (ja) | 1998-03-13 | 1999-09-21 | Dainippon Printing Co Ltd | コレステリック液晶性フォトクロミック高分子材料及びそれを用いた光機能性媒体 |
| US6479604B1 (en) | 1998-08-17 | 2002-11-12 | Korea Research Institute Of Chemical Technology | Diarylethene compound, photochromic diarylethene type copolymer and method for the production of the same |
| US6884553B2 (en) | 1999-03-11 | 2005-04-26 | Mitsubishi Chemical Corporation | Near-field optical recording medium and near-field optical recording method |
| US6359150B1 (en) | 1999-08-31 | 2002-03-19 | Kyocera Corporation | Photochromic compound and optical function device using the same |
| CA2416016C (en) | 2000-07-14 | 2010-01-26 | Simon Fraser University | Novel photochromic polymers and methods of synthesizing same |
| FR2813697A1 (fr) | 2000-09-04 | 2002-03-08 | Dixet | Support securise de donnees a lecture optique |
| CN1152110C (zh) | 2000-12-13 | 2004-06-02 | 中国科学院感光化学研究所 | 杂环取代俘精酸酐类光致变色材料及其合成方法 |
| JP4025920B2 (ja) | 2001-03-05 | 2007-12-26 | 入江 正浩 | フォトクロミック材料 |
| KR100424862B1 (ko) | 2001-03-06 | 2004-03-31 | 한국화학연구원 | 이속사졸기로 치환된 신규한 광변색성 디아릴에텐계 화합물 |
| JP3870703B2 (ja) | 2001-03-14 | 2007-01-24 | ダイソー株式会社 | 新規ホトクロミック化合物、およびその製造法と用途 |
| DE60238405D1 (de) | 2001-06-15 | 2011-01-05 | Masahiro Irie | Photochromes material und darauf basierender farbdosimeter |
| KR100501829B1 (ko) | 2001-07-30 | 2005-07-20 | 한국화학연구원 | 디아릴에텐 유도체와 이를 이용한 광변색 박막 |
| KR100482654B1 (ko) | 2001-09-18 | 2005-04-13 | 한국화학연구원 | 광변색 나노 캡슐 및 그의 제조방법 |
| KR20030025622A (ko) | 2001-09-21 | 2003-03-29 | 한국화학연구원 | 비닐기 함유 디아릴에텐 단량체 및 이를 이용하여 제조한광활성 고분자 |
| CN1206308C (zh) * | 2002-02-06 | 2005-06-15 | 清华大学 | 二芳基乙烯类光致变色化合物及其制备方法和用途 |
| KR20030085251A (ko) | 2002-04-29 | 2003-11-05 | 한국화학연구원 | 광변색 형광 중합체와 그 제조방법 |
| JP4410108B2 (ja) * | 2002-08-09 | 2010-02-03 | スイッチ マテリアルズ インコーポレイテッド | フォトクロミックかつエレクトロクロミックな化合物、該化合物の合成方法及び該化合物の使用方法 |
| JP2004277416A (ja) | 2003-02-27 | 2004-10-07 | Masahiro Irie | ジアリールエテン系化合物、フォトクロミック材料および光機能素子 |
| JP2005326503A (ja) | 2004-05-12 | 2005-11-24 | Tokai Rubber Ind Ltd | 調光材用着色部材 |
| FR2882282B1 (fr) | 2005-02-21 | 2008-10-17 | Snecma Moteurs Sa | Procede pour le corroyage d'un lopin metallique, chemise pour la mise en oeuvre du procede et ensemble d'une chemise et d'un couvercle pour la mise en oeuvre du procede |
| CA2609887C (en) * | 2005-05-25 | 2015-12-29 | Switch Materials Inc. | Photochromic and electrochromic compounds and synthesis and use thereof |
| US20070115762A1 (en) | 2005-11-21 | 2007-05-24 | Wisnudel Marc B | Optical article having anti-theft feature and a system and method for inhibiting theft of same |
| WO2007105620A1 (ja) * | 2006-03-10 | 2007-09-20 | Kyoto University | ジアリールエテン化合物の製造方法、及び新規ジアリールエテン化合物 |
| JP2008162895A (ja) * | 2006-12-26 | 2008-07-17 | Masahiro Irie | ジアリールエテン系化合物 |
| KR100938491B1 (ko) | 2007-10-24 | 2010-01-25 | 한국생명공학연구원 | 생체분자 표지용 수용성 광변색 화합물 및 이를 이용한생체분자의 검출방법 |
| CN105182569B (zh) * | 2009-06-11 | 2018-08-07 | 思维奇材料公司 | 可变透光率滤光片及其应用 |
| CN101851232B (zh) * | 2010-05-31 | 2012-01-25 | 江西科技师范学院 | 光致变色异噁唑噻吩混联型全氟环戊烯化合物及合成方法和应用 |
| AU2011274293B2 (en) * | 2010-06-28 | 2016-01-28 | David Daniel Williams | Temporary fence base |
| CN102079742B (zh) * | 2010-11-01 | 2012-11-14 | 江西科技师范学院 | 光致变色萘环-噻吩混联型全氟环戊烯化合物及合成方法和应用 |
| US9176357B2 (en) | 2010-12-15 | 2015-11-03 | Switch Materials, Inc. | Variable transmittance optical devices |
| EP2652547B1 (en) * | 2010-12-15 | 2019-10-23 | Switch Materials, Inc. | Variable transmittance optical filter with substantially co- planar electrode system |
| CN103492515B (zh) | 2011-03-24 | 2016-06-29 | 琳得科株式会社 | 一种粘着剂组合物以及粘着片 |
| KR102038447B1 (ko) | 2011-09-30 | 2019-11-29 | 스위치 머티리얼즈 인코퍼레이티드 | 디아릴에텐 화합물 및 그것의 이용 |
| US10054835B2 (en) * | 2012-04-09 | 2018-08-21 | Switch Materials, Inc. | Switching materials, and compositions and methods for making same |
-
2012
- 2012-09-28 KR KR1020147011590A patent/KR102038447B1/ko not_active Expired - Fee Related
- 2012-09-28 US US14/348,344 patent/US9227986B2/en active Active
- 2012-09-28 EP EP12836363.7A patent/EP2760969B1/en not_active Not-in-force
- 2012-09-28 EP EP18169652.7A patent/EP3385354A1/en not_active Withdrawn
- 2012-09-28 CN CN201280047935.4A patent/CN103890133A/zh active Pending
- 2012-09-28 KR KR1020197030994A patent/KR20190124800A/ko not_active Ceased
- 2012-09-28 JP JP2014532194A patent/JP6208137B2/ja not_active Expired - Fee Related
- 2012-09-28 CN CN201810686687.7A patent/CN108690045B/zh not_active Expired - Fee Related
- 2012-09-28 WO PCT/CA2012/000910 patent/WO2013044371A1/en not_active Ceased
- 2012-09-28 CA CA2832149A patent/CA2832149C/en not_active Expired - Fee Related
-
2015
- 2015-11-20 US US14/947,230 patent/US10072023B2/en active Active
-
2017
- 2017-09-06 JP JP2017171192A patent/JP6480997B2/ja not_active Expired - Fee Related
-
2018
- 2018-07-25 US US16/045,186 patent/US10556912B2/en active Active
-
2019
- 2019-02-08 JP JP2019021745A patent/JP2019123713A/ja active Pending
- 2019-04-03 US US16/374,571 patent/US11124524B2/en not_active Expired - Fee Related
-
2020
- 2020-11-05 JP JP2020185146A patent/JP2021042212A/ja active Pending
-
2022
- 2022-05-10 JP JP2022077367A patent/JP2022110051A/ja active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015501292A5 (https=) | ||
| BRPI0721051B1 (pt) | complexos catalíticos à base de rutênio e reciláveis, assim como seu processo de síntese | |
| JP2010525122A5 (https=) | ||
| JP6811949B2 (ja) | 光硬化性組成物 | |
| JP2017533203A (ja) | 半合成法 | |
| JP6651854B2 (ja) | シクロブタンテトラカルボン酸誘導体の製造方法 | |
| KR102065710B1 (ko) | 많은 가교 작용기를 가지는 아지드 유형의 가교제 | |
| Zhang et al. | Structure and Photochemical Properties of r‐1, c‐2, t‐3, t‐4‐l, 3‐Bis [2‐(5‐R‐benzoxazolyl)]− 2, 4‐di (4‐R'‐phenyl) cyclobutane | |
| JP5108383B2 (ja) | 光学活性モノスルホネート化合物の製造方法 | |
| CN108530474A (zh) | 一类吡咯腙肼双氟硼强荧光染料及其制备方法 | |
| JP6877791B2 (ja) | 塩基変換増殖剤 | |
| BR112015015880B1 (pt) | Processos de produção de um composto e compostos | |
| JP6854839B2 (ja) | カリケアマイシン誘導体を合成するための中間体および方法 | |
| JP5192730B2 (ja) | メルカプト複素環化合物の製造方法 | |
| ES2432525T3 (es) | Pirroles sustituidos terapéuticos | |
| JP2022188858A (ja) | 新規化合物 | |
| JP6159415B2 (ja) | 含臭素ｎ−フェニルジアクリルイミド誘導体及びその製造方法 | |
| JP2015040176A (ja) | ビス−ボロンジピロメテン系色素 | |
| JP4018066B2 (ja) | 新規なへキサペリヘキサベンゾコロネン誘導体 | |
| JP3256743B2 (ja) | 包摂超分子錯体のホスト化合物および包摂超分子錯体 | |
| JP7475638B2 (ja) | 光学活性化合物およびその製造方法、光学活性化合物を含む配位化合物、環状化合物、ならびに中間体化合物 | |
| RU2014101999A (ru) | Производные пиперазина, способы их получения и их применение в лечении инсулинорезистентности | |
| JP2015110771A (ja) | 造影剤の製造方法 | |
| CN109096324B (zh) | 一种二烷基酰基氯化锗合成方法与应用 | |
| CN103058952A (zh) | 一种具有强双光子效应的噻唑化合物及其合成方法 |