KR101418655B1 - 신규한 화합물 및 이를 이용한 철 이온 검출 방법 - Google Patents
신규한 화합물 및 이를 이용한 철 이온 검출 방법 Download PDFInfo
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- KR101418655B1 KR101418655B1 KR1020120147846A KR20120147846A KR101418655B1 KR 101418655 B1 KR101418655 B1 KR 101418655B1 KR 1020120147846 A KR1020120147846 A KR 1020120147846A KR 20120147846 A KR20120147846 A KR 20120147846A KR 101418655 B1 KR101418655 B1 KR 101418655B1
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- iron ions
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- iron
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title claims abstract description 63
- 150000001875 compounds Chemical class 0.000 title claims abstract description 61
- 229910052742 iron Inorganic materials 0.000 title claims abstract description 46
- 238000001514 detection method Methods 0.000 title description 6
- -1 iron ions Chemical class 0.000 claims abstract description 38
- 230000008859 change Effects 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 12
- 230000003287 optical effect Effects 0.000 claims abstract description 8
- 239000000538 analytical sample Substances 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 230000008569 process Effects 0.000 abstract description 3
- 230000035945 sensitivity Effects 0.000 abstract description 3
- 238000003786 synthesis reaction Methods 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- 238000010521 absorption reaction Methods 0.000 description 10
- 229910021645 metal ion Inorganic materials 0.000 description 10
- 150000002500 ions Chemical class 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 4
- HKNSIVFWRXBWCK-UHFFFAOYSA-N [N].NC1=CC=CC=C1 Chemical group [N].NC1=CC=CC=C1 HKNSIVFWRXBWCK-UHFFFAOYSA-N 0.000 description 4
- 238000002835 absorbance Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 229940075933 dithionate Drugs 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 3
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 3
- 150000004056 anthraquinones Chemical class 0.000 description 3
- 238000004020 luminiscence type Methods 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 239000001000 anthraquinone dye Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000002371 ultraviolet--visible spectrum Methods 0.000 description 2
- KAFZOLYKKCWUBI-HPMAGDRPSA-N (2s)-2-[[(2s)-2-[[(2s)-1-[(2s)-3-amino-2-[[(2s)-2-[[(2s)-2-(3-cyclohexylpropanoylamino)-4-methylpentanoyl]amino]-5-methylhexanoyl]amino]propanoyl]pyrrolidine-2-carbonyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]butanediamide Chemical compound N([C@@H](CC(C)C)C(=O)N[C@@H](CCC(C)C)C(=O)N[C@@H](CN)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CC(N)=O)C(N)=O)C(=O)CCC1CCCCC1 KAFZOLYKKCWUBI-HPMAGDRPSA-N 0.000 description 1
- BJDDKZDZTHIIJB-UHFFFAOYSA-N 4,5,6,7-tetrafluoro-2-benzofuran-1,3-dione Chemical compound FC1=C(F)C(F)=C2C(=O)OC(=O)C2=C1F BJDDKZDZTHIIJB-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920006061 Kelon® Polymers 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000012491 analyte Substances 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000005447 environmental material Substances 0.000 description 1
- 229910001448 ferrous ion Inorganic materials 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000004219 molecular orbital method Methods 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/14—Dithiocarbamic acids; Derivatives thereof
- C07C333/18—Esters of dithiocarbamic acids
- C07C333/20—Esters of dithiocarbamic acids having nitrogen atoms of dithiocarbamate groups bound to hydrogen atoms or to acyclic carbon atoms
-
- 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
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/33—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using ultraviolet light
-
- 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"
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- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- General Physics & Mathematics (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pathology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Optics & Photonics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Abstract
Description
도 2는 화학식 1로 표시되는 화합물에 철 이온을 첨가하였을때, 첨가량에 따른 스펙트라의 변화 및 색상변화를 나타낸 것이다.
도 3은 철이온을 포함한 다양한 금속이온과 화학식 1의 화합물을 반응시켰을때 발광특성의 변화를 나타낸 것이다.
도 4는 철이온과 결합한 화학식 1의 화합물의 구조를 도시한 그림이다.
Claims (5)
- 제1항의 화합물을 포함하는 철 이온(Fe3 +) 검출용 조성물.
- 제1항의 화합물에 철 이온을 포함하는 분석 시료를 첨가하는 단계; 및
상기 분석시료가 첨가된 화합물의 광학적 변화의 유무를 관측하는 단계를 포함하는 철 이온의 검출방법.
- 제4항에 있어서, 상기 광학적 변화는 UV-Vis(Ultraviolet-visible)분광기 또는 형광광도계 중 어느 하나 이상을 사용하여 관측하는 것을 특징으로 하는 철 이온의 검출 방법.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020120147846A KR101418655B1 (ko) | 2012-12-17 | 2012-12-17 | 신규한 화합물 및 이를 이용한 철 이온 검출 방법 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020120147846A KR101418655B1 (ko) | 2012-12-17 | 2012-12-17 | 신규한 화합물 및 이를 이용한 철 이온 검출 방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20140078466A KR20140078466A (ko) | 2014-06-25 |
KR101418655B1 true KR101418655B1 (ko) | 2014-07-10 |
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KR1020120147846A Active KR101418655B1 (ko) | 2012-12-17 | 2012-12-17 | 신규한 화합물 및 이를 이용한 철 이온 검출 방법 |
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KR (1) | KR101418655B1 (ko) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4647411A (en) | 1984-11-06 | 1987-03-03 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | 5,6,7,8-tetrafluoroanthraquinone derivatives |
KR20040050715A (ko) * | 2002-12-03 | 2004-06-16 | 롬 앤드 하스 캄파니 | 액체 탄화수소의 마킹방법 |
US6852680B2 (en) | 2001-10-26 | 2005-02-08 | Ethyl Corporation | Dithiocarbamates containing alkylthio and hydroxy substituents |
KR20070014292A (ko) * | 2005-07-28 | 2007-02-01 | 주식회사 아이센스 | 전기화학적 당화단백질 검출 시스템 |
-
2012
- 2012-12-17 KR KR1020120147846A patent/KR101418655B1/ko active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4647411A (en) | 1984-11-06 | 1987-03-03 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | 5,6,7,8-tetrafluoroanthraquinone derivatives |
US6852680B2 (en) | 2001-10-26 | 2005-02-08 | Ethyl Corporation | Dithiocarbamates containing alkylthio and hydroxy substituents |
KR20040050715A (ko) * | 2002-12-03 | 2004-06-16 | 롬 앤드 하스 캄파니 | 액체 탄화수소의 마킹방법 |
KR20070014292A (ko) * | 2005-07-28 | 2007-02-01 | 주식회사 아이센스 | 전기화학적 당화단백질 검출 시스템 |
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KR20140078466A (ko) | 2014-06-25 |
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