CN115651032A - 一种基于甲氧基嘧啶氮氧自由基配体的磁性Co配合物及其制备方法 - Google Patents
一种基于甲氧基嘧啶氮氧自由基配体的磁性Co配合物及其制备方法 Download PDFInfo
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- CN115651032A CN115651032A CN202211215500.8A CN202211215500A CN115651032A CN 115651032 A CN115651032 A CN 115651032A CN 202211215500 A CN202211215500 A CN 202211215500A CN 115651032 A CN115651032 A CN 115651032A
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- 239000003446 ligand Substances 0.000 title claims abstract description 43
- -1 methoxy pyrimidine nitroxide free radical Chemical class 0.000 title claims abstract description 34
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- 239000013078 crystal Substances 0.000 claims abstract description 31
- 150000003254 radicals Chemical class 0.000 claims abstract description 30
- QAMFBRUWYYMMGJ-UHFFFAOYSA-N hexafluoroacetylacetone Chemical compound FC(F)(F)C(=O)CC(=O)C(F)(F)F QAMFBRUWYYMMGJ-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000126 substance Substances 0.000 claims abstract description 5
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- 239000003960 organic solvent Substances 0.000 claims description 25
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 21
- 238000003756 stirring Methods 0.000 claims description 19
- 238000006243 chemical reaction Methods 0.000 claims description 18
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- 238000000034 method Methods 0.000 claims description 15
- 150000002500 ions Chemical class 0.000 claims description 14
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 12
- 101001018064 Homo sapiens Lysosomal-trafficking regulator Proteins 0.000 claims description 10
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 10
- 102100033472 Lysosomal-trafficking regulator Human genes 0.000 claims description 10
- 235000010703 Modiola caroliniana Nutrition 0.000 claims description 10
- 244000038561 Modiola caroliniana Species 0.000 claims description 10
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- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
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- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 7
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 7
- IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 6
- 235000019441 ethanol Nutrition 0.000 claims description 6
- 239000002243 precursor Substances 0.000 claims description 6
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 238000010992 reflux Methods 0.000 claims description 4
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- ZBYYWKJVSFHYJL-UHFFFAOYSA-L cobalt(2+);diacetate;tetrahydrate Chemical compound O.O.O.O.[Co+2].CC([O-])=O.CC([O-])=O ZBYYWKJVSFHYJL-UHFFFAOYSA-L 0.000 claims description 3
- 239000012634 fragment Substances 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000002245 particle Substances 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- RJNPRNCPYHCHHV-UHFFFAOYSA-N cobalt(2+) dinitrate tetrahydrate Chemical compound O.O.O.O.[Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O RJNPRNCPYHCHHV-UHFFFAOYSA-N 0.000 claims description 2
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 claims 2
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 claims 1
- 239000000696 magnetic material Substances 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 7
- 229910021645 metal ion Inorganic materials 0.000 abstract description 3
- 238000003860 storage Methods 0.000 abstract description 3
- 230000001808 coupling effect Effects 0.000 abstract description 2
- 231100000956 nontoxicity Toxicity 0.000 abstract description 2
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- 238000005859 coupling reaction Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000005290 antiferromagnetic effect Effects 0.000 description 3
- 238000002447 crystallographic data Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Chemical group C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229910020647 Co-O Inorganic materials 0.000 description 2
- 229910020704 Co—O Inorganic materials 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
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- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000001144 powder X-ray diffraction data Methods 0.000 description 2
- YLZYSVYZMDJYOT-UHFFFAOYSA-N 2-methoxypyrimidine Chemical compound COC1=NC=CC=N1 YLZYSVYZMDJYOT-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
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- 229910003460 diamond Inorganic materials 0.000 description 1
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- 125000000524 functional group Chemical group 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 238000002595 magnetic resonance imaging Methods 0.000 description 1
- 230000005389 magnetism Effects 0.000 description 1
- 239000008204 material by function Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 238000000634 powder X-ray diffraction Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
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- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
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Citations (1)
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CN104341458A (zh) * | 2014-10-09 | 2015-02-11 | 天津工业大学 | 一种Co(II)-氮氧自由基配合物及其制备方法 |
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CN104341458A (zh) * | 2014-10-09 | 2015-02-11 | 天津工业大学 | 一种Co(II)-氮氧自由基配合物及其制备方法 |
Non-Patent Citations (5)
Title |
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HIROKI MORI 等: "Magnetic behavior of copper(II) complexes of a nitronyl-nitroxide-substituted pyrimidine", 《POLYHEDRON》, vol. 20, 31 December 2001 (2001-12-31), pages 1663 - 1668, XP005258344, DOI: 10.1016/S0277-5387(01)00670-2 * |
JIAN WANG 等: "Syntheses and magnetic properties of a pyrimidyl-substituted nitronyl nitroxide radical and its cobalt(II) complexes", 《CHEM. COMMUN.》, vol. 52, 31 December 2016 (2016-12-31), pages 5033 - 5036 * |
KEIJI OKADA 等: "Preparation and Magnetic Properties of Mn(hfac) 2-Complexes of 2-(5-Pyrimidinyl)- and 2-(3-Pyridyl)-Substituted Nitronyl Nitroxides", 《INORG. CHEM.》, vol. 42, 31 December 2003 (2003-12-31), pages 3221 - 3228 * |
TATIANA SHERSTOBITOVA 等: "Ligand Structure Effects on Molecular Assembly and Magnetic Properties of Copper(II) Complexes with 3- Pyridyl-Substituted Nitronyl Nitroxide Derivatives", 《ACS OMEGA》, vol. 4, 31 December 2019 (2019-12-31), pages 17160 - 17170 * |
王超 等: "一个新的四自旋氮氧自由基-镍(II)配合物的合成、结构和磁性质", 《南开大学学报(自然科学版)》, vol. 45, no. 2, 31 December 2012 (2012-12-31), pages 100 - 104 * |
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