DD300106A5 - Verfahren zur herstellung von vanadiumarenen - Google Patents
Verfahren zur herstellung von vanadiumarenen Download PDFInfo
- Publication number
- DD300106A5 DD300106A5 DD340638A DD34063890A DD300106A5 DD 300106 A5 DD300106 A5 DD 300106A5 DD 340638 A DD340638 A DD 340638A DD 34063890 A DD34063890 A DD 34063890A DD 300106 A5 DD300106 A5 DD 300106A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- vanadium
- arene
- reaction
- heptane
- mesitylene
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 238000006243 chemical reaction Methods 0.000 claims abstract description 24
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 21
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 18
- -1 Vanadium arenes Chemical class 0.000 claims abstract description 15
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 13
- 241001120493 Arene Species 0.000 claims abstract description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 9
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims abstract description 9
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011701 zinc Substances 0.000 claims abstract description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000011572 manganese Substances 0.000 claims abstract description 5
- 229910052742 iron Inorganic materials 0.000 claims abstract description 4
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 4
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 4
- 150000001555 benzenes Chemical class 0.000 claims abstract description 3
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims abstract description 3
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052751 metal Inorganic materials 0.000 claims abstract description 3
- 239000002184 metal Substances 0.000 claims abstract description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 29
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 20
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 239000003638 chemical reducing agent Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 150000004292 cyclic ethers Chemical class 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 claims description 3
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 239000000376 reactant Substances 0.000 claims description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 7
- 239000005977 Ethylene Substances 0.000 abstract description 7
- 239000003054 catalyst Substances 0.000 abstract description 5
- 238000007334 copolymerization reaction Methods 0.000 abstract description 4
- 238000006116 polymerization reaction Methods 0.000 abstract description 3
- 239000004711 α-olefin Substances 0.000 abstract description 3
- GVHUQXQVSWGYSH-UHFFFAOYSA-N 4-(3-bromophenyl)-2-methyl-1,3-thiazole Chemical compound S1C(C)=NC(C=2C=C(Br)C=CC=2)=C1 GVHUQXQVSWGYSH-UHFFFAOYSA-N 0.000 abstract 1
- 239000007787 solid Substances 0.000 description 17
- 239000000725 suspension Substances 0.000 description 17
- LDMUQJXXTXSGMW-UHFFFAOYSA-I [I-].C1(=CC(=CC(=C1)C)C)C.[V+5].[I-].[I-].[I-].[I-] Chemical group [I-].C1(=CC(=CC(=C1)C)C)C.[V+5].[I-].[I-].[I-].[I-] LDMUQJXXTXSGMW-UHFFFAOYSA-I 0.000 description 10
- PSPFISPBMSHMFV-UHFFFAOYSA-N [V].C1(=CC(=CC(=C1)C)C)C Chemical group [V].C1(=CC(=CC(=C1)C)C)C PSPFISPBMSHMFV-UHFFFAOYSA-N 0.000 description 7
- 239000013078 crystal Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 239000012452 mother liquor Substances 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- 229910001516 alkali metal iodide Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Chemical compound [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- QZGUOBOGFWZQPL-UHFFFAOYSA-N 1,3,5-trimethylbenzene hydroiodide Chemical compound I.CC1=CC(C)=CC(C)=C1 QZGUOBOGFWZQPL-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- BDEDPKFUFGCVCJ-UHFFFAOYSA-N 3,6-dihydroxy-8,8-dimethyl-1-oxo-3,4,7,9-tetrahydrocyclopenta[h]isochromene-5-carbaldehyde Chemical compound O=C1OC(O)CC(C(C=O)=C2O)=C1C1=C2CC(C)(C)C1 BDEDPKFUFGCVCJ-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910021550 Vanadium Chloride Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- RPESBQCJGHJMTK-UHFFFAOYSA-I pentachlorovanadium Chemical compound [Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[V+5] RPESBQCJGHJMTK-UHFFFAOYSA-I 0.000 description 1
- NFVUDQKTAWONMJ-UHFFFAOYSA-I pentafluorovanadium Chemical compound [F-].[F-].[F-].[F-].[F-].[V+5] NFVUDQKTAWONMJ-UHFFFAOYSA-I 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G9/00—Compounds of zinc
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Polymerisation Methods In General (AREA)
- Bridges Or Land Bridges (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT8920522A IT1229737B (it) | 1989-05-16 | 1989-05-16 | Procedimento per la produzione di vanadio areni. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD300106A5 true DD300106A5 (de) | 1992-05-21 |
Family
ID=11168205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD340638A DD300106A5 (de) | 1989-05-16 | 1990-05-14 | Verfahren zur herstellung von vanadiumarenen |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US4980491A (ko) |
| EP (1) | EP0398402B1 (ko) |
| JP (1) | JP2873718B2 (ko) |
| KR (1) | KR930005258B1 (ko) |
| CN (1) | CN1024800C (ko) |
| AT (1) | ATE113954T1 (ko) |
| BR (1) | BR9002122A (ko) |
| CA (1) | CA2015997C (ko) |
| CZ (1) | CZ280389B6 (ko) |
| DD (1) | DD300106A5 (ko) |
| DE (1) | DE69013977T2 (ko) |
| DK (1) | DK0398402T3 (ko) |
| ES (1) | ES2063898T3 (ko) |
| FI (1) | FI97620C (ko) |
| HU (1) | HU208698B (ko) |
| IT (1) | IT1229737B (ko) |
| NO (1) | NO174671C (ko) |
| PL (1) | PL163355B1 (ko) |
| RU (1) | RU1838319C (ko) |
| SK (1) | SK280716B6 (ko) |
| ZA (1) | ZA903154B (ko) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1238071B (it) * | 1990-01-19 | 1993-07-03 | Enichem Anic Srl | Procedimento perfezionato per la produzione di vanadio areni |
| AU647296B2 (en) * | 1991-07-12 | 1994-03-17 | Ecp Enichem Polimeri S.R.L. | Procedure for the producing of vanadium bis-arenes from vanadium oxychloride |
| IT1269805B (it) * | 1994-05-20 | 1997-04-15 | Enichem Spa | Catalizzatore per la (co)polimerizzazione dell'etilene e procedimento per il suo ottenimento |
| JP4906480B2 (ja) * | 2006-11-27 | 2012-03-28 | 株式会社三共 | 遊技機 |
| IT1403290B1 (it) | 2010-12-27 | 2013-10-17 | Polimeri Europa Spa | Componente solido di catalizzatore, catalizzatore comprendente detto componente solido, e procedimento di (co)polimerizzazione delle alfa-olefine |
| ITMI20121724A1 (it) | 2012-10-12 | 2014-04-13 | Versalis Spa | Catalizzatore a base di rutenio e suo impiego nell'idrogenazione selettiva di composti aromatici o poliinsaturi |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3123571A (en) * | 1964-03-03 | Di-akene metal catalysts | ||
| BE551488A (ko) * | 1955-10-05 | |||
| US4526724A (en) * | 1983-09-30 | 1985-07-02 | Standard Oil Company (Indiana) | Process for the preparation of zero valent bis-arene transition metal compounds |
-
1989
- 1989-05-16 IT IT8920522A patent/IT1229737B/it active
-
1990
- 1990-04-18 DK DK90200953.9T patent/DK0398402T3/da active
- 1990-04-18 AT AT90200953T patent/ATE113954T1/de not_active IP Right Cessation
- 1990-04-18 DE DE69013977T patent/DE69013977T2/de not_active Expired - Lifetime
- 1990-04-18 ES ES90200953T patent/ES2063898T3/es not_active Expired - Lifetime
- 1990-04-18 EP EP90200953A patent/EP0398402B1/en not_active Expired - Lifetime
- 1990-04-25 ZA ZA903154A patent/ZA903154B/xx unknown
- 1990-04-25 PL PL90284934A patent/PL163355B1/pl unknown
- 1990-04-30 US US07/516,267 patent/US4980491A/en not_active Expired - Lifetime
- 1990-05-03 BR BR909002122A patent/BR9002122A/pt not_active IP Right Cessation
- 1990-05-03 CA CA002015997A patent/CA2015997C/en not_active Expired - Lifetime
- 1990-05-10 FI FI902351A patent/FI97620C/fi active IP Right Grant
- 1990-05-10 KR KR1019900006575A patent/KR930005258B1/ko not_active IP Right Cessation
- 1990-05-10 SK SK2308-90A patent/SK280716B6/sk not_active IP Right Cessation
- 1990-05-10 CZ CS902308A patent/CZ280389B6/cs not_active IP Right Cessation
- 1990-05-11 JP JP2120127A patent/JP2873718B2/ja not_active Expired - Fee Related
- 1990-05-14 NO NO902129A patent/NO174671C/no not_active IP Right Cessation
- 1990-05-14 DD DD340638A patent/DD300106A5/de unknown
- 1990-05-15 CN CN90103521A patent/CN1024800C/zh not_active Expired - Lifetime
- 1990-05-15 HU HU903046A patent/HU208698B/hu unknown
- 1990-05-15 RU SU904743897A patent/RU1838319C/ru active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2626097C2 (ko) | ||
| DE3853556T2 (de) | Homogener Zweikomponenten-Katalysator und Verfahren zur Herstellung linearer alpha-Olefine. | |
| EP0002221B1 (de) | Verfahren zur Herstellung eines Mischkatalysators und seine Verwendung zur Polymerisation von 1-Olefinen | |
| DD300106A5 (de) | Verfahren zur herstellung von vanadiumarenen | |
| DE2026032C3 (de) | Organische Zirkon und Hafnium verbindungen und deren Verwendung | |
| DE2116439A1 (de) | Verfahren zur Herstellung von Tn alkylphosphinen | |
| DE2703604C3 (de) | Verfahren zur Herstellung von Titan, oder Vanadiumtrichlorid enthaltenden Metallchloridgemischen und deren Verwendung in Polymerisationskatalysatoren für Olefine | |
| DE2007535A1 (de) | Verfahren zur Herstellung von Triarylphosphinen | |
| DE1132923B (de) | Verfahren zur Herstellung von metallorganischen Komplexverbindungen des Palladiums | |
| DE69022207T2 (de) | Verfahren zur Herstellung von Vanadium-arenen. | |
| DE69213605T2 (de) | Verfahren zur Herstellung von Vanadium-bisarenen aus Vanadiumoxychlorid | |
| EP0250860A2 (de) | Verfahren zum Herstellen von Homo-sowie Copolymerisaten des Ethens durch Phillips-Katalyse | |
| DE1090662B (de) | Verfahren zur Herstellung von Aluminiumtrialkylen | |
| DE1176867B (de) | Verfahren zur Herstellung von Polybuten | |
| DE2828953A1 (de) | Chemische verbindungen auf der basis von titantrihalogeniden, verfahren zu ihrer herstellung und ihre verwendung als katalysatoren | |
| DE1805318C3 (de) | Verfahren zur Herstellung von Vinylfluorid und 1,1-Difluoräthan | |
| Klepp et al. | Na2HgS2 und K2HgS2, zwei Thiomercurate mit isolierten Anionen/Na2HgS2 and K2HgS2, Two Thiomercurates with Discrete Anions | |
| DE2516857C3 (de) | Katalysator zur Polymerisation von a -Olefinen auf der Basis von Aluminium-, Mangan - und Titanverbindungen, Verfahren zu dessen Herstellung und seine Verwendung | |
| DE4415725A1 (de) | Verfahren zur Herstellung von Komplexen des Nickel(II), enthaltend einen heterodifunktionellen Chelatliganden und Verfahren zur Polymerisation von Ethylen mit den derart erhaltenen Komplexen | |
| AT224904B (de) | Verfahren zur Polymerisation von α-Olefinen | |
| DE2808074A1 (de) | Neue, substituierte, methylenueberbrueckte aluminiumoligomere | |
| AT231154B (de) | Verfahren zur Herstellung einer kristallinen Polymerisationskatalysatorzusammensetzung | |
| AT234381B (de) | Verfahren zur Polymerisation von Vinylchlorid zu kristallinen Polymeren | |
| AT202766B (de) | Verfahren zur Herstellung von hochmolekularen Polyäthylenen | |
| DE1593549C (de) | Verfahren zur Herstellung von Bis-(pi-allyl)-nickelverbindungen |