GB935716A - Complexes of transition metals and the production thereof - Google Patents
Complexes of transition metals and the production thereofInfo
- Publication number
- GB935716A GB935716A GB14157/61A GB1415761A GB935716A GB 935716 A GB935716 A GB 935716A GB 14157/61 A GB14157/61 A GB 14157/61A GB 1415761 A GB1415761 A GB 1415761A GB 935716 A GB935716 A GB 935716A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nickel
- triphenylphosphine
- complex
- bis
- 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.)
- Expired
Links
- 229910052723 transition metal Inorganic materials 0.000 title abstract 7
- 150000003624 transition metals Chemical class 0.000 title abstract 7
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 18
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 14
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 abstract 4
- -1 iron group metals Chemical class 0.000 abstract 4
- 150000002902 organometallic compounds Chemical class 0.000 abstract 4
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 abstract 4
- 230000000737 periodic effect Effects 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 3
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 3
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 abstract 2
- FSJSYDFBTIVUFD-SUKNRPLKSA-N (z)-4-hydroxypent-3-en-2-one;oxovanadium Chemical compound [V]=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FSJSYDFBTIVUFD-SUKNRPLKSA-N 0.000 abstract 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 239000011651 chromium Substances 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- FGOJWZOJZYATBO-UHFFFAOYSA-N cycloocta-1,3-diene nickel triphenylphosphane Chemical compound [Ni].C1CCC=CC=CC1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 FGOJWZOJZYATBO-UHFFFAOYSA-N 0.000 abstract 2
- KDUIUFJBNGTBMD-VXMYFEMYSA-N cyclooctatetraene Chemical compound C1=C\C=C/C=C\C=C1 KDUIUFJBNGTBMD-VXMYFEMYSA-N 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 229910052759 nickel Inorganic materials 0.000 abstract 2
- KFBKRCXOTTUAFS-UHFFFAOYSA-N nickel;triphenylphosphane Chemical compound [Ni].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 KFBKRCXOTTUAFS-UHFFFAOYSA-N 0.000 abstract 2
- UYLRKRLDQUXYKB-UHFFFAOYSA-N nickel;triphenylphosphane Chemical compound [Ni].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 UYLRKRLDQUXYKB-UHFFFAOYSA-N 0.000 abstract 2
- MFWFDRBPQDXFRC-LNTINUHCSA-N (z)-4-hydroxypent-3-en-2-one;vanadium Chemical compound [V].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O MFWFDRBPQDXFRC-LNTINUHCSA-N 0.000 abstract 1
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 abstract 1
- JHLUZZZZJZJUTJ-UHFFFAOYSA-N 3-methylhepta-1,3,5-triene Chemical compound CC=CC=C(C)C=C JHLUZZZZJZJUTJ-UHFFFAOYSA-N 0.000 abstract 1
- YASRNBSGIQYQBR-UHFFFAOYSA-N C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.[Ni].C1(=CC=CC=C1)C=CC1=CC=CC=C1 Chemical compound C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)P(C1=CC=CC=C1)C1=CC=CC=C1.[Ni].C1(=CC=CC=C1)C=CC1=CC=CC=C1 YASRNBSGIQYQBR-UHFFFAOYSA-N 0.000 abstract 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 abstract 1
- 239000007983 Tris buffer Substances 0.000 abstract 1
- OXWQZBNKPCTXDU-UHFFFAOYSA-N [Ni].C1(=CC=CC=C1)C=CC1=CC=CC=C1.C1(=CC=CC=C1)C=CC1=CC=CC=C1.C1(=CC=CC=C1)C=CC1=CC=CC=C1 Chemical compound [Ni].C1(=CC=CC=C1)C=CC1=CC=CC=C1.C1(=CC=CC=C1)C=CC1=CC=CC=C1.C1(=CC=CC=C1)C=CC1=CC=CC=C1 OXWQZBNKPCTXDU-UHFFFAOYSA-N 0.000 abstract 1
- 125000005595 acetylacetonate group Chemical group 0.000 abstract 1
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Natural products CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001399 aluminium compounds Chemical class 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 229940077746 antacid containing aluminium compound Drugs 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- DEQICGUGLGTBOG-UHFFFAOYSA-N chromium;1,2,3,4,5,6-hexamethylbenzene Chemical compound [Cr].CC1=C(C)C(C)=C(C)C(C)=C1C.CC1=C(C)C(C)=C(C)C(C)=C1C DEQICGUGLGTBOG-UHFFFAOYSA-N 0.000 abstract 1
- 229910017052 cobalt Inorganic materials 0.000 abstract 1
- 239000010941 cobalt Substances 0.000 abstract 1
- FJDJVBXSSLDNJB-LNTINUHCSA-N cobalt;(z)-4-hydroxypent-3-en-2-one Chemical compound [Co].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FJDJVBXSSLDNJB-LNTINUHCSA-N 0.000 abstract 1
- AIDLQXQSZXEEKY-UHFFFAOYSA-N cobalt;triphenylphosphane Chemical compound [Co].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 AIDLQXQSZXEEKY-UHFFFAOYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 150000004292 cyclic ethers Chemical class 0.000 abstract 1
- ZOLLIQAKMYWTBR-RYMQXAEESA-N cyclododecatriene Chemical compound C/1C\C=C\CC\C=C/CC\C=C\1 ZOLLIQAKMYWTBR-RYMQXAEESA-N 0.000 abstract 1
- UESBLKLLGXUHTC-UHFFFAOYSA-N cyclooctatetraene manganese Chemical compound [Mn].[Mn].C1=CC=CC=CC=C1 UESBLKLLGXUHTC-UHFFFAOYSA-N 0.000 abstract 1
- LAXQRXAXGJFQJS-UHFFFAOYSA-N cyclooctatetraene titanium Chemical compound [Ti].[Ti].C1=CC=CC=CC=C1.C1=CC=CC=CC=C1.C1=CC=CC=CC=C1 LAXQRXAXGJFQJS-UHFFFAOYSA-N 0.000 abstract 1
- 150000001993 dienes Chemical class 0.000 abstract 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 abstract 1
- 125000005594 diketone group Chemical group 0.000 abstract 1
- 239000000539 dimer Substances 0.000 abstract 1
- 238000006471 dimerization reaction Methods 0.000 abstract 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 abstract 1
- 125000002534 ethynyl group Chemical class [H]C#C* 0.000 abstract 1
- LZKLAOYSENRNKR-LNTINUHCSA-N iron;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Fe].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O LZKLAOYSENRNKR-LNTINUHCSA-N 0.000 abstract 1
- 229910052748 manganese Inorganic materials 0.000 abstract 1
- 239000011572 manganese Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- WIKHEOPGBUXIRS-UHFFFAOYSA-N nickel 1,2,3-triphenyl-4-(2-phenylethenyl)benzene Chemical compound [Ni].C1(=CC=CC=C1)C1=C(C(=C(C=C1)C=CC1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)C1=C(C(=C(C=C1)C=CC1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)C1=C(C(=C(C=C1)C=CC1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1.C1(=CC=CC=C1)C1=C(C(=C(C=C1)C=CC1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1 WIKHEOPGBUXIRS-UHFFFAOYSA-N 0.000 abstract 1
- HSZUNZSKBHOIAA-UHFFFAOYSA-N nickel triphenylarsane Chemical compound [Ni].c1ccc(cc1)[As](c1ccccc1)c1ccccc1.c1ccc(cc1)[As](c1ccccc1)c1ccccc1.c1ccc(cc1)[As](c1ccccc1)c1ccccc1.c1ccc(cc1)[As](c1ccccc1)c1ccccc1 HSZUNZSKBHOIAA-UHFFFAOYSA-N 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 150000003623 transition metal compounds Chemical class 0.000 abstract 1
- GEQBPMNDDHGGPJ-UHFFFAOYSA-N tri(piperidin-1-yl)phosphane Chemical compound C1CCCCN1P(N1CCCCC1)N1CCCCC1 GEQBPMNDDHGGPJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000013638 trimer Substances 0.000 abstract 1
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 abstract 1
- 229910052720 vanadium Inorganic materials 0.000 abstract 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
- B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
- B01J31/2234—Beta-dicarbonyl ligands, e.g. acetylacetonates
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2282—Unsaturated compounds used as ligands
- B01J31/2291—Olefins
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- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2282—Unsaturated compounds used as ligands
- B01J31/2295—Cyclic compounds, e.g. cyclopentadienyls
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- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
- B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
- C07C2/38—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of dienes or alkynes
- C07C2/40—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of dienes or alkynes of conjugated dienes
- C07C2/403—Catalytic processes
- C07C2/406—Catalytic processes with hydrides or organic compounds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/42—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons homo- or co-oligomerisation with ring formation, not being a Diels-Alder conversion
- C07C2/44—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons homo- or co-oligomerisation with ring formation, not being a Diels-Alder conversion of conjugated dienes only
- C07C2/46—Catalytic processes
- C07C2/465—Catalytic processes with hydrides or organic compounds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
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- C07C2/52—Catalytic processes
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/02—Iron compounds
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/02—Iron compounds
- C07F15/025—Iron compounds without a metal-carbon linkage
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/04—Nickel compounds
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
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- C07F15/045—Nickel compounds without a metal-carbon linkage
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/06—Cobalt compounds
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/06—Cobalt compounds
- C07F15/065—Cobalt compounds without a metal-carbon linkage
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- C07F17/00—Metallocenes
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/005—Compounds of elements of Group 5 of the Periodic Table without metal-carbon linkages
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
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- C—CHEMISTRY; METALLURGY
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- 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
- C07F9/50—Organo-phosphines
- C07F9/5045—Complexes or chelates of phosphines with metallic compounds or metals
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/845—Cobalt
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/847—Nickel
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- C07C2531/22—Organic complexes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- C07C2531/24—Phosphines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/18—Systems containing only non-condensed rings with a ring being at least seven-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (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)
- Catalysts (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEM0069381 | 1959-12-22 | ||
| DE1960ST016427 DE1191375C2 (de) | 1959-12-22 | 1960-04-28 | Verfahren zur Herstellung von CO- und NO-freien Komplexverbindungen der UEbergangsmetalle |
| US53290066A | 1966-03-09 | 1966-03-09 | |
| US05/573,198 US4017526A (en) | 1959-12-22 | 1975-04-30 | Metal complexes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB935716A true GB935716A (en) | 1963-09-04 |
Family
ID=27437240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB14157/61A Expired GB935716A (en) | 1959-12-22 | 1961-04-19 | Complexes of transition metals and the production thereof |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US3450732A (enExample) |
| BE (1) | BE603146A (enExample) |
| CH (2) | CH436284A (enExample) |
| DE (1) | DE1191375C2 (enExample) |
| GB (1) | GB935716A (enExample) |
| IT (1) | IT649440A (enExample) |
| NL (2) | NL263960A (enExample) |
| SE (1) | SE307577B (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3489590A (en) * | 1966-05-05 | 1970-01-13 | Hoechst Ag | Process for nickeling plastics materials |
| JP2022542677A (ja) * | 2019-07-30 | 2022-10-06 | シュトゥディエンゲゼルシャフト・コーレ・ミット・ベシュレンクテル・ハフツング | 空気安定性Ｎｉ（０）－オレフィン錯体及び触媒または触媒前駆体としてのそれらの使用 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4120882A (en) * | 1959-12-22 | 1978-10-17 | Studiengesellschaft Kohle M.B.H. | Metal complexes |
| DE1297600B (de) * | 1960-06-30 | 1969-06-19 | Studiengesellschaft Kohle Mbh | Verfahren zur Cyclodimerisation von 1, 3-Diolefinen in Gegenwart eines Katalysators aus kohlenoxydfreien Verbindungen des Nickels und Metallalkylen und Triphenylphosphin |
| US3507926A (en) * | 1967-12-28 | 1970-04-21 | Columbian Carbon | Process for cyclooligomerizing conjugated dienes |
| US3622644A (en) * | 1968-11-25 | 1971-11-23 | Phillips Petroleum Co | Oligomerization of olefins using a rhenium complex catalyst system |
| US3997579A (en) * | 1975-10-15 | 1976-12-14 | E. I. Du Pont De Nemours And Company | Selected phosphorus complexes of zerovalent iron |
| US4529553A (en) * | 1981-12-14 | 1985-07-16 | General Electric Company | Nickel complex catalyst for hydrosilation reaction |
| DE3205550A1 (de) * | 1982-02-17 | 1983-08-25 | Studiengesellschaft Kohle mbH, 4330 Mülheim | Herstellung von uebergangsmetallkomplexen |
| US4550152A (en) * | 1983-10-28 | 1985-10-29 | General Electric Company | Nickel complex catalyst for hydrosilation reactions |
| US5041574A (en) * | 1990-08-09 | 1991-08-20 | E. I. Du Pont De Nemours And Company | Process for the preparation of phosphine containing cobalt carbonyl complexes |
| US8940940B2 (en) | 2012-06-13 | 2015-01-27 | Basf Se | Process for preparing macrocyclic ketones |
| EP3771707A1 (en) | 2019-07-30 | 2021-02-03 | Studiengesellschaft Kohle mbH | Air-stable ni(0)-olefin complex and its use as catalyst and precatalyst |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE551488A (enExample) * | 1955-10-05 | |||
| US2916505A (en) * | 1957-11-18 | 1959-12-08 | Ethyl Corp | Manufacture of cyclopentadienyl-manganese carbonyl compounds |
| FR1215360A (fr) * | 1957-11-27 | 1960-04-19 | Union Carbide Corp | Procédé de fabrication de cyclopentadiénylmanganèse-tricarbonyles |
| NL134223C (enExample) * | 1960-12-05 | 1900-01-01 |
-
0
- NL NL129643D patent/NL129643C/xx active
- BE BE603146D patent/BE603146A/xx unknown
- IT IT649440D patent/IT649440A/it unknown
- NL NL263960D patent/NL263960A/xx unknown
-
1960
- 1960-04-28 DE DE1960ST016427 patent/DE1191375C2/de not_active Expired
-
1961
- 1961-04-17 CH CH451061A patent/CH436284A/de unknown
- 1961-04-17 CH CH1529365A patent/CH464915A/de unknown
- 1961-04-19 GB GB14157/61A patent/GB935716A/en not_active Expired
- 1961-04-28 SE SE4462/61A patent/SE307577B/xx unknown
-
1968
- 1968-08-21 US US755508A patent/US3450732A/en not_active Expired - Lifetime
-
1975
- 1975-04-30 US US05/573,198 patent/US4017526A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3489590A (en) * | 1966-05-05 | 1970-01-13 | Hoechst Ag | Process for nickeling plastics materials |
| JP2022542677A (ja) * | 2019-07-30 | 2022-10-06 | シュトゥディエンゲゼルシャフト・コーレ・ミット・ベシュレンクテル・ハフツング | 空気安定性Ｎｉ（０）－オレフィン錯体及び触媒または触媒前駆体としてのそれらの使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| US3450732A (en) | 1969-06-17 |
| NL129643C (enExample) | 1900-01-01 |
| BE603146A (enExample) | 1900-01-01 |
| CH436284A (de) | 1967-05-31 |
| US4017526A (en) | 1977-04-12 |
| SE307577B (enExample) | 1969-01-13 |
| IT649440A (enExample) | 1900-01-01 |
| DE1191375B (de) | 1965-04-22 |
| NL263960A (enExample) | 1900-01-01 |
| DE1191375C2 (de) | 1965-12-16 |
| CH464915A (de) | 1968-11-15 |
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