CN111795960B - Molecular platform for detecting different forms of iodine by spectrometry and colorimetry, and preparation method and application thereof - Google Patents

Molecular platform for detecting different forms of iodine by spectrometry and colorimetry, and preparation method and application thereof Download PDF

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CN111795960B
CN111795960B CN202010794666.4A CN202010794666A CN111795960B CN 111795960 B CN111795960 B CN 111795960B CN 202010794666 A CN202010794666 A CN 202010794666A CN 111795960 B CN111795960 B CN 111795960B
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iodine
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CN111795960A (en
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赵冰
李安然
孔祥东
杜佳慧
阚伟
卜凡强
王丽艳
孙立
王秀文
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Qiqihar University
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Abstract

A molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method, a preparation method and application thereof relate to a molecular platform for detecting iodine and a preparation and detection method thereof. The invention aims to solve the technical problems that the existing iodine detection material has few types, can only detect one form of iodine, has single detection mechanism and high detection limit and is easily interfered by external environment, and the molecular platform has the structural formula as follows:
Figure DDA0002625100040000011
the preparation method comprises the following steps: reacting 2- (3-amino-6-hydroxyphenyl) phenanthroimidazole with terephthalaldehyde to obtain an organic compound A, and reacting the organic compound A with mercury nitrate to obtain the molecular platform. The molecular platform can be used for qualitative or quantitative detection of iodide ions, iodine simple substances or/and iodine vapor in different media. Convenient use and quick response, and can be used in the detection field of iodide ions, iodine simple substances and iodine vapor.

Description

Molecular platform for detecting different forms of iodine by spectrometry and colorimetry, and preparation method and application thereof
Technical Field
The invention relates to an iodine detection reagent and a preparation method and application thereof.
Background
Iodine is a trace element on earth, and plays an important role in environmental and life sciences because it is widely distributed and can exist in the form of iodine simple substance (solid state), iodine vapor (gaseous state) and iodine ion (liquid state). Iodine has toxicity and corrosiveness to human body, and inhalation of iodine vapor has strong irritation and corrosiveness to skin, mucosa and respiratory tract of human body. In addition, the monitoring of iodine is of great importance because abnormal iodide ion concentration levels in humans usually cause diseases, and iodine deficiency or iodine excess can cause diseases such as goiter, hypothyroidism and hyperthyroidism, which affect human health.
In 2012, Zhuying et al synthesized a DNA fluorescent probe for detection of iodide ions by using a T-rich sequence, and found that the compound has good selective recognition on iodide ions in a 0.010mmol/L MOPS solution, but the detection limit of the fluorescent probe is higher than 30 mol/L. In 2016, pages 147-152 of Inorganic Chemistry Communications 70 (Inorganic Chemistry Communications), colorimetric chemical sensors for continuous identification of mercury (II) and iodide in aqueous media, reported a Schiff base compound whose probe can identify Hg by a color change 2+ And has relay identification performance on iodide ions, and Hg is added into the probe 2+ The color of the solution changed from light yellow to orange, and then changed to light yellow when iodide ion was added. In addition, the detection limit of iodide ion reaches 2.1 × 10 –7 mol/L, has potential application value. Documents "American society for chemistry applications Materials and interfaces" (ACS Applied Materials)&Interfaces) published a paper entitled "sensor of novel metal organic framework for direct electrical detection of iodine vapor" on 44649-44655, vol.51, No. 9, 2017, and discloses that a synthesized novel metal organic framework zeolite imidazolate framework (ZIF-8) is exposed to air at 25 ℃ to detect iodine simple substance within 720 seconds, and an impedance spectroscopy technology is used to directly detect real-time adsorption of the ZIF-8 to iodine ions, but the instrument is expensive, complex to operate and not beneficial to practical application. Recently, the report on the real-time detection and effective capture of volatile iodine by the fluorescent conjugated mesoporous polymer modified by N, N-diethylpropylamine on page 1974 of 1966-No. 4 of the journal of Material chemistry ACarbon-carbon triple bond linked triazine polymers (CMPN), which exhibit detection of iodine vapor by the phenomenon of fluorescence quenching. When the minimum concentration of iodine vapor is 24mg/L, the fluorescence quenching rate is 19.7%. In addition, CMPN still exhibits high selectivity for iodine vapor in the presence of water vapor and ethanol vapor, but it can only detect one form of iodine vapor, limiting the utility of this class of materials.
According to the reported literature, the iodine detection mainly has the following defects:
1. most iodine detection materials are inorganic mesoporous materials, and the types of the iodine detection materials are few;
2. most materials have the function of detecting only one form of iodine;
3. the detection mechanism of the material to iodine is single;
4. the detection limit of iodine is high, and the detection of low-concentration iodine is not suitable;
5. most materials have high requirements on iodine detection environment and are easily interfered by external environment;
disclosure of Invention
The invention provides a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method, a preparation method and application, and aims to solve the technical problems that the existing iodine detection material is few in types, can only detect one form of iodine, is single in detection mechanism, high in detection limit, and easy to be interfered by external environment. The molecular platform for detecting different forms of iodine by using the spectrometry and the colorimetry provided by the invention has the advantages of simple preparation, detection of various forms of iodine, low detection limit, convenience in use, visual phenomenon and the like.
The structural formula of the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry is as follows:
Figure GDA0003715323480000021
the preparation method of the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry comprises the following steps:
firstly, the ratio of 2- (3-amino-6-hydroxyphenyl) phenanthroimidazole to terephthalaldehyde according to the mass is (1-6): 1, adding the mixture into an organic solvent I, and reacting for 1-8 hours at the temperature of 20-80 ℃, wherein solids are separated out in the reaction process; after the reaction is finished, filtering, washing a filter cake by using an organic solvent II and distilled water in sequence, and drying the filter cake to obtain a crude product; recrystallizing the crude product by using an organic solvent III to obtain an organic compound A, wherein the structural formula of the organic compound A is as follows:
Figure GDA0003715323480000022
dissolving an organic compound A and mercury nitrate in an organic solvent IV according to the mass ratio of 1 (2-10), and stirring at room temperature until solid is separated out; filtering, washing a filter cake with ethanol and water in sequence, and drying to obtain a molecular platform for detecting iodine in different forms by a spectrometry method and a colorimetric method.
Furthermore, the organic solvent I is glacial acetic acid, methanol, ethanol, N-dimethylformamide, benzene or toluene.
Furthermore, the organic solvent II for washing the filter cake is ethyl acetate, acetone, acetonitrile, diethyl ether, dichloromethane or chloroform.
Furthermore, the organic solvent III for recrystallizing the crude product is ethyl acetate, or the volume ratio of ethyl acetate to petroleum ether is 1: (1-2), or the mixture of ethyl acetate and diethyl ether according to the volume ratio of 1: (1-3), or the volume ratio of ethyl acetate to dichloromethane is 1: (1-5).
Further, the organic solvent IV is methanol, ethanol, N-dimethylformamide, benzene, toluene or dimethyl sulfoxide.
The preparation process of the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry is represented by the following formula:
Figure GDA0003715323480000031
the application of the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry is to use the molecular platform for qualitatively or quantitatively detecting iodide ions, iodine simple substances or/and iodine vapor in different media.
A method for detecting iodide ions by a colorimetric method by utilizing a molecular platform for detecting different forms of iodine by a spectroscopic method and a colorimetric method comprises the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a platform stock solution A with the concentration of 0.50-1.00 multiplied by 10 –3 mol/L;
Secondly, diluting the platform stock solution A obtained in the first step into a solution with the concentration of 0.10-0.50 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, fully mixing the platform solution B obtained in the second step with a solution to be tested to obtain a test solution C;
and fourthly, under the irradiation of a handheld ultraviolet lamp, the platform solution B is a bright blue clear solution, and if the blue color of the test solution C is dark and black precipitate is generated, the solution to be tested contains iodide ions.
Further, the water-miscible organic solvent is glacial acetic acid, methanol, ethanol, N-dimethylformamide or dimethyl sulfoxide.
A method for detecting iodide ions by a fluorescence spectrometry method by utilizing a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method comprises the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a platform stock solution A with the concentration of 0.50-1.00 multiplied by 10 –3 mol/L;
Secondly, diluting the platform stock solution A obtained in the first step into a solution with the concentration of 0.10-0.50 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, fully mixing the platform solution B obtained in the second step with a solution to be tested to obtain a test solution C;
fourthly, measuring the fluorescence emission light of the platform solution B by taking 315nm as the excitation wavelengthThe emission intensity of the spectrum at an emission wavelength of 495nm is denoted T B
Fifthly, with 315nm as the excitation wavelength, the emission intensity of the fluorescence emission spectrum of the test solution C at the emission wavelength of 495nm is measured and is marked as T C
Sixthly, comparing T B And T C ,T B >73T C And judging that the solution to be detected contains iodide ions.
Further, the water-miscible organic solvent is glacial acetic acid, methanol, ethanol, N-dimethylformamide or dimethyl sulfoxide.
The method for detecting the elementary substance of iodine by ultraviolet spectrometry by utilizing the molecular platform for detecting iodine in different forms by spectrometry and colorimetry comprises the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a solution with a concentration of 0.10-0.50 multiplied by 10 –4 mmol/L of the platform solution A;
secondly, adding the object to be tested into the platform solution A, and standing for 0.5-10 hours to obtain a test sample B;
thirdly, measuring the ultraviolet spectrum of the platform solution A, and recording the absorbance at the position with the absorption wavelength of 530nm as A A
Fourthly, taking the supernatant of the test sample B, measuring the ultraviolet spectrum of the supernatant, and recording the absorbance A at the position of the absorption wavelength of 530nm B
Fifth, compare A A And A B If A is A >6A B Then, the iodine simple substance is judged to be contained in the object to be detected.
Further, the water-miscible organic solvent is glacial acetic acid, methanol, ethanol, N-dimethylformamide or dimethyl sulfoxide.
The method for detecting the elementary substance of iodine by using the molecular platform for detecting different forms of iodine by using a spectrometry method and a colorimetric method through a fluorescence spectrometry method comprises the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a concentrated solutionThe degree of the reaction is 0.10 to 0.50X 10 –4 mmol/L of the platform solution A;
secondly, adding the object to be tested into the platform solution A, and standing for 0.5-10 hours to obtain a test sample B;
thirdly, measuring the fluorescence spectrum of the platform solution A, and respectively recording the fluorescence intensity at the position with the emission wavelength of 500nm as I A
Fourthly, taking the supernatant of the test sample B, measuring the fluorescence spectrum of the supernatant, and measuring the fluorescence intensity I at the position of the emission wavelength of 500nm B
Fifth, compare I A And I B If I is A >18I B Then, the iodine simple substance is judged to be contained in the object to be detected.
Further, the water-miscible organic solvent is glacial acetic acid, methanol, ethanol, N-dimethylformamide or dimethyl sulfoxide.
A method for detecting iodine vapor by a colorimetric method by utilizing a molecular platform for detecting iodine in different forms by a spectroscopic method and a colorimetric method comprises the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a platform stock solution A with the concentration of 0.50-1.00 multiplied by 10 –3 mol/L;
Secondly, diluting the platform stock solution A obtained in the first step into a solution with the concentration of 0.10-0.50 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, cutting qualitative filter paper into strips, soaking the strips in the platform solution B for 1-2 hours, and drying to obtain molecular platform test paper strips for detecting iodine in different forms by using a spectrometry method and a colorimetric method;
fourthly, under the irradiation of natural light, the platform test strip is colorless; under the irradiation of a handheld ultraviolet lamp, the platform test strip is green;
fifthly, after the platform test strip obtained in the third step is placed in a test sample environment for 30-150 minutes, observing the platform test strip under natural light, and if the platform test strip is changed from colorless to yellow, indicating that iodine vapor is contained in the test sample; and observing under a handheld ultraviolet lamp, and if the platform test strip is changed from bright green to dark yellow, indicating that iodine vapor is contained in the test sample.
Further, the water-miscible organic solvent is glacial acetic acid, methanol, ethanol, N-dimethylformamide or dimethyl sulfoxide.
The method for quantitatively detecting iodide ions by using a molecular platform fluorescence method for detecting different forms of iodine by using a spectrometry method and a colorimetric method is a standard curve method.
The molecular platform for detecting different forms of iodine by using the spectrometry and the colorimetry provided by the invention is simple to prepare, stable in structure and low in cost, and is preserved. The detection of the iodide ions, the iodine simple substance and the iodine vapor is not interfered by other analogues, the detection effect is obvious, the use is convenient, the response is rapid, the sensitivity is high, the detection limit reaches 43.1nM, and the qualitative and quantitative detection can be realized. Can be used in the detection field of iodide ions, iodine simple substances and iodine vapor.
Drawings
FIG. 1 is the plateau solution B (0.10X 10) of example 1 –4 mol/L,V DMF :V HEPES 1:1, pH 7.40) and test solution C, the abscissa is emission wavelength and the ordinate is fluorescence intensity; in the figure, the organic compound A.2 Hg 2+ Is a plateau solution B, an organic compound A.2Hg 2+ The iodide ions are the solution C to be detected;
FIG. 2 shows the plateau solution B (0.10X 10) of example 1 –4 mol/L,V DMF :V HEPES 1:1, pH 7.40) and adding fluorescence emission spectra of different anions (0.1mol/L) respectively; the abscissa is the emission wavelength and the ordinate is the fluorescence intensity;
FIG. 3 shows the results of the test solutions C of example 1 at different concentrations of iodide ion (0-1.0X 10) –5 A fluorescence emission spectrogram under the condition of mol/L), wherein the abscissa is emission wavelength, and the ordinate is fluorescence intensity;
FIG. 4 is a standard curve of molecular platform fluorescence detection of iodide ions for the spectroscopic and colorimetric detection of different forms of iodine prepared in example 1.
FIG. 5 is a photograph of the platform solution B and the test solution C under irradiation of the UV lamp in example 1;
FIG. 6 is a photograph of the color change under natural light and under UV light when iodine vapor is detected by the platform strip of example 1.
Detailed Description
The following examples are used to demonstrate the beneficial effects of the present invention:
example 1: the preparation method of the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry of the embodiment is carried out according to the following method:
firstly, adding 0.81 g of 2- (3-amino-6-hydroxyphenyl) phenanthroimidazole and 0.13 g of terephthalaldehyde into 15.0mL of ethanol, and reacting at the temperature of 60 ℃ for 5 hours, wherein solids are separated out in the reaction process; after the reaction is finished, filtering, washing a filter cake for 3 times by using methanol and distilled water respectively in sequence, and drying the filter cake for 8 hours at the temperature of 80 ℃ to obtain a crude product; and (3) mixing the crude product with ethyl acetate and petroleum ether according to a volume ratio of 1: 2 to obtain an organic compound A, wherein the structural formula of the organic compound A is shown in the specification
Figure GDA0003715323480000061
Yield 92% and melting point 320 ℃.
Second, 0.75 g of organic compound A and 1.63 g of mercuric nitrate were dissolved in 15mL of N, N-dimethylformamide, and the mixture was stirred at room temperature until a large amount of solid precipitated. Filtering, washing the filter cake with ethanol for 3 times, washing with water for 3 times, drying the filter cake at 80 deg.C for 8 hr to obtain molecular platform for detecting iodine with different forms by spectrometry and colorimetry, with yield of 65% and melting point of more than 320 deg.C.
The structural characterization data for the preparation of organic compound a in this example is as follows: 1 HNMR(600MHz,DMSO-d 6 ):δ(ppm):13.84(s,2H),13.24(s,2H),8.93~8.97(m,6H),8.64(d,J=8.0Hz,2H),8.54(d,J=7.5Hz,2H),8.38(d,J=8.4Hz,2H),8.20(s,4H),7.81~7.84(m,4H),7.72~7.75(m,4H)7.55(d,J=6.0Hz,2H),7.19(d,J=8.5Hz,2H); 13 C NMR(600MHz,DMSO):δ(ppm):193.4,158.4,158.0,156.9,149.5,149.4,143.2,141.7,138.9,134.7,130.5,129.6,128.5,128.2,128.1,127.8,126.9,126.5,125.9,124.7,124.4,123.6,122.7,122.4,122.5,120.9,118.5,113.6;IR(KBr,cm –1 ):3306,3055,1689,1622,1589,1543,1493,1428,1388,1362,1262,1208,1063,967,892,826,794,755,722,673,631,595,565。
the structural characterization data of the molecular platform for detecting different forms of iodine by the preparative spectrometry and the colorimetry in this example are as follows: 1 HNMR(600MHz,DMSO-d 6 ):δ(ppm):8.90~8.99(m,6H),8.67(d,J=8.01Hz,2H),8.58(d,J=7.5Hz,2H),8.39(d,J=7.4Hz,2H),8.21(d,J=7.4Hz,1H),8.20(s,4H),8.11(d,J=7.4Hz,1H),7.81~7.89(m,4H),7.72~7.75(m,4H),7.55(d,J=6.0Hz,2H),7.19(d,J=8.4Hz,2H);IR(KBr,cm –1 ):1685,1617,1585,1546,1497,1431,1392,1360,1278,1220,1039,960,887,830,789,746,721,686,621,596. High resolution mass spectrum HR-MS (ESI) to obtain peak with mass-to-mass ratio of 1257.4474 and molecular weight of [ organic compound A-2H ] + +2Hg 2+ +2Cl +K + ] + The organic compound a was again determined in a mass amount of 1: the complexation ratio of 2 formed the metal complex a-2 Hg.
From the above characterization results, the structural formula of the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry prepared in this example is:
Figure GDA0003715323480000071
the following tests were carried out for detection of iodide ions by one of the molecular platform fluorescence spectrometry methods for detection of different forms of iodine prepared in example 1:
dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in N, N-dimethylformamide to prepare a platform stock solution A with the concentration of 0.50 multiplied by 10 –3 mol/L;
Secondly, the platform stock solution A obtained in the first step is diluted into a solution with the concentration of 0.10 multiplied by 10 by using a HEPES solution with the concentration of 0.01mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, fully mixing the platform solution B obtained in the second step with a solution to be tested to obtain a test solution C;
fourthly, taking 315nm as excitation wavelengthThe fluorescence emission spectrum of the platform solution B was measured for emission intensity at an emission wavelength of 495nm and was designated as T B ,T B 110 a.u.; the fluorescence emission spectrum of the platform solution B is shown in FIG. 1; the abscissa is the emission wavelength and the ordinate is the fluorescence intensity;
fifthly, with 315nm as the excitation wavelength, the emission intensity of the fluorescence emission spectrum of the test solution C at the emission wavelength of 495nm is measured and is marked as T C 1.5 a.u.; the fluorescence emission spectrum of test solution C is also plotted in fig. 1;
sixthly, comparing T B And T C ,T B >73T C And judging that the solution to be detected contains iodide ions.
The method for detecting the fluorescence emission spectrum of the molecular platform of iodine in different forms after the molecular platform reacts with different anions by the spectrometry and the colorimetry prepared in the example 1 comprises the following specific steps:
the spectroscopic and colorimetric methods prepared in example 1 were used to detect molecular plateau solutions of different forms of iodine (concentration 0.10X 10) –4 mol/L) are respectively added with different anion solutions (with the concentration of 0.10mol/L), wherein the anion is F ,Cl ,Br ,I ,S 2– ,HS ,SO 3 2– ,HSO 3 ,SO 4 2– ,HPO 4 3– ,H 2 PO 3 ,NO 2 ,NO 3 ,AcO ,CO 3 2– And SCN The fluorescence emission spectra of the plateau solution before and after addition of the anion were measured separately, as shown in FIG. 2. The fluorescence intensity of the platform solution A at the excitation wavelength of 315nm is I at the emission wavelength of 495nm A Fluorescence intensity after addition of anion is I B As can be seen from FIG. 2, the fluorescence intensities of the solutions with other anions besides iodide were all above 80a.u., and only the sample solution B with iodide added had a fluorescence intensity I at 495nm B 1.5a.u., when I A >73I B It is stated that the molecular platform does not suffer from F when detecting iodide ions ,Cl ,Br ,S 2– ,HS ,SO 3 2– ,HSO 3 ,SO 4 2– ,HPO 4 3– ,H 2 PO 3 ,NO 2 ,NO 3 ,AcO ,CO 3 2– And SCN Influence of ions.
The relationship between the concentration of iodide ions and the fluorescence intensity in the molecular platform detection for detecting different forms of iodine by the spectroscopic method and the colorimetric method prepared in example 1 was determined as follows:
dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in N, N-dimethylformamide to prepare a platform stock solution A with the concentration of 0.50 multiplied by 10 –3 mol/L;
Secondly, the platform stock solution A obtained in the first step is diluted to be 0.10 multiplied by 10 by using HEPES solution with the concentration of 0.01mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, fully mixing the platform solution B obtained in the second step with iodine ion solutions with different concentrations, wherein the concentration of the iodine ion solution is 0-2.0 multiplied by 10 –6 mol/L to obtain a test solution C;
fourthly, measuring the emission intensity of the fluorescence emission spectrum of the test solution C when the emission wavelength is 495nm by taking 315nm as the excitation wavelength; the fluorescence emission spectrum of test solution C is shown in fig. 3; the abscissa is the emission wavelength and the ordinate is the fluorescence intensity;
as can be seen from FIG. 3, the fluorescence intensity of test solution C at 495nm gradually increased with the increase in the iodide ion concentration, and the iodide ion concentration increased to 2.0X 10 –6 The fluorescence intensity reaches the maximum value at mol/L. In the concentration of iodide ion of 0-0.9 × 10 –6 The results of the linear relationship between the fluorescence intensity at 495nm of the test solution C and the change in the iodide ion concentration in the mol/L range are shown in FIG. 4. Calculation formula (C) based on detection limit DL =3S b M), fitting to obtain a linear regression equation y of-0.6912 x +1.0492 with standard deviation R from blank parallel experiment 2 0.9940, spectroscopic and colorimetric detection of different formsThe detection limit of the molecular platform of iodine reached 43.1 nM. The molecular platform fluorescence spectrometry for detecting the iodide ions in different forms by the spectrometry and the colorimetry has good linear relation.
The method for detecting iodide ions by a colorimetric method by utilizing the molecular platform for detecting different forms of iodine by the spectroscopic method and the colorimetric method prepared in example 1 comprises the following steps:
dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in N, N-dimethylformamide to prepare a platform stock solution A with the concentration of 1.00 multiplied by 10 –3 mol/L;
Secondly, the platform stock solution A obtained in the first step is diluted into a solution with the concentration of 0.10 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, fully mixing the platform solution B obtained in the second step with a solution to be tested to obtain a test solution C;
fourthly, under the irradiation of a handheld ultraviolet lamp, the color changes of the platform solution B and the test solution C under the irradiation of the ultraviolet lamp are shown in the figure 5; the platform solution B was a bright blue clear solution, while the test solution C was dark blue with black precipitate formation, indicating that the solution to be tested contained iodide ions.
A method for colorimetric detection of iodine vapor using the spectroscopic and colorimetric molecular platform prepared in example 1 for detection of different forms of iodine, comprising the steps of:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a platform stock solution A with the concentration of 1.00 multiplied by 10 –3 mol/L;
Secondly, the platform stock solution A obtained in the first step is diluted into a solution with the concentration of 0.10 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, cutting qualitative filter paper into strips, soaking the strips in the platform solution B for 2 hours, and drying the strips for 8 hours at the temperature of 25 ℃ to obtain molecular platform test strips for detecting iodine in different forms by using a spectrometry method and a colorimetric method;
fourthly, under the irradiation of natural light, the platform test strip is colorless; under the irradiation of a handheld ultraviolet lamp, the platform test strip is green;
fifthly, after the platform test strip obtained in the third step is placed in a test sample environment for 60 minutes, observing the platform test strip under natural light, and if the platform test strip is changed from colorless to yellow, indicating that iodine vapor is contained in the test sample; if the platform test strip is observed under a handheld ultraviolet lamp, the platform test strip is changed from bright green to dark yellow, and the situation that iodine vapor is contained in the test sample is also indicated. The color change of the platform strip under natural light and under an ultraviolet lamp is shown in fig. 6.
Example 2: the method for synthesizing the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry in the embodiment is as follows:
firstly, adding 1.62 g of 2- (3-amino-6-hydroxyphenyl) phenanthroimidazole and 0.13 g of terephthalaldehyde into methanol, and reacting at the temperature of 40 ℃ for 8 hours, wherein solids are separated out in the reaction process; after the reaction is finished, filtering, washing a filter cake by using methanol and distilled water in sequence, and drying the filter cake for 8 hours at the temperature of 80 ℃ to obtain a crude product; the crude product was purified by using ethyl acetate and dichloromethane ether at a volume ratio of 1: 5 to obtain the organic compound A with the yield of 75 percent and the melting point of 320 ℃.
Secondly, 0.75 g of organic compound A and 0.65 g of mercuric nitrate are dissolved in ethanol and stirred at room temperature until a large amount of solid is separated out. Filtering, washing the filter cake with ethanol for 3 times, washing with water for 3 times, drying the filter cake at 80 deg.C for 8 hr to obtain molecular platform for detecting iodine with different forms by spectrometry and colorimetry, with yield of 57% and melting point of > 320 deg.C.
Example 3: the synthesis method of the molecular platform for detecting different forms of iodine by the spectrometry and the colorimetry in the embodiment is as follows:
firstly, adding 1.95 g of 2- (3-amino-6-hydroxyphenyl) phenanthroimidazole and 0.13 g of terephthalaldehyde into benzene, and reacting at 70 ℃ for 3 hours, wherein solids are separated out in the reaction process; after the reaction is finished, filtering, washing a filter cake by using methanol and distilled water in sequence, and drying the filter cake for 8 hours at the temperature of 80 ℃ to obtain a crude product; and (3) mixing the crude product with ethyl acetate and ether according to a volume ratio of 1: 3 to obtain the organic compound A with the yield of 40 percent and the melting point of 320 ℃.
Secondly, 0.75 g of organic compound A and 2.93 g of mercury nitrate are dissolved in dimethyl sulfoxide, and the mixture is stirred at room temperature until a large amount of solid is separated out. Filtering, washing the filter cake with ethanol and water in sequence, drying the filter cake for 8 hours at 80 ℃ to obtain a molecular platform for detecting different forms of iodine by a spectrometry and a colorimetry, wherein the yield is 63%, and the melting point is more than 320 ℃. .

Claims (10)

1. A molecular platform for detecting different forms of iodine by spectrometry and colorimetry is characterized in that the structural formula of the molecular platform is as follows:
Figure FDA0003715323470000011
2. a method of preparing a molecular platform for spectroscopic and colorimetric detection of different forms of iodine according to claim 1, wherein the method is performed by the steps of:
firstly, the ratio of 2- (3-amino-6-hydroxyphenyl) phenanthroimidazole to terephthalaldehyde according to the mass is (1-6): 1, adding the mixture into an organic solvent I, and reacting for 1-8 hours at the temperature of 20-80 ℃, wherein solids are separated out in the reaction process; after the reaction is finished, filtering, washing a filter cake by using an organic solvent II and distilled water in sequence, and drying the filter cake to obtain a crude product; recrystallizing the crude product with organic solvent III to obtain organic compound A with structural formula
Figure FDA0003715323470000012
Dissolving an organic compound A and mercury nitrate in an organic solvent IV according to the mass ratio of 1 (2-10), and stirring at room temperature until solid is separated out; filtering, washing a filter cake with ethanol and water in sequence, and drying to obtain a molecular platform for detecting iodine in different forms by a spectrometry method and a colorimetric method.
3. The method according to claim 2, wherein the organic solvent I is glacial acetic acid, methanol, ethanol, N-dimethylformamide, benzene or toluene.
4. The method of claim 2, wherein the organic solvent II used to wash the filter cake is ethyl acetate, acetone, acetonitrile, diethyl ether, dichloromethane or chloroform.
5. The use of a spectroscopic and colorimetric molecular platform for the detection of different forms of iodine according to claim 1 in the qualitative or quantitative detection of iodide ions or iodine simple substances in different media.
6. Use of a molecular platform for spectroscopic and colorimetric detection of different forms of iodine according to claim 5, wherein the method for colorimetric detection of iodide ions using the molecular platform is performed according to the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a platform stock solution A with the concentration of 0.50-1.00 multiplied by 10 –3 mol/L;
Secondly, diluting the platform stock solution A obtained in the first step into a solution with the concentration of 0.10-0.50 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, fully mixing the platform solution B obtained in the second step with a solution to be tested to obtain a test solution C;
and fourthly, under the irradiation of a handheld ultraviolet lamp, the platform solution B is a bright blue clear solution, and if the blue color of the test solution C is dark and black precipitate is generated, the solution to be tested contains iodide ions.
7. The use of a molecular platform for spectroscopic and colorimetric detection of different forms of iodine according to claim 5, wherein the molecular platform is used in a method for detection of iodide ions by fluorescence spectroscopy, according to the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a platform stock solution A with the concentration of 0.50-1.00 multiplied by 10 –3 mol/L;
Secondly, diluting the platform stock solution A obtained in the first step into a solution with the concentration of 0.10-0.50 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, fully mixing the platform solution B obtained in the second step with a solution to be tested to obtain a test solution C;
fourthly, with 315nm as the excitation wavelength, the emission intensity of the fluorescence emission spectrum of the platform solution B when the emission wavelength is 495nm is measured and is marked as T B
Fifthly, with 315nm as the excitation wavelength, the emission intensity of the fluorescence emission spectrum of the test solution C at the emission wavelength of 495nm is measured and is marked as T C
Sixthly, comparing T B And T C ,T B >18T C And judging that the solution to be detected contains iodide ions.
8. The use of the molecular platform for spectroscopic and colorimetric detection of iodine of different forms as claimed in claim 5, wherein the molecular platform is used in the detection of elemental iodine by UV spectroscopy by the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a solution with a concentration of 0.10-0.50 multiplied by 10 –4 mmol/L of the platform solution A;
secondly, adding the object to be tested into the platform solution A, and standing for 0.5-10 hours to obtain a test sample B;
thirdly, measuring the ultraviolet spectrum of the platform solution A, and recording the absorbance at the position with the absorption wavelength of 530nm as A A
Fourthly, taking the supernatant of the test sample B, measuring the ultraviolet spectrum of the supernatant, and recording the absorbance A at the position of the absorption wavelength of 530nm B
Fifth, compare A A And A B If A is A >6A B Then, the iodine simple substance is judged to be contained in the object to be detected.
9. The use of the molecular platform for spectroscopic and colorimetric detection of different forms of iodine as claimed in claim 5, wherein the molecular platform is used in a method for detecting elemental iodine by fluorescence spectroscopy, comprising the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a solution with a concentration of 0.10-0.50 multiplied by 10 –4 mmol/L of the platform solution A;
secondly, adding the object to be tested into the platform solution A, and standing for 0.5-10 hours to obtain a test sample B;
thirdly, measuring the fluorescence spectrum of the platform solution A, and respectively recording the fluorescence intensity at the position with the emission wavelength of 500nm as I A
Fourthly, taking the supernatant of the test sample B, measuring the fluorescence spectrum of the supernatant, and measuring the fluorescence intensity I at the position of the emission wavelength of 500nm B
Fifth, compare I A And I B If I is A >18I B Then, the iodine simple substance is judged to be contained in the object to be detected.
10. Use of a molecular platform for spectroscopic and colorimetric detection of different forms of iodine according to claim 5, wherein the method for colorimetric detection of iodine vapor using the molecular platform is carried out according to the following steps:
firstly, dissolving a molecular platform for detecting different forms of iodine by a spectrometry method and a colorimetric method in an organic solvent which can be mutually dissolved with water to prepare a platform stock solution A with the concentration of 0.50-1.00 multiplied by 10 –3 mol/L;
Secondly, diluting the platform stock solution A obtained in the first step into a solution with the concentration of 0.10-0.50 multiplied by 10 by using a HEPES solution with the concentration of 0.010mol/L, pH-7.40 –4 A platform solution B of mol/L;
thirdly, cutting qualitative filter paper into strips, soaking the strips in the platform solution B for 1-2 hours, and drying to obtain molecular platform test paper strips for detecting iodine in different forms by using a spectrometry method and a colorimetric method;
fourthly, under the irradiation of natural light, the platform test strip is colorless; under the irradiation of a handheld ultraviolet lamp, the platform test strip is green;
fifthly, after the platform test strip obtained in the third step is placed in a test sample environment for 30-150 minutes, observing the platform test strip under natural light, and if the platform test strip is changed from colorless to yellow, indicating that iodine vapor is contained in the test sample; and observing under a handheld ultraviolet lamp, and if the platform test strip is changed from bright green to dark yellow, indicating that iodine vapor is contained in the test sample.
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113024799B (en) * 2021-03-01 2022-05-06 山东大学 Application of soluble polymer with micropores in iodine vapor detection
CN113004206B (en) * 2021-03-11 2022-06-17 齐齐哈尔大学 Naphthalene derivative fluorescent probe and preparation method and application thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0874242A1 (en) * 1997-04-21 1998-10-28 Randox Laboratories Ltd. Device and apparatus for the simultaneous detection of multiple analytes
EP1577010A2 (en) * 1995-12-05 2005-09-21 Tecan Trading AG Microsystem platform and its use
CN101084235A (en) * 2002-04-17 2007-12-05 迪纳米斯治疗公司 3-deoxyglucosone and skin
JP2014136675A (en) * 2013-01-15 2014-07-28 Nara Women's Univ Metal ion fluorescence probe

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69233146T2 (en) * 1991-05-22 2004-04-29 Dade Behring Marburg Gmbh Particles containing a composition comprising a chemiluminescent compound
DE60219812T8 (en) * 2001-10-17 2008-05-21 Ciba Specialty Chemicals Holding Inc. PHOTOACTIVABLE NITROGEN BOTTOMS
US7445894B2 (en) * 2002-05-03 2008-11-04 Molecular Probes, Inc. Compositions and methods for detection and isolation of phosphorylated molecules
US20040171034A1 (en) * 2002-05-03 2004-09-02 Brian Agnew Compositions and methods for detection and isolation of phosphorylated molecules
JP2005104148A (en) * 2003-09-11 2005-04-21 Fuji Photo Film Co Ltd Cellulose acylate film and solution film forming method
US20070004679A1 (en) * 2004-05-17 2007-01-04 Nathalie Schlienger Androgen receptor modulators and methods of treating disease using the same
AU2013200142C1 (en) * 2005-08-30 2016-07-07 Takeda Pharmaceutical Company Limited 1-Heterocyclylsulfonyl, 3-aminomethyl, 5-(hetero-)aryl substituted 1-H-pyrrole derivatives as acid secretion inhibitors
JP2008170422A (en) * 2006-12-15 2008-07-24 Fujifilm Corp Immunoassay method
US8697714B2 (en) * 2010-07-28 2014-04-15 Nanyang Technological University Quinazolinone based fluorogenic probes
US20140170735A1 (en) * 2011-09-25 2014-06-19 Elizabeth A. Holmes Systems and methods for multi-analysis
US10012664B2 (en) * 2011-09-25 2018-07-03 Theranos Ip Company, Llc Systems and methods for fluid and component handling
US9810704B2 (en) * 2013-02-18 2017-11-07 Theranos, Inc. Systems and methods for multi-analysis
US10550068B2 (en) * 2015-07-23 2020-02-04 Mitsubishi Gas Chemical Company, Inc. Compound and method for producing same
CN105255481B (en) * 2015-11-16 2017-04-05 齐齐哈尔大学 A kind of phenanthro- imidazoles coumarin pair fluorophor ratio fluorescent molecular probe and its synthesis and using method for iron ion detection
US10605799B2 (en) * 2016-05-17 2020-03-31 The Regents Of The University Of California Systems and methods for detecting metal ion concentrations in subjects
CN106699734B (en) * 2016-12-19 2020-03-10 中南大学 Fluorescent molecular probe and nano probe as well as preparation method and application thereof
TW201930298A (en) * 2017-11-17 2019-08-01 美商史基普研究協會 Bis-benzimidazole compounds and methods of using the same
CN108863945A (en) * 2018-06-12 2018-11-23 齐齐哈尔大学 A kind of phenanthro- imidazoles Fe3+Probe and its preparation and application
CN109470671A (en) * 2018-11-30 2019-03-15 齐齐哈尔大学 One kind being used for H2The fluorescent test paper strip and its preparation and application of S detection
CN111777598B (en) * 2020-08-10 2023-03-17 齐齐哈尔大学 Detect Cu 2+ And can utilize Cu 2+ Detection of HPO4 2– Fluorescent probe and preparation method and application thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1577010A2 (en) * 1995-12-05 2005-09-21 Tecan Trading AG Microsystem platform and its use
EP0874242A1 (en) * 1997-04-21 1998-10-28 Randox Laboratories Ltd. Device and apparatus for the simultaneous detection of multiple analytes
CN101084235A (en) * 2002-04-17 2007-12-05 迪纳米斯治疗公司 3-deoxyglucosone and skin
JP2014136675A (en) * 2013-01-15 2014-07-28 Nara Women's Univ Metal ion fluorescence probe

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