DE10306617A1 - Salze mit Cyanoborat-Anionen - Google Patents
Salze mit Cyanoborat-Anionen Download PDFInfo
- Publication number
- DE10306617A1 DE10306617A1 DE10306617A DE10306617A DE10306617A1 DE 10306617 A1 DE10306617 A1 DE 10306617A1 DE 10306617 A DE10306617 A DE 10306617A DE 10306617 A DE10306617 A DE 10306617A DE 10306617 A1 DE10306617 A1 DE 10306617A1
- Authority
- DE
- Germany
- Prior art keywords
- alkali metal
- proviso
- salt
- carbon atoms
- group
- 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- Withdrawn
Links
- -1 alkali metal salt Chemical class 0.000 title claims abstract description 77
- 229910052783 alkali metal Inorganic materials 0.000 title claims abstract description 44
- 239000002608 ionic liquid Substances 0.000 title claims description 16
- 150000001875 compounds Chemical class 0.000 title claims description 9
- 239000004973 liquid crystal related substance Substances 0.000 title claims description 3
- 239000011255 nonaqueous electrolyte Substances 0.000 title claims description 3
- 239000003444 phase transfer catalyst Substances 0.000 title claims description 3
- 239000011814 protection agent Substances 0.000 title claims 2
- HZXXSCOUSGLRRX-UHFFFAOYSA-N cyanoboronic acid Chemical class OB(O)C#N HZXXSCOUSGLRRX-UHFFFAOYSA-N 0.000 title description 3
- 239000000543 intermediate Substances 0.000 title 1
- 150000002892 organic cations Chemical class 0.000 claims abstract description 16
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 150000003839 salts Chemical class 0.000 claims description 43
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 26
- 229910052744 lithium Inorganic materials 0.000 claims description 20
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 15
- 125000005842 heteroatom Chemical group 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 229910052792 caesium Inorganic materials 0.000 claims description 13
- 239000000460 chlorine Substances 0.000 claims description 13
- 229910052700 potassium Inorganic materials 0.000 claims description 13
- 229910052701 rubidium Inorganic materials 0.000 claims description 13
- 229910052708 sodium Inorganic materials 0.000 claims description 13
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 12
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000001768 cations Chemical class 0.000 claims description 8
- 150000002367 halogens Chemical group 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 238000003786 synthesis reaction Methods 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 claims description 5
- 238000003746 solid phase reaction Methods 0.000 claims description 5
- 238000010671 solid-state reaction Methods 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000000010 aprotic solvent Substances 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 150000001340 alkali metals Chemical class 0.000 abstract 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 51
- 238000005481 NMR spectroscopy Methods 0.000 description 22
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 18
- 239000002904 solvent Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- 239000000155 melt Substances 0.000 description 14
- 239000011734 sodium Substances 0.000 description 14
- 238000000921 elemental analysis Methods 0.000 description 13
- 238000003756 stirring Methods 0.000 description 13
- 239000000126 substance Substances 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 9
- 125000001424 substituent group Chemical group 0.000 description 9
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000012074 organic phase Substances 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 239000013558 reference substance Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000004009 13C{1H}-NMR spectroscopy Methods 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000006555 catalytic reaction Methods 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- AIYUHDOJVYHVIT-UHFFFAOYSA-M caesium chloride Chemical compound [Cl-].[Cs+] AIYUHDOJVYHVIT-UHFFFAOYSA-M 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- YZPHGBCZBFZOSC-UHFFFAOYSA-N dichloromethane;n,n-dipropylpropan-1-amine Chemical compound ClCCl.CCCN(CCC)CCC YZPHGBCZBFZOSC-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000005496 eutectics Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- BKCCIUKIEWNJBW-UHFFFAOYSA-N 1-butyl-3-methylimidazol-3-ium;difluoroboranylformonitrile Chemical compound FB(F)C#N.FB(F)C#N.CCCCN1C=C[N+](C)=C1 BKCCIUKIEWNJBW-UHFFFAOYSA-N 0.000 description 1
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 1
- NNLHWTTWXYBJBQ-UHFFFAOYSA-N 1-butyl-4-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=C(C)C=C1 NNLHWTTWXYBJBQ-UHFFFAOYSA-N 0.000 description 1
- HNQODRCNFCISOV-UHFFFAOYSA-N 1-butyl-4-methylpyridin-1-ium;difluoroboranylformonitrile Chemical compound FB(F)C#N.FB(F)C#N.CCCC[N+]1=CC=C(C)C=C1 HNQODRCNFCISOV-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 101710134784 Agnoprotein Proteins 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 1
- 238000005863 Friedel-Crafts acylation reaction Methods 0.000 description 1
- 238000003547 Friedel-Crafts alkylation reaction Methods 0.000 description 1
- 238000007341 Heck reaction Methods 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 description 1
- 229910013553 LiNO Inorganic materials 0.000 description 1
- 229910019093 NaOCl Inorganic materials 0.000 description 1
- 238000001237 Raman spectrum Methods 0.000 description 1
- 241001620634 Roger Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000009841 combustion method Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000006352 cycloaddition reaction Methods 0.000 description 1
- 238000011157 data evaluation Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- 239000002027 dichloromethane extract Substances 0.000 description 1
- XUOUWPSYFXADTP-UHFFFAOYSA-N difluoroboranylformonitrile;1-ethyl-3-methylimidazol-3-ium Chemical compound FB(F)C#N.FB(F)C#N.CC[N+]=1C=CN(C)C=1 XUOUWPSYFXADTP-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229910001412 inorganic anion Inorganic materials 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- JORQDGTZGKHEEO-UHFFFAOYSA-N lithium cyanide Chemical compound [Li+].N#[C-] JORQDGTZGKHEEO-UHFFFAOYSA-N 0.000 description 1
- HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Inorganic materials [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000004452 microanalysis Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical group 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 229910001495 sodium tetrafluoroborate Inorganic materials 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- CCZXMDQFIVMWMF-UHFFFAOYSA-N trifluoromethoxyboronic acid Chemical class OB(O)OC(F)(F)F CCZXMDQFIVMWMF-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
- C07D213/16—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing only one pyridine ring
- C07D213/20—Quaternary compounds thereof
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/62—Quaternary ammonium compounds
- C07C211/63—Quaternary ammonium compounds having quaternised nitrogen atoms bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/62—Quaternary ammonium compounds
- C07C211/64—Quaternary ammonium compounds having quaternised nitrogen atoms bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- 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
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
-
- 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
- C07F5/027—Organoboranes and organoborohydrides
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/54—Quaternary phosphonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Priority Applications (24)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10306617A DE10306617A1 (de) | 2003-02-14 | 2003-02-14 | Salze mit Cyanoborat-Anionen |
| DE502004004472T DE502004004472D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
| KR1020107026021A KR101105618B1 (ko) | 2003-02-14 | 2004-01-15 | 시아노보레이트 음이온을 갖는 염 |
| EP06016495A EP1726594B1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
| RU2005128348/04A RU2337912C2 (ru) | 2003-02-14 | 2004-01-15 | Соли с цианоборатными анионами |
| AT04702317T ATE340799T1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| CNB2007101361308A CN100572385C (zh) | 2003-02-14 | 2004-01-15 | 具有氰基硼酸根阴离子的盐 |
| AT06016495T ATE368045T1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| KR1020117022210A KR20110110873A (ko) | 2003-02-14 | 2004-01-15 | 시아노보레이트 음이온을 갖는 염 |
| PCT/EP2004/000231 WO2004072089A1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| DE502004004471T DE502004004471D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
| CN2007101361295A CN101108861B (zh) | 2003-02-14 | 2004-01-15 | 具有氰基硼酸根阴离子的盐 |
| KR1020057014965A KR101010558B1 (ko) | 2003-02-14 | 2004-01-15 | 시아노보레이트 음이온을 갖는 염 |
| EP06016494A EP1726593B1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
| JP2006501548A JP4718438B2 (ja) | 2003-02-14 | 2004-01-15 | シアノボレートアニオンを有する塩 |
| CA2771069A CA2771069C (en) | 2003-02-14 | 2004-01-15 | Salts comprising cyanoborate anions |
| CNB2004800041330A CN100361997C (zh) | 2003-02-14 | 2004-01-15 | 具有氰基硼酸根阴离子的盐 |
| ES04702317T ES2271837T3 (es) | 2003-02-14 | 2004-01-15 | Sales que contienen aniones de cianoborato. |
| AT06016494T ATE368044T1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| US10/545,690 US7645434B2 (en) | 2003-02-14 | 2004-01-15 | Salts comprising cyanoborate anions |
| EP04702317A EP1592696B1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| DE502004001603T DE502004001603D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| CA2515856A CA2515856C (en) | 2003-02-14 | 2004-01-15 | Salts comprising cyanoborate anions |
| KR1020127017205A KR101287689B1 (ko) | 2003-02-14 | 2004-01-15 | 시아노보레이트 음이온을 갖는 염 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10306617A DE10306617A1 (de) | 2003-02-14 | 2003-02-14 | Salze mit Cyanoborat-Anionen |
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| Publication Number | Publication Date |
|---|---|
| DE10306617A1 true DE10306617A1 (de) | 2004-08-26 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10306617A Withdrawn DE10306617A1 (de) | 2003-02-14 | 2003-02-14 | Salze mit Cyanoborat-Anionen |
| DE502004004471T Expired - Lifetime DE502004004471D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
| DE502004001603T Expired - Lifetime DE502004001603D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| DE502004004472T Expired - Lifetime DE502004004472D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
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| DE502004004471T Expired - Lifetime DE502004004471D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
| DE502004001603T Expired - Lifetime DE502004001603D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit cyanoborat-anionen |
| DE502004004472T Expired - Lifetime DE502004004472D1 (de) | 2003-02-14 | 2004-01-15 | Salze mit Cyanoborat-Anionen |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7645434B2 (https=) |
| EP (3) | EP1592696B1 (https=) |
| JP (1) | JP4718438B2 (https=) |
| KR (4) | KR20110110873A (https=) |
| CN (3) | CN100572385C (https=) |
| AT (3) | ATE368045T1 (https=) |
| CA (2) | CA2515856C (https=) |
| DE (4) | DE10306617A1 (https=) |
| ES (1) | ES2271837T3 (https=) |
| RU (1) | RU2337912C2 (https=) |
| WO (1) | WO2004072089A1 (https=) |
Cited By (2)
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|---|---|---|---|---|
| WO2005097731A3 (en) * | 2004-04-07 | 2005-11-24 | Univ York | Ionic liquids comprising nitrogen containing cations |
| EP1819005A1 (en) * | 2006-02-13 | 2007-08-15 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Ionic liquid electrolyte |
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| DE102015016400A1 (de) | 2015-12-18 | 2017-06-22 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Salzen mit Perfluoralkyltricyanoboratanionen oder Tetracyanoboratanionen |
| DE102015016401A1 (de) | 2015-12-18 | 2017-06-22 | Julius-Maximilians-Universität Würzburg | Verfahren zur Herstellung von Salzen mit Monofluorotricyanoboratanionen |
| DE102016009846A1 (de) | 2016-08-16 | 2018-02-22 | Julius-Maximilians-Universität Würzburg | Fluoralkylhydrido- und Fluoralkylcyanohydridoborate |
| EP4243122A3 (en) | 2016-12-02 | 2023-11-15 | Fastcap Systems Corporation | Composite electrode |
| JP2021141101A (ja) * | 2020-03-02 | 2021-09-16 | 日清紡ホールディングス株式会社 | 蓄電デバイス用電解液およびイオン液体 |
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| US4301129A (en) * | 1978-09-18 | 1981-11-17 | Thiokol Corporation | Synthesis of NaBH3 CN and related compounds |
| JPS5542292A (en) | 1978-09-18 | 1980-03-25 | Thiokol Chemical Corp | Method of synthesizing nabh3cn and related compounds |
| JPH07116113B2 (ja) | 1987-05-14 | 1995-12-13 | 三菱化学株式会社 | 四級アンモニウム無機酸塩の製造方法 |
| US4892944A (en) * | 1987-05-13 | 1990-01-09 | Mitsubishi Petrochemical Co., Ltd. | Process for producing quaternary salts |
| DE10055811A1 (de) * | 2000-11-10 | 2002-05-29 | Merck Patent Gmbh | Tetrakisfluoroalkylborat-Salze und deren Verwendung als Leitsalze |
| CN1449069A (zh) * | 2002-04-02 | 2003-10-15 | 株式会社日本触媒 | 电解质溶液用材料及其用途 |
| JP4467247B2 (ja) | 2002-04-02 | 2010-05-26 | 株式会社日本触媒 | 新規溶融塩を用いたイオン伝導体 |
| JP4127788B2 (ja) * | 2002-11-22 | 2008-07-30 | 株式会社トクヤマ | オニウム塩 |
-
2003
- 2003-02-14 DE DE10306617A patent/DE10306617A1/de not_active Withdrawn
-
2004
- 2004-01-15 KR KR1020117022210A patent/KR20110110873A/ko not_active Ceased
- 2004-01-15 AT AT06016495T patent/ATE368045T1/de not_active IP Right Cessation
- 2004-01-15 KR KR1020057014965A patent/KR101010558B1/ko not_active Expired - Fee Related
- 2004-01-15 RU RU2005128348/04A patent/RU2337912C2/ru not_active IP Right Cessation
- 2004-01-15 KR KR1020107026021A patent/KR101105618B1/ko not_active Expired - Fee Related
- 2004-01-15 ES ES04702317T patent/ES2271837T3/es not_active Expired - Lifetime
- 2004-01-15 DE DE502004004471T patent/DE502004004471D1/de not_active Expired - Lifetime
- 2004-01-15 CN CNB2007101361308A patent/CN100572385C/zh not_active Expired - Fee Related
- 2004-01-15 AT AT06016494T patent/ATE368044T1/de not_active IP Right Cessation
- 2004-01-15 EP EP04702317A patent/EP1592696B1/de not_active Expired - Lifetime
- 2004-01-15 CN CN2007101361295A patent/CN101108861B/zh not_active Expired - Fee Related
- 2004-01-15 EP EP06016494A patent/EP1726593B1/de not_active Expired - Lifetime
- 2004-01-15 CA CA2515856A patent/CA2515856C/en not_active Expired - Fee Related
- 2004-01-15 CA CA2771069A patent/CA2771069C/en not_active Expired - Fee Related
- 2004-01-15 CN CNB2004800041330A patent/CN100361997C/zh not_active Expired - Fee Related
- 2004-01-15 WO PCT/EP2004/000231 patent/WO2004072089A1/de not_active Ceased
- 2004-01-15 US US10/545,690 patent/US7645434B2/en not_active Expired - Fee Related
- 2004-01-15 AT AT04702317T patent/ATE340799T1/de active
- 2004-01-15 DE DE502004001603T patent/DE502004001603D1/de not_active Expired - Lifetime
- 2004-01-15 JP JP2006501548A patent/JP4718438B2/ja not_active Expired - Fee Related
- 2004-01-15 KR KR1020127017205A patent/KR101287689B1/ko not_active Expired - Fee Related
- 2004-01-15 EP EP06016495A patent/EP1726594B1/de not_active Expired - Lifetime
- 2004-01-15 DE DE502004004472T patent/DE502004004472D1/de not_active Expired - Lifetime
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005097731A3 (en) * | 2004-04-07 | 2005-11-24 | Univ York | Ionic liquids comprising nitrogen containing cations |
| EP2322497A1 (en) * | 2004-04-07 | 2011-05-18 | Innovia Films Limited | Ionic liquids comprising nitrogen containing cations |
| US8784686B2 (en) | 2004-04-07 | 2014-07-22 | Innovia Films Limited | Liquids |
| US8992798B2 (en) | 2004-04-07 | 2015-03-31 | Innovia Films Limited | Liquids |
| US9328220B2 (en) | 2004-04-07 | 2016-05-03 | Innovia Films Limited | Liquids |
| EP1819005A1 (en) * | 2006-02-13 | 2007-08-15 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Ionic liquid electrolyte |
| WO2007093961A1 (en) * | 2006-02-13 | 2007-08-23 | Ecole Polytechnique Federale De Lausanne (Epfl) | Ionic liquid electrolyte |
| AU2007216216B2 (en) * | 2006-02-13 | 2011-11-03 | Ecole Polytechnique Federale De Lausanne (Epfl) | Ionic liquid electrolyte |
| US8114318B2 (en) | 2006-02-13 | 2012-02-14 | Ecole Polytechnique Federale De Lausanne (Epfl) | Ionic liquid electrolyte |
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