NL8020087A - Carbonyleringswerkwijze en nieuwe overgangs- metaalkatalysatoren. - Google Patents
Carbonyleringswerkwijze en nieuwe overgangs- metaalkatalysatoren. Download PDFInfo
- Publication number
- NL8020087A NL8020087A NL8020087A NL8020087A NL8020087A NL 8020087 A NL8020087 A NL 8020087A NL 8020087 A NL8020087 A NL 8020087A NL 8020087 A NL8020087 A NL 8020087A NL 8020087 A NL8020087 A NL 8020087A
- Authority
- NL
- Netherlands
- Prior art keywords
- group
- carbon atoms
- formula
- rhodium
- ligand
- Prior art date
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- 239000003054 catalyst Substances 0.000 title claims abstract description 285
- 238000000034 method Methods 0.000 title claims abstract description 180
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- 229910052723 transition metal Inorganic materials 0.000 title claims description 11
- 150000003624 transition metals Chemical class 0.000 title claims description 8
- 238000005810 carbonylation reaction Methods 0.000 title description 14
- 230000006315 carbonylation Effects 0.000 title description 12
- 239000010948 rhodium Substances 0.000 claims abstract description 260
- 239000003446 ligand Substances 0.000 claims abstract description 257
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- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims abstract description 143
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- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 28
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- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- JYVHOGDBFNJNMR-UHFFFAOYSA-N hexane;hydrate Chemical compound O.CCCCCC JYVHOGDBFNJNMR-UHFFFAOYSA-N 0.000 description 1
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- JFZUABNDWZQLIJ-UHFFFAOYSA-N methyl 2-[(2-chloroacetyl)amino]benzoate Chemical compound COC(=O)C1=CC=CC=C1NC(=O)CCl JFZUABNDWZQLIJ-UHFFFAOYSA-N 0.000 description 1
- HCZDSQSBFCVXFG-UHFFFAOYSA-N methyl 3-diphenylphosphanylpropanoate Chemical compound C=1C=CC=CC=1P(CCC(=O)OC)C1=CC=CC=C1 HCZDSQSBFCVXFG-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
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- 125000001802 myricyl 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])C([H])([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])C([H])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
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- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 1
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- 238000005191 phase separation Methods 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
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- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical group OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
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- 239000001294 propane Substances 0.000 description 1
- 239000012629 purifying agent Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000007420 reactivation Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 150000003284 rhodium compounds Chemical class 0.000 description 1
- BDDWSAASCFBVBK-UHFFFAOYSA-N rhodium;triphenylphosphane Chemical class [Rh].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 BDDWSAASCFBVBK-UHFFFAOYSA-N 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 150000003376 silicon Chemical class 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 125000005353 silylalkyl group Chemical group 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- ZGNPLWZYVAFUNZ-UHFFFAOYSA-N tert-butylphosphane Chemical group CC(C)(C)P ZGNPLWZYVAFUNZ-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 238000006257 total synthesis reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical class CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- TYLYVJBCMQFRCB-UHFFFAOYSA-K trichlororhodium;trihydrate Chemical compound O.O.O.[Cl-].[Cl-].[Cl-].[Rh+3] TYLYVJBCMQFRCB-UHFFFAOYSA-K 0.000 description 1
- 125000002469 tricosyl 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])C([H])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HYWCXWRMUZYRPH-UHFFFAOYSA-N trimethyl(prop-2-enyl)silane Chemical compound C[Si](C)(C)CC=C HYWCXWRMUZYRPH-UHFFFAOYSA-N 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Classifications
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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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- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/1608—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes the ligands containing silicon
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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
- B01J31/24—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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- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C07C45/74—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with dehydration
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- C07F9/54—Quaternary phosphonium compounds
- C07F9/5407—Acyclic saturated phosphonium compounds
- C07F9/5414—Acyclic saturated phosphonium compounds substituted by B, Si, P or a metal
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- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/011,238 US4298541A (en) | 1979-02-12 | 1979-02-12 | Trihydrocarbyl silyl-substituted alkyl diaryl phosphine transition metal complexes and their use as homogeneous catalysts |
US1123879 | 1979-02-12 | ||
US4354879A | 1979-05-29 | 1979-05-29 | |
US4354879 | 1979-05-29 | ||
US06/114,627 US4302401A (en) | 1980-01-23 | 1980-01-23 | Tetraalkyl phosphonium substituted phosphine and amine transition metal complexes |
US11462780 | 1980-01-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
NL8020087A true NL8020087A (nl) | 1980-12-31 |
Family
ID=27359388
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL8020079A NL8020079A (nl) | 1979-02-12 | 1980-02-12 | Werkwijze ter bereiding van aldehyden. |
NL8020088A NL8020088A (nl) | 1979-02-12 | 1980-02-12 | Tetraaelkylfosfonium-gesubstitueerde overgangsmetaal- complexen. |
NL8020087A NL8020087A (nl) | 1979-02-12 | 1980-02-12 | Carbonyleringswerkwijze en nieuwe overgangs- metaalkatalysatoren. |
NL8020086A NL8020086A (nl) | 1979-02-12 | 1980-02-12 | Fosfine- en fosforniumverbindingen en katalysator. |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL8020079A NL8020079A (nl) | 1979-02-12 | 1980-02-12 | Werkwijze ter bereiding van aldehyden. |
NL8020088A NL8020088A (nl) | 1979-02-12 | 1980-02-12 | Tetraaelkylfosfonium-gesubstitueerde overgangsmetaal- complexen. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL8020086A NL8020086A (nl) | 1979-02-12 | 1980-02-12 | Fosfine- en fosforniumverbindingen en katalysator. |
Country Status (8)
Country | Link |
---|---|
EP (6) | EP0159460A1 (fr) |
JP (3) | JPS56500167A (fr) |
BR (3) | BR8006681A (fr) |
DE (4) | DE3034353A1 (fr) |
GB (3) | GB2057906B (fr) |
NL (4) | NL8020079A (fr) |
SE (6) | SE8007079L (fr) |
WO (4) | WO1980001689A1 (fr) |
Families Citing this family (57)
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US4429161A (en) * | 1981-08-17 | 1984-01-31 | Union Carbide Corporation | Process for preparing organic tertiary polyphosphine monooxides |
US4522933A (en) * | 1981-08-17 | 1985-06-11 | Union Carbide Corporation | Hydroformylation catalyst containing bisphosphine monooxide ligands |
US4491675A (en) * | 1981-08-17 | 1985-01-01 | Union Carbide Corporation | Hydroformylation process using triarylphosphine and bisphosphine monooxide ligands |
US4400548A (en) * | 1981-08-17 | 1983-08-23 | Union Carbide Corporation | Hydroformylation process using bisphosphine monooxide ligands |
US4593011A (en) * | 1981-08-17 | 1986-06-03 | Union Carbide Corporation | Hydroformylation process using triarylphosphine and bisphosphine monooxide ligands |
DE3264581D1 (en) * | 1981-10-28 | 1985-08-08 | Monsanto Co | Synthesis of isoprene from linear butenes |
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US5110990A (en) * | 1984-03-30 | 1992-05-05 | Union Carbide Chemicals & Plastics Technology Corporation | Process for recovery of phosphorus ligand from vaporized aldehyde |
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CA1237728A (fr) * | 1984-07-20 | 1988-06-07 | Anthony G. Abatjoglou | Preparation d'acides carboxyliques a partir d'alcools en presence de catalyseurs a base de complexe de rhodium |
US4927967A (en) * | 1984-07-20 | 1990-05-22 | Union Carbide Chemicals And Plastics Company Inc. | Production of carboxylic acids from organic formate esters using rhodium complex catalysts |
CA1248549A (fr) * | 1984-08-16 | 1989-01-10 | Richard W. Wegman | Preparation d'acides carboxyliques anhydres a partir d'alcools en presence de catalyseurs a base de complexe de rhodium, et d'une source d'ester organique |
US4593127A (en) * | 1985-01-11 | 1986-06-03 | Union Carbide Corporation | Hydroformylation process |
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DE3546123A1 (de) * | 1985-12-24 | 1987-06-25 | Ruhrchemie Ag | Verfahren zur herstellung von aldehyden |
GB8614910D0 (en) * | 1986-06-19 | 1986-07-23 | British Petroleum Co Plc | Preparation of ketones |
EP0320546A1 (fr) * | 1987-12-15 | 1989-06-21 | Council of Scientific and Industrial Research | Catalyseur d'hydrogénation |
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US5001274A (en) * | 1989-06-23 | 1991-03-19 | Union Carbide Chemicals And Plastics Company Inc. | Hydroformylation process |
JPH0520984U (ja) * | 1991-03-04 | 1993-03-19 | 日本フルハーフ株式会社 | 貨物自動車における煽 |
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FR2743010B1 (fr) * | 1995-12-29 | 1998-02-20 | Rhone Poulenc Fibres | Procede de preparation par hydrogenation de catalyseurs a base de metal de transition et de phosphine |
ES2253552T3 (es) * | 2001-03-29 | 2006-06-01 | Basf Aktiengesellschaft | Ligandos para complejos de quelato de pnicogeno con un metal del grupo viii secundario y empleo de los complejos como catalizadores para la hidroformilacion, la carbonilacion, la hidrocianacion o la hidrogenacion. |
AU2002324067A1 (en) * | 2001-08-24 | 2003-03-10 | Basf Aktiengesellschaft | Method for the production of 2-propylheptanol and hydroformylating catalysts and the further use thereof for carbonylation, hydrocyanation and hydrogenation |
DE10355066A1 (de) | 2003-11-25 | 2005-06-23 | Basf Ag | Verfahren zur asymmetrischen Synthese |
KR101141634B1 (ko) * | 2004-07-20 | 2012-05-04 | 엘지전자 주식회사 | 세탁장치 |
US7294745B2 (en) | 2004-12-30 | 2007-11-13 | Council Of Scientific And Industrial Research | Process for preparing aldol derivatives from alkenes using catalyst |
CN101094826B (zh) * | 2004-12-31 | 2011-02-09 | 科学与工业研究委员会 | 使用催化剂从烯烃制备羟醛衍生物的方法 |
FR2894251B1 (fr) * | 2005-12-05 | 2008-01-04 | Air Liquide | Procede de synthese de methanol permettant un recyclage du gaz residuaire |
US9251837B2 (en) | 2012-04-25 | 2016-02-02 | Seagate Technology Llc | HAMR NFT materials with improved thermal stability |
US9224416B2 (en) | 2012-04-24 | 2015-12-29 | Seagate Technology Llc | Near field transducers including nitride materials |
US8427925B2 (en) | 2010-02-23 | 2013-04-23 | Seagate Technology Llc | HAMR NFT materials with improved thermal stability |
DE102011081074A1 (de) * | 2011-08-17 | 2013-02-21 | Areva Np Gmbh | Verfahren zur Herstellung eines Uranoxid als aktive Komponente enthaltenden Katalysators |
KR101611113B1 (ko) | 2011-12-20 | 2016-04-08 | 다우 테크놀로지 인베스트먼츠 엘엘씨. | 하이드로포밀화 방법 |
US20140376351A1 (en) | 2013-06-24 | 2014-12-25 | Seagate Technology Llc | Materials for near field transducers and near field transducers containing same |
US9245573B2 (en) | 2013-06-24 | 2016-01-26 | Seagate Technology Llc | Methods of forming materials for at least a portion of a NFT and NFTs formed using the same |
US9058824B2 (en) | 2013-06-24 | 2015-06-16 | Seagate Technology Llc | Devices including a gas barrier layer |
US8976634B2 (en) | 2013-06-24 | 2015-03-10 | Seagate Technology Llc | Devices including at least one intermixing layer |
US9570098B2 (en) | 2013-12-06 | 2017-02-14 | Seagate Technology Llc | Methods of forming near field transducers and near field transducers formed thereby |
US9697856B2 (en) | 2013-12-06 | 2017-07-04 | Seagate Techology LLC | Methods of forming near field transducers and near field transducers formed thereby |
BR112016013001B1 (pt) | 2013-12-19 | 2020-12-29 | Dow Technology Investments Llc | processo de hidroformilação |
DE102014201122A1 (de) * | 2014-01-22 | 2015-07-23 | Leibniz-Institut Für Katalyse E.V. An Der Universität Rostock (Likat) | Verfahren zur katalytischen Herstellung von ungesättigten Aldehyden |
US9620150B2 (en) | 2014-11-11 | 2017-04-11 | Seagate Technology Llc | Devices including an amorphous gas barrier layer |
US9552833B2 (en) | 2014-11-11 | 2017-01-24 | Seagate Technology Llc | Devices including a multilayer gas barrier layer |
US9822444B2 (en) | 2014-11-11 | 2017-11-21 | Seagate Technology Llc | Near-field transducer having secondary atom higher concentration at bottom of the peg |
US10510364B2 (en) | 2014-11-12 | 2019-12-17 | Seagate Technology Llc | Devices including a near field transducer (NFT) with nanoparticles |
TWI788364B (zh) | 2017-06-23 | 2023-01-01 | 美商陶氏科技投資有限公司 | 氫甲醯化反應製程 |
CN110975941B (zh) * | 2019-12-17 | 2022-08-05 | 万华化学集团股份有限公司 | 一种氢甲酰化反应催化剂组合物及丙烯氢甲酰化反应制备醛的方法 |
WO2022025562A1 (fr) | 2020-07-30 | 2022-02-03 | 주식회사 엘지화학 | Procédé d'hydroformylation |
JP2024500349A (ja) | 2020-12-22 | 2024-01-09 | ダウ テクノロジー インベストメンツ リミティド ライアビリティー カンパニー | ヒドロホルミル化反応方法 |
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-
1980
- 1980-02-12 DE DE803034353T patent/DE3034353A1/de not_active Withdrawn
- 1980-02-12 NL NL8020079A patent/NL8020079A/nl not_active Application Discontinuation
- 1980-02-12 WO PCT/US1980/000212 patent/WO1980001689A1/fr active IP Right Grant
- 1980-02-12 JP JP50065180A patent/JPS56500167A/ja active Pending
- 1980-02-12 BR BR8006681A patent/BR8006681A/pt unknown
- 1980-02-12 WO PCT/US1980/000213 patent/WO1980001690A1/fr active IP Right Grant
- 1980-02-12 BR BR8006679A patent/BR8006679A/pt unknown
- 1980-02-12 DE DE803034352T patent/DE3034352A1/de not_active Withdrawn
- 1980-02-12 EP EP85100028A patent/EP0159460A1/fr not_active Withdrawn
- 1980-02-12 NL NL8020088A patent/NL8020088A/nl not_active Application Discontinuation
- 1980-02-12 WO PCT/US1980/000215 patent/WO1980001692A1/fr active IP Right Grant
- 1980-02-12 BR BR8006680A patent/BR8006680A/pt unknown
- 1980-02-12 GB GB8031135A patent/GB2057906B/en not_active Expired
- 1980-02-12 GB GB8031137A patent/GB2056989B/en not_active Expired
- 1980-02-12 EP EP82107978A patent/EP0071281B1/fr not_active Expired
- 1980-02-12 NL NL8020087A patent/NL8020087A/nl not_active Application Discontinuation
- 1980-02-12 DE DE803034354T patent/DE3034354A1/de not_active Ceased
- 1980-02-12 JP JP50065080A patent/JPS55501178A/ja active Pending
- 1980-02-12 WO PCT/US1980/000216 patent/WO1980001691A1/fr active Application Filing
- 1980-02-12 JP JP55500652A patent/JPS6332079B2/ja not_active Expired
- 1980-02-12 GB GB8031136A patent/GB2086906B/en not_active Expired
- 1980-02-12 NL NL8020086A patent/NL8020086A/nl not_active Application Discontinuation
- 1980-02-12 DE DE803034351T patent/DE3034351A1/de not_active Ceased
- 1980-08-25 EP EP80900540A patent/EP0024091B1/fr not_active Expired
- 1980-08-25 EP EP80900539A patent/EP0023923B1/fr not_active Expired
- 1980-08-25 EP EP80900484A patent/EP0024088A1/fr not_active Withdrawn
- 1980-08-25 EP EP80900541A patent/EP0023924B1/fr not_active Expired
- 1980-10-09 SE SE8007079A patent/SE8007079L/xx not_active Application Discontinuation
- 1980-10-09 SE SE8007080A patent/SE439439B/sv not_active IP Right Cessation
- 1980-10-10 SE SE8007140A patent/SE449093B/sv not_active IP Right Cessation
- 1980-10-10 SE SE8007139A patent/SE449750B/sv not_active IP Right Cessation
-
1982
- 1982-01-22 SE SE8200371A patent/SE8200371L/xx not_active Application Discontinuation
- 1982-07-23 SE SE8204443A patent/SE8204443D0/xx not_active Application Discontinuation
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BB | A search report has been drawn up | ||
BV | The patent application has lapsed |