CN113880867A - 一种可检测水中Cu2+、Zn2+分子传感器及应用 - Google Patents
一种可检测水中Cu2+、Zn2+分子传感器及应用 Download PDFInfo
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- CN113880867A CN113880867A CN202111190528.6A CN202111190528A CN113880867A CN 113880867 A CN113880867 A CN 113880867A CN 202111190528 A CN202111190528 A CN 202111190528A CN 113880867 A CN113880867 A CN 113880867A
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- molecular sensor
- phenylenediamine
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- tetramethyljulolidine
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- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 title description 24
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 title description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 38
- 238000001514 detection method Methods 0.000 claims abstract description 20
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 20
- 150000002500 ions Chemical class 0.000 claims abstract description 18
- 150000002466 imines Chemical class 0.000 claims abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
- 150000001412 amines Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 6
- 238000002360 preparation method Methods 0.000 abstract description 6
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 abstract description 5
- 230000035945 sensitivity Effects 0.000 abstract description 5
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
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- 239000002994 raw material Substances 0.000 abstract description 2
- 238000003786 synthesis reaction Methods 0.000 abstract description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 15
- 239000010949 copper Substances 0.000 description 14
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 10
- 229910001385 heavy metal Inorganic materials 0.000 description 9
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- 150000001875 compounds Chemical class 0.000 description 8
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- 230000003287 optical effect Effects 0.000 description 7
- 239000011701 zinc Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 241000282414 Homo sapiens Species 0.000 description 6
- 239000008399 tap water Substances 0.000 description 6
- 235000020679 tap water Nutrition 0.000 description 5
- 238000011161 development Methods 0.000 description 4
- JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 150000002085 enols Chemical class 0.000 description 3
- 238000002189 fluorescence spectrum Methods 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 238000003419 tautomerization reaction Methods 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 229940126062 Compound A Drugs 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000036737 immune function Effects 0.000 description 2
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 206010003445 Ascites Diseases 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 208000035240 Disease Resistance Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 206010016654 Fibrosis Diseases 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
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- 125000003118 aryl group Chemical group 0.000 description 1
- 238000001391 atomic fluorescence spectroscopy Methods 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 231100000739 chronic poisoning Toxicity 0.000 description 1
- 230000007882 cirrhosis Effects 0.000 description 1
- 208000019425 cirrhosis of liver Diseases 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- MAEBCGDGGATMSC-OSHGGGOQSA-N cyclamine Chemical compound O([C@H]1CO[C@H]([C@@H]([C@H]1O[C@@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O[C@@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@H]1CC[C@]2(C)[C@H]3CCC45OCC6([C@@H](C[C@@]4(C)[C@]3(C)CCC2C1(C)C)O)CC[C@@](C[C@@H]65)(C)C=O)[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O MAEBCGDGGATMSC-OSHGGGOQSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N deuterated chloroform Substances [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000002440 hepatic effect Effects 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 125000000879 imine group Chemical group 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 238000009616 inductively coupled plasma Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- DZFWNZJKBJOGFQ-UHFFFAOYSA-N julolidine Chemical group C1CCC2=CC=CC3=C2N1CCC3 DZFWNZJKBJOGFQ-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
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- -1 schiff base compound Chemical class 0.000 description 1
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- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N21/643—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" non-biological material
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- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
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Abstract
Description
水样 | 加入Cu<sup>2+</sup> (M ) | 检测 Cu<sup> 2+</sup> (M ) | 重现率 (%) | R.S.D.<sup>a</sup> (%) |
河水 | -- | -- | ||
合成水 1<sup>b</sup> | 1.0 × 10<sup>-6</sup> | (1.02 ± 0.02) × 10<sup>-6</sup> | 102 | 2.0 |
合成水 2<sup>b</sup> | 1.0 × 10<sup>-5</sup> | (1.01 ± 0.06) × 10<sup>-5</sup> | 101 | 1.0 |
合成水 3<sup>b</sup> | 1.0 × 10<sup>-4</sup> | (1.01 ± 0.05) × 10<sup>-4</sup> | 101 | 1.0 |
加入Zn<sup>2+</sup> (M ) | 检测Zn<sup>2+</sup> (M ) | 重现率 (%) | R.S.D.<sup>a</sup> (%) | |
自来水 | -- | -- | ||
合成水 1<sup>b</sup> | 1.0 × 10<sup>-6</sup> | (1.01 ± 0.10) × 10<sup>-6</sup> | 101 | 1.0 |
合成水 2<sup>b</sup> | 1.0 × 10<sup>-5</sup> | (1.02 ± 0.06) × 10<sup>-5</sup> | 102 | 2.0 |
合成水 3<sup>b</sup> | 1.0 × 10<sup>-4</sup> | (0.99 ± 0.05) × 10<sup>-4</sup> | 99 | 1.0 |
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CN202111190528.6A CN113880867B (zh) | 2021-10-13 | 2021-10-13 | 一种可检测水中Cu2+、Zn2+分子传感器及应用 |
LU501426A LU501426B1 (en) | 2021-10-13 | 2022-02-09 | MOLECULAR SENSOR CAPABLE OF DETECTING Cu2+ AND Zn2+ IN WATER AND USE THEREOF |
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CN202111190528.6A CN113880867B (zh) | 2021-10-13 | 2021-10-13 | 一种可检测水中Cu2+、Zn2+分子传感器及应用 |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116751218A (zh) * | 2022-07-29 | 2023-09-15 | 德州学院 | 一种久洛尼定聚集发光材料及制备方法与应用 |
CN117050097A (zh) * | 2023-10-11 | 2023-11-14 | 德州学院 | 一种可检测水中Fe3+、Cu2+及Zn2+离子的分子传感器及应用 |
CN118994143A (zh) * | 2024-10-24 | 2024-11-22 | 德州学院 | 一种分子传感器及其在检测金属离子中的应用 |
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US3489558A (en) * | 1967-09-18 | 1970-01-13 | Ibm | Photoconductive benzobisthiazoles and their use in electrophotographic processes |
FR3024730A1 (fr) * | 2014-08-06 | 2016-02-12 | Imra Europ Sas | Espaceurs moleculaires a base de spiroxazines chromogenes non-symetriques |
CN113121576A (zh) * | 2021-04-15 | 2021-07-16 | 德州学院 | 一种对酸、碱环境具有不同检测信号的分子传感器及应用 |
CN113366063A (zh) * | 2019-02-01 | 2021-09-07 | 巴斯夫欧洲公司 | 用于液晶组合物的二色性偶氮-偶氮甲碱染料 |
-
2021
- 2021-10-13 CN CN202111190528.6A patent/CN113880867B/zh active Active
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2022
- 2022-02-09 LU LU501426A patent/LU501426B1/en active IP Right Grant
Patent Citations (4)
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US3489558A (en) * | 1967-09-18 | 1970-01-13 | Ibm | Photoconductive benzobisthiazoles and their use in electrophotographic processes |
FR3024730A1 (fr) * | 2014-08-06 | 2016-02-12 | Imra Europ Sas | Espaceurs moleculaires a base de spiroxazines chromogenes non-symetriques |
CN113366063A (zh) * | 2019-02-01 | 2021-09-07 | 巴斯夫欧洲公司 | 用于液晶组合物的二色性偶氮-偶氮甲碱染料 |
CN113121576A (zh) * | 2021-04-15 | 2021-07-16 | 德州学院 | 一种对酸、碱环境具有不同检测信号的分子传感器及应用 |
Non-Patent Citations (4)
Title |
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DARIO GARGIULO,等: "CD Exciton Chirality Method: Schiff Base and Cyanine Dye-Type Chromophores", 《J. AM. CHEM. SOC.》 * |
MAKESH MOHAN,等: "Design, Synthesis and Characterization of N-Substituted Heteroaromatics: DFT-Studies and Organic Light Emitting Device Application", 《CHEMISTRYSELECT》 * |
MD. SERAJUL HAQUE FAIZI,等: "Crystal structure of 9,90-{(1E,10E)-[1,4-phenylphenylenebis(2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]-quinolin-8-ol)", 《ACTA CRYSTALLOGRAPHICA, SECTION E: CRYSTALLOGRAPHIC COMMUNICATIONS》 * |
SANGEETA DEY,等: "Double-Cuvette ISES: In Situ Estimation of Enantioselectivity and Relative Rate for Catalyst Screening", 《JOURNAL OF THE AMERICAN CHEMICAL SOCIETY》 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116751218A (zh) * | 2022-07-29 | 2023-09-15 | 德州学院 | 一种久洛尼定聚集发光材料及制备方法与应用 |
CN117050097A (zh) * | 2023-10-11 | 2023-11-14 | 德州学院 | 一种可检测水中Fe3+、Cu2+及Zn2+离子的分子传感器及应用 |
CN118994143A (zh) * | 2024-10-24 | 2024-11-22 | 德州学院 | 一种分子传感器及其在检测金属离子中的应用 |
CN118994143B (zh) * | 2024-10-24 | 2025-02-28 | 德州学院 | 一种分子传感器及其在检测金属离子中的应用 |
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