JP2015535809A5 - - Google Patents
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- JP2015535809A5 JP2015535809A5 JP2015528642A JP2015528642A JP2015535809A5 JP 2015535809 A5 JP2015535809 A5 JP 2015535809A5 JP 2015528642 A JP2015528642 A JP 2015528642A JP 2015528642 A JP2015528642 A JP 2015528642A JP 2015535809 A5 JP2015535809 A5 JP 2015535809A5
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- JP
- Japan
- Prior art keywords
- group
- membered
- nitrogen
- optionally substituted
- oxygen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 52
- 229920006395 saturated elastomer Polymers 0.000 claims description 38
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 34
- 125000005842 heteroatom Chemical group 0.000 claims description 34
- 229910052757 nitrogen Inorganic materials 0.000 claims description 34
- 229910052760 oxygen Inorganic materials 0.000 claims description 32
- 239000001301 oxygen Chemical group 0.000 claims description 32
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 30
- 229910052717 sulfur Chemical group 0.000 claims description 30
- 239000011593 sulfur Chemical group 0.000 claims description 30
- 125000000623 heterocyclic group Chemical group 0.000 claims description 17
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 14
- 229920000515 polycarbonate Polymers 0.000 claims description 14
- 239000004417 polycarbonate Substances 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- 150000004696 coordination complex Chemical class 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 6
- 239000001569 carbon dioxide Substances 0.000 claims description 6
- 150000002118 epoxides Chemical class 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
- 125000003367 polycyclic group Chemical group 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 238000004587 chromatography analysis Methods 0.000 claims description 4
- 125000001072 heteroaryl group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 239000003446 ligand Substances 0.000 claims description 4
- VEUMANXWQDHAJV-UHFFFAOYSA-N 2-[2-[(2-hydroxyphenyl)methylideneamino]ethyliminomethyl]phenol Chemical compound OC1=CC=CC=C1C=NCCN=CC1=CC=CC=C1O VEUMANXWQDHAJV-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000002619 bicyclic group Chemical group 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 125000002837 carbocyclic group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000005587 carbonate group Chemical group 0.000 claims description 2
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 238000010276 construction Methods 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- 125000005549 heteroarylene group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002346 iodo group Chemical group I* 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 125000005647 linker group Chemical group 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 125000001620 monocyclic carbocycle group Chemical group 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 238000001556 precipitation Methods 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims 1
- 150000004679 hydroxides Chemical class 0.000 claims 1
- 150000002823 nitrates Chemical class 0.000 claims 1
- 235000021317 phosphate Nutrition 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000000909 amidinium group Chemical group 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261693000P | 2012-08-24 | 2012-08-24 | |
| US61/693,000 | 2012-08-24 | ||
| PCT/US2013/056102 WO2014031811A1 (en) | 2012-08-24 | 2013-08-22 | Metal complexes |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018004171A Division JP2018052995A (ja) | 2012-08-24 | 2018-01-15 | 金属錯体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015535809A JP2015535809A (ja) | 2015-12-17 |
| JP2015535809A5 true JP2015535809A5 (enExample) | 2016-09-29 |
| JP6313305B2 JP6313305B2 (ja) | 2018-04-18 |
Family
ID=50150376
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015528642A Active JP6313305B2 (ja) | 2012-08-24 | 2013-08-22 | 金属錯体 |
| JP2018004171A Withdrawn JP2018052995A (ja) | 2012-08-24 | 2018-01-15 | 金属錯体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018004171A Withdrawn JP2018052995A (ja) | 2012-08-24 | 2018-01-15 | 金属錯体 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US9771388B2 (enExample) |
| EP (1) | EP2888271B1 (enExample) |
| JP (2) | JP6313305B2 (enExample) |
| KR (1) | KR102096761B1 (enExample) |
| CN (1) | CN104781268B (enExample) |
| ES (1) | ES2761880T3 (enExample) |
| WO (1) | WO2014031811A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2879498T3 (es) | 2008-08-22 | 2021-11-22 | Saudi Aramco Tech Co | Catalizadores y métodos para la síntesis de polímeros |
| EP3838403A1 (en) | 2011-05-13 | 2021-06-23 | Novomer, Inc. | Carbonylation catalysts and method |
| CN103827128B (zh) | 2011-07-18 | 2017-08-08 | 诺沃梅尔公司 | 金属络合物 |
| US9359474B2 (en) | 2011-11-04 | 2016-06-07 | Novomer, Inc. | Catalysts and methods for polymer synthesis |
| WO2013090276A1 (en) | 2011-12-11 | 2013-06-20 | Novomer, Inc. | Salen complexes with dianionic counterions |
| US9771388B2 (en) | 2012-08-24 | 2017-09-26 | Saudi Aramco Technologies Company | Metal complexes |
| WO2019126221A1 (en) | 2017-12-22 | 2019-06-27 | Saudi Aramco Technologies Company | Catalysts for polycarbonate production |
| KR102747154B1 (ko) | 2018-04-18 | 2024-12-31 | 사우디 아람코 테크놀로지스 컴퍼니 | 폴리(알킬렌 카보네이트) 중합체의 말단 그룹 이성질체화 |
| US11180609B2 (en) | 2018-08-02 | 2021-11-23 | Saudi Aramco Technologies Company | Sustainable polymer compositions and methods |
| US11634539B2 (en) | 2018-09-24 | 2023-04-25 | Saudi Aramco Technologies Company | Polycarbonate block copolymers and methods thereof |
| TWI906317B (zh) | 2020-06-24 | 2025-12-01 | 沙烏地阿拉伯商沙烏地阿美科技公司 | 多元醇組合物及方法 |
| WO2022153149A1 (en) | 2021-01-12 | 2022-07-21 | Saudi Aramco Technologies Company | Continuous manufacturing of polyol |
| TW202302704A (zh) | 2021-06-23 | 2023-01-16 | 沙烏地阿拉伯商沙烏地阿美科技公司 | 多元醇組合物及方法 |
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-
2013
- 2013-08-22 US US14/422,780 patent/US9771388B2/en active Active
- 2013-08-22 JP JP2015528642A patent/JP6313305B2/ja active Active
- 2013-08-22 EP EP13830629.5A patent/EP2888271B1/en active Active
- 2013-08-22 ES ES13830629T patent/ES2761880T3/es active Active
- 2013-08-22 KR KR1020157007284A patent/KR102096761B1/ko active Active
- 2013-08-22 WO PCT/US2013/056102 patent/WO2014031811A1/en not_active Ceased
- 2013-08-22 CN CN201380053750.9A patent/CN104781268B/zh active Active
-
2017
- 2017-08-22 US US15/683,496 patent/US20170349616A1/en not_active Abandoned
-
2018
- 2018-01-15 JP JP2018004171A patent/JP2018052995A/ja not_active Withdrawn
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| Wang et al. | Syntheses and structural characterization of three new coordination polymers of [Ag (PPIA)· H2O] n,[Cu (PPIA) 2· 2H2O] n and [Zn (PPIA) 2 (H2O) 2] n; PPIA= 3-pyridinepropionic acid | |
| Kim et al. | New topological 3D copper (ii) coordination networks: catechol oxidation catalysis and solvent adsorption via porous properties | |
| Shahverdizadeh et al. | Four mixed-ligands lead (II) complexes based on 8-hydroxyquinolin (8-HQuin),[Pb (8-Quin) X]; X= 4-pyridinecarboxylate, acetate, thiocyanate and nitrate; structural and thermal studies | |
| Rogers et al. | Divalent metal homophthalate coordination polymers with long-spanning dipyridyl ligands containing piperazine moieties | |
| Paul et al. | (μ-O, O′)-nitrito bridged 3-D coordination frameworks of M2+ (Mn Co, Zn) with mab and jsm topology | |
| Verma et al. | Microwave assisted synthesis, spectral and antibacterial studies of complexes of 2-hydroxy-6-methylnicotinic acid with Co (II), Ni (II) and Cu (II) |