CN109959690A - 一种用于电化学识别色氨酸对映体的环己烷二甲酸衍生物修饰电极的制备方法 - Google Patents
一种用于电化学识别色氨酸对映体的环己烷二甲酸衍生物修饰电极的制备方法 Download PDFInfo
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- CN109959690A CN109959690A CN201910291488.0A CN201910291488A CN109959690A CN 109959690 A CN109959690 A CN 109959690A CN 201910291488 A CN201910291488 A CN 201910291488A CN 109959690 A CN109959690 A CN 109959690A
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- Prior art keywords
- cyclohexane cyclohexanedimethanodibasic
- electrode
- derivatives modified
- cyclohexane
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- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 title claims abstract description 41
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical class C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 title claims abstract description 23
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 6
- 230000008569 process Effects 0.000 claims abstract description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- 239000000243 solution Substances 0.000 claims description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 claims description 5
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 claims description 5
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims description 5
- 238000001548 drop coating Methods 0.000 claims description 5
- 229910021397 glassy carbon Inorganic materials 0.000 claims description 5
- 239000008055 phosphate buffer solution Substances 0.000 claims description 5
- 238000010408 sweeping Methods 0.000 claims description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 238000002484 cyclic voltammetry Methods 0.000 claims description 3
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical class OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 claims description 3
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical class Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 claims description 3
- 238000004090 dissolution Methods 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 238000002390 rotary evaporation Methods 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- IZRBAWXNLPBYKE-UHFFFAOYSA-N cyclohexane dioctyl benzene-1,2-dicarboxylate Chemical compound C(C=1C(C(=O)OCCCCCCCC)=CC=CC1)(=O)OCCCCCCCC.C1CCCCC1 IZRBAWXNLPBYKE-UHFFFAOYSA-N 0.000 claims description 2
- 229960000935 dehydrated alcohol Drugs 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 125000004494 ethyl ester group Chemical group 0.000 claims 1
- 230000009286 beneficial effect Effects 0.000 abstract description 2
- 239000003349 gelling agent Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- DWNBOPVKNPVNQG-LURJTMIESA-N (2s)-4-hydroxy-2-(propylamino)butanoic acid Chemical compound CCCN[C@H](C(O)=O)CCO DWNBOPVKNPVNQG-LURJTMIESA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 238000005557 chiral recognition Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- QIVBCDIJIAJPQS-SECBINFHSA-N D-tryptophane Chemical compound C1=CC=C2C(C[C@@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-SECBINFHSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- UWKWMTBKFCNDDH-UHFFFAOYSA-N N(=NC=NN)CCCCCCN=NC=NN Chemical compound N(=NC=NN)CCCCCCN=NC=NN UWKWMTBKFCNDDH-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000008827 biological function Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 230000005518 electrochemistry Effects 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000001338 self-assembly Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000759 toxicological effect Toxicity 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/28—Electrolytic cell components
- G01N27/30—Electrodes, e.g. test electrodes; Half-cells
- G01N27/308—Electrodes, e.g. test electrodes; Half-cells at least partially made of carbon
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/28—Electrolytic cell components
- G01N27/30—Electrodes, e.g. test electrodes; Half-cells
- G01N27/327—Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
- G01N27/3275—Sensing specific biomolecules, e.g. nucleic acid strands, based on an electrode surface reaction
- G01N27/3277—Sensing specific biomolecules, e.g. nucleic acid strands, based on an electrode surface reaction being a redox reaction, e.g. detection by cyclic voltammetry
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Abstract
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CN201910291488.0A CN109959690B (zh) | 2019-04-12 | 2019-04-12 | 一种用于电化学识别色氨酸对映体的环己烷二甲酸衍生物修饰电极的制备方法 |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105758915A (zh) * | 2016-03-02 | 2016-07-13 | 常州大学 | 一种羧甲基纤维素-壳聚糖复合材料的制备及其修饰电极电化学法识别色氨酸对映体 |
CN108017725A (zh) * | 2018-01-18 | 2018-05-11 | 西北师范大学 | 多壁碳纳米管-n-羧甲基壳聚糖手性材料的制备及应用 |
CN108490048A (zh) * | 2018-03-16 | 2018-09-04 | 常州大学 | 一种用于电化学识别氨基酸对映体的ctab自组装杯芳烃的手性传感器的制备方法 |
CN108645902A (zh) * | 2018-05-16 | 2018-10-12 | 常州大学 | 一种用于电化学法识别色氨酸对映体的手性杯芳烃衍生物修饰电极的制备方法 |
CN108918621A (zh) * | 2018-05-16 | 2018-11-30 | 常州大学 | 一种用于电化学识别色氨酸对映体的ctab自组装杯芳烃衍生物的手性传感器的制备方法 |
-
2019
- 2019-04-12 CN CN201910291488.0A patent/CN109959690B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105758915A (zh) * | 2016-03-02 | 2016-07-13 | 常州大学 | 一种羧甲基纤维素-壳聚糖复合材料的制备及其修饰电极电化学法识别色氨酸对映体 |
CN108017725A (zh) * | 2018-01-18 | 2018-05-11 | 西北师范大学 | 多壁碳纳米管-n-羧甲基壳聚糖手性材料的制备及应用 |
CN108490048A (zh) * | 2018-03-16 | 2018-09-04 | 常州大学 | 一种用于电化学识别氨基酸对映体的ctab自组装杯芳烃的手性传感器的制备方法 |
CN108645902A (zh) * | 2018-05-16 | 2018-10-12 | 常州大学 | 一种用于电化学法识别色氨酸对映体的手性杯芳烃衍生物修饰电极的制备方法 |
CN108918621A (zh) * | 2018-05-16 | 2018-11-30 | 常州大学 | 一种用于电化学识别色氨酸对映体的ctab自组装杯芳烃衍生物的手性传感器的制备方法 |
Non-Patent Citations (4)
Title |
---|
LILI GUO ET AL.: "Chiral Sensing Platform Based on the Self-Assemblies of Diphenylalanine and Oxalic Acid", 《ANAL. CHEM.》 * |
LILI GUO ET AL.: "Electrochemical recognition of tryptophan enantiomers using self-assembled diphenylalanine structures induced by graphene quantum dots, chitosan and CTAB", 《ELECTROCHEMISTRY COMMUNICATIONS》 * |
MARK D. DOHERTY ET AL.: "Small Molecule Cyclic Amide and Urea Based Thickeners for Organic and sc-CO2/Organic Solutions", 《ENERGY FUELS》 * |
靳清贤 等: "超分子凝胶的手性功能应用:手性分子识别与不对称催化", 《化学进展》 * |
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Application publication date: 20190702 Assignee: Shandong Hongde Yuheng Information Technology Co.,Ltd. Assignor: CHANGZHOU University Contract record no.: X2024980008518 Denomination of invention: Preparation method of cyclohexane dicarboxylic acid derivative modified electrode for electrochemical recognition of tryptophan enantiomers Granted publication date: 20210316 License type: Common License Record date: 20240702 |
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