JP2018507843A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2018507843A5 JP2018507843A5 JP2017541087A JP2017541087A JP2018507843A5 JP 2018507843 A5 JP2018507843 A5 JP 2018507843A5 JP 2017541087 A JP2017541087 A JP 2017541087A JP 2017541087 A JP2017541087 A JP 2017541087A JP 2018507843 A5 JP2018507843 A5 JP 2018507843A5
- Authority
- JP
- Japan
- Prior art keywords
- acid
- ion
- group
- cao
- compound
- 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
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 20
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 14
- 239000011575 calcium Substances 0.000 claims description 11
- 239000013078 crystal Substances 0.000 claims description 10
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000007800 oxidant agent Substances 0.000 claims description 9
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000002244 precipitate Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 159000000007 calcium salts Chemical class 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 238000001953 recrystallisation Methods 0.000 claims description 2
- 239000011572 manganese Substances 0.000 claims 25
- -1 small molecule esters Chemical class 0.000 claims 25
- 238000000034 method Methods 0.000 claims 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 10
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 claims 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 6
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 6
- 150000007942 carboxylates Chemical class 0.000 claims 6
- 238000002425 crystallisation Methods 0.000 claims 6
- 230000008025 crystallization Effects 0.000 claims 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 6
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 5
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 claims 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 4
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 claims 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 4
- 239000003446 ligand Substances 0.000 claims 4
- 230000007935 neutral effect Effects 0.000 claims 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 3
- 150000002825 nitriles Chemical class 0.000 claims 3
- 229950010765 pivalate Drugs 0.000 claims 3
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 claims 2
- 229910020366 ClO 4 Inorganic materials 0.000 claims 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- 150000002500 ions Chemical class 0.000 claims 2
- 150000002576 ketones Chemical class 0.000 claims 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims 2
- 235000019260 propionic acid Nutrition 0.000 claims 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 2
- 229940070710 valerate Drugs 0.000 claims 2
- 229940005605 valeric acid Drugs 0.000 claims 2
- 239000003643 water by type Substances 0.000 claims 2
- UHOPWFKONJYLCF-UHFFFAOYSA-N 2-(2-sulfanylethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CCS)C(=O)C2=C1 UHOPWFKONJYLCF-UHFFFAOYSA-N 0.000 claims 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 235000011054 acetic acid Nutrition 0.000 claims 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims 1
- 239000012467 final product Substances 0.000 claims 1
- 235000019253 formic acid Nutrition 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 150000002696 manganese Chemical class 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000013110 organic ligand Substances 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 230000035484 reaction time Effects 0.000 claims 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 229910001424 calcium ion Inorganic materials 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510065238.7 | 2015-02-06 | ||
| CN201510065238.7A CN104761591B (zh) | 2015-02-06 | 2015-02-06 | 一种含有Mn4CaO4核心结构的水裂解催化剂，其制备方法及其应用 |
| PCT/CN2016/073203 WO2016124133A1 (zh) | 2015-02-06 | 2016-02-02 | 一种含有Mn4CaO4核心结构的水裂解催化剂，其制备方法及其应用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018507843A JP2018507843A (ja) | 2018-03-22 |
| JP2018507843A5 true JP2018507843A5 (enExample) | 2020-04-02 |
| JP6795508B2 JP6795508B2 (ja) | 2020-12-02 |
Family
ID=53643725
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017541087A Active JP6795508B2 (ja) | 2015-02-06 | 2016-02-02 | Ｍｎ４ＣａＯ４核構造を含む水分解触媒、その製造方法及びその使用 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US10421065B2 (enExample) |
| EP (1) | EP3255053B1 (enExample) |
| JP (1) | JP6795508B2 (enExample) |
| KR (1) | KR101991755B1 (enExample) |
| CN (1) | CN104761591B (enExample) |
| AU (1) | AU2016214806B2 (enExample) |
| CA (1) | CA2975919C (enExample) |
| WO (1) | WO2016124133A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104761591B (zh) | 2015-02-06 | 2017-07-21 | 中国科学院化学研究所 | 一种含有Mn4CaO4核心结构的水裂解催化剂，其制备方法及其应用 |
| CN109748939B (zh) * | 2017-11-01 | 2020-07-14 | 中国科学院化学研究所 | 含有[Mn3SrO4]和[Mn4SrO4]核心结构的簇合物及其制备方法和应用 |
| US11511266B2 (en) | 2017-11-01 | 2022-11-29 | Institute Of Chemistry, Chinese Academy Of Sciences | Cluster compounds containing [Mn3SrO4] and [Mn4SrO4] core structures, preparation method and application thereof |
| CN110219015A (zh) * | 2019-05-05 | 2019-09-10 | 南京航空航天大学 | 仿生锰核立方烷催化剂复合钒酸铋光电极及其制备方法 |
| TWI794836B (zh) * | 2021-06-16 | 2023-03-01 | 國立成功大學 | 高熵複合甘油酸酯及其製法和包含其的電催化劑 |
| CN115710292B (zh) * | 2021-08-23 | 2025-10-24 | 中国科学院化学研究所 | 含稀土离子的仿生水裂解催化剂及其制备方法和应用 |
| WO2023023898A1 (zh) * | 2021-08-23 | 2023-03-02 | 中国科学院化学研究所 | 含稀土离子的仿生水裂解催化剂及其制备方法和应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101134723A (zh) * | 2006-08-29 | 2008-03-05 | 惠州市昆泰精细化工有限公司 | 没食子酸与二价金属离子的复合物及其制备方法与应用 |
| US9365600B2 (en) * | 2011-05-06 | 2016-06-14 | University Of Florida Research Foundation, Inc. | Polynuclear metal clusters, methods of making, and methods of use thereof |
| CN104761591B (zh) * | 2015-02-06 | 2017-07-21 | 中国科学院化学研究所 | 一种含有Mn4CaO4核心结构的水裂解催化剂，其制备方法及其应用 |
-
2015
- 2015-02-06 CN CN201510065238.7A patent/CN104761591B/zh active Active
-
2016
- 2016-02-02 CA CA2975919A patent/CA2975919C/en active Active
- 2016-02-02 AU AU2016214806A patent/AU2016214806B2/en active Active
- 2016-02-02 JP JP2017541087A patent/JP6795508B2/ja active Active
- 2016-02-02 US US15/549,256 patent/US10421065B2/en active Active
- 2016-02-02 KR KR1020177021848A patent/KR101991755B1/ko active Active
- 2016-02-02 WO PCT/CN2016/073203 patent/WO2016124133A1/zh not_active Ceased
- 2016-02-02 EP EP16746128.4A patent/EP3255053B1/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2018507843A5 (enExample) | ||
| JP6795508B2 (ja) | Ｍｎ４ＣａＯ４核構造を含む水分解触媒、その製造方法及びその使用 | |
| JP2014523898A (ja) | 亜鉛メチルイミダゾラートからなる多孔性金属有機構造体の製造方法 | |
| JP2012530672A5 (enExample) | ||
| CN103551175A (zh) | 磷酸氧钒催化剂及其制备方法与用途 | |
| CN107108553A (zh) | 制备二芳基硫代乙内酰脲化合物的方法 | |
| JPH039773B2 (enExample) | ||
| CN102399182A (zh) | 喹啉酸的生产方法 | |
| JP2018203639A (ja) | Ｎ−カルバメート保護カルボキシ無水物の製造方法 | |
| WO2019084845A1 (zh) | 含有[Mn3SrO4]和[Mn4SrO4]核心结构的簇合物及其制备方法和应用 | |
| CN105175446B (zh) | 一种治疗骨质疏松的米诺膦酸的制备方法 | |
| JP2016515555A5 (enExample) | ||
| CN109748939B (zh) | 含有[Mn3SrO4]和[Mn4SrO4]核心结构的簇合物及其制备方法和应用 | |
| JPS5980633A (ja) | ハロ酸エステル及びその製法 | |
| CN105061421A (zh) | 一种制备2-氯-1, 8-萘啶类衍生物的方法 | |
| JP4298864B2 (ja) | ビフェニルテトラカルボン酸エステルの製造方法 | |
| JP2010043053A (ja) | 高純度のレバミピドの製造方法 | |
| CN110156760A (zh) | 一种4-(1,4-二氧六环-2-基)喹啉-2-甲酸甲酯衍生物的制备方法 | |
| CN106518865A (zh) | 一种1‑烯基中氮茚衍生物的制备方法 | |
| CN111205222B (zh) | 吡啶环化合物的制备方法 | |
| King et al. | The Reaction of Diazoketones with Heterocyclic Amine Salts | |
| CN103920523B (zh) | 一种介孔固体强碱催化剂的制备方法 | |
| CN112745211A (zh) | 一种异壬酸的制备方法 | |
| CN103265514A (zh) | 一种制备吗替麦考酚酯的方法 | |
| CN101468951A (zh) | 制备2-氯-5-(2-氯-4-三氟甲基苯氧基)苯甲酰基-l-乳酸乙酯的方法 |