KR20160011848A - 퀴놀린 화합물, 이를 이용한 아연이온, 카드뮴이온 및 코발트 이온 검출제, 검출 방법 및 검출장치 - Google Patents
퀴놀린 화합물, 이를 이용한 아연이온, 카드뮴이온 및 코발트 이온 검출제, 검출 방법 및 검출장치 Download PDFInfo
- Publication number
- KR20160011848A KR20160011848A KR1020140093025A KR20140093025A KR20160011848A KR 20160011848 A KR20160011848 A KR 20160011848A KR 1020140093025 A KR1020140093025 A KR 1020140093025A KR 20140093025 A KR20140093025 A KR 20140093025A KR 20160011848 A KR20160011848 A KR 20160011848A
- Authority
- KR
- South Korea
- Prior art keywords
- ion
- compound
- formula
- cadmium
- ions
- 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.)
- Granted
Links
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 title claims abstract description 55
- WLZRMCYVCSSEQC-UHFFFAOYSA-N cadmium(2+) Chemical compound [Cd+2] WLZRMCYVCSSEQC-UHFFFAOYSA-N 0.000 title claims abstract description 53
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 14
- 238000000034 method Methods 0.000 title claims description 10
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 title 1
- 229910001431 copper ion Inorganic materials 0.000 title 1
- 125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 title 1
- 229910001429 cobalt ion Inorganic materials 0.000 claims abstract description 51
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 claims abstract description 51
- 238000001514 detection method Methods 0.000 claims abstract description 26
- 239000000126 substance Substances 0.000 claims abstract description 15
- -1 quinoline compound Chemical class 0.000 claims abstract description 13
- SMWDFEZZVXVKRB-UHFFFAOYSA-N anhydrous quinoline Natural products N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims abstract description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 93
- 150000001875 compounds Chemical class 0.000 claims description 89
- 239000011701 zinc Substances 0.000 claims description 62
- 239000000243 solution Substances 0.000 claims description 28
- 239000002904 solvent Substances 0.000 claims description 17
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 6
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 229910052793 cadmium Inorganic materials 0.000 claims description 5
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 5
- 150000002500 ions Chemical class 0.000 claims description 5
- 239000000523 sample Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- SKKQYKWIJVYCNX-UHFFFAOYSA-N 2-[(2-hydroxyphenyl)methyl-(pyridin-2-ylmethyl)amino]-N-quinolin-8-ylacetamide Chemical compound OC1=C(CN(CC(=O)NC=2C=CC=C3C=CC=NC=23)CC2=NC=CC=C2)C=CC=C1 SKKQYKWIJVYCNX-UHFFFAOYSA-N 0.000 abstract 1
- 150000001455 metallic ions Chemical class 0.000 abstract 1
- 229910021645 metal ion Inorganic materials 0.000 description 38
- 230000008859 change Effects 0.000 description 24
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- 238000002835 absorbance Methods 0.000 description 13
- 238000004458 analytical method Methods 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- 239000011575 calcium Substances 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 229910017052 cobalt Inorganic materials 0.000 description 5
- 239000010941 cobalt Substances 0.000 description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
- ILSCGIHFKLZTME-UHFFFAOYSA-N 2-chloro-n-quinolin-8-ylacetamide Chemical compound C1=CN=C2C(NC(=O)CCl)=CC=CC2=C1 ILSCGIHFKLZTME-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 241000282414 Homo sapiens Species 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000747 cardiac effect Effects 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000012921 fluorescence analysis Methods 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 150000003248 quinolines Chemical class 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 102000001554 Hemoglobins Human genes 0.000 description 1
- 108010054147 Hemoglobins Proteins 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 208000019693 Lung disease Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 206010062237 Renal impairment Diseases 0.000 description 1
- 206010047141 Vasodilatation Diseases 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 1
- XIEPJMXMMWZAAV-UHFFFAOYSA-N cadmium nitrate Inorganic materials [Cd+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XIEPJMXMMWZAAV-UHFFFAOYSA-N 0.000 description 1
- 208000015202 calcium metabolic disease Diseases 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- FDJOLVPMNUYSCM-UVKKECPRSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2,7, Chemical compound [Co+3].N#[C-].C1([C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)[N-]\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O FDJOLVPMNUYSCM-UVKKECPRSA-L 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 230000009918 complex formation Effects 0.000 description 1
- 238000003271 compound fluorescence assay Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 208000037765 diseases and disorders Diseases 0.000 description 1
- 239000005447 environmental material Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001917 fluorescence detection Methods 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000005977 kidney dysfunction Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- XCVNDBIXFPGMIW-UHFFFAOYSA-N n-ethylpropan-1-amine Chemical compound CCCNCC XCVNDBIXFPGMIW-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 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
- 239000000049 pigment Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000000159 protein binding assay Methods 0.000 description 1
- 239000002096 quantum dot Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 230000005062 synaptic transmission Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000024883 vasodilation Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
- C07D215/46—Nitrogen atoms attached in position 4 with hydrocarbon radicals, substituted by nitrogen atoms, attached to said nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- 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"
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Immunology (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Optics & Photonics (AREA)
- Chemical Kinetics & Catalysis (AREA)
Abstract
Description
도 2는 아세토나이트릴 용매에서, 화학식 1의 화합물에 다양한 금속 이온을 각각 넣었을 때의 색변화를 나타낸 것이다.
도 3은 아세토나이트릴 수용액에서, 화학식 1의 화합물에 다양한 금속 이온을 각각 첨가하여 형광의 세기를 측정한 그래프이다.
도 4는 화학식 1의 화합물에 아연이온(Zn2+)의 양을 점점 증가시키면서 형광의 세기를 측정한 그래프이다.
도 5는 화학식 1의 화합물에 아연이온(Zn2+)의 농도를 점점 증가시켰을 때 흡광도의 변화를 나타낸 그래프이다.
도 6은 화학식 1의 화합물과 아연이온(Zn2+)의 결합비를 알아보기 위한 잡플랏(Job's Plot)이다.
도 7은 다양한 금속이온이 존재할 때 화학식 1의 화합물이 아연이온(Zn2+)을 검출하는데 방해를 받는지 확인하기 위한 형광세기 실험결과를 막대그래프로 나타낸 것이다.
도 8은 화학식 1의 화합물에 카드뮴이온(Cd2+)의 농도를 점점 증가시키면서 형광의 세기를 측정한 그래프이다.
도 9는 화학식 1의 화합물과 카드뮴이온(Cd2+)의 결합비를 알아보기 위한 잡플랏(Job's Plot)이다.
도 10은 다양한 금속이온이 존재할 때 화학식 1의 화합물이 카드뮴이온(Cd2+)을 검출하는데 방해를 받는지를 확인하기 위한 형광세기 실험결과를 막대그래프로 나타낸 것이다.
도 11은 화학식 1의 화합물과 카드뮴 이온(Cd2 +) 착물의 결정구조를 나타낸 것이다.
도 12는 화학식 1의 화합물에 코발트이온(Co2+)의 농도를 점점 증가시켰을 때 흡광도의 변화를 나타낸 그래프이다.
도 13은 화학식 1의 화합물과 코발트 이온(Co2 +)의 결합형태를 알아보기 위한 ESI-MS 결과이다.
도 14는 화학식 1의 화합물과 코발트이온(Co2+)의 결합비를 알아보기 위한 잡플랏(Job's Plot)이다.
도 15는 다양한 금속이온이 존재할 때 화학식 1의 화합물이 코발트이온 (Co2+)을 검출하는데 방해를 받는지를 확인하기 위한 색 변화 실험 결과를 나타낸 것이다.
Claims (9)
- 2-클로로-N-(퀴놀린-8-일)아세트아마이드, 2-(((피리딘-2-일)메틸아미노)메틸)페놀 및 N, N-다이아이소프로필에틸아민을 반응시키는 것을 특징으로 하는 청구항 1의 상기 화학식 1의 화합물 제조 방법.
- 청구항 1의 화학식 1의 화합물을 포함하는 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 코발트이온(Co2 +) 검출제.
- 청구항 3에 있어서,
상기 검출제는 추가로 용매를 포함할 수 있는 것을 특징으로 하는 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 코발트이온(Co2 +) 검출제. - 청구항 4에 있어서,
상기 용매는 아세토나이트릴 또는 아세토나이트릴 수용액으로 이루어진 군으로부터 선택되는 1종인 것을 특징으로 하는 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 코발트이온(Co2 +) 검출제. - 청구항 5에 있어서,
상기 아세토나이트릴 수용액은 물의 부피에 대한 아세토나이트릴의 부피 비율이 1 이상인 것을 특징으로 하는 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 카드뮴이온(Cd2 +) 검출제. - 청구항 1의 화학식 1의 화합물을 사용하는 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 코발트이온(Co2 +) 검출 방법.
- 청구항 3의 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 코발트이온(Co2 +) 검출제를 포함하는 포함하는 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 코발트이온(Co2 +) 검출 장치.
- 청구항 8에 있어서,
상기 검출 장치는 프로브(probe)인 것을 특징으로 하는 아연이온(Zn2 +), 카드뮴이온(Cd2 +) 또는 코발트이온(Co2 +) 검출 장치.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020140093025A KR101638682B1 (ko) | 2014-07-23 | 2014-07-23 | 퀴놀린 화합물, 이를 이용한 아연이온, 카드뮴이온 및 코발트 이온 검출제, 검출 방법 및 검출장치 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020140093025A KR101638682B1 (ko) | 2014-07-23 | 2014-07-23 | 퀴놀린 화합물, 이를 이용한 아연이온, 카드뮴이온 및 코발트 이온 검출제, 검출 방법 및 검출장치 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20160011848A true KR20160011848A (ko) | 2016-02-02 |
KR101638682B1 KR101638682B1 (ko) | 2016-07-11 |
Family
ID=55354372
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020140093025A Expired - Fee Related KR101638682B1 (ko) | 2014-07-23 | 2014-07-23 | 퀴놀린 화합물, 이를 이용한 아연이온, 카드뮴이온 및 코발트 이온 검출제, 검출 방법 및 검출장치 |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR101638682B1 (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106565601A (zh) * | 2016-10-14 | 2017-04-19 | 河南理工大学 | 一种基于喹啉酰腙衍生物的荧光探针及其制备方法与应用 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101732280B1 (ko) | 2015-12-22 | 2017-05-02 | 서울과학기술대학교 산학협력단 | 신규한 쿠마린계 화합물, 이를 이용한 코발트 이온 검출제, 회수 방법 및 검출 장치 |
-
2014
- 2014-07-23 KR KR1020140093025A patent/KR101638682B1/ko not_active Expired - Fee Related
Non-Patent Citations (2)
Title |
---|
Dyes and Pigments, Vol.102, pp.301-307 (온라인 게시일: 2013.11.20.)* * |
Jin Hoon Kim; In Hong Hwang; Seung Pyo Jang; Juhye Kang; Sumi Kim; Insup Noh; Youngmee Kim; Cheal Kim; Roger G. Harrison; Dalton Transactions, 2013, 42, 5500-5507. |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106565601A (zh) * | 2016-10-14 | 2017-04-19 | 河南理工大学 | 一种基于喹啉酰腙衍生物的荧光探针及其制备方法与应用 |
Also Published As
Publication number | Publication date |
---|---|
KR101638682B1 (ko) | 2016-07-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Tsui et al. | Azo dyes featuring with nitrobenzoxadiazole (NBD) unit: a new selective chromogenic and fluorogenic sensor for cyanide ion | |
Park et al. | A new coumarin-based chromogenic chemosensor for the detection of dual analytes Al 3+ and F− | |
Samanta et al. | An aggregation-induced emission (AIE) active probe for multiple targets: a fluorescent sensor for Zn 2+ and Al 3+ & a colorimetric sensor for Cu 2+ and F− | |
Lim et al. | Fluorescent probe for sequential recognition of Ga3+ and pyrophosphate anions | |
Wang et al. | A novel fluorescent and colorimetric dual-channel sensor for the fast, reversible and simultaneous detection of Fe3+ and Cu2+ based on terthiophene derivative with high sensitivity and selectivity | |
Duarte et al. | A selective proton transfer optical sensor for copper II based on chelation enhancement quenching effect (CHEQ) | |
Guang et al. | A novel turn-on fluorescent probe for the multi-channel detection of Zn 2+ and Bi 3+ with different action mechanisms | |
Beneto et al. | A phenanthroimidazole based effective colorimetric chemosensor for copper (II) and fluoride ions | |
Gupta et al. | Azoaniline-based rapid and selective dual sensor for copper and fluoride ions with two distinct output modes of detection | |
KR101980973B1 (ko) | 로다민 하이드라자이드 유도체 및 이를 이용한 구리 및 차아염소산염 검출방법 | |
Zuo et al. | A dual responsive colorimetric/fluorescent turn-on sensor for highly selective, sensitive and fast detection of Fe3+ ions and its applications | |
Patra et al. | A highly selective benzildihydrazone based Schiff base chromogenic chemosensor for rapid detection of Cu2+ in aqueous solution | |
Zhou et al. | A highly selective colorimetric chemosensor for cobalt (II) ions based on a tripodal amide ligand | |
CN104529890B (zh) | 特异性识别锌离子的水溶性荧光探针的制备方法及其应用 | |
Sahin et al. | A phenanthrene-based calix [4] arene as a fluorescent sensor for Cu2+ and F− | |
CN108658862B (zh) | 基于萘二甲酰亚胺衍生物的传感器分子及其合成和应用 | |
Amirnasr et al. | A fluorescent carboxamide ligand, having combined ionophore/fluorophore moieties, exhibiting “On-Off” switching toward Zn2+ ion | |
Wang et al. | A near-infrared squaraine dye for cascade recognition of copper ion and biological phosphate and its application in IMPLICATION logic gate | |
CN110964515A (zh) | 一种双席夫碱铝离子荧光探针、其合成方法及其应用 | |
Chemate et al. | Highly sensitive and selective chemosensors for Cu 2+ and Al 3+ based on photoinduced electron transfer (PET) mechanism | |
Shamsipur et al. | An efficient and selective flourescent optode membrane based on 7-[(5-chloro-8-hydroxy-7-quinolinyl) methyl]-5, 6, 7, 8, 9, 10-hexahydro-2H-1, 13, 4, 7, 10-benzodioxatriazacyclopentadecine-3, 11 (4H, 12H)-dione as a novel fluoroionophore for determination of cobalt (II) ions | |
Jeyanthi et al. | Crystal structure and chemosensing property of benzimidazole-based probe towards detection of multiple analytes–A combined experimental and DFT approach | |
KR101638682B1 (ko) | 퀴놀린 화합물, 이를 이용한 아연이온, 카드뮴이온 및 코발트 이온 검출제, 검출 방법 및 검출장치 | |
Algohary et al. | Novel colorimetric chemosensors containing pyridine moiety for detection of some cations in water and crops samples: Design, synthesis, and evaluation | |
KR101171802B1 (ko) | 수은 이온 선택성을 갖는 파이렌계 화합물 및 이를 이용한 수은 이온 검출 시스템 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20140723 |
|
PA0201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20151202 Patent event code: PE09021S01D |
|
PG1501 | Laying open of application | ||
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20160630 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20160705 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20160705 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20200630 Start annual number: 5 End annual number: 5 |
|
PC1903 | Unpaid annual fee |
Termination category: Default of registration fee Termination date: 20220416 |