CN102041000A - Blue-light-excited nickel-chelidamic acid fluorescent film - Google Patents
Blue-light-excited nickel-chelidamic acid fluorescent film Download PDFInfo
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- CN102041000A CN102041000A CN2009101126468A CN200910112646A CN102041000A CN 102041000 A CN102041000 A CN 102041000A CN 2009101126468 A CN2009101126468 A CN 2009101126468A CN 200910112646 A CN200910112646 A CN 200910112646A CN 102041000 A CN102041000 A CN 102041000A
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- film
- blue
- light
- nickel
- excited
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- 0 *c1cc(O)cc(C(O)=O)n1 Chemical compound *c1cc(O)cc(C(O)=O)n1 0.000 description 1
Abstract
The invention relates to a blue-light-excited nickel-chelidamic acid fluorescent film, introduces the bioinorganic chemical research result of nickel-chelidamic acid complex into the film production technology and discovers that the compound film is luminescent when excited by blue light (460nm). Since the blue light (460nm) is safe for organism, 460nm can be used as exciting light to detect the fluorescent characteristic of a film. Therefore, the compound film can be safely used for biological fluorescence detection.
Description
Technical field:
The present invention relates to a kind of available blue-light excited luminous nickel-chelidonamic acid film.
Background technology:
2,6-dicarboxyl-4-pyridone (chelidonamic acid), English name 2,6-dicarboxy-4-hydroxypyridine or chelidamic acid are called for short H
3Chel (following) with being called for short.H
3Chel is the complex ligand in a typical polygamy site, simultaneously is again the material of biologically active in vivo, and the research of title complex for it all has wide application prospect in coordination chemistry and bio-inorganic chemistry field.U.S. scientist has been found that with H
3The metal complexes of Chel is as the macromole probe of one of major portion, and DNA isolates effect for organism.The environmentalist also finds, at H
3Chel and Ni
2+After the coordination, reduced Ni
2+With contacting of cell surface, thereby alleviated the toxic action of nickel to microorganism.Simultaneously, nickel is again the necessary trace elements of organism (bacterium, plant, animal and human), has been found that at present 4 kinds of bacterial enzymes are to rely on nickel, as urine enzyme (also finding in the plant), CO desaturase (CODH), hydrogen enzyme (H
2-ASE) and contain the methyl reductase enzyme (MCR) of enzyme prothetic group (F430), the coordination environment of nickel is different in above-mentioned 4 kinds of enzymes, but the nickel center all is positioned at the reactive site of these enzymes.
Summary of the invention:
The present invention has introduced masking technique the bio-inorganic chemistry research of nickel complex first, and has successfully introduced H
3Chel has found simultaneously that as complex ligand this closes film forming fluorescent characteristic, for nickeliferous metalloprotein of chemical simulation and metalloenzyme, and further investigation H
3The function of Chel all has great importance.Purpose of the present invention just is to disclose this and closes film forming synthetic and making method.
Technical scheme: use H
3Chel is as complex ligand and NiCl
3Reaction obtains blue-light excited nickel-chelidonamic acid fluorescent material Ni (C
7H
2NO
5) (H
2O)
3H
2O0.25MeCN.At Ni (C
7H
2NO
5) (H
2O)
3H
2The interpolation gelifying agent can be made and obtain fluorescence membrane in the homogeneous phase solution of O0.25MeCN.Gelifying agent can be selected H for use
2NC
6H
4CH
2C
6H
4NH
2
Embodiment:
1, Ni (C
7H
2NO
5) (H
2O)
3H
2O0.25MeCN's is synthetic
Under the condition of 70 ℃ of heating, with the H of 20mL distilled water/3: 1 mixing solutions stirring and dissolving of acetonitrile volume ratio 50mg
3The Chel powder adds 59mg NiCl
36H
2O, 70 ℃ of heated and stirred 4 hours are cooled to room temperature, obtain Ni (C
7H
2NO
5) (H
2O)
3H
2The homogeneous phase solution of O0.25MeCN.Leave standstill and separate out Ni (C
7H
2NO
5) (H
2O)
3H
2The O0.25MeCN crystal.Reaction formula is as follows:
Ni (C
7H
2NO
5) (H
2O)
3H
2The O0.25MeCN crystal is through infrared and its crystalline structure of X-ray measuring, and its significant parameter is:
2, the making of film
At Ni (C
7H
2NO
5) (H
2O)
3H
2Before the O0.25MeCN green crystal is not separated out, add 50mgH
2NC
6H
4CH
2C
6H
4NH
2Powder stirred 4 hours as gelifying agent.Under the normal temperature, solvent flashing.When treating that solution becomes the semi-gelled state, get mixing drop 1-2 with glue head dropper and drip on the slide glass of 0.8 * 2.0 (cm).Slide glass is placed on the sol evenning machine, and 100 rev/mins of rotating speeds rotated three seconds.Take off slide glass, vacuum-drying evaporates into film and does typing under the normal temperature, gets the yellow-green colour transparent film.
By above step, success of the present invention synthetic also made nickel-chelidonamic acid film.Simultaneously, we have also carried out ultimate analysis to this film, and have measured its fluorescent characteristic.The results of elemental analyses of this film is: N (%): 7.86; C (%): 45.07; O (%): 4.65.
3, the bioluminescence of safety detects
We can clearly see by fluorometric investigation, and this synthetic film has a fluorescence excitation peak significantly at the 460nm place, a sharp-pointed fluorescence emission peak is arranged at the 502nm place.Because the blue light of 460nm is safe for organism, adopt 460nm to make exciting light, the 502nm emitting fluorescence of detected characteristics, therefore, this compound film can be applied to safe bioluminescence and detect.
Claims (4)
2. fluorescent material as claimed in claim 1, the building-up process that it is characterized by this material is to use chelidonamic acid as part.
3. a fluorescence membrane is characterized by: contain the fluorescent material described in claim 1 or 2 in this film.
4. a fluorescence membrane as claimed in claim 3 is characterized by: this film use H
2NC
6H
4CH
2C
6H
4NH
2As gelifying agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2009101126468A CN102041000A (en) | 2009-10-15 | 2009-10-15 | Blue-light-excited nickel-chelidamic acid fluorescent film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2009101126468A CN102041000A (en) | 2009-10-15 | 2009-10-15 | Blue-light-excited nickel-chelidamic acid fluorescent film |
Publications (1)
Publication Number | Publication Date |
---|---|
CN102041000A true CN102041000A (en) | 2011-05-04 |
Family
ID=43907552
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2009101126468A Pending CN102041000A (en) | 2009-10-15 | 2009-10-15 | Blue-light-excited nickel-chelidamic acid fluorescent film |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN102041000A (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB559089A (en) * | 1942-08-04 | 1944-02-03 | Wellcome Found | Improvements in and relating to the preparation of compounds of iron suitable for therapeutic injection |
US5069812A (en) * | 1990-12-10 | 1991-12-03 | Lever Brothers Company | Bleach/builder precursors |
US5300657A (en) * | 1992-12-07 | 1994-04-05 | Lever Brothers Company, Division Of Conopco, Inc. | Process for preparing chelidonic acid |
CN1683378A (en) * | 2004-04-13 | 2005-10-19 | 中国科学院福建物质结构研究所 | Synthesis and preparation of nickel-chelidonamic acid film with fluorescent property |
CN101492417A (en) * | 2009-03-10 | 2009-07-29 | 南昌航空大学 | Metallic copper chelidonamic acid complex and method for preparing the same |
-
2009
- 2009-10-15 CN CN2009101126468A patent/CN102041000A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB559089A (en) * | 1942-08-04 | 1944-02-03 | Wellcome Found | Improvements in and relating to the preparation of compounds of iron suitable for therapeutic injection |
US5069812A (en) * | 1990-12-10 | 1991-12-03 | Lever Brothers Company | Bleach/builder precursors |
US5300657A (en) * | 1992-12-07 | 1994-04-05 | Lever Brothers Company, Division Of Conopco, Inc. | Process for preparing chelidonic acid |
CN1683378A (en) * | 2004-04-13 | 2005-10-19 | 中国科学院福建物质结构研究所 | Synthesis and preparation of nickel-chelidonamic acid film with fluorescent property |
CN101492417A (en) * | 2009-03-10 | 2009-07-29 | 南昌航空大学 | Metallic copper chelidonamic acid complex and method for preparing the same |
Non-Patent Citations (1)
Title |
---|
GUO-WEI ZHOU等: "3-D Hydrogen-Bonded Frameworks of Two Metal Complexes with Chelidamic Acid:Syntheses, Structures and Magnetism", 《BULL. KOREAN CHEM. SOC.》 * |
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Application publication date: 20110504 |