DE102006008020A1 - Ionische Flüssigkeiten auf Basis asymmetrischer Semichelatoborate - Google Patents
Ionische Flüssigkeiten auf Basis asymmetrischer Semichelatoborate Download PDFInfo
- Publication number
- DE102006008020A1 DE102006008020A1 DE200610008020 DE102006008020A DE102006008020A1 DE 102006008020 A1 DE102006008020 A1 DE 102006008020A1 DE 200610008020 DE200610008020 DE 200610008020 DE 102006008020 A DE102006008020 A DE 102006008020A DE 102006008020 A1 DE102006008020 A1 DE 102006008020A1
- Authority
- DE
- Germany
- Prior art keywords
- ionic liquid
- compound
- cation
- anion
- liquid according
- 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.)
- Withdrawn
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- 239000002608 ionic liquid Substances 0.000 title claims abstract description 38
- -1 nitride ion compound Chemical class 0.000 title claims abstract description 29
- 150000001768 cations Chemical class 0.000 title claims abstract description 19
- 150000001450 anions Chemical class 0.000 title claims abstract description 15
- 239000003792 electrolyte Substances 0.000 title claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract 4
- 125000002947 alkylene group Chemical group 0.000 claims abstract 4
- 229910052794 bromium Inorganic materials 0.000 claims abstract 4
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 4
- 229910052731 fluorine Inorganic materials 0.000 claims abstract 4
- 229910052740 iodine Inorganic materials 0.000 claims abstract 4
- 125000002577 pseudohalo group Chemical group 0.000 claims abstract 4
- 125000000732 arylene group Chemical group 0.000 claims abstract 3
- 125000004653 anthracenylene group Chemical group 0.000 claims abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract 2
- 125000005842 heteroatom Chemical group 0.000 claims abstract 2
- 125000004957 naphthylene group Chemical group 0.000 claims abstract 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract 2
- 125000005550 pyrazinylene group Chemical group 0.000 claims abstract 2
- 125000005551 pyridylene group Chemical group 0.000 claims abstract 2
- 125000005576 pyrimidinylene group Chemical group 0.000 claims abstract 2
- 238000003786 synthesis reaction Methods 0.000 claims description 10
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 4
- 238000009713 electroplating Methods 0.000 claims description 3
- SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical compound CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 claims description 3
- UINDRJHZBAGQFD-UHFFFAOYSA-O 2-ethyl-3-methyl-1h-imidazol-3-ium Chemical compound CCC1=[NH+]C=CN1C UINDRJHZBAGQFD-UHFFFAOYSA-O 0.000 claims description 2
- 239000003990 capacitor Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 claims 2
- 150000004820 halides Chemical class 0.000 claims 2
- PXELHGDYRQLRQO-UHFFFAOYSA-N 1-butyl-1-methylpyrrolidin-1-ium Chemical compound CCCC[N+]1(C)CCCC1 PXELHGDYRQLRQO-UHFFFAOYSA-N 0.000 claims 1
- NIHOUJYFWMURBG-UHFFFAOYSA-N 1-ethyl-1-methylpyrrolidin-1-ium Chemical compound CC[N+]1(C)CCCC1 NIHOUJYFWMURBG-UHFFFAOYSA-N 0.000 claims 1
- YQFWGCSKGJMGHE-UHFFFAOYSA-N 1-methyl-1-propylpyrrolidin-1-ium Chemical compound CCC[N+]1(C)CCCC1 YQFWGCSKGJMGHE-UHFFFAOYSA-N 0.000 claims 1
- DECWYWSYTFTUAV-UHFFFAOYSA-O 3-methyl-2-propyl-1h-imidazol-3-ium Chemical compound CCCC=1NC=C[N+]=1C DECWYWSYTFTUAV-UHFFFAOYSA-O 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical class C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 239000000956 alloy Substances 0.000 claims 1
- 229910045601 alloy Inorganic materials 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 230000008021 deposition Effects 0.000 claims 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- 239000000615 nonconductor Substances 0.000 claims 1
- 239000004065 semiconductor Substances 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 8
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 238000005160 1H NMR spectroscopy Methods 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000013522 chelant Substances 0.000 description 3
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 2
- WEVYAHXRMPXWCK-FIBGUPNXSA-N acetonitrile-d3 Chemical compound [2H]C([2H])([2H])C#N WEVYAHXRMPXWCK-FIBGUPNXSA-N 0.000 description 2
- 238000001897 boron-11 nuclear magnetic resonance spectrum Methods 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229910001416 lithium ion Inorganic materials 0.000 description 2
- 229910003002 lithium salt Inorganic materials 0.000 description 2
- 159000000002 lithium salts Chemical class 0.000 description 2
- 238000005649 metathesis reaction Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- BMQZYMYBQZGEEY-UHFFFAOYSA-M 1-ethyl-3-methylimidazolium chloride Chemical compound [Cl-].CCN1C=C[N+](C)=C1 BMQZYMYBQZGEEY-UHFFFAOYSA-M 0.000 description 1
- QSVCPXPVEZVSPY-UHFFFAOYSA-N 2-ethyl-1-methyl-1h-imidazol-1-ium;chloride Chemical compound [Cl-].CCC1=[NH+]C=CN1C QSVCPXPVEZVSPY-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910013075 LiBF Inorganic materials 0.000 description 1
- CKSNGRFEJKNBMU-UHFFFAOYSA-N O=C(C(O1)=O)O[B-]1(F)F Chemical compound O=C(C(O1)=O)O[B-]1(F)F CKSNGRFEJKNBMU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 230000005518 electrochemistry Effects 0.000 description 1
- AHRQMWOXLCFNAV-UHFFFAOYSA-O ethylammonium nitrate Chemical compound CC[NH3+].[O-][N+]([O-])=O AHRQMWOXLCFNAV-UHFFFAOYSA-O 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 150000008040 ionic compounds Chemical group 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011829 room temperature ionic liquid solvent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/022—Boron compounds without C-boron linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Secondary Cells (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE200610008020 DE102006008020A1 (de) | 2006-02-21 | 2006-02-21 | Ionische Flüssigkeiten auf Basis asymmetrischer Semichelatoborate |
| PCT/EP2007/001413 WO2007096113A1 (fr) | 2006-02-21 | 2007-02-19 | Liquides ioniques à base de borates semi-chélatés asymétriques |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE200610008020 DE102006008020A1 (de) | 2006-02-21 | 2006-02-21 | Ionische Flüssigkeiten auf Basis asymmetrischer Semichelatoborate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102006008020A1 true DE102006008020A1 (de) | 2007-08-23 |
Family
ID=37984315
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE200610008020 Withdrawn DE102006008020A1 (de) | 2006-02-21 | 2006-02-21 | Ionische Flüssigkeiten auf Basis asymmetrischer Semichelatoborate |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE102006008020A1 (fr) |
| WO (1) | WO2007096113A1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102008028331A1 (de) | 2008-06-13 | 2009-12-17 | Universität Regensburg | Verfahren zur Darstellung ionischer Verbindungen mit Anionen mit unterschiedlichen Liganden |
| US10450329B2 (en) | 2016-02-05 | 2019-10-22 | Gotion Inc. | Preparation of difluoro chelato borate salts |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102008021271A1 (de) * | 2008-04-29 | 2010-01-28 | Merck Patent Gmbh | Reaktive ionische Flüssigkeiten |
| JP2014122185A (ja) * | 2012-12-21 | 2014-07-03 | Central Glass Co Ltd | 有機化合物を配位子とするイオン性金属錯体塩の製造方法 |
| CN118063514A (zh) * | 2024-04-22 | 2024-05-24 | 蓝固(湖州)新能源科技有限公司 | 一种原位固态化单体、电解液和混合固液电池 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005090362A1 (fr) * | 2004-03-18 | 2005-09-29 | Ciba Specialty Chemicals Holding Inc. | Support d'enregistrement optique a performance elevee |
-
2006
- 2006-02-21 DE DE200610008020 patent/DE102006008020A1/de not_active Withdrawn
-
2007
- 2007-02-19 WO PCT/EP2007/001413 patent/WO2007096113A1/fr active Application Filing
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102008028331A1 (de) | 2008-06-13 | 2009-12-17 | Universität Regensburg | Verfahren zur Darstellung ionischer Verbindungen mit Anionen mit unterschiedlichen Liganden |
| US10450329B2 (en) | 2016-02-05 | 2019-10-22 | Gotion Inc. | Preparation of difluoro chelato borate salts |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007096113A1 (fr) | 2007-08-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8139 | Disposal/non-payment of the annual fee |