JP6052768B2 - 陰イオン交換体 - Google Patents
陰イオン交換体 Download PDFInfo
- Publication number
- JP6052768B2 JP6052768B2 JP2012189551A JP2012189551A JP6052768B2 JP 6052768 B2 JP6052768 B2 JP 6052768B2 JP 2012189551 A JP2012189551 A JP 2012189551A JP 2012189551 A JP2012189551 A JP 2012189551A JP 6052768 B2 JP6052768 B2 JP 6052768B2
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- JP
- Japan
- Prior art keywords
- group
- ion
- anion
- metal
- metal complex
- 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.)
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- 150000001450 anions Chemical class 0.000 title claims description 76
- -1 monoalkylamino group Chemical group 0.000 claims description 91
- 150000004696 coordination complex Chemical class 0.000 claims description 71
- 229910021645 metal ion Inorganic materials 0.000 claims description 50
- 239000013110 organic ligand Substances 0.000 claims description 50
- 125000001424 substituent group Chemical group 0.000 claims description 27
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Chemical compound [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 25
- 229910052751 metal Inorganic materials 0.000 claims description 23
- 239000002184 metal Substances 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- 125000004423 acyloxy group Chemical group 0.000 claims description 16
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 16
- 125000003277 amino group Chemical group 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 15
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 14
- 125000004442 acylamino group Chemical group 0.000 claims description 13
- 150000002500 ions Chemical class 0.000 claims description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 13
- 125000002883 imidazolyl group Chemical group 0.000 claims description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 7
- 230000000737 periodic effect Effects 0.000 claims description 7
- 150000002739 metals Chemical class 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000001425 triazolyl group Chemical group 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 5
- 229940077388 benzenesulfonate Drugs 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 3
- 229940006460 bromide ion Drugs 0.000 claims description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 claims description 3
- 229940006461 iodide ion Drugs 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 description 35
- 238000003786 synthesis reaction Methods 0.000 description 35
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 239000013078 crystal Substances 0.000 description 16
- 235000002639 sodium chloride Nutrition 0.000 description 15
- 125000004432 carbon atom Chemical group C* 0.000 description 14
- 229910001429 cobalt ion Inorganic materials 0.000 description 14
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 12
- 230000008859 change Effects 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 238000005571 anion exchange chromatography Methods 0.000 description 9
- KQJVBDLESMDEHN-UHFFFAOYSA-N 1-[[3-(imidazol-1-ylmethyl)-2,4,6-trimethylphenyl]methyl]imidazole Chemical compound CC1=C(CN2C=NC=C2)C(C)=CC(C)=C1CN1C=CN=C1 KQJVBDLESMDEHN-UHFFFAOYSA-N 0.000 description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 229910001431 copper ion Inorganic materials 0.000 description 7
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 7
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000000470 constituent Substances 0.000 description 6
- 125000000623 heterocyclic group Chemical group 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 125000004434 sulfur atom Chemical group 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 4
- 238000005349 anion exchange Methods 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 4
- 229910001495 sodium tetrafluoroborate Inorganic materials 0.000 description 4
- 238000012916 structural analysis Methods 0.000 description 4
- 238000000967 suction filtration Methods 0.000 description 4
- UIANYESDIYVJNS-UHFFFAOYSA-N 1-[[4-(imidazol-1-ylmethyl)-2,3,5,6-tetramethylphenyl]methyl]imidazole Chemical class CC=1C(C)=C(CN2C=NC=C2)C(C)=C(C)C=1CN1C=CN=C1 UIANYESDIYVJNS-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 3
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 3
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 3
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000006606 n-butoxy group Chemical group 0.000 description 3
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 0 *c1c(*)c(*)c(*)c(*)c1* Chemical compound *c1c(*)c(*)c(*)c(*)c1* 0.000 description 2
- YBXNRUYDSYXYFU-UHFFFAOYSA-N 1-(2-imidazol-1-ylethyl)imidazole Chemical compound C1=CN=CN1CCN1C=CN=C1 YBXNRUYDSYXYFU-UHFFFAOYSA-N 0.000 description 2
- KNGUTJAUDYHCQH-UHFFFAOYSA-N 4-[[2,4,6-trimethyl-3-(pyridin-4-ylmethyl)phenyl]methyl]pyridine Chemical compound Cc1cc(C)c(Cc2ccncc2)c(C)c1Cc1ccncc1 KNGUTJAUDYHCQH-UHFFFAOYSA-N 0.000 description 2
- KSCMYJXTGSEZEI-UHFFFAOYSA-N 5-[2-(2h-tetrazol-5-yl)ethyl]-2h-tetrazole Chemical compound N1=NNN=C1CCC=1N=NNN=1 KSCMYJXTGSEZEI-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 150000001244 carboxylic acid anhydrides Chemical group 0.000 description 2
- 239000013522 chelant Substances 0.000 description 2
- 150000001868 cobalt Chemical class 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 150000001879 copper Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002696 manganese Chemical class 0.000 description 2
- 229910001437 manganese ion Inorganic materials 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000002815 nickel Chemical class 0.000 description 2
- 229910001453 nickel ion Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000036962 time dependent Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- ISXPITWIJWSEKJ-UHFFFAOYSA-N 1-(3-imidazol-1-ylpropyl)imidazole Chemical compound C1=CN=CN1CCCN1C=CN=C1 ISXPITWIJWSEKJ-UHFFFAOYSA-N 0.000 description 1
- LGCPYQSYWVJQCJ-UHFFFAOYSA-N 1-(4-imidazol-1-ylbutyl)imidazole Chemical compound C1=CN=CN1CCCCN1C=CN=C1 LGCPYQSYWVJQCJ-UHFFFAOYSA-N 0.000 description 1
- WSQVBAYVVJVLEE-UHFFFAOYSA-N 1-[[4-(benzimidazol-1-ylmethyl)-1,2,3,5-tetramethylcyclohexa-2,4-dien-1-yl]methyl]benzimidazole Chemical compound N1(C=NC2=C1C=CC=C2)CC2=C(CC(C(=C2C)C)(C)CN2C=NC1=C2C=CC=C1)C WSQVBAYVVJVLEE-UHFFFAOYSA-N 0.000 description 1
- DQRKTVIJNCVZAX-UHFFFAOYSA-N 4-(2-pyridin-4-ylethyl)pyridine Chemical compound C=1C=NC=CC=1CCC1=CC=NC=C1 DQRKTVIJNCVZAX-UHFFFAOYSA-N 0.000 description 1
- OGNCVVRIKNGJHQ-UHFFFAOYSA-N 4-(3-pyridin-4-ylpropyl)pyridine Chemical compound C=1C=NC=CC=1CCCC1=CC=NC=C1 OGNCVVRIKNGJHQ-UHFFFAOYSA-N 0.000 description 1
- XEWYLBJSCXVMCJ-UHFFFAOYSA-N 4-(4-pyridin-4-ylbutyl)pyridine Chemical compound C=1C=NC=CC=1CCCCC1=CC=NC=C1 XEWYLBJSCXVMCJ-UHFFFAOYSA-N 0.000 description 1
- XWPVTMQDKLGEGM-UHFFFAOYSA-N 4-[[2,3,5,6-tetramethyl-4-(pyridin-4-ylmethyl)phenyl]methyl]pyridine Chemical compound Cc1c(C)c(Cc2ccncc2)c(C)c(C)c1Cc1ccncc1 XWPVTMQDKLGEGM-UHFFFAOYSA-N 0.000 description 1
- RZYDLVDZJFHULI-UHFFFAOYSA-N 5-[2-(1h-1,2,4-triazol-5-yl)ethyl]-1h-1,2,4-triazole Chemical compound N=1C=NNC=1CCC1=NC=NN1 RZYDLVDZJFHULI-UHFFFAOYSA-N 0.000 description 1
- ZTOVUOVWUQVXIM-UHFFFAOYSA-N 5-[3-(1H-1,2,4-triazol-5-yl)propyl]-1H-1,2,4-triazole Chemical compound C(CCC1=NNC=N1)C1=NNC=N1 ZTOVUOVWUQVXIM-UHFFFAOYSA-N 0.000 description 1
- ZSDFUHKAFFDSKW-UHFFFAOYSA-N 5-[3-(2h-tetrazol-5-yl)propyl]-2h-tetrazole Chemical compound N1=NNN=C1CCCC=1N=NNN=1 ZSDFUHKAFFDSKW-UHFFFAOYSA-N 0.000 description 1
- YBEQMBOBWUJWTB-UHFFFAOYSA-N 5-[4-(1h-1,2,4-triazol-5-yl)butyl]-1h-1,2,4-triazole Chemical compound N1=CNN=C1CCCCC=1N=CNN=1 YBEQMBOBWUJWTB-UHFFFAOYSA-N 0.000 description 1
- CXQSAFJKCHJMQV-UHFFFAOYSA-N 5-[4-(2h-tetrazol-5-yl)butyl]-2h-tetrazole Chemical compound N1=NNN=C1CCCCC=1N=NNN=1 CXQSAFJKCHJMQV-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- JYKZTQOOXYPGDM-UHFFFAOYSA-N CC.N1(N=CN=C1)N1N=CN=C1 Chemical compound CC.N1(N=CN=C1)N1N=CN=C1 JYKZTQOOXYPGDM-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 235000015842 Hesperis Nutrition 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 235000012633 Iberis amara Nutrition 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- WAEMQWOKJMHJLA-UHFFFAOYSA-N Manganese(2+) Chemical compound [Mn+2] WAEMQWOKJMHJLA-UHFFFAOYSA-N 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- VEQPNABPJHWNSG-UHFFFAOYSA-N Nickel(2+) Chemical compound [Ni+2] VEQPNABPJHWNSG-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000003957 anion exchange resin Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 229940063013 borate ion Drugs 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001661 cadmium Chemical class 0.000 description 1
- WLZRMCYVCSSEQC-UHFFFAOYSA-N cadmium(2+) Chemical compound [Cd+2] WLZRMCYVCSSEQC-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M chlorate Inorganic materials [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- GFHNAMRJFCEERV-UHFFFAOYSA-L cobalt chloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Co+2] GFHNAMRJFCEERV-UHFFFAOYSA-L 0.000 description 1
- QGUAJWGNOXCYJF-UHFFFAOYSA-N cobalt dinitrate hexahydrate Chemical compound O.O.O.O.O.O.[Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O QGUAJWGNOXCYJF-UHFFFAOYSA-N 0.000 description 1
- DAYYOITXWWUZCV-UHFFFAOYSA-L cobalt(2+);sulfate;hexahydrate Chemical compound O.O.O.O.O.O.[Co+2].[O-]S([O-])(=O)=O DAYYOITXWWUZCV-UHFFFAOYSA-L 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- JZCCFEFSEZPSOG-UHFFFAOYSA-L copper(II) sulfate pentahydrate Chemical compound O.O.O.O.O.[Cu+2].[O-]S([O-])(=O)=O JZCCFEFSEZPSOG-UHFFFAOYSA-L 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 208000010643 digestive system disease Diseases 0.000 description 1
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007102 metabolic function Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000002940 palladium Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 229910001487 potassium perchlorate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 150000003283 rhodium Chemical class 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- 150000003303 ruthenium Chemical class 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000004449 solid propellant Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 238000012982 x-ray structure analysis Methods 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Description
(1)周期表の2族及び7〜12族に属する金属のイオンから選択される少なくとも1種の金属イオンと、該金属イオンに二座配位可能な有機配位子とを、金属イオン:二座配位可能な有機配位子=1:3の組成比で含み、前記二座配位可能な有機配位子が2つの金属イオンに配位する金属錯体からなる陰イオン交換体。
(2)該二座配位可能な有機配位子が、少なくとも1つの窒素原子を環内に有する複素環基を少なくとも2つ有する含窒素複素環化合物である(1)に記載の陰イオン交換体。
(3)該二座配位可能な有機配位子が、下記一般式(I);
(4)該二座配位可能な有機配位子が、下記一般式(II);
(5)硝酸イオン、硫酸イオン、フッ化物イオン、塩化物イオン、臭化物イオン、ヨウ化物イオンから選択される少なくとも一種の陰イオンを含む(1)〜(4)のいずれかに記載の陰イオン交換体
(6)(1)〜(5)のいずれかに記載の陰イオン交換体からなる陰イオン除去材。
(7)該陰イオン除去材が、過塩素酸イオン、テトラフルオロホウ酸イオン、ヘキサフルオロリン酸イオン、ヘキサフルオロヒ酸イオン、ヘキサフルオロアンチモン酸イオン、メタンスルホン酸イオン、ベンゼンスルホン酸イオン、トリフルオロ酢酸イオンまたはトリフルオロメタンスルホン酸イオンを除去するための除去材である(5)に記載の陰イオン除去材。
得られた単結晶をゴニオヘッドにマウントし、単結晶X線回折装置を用いて測定した。分析条件の詳細を以下に示す。
<分析条件>
装置:株式会社リガク製Mercury CCD system
X線源:MoKα(λ=0.71073Å) 50kV 40mA
検出器:CCD
コリメータ:Φ0.50mm
測定温度:293K
解析ソフト:SHELXL97
陰イオンを含む溶液200μLを採取し、超純水で25倍に希釈し、陰イオンクロマトグラフを用いて測定した。
<分析条件>
装置:メトローム社製861 Advanced Compact IC
硝酸コバルト六水和物15.0mg(0.052mmol)を水30mLに溶解させ、これに1,3−ビス(イミダゾール−1−イルメチル)−2,4,6−トリメチルベンゼン28.0mg(0.10mmol)を溶解させたメタノール30mLを加え、298Kで3日間静置した。析出した薄桃色の金属錯体を吸引濾過により回収した後、メタノールで洗浄し、目的の金属錯体78.6mg(収率25%)を得た。得られた金属錯体について単結晶X線構造解析を行った結果を以下に示す。また、結晶構造を図1に示す。図1より、得られた金属錯体の組成は、コバルトイオン:硝酸イオン:1,3−ビス(イミダゾール−1−イルメチル)−2,4,6−トリメチルベンゼン=1:1:3であることが分かる。
Monoclinic(C2/c)
a=26.330(18)Å
b=20.406(13)Å
c=14.273(10)Å
α=90.0000°
β=118.146(9)°
γ=90.0000°
V=6762(8)Å3
Z=4
R=0.0958
wR=0.2102
硫酸コバルト六水和物169mg(0.60mmol)を水10mLに溶解させ、これに1,3−ビス(イミダゾール−1−イルメチル)−2,4,6−トリメチルベンゼン505mg(1.8mmol)を溶解させたメタノール10mLを加え、298Kで3日間静置した。析出した桃色の金属錯体を吸引濾過により回収した後、メタノールで洗浄し、目的の金属錯体258mg(収率42%)を得た。得られた金属錯体について単結晶X線構造解析を行った結果を以下に示す。また、結晶構造を図2に示す。図2より、得られた金属錯体の組成は、コバルトイオン:硫酸イオン:1,3−ビス(イミダゾール−1−イルメチル)−2,4,6−トリメチルベンゼン=1:1:3であることが分かる。
Monoclinic(C2/c)
a=26.356(11)Å
b=20.418(8)Å
c=14.319(6)Å
α=90.0000°
β=118.174(6)°
α=90.0000°
V=6792(5)Å3
Z=4
R=0.0842
wR=0.1706
塩化コバルト六水和物36.0mg(0.15mmol)を水10mLに溶解させ、これに1,3−ビス(イミダゾール−1−イルメチル)−2,4,6−トリメチルベンゼン84.0mg(0.30mmol)を溶解させたメタノール10mLを加え、298Kで3日間静置した。析出した薄桃色の金属錯体を吸引濾過により回収した後、メタノールで洗浄し、目的の金属錯体49.0mg(収率50%)を得た。得られた金属錯体について単結晶X線構造解析を行った結果を以下に示す。また、結晶構造を図3に示す。図3より、得られた金属錯体の組成は、コバルトイオン:塩化物イオン:1,3−ビス(イミダゾール−1−イルメチル)−2,4,6−トリメチルベンゼン=1:2:3であることが分かる。
Trigonal(R−3(h))
a=16.886(9)Å
b=16.886(9)Å
c=42.25(3)Å
α=90.0000°
β=90.0000°
γ=120.0000°
V=10432(10)Å3
Z=6
R=0.0975
wR=0.2089
硫酸銅5水和物31.2mg(0.13mmol)を水25mLに、1,4−ビス(イミダゾール−1−イルメチル)−2,3,5,6−テトラメチルベンゼン73.6mg(0.25mmol)をN,N−ジメチルホルムアミド25mLに、それぞれ溶解させ、これらの溶液を混合し7日間、298Kで静置することで金属錯体89mg(収率85%)を青色の板状結晶として得た。得られた金属錯体について単結晶X線構造解析を行った結果を以下に示す。また、結晶構造を図4に示す。図4より、得られた金属錯体の組成は、銅イオン:硫酸イオン:1,4−ビス(イミダゾール−1−イルメチル)−2,3,5,6−テトラメチルベンゼン=1:1:2であることが分かる。
Monoclinic(C2/m)
a=12.3507(17)Å
b=27.263(3)Å
c=14.377(3)Å
β=118.774°
V=4243.4(10)Å3
Z=2
R=0.0644
wR=0.0722
1mM過塩素酸ナトリウム水溶液100mLに合成例1で得た金属錯体52.1mg(コバルトイオンを0.050mmol含有)を加え、303Kにおける過塩素酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図5に示す。
1mM過塩素酸ナトリウム水溶液100mLに合成例2で得た金属錯体51.6mg(コバルトイオンを0.050mmol含有)を加え、303Kにおける過塩素酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図5に示す。
1mM過塩素酸ナトリウム水溶液100mLに合成例3で得た金属錯体48.5mg(コバルトイオンを0.050mmol含有)を加え、303Kにおける過塩素酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図5に示す。
1mM過塩素酸ナトリウム水溶液100mLに比較合成例1で得た金属錯体38.3mg(銅イオンを0.050mmol含有)を加え、303Kにおける過塩素酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図5に示す。
1mMテトラフルオロホウ酸ナトリウム水溶液100mLに合成例1で得た金属錯体52.1mg(コバルトイオンを0.050mmol含有)を加え、303Kにおけるテトラフルオロホウ酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図6に示す。
1mMテトラフルオロホウ酸ナトリウム水溶液100mLに合成例2で得た金属錯体51.6mg(コバルトイオンを0.050mmol含有)を加え、303Kにおけるテトラフルオロホウ酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図6に示す。
1mMテトラフルオロホウ酸ナトリウム水溶液100mLに合成例3で得た金属錯体48.5mg(コバルトイオンを0.050mmol含有)を加え、303Kにおけるテトラフルオロホウ酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図6に示す。
1mMテトラフルオロホウ酸ナトリウム水溶液100mLに比較合成例1で得た金属錯体38.3mg(銅イオンを0.050mmol含有)を加え、303Kにおけるテトラフルオロホウ酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図6に示す。
過塩素酸ナトリウム、塩化ナトリウム、硝酸ナトリウム及び硫酸ナトリウムをそれぞれ1mMずつ含む水溶液100mLに合成例1で得た金属錯体52.1mg(コバルトイオンを0.050mmol含有)を加え、303Kにおける過塩素酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図7に示す。
1mM過塩素酸ナトリウム水溶液100mLに合成例2で得た金属錯体51.6mg(コバルトイオンを0.050mmol含有)を加え、303Kにおける過塩素酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図8に示す。
1mM過塩素酸ナトリウム水溶液100mLに合成例3で得た金属錯体48.5mg(コバルトイオンを0.050mmol含有)を加え、303Kにおける過塩素酸イオン濃度の経時変化を陰イオンクロマトグラフで追跡した。結果を図9に示す。
Claims (3)
- 周期表の2族及び7〜12族に属する金属のイオンから選択される少なくとも1種の金属イオンと、該金属イオンに二座配位可能な有機配位子とを、金属イオン:二座配位可能な有機配位子=1:3の組成比で含み、前記二座配位可能な有機配位子が2つの金属イオンに配位する金属錯体からなり、
該二座配位可能な有機配位子が、下記一般式(I);
硝酸イオン、硫酸イオン、炭酸イオン、炭酸水素イオン、フッ化物イオン、塩化物イオン、臭化物イオン及びヨウ化物イオンから選択される少なくとも一種の陰イオンを該金属錯体中に有する陰イオン交換体。 - 請求項1に記載の陰イオン交換体からなる陰イオン除去材。
- 該陰イオン除去材が、過塩素酸イオン、テトラフルオロホウ酸イオン、ヘキサフルオロリン酸イオン、ヘキサフルオロヒ酸イオン、ヘキサフルオロアンチモン酸イオン、メタンスルホン酸イオン、ベンゼンスルホン酸イオン、トリフルオロ酢酸イオンまたはトリフルオロメタンスルホン酸イオンを除去するための除去材である請求項2に記載の陰イオン除去材。
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