JP2002509960A5 - - Google Patents
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- JP2002509960A5 JP2002509960A5 JP2000541227A JP2000541227A JP2002509960A5 JP 2002509960 A5 JP2002509960 A5 JP 2002509960A5 JP 2000541227 A JP2000541227 A JP 2000541227A JP 2000541227 A JP2000541227 A JP 2000541227A JP 2002509960 A5 JP2002509960 A5 JP 2002509960A5
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- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- compound
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- atom
- 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.)
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- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 11
- 150000001925 cycloalkenes Chemical class 0.000 description 6
- 239000003446 ligand Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 238000005649 metathesis reaction Methods 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical group [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- 125000001072 heteroaryl group Chemical group 0.000 description 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052762 osmium Inorganic materials 0.000 description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical group [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 1
- 125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH77498 | 1998-03-31 | ||
| CH774/98 | 1998-03-31 | ||
| PCT/EP1999/001914 WO1999050330A2 (en) | 1998-03-31 | 1999-03-22 | Ruthenium and osmium carbene carbonyl catalysts |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002509960A JP2002509960A (ja) | 2002-04-02 |
| JP2002509960A5 true JP2002509960A5 (https=) | 2006-04-27 |
Family
ID=4194877
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000541227A Withdrawn JP2002509960A (ja) | 1998-03-31 | 1999-03-22 | ルテニウムおよびオスミウムカルベンカルボニル触媒 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6465554B1 (https=) |
| EP (1) | EP1070091B1 (https=) |
| JP (1) | JP2002509960A (https=) |
| AU (1) | AU3519899A (https=) |
| DE (1) | DE69916817T2 (https=) |
| WO (1) | WO1999050330A2 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7507854B2 (en) | 1998-09-01 | 2009-03-24 | Materia, Inc. | Impurity reduction in Olefin metathesis reactions |
| US6900347B2 (en) | 1998-09-01 | 2005-05-31 | Tilliechem, Inc. | Impurity inhibition in olefin metathesis reactions |
| US6696597B2 (en) | 1998-09-01 | 2004-02-24 | Tilliechem, Inc. | Metathesis syntheses of pheromones or their components |
| EP1263833A1 (en) | 2000-02-22 | 2002-12-11 | Ciba SC Holding AG | Romp with oligomeric uv-absorbers |
| AU2003232067A1 (en) | 2002-05-06 | 2003-11-17 | Kerr Corporation | Composition curable by metathesis reaction |
| US7060770B2 (en) * | 2003-05-06 | 2006-06-13 | Kerr Corporation | Metathesis-curable composition with a reaction control agent |
| US7173097B2 (en) | 2003-05-06 | 2007-02-06 | Kerr Corporation | Metathesis-curable composition with a reaction control agent |
| US7683148B2 (en) | 2003-05-06 | 2010-03-23 | Kerr Corporation | Metathesis-curable composition with a reaction control agent |
| US7060769B2 (en) | 2003-05-06 | 2006-06-13 | Kerr Corporation | Method of curing composition by metathesis reaction using reaction control agent |
| US7001590B1 (en) | 2004-11-15 | 2006-02-21 | Kerr Corporation | Metathesis-curable composition |
| US7625551B2 (en) * | 2004-11-15 | 2009-12-01 | Kerr Corporation | Polyether-based dental impression material curable by metathesis reaction |
| US7645443B2 (en) * | 2004-11-15 | 2010-01-12 | Kerr Corporation | Polyether-based composition curable by metathesis reaction |
| US8461223B2 (en) | 2005-04-07 | 2013-06-11 | Aspen Aerogels, Inc. | Microporous polycyclopentadiene-based aerogels |
| EP1847245A1 (en) * | 2006-02-21 | 2007-10-24 | Kerr Corporation | Method for making alkoxy-siloxane polyether carboxylates terminated with functional olefin groups |
| US8241575B2 (en) | 2008-01-28 | 2012-08-14 | The Johns Hopkins University | Molecularly imprinted polymer sensor device |
| US9786409B2 (en) | 2013-06-27 | 2017-10-10 | Basf Se | Metathesis polymers as dielectrics |
| EP4045560A1 (en) | 2019-10-14 | 2022-08-24 | 3M Innovative Properties Company | Compositions comprising cyclic olefins and thermally conductive filler |
| US12312509B2 (en) | 2019-12-20 | 2025-05-27 | 3M Innovative Properties Company | Adhesive article comprising polymer and polymerizable cyclic olefins, adhesive compositions and methods |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8902362D0 (en) * | 1989-02-03 | 1989-03-22 | Amersham Int Plc | Cationic complexes of technetium-99m |
| US5312940A (en) * | 1992-04-03 | 1994-05-17 | California Institute Of Technology | Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization |
| US5710298A (en) * | 1992-04-03 | 1998-01-20 | California Institute Of Technology | Method of preparing ruthenium and osmium carbene complexes |
| JP3067031B2 (ja) * | 1992-04-03 | 2000-07-17 | カリフォルニア インスティチュート オブ テクノロジー | オレフィンメタセシス重合方法 |
| EP0722468A1 (en) * | 1993-09-10 | 1996-07-24 | Ciba SC Holding AG | Process for the polymerization of cyclic olefins and a polymerizable composition |
| US5639900A (en) * | 1993-12-29 | 1997-06-17 | Metton America, Inc. | Thermally activated olefin metathesis catalyst precursor |
| US5728785A (en) * | 1995-07-07 | 1998-03-17 | California Institute Of Technology | Romp polymerization in the presence of peroxide crosslinking agents to form high-density crosslinked polymers |
| EP0771830B1 (de) | 1995-11-02 | 2003-01-29 | Ciba Specialty Chemicals Holding Inc. | Härtbare Zusammensetzung enthaltend Cycloolefin, Silan und Füllstoff |
| US5939504A (en) * | 1995-12-07 | 1999-08-17 | Advanced Polymer Technologies | Method for extending the pot life of an olefin metathesis polymerization reaction |
| EP0844263B1 (de) * | 1996-11-15 | 2003-01-15 | Ciba SC Holding AG | Katalysatorgemisch für die ringöffnende Metathesepolymerisation |
| EP0853099A3 (de) * | 1996-12-10 | 2000-12-27 | Ciba SC Holding AG | Thixotropiermittel für gefüllte Cycloolefine |
| DE19654074C2 (de) * | 1996-12-23 | 2001-01-25 | Bayer Ag | Verfahren zur Herstellung hydrierter ringgeöffneter Metathesepolymeren |
| US6284852B1 (en) * | 1997-10-30 | 2001-09-04 | California Institute Of Technology | Acid activation of ruthenium metathesis catalysts and living ROMP metathesis polymerization in water |
| US6225488B1 (en) * | 1999-04-02 | 2001-05-01 | Nippon Zeon Co., Ltd. | Ruthenium or osmium catalysts for olefin metathesis reactions |
| US6291616B1 (en) * | 1999-06-17 | 2001-09-18 | Wisconsin Alumni Research Foundation | Methods and reagents for capping ruthenium or osmium carbene-catalyzed ROMP products |
-
1999
- 1999-03-22 DE DE69916817T patent/DE69916817T2/de not_active Expired - Fee Related
- 1999-03-22 AU AU35198/99A patent/AU3519899A/en not_active Abandoned
- 1999-03-22 JP JP2000541227A patent/JP2002509960A/ja not_active Withdrawn
- 1999-03-22 EP EP99916859A patent/EP1070091B1/en not_active Expired - Lifetime
- 1999-03-22 US US09/647,031 patent/US6465554B1/en not_active Expired - Lifetime
- 1999-03-22 WO PCT/EP1999/001914 patent/WO1999050330A2/en not_active Ceased
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