JP2014522397A5 - - Google Patents
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- JP2014522397A5 JP2014522397A5 JP2014513074A JP2014513074A JP2014522397A5 JP 2014522397 A5 JP2014522397 A5 JP 2014522397A5 JP 2014513074 A JP2014513074 A JP 2014513074A JP 2014513074 A JP2014513074 A JP 2014513074A JP 2014522397 A5 JP2014522397 A5 JP 2014522397A5
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- JP
- Japan
- Prior art keywords
- atoms
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- cation
- Prior art date
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 52
- -1 silver tricyano-borate Chemical compound 0.000 claims description 41
- 150000001875 compounds Chemical class 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 229910052783 alkali metal Inorganic materials 0.000 claims description 30
- 150000001768 cations Chemical class 0.000 claims description 13
- 150000002892 organic cations Chemical class 0.000 claims description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- 229910021538 borax Inorganic materials 0.000 claims description 5
- 150000001767 cationic compounds Chemical class 0.000 claims description 5
- 239000003792 electrolyte Substances 0.000 claims description 5
- 150000003839 salts Chemical group 0.000 claims description 5
- 229910001411 inorganic cation Inorganic materials 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 3
- 229910052776 Thorium Inorganic materials 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052770 Uranium Inorganic materials 0.000 claims description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 238000009472 formulation Methods 0.000 claims description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052737 gold Inorganic materials 0.000 claims description 3
- 239000010931 gold Substances 0.000 claims description 3
- 229910052735 hafnium Inorganic materials 0.000 claims description 3
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 229910052741 iridium Inorganic materials 0.000 claims description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 239000003446 ligand Substances 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910000510 noble metal Inorganic materials 0.000 claims description 3
- 229910052762 osmium Inorganic materials 0.000 claims description 3
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 229910052703 rhodium Inorganic materials 0.000 claims description 3
- 239000010948 rhodium Substances 0.000 claims description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052723 transition metal Inorganic materials 0.000 claims description 3
- 150000003624 transition metals Chemical class 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 claims description 2
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 claims description 2
- MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-O oxonium Chemical compound [OH3+] XLYOFNOQVPJJNP-UHFFFAOYSA-O 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052722 tritium Inorganic materials 0.000 claims description 2
- 125000005500 uronium group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 22
- 150000002367 halogens Chemical class 0.000 claims 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 15
- 125000000753 cycloalkyl group Chemical group 0.000 claims 14
- 125000001424 substituent group Chemical group 0.000 claims 13
- 150000001340 alkali metals Chemical class 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000000304 alkynyl group Chemical group 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- 229920006395 saturated elastomer Polymers 0.000 claims 8
- 125000004429 atom Chemical group 0.000 claims 5
- 125000005843 halogen group Chemical group 0.000 claims 5
- 239000000654 additive Substances 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000010720 hydraulic oil Substances 0.000 claims 2
- 239000000314 lubricant Substances 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 229910052700 potassium Inorganic materials 0.000 claims 2
- 239000011591 potassium Substances 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- 239000006227 byproduct Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- 238000010538 cationic polymerization reaction Methods 0.000 claims 1
- 210000000170 cell membrane Anatomy 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- JPBGLQJDCUZXEF-UHFFFAOYSA-N chromenylium Chemical compound [O+]1=CC=CC2=CC=CC=C21 JPBGLQJDCUZXEF-UHFFFAOYSA-N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- DQZLFOAQOCSCBJ-UHFFFAOYSA-N isochromenylium Chemical compound C1=[O+]C=CC2=CC=CC=C21 DQZLFOAQOCSCBJ-UHFFFAOYSA-N 0.000 claims 1
- 239000003607 modifier Substances 0.000 claims 1
- 230000005693 optoelectronics Effects 0.000 claims 1
- 239000003444 phase transfer catalyst Substances 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 239000003505 polymerization initiator Substances 0.000 claims 1
- 238000000746 purification Methods 0.000 claims 1
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000003115 supporting electrolyte Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000004753 textile Substances 0.000 claims 1
- OLFPYUPGPBITMH-UHFFFAOYSA-N tritylium Chemical compound C1=CC=CC=C1[C+](C=1C=CC=CC=1)C1=CC=CC=C1 OLFPYUPGPBITMH-UHFFFAOYSA-N 0.000 claims 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 4
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 3
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- TXNLQUKVUJITMX-UHFFFAOYSA-N 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine Chemical group CC(C)(C)C1=CC=NC(C=2N=CC=C(C=2)C(C)(C)C)=C1 TXNLQUKVUJITMX-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical class [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000002496 iodine Chemical class 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WRTMQOHKMFDUKX-UHFFFAOYSA-N triiodide Chemical compound I[I-]I WRTMQOHKMFDUKX-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11004431 | 2011-05-31 | ||
| EP11004431.0 | 2011-05-31 | ||
| PCT/EP2012/002179 WO2012163489A1 (en) | 2011-05-31 | 2012-05-23 | Compounds containing hydrido-tricyano-borate anions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014522397A JP2014522397A (ja) | 2014-09-04 |
| JP2014522397A5 true JP2014522397A5 (https=) | 2015-07-09 |
| JP5990262B2 JP5990262B2 (ja) | 2016-09-07 |
Family
ID=46149387
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014513074A Expired - Fee Related JP5990262B2 (ja) | 2011-05-31 | 2012-05-23 | ヒドリド−トリシアノ−ボラートアニオンを含む化合物 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US9518068B2 (https=) |
| EP (1) | EP2714698B1 (https=) |
| JP (1) | JP5990262B2 (https=) |
| KR (1) | KR20140034256A (https=) |
| CN (1) | CN103582647A (https=) |
| AU (1) | AU2012265219B2 (https=) |
| BR (1) | BR112013030741A2 (https=) |
| IL (1) | IL229328A (https=) |
| SG (1) | SG195086A1 (https=) |
| TW (1) | TWI567084B (https=) |
| WO (1) | WO2012163489A1 (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2925767A1 (en) * | 2012-11-30 | 2015-10-07 | Merck Patent GmbH | Cobalt complexes with tricyanoborate or dicyanoborate counter-anions for electrochemical or optoelectronic devices |
| EP2925768B1 (en) * | 2012-11-30 | 2016-12-21 | Merck Patent GmbH | Cobaltcomplex salts |
| DE102013009959A1 (de) | 2013-06-14 | 2014-12-31 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Salzen mit Hydridocyanoborat-Anionen |
| DE102013013502A1 (de) * | 2013-08-16 | 2015-03-12 | Julius-Maximilians-Universität Würzburg | Hexacyanodiborate |
| DE102014008131A1 (de) | 2014-06-06 | 2015-12-17 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Salzen mit Monoydridocyanoborat-Anionen |
| DE102014011089A1 (de) | 2014-07-30 | 2016-02-04 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Salzen mit Hydridocyanoborat-Anionen |
| DE102014014967A1 (de) | 2014-10-14 | 2016-04-14 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Verbindungen mit Monofluorotricyanoborat-Anionen |
| DE102014016681A1 (de) | 2014-11-12 | 2016-05-12 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Salzen mit Hydridocyanoborat-Anionen |
| DE102014018103A1 (de) | 2014-12-09 | 2016-06-09 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Verbindungen mit Tricyanoborat-Dianionen |
| CA3001974A1 (en) | 2015-10-14 | 2017-04-20 | Bristol-Myers Squibb Company | 2,4-dihydroxy-nicotinamides as apj agonists |
| CN106750839B (zh) * | 2015-11-20 | 2019-04-05 | 中国石油天然气股份有限公司 | 滴灌带专用料及其制备方法 |
| TW201725203A (zh) | 2015-12-16 | 2017-07-16 | 必治妥美雅史谷比公司 | 作為ａｐｊ受體促效劑之雜芳基羥基嘧啶酮 |
| SG11201808163WA (en) | 2016-03-24 | 2018-10-30 | Bristol Myers Squibb Co | 6-hydroxy-4-oxo-1,4-dihydropyrimidine-5-carboxamides as apj agonists |
| CA3026149A1 (en) | 2016-06-02 | 2017-12-07 | Cadent Therapeutics, Inc. | Potassium channel modulators |
| DE102016009846A1 (de) | 2016-08-16 | 2018-02-22 | Julius-Maximilians-Universität Würzburg | Fluoralkylhydrido- und Fluoralkylcyanohydridoborate |
| DE102016010488A1 (de) | 2016-08-30 | 2018-03-01 | Julius-Maximilians-Universität Würzburg | Verbindungen mit ein-, bis- und mehrfach geladenen schwach koordinierenden Anionen |
| SI3571193T1 (sl) | 2017-01-23 | 2022-04-29 | Cadent Therapeutics, Inc. | Modulatorji kalijevega kanalčka |
| BR112020018094A2 (pt) | 2018-03-08 | 2020-12-22 | Incyte Corporation | Compostos de aminopirazina diol como inibidores de pi3k-¿ |
| US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
| JP2021534196A (ja) | 2018-08-23 | 2021-12-09 | シージェン インコーポレイテッド | 抗ｔｉｇｉｔ抗体 |
| CA3116339A1 (en) | 2018-10-22 | 2020-04-30 | Cadent Therapeutics, Inc. | Crystalline forms of potassium channel modulators |
| WO2020219049A1 (en) * | 2019-04-25 | 2020-10-29 | Exxonmobil Chemical Patents Inc. | Non-coordinating anion type indolinium activators in aliphatic and alicyclic hydrocarbon solvents |
| PT4426434T (pt) | 2021-11-02 | 2025-11-24 | Flare Therapeutics Inc | Agonistas inversos de pparg e suas utilizações |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10055811A1 (de) * | 2000-11-10 | 2002-05-29 | Merck Patent Gmbh | Tetrakisfluoroalkylborat-Salze und deren Verwendung als Leitsalze |
| TWI263235B (en) | 2002-04-02 | 2006-10-01 | Nippon Catalytic Chem Ind | Material for electrolytic solutions and use thereof |
| JP4439797B2 (ja) * | 2002-10-03 | 2010-03-24 | 株式会社日本触媒 | イオン伝導体用材料 |
| JP2004123652A (ja) * | 2002-10-04 | 2004-04-22 | Nippon Shokubai Co Ltd | イオン性物質の製造方法 |
| JP2004123653A (ja) * | 2002-10-04 | 2004-04-22 | Nippon Shokubai Co Ltd | イオン性物質の製造方法 |
| EP1528580B2 (en) | 2003-01-15 | 2015-07-01 | Nippon Shokubai Co., Ltd. | Dye-sensitized type solar cell |
| DE10306617A1 (de) * | 2003-02-14 | 2004-08-26 | Merck Patent Gmbh | Salze mit Cyanoborat-Anionen |
| JP2006173014A (ja) * | 2004-12-17 | 2006-06-29 | Nippon Shokubai Co Ltd | イオン性物質含有組成物、イオン伝導性材料及びその用途 |
| JP4883903B2 (ja) * | 2004-05-10 | 2012-02-22 | 株式会社日本触媒 | 電解液材料 |
| CN1331840C (zh) * | 2004-11-11 | 2007-08-15 | 中国科学院大连化学物理研究所 | 一种催化合成苯胲类化合物的方法 |
| JP2006202646A (ja) * | 2005-01-21 | 2006-08-03 | Nippon Shokubai Co Ltd | イオン性液体組成物、イオン伝導性材料及び電解液材料 |
| JP2007134184A (ja) * | 2005-11-10 | 2007-05-31 | Nippon Shokubai Co Ltd | イオン性組成物 |
| JP4187113B2 (ja) | 2006-12-25 | 2008-11-26 | 株式会社日本触媒 | イオン性化合物 |
| EP2327707A4 (en) * | 2008-08-22 | 2012-05-30 | Nippon Catalytic Chem Ind | IONIC CONNECTION, MANUFACTURING METHOD AND ION-LEADING MATERIAL THEREFOR |
| AU2010209972B9 (en) * | 2009-02-02 | 2013-10-17 | Lonza Ltd | Novel tricyanoborates |
| JPWO2010092962A1 (ja) * | 2009-02-12 | 2012-08-16 | アステラス製薬株式会社 | へテロ環誘導体 |
-
2012
- 2012-05-23 EP EP12723382.3A patent/EP2714698B1/en not_active Not-in-force
- 2012-05-23 KR KR1020137034534A patent/KR20140034256A/ko not_active Ceased
- 2012-05-23 SG SG2013086186A patent/SG195086A1/en unknown
- 2012-05-23 US US14/119,893 patent/US9518068B2/en not_active Expired - Fee Related
- 2012-05-23 JP JP2014513074A patent/JP5990262B2/ja not_active Expired - Fee Related
- 2012-05-23 BR BR112013030741A patent/BR112013030741A2/pt not_active IP Right Cessation
- 2012-05-23 WO PCT/EP2012/002179 patent/WO2012163489A1/en not_active Ceased
- 2012-05-23 CN CN201280026258.8A patent/CN103582647A/zh active Pending
- 2012-05-23 TW TW101118337A patent/TWI567084B/zh not_active IP Right Cessation
- 2012-05-23 AU AU2012265219A patent/AU2012265219B2/en not_active Ceased
-
2013
- 2013-11-07 IL IL229328A patent/IL229328A/en not_active IP Right Cessation
-
2016
- 2016-02-19 US US15/048,381 patent/US9409925B2/en not_active Expired - Fee Related
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