JPS6261959A - 導電性有機化合物 - Google Patents

導電性有機化合物

Info

Publication number: JPS6261959A
Authority: JP; Japan
Prior art keywords: complex; tcnq; formula; electrically conductive; compound
Prior art date: 1985-09-11
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

Application number

JP20083985A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0515700B2 (fr

Inventor

Toshio Mukai

向井　利夫

Takao Yamashita

敬郎山下

Koju Hagitani

弘寿萩谷

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Takasago International Corp

Takasago Corp

Original Assignee

Takasago Perfumery Industry Co

Takasago Corp

Priority date (The priority date 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 date listed.)

1985-09-11

Filing date

1985-09-11

Publication date

1987-03-18

1985-09-11 Application filed by Takasago Perfumery Industry Co, Takasago Corp filed Critical Takasago Perfumery Industry Co

1985-09-11 Priority to JP20083985A priority Critical patent/JPS6261959A/ja

1987-03-18 Publication of JPS6261959A publication Critical patent/JPS6261959A/ja

1993-03-02 Publication of JPH0515700B2 publication Critical patent/JPH0515700B2/ja

Status Granted legal-status Critical Current

Links

150000002894 organic compounds Chemical class 0.000 title abstract description 15
125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 3
239000000126 substance Substances 0.000 claims description 6
125000003277 amino group Chemical class 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 abstract description 43
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract description 27
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 24
238000009835 boiling Methods 0.000 abstract description 22
-1 tetrafluoroborate Chemical compound 0.000 abstract description 21
150000001875 compounds Chemical class 0.000 abstract description 16
239000000463 material Substances 0.000 abstract description 9
OJOSABWCUVCSTQ-UHFFFAOYSA-N cyclohepta-2,4,6-trienylium Chemical compound C1=CC=C[CH+]=C[CH]1 OJOSABWCUVCSTQ-UHFFFAOYSA-N 0.000 abstract description 8
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 abstract description 4
239000002994 raw material Substances 0.000 abstract description 4
239000000470 constituent Substances 0.000 abstract description 2
239000012799 electrically-conductive coating Substances 0.000 abstract 1
239000000976 ink Substances 0.000 abstract 1
239000004973 liquid crystal related substance Substances 0.000 abstract 1
238000002360 preparation method Methods 0.000 abstract 1
125000002924 primary amino group Chemical class [H]N([H])* 0.000 abstract 1
239000013078 crystal Substances 0.000 description 13
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
230000015572 biosynthetic process Effects 0.000 description 8
238000003786 synthesis reaction Methods 0.000 description 8
230000000704 physical effect Effects 0.000 description 7
FHCPAXDKURNIOZ-UHFFFAOYSA-N tetrathiafulvalene Chemical compound S1C=CSC1=C1SC=CS1 FHCPAXDKURNIOZ-UHFFFAOYSA-N 0.000 description 5
238000000034 method Methods 0.000 description 4
MMSNCFMJAHZABL-UHFFFAOYSA-N CN[C+]1C=CC=CC=C1 Chemical compound CN[C+]1C=CC=CC=C1 MMSNCFMJAHZABL-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
FEPMURGXOVQVMU-UHFFFAOYSA-N CS[C+]1C=CC=CC=C1 Chemical compound CS[C+]1C=CC=CC=C1 FEPMURGXOVQVMU-UHFFFAOYSA-N 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
ICMGEDLKPRIZQA-UHFFFAOYSA-N cyclohepta-2,4,6-trien-1-ylidene(ethyl)oxidanium Chemical compound C(C)O[C+]1C=CC=CC=C1 ICMGEDLKPRIZQA-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000000465 moulding Methods 0.000 description 2
239000000843 powder Substances 0.000 description 2
KFQLMCTXXYOOPK-UHFFFAOYSA-N (2-methoxycyclohepta-2,4,6-trien-1-ylidene)-methyloxidanium Chemical compound COC1=CC=CC=CC1=[O+]C KFQLMCTXXYOOPK-UHFFFAOYSA-N 0.000 description 1
XZPNVGKRRGOOMS-UHFFFAOYSA-N 10-methyl-5h-phenazine Chemical compound C1=CC=C2N(C)C3=CC=CC=C3NC2=C1 XZPNVGKRRGOOMS-UHFFFAOYSA-N 0.000 description 1
YMWLPMGFZYFLRP-UHFFFAOYSA-N 2-(4,5-dimethyl-1,3-diselenol-2-ylidene)-4,5-dimethyl-1,3-diselenole Chemical compound [Se]1C(C)=C(C)[Se]C1=C1[Se]C(C)=C(C)[Se]1 YMWLPMGFZYFLRP-UHFFFAOYSA-N 0.000 description 1
BAEWLQWSDPXZDM-UHFFFAOYSA-N 2-[2-(dimethylamino)ethyldisulfanyl]-n,n-dimethylethanamine Chemical compound CN(C)CCSSCCN(C)C BAEWLQWSDPXZDM-UHFFFAOYSA-N 0.000 description 1
KTHCAULZPANDON-UHFFFAOYSA-N CN(C)[C+]1C=CC=CC=C1 Chemical compound CN(C)[C+]1C=CC=CC=C1 KTHCAULZPANDON-UHFFFAOYSA-N 0.000 description 1
101100258233 Caenorhabditis elegans sun-1 gene Proteins 0.000 description 1
BBHWMHOTBMSPFJ-UHFFFAOYSA-M Cl(=O)(=O)(=O)[O-].Cl[C+]1C=CC=CC=C1 Chemical compound Cl(=O)(=O)(=O)[O-].Cl[C+]1C=CC=CC=C1 BBHWMHOTBMSPFJ-UHFFFAOYSA-M 0.000 description 1
241000934653 Dero Species 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
238000007385 chemical modification Methods 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
QMPFGJUWNZILPF-UHFFFAOYSA-N cyclohepta-2,4,6-trien-1-ylidene(methyl)oxidanium Chemical compound C[O+]=C1C=CC=CC=C1 QMPFGJUWNZILPF-UHFFFAOYSA-N 0.000 description 1
238000009795 derivation Methods 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
239000003205 fragrance Substances 0.000 description 1
230000000968 intestinal effect Effects 0.000 description 1
230000015654 memory Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
238000012552 review Methods 0.000 description 1
230000002269 spontaneous effect Effects 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 1
ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP20083985A 1985-09-11 1985-09-11 導電性有機化合物 Granted JPS6261959A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP20083985A JPS6261959A (ja)	1985-09-11	1985-09-11	導電性有機化合物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP20083985A JPS6261959A (ja)	1985-09-11	1985-09-11	導電性有機化合物

Publications (2)

Publication Number	Publication Date
JPS6261959A true JPS6261959A (ja)	1987-03-18
JPH0515700B2 JPH0515700B2 (fr)	1993-03-02

Family

ID=16431063

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP20083985A Granted JPS6261959A (ja)	1985-09-11	1985-09-11	導電性有機化合物

Country Status (1)

Country	Link
JP (1)	JPS6261959A (fr)

1985
- 1985-09-11 JP JP20083985A patent/JPS6261959A/ja active Granted

Also Published As

Publication number	Publication date
JPH0515700B2 (fr)	1993-03-02

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