EP2618930A2 - Nouvelle classe de catalyseurs de métathèse d'oléfines, méthodes de préparation, et procédés d'utilisation - Google Patents
Nouvelle classe de catalyseurs de métathèse d'oléfines, méthodes de préparation, et procédés d'utilisationInfo
- Publication number
- EP2618930A2 EP2618930A2 EP11827288.9A EP11827288A EP2618930A2 EP 2618930 A2 EP2618930 A2 EP 2618930A2 EP 11827288 A EP11827288 A EP 11827288A EP 2618930 A2 EP2618930 A2 EP 2618930A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- oil
- group
- olefin
- dihydrogen
- metathesis
- 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.)
- Withdrawn
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 162
- 238000000034 method Methods 0.000 title claims description 89
- 230000008569 process Effects 0.000 title claims description 66
- 238000005865 alkene metathesis reaction Methods 0.000 title description 9
- 238000002360 preparation method Methods 0.000 title description 4
- -1 aryloxides Chemical class 0.000 claims abstract description 154
- 238000005649 metathesis reaction Methods 0.000 claims abstract description 136
- 239000003446 ligand Substances 0.000 claims abstract description 102
- 229910052751 metal Inorganic materials 0.000 claims abstract description 101
- 239000002184 metal Substances 0.000 claims abstract description 101
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 75
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 69
- 239000001257 hydrogen Substances 0.000 claims abstract description 50
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 50
- 150000004820 halides Chemical class 0.000 claims abstract description 36
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 30
- 150000004703 alkoxides Chemical class 0.000 claims abstract description 20
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims abstract description 16
- 150000008052 alkyl sulfonates Chemical class 0.000 claims abstract description 16
- 125000000129 anionic group Chemical group 0.000 claims abstract description 13
- 230000007935 neutral effect Effects 0.000 claims abstract description 13
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 126
- 150000001336 alkenes Chemical class 0.000 claims description 113
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 claims description 100
- 239000000203 mixture Substances 0.000 claims description 93
- 239000003921 oil Substances 0.000 claims description 92
- 235000019198 oils Nutrition 0.000 claims description 88
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 claims description 80
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 claims description 66
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 54
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 47
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 42
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 36
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 28
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 claims description 25
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 21
- 125000004122 cyclic group Chemical group 0.000 claims description 20
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 claims description 20
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims description 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
- 239000004913 cyclooctene Substances 0.000 claims description 14
- 229910052707 ruthenium Inorganic materials 0.000 claims description 13
- 235000012424 soybean oil Nutrition 0.000 claims description 13
- 239000003549 soybean oil Substances 0.000 claims description 13
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 12
- 235000019486 Sunflower oil Nutrition 0.000 claims description 12
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000002600 sunflower oil Substances 0.000 claims description 12
- 239000004711 α-olefin Substances 0.000 claims description 12
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical group [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 11
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical group ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 10
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 10
- 241000195493 Cryptophyta Species 0.000 claims description 9
- 239000000828 canola oil Substances 0.000 claims description 9
- 235000019519 canola oil Nutrition 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 150000002466 imines Chemical class 0.000 claims description 9
- 239000000944 linseed oil Substances 0.000 claims description 9
- 235000021388 linseed oil Nutrition 0.000 claims description 9
- 229910052762 osmium Chemical group 0.000 claims description 9
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical group [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 9
- 241000221089 Jatropha Species 0.000 claims description 8
- 235000019482 Palm oil Nutrition 0.000 claims description 8
- 240000000528 Ricinus communis Species 0.000 claims description 8
- 235000004443 Ricinus communis Nutrition 0.000 claims description 8
- 239000002540 palm oil Substances 0.000 claims description 8
- 150000003003 phosphines Chemical class 0.000 claims description 8
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 8
- ADLVDYMTBOSDFE-UHFFFAOYSA-N 5-chloro-6-nitroisoindole-1,3-dione Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC2=C1C(=O)NC2=O ADLVDYMTBOSDFE-UHFFFAOYSA-N 0.000 claims description 7
- 241001465754 Metazoa Species 0.000 claims description 7
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 7
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical group O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 6
- 235000019485 Safflower oil Nutrition 0.000 claims description 6
- 229910000074 antimony hydride Inorganic materials 0.000 claims description 6
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 claims description 6
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 6
- 125000005538 phosphinite group Chemical group 0.000 claims description 6
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 6
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 6
- 235000005713 safflower oil Nutrition 0.000 claims description 6
- 239000003813 safflower oil Substances 0.000 claims description 6
- OUULRIDHGPHMNQ-UHFFFAOYSA-N stibane Chemical compound [SbH3] OUULRIDHGPHMNQ-UHFFFAOYSA-N 0.000 claims description 6
- 150000003462 sulfoxides Chemical class 0.000 claims description 6
- 239000003760 tallow Substances 0.000 claims description 6
- 150000007970 thio esters Chemical class 0.000 claims description 6
- 239000002699 waste material Substances 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 150000001805 chlorine compounds Chemical group 0.000 claims description 5
- 239000003784 tall oil Substances 0.000 claims description 5
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 claims description 4
- 239000004912 1,5-cyclooctadiene Substances 0.000 claims description 4
- CXOZQHPXKPDQGT-UHFFFAOYSA-N 3-Methylcyclopentene Chemical compound CC1CCC=C1 CXOZQHPXKPDQGT-UHFFFAOYSA-N 0.000 claims description 4
- 235000000832 Ayote Nutrition 0.000 claims description 4
- 240000008067 Cucumis sativus Species 0.000 claims description 4
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 claims description 4
- 240000004244 Cucurbita moschata Species 0.000 claims description 4
- 235000009854 Cucurbita moschata Nutrition 0.000 claims description 4
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 claims description 4
- 241001072282 Limnanthes Species 0.000 claims description 4
- 235000019483 Peanut oil Nutrition 0.000 claims description 4
- 235000004347 Perilla Nutrition 0.000 claims description 4
- 244000124853 Perilla frutescens Species 0.000 claims description 4
- 241000390166 Physaria Species 0.000 claims description 4
- 235000019498 Walnut oil Nutrition 0.000 claims description 4
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 claims description 4
- 235000015278 beef Nutrition 0.000 claims description 4
- 235000005687 corn oil Nutrition 0.000 claims description 4
- 239000002285 corn oil Substances 0.000 claims description 4
- 235000012343 cottonseed oil Nutrition 0.000 claims description 4
- 239000002385 cottonseed oil Substances 0.000 claims description 4
- 239000008169 grapeseed oil Substances 0.000 claims description 4
- 239000008164 mustard oil Substances 0.000 claims description 4
- 239000000312 peanut oil Substances 0.000 claims description 4
- 239000010491 poppyseed oil Substances 0.000 claims description 4
- 235000015136 pumpkin Nutrition 0.000 claims description 4
- 239000008159 sesame oil Substances 0.000 claims description 4
- 235000011803 sesame oil Nutrition 0.000 claims description 4
- 239000002383 tung oil Substances 0.000 claims description 4
- 235000019871 vegetable fat Nutrition 0.000 claims description 4
- 239000008170 walnut oil Substances 0.000 claims description 4
- NYPKZCJJKHGKEU-UHFFFAOYSA-N 5-(2,6-diethylphenyl)-2,2,4,4-tetramethylpyrrolidine;tricyclohexylphosphane Chemical compound CCC1=CC=CC(CC)=C1C1C(C)(C)CC(C)(C)N1.C1CCCCC1P(C1CCCCC1)C1CCCCC1 NYPKZCJJKHGKEU-UHFFFAOYSA-N 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 87
- 239000000194 fatty acid Substances 0.000 description 87
- 229930195729 fatty acid Natural products 0.000 description 87
- 238000006243 chemical reaction Methods 0.000 description 73
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 70
- 238000005686 cross metathesis reaction Methods 0.000 description 50
- 150000004665 fatty acids Chemical class 0.000 description 48
- 239000000047 product Substances 0.000 description 36
- 239000000243 solution Substances 0.000 description 36
- 238000007152 ring opening metathesis polymerisation reaction Methods 0.000 description 35
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 27
- 238000005481 NMR spectroscopy Methods 0.000 description 27
- 239000000463 material Substances 0.000 description 27
- 150000002148 esters Chemical class 0.000 description 23
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 22
- UURSXESKOOOTOV-MDZDMXLPSA-N (e)-dec-5-ene Chemical compound CCCC\C=C\CCCC UURSXESKOOOTOV-MDZDMXLPSA-N 0.000 description 21
- UURSXESKOOOTOV-KTKRTIGZSA-N (z)-dec-5-ene Chemical compound CCCC\C=C/CCCC UURSXESKOOOTOV-KTKRTIGZSA-N 0.000 description 21
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 19
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 18
- 239000002904 solvent Substances 0.000 description 17
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 16
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 15
- 150000003626 triacylglycerols Chemical class 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- 239000003225 biodiesel Substances 0.000 description 14
- 239000000376 reactant Substances 0.000 description 14
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 13
- 239000005977 Ethylene Substances 0.000 description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 13
- 238000011068 loading method Methods 0.000 description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 11
- YMWUJEATGCHHMB-DICFDUPASA-N dichloromethane-d2 Chemical compound [2H]C([2H])(Cl)Cl YMWUJEATGCHHMB-DICFDUPASA-N 0.000 description 11
- 238000006317 isomerization reaction Methods 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 125000002524 organometallic group Chemical group 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 125000001424 substituent group Chemical group 0.000 description 10
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- 230000008719 thickening Effects 0.000 description 9
- 239000011345 viscous material Substances 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 8
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 8
- 235000021313 oleic acid Nutrition 0.000 description 8
- 238000007142 ring opening reaction Methods 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 7
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 7
- 125000005842 heteroatom Chemical group 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 6
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 6
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 235000020778 linoleic acid Nutrition 0.000 description 6
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 6
- 229940073769 methyl oleate Drugs 0.000 description 6
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- 238000006798 ring closing metathesis reaction Methods 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 5
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 5
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 5
- 239000005642 Oleic acid Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 235000021588 free fatty acids Nutrition 0.000 description 5
- 125000000524 functional group Chemical group 0.000 description 5
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 5
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 5
- 230000009466 transformation Effects 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 4
- 238000010535 acyclic diene metathesis reaction Methods 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical compound C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 4
- 239000000539 dimer Substances 0.000 description 4
- 238000005886 esterification reaction Methods 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- RYPKRALMXUUNKS-UHFFFAOYSA-N hex-2-ene Chemical compound CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 4
- 235000021281 monounsaturated fatty acids Nutrition 0.000 description 4
- 150000002894 organic compounds Chemical class 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation 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
- 238000000844 transformation Methods 0.000 description 4
- 239000008158 vegetable oil Substances 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 3
- 239000001149 (9Z,12Z)-octadeca-9,12-dienoate Substances 0.000 description 3
- WTTJVINHCBCLGX-UHFFFAOYSA-N (9trans,12cis)-methyl linoleate Natural products CCCCCC=CCC=CCCCCCCCC(=O)OC WTTJVINHCBCLGX-UHFFFAOYSA-N 0.000 description 3
- LNJCGNRKWOHFFV-UHFFFAOYSA-N 3-(2-hydroxyethylsulfanyl)propanenitrile Chemical compound OCCSCCC#N LNJCGNRKWOHFFV-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- PKIXXJPMNDDDOS-UHFFFAOYSA-N Methyl linoleate Natural products CCCCC=CCCC=CCCCCCCCC(=O)OC PKIXXJPMNDDDOS-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 150000001923 cyclic compounds Chemical class 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- 125000002704 decyl group Chemical group [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])* 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 3
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 3
- 229960004488 linolenic acid Drugs 0.000 description 3
- 125000005481 linolenic acid group Chemical group 0.000 description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
- 125000004043 oxo group Chemical group O=* 0.000 description 3
- 230000037361 pathway Effects 0.000 description 3
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 150000003573 thiols Chemical class 0.000 description 3
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 description 2
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- IBXNCJKFFQIKKY-UHFFFAOYSA-N 1-pentyne Chemical group CCCC#C IBXNCJKFFQIKKY-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229930194542 Keto Natural products 0.000 description 2
- 238000012565 NMR experiment Methods 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000012327 Ruthenium complex Substances 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 125000003302 alkenyloxy group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 125000005133 alkynyloxy group Chemical group 0.000 description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
- 229910000323 aluminium silicate Inorganic materials 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical group CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 150000007942 carboxylates Chemical group 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000012320 chlorinating reagent Substances 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- ZBCKWHYWPLHBOK-UHFFFAOYSA-N cyclohexylphosphane Chemical group PC1CCCCC1 ZBCKWHYWPLHBOK-UHFFFAOYSA-N 0.000 description 2
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 150000008049 diazo compounds Chemical class 0.000 description 2
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 235000003869 genetically modified organism Nutrition 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000001282 iso-butane Substances 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000000468 ketone group Chemical group 0.000 description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000007040 multi-step synthesis reaction Methods 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 2
- 230000000269 nucleophilic effect Effects 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 150000002889 oleic acids Chemical class 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
- LQAVWYMTUMSFBE-UHFFFAOYSA-N pent-4-en-1-ol Chemical compound OCCCC=C LQAVWYMTUMSFBE-UHFFFAOYSA-N 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 229920003245 polyoctenamer Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 150000003738 xylenes Chemical class 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- ZIPDPGGBRDWAMG-UHFFFAOYSA-N (2-phenylcyclopropen-1-yl)benzene Chemical compound C1C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 ZIPDPGGBRDWAMG-UHFFFAOYSA-N 0.000 description 1
- CGHIBGNXEGJPQZ-UHFFFAOYSA-N 1-hexyne Chemical group CCCCC#C CGHIBGNXEGJPQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- UQRONKZLYKUEMO-UHFFFAOYSA-N 4-methyl-1-(2,4,6-trimethylphenyl)pent-4-en-2-one Chemical group CC(=C)CC(=O)Cc1c(C)cc(C)cc1C UQRONKZLYKUEMO-UHFFFAOYSA-N 0.000 description 1
- YCNYCBYHUAGZIZ-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]hept-2-ene Chemical compound O1C2CCC1C=C2 YCNYCBYHUAGZIZ-UHFFFAOYSA-N 0.000 description 1
- YKCNBNDWSATCJL-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]hepta-2,5-diene Chemical compound C1=CC2C=CC1O2 YKCNBNDWSATCJL-UHFFFAOYSA-N 0.000 description 1
- YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000252203 Clupea harengus Species 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 235000021319 Palmitoleic acid Nutrition 0.000 description 1
- 229920001153 Polydicyclopentadiene Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241001125046 Sardina pilchardus Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000004164 Wax ester Substances 0.000 description 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229940090047 auto-injector Drugs 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 239000010428 baryte Substances 0.000 description 1
- 229910052601 baryte Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000012455 biphasic mixture Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000012018 catalyst precursor Substances 0.000 description 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- 239000003034 coal gas Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- HYPABJGVBDSCIT-UPHRSURJSA-N cyclododecene Chemical compound C1CCCCC\C=C/CCCC1 HYPABJGVBDSCIT-UPHRSURJSA-N 0.000 description 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 125000006003 dichloroethyl group Chemical group 0.000 description 1
- 150000001993 dienes Chemical group 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
- 235000020673 eicosapentaenoic acid Nutrition 0.000 description 1
- 229960005135 eicosapentaenoic acid Drugs 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 239000011984 grubbs catalyst Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- YVXHZKKCZYLQOP-UHFFFAOYSA-N hept-1-yne Chemical group CCCCCC#C YVXHZKKCZYLQOP-UHFFFAOYSA-N 0.000 description 1
- WZHKDGJSXCTSCK-UHFFFAOYSA-N hept-3-ene Chemical compound CCCC=CCC WZHKDGJSXCTSCK-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000019514 herring Nutrition 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- LJDZFAPLPVPTBD-UHFFFAOYSA-N nitroformic acid Chemical compound OC(=O)[N+]([O-])=O LJDZFAPLPVPTBD-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000012434 nucleophilic reagent Substances 0.000 description 1
- 238000010534 nucleophilic substitution reaction Methods 0.000 description 1
- UMIPWJGWASORKV-UHFFFAOYSA-N oct-1-yne Chemical group CCCCCCC#C UMIPWJGWASORKV-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229940014569 pentam Drugs 0.000 description 1
- YBVNFKZSMZGRAD-UHFFFAOYSA-N pentamidine isethionate Chemical compound OCCS(O)(=O)=O.OCCS(O)(=O)=O.C1=CC(C(=N)N)=CC=C1OCCCCCOC1=CC=C(C(N)=N)C=C1 YBVNFKZSMZGRAD-UHFFFAOYSA-N 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000012041 precatalyst Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- NNNVXFKZMRGJPM-KHPPLWFESA-N sapienic acid Chemical compound CCCCCCCCC\C=C/CCCCC(O)=O NNNVXFKZMRGJPM-KHPPLWFESA-N 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- 238000005872 self-metathesis reaction Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000006257 total synthesis reaction Methods 0.000 description 1
- ZQDPJFUHLCOCRG-AATRIKPKSA-N trans-3-hexene Chemical compound CC\C=C\CC ZQDPJFUHLCOCRG-AATRIKPKSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- HSNQNPCNYIJJHT-ISLYRVAYSA-N trans-octadec-9-ene Chemical compound CCCCCCCC\C=C\CCCCCCCC HSNQNPCNYIJJHT-ISLYRVAYSA-N 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 125000006000 trichloroethyl group Chemical group 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 150000003657 tungsten Chemical class 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 235000019386 wax ester Nutrition 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- 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
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/002—Osmium compounds
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/46—Ruthenium, rhodium, osmium or iridium
- B01J23/462—Ruthenium
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/46—Ruthenium, rhodium, osmium or iridium
- B01J23/466—Osmium
-
- 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
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/121—Metal hydrides
-
- 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
- B01J31/2286—Alkynes, e.g. acetylides
-
- 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
- B01J31/24—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
- C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
- C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
-
- 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
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/04—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
- C08G61/06—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds
- C08G61/08—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
-
- 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
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
- B01J2231/54—Metathesis reactions, e.g. olefin metathesis
- B01J2231/543—Metathesis reactions, e.g. olefin metathesis alkene metathesis
-
- 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
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/821—Ruthenium
-
- 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
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/825—Osmium
-
- 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
- C07C2531/22—Organic complexes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/33—Monomer units or repeat units incorporating structural elements in the main chain incorporating non-aromatic structural elements in the main chain
- C08G2261/332—Monomer units or repeat units incorporating structural elements in the main chain incorporating non-aromatic structural elements in the main chain containing only carbon atoms
- C08G2261/3324—Monomer units or repeat units incorporating structural elements in the main chain incorporating non-aromatic structural elements in the main chain containing only carbon atoms derived from norbornene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/33—Monomer units or repeat units incorporating structural elements in the main chain incorporating non-aromatic structural elements in the main chain
- C08G2261/332—Monomer units or repeat units incorporating structural elements in the main chain incorporating non-aromatic structural elements in the main chain containing only carbon atoms
- C08G2261/3325—Monomer units or repeat units incorporating structural elements in the main chain incorporating non-aromatic structural elements in the main chain containing only carbon atoms derived from other polycyclic systems
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/40—Polymerisation processes
- C08G2261/41—Organometallic coupling reactions
- C08G2261/418—Ring opening metathesis polymerisation [ROMP]
Definitions
- This invention relates to a novel class of olefin metathesis catalysts, methods of preparation, and to processes using the olefin metathesis catalysts.
- CM cross- metathesis
- ROM ring-opening cross metathesis
- RCM ring-closing metathesis
- ADMET acyclic diene metathesis
- ROMP involves the formation of polyolefins from the ring opening of cyclic olefins
- ROCM involves a tandem sequence in which a cyclic olefin is opened and a second acyclic olefin is then cross metathesized onto the newly formed olefin termini
- RCM involves the intramolecular transformation of an alpha, omega-diene to a cyclic olefin
- ADMET involves the polymerization of terminal dienes to polyenes.
- ROMP read-only polymers
- trans-polyoctenamer polymer of cyclooctene, commercially available as Vestenamer® from Evonik Industries
- polynorbornene commercially available as Norsorex®
- polydicyclopentadiene commercially available as Telene®, Metton®, and Pentam®
- ethenolysis is the CM of ethylene and internal olefins to produce alpha-olefms. Metathesis reactions are therefore indispensable as a synthetic tool for the formation of new carbon-carbon bonds.
- Olefin metathesis may be catalyzed by one or more catalytic metals, usually one or more transition metals, such as the molybdenum-containing Schrock catalyst and the ruthenium- or osmium-containing Grubbs catalysts.
- Catalytic metals usually one or more transition metals, such as the molybdenum-containing Schrock catalyst and the ruthenium- or osmium-containing Grubbs catalysts.
- Transition metals such as the molybdenum-containing Schrock catalyst and the ruthenium- or osmium-containing Grubbs catalysts.
- Well-defined single component ruthenium or osmium catalysts have been previously described by, for example, U.S. Patent Nos. 5,312,940; 5,342,909; 5,728,917; 5,710,298; 5,750,815; 5,831,108; 7,329,758; and PCT Publications WO 97/20865 and WO 97/29135, which
- LAOs linear alpha-olefms
- LAOs are useful as monomers or comonomers to produce polyalphaolefms (PAOs) and/or as intermediates in the production of epoxides, amines, oxo alcohols, synthetic lubricants, synthetic fatty acids, and alkylated aromatics.
- LAOs of industrial importance include 1-butene, 1-hexene, 1-octene, 1-decene, 1-undecene, 1-dodecene, and 1-tetradecene.
- LAOs are often undesirably inefficient, creates unwanted by-products and wastes reactants and energy.
- the major source of the starting materials for these commercial routes to LAOs are nonrenewable feedstreams including petroleum, coal, and natural gas.
- LAOs may be produced from such renewable feedstreams by a CM reaction of the renewable feedstream, such as methyl oleate, with an olefin, such as ethylene, in the presence of a metathesis catalyst.
- CM catalysts reported thus far, for the ethenolysis of methyl oleate are typically ruthenium-based catalysts bearing phosphine or carbene ligands, such as those reported in Organometallics, 2004, Vol. 23, No. 9, pp. 2027-2047 and WO 2008/010961.
- these catalysts were reported to be too expensive for industrial consideration due to high costs associated with the catalysts being derived from a low yielding synthesis (See Final Technical Report entitled "Platform Chemicals from an Oilseed Biorefmery,” grant number DE-FG36-04GO14016, awarded by the Department of Energy).
- these ruthenium alkylidene catalysts are usually prepared by the reaction of ruthenium species with diazo compounds (J. Am. Chem. Soc, 1999, Vol. 121, No. 4, pp. 791-799). Therefore, cost and safety concerns associated with industrial scale reactions comprising diazo compounds have led to increased efforts to prepare ruthenium alkylidenes via alternate synthetic routes, such as using propargyl and vinyl chlorides (Organometallics, 1997, Vol. 16, No. 18, pp. 3867-3869). In order to obtain a commercially viable metathesis-based process, for example, LAO production via the CM of ethylene and biodiesel or natural oils, higher activity metathesis catalysts must be discovered.
- metathesis catalyst composition comprising a Group 8 metal hydride-dihydrogen complex and a ligand exchange agent and, optionally, an acetylene generates an active metathesis catalyst.
- the metathesis catalyst compositions of the present invention provide mild, affordable, and simple synthetic routes to desirable olefins and polyolefms, for example, LAOs, which in turn may be useful in the preparation of PAOs; poly(cyclic olefins); and other industrially relevant chemicals.
- This invention relates to a metathesis catalyst composition
- a metathesis catalyst composition comprising (preferably comprising the reaction product of): (i) a Group 8 metal hydride-dihydrogen complex represented by the formula:
- M is a Group 8 metal
- X is an anionic ligand
- Li and L 2 are neutral donor ligands
- a ligand exchange agent represented by the formula J-Y wherein J is selected from the group consisting of hydrogen, a C ⁇ to C 30 hydrocarbyl, and a C ⁇ to C 30 substituted hydrocarbyl; and Y is selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates.
- This invention also relates to a method for making a metathesis catalyst comprising contacting a Group 8 metal hydride-dihydrogen complex with a ligand exchange agent; wherein the Group 8 metal hydride-dihydrogen complex is represented by the formula:
- M is a Group 8 metal
- X is an anionic ligand
- L2 are neutral donor ligands
- the ligand exchange agent is represented by the formula J-Y, wherein J is selected from the group consisting of hydrogen, a C to C30 hydrocarbyl, and a C to C30 substituted hydrocarbyl; and Y is selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates.
- This invention further relates to a process for performing a metathesis reaction comprising contacting at least one olefin with a metathesis catalyst, wherein the metathesis catalyst comprises a Group 8 metal hydride-dihydrogen complex represented by the formula:
- M is a Group 8 metal
- X is an anionic ligand
- I and L2 are neutral donor ligands.
- Figure 1 is a representation of some of the possible outcomes of ring opening cross metathesis.
- a "substituted hydrocarbyl” is a radical made of carbon and hydrogen where at least one hydrogen is replaced by a heteroatom.
- alkoxides include those where the alkyl group is a C ⁇ to C 10 hydrocarbyl.
- the alkyl group may be straight chain, branched, or cyclic.
- the alkyl group may be saturated or unsaturated.
- the alkyl group may comprise at least one aromatic group.
- Preferred alkoxides include a C ⁇ to C 10 alkyl group, preferably methyl, ethyl, propyl, butyl, or isopropyl.
- Preferred alkoxides include those where the alkyl group is a phenol, substituted phenol (where the phenol may be substituted with up to 1 , 2, 3, 4, or 5 C to C 2 hydrocarbyl groups) or a C to C Q hydrocarbyl, preferably a C j to C 10 alkyl group, preferably methyl, ethyl, propyl, butyl, or phenyl.
- a polymer when referred to as “comprising an olefin,” the olefin present in the polymer is the polymerized form of the olefin.
- a “polymer” has one or more of the same or different mer units.
- a “copolymer” is a polymer having two or more mer units that are different from each other.
- An “oligomer” is a polymer having two to 100 mer units, where the mer units may be the same or different. Exemplary oligomers include dimers (two mer units), trimers (three mer units), tetramers (four mer units), decamers (ten mer units), and so on.
- An "olefin,” alternatively referred to as “alkene,” is a linear, branched, or cyclic compound of carbon and hydrogen having at least one double bond.
- An "alpha-olefm” is an olefin having a double bond at the alpha (or 1-) position.
- a “linear alpha-olefm” or “LAO” is an olefin with a double bond at the alpha position and a linear hydrocarbon chain.
- a “polyalphaolefm” or “PAO” is a polymer having at least 100 mer units.
- An “anionic ligand” is a negatively charged ligand which donates one or more pairs of electrons to a metal ion.
- a “neutral donor ligand” is a neutrally charged ligand which donates one or more pairs of electrons to a metal ion.
- catalyst compositions are described as comprising neutral stable forms of the components, it is well understood by one of ordinary skill in the art, that the ionic form of the component is the form that reacts with the monomers to produce polymers.
- the transition metal compound used for catalysis may be described as a catalyst precursor, a pre- catalyst compound, a catalyst, or a catalyst compound, and these terms are used interchangeably.
- a "reactor" is any container(s) in which a chemical reaction occurs.
- the present invention comprises novel catalyst compositions useful for the metathesis of olefins, methods of making such catalyst compositions, and processes for the use thereof. More particularly, the present invention comprises novel metathesis catalyst compositions which comprise the reaction product of: (i) a Group 8 metal hydride- dihydrogen complex; and (ii) a ligand exchange agent; methods of making such catalyst compositions and processes for the use thereof.
- the present invention comprises novel metathesis catalyst compositions useful to produce a linear alpha-olefm by a process comprising contacting at least one renewable feedstream with at least one lower olefin in the presence of the metathesis catalyst compositions of the present invention.
- the present invention comprises novel metathesis catalyst compositions useful to produce a polyolefm by a process comprising contacting at least one cyclic olefin with the metathesis catalyst compositions of the present invention.
- the inventors have discovered a new class of Group 8 metal catalyst compositions useful for metathesis reactions and an efficient and commercially economic route to these desirable Group 8 metal catalyst compositions, described herein.
- the inventors have further demonstrated utility of this class of Group 8 metal catalyst compositions for metathesis reactions, in particular, CM, ROCM, and ROMP.
- the new class of Group 8 metal catalyst compositions may be made in a single step and used in situ, thereby avoiding multistep synthesis and associated post-synthetic purification steps which tend to be costly, in terms of time, effort, and money.
- This invention relates to a metathesis catalyst composition
- a metathesis catalyst composition comprising: (i) a Group 8 metal hydride-dihydrogen complex represented by the formula:
- M is a Group 8 metal, preferably ruthenium or osmium, preferably ruthenium;
- X is an anionic ligand, preferably X is selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates; preferably X is a halide; preferably X is a chloride; and
- Li and L 2 are neutral donor ligands, preferably I and L 2 are independently selected from the group consisting of a phosphine, a sulfonated phosphine, a phosphite, a phosphinite, a phosphonite, an arsine, a stibine, an ether, an amine, an imine, a sulfoxide, a carboxyl, a nitrosyl, a pyridine, a thioester, a cyclic carbene, and substituted analogs thereof; preferably a phosphine, a sulfonated phosphine, an N-heterocyclic carbene, a cyclic alkyl amino carbene, and substituted analogs thereof; and
- J is selected from the group consisting of hydrogen, a C to C30 hydrocarbyl, and a Cj to C30 substituted hydrocarbyl;
- Y is an anionic group selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates.
- phosphines may be represented by the formula PR3, wherein R is independently selected from the group comprising hydrogen, C j to C 12 hydrocarbyl groups, substituted Cj to C 1 2 hydrocarbyl groups, and halides; preferably methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, pentyl, cyclopentyl, hexyl, cyclohexyl, heptyl, and substituted analogs and isomers thereof, preferably cyclohexyl.
- a "cyclic carbene” may defined as a cyclic compound with a neutral dicoordinate carbon center featuring a lone of electrons.
- Such cyclic carbenes may be represented by the formula II below:
- n is a linking group comprising from one to four ring vertices selected from the group consisting of C, Si, N, P, O, and S, with available valences optionally occupied by H, oxo, hydrocarbyl, or substituted hydrocarbyl groups; preferably, n comprises two ring vertices of carbon with available valences occupied by H, oxo, hydrocarbyl or substituted hydrocarbyl groups; preferably n is C 2 H 2 , C 2 H 4 , or substituted versions thereof;
- E is independently selected from the group comprising C, N, S, O, and P, with available valences optionally occupied by L X , L Y , L Z , and L Z >; preferably, at least one E is a C; preferably, one E is a C and the other E is a N; preferably, both E's are C; and
- L x , L y , L z , and L z > are independently selected from the group comprising hydrogen, hydrocarbyl groups, and substituted hydrocarbyl groups; preferably, L x , L y , L z , and L z > are independently selected from the group comprising a hydrocarbyl group and substituted hydrocarbyl group having 1 to 40 carbon atoms; preferably, L x , L y , L z , and L z > are independently selected from the group comprising ⁇ _ 10 alkyl, substituted ⁇ _ 10 alkyl, C 2- io alkenyl, substituted C 2 _io alkenyl, C 2 _io alkynyl, substituted C 2 _io alkynyl, aryl, and substituted aryl; preferably, L x , L y , L z , and L z > are independently selected from the group comprising methyl, ethyl, propyl, but
- Useful substituents include C I .I Q alkyl, C 2 _i0 alkenyl, C 2 _ IQ alkynyl, aryl, C ⁇ Q alkoxy, C 2 _ IQ alkenyloxy, C 2 _IQ alkynyloxy, aryloxy, C 2 _io alkoxycarbonyl, C I . I Q alkylthio, C I . I Q alkylsulfonyl, fluoro, chloro, bromo, iodo, oxo, amino, imine, nitrogen heterocycle, hydroxy, thiol, thiono, phosphorous, and carbene groups. Examples of cyclic carbenes useful in embodiments of the present invention
- L x , L y , and L z are as defined above.
- at least two of L x , L y , L z , and L z > may be joined to form a 3- to 12-membered spirocyclic ring, with available valences optionally occupied by H, oxo, halogens, hydrocarbyl or substituted hydrocarbyl groups.
- Useful substituents include ⁇ _ 10 alkyl, C 2- io alkenyl, C 2- io alkynyl, aryl, C ⁇ Q alkoxy, C 2 _ 10 alkenyloxy, C 2- io alkynyloxy, aryloxy, C 2 _io alkoxy carbonyl, C I . I Q alkylthio, C I . I Q alkylsulfonyl, fluoro, chloro, bromo, iodo, oxo, amino, imine, nitrogen heterocycle, hydroxy, thiol, thiono, phosphorous, and carbene groups.
- NHCs N-heterocyclic carbenes
- NHCs are cyclic carbenes of the types described in Formula II above, where each E is N and the available valences on the N are occupied by L x and L y .
- NHCs may be represented b the formula:
- n, L x , and L y are as described above.
- Some particularly useful NHCs include: where L x and L y are as described above.
- Other useful NHCs include the compounds described in Hermann, W. A. Chem. Eur. J., 1996, 2, 772 and 1627; Enders, D. et al, Angew. Chem. Int. Ed. 1995, 34, 1021; Alder R. W., Angew. Chem. Int. Ed., 1996, 35, 1121; and Bertrand, G. et al, Chem. Rev., 2000, 100, 39.
- CAACs cyclic alkyl amino carbines
- CAACs are cyclic carbenes of the types described in Formula II above, where one E is N and the other E is C, and the available valences on the N and C are occupied by L x , L y , and L .
- CAACs may be represented by the formula:
- L x , L y , and L z are as described above.
- CAACs include:
- CAACs include the compounds described in U.S. Patent No. 7,312,331 and Bertrand et al, Angew. Chem. Int. Ed., 2005, 44, 7236-7239.
- carbenes useful in embodiments of the present invention include thiazolyidenes, P-heterocyclic carbenes (PHCs), and cyclopropenylidenes.
- L 2 may be the same or different.
- Lj and L 2 are both cyclohexylphosphine groups (Cy 3 P).
- L 2 are different, that is is an ethoxy group and L 2 is a cyclohexylphosphine group.
- at least one of and L 2 is selected from a phosphine, an N-heterocyclic carbene, a cyclic alkyl amino carbene, and substituted analogs thereof.
- Group 8 metal hydride-dihydrogen complexes include: l,3-bis-(2,4,6-trimethylphenyl)-2-
- a "ligand exchange agent” is a compound represented by the formula J-Y, where J is selected from the group consisting of hydrogen, a C ⁇ to C 30 hydrocarbyl, and a C to C30 substituted hydrocarbyl, preferably a C2 to C 1 5 hydrocarbyl or a C 2 to C 15 substituted hydrocarbyl, preferably a C 2 to C 8 hydrocarbyl or a C 2 to C 8 substituted hydrocarbyl, preferably ethyl, chloroethyl, dichloroethyl, trichloroethyl, tetrachloroethyl, pentachloroethyl; and Y is an anionic group selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates, preferably a halide or an alkoxide, preferably a chloride.
- a "ligand exchange agent” is a compound represented by the formula R 3 C-CR 3 , where each R group is, independently, hydrogen, or a halide (preferably I, Br or CI, preferably CI), provided that at least three R groups are halide, preferably at least four R groups, preferably at least five R groups are halide, preferably six R groups are halide (preferably I, Br or CI, preferably CI).
- the ligand exchange agent is represented by the formula: R 3 C-CR 3 , where each R group is, independently, hydrogen or chloride, provided that at least three R groups are chloride.
- the ligand exchange agent is tetrachloroethane, pentachloroethane, hexachloroethane, preferably pentachloroethane, hexachloroethane or a mixture thereof.
- ligand exchange agents react with the Group 8 metal hydride-dihydrogen complex described above, by abstracting a ligand (I or L 2 ) and donating the heteroatom-containing group Y to the Group 8 metal hydride-dihydrogen complex.
- the hexachloroethane is thought to abstract a phosphine ligand (Cy3P) and donate a chloride heteroatom to the Group 8 metal hydride-dihydrogen complex.
- Hexachloroethane has been reported to act as a mild chlorinating agent for tungsten complexes in Organometallics 1984, 3, 476-484.
- the inventors demonstrate the utility of ligand exchange agents, such as hexachloroethane, for generating active Group 8 metal complexes by both abstracting a ligand and donating a heteroatom-containing group to the
- Useful ligand exchange agents include halogenating agents wherein
- Y is a halide, preferably chlorinating agents, wherein Y is a chloride, preferably the ligand exchange agent comprises tetrachloroethane, pentachloroethane, hexachloroethane, preferably pentachloroethane, hexachloroethane or a mixture thereof.
- the metathesis catalyst composition further comprises an acetylene compound represented by the formula:
- R j and R2 are independently selected from the group consisting of hydrogen, a C to C30 hydrocarbyl, and a C ⁇ to C 30 substituted hydrocarbyl; preferably from the group consisting of a hydrogen, a C2 to C 1 5 hydrocarbyl, and a C2 to C1 5 substituted hydrocarbyl; preferably from the group consisting of a hydrogen, a C 2 to C 6 hydrocarbyl, and a C 2 to C 6 substituted hydrocarbyl; preferably at least one of R j and R 2 is hydrogen; preferably at least one of R j and R 2 is ethyl, propyl, butyl, phenyl, hexyl, cyclohexyl.
- acetylene compounds include: acetylene, methylacetylene, ethylacetylene, propylacetylene, butylacetylene, pentylacetylene, hexylacetylene, phenylacetylene, isomers, and substituted analogs thereof, preferably acetylene or phenylacetylene.
- Exemplary catalyst compositions include a composition of a Group 8 metal hydride-dihydrogen complex and a ligand exchange agent; and a composition of a Group 8 metal hydride-dihydrogen complex, a ligand exchange agent, and an acetylene, more particularly, a composition of a Group 8 metal hydride-dihydrogen complex and hexachloroethane; and a composition of a Group 8 metal hydride-dihydrogen complex, hexachloroethane, and an acetylene, even more particularly, a composition of RuClH(H 2 )(PCy 3 ) 2 and pentachloroethane; and a composition of RuClH(H 2 )(PCy 3 ) 2 , hexachloroethane, and phenylacetylene.
- the catalyst composition employed in the process of this invention may be bound to or deposited on a solid support.
- the Group 8 metal hydride-dihydrogen complex may be bound to or deposited onto a solid support, which may simplify catalyst recovery.
- the support may increase catalyst strength and attrition resistance.
- Suitable catalyst supports include, without limitation, silicas, aluminas, silica-aluminas, aluminosilicates, including zeolites, and other crystalline porous aluminosilicates; as well as titanias, zirconia, magnesium oxide, carbon, and cross-linked polymeric resins, such as functionalized cross-linked polystyrenes, e.g., chloromethyl- functionalized cross-linked polystyrenes; preferably silica or alumina.
- the Group 8 metal hydride-dihydrogen complex may be deposited onto the support by any method known to those skilled in the art, including, for example, impregnation, ion-exchange, deposition- precipitation, and vapor deposition.
- a component of the catalyst composition such as the Group 8 metal hydride-dihydrogen complex
- the catalyst composition may be immobilized by one or more covalent bonds with one or more of substituents of a ligand of the Group 8 metal hydride-dihydrogen complex.
- the Group 8 metal hydride- dihydrogen complex may be deposited onto a silica support.
- the Group 8 metal hydride-dihydrogen complex may be preloaded onto the solid support before forming the catalyst composition of the present invention.
- the supported catalyst composition may be generated in situ.
- the catalyst compound may be loaded onto the catalyst support in any amount, provided that the metathesis process of this invention proceeds to the metathesis products.
- the catalyst compound is loaded onto the support in an amount based on the weight of the transition metal, preferably the Group 8 metal, preferably ruthenium or osmium, relative to the total weight of the catalysts plus support.
- the catalyst compound may be loaded onto the support in an amount greater than about 0.01 weight percent of the Group 8 metal, and preferably, greater than about 0.05 weight percent of the Group 8 metal.
- the catalyst compound is loaded onto the support in an amount that is less than about 20 weight percent of the Group 8 metal, and preferably, less than about 10 weight percent of the Group 8 metal.
- metathesis catalysts described herein may be synthesized by any methods known to those skilled in the art.
- the metathesis catalysts of the present invention are made by contacting a Group 8 metal hydride-dihydrogen complex of the formula
- the metathesis catalysts of the present invention are made by contacting a Group 8 metal hydride-dihydrogen complex of the formula
- each of the Group 8 metal hydride-dihydrogen complex, the ligand exchange agent, and the acetylene are as described above, and whereby the ligand exchange agent is believed to both abstract a ligand from the Group 8 metal hydride-dihydrogen complex and donate the heteroatom Y to the Group 8 metal hydride-dihydrogen complex.
- the Group 8 metal hydride-dihydrogen complex, the ligand exchange agent, and the acetylene may be made by any suitable method.
- Representative methods of synthesizing the Group 8 metal hydride-dihydrogen complex of the type described herein include, for example, those reported in Organometallics, 1997, 16, 3867.
- the metathesis catalysts of the present invention are made by contacting the Group 8 metal hydride-dihydrogen complex with a ligand exchange agent, and, optionally, an acetylene, as described above, where any of the reactants may be dissolved in a suitable solvent, include non-coordinating, inert liquids.
- Examples include straight and branched-chain hydrocarbons such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof; cyclic and alicyclic hydrocarbons such as cyclohexane, cycloheptane, methylcyclohexane, methylcycloheptane, and mixtures thereof, including those that can be found commercially (IsoparTM); perhalogenated hydrocarbons such as perfluorinated C 4 .
- straight and branched-chain hydrocarbons such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof
- cyclic and alicyclic hydrocarbons such as cyclohexane, cyclohept
- alkanes such as benzene, toluene, mesitylene, and xylene.
- Suitable diluents/solvents also include aromatic hydrocarbons, such as toluene or xylenes, and chlorinated solvents, such as dichloromethane.
- the reactants may be used neat, that is, in the absence of a carrier solvent.
- the metathesis catalysts of the present invention are made by contacting the Group 8 metal hydride-dihydrogen complex with a ligand exchange agent, and, optionally, an acetylene, as described above, in any amount sufficient to form the metathesis products.
- the "catalyst loading" is the number of moles of olefin relative to the number of moles of Group 8 metal hydride-dihydrogen complex.
- the catalyst loading is typically greater than 10: 1; preferably, greater than 100: 1; preferably, greater than 1,000: 1; preferably, greater than 10,000: 1; preferably, greater than 25,000: 1; preferably, greater than 50,000: 1; preferably, greater than 100,000: 1.
- the molar ratio of renewable feedstream to metathesis catalyst is typically less than 10,000,000: 1; preferably, less than 1,000,000: 1; and more preferably, less than 500,000: 1.
- the ligand exchange agent, and, optionally, an acetylene may be used in equimolar amounts, relative to the amount of olefin used.
- an excess of the ligand-exchange agent, and, optionally, an acetylene may be used, relative to the amount of olefin used, for example, the ligand-exchange agent and, optionally, the acetylene may be used in amounts of 5 molar equivalents, 10 molar equivalents, 15 molar equivalents, 50 molar equivalents, 100 molar equivalents; preferably 10 molar equivalents, 50 molar equivalents.
- the catalyst loading is less than 100,000: 1 and the ligand exchange agent, and, optionally, an acetylene are used in equimolar amounts, relative to the amount of olefin used. In other embodiments, the catalyst loading is less than 100,000: 1 and the ligand exchange agent, and, optionally, an acetylene are used in a 10 molar equivalent amount, relative to the amount of olefin used in the reaction.
- the contacting process may occur in the presence of heat, for example, heat to reflux, for a time period appropriate to yield the desired metathesis catalyst.
- the ligand exchange reaction may occur faster in such embodiments.
- the contacting process may occur at a temperature of 20 to 300°C (preferably, 20 to 200°C; preferably, 25 to 100°C; preferably, 25 to 60°C) for a contacting time of 0.5 seconds to 48 hours (preferably, 0.25 to 24 hours; preferably, 30 minutes to 2 hours).
- the active metathesis catalysts are generated due to the ligand exchange agent, for example, hexachloroethane, serving two functions, specifically, to remove a ligand, for example, a phosphine, from the Group 8 metal hydride-dihydrogen complex and to donate a heteroatom, for example, a chloride, to the Group 8 metal hydride-dihydrogen complex.
- the active metathesis catalyst may be generated through reaction with olefin reactant or, embodiments where an acetylene is part of the catalyst composition, by rapid insertion of acetylene into the Group 8 metal hydride, as shown below:
- L 1 ? L 2 , M, X, J, and Y are as defined above and R is a hydrocarbyl group derived from the acetylene or the olefin, and is also described as above.
- the inventors conducted NMR experiments to investigate the behavior of the ligand exchange agents pentachloroethane and hexachloroethane.
- Contacting the free phosphine ligand tricyclohexylphosphine (Cy3P) with hexachloroethane generated the species Cy 3 PCl 2 ( 3 1 P NMR (CH 2 C1 2 ): ⁇ 107.4).
- contacting the free phosphine ligand tricyclohexylphosphine (Cy3P) with pentachloroethane generated the species Cy3PCl 2 ( 3 1 P NMR (CH 2 C1 2 ): ⁇ 107.3).
- a Group 8 metal hydride-dihydrogen complex of the formula (Cy3P) 2 RuH(H 2 )Cl was found to be stable in deuterated dichloromethane ( 3 1 P NMR (CH 2 C1 2 ): ⁇ 53.8). However, on contacting the (Cy3P) 2 RuH(H 2 )Cl with the ligand exchange agent hexachloroethane, a reaction occurred, producing Cy3PCl 2 ( 1 P NMR (CH 2 C1 2 ): ⁇ 1 17.4, 107.9 (Cy 3 PCl 2 ), and 92.3 (br)).
- the inventors suggest that the reaction indicates that hexachloroethane abstracts a phosphine ligand from (Cy3P) 2 Ru(H 2 )HCl through an oxidation pathway and donates a chloride heteroatom to the ruthenium complex, producing Cy 3 PCl 2 as a byproduct.
- metathesis catalyst compositions comprising: (i) a Group 8 metal hydride-dihydrogen complex; and (ii) a ligand exchange agent, as previously described, generate an active catalyst suitable for metathesis reactions.
- the catalysts of the present invention may be used for any metathesis reaction, including ROMP, RCM, CM, ROCM, and so on, by contacting the inventive catalysts with olefins.
- a process for performing a metathesis reaction comprises contacting at least one olefin with a metathesis catalyst, wherein the metathesis catalyst comprises a Group 8 metal hydride-dihydrogen complex represented by the formula:
- a method for performing a metathesis reaction comprises contacting at least one olefin with a metathesis catalyst, wherein the metathesis catalyst comprises (i) a Group 8 metal hydride-dihydrogen complex represented by the formula:
- J is selected from the group consisting of hydrogen, a C to C30 hydrocarbyl, and a Cj to C30 substituted hydrocarbyl;
- Y is selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates.
- a method for performing a metathesis reaction comprises contacting at least one olefin with a metathesis catalyst, wherein the metathesis catalyst comprises (i) a Group 8 metal hydride-dihydrogen complex represented by the formula:
- a ligand exchange agent represented by the formula J-Y where J is selected from the group consisting of hydrogen, a C to C30 hydrocarbyl, and a C j to C30 substituted hydrocarbyl; and Y is selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates; and
- R j and R 2 are independently selected from the group consisting of hydrogen, a C j to C30 hydrocarbyl, and a C j to C30 substituted hydrocarbyl.
- a method for performing a metathesis reaction comprises contacting at least one olefin with a metathesis catalyst, wherein the metathesis catalyst comprises (i) a Group 8 metal hydride-dihydrogen complex as described above; (ii) hexachloroethane; and (iii) phenylacetylene.
- the metathesis reaction proceeds slowly in the presence of the Group 8 metal hydride-dihydrogen complex, for example, in Example 6 the polymerization to a viscous poly(dicyclopentadiene) (poly-DCPD) takes three hours.
- the metathesis reaction proceeds at about the same rate in the presence of the Group 8 metal hydride-dihydrogen complex and the ligand exchange agent, for example, in Example 8 the polymerization to a viscous poly-DCPD also takes three hours.
- the metathesis reaction proceeds faster in the presence of the Group 8 metal hydride-dihydrogen complex, the ligand exchange agent, and acetylene, for example, in Examples 1 and 4 the polymerization to a viscous poly-DCPD takes just 6 minutes and four minutes, respectively.
- the CM reaction proceeds slowly in the presence of the Group 8 metal hydride-dihydrogen complex, for example, Example 18, with a conversion of 1-hexene to cis/trans-5-decene of 2.2%.
- the CM reaction proceeds at about the same rate in the presence of the Group 8 metal hydride-dihydrogen complex and the ligand exchange agent, for example, Example 20, with a conversion of 1-hexene to cis/trans-5-decene of 2.1%.
- the CM reaction proceeds even faster in the presence of the Group 8 metal hydride-dihydrogen complex, the ligand exchange agent, and acetylene, for example, Examples 16 and 17, with a conversion of 1-hexene to cis/trans-5-decene of 7.4% and 4.5%, respectively.
- the metathesis catalyst compositions of the present invention are also useful as isomerization catalysts.
- the isomerization catalysts isomerizes an alpha olefin into its respective internal isomers.
- 1-hexene was isomerized to internal isomers, such as hex-2-ene, hex-3-ene, and so on.
- Example 16 31.0% of the 1-hexene was converted to internal olefins, while 7.4% of the 1-hexene was converted to the cross- metathesis product of cis/trans-5-decene.
- Any olefin may be used in the processes for performing a metathesis reaction of this invention.
- the olefin may have one carbon-carbon double bond, or alternatively, two or more carbon-carbon double bonds. Since the metathesis reaction can occur at any double bond, olefins having more than one double bond will produce more metathesis products. Accordingly, in some embodiments, it is preferred to employ an olefin having only one carbon-carbon double bond.
- the double bond may be, without limitation, a terminal double bond or an internal double bond.
- the olefin may also be substituted at any position along the carbon chain with one or more substituents. In some embodiments, the one or more substituents are essentially inert with respect to the metathesis process.
- Suitable substituents include, without limitation, alkyl, preferably, Ci .g alkyl; cycloalkyl, preferably, C 3 . 6 cycloalkyl; as well as hydroxy, ether, keto, aldehyde, and halogen functionalities.
- the reactant olefin may be chosen, depending on the application the metathesis product may be employed in, as illustrated in the applications below.
- the reactant olefin may be at least one of an acyclic olefin, an alpha olefin, a renewable feedstream, a cyclic olefin, and an internal olefin. Production of LAOs From Renewable Feedstreams by Cross Metathesis
- the present invention involves a process for performing a metathesis reaction, as described above, wherein the at least one olefin comprises at least one lower olefin and at least one renewable feedstream.
- the metathesis product comprises a linear alphaolefm (LAO).
- lower olefin refers to an organic compound containing at least one carbon-carbon double bond and having 6 carbon atoms or less.
- both R* are the same; preferably, both R* are hydrogen.
- ethylene is a lower olefin that is particularly useful in embodiments herein.
- Non-limiting examples of suitable lower olefins include ethylene, propylene, butene, butadiene, and isomers thereof.
- the lower olefin is ethylene.
- renewable feedstreams means starting materials that are derived from renewable sources. A source is considered renewable if it is replenished by natural means.
- Renewable feedstreams useful herein include fatty acids, fatty acid esters, natural oils, biodiesel, triacylglycerides, or mixtures thereof.
- Natural oils includes oils derived from biological sources, including animals, plants, algae, and fungi. Natural oils typically comprise mixtures of fatty acids and fatty acid esters, which are discussed below. These fatty acids often naturally occur as esters of three fatty acids and glycerol, known as triglycerides, also discussed below.
- Natural oils useful herein preferably contain fatty acids and fatty acid esters with at least one site of unsaturation and include, but are not limited to, canola oil, corn oil, soybean oil, rapeseed oil, algae oil, peanut oil, mustard oil, sunflower oil, tung oil, tall oil, perilla oil, grapeseed oil, linseed oil, saffiower oil, pumpkin oil, palm oil, Jatropha oil, high- oleic soybean oil, high-oleic saffiower oil, high-oleic sunflower oil, mixtures of animal and vegetable fats and oils, beef tallow, castor bean oil, dehydrated castor bean oil, cucumber oil, poppyseed oil, flaxseed oil, lesquerella oil, walnut oil, cottonseed oil, meadowfoam, tuna oil, sesame oils, waste oils/greases, and mixtures thereof.
- fatty acids and fatty acid esters available from animal fats including, without limitation, lard, and fish oils, such as sardine oil, tuna oil, herring oil, and the like, may be employed in embodiments herein.
- particular fatty acids or fatty acid precursors may also be advantageously available from genetically modified organisms, such as genetically modified plants, particularly genetically modified algae.
- genetically modified organisms are typically designed to produce a desired fatty acid or fatty acid precursor biosynthetically or to advantageously produce increased amounts of such compounds.
- Preferred natural oils include palm oil, soybean oil, sunflower oil, canola oil, Jatropha oil, and algae oil.
- Fatty acids are carboxylic acids with saturated or unsaturated aliphatic tails that occur naturally in many different natural oils.
- Fatty acid esters are alkyl esters of fatty acids; preferably, C j to C 2 esters; preferably, C j to C5 esters; preferably, methyl, ethyl, n-propyl, n-butyl esters; more preferably, methyl or ethyl esters.
- An unsaturated fatty acid comprises a long carbon chain containing at least one carbon-carbon double bond and terminating in a carboxylic acid group.
- An unsaturated fatty acid ester also comprises a long carbon chain containing at least one carbon-carbon double bond but terminates in a carboxylate group.
- Unsaturated fatty acids, unsaturated fatty acid esters, and mixtures thereof are of particular importance in embodiments herein. Any unsaturated fatty acid or fatty acid ester may be suitably employed to produce LAOs, provided that the unsaturated fatty acid or fatty acid ester can be metathesized in the manner disclosed herein. At least one carbon-carbon double bond may occur at any internal location, usually about the middle of the aliphatic tail. A terminal carbon-carbon double bond, at the opposite end of the carbon chain relative to the carboxylic acid or carboxylate group, is also suitably employed, although terminal carbon- carbon double bonds occur less commonly in fatty acids.
- Monounsaturated fatty acids and fatty acid esters contain one carbon-carbon double bond in the long aliphatic tail.
- Examples of monounsaturated fatty acids and fatty acid esters useful herein include myristoleic acid, palmitoleic acid, sapienic acid, oleic acid, erucic acid, and alkyl esters thereof.
- Polyunsaturated fatty acids and fatty acid esters contain two or more carbon-carbon double bonds in the long aliphatic tail.
- polyunsaturated fatty acids and esters useful herein include linoleic acid, linolenic acid, arachidonic acid, eicosapentaenoic acid, docosahexaenoic acid, and alkyl esters thereof.
- Some natural oils may contain fatty acids and fatty acid esters that are polyunsaturated, and some of the sites of unsaturation may be internal.
- oleic acid, linoleic acid, and linolenic acid, and their respective esters are examples of fatty acid and fatty acid esters with internal sites of unsaturation.
- Methyl oleate has one internal double bond
- methyl linoleate has two internal double bonds
- methyl linolenoate has three internal double bonds, as shown below.
- Fatty acids and fatty acid esters useful herein include monounsaturated fatty acids and esters thereof, polyunsaturated fatty acids and esters thereof, and mixtures of monounsaturated and polyunsaturated fatty acids and esters thereof.
- the unsaturated fatty acid will contain greater than 8 carbon atoms; preferably, greater than 10 carbon atoms; and more preferably, greater than 12 carbon atoms.
- the unsaturated fatty acid will contain less than 50 carbon atoms; preferably, less than 35 carbon atoms; and more preferably, less than 25 carbon atoms.
- the unsaturated fatty acid may be straight or branched, and may be substituted along the fatty acid chain with one or more substituents, provided that the one or more substituents are substantially inert with respect to the metathesis process.
- suitable substituents include alkyl moieties, preferably, ⁇ _ 10 alkyl moieties, including, for example, methyl, ethyl, propyl, butyl, and the like; cycloalkyl moieties, preferably, C 4 .
- cycloalkyl moieties including for example, cyclobutyl, cyclopentyl, cyclohexyl and cyclooctyl; monocyclic aromatic moieties, preferably, C ⁇ aromatic moieties, including for example, phenyl; and alkylaryl moieties, preferably, C 7 _ 16 alkylaryl moieties, including, for example, tolyl, ethylphenyl, xylyl, and the like; as well as hydroxyl, ether, keto, aldehyde, and halide, preferably, chloride and bromide, functionalities.
- Non-limiting examples of suitable unsaturated fatty acid and fatty acid esters include 3-hexenoic (hydrosorbic), trans-2-heptenoic, 2-octenoic, 2-nonenoic, cis-and trans-4- decenoic, 9-decenoic (caproleic), 10-undecenoic (undecylenic), trans-3-dodecenoic (linderic), tridecenoic, cis-9-tetradeceonic (myristoleic), pentadecenoic, cis-9-hexadecenoic (cis-9- palmitoelic), trans-9-hexadecenoic (trans-9-palmitoleic), 9-heptadecenoic, cis-6-octadecenoic (petroselinic), trans-6-octadecenoic (petroselaidic), cis-9-octadecenoic (oleic), trans-9- oct
- the natural oils useful in the processes described herein typically include a mixture of saturated (Cn:0), monounsaturated (Cn: l), and polyunsaturated (Cn:2, 3, etc.) fatty acids, where n is the number of carbon atoms present in the fatty acid.
- Cn:0 saturated
- Cn: l monounsaturated
- Cn:2, 3, etc. polyunsaturated
- Table 1 the fatty acid profiles of several potential natural oil feedstreams are shown in Table 1 , below.
- the renewable feedstream comprises a combination of natural oils.
- Preferred combinations include two or more of tall oil, palm oil, tallow, waste grease, rapeseed oil, canola oil, soybean oil, sunflower oil, Jatropha oil, and algae oil.
- Alternate useful combinations include two (three or four) or more of soybean oil, sunflower oil, palm oil, canola oil, rapeseed oil, algae oil, Jatropha oil, and tallow.
- TAGs Triacylglycerides
- TAGs triacylglycerides
- TAGs are a naturally occurring ester of three fatty acids and glycerol.
- the three fatty acids can be all different, all the same, or only two the same. They can be saturated or unsaturated fatty acids, and the saturated fatty acids may have one or multiple sites of unsaturations.
- Chain lengths of the fatty acids in naturally occurring TAGs can be of varying lengths, but 16, 18, and 20 carbons are the most common.
- Natural fatty acids found in plants and animals are typically composed of even numbers of carbon atoms due to the way they are bio-synthesized. Most natural fats contain a complex mixture of individual triglycerides and because of this, they melt over a broad range of temperatures.
- TAGs typically have the chemical structure:
- R a , R b , and R c each, independently, represent a saturated or non-saturated hydrocarbon chain (preferably, R a , Rb, and R c each, independently, are a C ⁇ to C28 alkyl or olefin, preferably, Ci g to C22 alkyl or olefin).
- Different vegetable oils have different fatty acid profiles, with the same or different fatty acids occurring on a single glycerol.
- an oil can have linoleic, oleic, and stearic acids attached to the same glycerol, with each of R a , Rb, and R c representing one of these three fatty acids.
- a useful TAG consists of three unsaturated fatty acids, where at least one fatty acid is oleic acid. In another embodiment, a useful TAG consists of three unsaturated fatty acids, where at least one fatty acid is linoleic acid. In yet another embodiment, a useful TAG consists of three unsaturated fatty acids, where at least one fatty acid is oleic acid and at least one fatty acid is linoleic acid. In other embodiments, a mixture of different TAGs may be used.
- fatty acid glycerides or other fatty acid esters can also be used, including phospholipids, lysophospho lipids, and fatty acid wax esters.
- the free fatty acid content of useful natural oils is preferably about 0.1 wt% or less when employed in a basic homogeneous catalyst esterification reaction. Higher levels can be utilized as well, and levels up to about 3.0 wt%, or even as high as about 15.0 wt% or more may be tolerated.
- TAGs may be processed by transesterification with alcohols to give biodiesel.
- Biodiesel is typically a mixture of mono-alkyl fatty acid esters, and is useful as a renewable feedstream for methods disclosed herein. The processing of natural oils is discussed in greater detail below.
- Raw or unrefined oils can be used in certain embodiments. However, filtered and refined oils are typically preferred. Use of degummed and filtered feedstreams minimizes the potential for emulsification and blockage in the reactor systems.
- Feedstreams with high water content can be dried before use.
- Feedstreams with high free fatty acid content can be passed through an esterification process to reduce the free fatty acid content before the process of esterification to convert fatty acid glycerides to monoalkyl esters. The reduction of free fatty acids and the conversion of fatty acid glycerides can be accomplished in the same processing step.
- Feedstreams containing other organic compounds such as hexane, heptane, isohexane, etc.
- processed oils such as blown oils
- Blown oils are processed through partial oxidation.
- Common blown oils available include linseed oil, castor oil, fish oil, and soybean oil.
- Natural oils may be further processed before use in the present invention, for example, natural oils may be esterified with alcohols to convert any fatty acids present to fatty acid esters, to produce biodiesel.
- Biodiesel is a mixture of mono-alkyl fatty acid esters typically derived from the transesterification of natural oils and alcohols. While natural oils and alcohols are commonly employed as reactants in esterification reactions, any fatty acid source, such as free fatty acids, soaps, esters, glycerides (mono-, di-, and tri-), phospholipids, lysophospholipids, or amides and a monohydric alcohol source, such as an alcohol, can be esterified.
- Biodiesel compositions that are particularly useful in this invention are those which have high concentrations of oleic acids, erucic acids, and esters thereof. These fatty acids and esters have one site of unsaturation such that CM with ethylene yields the LAO, 1- decene, as the coproduct.
- Preferred biodiesel compositions are those produced from natural oils such as canola oil, rapeseed oil, palm oil, and other high oleic or high erucic oils.
- Particularly preferred natural oils include those having at least 30 mol% combined oleic and erucic fatty acid or esters of all fatty acid and fatty acid esters combined, preferably at least 40%, preferably at least 50%, preferably at least 60%>, preferably at least 70%>, preferably at least 80%, preferably at least 90%.
- biodiesel compositions that are particularly useful in this invention are those which have high concentrations of oleic, erucic, linoleic, and linolenic acids and respective esters thereof.
- Preferred biodiesel compositions are those produced from vegetable oils such as canola oil, soybean oil, sunflower oil, Jatropha oil, and other oils having a high concentration of oleic, erucic, linoleic, and linolenic acids and respective esters thereof.
- Particularly preferred vegetable oils include those having at least 50 mol% oleic, erucic, linoleic, and linolenic acids and respective esters thereof of all fatty acid and fatty acid ester chains combined, preferably at least 60%, preferably at least 70%, preferably at least 80%, preferably at least 90%.
- LAOs Linear Alpha Olefins
- the metathesis catalyst may be combined with the lower olefin and renewable feedstream in any manner known in the art.
- the metathesis catalysts described herein may be combined directly with the lower olefin and renewable feedstreams to produce alpha-olefms, preferably LAOs, preferably C4 to C24 alpha-olefms, preferably C4 to C 2 4 LAOs, such as preferably 1-decene, 1-heptene, and/or 1-butene.
- the molar ratio of lower olefin to renewable feedstream is greater than 0.8: 1.0, preferably, greater than 0.9: 1.0, greater than 1.0: 1.0, greater than 1.5: 1.0, greater than 2.0: 1.0.
- the molar ratio of lower olefin to feed material is less than 3.0: 1.0, preferably, less than 2.0: 1.0, less than 1.5: 1.0.
- other molar ratios may also be suitable.
- the molar ratio of ethylene to renewable feedstream may range from greater than 0.8: 1 to typically less than 20: 1.
- the renewable feedstream comprises unsaturated fatty acid esters and/or unsaturated fatty acids and is provided as a liquid at the process temperature, and it is generally preferred to be used neat, that is, without a diluent or solvent.
- a solvent usually increases recycle requirements and increases costs.
- a solvent can be employed with the lower olefin and/or renewable feedstream.
- a solvent may be desirable, for instance, where liquid feed material and lower olefin are not entirely miscible, and both then can be solubilized in a suitable solvent.
- the CM reaction of the lower olefin and the renewable feedstream may be run in a biphasic mixture of solvents, in an emulsion or suspension, or in a lipid vesicle, or bilayer.
- Suitable diluents/solvents for the process include non-coordinating, inert liquids.
- Examples include straight and branched-chain hydrocarbons, such as isobutane, butane, pentane, isopentane, hexanes, isohexane, heptane, octane, dodecane, and mixtures thereof; cyclic and alicyclic hydrocarbons, such as cyclohexane, cycloheptane, methylcyclohexane, methylcycloheptane, and mixtures thereof, including those that can be found commercially (IsoparTM); perhalogenated hydrocarbons, such as perfluorinated C 4 .
- the feed for the process comprises 60 vol% solvent or less, based on the total volume of the feed, preferably 40 vol% or less, preferably 20 vol% or less.
- the quantity of metathesis catalyst that is employed in the process of this invention is any quantity that provides for an operable metathesis reaction.
- the ratio of moles of renewable feedstream (such as unsaturated fatty acid or fatty acid ester) to moles of metathesis catalyst is typically greater than 10: 1; preferably, greater than 100: 1; preferably, greater than 1,000: 1; preferably, greater than 10,000: 1; preferably, greater than 25,000: 1; preferably, greater than 50,000: 1; preferably, greater than 100,000: 1.
- from 0.005 nmoles to 500 nmoles, preferably from 0.1 to 250 nmoles, and most preferably from 1 to 50 nmoles of the metathesis catalyst are charged to the reactor per 3 mmoles of renewable feedstream (such as TAGs, biodiesel, fatty acids, fatty acid esters, and/or fatty acid alkyl esters, or mixtures thereof; preferably, fatty acid esters) charged.
- renewable feedstream such as TAGs, biodiesel, fatty acids, fatty acid esters, and/or fatty acid alkyl esters, or mixtures thereof; preferably, fatty acid esters
- the process may be batch, semi-batch, or continuous.
- continuous means a system that operates without interruption or cessation.
- a continuous process to produce a metathesis product would be one where the reactants are continually introduced into one or more reactors and metathesis products are continually withdrawn.
- the processes may be conducted in any of glass lined, stainless steel, or similar type reaction equipment.
- Useful reaction vessels include reactors (including continuous stirred tank reactors, batch reactors, reactive extruder, pipe, or pump, continuous flow fixed bed reactors, slurry reactors, fluidized bed reactors, and catalytic distillation reactors).
- the reaction zone may be fitted with one or more internal and/or external heat exchanger(s) in order to control temperature fluctuations.
- the contacting time of the renewable feedstream and catalyst can be of any duration, provided that the desired olefin metathesis products are obtained.
- the contacting time in a reactor is greater than 5 minutes; and preferably, greater than 10 minutes.
- the contacting time in a reactor is less than 25 hours; preferably, less than 15 hours; and more preferably, less than 10 hours.
- the reactants for example, metathesis catalyst; renewable feedstream; lower olefin, optional diluent, etc.
- a reaction vessel at a temperature of 20 to 300°C (preferably, 20 to 200°C; preferably, 30 to 100°C; preferably, 40 to 60°C) and an olefin (such as ethylene) at a pressure of 0.1 to 1000 psi (0.7 kPa to 6.9 MPa) (preferably, 20 to 400 psi (0.14 MPa to 2.8MPa); preferably, 50 to 250 psi (0.34 MPa to 1.7MPa)), if the olefin is present, for a residence time of 0.5 seconds to 48 hours (preferably, 0.25 to 5 hours; preferably, 30 minutes to 2 hours).
- the olefin pressure is greater than 5 psig (34.5 kPa); preferably, greater than 10 psig (68.9 kPa); and more preferably, greater than 45 psig (310 kPa).
- the aforementioned pressure ranges may also be suitably employed as the total pressure of olefin and diluent.
- the aforementioned pressure ranges may be suitably employed for the inert gas pressure.
- the process is typically a solution process, although it may be a bulk or high pressure process. Homogeneous processes are preferred. (A homogeneous process is defined to be a process where at least 90 wt% of the product is soluble in the reaction media.) A bulk homogeneous process is particularly preferred. (A bulk process is defined to be a process where reactant concentration in all feeds to the reactor is 70 vol% or more.) Alternately, no solvent or diluent is present or added in the reaction medium, (except for the small amounts used as the carrier for the catalyst or other additives, or amounts typically found with the reactants, e.g., propane in propylene).
- the conversion of the renewable feedstream (preferably, fatty acid ester) to the desired LAO products can vary widely depending upon the specific reagents, such as, for example, the lower olefins, the specific metathesis catalyst, the specific process conditions employed, and the specific chemical makeup of the fatty acid ester.
- “conversion” is defined as the mole percentage of feed material that is converted to the CM products, that is, LAOs.
- the conversion of the renewable feedstream (preferably, fatty acid ester) to LAOs is greater than 50 mol%; preferably, greater than 60 mol%; and more preferably, greater than 70 mol%.
- the conversion of the renewable feedstream (preferably, fatty acid ester) to LAOs is greater than 50 mol%; preferably, greater than 60 mol%; and more preferably, greater than 70 mol%.
- the yields of the LAO can also vary depending upon the specific reagent olefins, catalyst, and process conditions employed.
- Yield will be defined as the mole percentage of LAOs formed relative to the initial moles of renewable feedstream (such as, fatty acid ester in the feed).
- renewable feedstock comprises TAGs (as represented in the formula below):
- R a , R b , and R c each, independently, represent a saturated or unsaturated hydrocarbon chain (preferably, R a , R b , and R c each, independently, are a C 2 to C28 alkyl or olefin; preferably, Ci g to C22 alkyl or olefin)
- the yield may be defined as the mole percentage of LAOs formed relative to the initial moles of starting fatty acid ester (unsaturated R a + moles of unsaturated B + moles of unsaturated R c ) introduced into the reactor.
- the yield may be defined by the mole percentage of LAOs formed relative to the initial moles of starting fatty acid ester.
- the yield of LAOs is greater than 30 mol% or more; preferably, greater than 35 mol% or more; preferably, greater than 40 mol% or more; preferably, greater than 45 mol% or more; preferably, greater than 50 mol% or more; preferably, greater than 55 mol% or more; preferably, greater than 60 mol% or more.
- the yield of LAOs is greater than 30 mol% or more; preferably, greater than 35 mol% or more; preferably, greater than 40 mol% or more; preferably, greater than 45 mol% or more; preferably, greater than 50 mol% or more; preferably, greater than 55 mol% or more; preferably, greater than 60 mol% or more.
- productivity is defined to be the amount in grams of LAO produced per mmol of catalyst introduced into the reactor, per hour.
- productivity of the process is at least 200 g of LAO (such as, decene-1) per mmol of catalyst per hour; preferably, at least 5000 g/mmol/hour; preferably, at least 10,000 g/mmol/hour; preferably, at least 300,000 g/mmol/hour.
- selectivity is a measure of conversion of lower olefin and renewable feedstream to the LAO products, and is defined by the mole percentage of LAOs formed relative to the initial moles of lower olefin or renewable feedstream. In a preferred embodiment, the selectivity of the process is at least 20 wt%
- LAOs based upon the weight of the material exiting the reactor, preferably, at least 25 wt%; preferably, at least 30 wt%; preferably, at least 35 wt%., preferably, at least 40 wt%; preferably, at least 45 wt%; preferably, at least 50 wt%; preferably, at least 60 wt%; preferably, at least 70 wt%; preferably, at least 80 wt%; preferably, at least 85 wt%; preferably, at least 90 wt%; preferably, at least 95 wt%.
- TON catalyst turnover number
- the (TON) of the process is at least 5,000; preferably, at least 10,000; preferably, at least 50,000; preferably, at least 100,000; preferably, at least 1 ,000,000.
- a fatty acid or a fatty acid ester which is monosaturated may be cross-metathesized with a lower olefin in the presence of metathesis catalysts of the present invention to produce a desired C4 to C40 LAO.
- metathesis catalysts of the present invention For example, methyl oleate and ethylene may be cross-metathesized using a suitable metathesis catalyst to produce major CM products of 1-decene and methyl-9-decanoate. Both products are alpha-olefms; however, the decanoate terminates in an ester moiety at the opposite end of the chain from the carbon-carbon double bond.
- the methyl oleate may self- metathesize to produce small amounts of 9-octadecene, a less desirable product, and dimethyl-9-octadecene-l,18-dioate, a second less desirable product.
- mixtures of fatty acids, or fatty acid esters, or a natural oil comprising mixtures of monosaturated and polyunsaturated fatty acids and/or esters, or a mixture of natural oils may be cross-metathesized with a lower olefin in the presence of a suitable metathesis catalyst to produce a desired LAO.
- a mixture of methyl oleate and methyl linoleate may be cross-metathesized with ethylene to produce 1-decene.
- Ring-Opening Metathesis Polymerization (ROMP)
- the present invention involves a process for performing a metathesis reaction, as described above, wherein the at least one olefin comprises at least one cyclic olefin.
- the metathesis product comprises a polyolefm.
- the cyclic olefin may be a single cyclic olefin, or a combination of cyclic olefins, that is a mixture of two or more different cyclic olefins.
- the cyclic olefins may be strained or unstrained, monocyclic, or polycyclic; and may optionally include hetero atoms and/or one or more functional groups.
- Suitable cyclic olefins include, but are not limited to norbornene, norbomadiene, dicyclopentadiene, cyclopentene, cycloheptene, cyclooctene, cyclooctadiene, cyclododecene, 7-oxanorbornene, 7-oxanorbornadiene, and substituted derivatives therefrom.
- substituents include, but are not limited to, hydroxyl, thiol, ketone, aldehyde, ester, ether, amine, imine, amide, nitro, carboxylic acid, disulfide, carbonate, isocyanate, carbodiimide, carboalkoxy, and halogen.
- Preferred cyclic olefins include cyclooctene, 1,5 -cyclooctadiene, l-hydroxy-4-cyclooctene, l-acetoxy-4-cyclooctene, 5-methylcyclopentene, cyclopentene, dicyclopentadiene, norbornene, norbomadiene, and their respective homologs and derivatives, preferably norbornene, norbomadiene, and dicyclopentadiene, as shown below.
- the cyclic olefins discussed above may undergo ROMP to form a polyolefm.
- the ROMP reaction may occur either in the presence or absence of solvent and may optionally include additives.
- additives include antistatics, antioxidants, light stabilizers, plasticizers, dyes, pigments, fillers, reinforcing fibers, lubricants, adhesion promoters, viscosity-increasing agents, and demolding enhancers.
- fillers for improving the optical physical, mechanical and electrical properties include glass and quartz in the form of powders, beads and fibers, metal and semi-metal oxides, carbonates (i.e., MgC03, CaC03), dolomite, metal sulfates (such as, gypsum and barite), natural and synthetic silicates (i.e., zeolites, wollastonite, feldspars), carbon fibers, and plastic fibers or powders.
- NBD norbornadiene
- the present invention involves a process for performing a metathesis reaction, as described above, wherein the at least one olefin comprises at least one cyclic olefin and at least one second olefin.
- the metathesis product comprises a ROCM product of the cyclic olefin and the second olefin.
- the cyclic olefin may be a single cyclic olefin, or a combination of cyclic olefins, that is a mixture of two or more different cyclic olefins, as described above.
- Any olefin may be used for the ROCM reaction with the at least one cyclic olefin.
- terminal olefin may be used.
- terminal olefin refers to an organic compound containing at least one carbon-carbon double bond, where the at least one carbon-carbon double bond occurs between the alpha and beta carbons of the chain.
- R* is independently, hydrogen or a C to C30 hydrocarbyl; preferably, a C 2 to C 2 o hydrocarbyl; preferably, a C 2 to C 12 hydrocarbyl; preferably, methyl, ethyl, propyl, butyl, pentyl, hexyl, and substituted and cyclic analogs thereof.
- 1-hexene, 1-heptene, and 1-decene are terminal olefins that are particularly useful in embodiments herein.
- internal olefins may be used.
- internal olefin refers to an organic compound containing at least one carbon-carbon double bond, where the at least one carbon-carbon double bond does not occur between the alpha and beta carbons of the chain.
- TBS means "tert-but
- ROCM involves a tandem sequence in which a cyclic olefin is opened and a second, acyclic olefin is crossed onto the newly formed termini.
- the Group 8 metal-bound intermediate has two options: reaction with another cyclic olefin or reaction with the other olefin.
- a cyclic olefin will undergo a ring opening reaction in the presence of the catalyst at a rate constant k RO
- the second olefin reactant will undergo a cross- metathesis reaction with the ring opened cyclic olefin at a rate constant k ⁇ j j
- k ⁇ is greater than or equal to k RO
- the ROCM product is predominantly a monomer, dimer, and/or oligomer, but not a polymer. More specifically, when k CM is approximately equal to k RO , the ROCM product is predominantly a dimer or oligomer, while when k RO is greater than 13 ⁇ 4M > the ROCM product is predominantly a polymer. Dimers and oligomers are of particular interest because their internal olefin moieties may be further functionalized by metathesis or other transformations.
- Monomers are also of interest, particularly when they can be prepared so as to be end differentiated, i.e., asymmetric with regard to the two terminal olefinic groups resulting from the ROCM reaction. It should be appreciated that k RO will be higher for moderately and highly strained cyclic olefins such as cyclooctadiene, but lower for low-strain olefins such as cyclopentene and cyclohexene.
- metathesis catalyst composition comprises (Cy3P)2Ru(H 2 )HCl, hexachloroethane, and, optionally, phenylacetylene.
- the choice of the cyclic olefin and the second olefin used in a ROCM reaction may allow for tailoring of the resultant capped poly(cyclic olefin).
- Use of olefins with protected functionalities, for example, TBS-protected 4-penten-l-ol, may allow for introduction of functional groups to the capped poly(cyclic olefin).
- Some examples of functionalized poly(cyclic olefin)s include those that are functionalized with maleic acid or maleic anhydride groups.
- the functionalized capped poly(cyclic olefin) can in turn be derivatized with a derivatizing compound, such as described in U.S. Patent No. 6,022,929; A. Toyota, T. Tsutsui, and N. Kashiwa, Polymer Bulletin 48, 213-219, 2002; and J. Am. Chem. Soc, 1990, 112, 7433-7434.
- the derivatizing compound can react with the functional groups of the functionalized capped poly(cyclic olefin) by any means known in the art, such as nucleophilic substitution, Mannich Base condensation, and the like.
- the derivatizing compound can be polar and/or contain reactive derivative groups.
- Preferred derivatizing compounds are selected from hydroxy containing compounds, amines, metal salts, anhydride containing compounds, and acetyl halide containing compounds.
- the derivatizing compounds can comprise at least one nucleophilic group and preferably at least two nucleophilic groups.
- An exemplary derivatized capped poly(cyclic olefin) may be made by contacting a functionalized capped poly(cyclic olefin), for example, one substituted with a carboxylic acid/anhydride or ester, with a nucleophilic reagent, for example, amines, alcohols (including polyols), amino alcohols, reactive metal compounds and the like. (For more information, please see U.S. Patent No. 6,022,929, column 33, line 27 to column 74, line 63.)
- this invention relates to:
- a metathesis catalyst comprising (preferably comprising the reaction product of): i. a Group 8 metal hydride-dihydrogen complex represented by the formula:
- M is a Group 8 metal; preferably, M is ruthenium or osmium;
- X is an anionic ligand; preferably, selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates; and
- Li and L 2 are neutral donor ligands; preferably, and L 2 are independently selected from the group consisting of a phosphine, a sulfonated phosphine, a phosphite, a phosphinite, a phosphonite, an arsine, a stibine, an ether, an amine, an imine, a sulfoxide, a carboxyl, a nitrosyl, a pyridine, a thioester, a cyclic carbene, and substituted analogs thereof; preferably, at least one of L j and L 2 is selected from a phosphine, an N-heterocyclic carbene, a cyclic alkyl amino carbene, and substituted analogs thereof; and
- J is selected from the group consisting of hydrogen, a C ⁇ to C 30 hydrocarbyl, and a C ⁇ to C30 substituted hydrocarbyl;
- Y is selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates; preferably, Y is a halide; preferably, Y is chloride, preferably the ligand exchange agent represented by the formula R3C-CR3, where each R group is, independently, hydrogen, or a halide (preferably I, Br or CI, preferably CI), provided that at least three R groups are halide, preferably at least four R groups, preferably at least five R groups are halide, preferably six R groups are halide (preferably I, Br, or CI, preferably CI).
- the metathesis catalyst composition of paragraph 1, wherein the Group 8 metal hydride-dihydrogen complex is selected from l,3-bis-(2,4,6-trimethylphenyl)-2- (imidazolidinylidene)(tricyclohexylphosphine)(dihydrogen) rutheniumhydridochloride, bis- (tricyclohexylphosphine)(dihydrogen)rutheniumhydridochloride, (l-mesityl-3-methyl-2H- 4,5-dihydroimidazol-2-ylidene)(tricyclohexylphosphine)-(dihydrogen)
- R j and R 2 are independently selected from the group consisting of hydrogen, a C ⁇ to C30 hydrocarbyl, and a C to C30 substituted hydrocarbyl; preferably, at least one of R j and R 2 is hydrogen; preferably, the acetylene compound is acetylene or phenylacetylene.
- a method for making the metathesis catalyst composition of paragraphs 1 to 3, comprising:
- R j and R 2 are independently selected from the group consisting of hydrogen, a C ⁇ to C30 hydrocarbyl, and a C to C30 substituted hydrocarbyl; preferably, at least one of R j and R 2 is hydrogen; preferably, the acetylene compound is acetylene or phenylacetylene.
- a process for performing a metathesis reaction comprising:
- metathesis catalyst comprises a Group 8 metal hydride-dihydrogen complex represented by the formula:
- M is a Group 8 metal; preferably, M is ruthenium or osmium; X is an anionic ligand; preferably, selected from the group consisting of halides, alkoxides, aryloxides, and alkyl sulfonates; and
- I and L 2 are neutral donor ligands; preferably, I and L 2 are independently selected from the group consisting of a phosphine, a sulfonated phosphine, a phosphite, a phosphinite, a phosphonite, an arsine, a stibine, an ether, an amine, an imine, a sulfoxide, a carboxyl, a nitrosyl, a pyridine, a thioester, a cyclic carbene, and substituted analogs thereof; preferably, at least one of I and L 2 is selected from a phosphine, an N-heterocyclic carbene, a cyclic alkyl amino carbene, and substituted analogs thereof.
- a process for performing a metathesis reaction comprising:
- R 2 are independently selected from the group consisting of hydrogen, a C ⁇ to C30 hydrocarbyl, and a C to C30 substituted hydrocarbyl; preferably, at least one of R j and R 2 is hydrogen; preferably, the acetylene compound is acetylene or phenylacetylene.
- the at least one olefin comprises at least one cyclic olefin, selected from cyclooctene, 1,5-cyclooctadiene, l-hydroxy-4- cyclooctene, l-acetoxy-4-cyclooctene, 5-methylcyclopentene, cyclopentene, dicyclopentadiene, norbornene, and norbornadiene; and wherein a polyolefm is produced.
- the at least one olefin is a linear alpha olefin, and wherein the linear alpha olefin is isomerized to internal isomers thereof.
- Cy is cyclohexyl
- DCM dichloromethane
- DCPD is dicyclopentadiene
- NB is norbornene
- NBD is norbornadiene
- HCE hexachloroethane
- PCE pentachloroethane
- PhAc is phenyl acetate.
- Typical dry-box procedures for synthesis of air-sensitive compounds were followed, including using dried glassware (90°C, 4 hours) and using anhydrous solvents purchased from Sigma Aldrich (St. Louis, MO), which were further dried over 3 A sieves. All reagents were purchased from Sigma-Aldrich and used as received, unless otherwise noted. 1-hexene was obtained from Aldrich and dried over a NaK alloy prior to use.
- a sample of the metathesis product will be taken and analyzed by GC.
- An internal standard usually tetradecane, is used to derive the amount of metathesis product that is obtained.
- the amount of metathesis product is calculated from the area under the desired peak on the GC trace, relative to the internal standard. Yield or conversion is reported as a percentage and defined as 100 x [micromoles of metathesis products obtained by GC]/[micromoles of feed material weighed into reaction vessel].
- Yields of isomerized product were obtained by subtraction of the yield of metathesis product obtained (determined from GC spectra, above) from the yield of total internal olefins (determined from 3 ⁇ 4 NMR data, above).
- Catalyst compositions described herein were used for the ROMP of DCPD (dicyclopentadiene), norbornadiene (NBD or bicyclo[2.2.1]hepta-2,5-diene), or norbornene (NB or bicyclo[2.2.1]hept-2-ene).
- the Group 8 metal hydride-dihydrogen complex used was RuClH(H 2 )(PCy3) 2 , which was prepared as described in Organometallics 1997, 16, 3867.
- the ligand exchange agent used was hexachloroethane or pentachloroethane.
- the acetylene used was phenylacetylene.
- Example 1 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added. One equivalent of phenylacetylene and hexachloroethane per equivalent of RuClH(H 2 )(PCy3) 2 was charged via the addition of 0.1 mis each of a 72 mM stock solution of phenylacetylene and hexachloroethane, respectively. The ring opening polymerization of dicyclopentadiene was observed by a gradual thickening of the solution to a rubbery viscous material after six minutes. After one hour a solid rubbery material had formed.
- Example 2 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added. Five equivalents of phenylacetylene and hexachloroethane per equivalent of RuClH(H 2 )(PCy3) 2 were added via the addition of 0.5 mis of 72 mM solution of phenylacetylene and hexachloroethane, respectively.
- the ring- opening polymerization of dicyclopentadiene was observed by a rapid thickening of the solution to a rubbery viscous material. After 4 minutes, the material was a rubbery solid. After 24 hours, the material was a hard rubbery solid.
- Example 3 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy 3 ) 2 was added. One equivalent of phenylacetylene per equivalent of RuClH(H 2 )(PCy3) 2 was added via the addition of 0.1 mis of 72 mM solution of phenylacetylene. Ten equivalents of hexachloroethane per equivalent of RuClH(H 2 )(PCy3) 2 were charged via the addition of 1.0 mis of a 72 mM solution. The ring opening polymerization of dicyclopentadiene was observed by a gradual thickening of the solution to a rubbery viscous material after six minutes. After one hour, a solid rubbery material had formed.
- Example 4 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3) 2 was added. Ten equivalents of phenylacetylene and hexachloroethane per equivalent of RuClH(H2)(PCy3)2 were added via the addition of 1.0 mis each of a 72 mM solution of phenylacetylene and hexachloroethane, respectively. The ring opening polymerization of dicyclopentadiene was observed by a rapid thickening of the solution to a rubbery viscous material. After 4 minutes, the material was a rubbery solid. After 24 hours, a hard rubbery solid was obtained.
- Example 5 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 1.2 milligram (1.7 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added. One equivalent of phenylacetylene per equivalent of RuClH(H 2 )(PCy3) 2 was added via the addition of 0.1 mis of 72 mM solution of phenylacetylene. 100 equivalents of hexachloroethane (170 mg) was added. The ring opening polymerization of dicyclopentadiene was observed slowly by a gradual thickening of the solution to a rubbery viscous material after three hours. After 24 hours, the material was gel-like.
- Example 6 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added. The ring opening polymerization of dicyclopentadiene was observed slowly by a gradual thickening of the solution to a rubbery viscous material after three hours. After 24 hours, the material was a soft rubbery material.
- Example 7 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added. One equivalent of phenylacetylene per equivalent of RuClH(H 2 )(PCy3) 2 was added via the addition of 0.1 mis of a 72 mM solution of phenylacetylene. The ring opening polymerization of dicyclopentadiene was observed slowly by a gradual thickening of the solution to a rubbery viscous material after three hours. After 24 hours, the material was soft and rubbery.
- Example 8 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H2)(PCy3)2 was added. One equivalent of hexachloroethane was charged per equivalent of RuClH(H 2 )(PCy3)2 via the addition of 0.1 mis of a 72 mM hexachloroethane solution. The ring opening polymerization of dicyclopentadiene was observed slowly by a gradual thickening of the solution to a rubbery viscous material after three hours. After 24 hours, the material was a soft rubbery material.
- Example 9 ROMP of DCPD: A 10.0 gram (75.6 mmol) amount of dicyclopentadiene was added to a 100 ml round-bottom flask. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2, ten equivalents of hexachloroethane, and ten equivalents of phenylacetylene were added via the addition of a 0.5 mis stock solution containing 2.5 mis of CH 2 C1 2 , 25 mg RuClH(H 2 )(PCy 3 ) 2 , 86 mg of hexachloroethane and 36 mg of phenylacetylene. The ring opening polymerization of dicyclopentadiene was observed slowly by a gradual thickening of the solution to a rubbery viscous material after three hours. After 24 hours, it had become a soft rubbery material.
- Example 10 ROMP of Norbornadiene: A 10.0 gram (108 mmol) amount of bicyclo[2.2.1]hepta-2,5-diene was added to a lOOmL round-bottom flask. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H2)(PCy3)2, ten equivalents of hexachloroethane and ten equivalents of phenylacetylene were added. The material was very viscous after two minutes at which point the material foamed and became a sponge-like material.
- Example 11 ROMP of Norbornadiene: A 10.0 gram (108 mmol) amount of bicyclo[2.2.1]hepta-2,5-diene was added to a 100 mL round-bottom flask. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2, ten equivalents of pentachloroethane and ten equivalents of phenylacetylene were added. The material became very viscous after two minutes, at which point the material foamed and became sponge-like.
- Example 12 ROMP of Norbornene: A 10.0 gram (106 mmol) amount of bicyclo[2.2.1]hept-2-ene was added to a lOOmL round-bottom flask. A 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2, ten equivalents of hexachloroethane and ten equivalents of phenylacetylene were added. Immediately upon the dropwise addition of the catalyst solution, a sponge-like rubbery material formed. Twenty minutes after catalyst addition all the monomer had been converted into the rubbery material. TABLE 2: Summary Of ROMP Reactions Using Metathesis Catalysts
- Example 13 Cross-metathesis of 1-hexene.
- a 10.0 gram (119 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial.
- a 5.0 milligram (7.2 ⁇ ) amount of RuClH(H2)(PCy3)2 was added.
- One equivalent of phenylacetylene and hexachloroethane per equivalent of RuClH(H 2 )(PCy3)2 was charged to the vial via the addition of 0.1 mis each of a 72 mM solution of phenylacetylene and hexachloroethane, respectively.
- the conversion to cis/trans-5-decene was monitored by GC & 3 ⁇ 4 NMR.
- Example 14 Cross-metathesis of 1-hexene.
- a 10.0 gram (119 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial.
- a 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added.
- Five equivalents of phenylacetylene and hexachloroethane per equivalent of RuClH(H2)(PCy3)2 were added via the addition of 0.1 mis each of a 72 mM solution of phenylacetylene and hexachloroethane, respectively.
- the conversion to cis/trans- 5-decene was monitored by GC & 3 ⁇ 4 NMR.
- Example 15 Cross-metathesis of 1-hexene.
- a 10.0 gram (1 19 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial.
- a 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added.
- RuClH(H 2 )(PCy3)2 was added via the addition of 0.1 mis of a 72 mM solution of phenylacetylene. Ten equivalents of hexachloroethane per equivalent of RuClH(H 2 )(PCy3)2 was added via the addition 1.0 mis of a 72 mM solution. The conversion to cis/trans-5- decene was monitored by GC & ⁇ NMR. The reactions were performed at room temperature and sampled after two days stirring. Isomerization of 1-hexene to internal olefins was observed as well as some cross metathesis: cis/trans-5 -decene 5.7% yield; internal olefins 20.7% yield.
- Example 16 Cross-metathesis of 1-hexene.
- a 10.0 gram (119 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial.
- a 5.0 milligram (7.2 ⁇ ) amount of RuClH(H2)(PCy3)2 was added.
- Ten equivalents of phenylacetylene and hexachloroethane per equivalent of RuClH(H 2 )(PCy3)2 were added via the addition of 1.0 mis each of a 72 mM solution of phenylacetylene and hexachloroethane, respectively.
- the conversion to cis/trans- 5 -decene was monitored by GC & 3 ⁇ 4 NMR.
- Example 17 Cross-metathesis of 1-hexene.
- a 10.0 gram (1 19 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial.
- a 1.2 milligram (1.4 ⁇ ) amount of RuClH(H 2 )(PCy3)2 was added.
- One equivalent of phenylacetylene per equivalent of RuClH(H 2 )(PCy3) 2 was added via the addition of 0.1 mis of a 72 mM solution of phenylacetylene.
- One hundred equivalents of hexachloroethane (170 mg) per equivalent of RuClH(H 2 )(PCy3) 2 were added.
- Example 18 Cross-metathesis of 1-hexene.
- a 10.0 gram (119 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial.
- a 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3) 2 was added.
- the conversion to cis/trans-5 -decene was monitored by GC & 3 ⁇ 4 NMR. The reactions were performed at room temperature and sampled after two days stirring. Isomerization of 1-hexene to internal olefins was observed as well as some cross metathesis: cis/trans-5 -decene 2.2% yield; internal olefins 11.9% yield.
- Example 19 Cross-metathesis of 1-hexene. A 10.0 gram (1 19 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial. A 5.0 milligram (7.2 ⁇ ) amount of
- RuClH(H 2 )(PCy3) 2 was added via the addition of 0.1 mis of a 72 mM solution of phenylacetylene.
- the conversion to cis/trans-5 -decene was monitored by GC & 3 ⁇ 4 NMR. The reactions were performed at room temperature and sampled after two days stirring. Isomerization of 1-hexene to internal olefins was observed as well as some cross metathesis: cis/trans-5-decene 3.4% yield, internal olefins 13.5% yield.
- Example 20 Cross-metathesis of 1-hexene.
- a 10.0 gram (1 19 mmoles) amount of 1-hexene was added to a 20 ml scintillation vial.
- a 5.0 milligram (7.2 ⁇ ) amount of RuClH(H 2 )(PCy3) 2 was added.
- One equivalent of hexachloro ethane was added via the addition of 0.1 mis of a 72 mM hexachloroethane solution.
- the conversion to cis/trans-5- decene was monitored by GC & 3 ⁇ 4 NMR. The reactions were performed at room temperature and sampled after two days stirring. Isomerization of 1-hexene to internal olefins was observed as well as some cross metathesis: cis/trans-5-decene 2.1% yield; internal olefins 10.2% yield.
- PhAc phenylacetylene
- the Group 8 metal hydride-dihydrogen complex used was RuClH(H 2 )(PCy3)2, which was prepared as described in Organometallics, 1997, 16, 3867.
- the ligand exchange agent used was hexachloroethane.
- the acetylene used was phenylacetylene.
- Example 21 Ring-Opening Cross Metathesis of Norbornadiene and 1- Decene.
- a 28.0 g (0.199 mol) amount of 1-decene was combined with 1 1.0 g (0.199 mol) of norbornadiene.
- a 6.8 mgs (9.8 ⁇ ⁇ ⁇ ) amount of RuClH(H 2 )(PCy3) 2 was combined in a 20 ml vial with 140 mgs (60 equivalents) of hexachloroethane and 5.0 mgs (5 equivalents) of phenylacetylene in 1 ml of dichloromethane.
- the catalyst solution was combined into the 1- decene/norbornadiene mixture. An exo therm resulted.
- compositions encompasses the terms “consisting essentially of,” “is,” and “consisting of and anyplace “comprising” is used “consisting essentially of,” “is,” or “consisting of may be substituted therefor.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Catalysts (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11827288.9A EP2618930A4 (fr) | 2010-09-24 | 2011-09-19 | Nouvelle classe de catalyseurs de métathèse d'oléfines, méthodes de préparation, et procédés d'utilisation |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/890,315 US8227371B2 (en) | 2010-09-24 | 2010-09-24 | Class of olefin metathesis catalysts, methods of preparation, and processes for the use thereof |
EP10194264 | 2010-12-09 | ||
EP11827288.9A EP2618930A4 (fr) | 2010-09-24 | 2011-09-19 | Nouvelle classe de catalyseurs de métathèse d'oléfines, méthodes de préparation, et procédés d'utilisation |
PCT/US2011/052109 WO2012040088A2 (fr) | 2010-09-24 | 2011-09-19 | Nouvelle classe de catalyseurs de métathèse d'oléfines, méthodes de préparation, et procédés d'utilisation |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2618930A2 true EP2618930A2 (fr) | 2013-07-31 |
EP2618930A4 EP2618930A4 (fr) | 2014-04-02 |
Family
ID=45874302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP11827288.9A Withdrawn EP2618930A4 (fr) | 2010-09-24 | 2011-09-19 | Nouvelle classe de catalyseurs de métathèse d'oléfines, méthodes de préparation, et procédés d'utilisation |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP2618930A4 (fr) |
CN (1) | CN103079699B (fr) |
WO (1) | WO2012040088A2 (fr) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2742074A4 (fr) * | 2011-08-12 | 2015-04-01 | Exxonmobil Chem Patents Inc | Polymères préparés par ouverture de cycle/métathèse croisée |
MX2015017461A (es) * | 2013-06-24 | 2016-08-12 | Materia Inc | Aislante térmico. |
CN110170077B (zh) * | 2019-03-26 | 2021-09-28 | 南京理工大学 | 一种聚离子型生物润滑剂及其制备方法 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5599962A (en) * | 1995-01-31 | 1997-02-04 | E. I. Du Pont De Nemours And Company | Process for the preparation of ruthenium hydrogenation catalysts and products thereof |
US5917071A (en) * | 1996-11-15 | 1999-06-29 | California Institute Of Technology | Synthesis of ruthenium or osmium metathesis catalysts |
DE19820652A1 (de) * | 1998-05-08 | 1999-11-11 | Basf Ag | Kationische Rutheniumkomplexe, Verfahren zu ihrer Herstellung und ihre Verwendung |
AU2002307089A1 (en) * | 2001-04-02 | 2002-10-15 | California Institute Of Technology | One-pot synthesis of group 8 transition metal carbene complexes useful as olefin metathesis catalysts |
-
2011
- 2011-09-19 WO PCT/US2011/052109 patent/WO2012040088A2/fr active Application Filing
- 2011-09-19 EP EP11827288.9A patent/EP2618930A4/fr not_active Withdrawn
- 2011-09-19 CN CN201180041259.5A patent/CN103079699B/zh not_active Expired - Fee Related
Non-Patent Citations (5)
Title |
---|
BERGENS ET AL: "A Ruthenium-Dihydrogen Putative Intermediate in Ketone Hydrogenation", J. AM.CHEM. SOC, vol. 127, 1 March 2005 (2005-03-01), pages 4152-4153, XP002619901, * |
FOGG ET AL: "Carbonyl-Amplified Catalyst Performance: Balancing Stability against Activity for Five-Coordinate Ruthenium Hydride and Hydridocarbonyl Catalysts", ORGANOMETALLICS, vol. 28, 19 December 2008 (2008-12-19), pages 441-447, XP002619900, * |
See also references of WO2012040088A2 * |
STUER W ET AL: "A tertiary phosphine that is too bulky: preparation of catalytically less active carbene and vinylidene ruthenium(II) complexes", JOURNAL OF ORGANOMETALLIC CHEMISTRY, ELSEVIER-SEQUOIA S.A. LAUSANNE, CH, vol. 641, no. 1-2, 4 January 2002 (2002-01-04), pages 203-207, XP004326738, ISSN: 0022-328X, DOI: DOI:10.1016/S0022-328X(01)01300-6 * |
WILHELM T E ET AL: "REACTIVITY OF RU(H)(H2)CL(PCY3)2 WITH PROPARGYL AND VINYL CHLORIDES: NEW METHODOLOGY TO GIVE METATHESIS-ACTIVE RUTHENIUM CARBENES", ORGANOMETALLICS, ACS, WASHINGTON, DC, US, vol. 16, no. 18, 2 September 1997 (1997-09-02), pages 3867-3869, XP001027486, ISSN: 0276-7333, DOI: DOI:10.1021/OM9705259 * |
Also Published As
Publication number | Publication date |
---|---|
CN103079699A (zh) | 2013-05-01 |
CN103079699B (zh) | 2015-07-08 |
WO2012040088A2 (fr) | 2012-03-29 |
EP2618930A4 (fr) | 2014-04-02 |
WO2012040088A3 (fr) | 2012-06-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8227371B2 (en) | Class of olefin metathesis catalysts, methods of preparation, and processes for the use thereof | |
US8524930B2 (en) | Class of olefin metathesis catalysts, methods of preparation, and processes for the use thereof | |
AU2002252124B2 (en) | Metathesis of unsaturated fatty acid esters or unsaturated fatty acids with lower olefins | |
US8237003B2 (en) | Metathesis catalyst and process for use thereof | |
US8809563B2 (en) | Metathesis catalyst and process for use thereof | |
AU2002252124A1 (en) | Metathesis of unsaturated fatty acid esters or unsaturated fatty acids with lower olefins | |
EP2498909B1 (fr) | Catalyseur de métathèse et son procédé d'utilisation | |
JP2008542441A (ja) | α,ω−官能基を有するオレフィンを調製する複分解法 | |
CA2785897C (fr) | Catalyseur de metathese et procede d'utilisation associe | |
US8329921B2 (en) | Metathesis catalyst and process for use thereof | |
EP3129347A1 (fr) | Réactions en présence de complexes de ruthénium | |
EP2498908A2 (fr) | Catalyseurs de métathèse et leurs procédés d'utilisation | |
WO2012040088A2 (fr) | Nouvelle classe de catalyseurs de métathèse d'oléfines, méthodes de préparation, et procédés d'utilisation | |
US9024034B2 (en) | Metathesis catalysts and processes for use thereof | |
CA2777176C (fr) | Catalyseurs de metathese et leurs procedes d'utilisation | |
WO2012166259A2 (fr) | Nouvelle classe de catalyseurs de métathèse d'oléfine, procédés de préparation et procédés pour l'utilisation de celle-ci | |
WO2014004089A1 (fr) | Catalyseur de métathèse et son procédé d'utilisation | |
KR20150024396A (ko) | 불포화 화합물의 제조 방법 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20130418 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20140228 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: B01J 31/22 20060101AFI20140224BHEP Ipc: B01J 31/24 20060101ALI20140224BHEP |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
18W | Application withdrawn |
Effective date: 20170712 |