JP2014152114A - 有機金属錯体 - Google Patents
有機金属錯体 Download PDFInfo
- Publication number
- JP2014152114A JP2014152114A JP2013020800A JP2013020800A JP2014152114A JP 2014152114 A JP2014152114 A JP 2014152114A JP 2013020800 A JP2013020800 A JP 2013020800A JP 2013020800 A JP2013020800 A JP 2013020800A JP 2014152114 A JP2014152114 A JP 2014152114A
- Authority
- JP
- Japan
- Prior art keywords
- group
- atom
- carbon atoms
- organometallic complex
- mmol
- 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
- 125000002524 organometallic group Chemical group 0.000 title claims abstract description 50
- 125000001424 substituent group Chemical group 0.000 claims abstract description 65
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 50
- 125000004429 atom Chemical group 0.000 claims abstract description 29
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 26
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 25
- 229910052751 metal Inorganic materials 0.000 claims abstract description 23
- 239000002184 metal Substances 0.000 claims abstract description 23
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 21
- 125000003118 aryl group Chemical group 0.000 claims description 23
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
- 150000001721 carbon Chemical group 0.000 claims description 14
- 125000005842 heteroatom Chemical group 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000004122 cyclic group Chemical group 0.000 claims description 9
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 125000001769 aryl amino group Chemical group 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- 150000008282 halocarbons Chemical group 0.000 claims description 6
- 229910052782 aluminium Chemical group 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 239000011777 magnesium Chemical group 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- 239000011701 zinc Chemical group 0.000 claims description 4
- 229910052790 beryllium Inorganic materials 0.000 claims description 3
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical group [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 150000004696 coordination complex Chemical class 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 23
- 230000000737 periodic effect Effects 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 45
- -1 phenyloxy group Chemical group 0.000 description 23
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 20
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 18
- 239000000047 product Substances 0.000 description 16
- 238000005160 1H NMR spectroscopy Methods 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- 238000001914 filtration Methods 0.000 description 14
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical class ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 12
- 229910052938 sodium sulfate Inorganic materials 0.000 description 12
- 235000011152 sodium sulphate Nutrition 0.000 description 12
- 239000003446 ligand Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 238000005259 measurement Methods 0.000 description 10
- 239000012044 organic layer Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 8
- 125000000304 alkynyl group Chemical group 0.000 description 6
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 5
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000005281 excited state Effects 0.000 description 5
- 238000010898 silica gel chromatography Methods 0.000 description 5
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 description 4
- LBVKVHPNSXYVJM-UHFFFAOYSA-N 2-(1,2,4-triazol-1-yl)phenol Chemical compound OC1=CC=CC=C1N1N=CN=C1 LBVKVHPNSXYVJM-UHFFFAOYSA-N 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- UXVGOLIOXDSSBU-UHFFFAOYSA-N C1=CC=C(C=C1)C2=NN=NN2C3=CC=CC=C3O Chemical compound C1=CC=C(C=C1)C2=NN=NN2C3=CC=CC=C3O UXVGOLIOXDSSBU-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(i) oxide Chemical compound [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 239000007850 fluorescent dye Substances 0.000 description 4
- 239000003269 fluorescent indicator Substances 0.000 description 4
- 239000000976 ink Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 238000006467 substitution reaction Methods 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- 235000005074 zinc chloride Nutrition 0.000 description 4
- 239000011592 zinc chloride Substances 0.000 description 4
- HQFONKQSJMKSTJ-UHFFFAOYSA-N C1=CC=C(C=C1)C2=NC=NN2C3=CC=CC=C3O Chemical compound C1=CC=C(C=C1)C2=NC=NN2C3=CC=CC=C3O HQFONKQSJMKSTJ-UHFFFAOYSA-N 0.000 description 3
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 125000002015 acyclic group Chemical group 0.000 description 3
- RBHJBMIOOPYDBQ-UHFFFAOYSA-N carbon dioxide;propan-2-one Chemical compound O=C=O.CC(C)=O RBHJBMIOOPYDBQ-UHFFFAOYSA-N 0.000 description 3
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 3
- 125000004986 diarylamino group Chemical group 0.000 description 3
- 238000002189 fluorescence spectrum Methods 0.000 description 3
- 238000004770 highest occupied molecular orbital Methods 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 0 **1C(*)(*)COc2c(*)c(*)c(*)c(*)c2[*@]1*=** Chemical compound **1C(*)(*)COc2c(*)c(*)c(*)c(*)c2[*@]1*=** 0.000 description 2
- RRACAHMQZYFWLF-UHFFFAOYSA-N 1-(2-methoxyphenyl)-1,2,4-triazole Chemical compound COC1=CC=CC=C1N1N=CN=C1 RRACAHMQZYFWLF-UHFFFAOYSA-N 0.000 description 2
- WYSAWGCLEHCQLX-UHFFFAOYSA-N 2-azidophenol Chemical compound OC1=CC=CC=C1N=[N+]=[N-] WYSAWGCLEHCQLX-UHFFFAOYSA-N 0.000 description 2
- WWWLBYHLEISWKK-UHFFFAOYSA-N COC1=CC=CC=C1N2C(=NC=N2)C3=CC=CC=C3 Chemical compound COC1=CC=CC=C1N2C(=NC=N2)C3=CC=CC=C3 WWWLBYHLEISWKK-UHFFFAOYSA-N 0.000 description 2
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical group C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical group C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 239000013522 chelant Substances 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- DHRRIBDTHFBPNG-UHFFFAOYSA-L magnesium dichloride hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-] DHRRIBDTHFBPNG-UHFFFAOYSA-L 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 150000003852 triazoles Chemical class 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 2
- 238000003828 vacuum filtration Methods 0.000 description 2
- ROEQGIFOWRQYHD-UHFFFAOYSA-N (2-methoxyphenyl)boronic acid Chemical compound COC1=CC=CC=C1B(O)O ROEQGIFOWRQYHD-UHFFFAOYSA-N 0.000 description 1
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 1
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 description 1
- GGUWDWFMZXFXNY-UHFFFAOYSA-N 1-(2-methoxyphenyl)-5-phenyltetrazole Chemical compound COC1=CC=CC=C1N1C(C=2C=CC=CC=2)=NN=N1 GGUWDWFMZXFXNY-UHFFFAOYSA-N 0.000 description 1
- DVQWNQBEUKXONL-UHFFFAOYSA-N 1-iodo-2-methoxybenzene Chemical compound COC1=CC=CC=C1I DVQWNQBEUKXONL-UHFFFAOYSA-N 0.000 description 1
- 125000006017 1-propenyl group Chemical group 0.000 description 1
- 125000000530 1-propynyl group Chemical group [H]C([H])([H])C#C* 0.000 description 1
- BIOOHCOTKZDTIH-UHFFFAOYSA-N 2-(4-phenyltriazol-1-yl)phenol Chemical compound Oc1ccccc1-n1cc(nn1)-c1ccccc1 BIOOHCOTKZDTIH-UHFFFAOYSA-N 0.000 description 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical group N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- PPWNCLVNXGCGAF-UHFFFAOYSA-N 3,3-dimethylbut-1-yne Chemical group CC(C)(C)C#C PPWNCLVNXGCGAF-UHFFFAOYSA-N 0.000 description 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
- MARUHZGHZWCEQU-UHFFFAOYSA-N 5-phenyl-2h-tetrazole Chemical compound C1=CC=CC=C1C1=NNN=N1 MARUHZGHZWCEQU-UHFFFAOYSA-N 0.000 description 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- DANGZESZOLXEIQ-UHFFFAOYSA-N C(C)(C)(C)C=1N=NN(C=1)C1=C(C=CC=C1)O Chemical compound C(C)(C)(C)C=1N=NN(C=1)C1=C(C=CC=C1)O DANGZESZOLXEIQ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical class CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Chemical group C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 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
- 150000007960 acetonitrile Chemical class 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000005224 alkoxybenzenes Chemical class 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- YCOXTKKNXUZSKD-UHFFFAOYSA-N as-o-xylenol Natural products CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 1
- 229910000024 caesium carbonate Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 230000005283 ground state Effects 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000005446 heptyloxy 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])O* 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- SNHMUERNLJLMHN-UHFFFAOYSA-N iodobenzene Chemical compound IC1=CC=CC=C1 SNHMUERNLJLMHN-UHFFFAOYSA-N 0.000 description 1
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 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
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([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
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- LZWQNOHZMQIFBX-UHFFFAOYSA-N lithium;2-methylpropan-2-olate Chemical compound [Li+].CC(C)(C)[O-] LZWQNOHZMQIFBX-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005447 octyloxy 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])O* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- WUHLVXDDBHWHLQ-UHFFFAOYSA-N pentazole Chemical compound N=1N=NNN=1 WUHLVXDDBHWHLQ-UHFFFAOYSA-N 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052706 scandium Inorganic materials 0.000 description 1
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 125000003638 stannyl group Chemical group [H][Sn]([H])([H])* 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 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
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- DJWUNCQRNNEAKC-UHFFFAOYSA-L zinc acetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O DJWUNCQRNNEAKC-UHFFFAOYSA-L 0.000 description 1
Abstract
Description
以下に本発明を詳述する。
上記炭素数1〜20の炭化水素基は、メチル基、エチル基、プロピル基、イソプロピル基、ブチル基、イソブチル基、tert−ブチル基、ヘキシル基、オクチル基等の炭素数1〜12の直鎖状若しくは分岐鎖状アルキル基;ビニル基、1−プロペニル基、アリル基、スチリル基等の炭素数2〜12のアルケニル基;エチニル基、1−プロピニル基、プロパルギル基等の炭素数2〜12のアルキニル基;シクロペンチル基、シクロヘキシル基、シクロヘプチル基等の炭素数5〜12の環状アルキル基;アルキル基、アルケニル基、アルキニル基等で置換されていてもよい炭素数6〜20のアリール基が挙げられる。
上記炭素数1〜12のハロゲン化炭化水素基は、上述したもののうち、その炭素数が1〜8であることが好ましい。より好ましくは、1〜6である。
上記炭素数0〜12のヘテロ原子含有環基は、上述したもののうち、その炭素数が1〜8であることが好ましい。より好ましくは、1〜6である。
上記炭素数1〜12のアルコキシ基は、上述したもののうち、その炭素数が1〜8であることが好ましい。より好ましくは、1〜6である。更に好ましくは、1〜3である。
上記炭素数6〜12のアリールオキシ基は、上述したもののうち、その炭素数が6〜10であることが好ましい。より好ましくは、6〜8である。更に好ましくは、6である。
上記炭素数1〜12のアルキルアミノ基は、上述したもののうち、その炭素数が1〜8であることが好ましい。より好ましくは、1〜6である。更に好ましくは、1〜4である。
上記炭素数6〜18のアリールアミノ基は、上述したもののうち、その炭素数が8〜18であることが好ましい。より好ましくは、12〜18である。更に好ましくは、12である。
上記アルコキシ体は、例えば、環構成原子として窒素原子をもつ五員環の芳香族化合物と、オルト位の炭素上の水素がハロゲン原子等の反応性基に置換されたフェノールとを有機溶媒等の溶媒中で触媒の存在下反応させることにより得ることができる。また、オルト位の炭素上に置換基を有するアルコキシベンゼンにおいて、該置換基の一部を環化させて得ることもできる。
本発明の有機金属錯体は、上記配位子を、金属塩と中性若しくは塩基性条件下で反応させることにより得ることができる。ただし、本発明の有機金属錯体の製造方法は、これに制限されない。
本発明の有機金属錯体のHOMOとLUMOのエネルギー準位の差は、紫外可視分光分析(UV−Vis)により測定する方法で評価することができる。
(1H−NMR測定)
試料をテトラメチルシランを含有する重クロロホルムまたは重ジメチルスルホキシドに溶解し、核磁気共鳴装置(Gemini2000、400MHz、Varian社製)により測定した。
(蛍光スペクトル測定)
試料をジメチルホルムアミドの希薄溶液とし、蛍光分光光度計(F−7000、日立ハイテクノロジーズ社製)を用いて、蛍光スペクトルを測定した。励起波長は350nmとし、発光強度が最大となるところを蛍光波長(λmax)とした。
(熱分解温度測定)
示差熱熱重量同時測定装置(TG/DTA6200、セイコー・インスツル株式会社製)を用いて、約5mgの試料(錯体化合物)をアルミニウムパンにいれ、以下のようにして測定した。
測定温度の範囲:室温〜500℃
昇温速度:10℃/min
得られた熱分解曲線において急激に重量減少が見られたところを熱分解温度とした。
1−(2−メトキシフェニル)−1H−1,2,4−トリアゾール
1−(2−メトキシフェニル)−5−フェニル−1H−1,2,4−トリアゾール
1−(2−メトキシフェニル)−5−フェニル−1H−テトラゾール
2−(4−フェニル−1H−1,2,3−トリアゾール−1−イル)フェノール
2−(4−(tert−ブチル)−1H−1,2,3−トリアゾール−1−イル)フェノール
Claims (4)
- 下記一般式(1)で表されることを特徴とする有機金属錯体。
- 前記中心金属原子Mが、ベリリウム、マグネシウム、亜鉛、又は、アルミニウムを表す
ことを特徴とする請求項1に記載の有機金属錯体。 - 前記一般式(1)中、X1〜X3が有していてもよい1価の置換基、及び、R1〜R4における1価の置換基は、ハロゲン原子、炭素数1〜20の炭化水素基、炭素数1〜12のハロゲン化炭化水素基、炭素数0〜12のヘテロ原子含有環基、シアノ基、炭素数1〜12のアルコキシ基、炭素数6〜12のアリールオキシ基、炭素数1〜12のアルキルアミノ基、又は、炭素数6〜18のアリールアミノ基である
ことを特徴とする請求項1又は2に記載の有機金属錯体。 - 前記X1〜X3の1つ又は2つが窒素原子を表す
ことを特徴とする請求項1〜3のいずれかに記載の有機金属錯体。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013020800A JP6009957B2 (ja) | 2013-02-05 | 2013-02-05 | 有機金属錯体 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013020800A JP6009957B2 (ja) | 2013-02-05 | 2013-02-05 | 有機金属錯体 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2014152114A true JP2014152114A (ja) | 2014-08-25 |
JP6009957B2 JP6009957B2 (ja) | 2016-10-19 |
Family
ID=51574336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013020800A Expired - Fee Related JP6009957B2 (ja) | 2013-02-05 | 2013-02-05 | 有機金属錯体 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP6009957B2 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105694860A (zh) * | 2016-03-23 | 2016-06-22 | 桂林理工大学 | 发光材料[Cd(tidc)2]n及合成方法 |
CN105694861A (zh) * | 2016-03-23 | 2016-06-22 | 桂林理工大学 | 发光材料[Mn(tibc)2]n及合成方法 |
CN105694862A (zh) * | 2016-03-23 | 2016-06-22 | 桂林理工大学 | 发光材料[Zn(tibc)2]n及合成方法 |
CN105801504A (zh) * | 2016-03-23 | 2016-07-27 | 桂林理工大学 | 发光材料[Cd(tibc)2]n及合成方法 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105647521B (zh) * | 2016-03-23 | 2018-01-12 | 桂林理工大学 | 发光材料[Mn(tidc)2]n及合成方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11144872A (ja) * | 1997-11-11 | 1999-05-28 | Fuji Photo Film Co Ltd | 有機エレクトロルミネツセンス素子材料およびそれを使用した有機エレクトロルミネツセンス素子 |
JP2000302754A (ja) * | 1999-02-15 | 2000-10-31 | Fuji Photo Film Co Ltd | 含窒素ヘテロ環化合物、有機発光素子材料、有機発光素子 |
JP2001040346A (ja) * | 1999-07-30 | 2001-02-13 | Fuji Photo Film Co Ltd | 発光素子材料およびそれを使用した発光素子 |
JP2001271063A (ja) * | 2000-03-27 | 2001-10-02 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子用材料およびそれを使用した有機エレクトロルミネッセンス素子 |
JP2002305083A (ja) * | 2001-04-04 | 2002-10-18 | Mitsubishi Chemicals Corp | 有機電界発光素子 |
-
2013
- 2013-02-05 JP JP2013020800A patent/JP6009957B2/ja not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11144872A (ja) * | 1997-11-11 | 1999-05-28 | Fuji Photo Film Co Ltd | 有機エレクトロルミネツセンス素子材料およびそれを使用した有機エレクトロルミネツセンス素子 |
JP2000302754A (ja) * | 1999-02-15 | 2000-10-31 | Fuji Photo Film Co Ltd | 含窒素ヘテロ環化合物、有機発光素子材料、有機発光素子 |
JP2001040346A (ja) * | 1999-07-30 | 2001-02-13 | Fuji Photo Film Co Ltd | 発光素子材料およびそれを使用した発光素子 |
JP2001271063A (ja) * | 2000-03-27 | 2001-10-02 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子用材料およびそれを使用した有機エレクトロルミネッセンス素子 |
JP2002305083A (ja) * | 2001-04-04 | 2002-10-18 | Mitsubishi Chemicals Corp | 有機電界発光素子 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105694860A (zh) * | 2016-03-23 | 2016-06-22 | 桂林理工大学 | 发光材料[Cd(tidc)2]n及合成方法 |
CN105694861A (zh) * | 2016-03-23 | 2016-06-22 | 桂林理工大学 | 发光材料[Mn(tibc)2]n及合成方法 |
CN105694862A (zh) * | 2016-03-23 | 2016-06-22 | 桂林理工大学 | 发光材料[Zn(tibc)2]n及合成方法 |
CN105801504A (zh) * | 2016-03-23 | 2016-07-27 | 桂林理工大学 | 发光材料[Cd(tibc)2]n及合成方法 |
CN105801504B (zh) * | 2016-03-23 | 2018-01-12 | 桂林理工大学 | 发光材料[Cd(tibc)2]n及合成方法 |
Also Published As
Publication number | Publication date |
---|---|
JP6009957B2 (ja) | 2016-10-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR102349659B1 (ko) | 개질된 방출 스펙트럼을 갖는 인광성 네자리 금속 착물 | |
WO2018071697A1 (en) | Narrow band red phosphorescent tetradentate platinum (ii) complexes | |
JP6009957B2 (ja) | 有機金属錯体 | |
KR20190106811A (ko) | 청색 및 협대역 녹색 및 적색 발광 금속 착체 | |
JP5959171B2 (ja) | π共役有機ホウ素化合物及びその製造方法 | |
KR20110131200A (ko) | 피리딜트리아졸 리간드를 함유하는 인광성 발광 이리듐 착물 | |
JP2007045742A (ja) | 遷移金属錯体の製造方法及び遷移金属錯体 | |
Nie et al. | Two novel six-coordinated cadmium (II) and zinc (II) complexes from carbazate β-diketonate: crystal structures, enhanced two-photon absorption and biological imaging application | |
JP2005239648A (ja) | キノキサリン構造を含む有機金属化合物及び発光素子 | |
Zhan et al. | Mechanofluorochromism based on BOPIM complexes: the effect of substituents and regulation of the direction of the emission color changes | |
Francis et al. | Achieving visible light excitation in carbazole-based Eu 3+–β-diketonate complexes via molecular engineering | |
JP6551399B2 (ja) | 有機金属錯体の合成方法 | |
Tomashenko et al. | A new heterocyclic skeleton with highly tunable absorption/emission wavelength via H-bonding | |
JP7222517B2 (ja) | 新規化合物及びその製造方法 | |
JP2004331586A (ja) | 1,10−フェナントロリン誘導体、キレート配位子及び1,10−フェナントロリン誘導体の製造方法 | |
JP6009958B2 (ja) | 有機金属錯体 | |
JP3321599B2 (ja) | 発光材料 | |
FehÚr et al. | A modular synthesis of 1, 4, 5-trisubstituted 1, 2, 3-triazoles with ferrocene moieties | |
JP2019112387A (ja) | 有機発光素子材料合成用原料および化合物 | |
JP2014152119A (ja) | 有機金属錯体 | |
JP6059544B2 (ja) | 有機金属錯体 | |
Chen et al. | Fluorescent mesogenic boron difluoride complexes derived from heterocyclic benzoxazoles | |
JP2014152120A (ja) | 有機金属錯体 | |
US20230137820A1 (en) | PHOSPHORESCENT aNHC-BASED PLATINUM (II) COMPLEXES | |
JP6687240B2 (ja) | 新規化合物、化学センサー、センシング装置及びセンシング方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20151106 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20160607 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20160609 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20160803 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20160823 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20160915 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6009957 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
LAPS | Cancellation because of no payment of annual fees |