CN113666966A - Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide - Google Patents

Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide Download PDF

Info

Publication number
CN113666966A
CN113666966A CN202111116165.1A CN202111116165A CN113666966A CN 113666966 A CN113666966 A CN 113666966A CN 202111116165 A CN202111116165 A CN 202111116165A CN 113666966 A CN113666966 A CN 113666966A
Authority
CN
China
Prior art keywords
bpdc
tcpp
fluorescent probe
water
dimethyl sulfoxide
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
Application number
CN202111116165.1A
Other languages
Chinese (zh)
Other versions
CN113666966B (en
Inventor
张光耀
喻琨
颜廷义
周子杰
刘倩
王希雁
曲丽君
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Qingdao University
Original Assignee
Qingdao University
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Qingdao University filed Critical Qingdao University
Priority to CN202111116165.1A priority Critical patent/CN113666966B/en
Publication of CN113666966A publication Critical patent/CN113666966A/en
Application granted granted Critical
Publication of CN113666966B publication Critical patent/CN113666966B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F13/00Compounds containing elements of Groups 7 or 17 of the Periodic Table
    • C07F13/005Compounds without a metal-carbon linkage
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/6428Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
    • G01N21/643Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" non-biological material
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/18Metal complexes
    • C09K2211/188Metal complexes of other metals not provided for in one of the previous groups
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/6428Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
    • G01N2021/6432Quenching

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Molecular Biology (AREA)
  • Materials Engineering (AREA)
  • Engineering & Computer Science (AREA)
  • Optics & Photonics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)

Abstract

The invention belongs to the technical field of chemical analysis and detection, and relates to synthesis and application of a fluorescent probe for detecting trace water in dimethyl sulfoxide. Porphyrin and manganese ions can be used for preparing the Mn-TCPP (BPDC) material by a simple solvothermal method, and the material has stronger fluorescence response to water, no response to an organic solvent dimethyl sulfoxide (DMSO) and better fluorescence linear range response to the water content in the DMSO. The fluorescent probe is simple and convenient to prepare, and has the advantages of high sensitivity, large linear range, good stability and repeatability and the like for detecting moisture.

Description

Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide
Technical Field
The invention belongs to the technical field of chemical analysis and detection, and particularly relates to a preparation method and application of a porphyrin MOF fluorescent probe for detecting trace water in dimethyl sulfoxide (DMSO).
Background
The information in this background section is only for enhancement of understanding of the general background of the invention and is not necessarily to be construed as an admission or any form of suggestion that this information forms the prior art that is already known to a person of ordinary skill in the art.
Water is one of the most common impurities in organic solvents, seriously compromising laboratory chemistry and industrial manufacturing. Therefore, the development of a simple, fast and reliable sensor for detecting water in organic solvents is urgently needed. The traditional and widely used techniques for determining water content are karl fischer titration and gas chromatography. However, these methods have limitations including the need for specialized equipment, trained personnel, time consuming procedures, and the inability to monitor in real time on site. The fluorescence sensor has the characteristics of simple operation, quick response, high sensitivity, easy manufacture, capability of carrying out noninvasive in-situ detection and the like, and is considered as a potential substitute of the traditional analysis method.
In recent years, many fluorescent probes excited by water response have been reported. However, most probes are complex to synthesize, large in dosage, low in sensitivity, limited in detection range, and part of the probes are poor in stability, difficult to store and incapable of being recycled.
Disclosure of Invention
Aiming at the current detection situation of water in the organic solvent dimethyl sulfoxide, the invention aims to provide a synthesis and application research of a probe capable of rapidly detecting trace water in the organic solvent dimethyl sulfoxide.
In order to achieve the technical purpose, the invention adopts the following technical scheme:
in a first aspect of the present invention, a method for synthesizing a fluorescent probe Mn-tcpp (bpdc) for detecting trace amount of water in dimethyl sulfoxide is provided, which comprises:
TCPP, manganese salt and BPDC are taken as raw materials to carry out solvent thermal reaction, thus obtaining the catalyst.
The MOF material Mn-TCPP (BPDC) is synthesized by a solvothermal method, and the porphyrin TCPP in the MOF material generates fluorescence quenching effect due to electron transfer to metal ions (LMCT). The material can recognize and combine trace water molecules in organic solvent, and further recover fluorescence as a response signal. The technical method has the advantages of high detection speed, high sensitivity, simple operation, low cost and the like.
In a second aspect of the invention, there is provided a fluorescent probe Mn-TCPP (BPDC) synthesized by any of the above-described methods.
The synthesis of the porphyrin-based MOF only needs one step, the synthesis time is short, the raw materials are cheap and easy to obtain, and the dosage is very small. The porphyrin ligand in the material determines the fluorescence property of the material to be outstanding. The self fluorescence of the MOF probe formed by modification can be almost completely masked, and the fluorescence intensity is rapidly enhanced after the MOF probe reacts with water for several seconds, and the enhancement range is large. The material has the advantages of low detection limit (0.04%), high sensitivity, small dosage (0.25 mu g/mL) and no pollution.
In a third aspect of the present invention, there is provided a method for detecting the content of trace water in an organic solvent, comprising:
preparing organic solvents with different water contents as standard solutions;
adding the fluorescent probe Mn-TCPP (BPDC) into the standard solution, uniformly mixing, and detecting the fluorescent response;
establishing a corresponding relation between the water content and the fluorescence intensity according to the measured fluorescence intensity;
and adding the fluorescent probe Mn-TCPP (BPDC) into an organic solvent to be detected, uniformly mixing, detecting fluorescent response, and calculating the water content to obtain the fluorescent probe.
The invention has the beneficial effects that:
(1) compared with the prior art, the invention has the following remarkable advantages: the Mn-TCPP (BPDC) MOF composite material has the advantages of simple synthesis process, less time consumption and cheap and easily-obtained raw materials. The method is applied to the field of fluorescent probes, the property of the parent nucleus ligand is excellent, and a novel probe can be synthesized by derivation of the parent nucleus ligand. When the synthesized fluorescent probe MOF is used for detecting water, the fluorescence enhancement range is large, the sensitivity is high, the detection limit is low, the usage amount is small, and the like. In conclusion, the fluorescent probe is a tool which is low in cost, convenient, fast and sensitive, is suitable for detecting the concentration of trace water in the dimethyl sulfoxide organic solvent, and has wide application prospects in the field of chemical analysis and detection.
(2) The operation method is simple, low in cost, universal and easy for large-scale production.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of this specification, are included to provide a further understanding of the invention, and are incorporated in and constitute a part of this specification, illustrate exemplary embodiments of the invention and together with the description serve to explain the invention and not to limit the invention.
FIG. 1 is a diagram of the mechanism of Mn-TCPP (BPDC) synthesis and sensing;
FIG. 2 is a photograph of Mn-TCPP (BPDC) prepared in example 1, wherein (1) is a (Scanning Electron Microscope) SEM image of Mn-TCPP (BPDC), (2) is an X-ray diffraction (XRD) spectrum of Mn-TCPP (BPDC), and (3) is an infrared spectrum of Mn-TCPP (BPDC);
FIG. 3 shows fluorescence intensity of Mn-TCPP (BPDC) prepared in example 1 in different solvents;
FIG. 4 is a graph of the fluorescence spectra (1) of Mn-TCPP (BPDC) prepared in example 1 in DMSO at various water contents, and a linear relationship between the fluorescence intensity and the water content (2);
FIG. 5 is a structural diagram of Mn-TCPP (BPDC).
Detailed Description
It is to be understood that the following detailed description is exemplary and is intended to provide further explanation of the invention as claimed. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
A preparation method of MOF material Mn-TCPP (BPDC) is shown in figure 5.
The details of the preparation method are as follows:
meso-tetra (4-carboxyphenyl) porphine (TCPP), manganese nitrate tetrahydrate Mn (NO)3)2·4H2O and 4,4' -biphenyldicarboxylic acid (BPDC) were dissolved in N, N-Dimethylformamide (DMF) at room temperature, and the reaction mixture was dissolved inStirring for 1 hour at 150 ℃, cooling the reaction to room temperature, centrifuging, pouring out the mother liquor on the upper layer, washing with ethanol for 3 times, and vacuum-drying at 60 ℃.
The fluorescent probe of the invention has almost no fluorescence, and has strong fluorescence emission rapidly after water action, and the maximum emission wavelength is 650nm (lambda ex is 415 nm).
The fluorescent probe has good selectivity on water, the fluorescence is weak in acetone, DMF, DMSO, ethanol, isopropanol and methanol solutions, and the extremely strong fluorescence can be seen by naked eyes when the fluorescent probe is added into water under the same condition.
The fluorescent probe can be used for rapidly detecting the content of trace water in an organic solvent DMSO, and the method comprises the following steps:
adding Mn-TCPP (BPDC) into an organic solvent, adding quantitative water, shaking for 5min, and detecting a fluorescence response by using a fluorescence spectrometer.
Wherein the final concentration of Mn-TCPP (BPDC) is 2.5 mu g/mL, the excitation wavelength is 415nm, the emission wavelength is 650nm, and the volume content of water is 0.05-30% (v/v).
The fluorescent probes of the present invention exhibit high sensitivity for the detection of water. The fluorescence intensity of the probe solution increases with increasing water content. The fluorescence intensity reaches a peak at approximately 30% water content. In the range of 0 to 30 percent of water content, the fluorescence intensity of the probe solution has a good linear relation with the water content. The detection limit of the fluorescent probe in DMSO is 0.04%.
The stability research of the fluorescent probe disclosed by the invention shows that the detection of the probe on the water content is not influenced after the material is stored for 150 days.
The present invention is described in further detail below with reference to specific examples, which are intended to be illustrative of the invention and not limiting.
Example 1
Referring to FIG. 1, the preparation and sensing process of Mn-TCPP (BPDC) of the present invention is as follows:
(1) after 2mg of TCPP, 4.2mg of manganese nitrate tetrahydrate and 5mg of BPDC were dissolved in 12mL of DMF, the solution was added to a Schlenk tube under nitrogen protection, and stirred and refluxed at 150 ℃ for one hour;
(2) the reaction solution cooled to room temperature is centrifuged (rotation speed 7000r/min), washed with ethanol for 3 times, and dried in vacuum for 10h to obtain Mn-TCPP (BPDC).
(3) Ultrasonically dispersing the Mn-TCPP (BPDC) probe obtained in the step (2) in ethanol (1mg/mL) for later use. And (3) adding 2mL of the solution to be detected into 5 mu L of the probe solution, shaking for 5min, and measuring the fluorescence intensity.
(4) After the probe is added into DMSO with low water content, weak fluorescence can be seen under a 365nm ultraviolet lamp, because the fluorescence is weakly recovered due to ligand exchange between water molecules in the DMSO and BPDC and binding to a metal node. When the water content is higher, the water molecules break the metal nodes, so that porphyrin is released, and the fluorescence is enhanced violently.
Example 2
Appearance and structure characterization of Mn-TCPP (BPDC) material
The MOF probe Mn-tcpp (bpdc) prepared in example 1 was morphologically characterized by scanning electron microscopy, as shown in (1) of fig. 2, and it can be seen from (1) of fig. 2 that the MOF material was in the shape of regular square biscuit and was uniform in morphology. The XRD pattern shows that Mn-TCPP (BPDC) has a uniform crystal structure. Molecular binding patterns of probes were determined using infrared spectroscopy, including 1580cm-1Turbine structure representing metal node, 1009cm-1Formation of metalloporphyrin and 965cm-1The presence of hollow porphyrin was confirmed, and the microstructure of the material Mn-TCPP (BPDC) was confirmed.
Example 3
Mn-TCPP (BPDC) material selectivity and application
The dispersed MOF material Mn-TCPP (BPDC) prepared in example 1 is added with 2mL of water, DMSO, methanol, ethanol, isopropanol, acetone and DMF respectively, vibrated for 5min at normal temperature, transferred to a quartz cuvette, and the fluorescence intensity at 650nm is measured at the excitation wavelength of 415 nm. The test solution was irradiated with a 365nm ultraviolet lamp and observed for fluorescence. The detection result is shown in (figure 3), the photo of the fluorescence intensity at 650nm and the photo under 365nm ultraviolet lamp shows that the material has no fluorescence response in the anhydrous organic solvent and only emits light in water, thus having good selectivity.
Preparing a DMSO solution with the water content of 0-40%, adding the dispersed MOF material Mn-TCPP (BPDC) into 2mL of the prepared solution, oscillating for 5min at normal temperature, transferring to a quartz cuvette, and measuring the fluorescence spectrum of 600-800 nm under the excitation wavelength of 415 nm. As shown in fig. 4 (1), the fluorescence intensity of the solution increased with the increase in the water content of the test solution, and thus a good linear relationship between the water content and the fluorescence intensity at 650nm was obtained (fig. 4 (2) and (3)), where the linear equation is y 550x +143(C < 10%), y 23979 x-249178 (C > 10%), the linear range is 0.05% to 30%, and the minimum detection limit is 0.04%. The MOF material Mn-TCPP (BPDC) has low lower limit of fluorescence detection on water, wide detection range and good application value.
It should be noted that the above-mentioned embodiments are only preferred embodiments of the present invention, and the present invention is not limited thereto, and although the present invention has been described in detail with reference to the foregoing embodiments, it will be apparent to those skilled in the art that modifications and equivalents can be made in the technical solutions described in the foregoing embodiments, or equivalents thereof. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.

Claims (10)

1. A synthetic method of a fluorescent probe Mn-TCPP (BPDC) for detecting trace water in dimethyl sulfoxide is characterized by comprising the following steps:
TCPP, manganese salt and BPDC are taken as raw materials to carry out solvent thermal reaction, thus obtaining the catalyst.
2. The method for synthesizing a fluorescent probe Mn-TCPP (BPDC) for detecting trace amount of water in dimethyl sulfoxide according to claim 1, wherein the manganese salt is manganese nitrate tetrahydrate.
3. The method for synthesizing the fluorescent probe Mn-TCPP (BPDC) for detecting trace water in dimethyl sulfoxide according to claim 1, wherein the specific conditions of the solvothermal method are as follows: reacting at 150-180 ℃ for 1-1.5 hours, preferably stirring at 150 ℃ for 1 hour.
4. The method for synthesizing a fluorescent probe Mn-TCPP (BPDC) for detecting trace amount of water in dimethyl sulfoxide according to claim 1, further comprising: cooling, solid-liquid separation, washing and drying.
5. The method for synthesizing the fluorescent probe Mn-TCPP (BPDC) for detecting trace water in dimethyl sulfoxide according to claim 1, wherein the mass ratio of TCPP to manganese salt to BPDC is 2-5: 4-8: 5-10, preferably, the mass ratio is 2: 4.2: 5.
6. the method for synthesizing the fluorescent probe Mn-TCPP (BPDC) for detecting trace water in dimethyl sulfoxide according to claim 1, wherein the solvothermal reaction is performed in an inert gas atmosphere, and preferably, the inert gas is nitrogen.
7. The method for synthesizing the fluorescent probe Mn-TCPP (BPDC) for detecting trace water in dimethyl sulfoxide according to claim 1, wherein the fluorescent probe Mn-TCPP (BPDC) is washed by ethanol for 3-4 times and dried in vacuum for 10-12 hours.
8. A fluorescent probe Mn-TCPP (BPDC) synthesized according to the method of any one of claims 1 to 7.
9. A method for detecting the content of trace water in an organic solvent rapidly is characterized by comprising the following steps:
preparing organic solvents with different water contents as standard solutions;
adding the fluorescent probe Mn-TCPP (BPDC) of claim 8 into the standard solution, uniformly mixing, and detecting a fluorescent response;
establishing a corresponding relation between the water content and the fluorescence intensity according to the measured fluorescence intensity;
adding the fluorescent probe Mn-TCPP (BPDC) of claim 8 into an organic solvent to be detected, uniformly mixing, detecting fluorescence response, and calculating the water content to obtain the fluorescent probe.
10. The method for detecting the content of trace water in the organic solvent according to claim 9, wherein the organic solvent is acetone, N-dimethylformamide, dimethyl sulfoxide, ethanol, isopropanol or methanol;
preferably, the concentration of Mn-TCPP (BPDC) is 2-3 mug/mL; most preferably, the concentration of Mn-TCPP (BPDC) is 2.5. mu.g/mL;
or, the excitation wavelength is 415nm, and the emission wavelength is 650 nm;
or the water volume content is 0.05-30% v/v.
CN202111116165.1A 2021-09-23 2021-09-23 Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide Active CN113666966B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111116165.1A CN113666966B (en) 2021-09-23 2021-09-23 Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111116165.1A CN113666966B (en) 2021-09-23 2021-09-23 Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide

Publications (2)

Publication Number Publication Date
CN113666966A true CN113666966A (en) 2021-11-19
CN113666966B CN113666966B (en) 2023-07-25

Family

ID=78550181

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111116165.1A Active CN113666966B (en) 2021-09-23 2021-09-23 Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide

Country Status (1)

Country Link
CN (1) CN113666966B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115594856A (en) * 2021-11-30 2023-01-13 青岛大学(Cn) Preparation method and application of ratiometric fluorescent probe

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130184456A1 (en) * 2011-06-20 2013-07-18 University Of South Florida Heterocyclic macrocycle templated metal-organic materials
CN111282405A (en) * 2018-12-09 2020-06-16 中国科学院大连化学物理研究所 Modified metal organic framework nanosheet and preparation method thereof
CN111905824A (en) * 2020-08-18 2020-11-10 苏州荣格君新材料有限公司 Double-ligand metal organic framework photocatalyst and application thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130184456A1 (en) * 2011-06-20 2013-07-18 University Of South Florida Heterocyclic macrocycle templated metal-organic materials
CN111282405A (en) * 2018-12-09 2020-06-16 中国科学院大连化学物理研究所 Modified metal organic framework nanosheet and preparation method thereof
CN111905824A (en) * 2020-08-18 2020-11-10 苏州荣格君新材料有限公司 Double-ligand metal organic framework photocatalyst and application thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
YUEWU ZHAO ET AL.: "Synthesis of porphyrin-based two-dimensional metal–organic framework nanodisk with small size and few layers", 《J. MATER. CHEM. A》, vol. 6, pages 2828 *
ZHI-WEI HUANG ET AL.: "Mixed-Ligands Strategy Regulates Thorium-based MOFs", 《DALTON TRANSACTIONS》, pages 983 - 987 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115594856A (en) * 2021-11-30 2023-01-13 青岛大学(Cn) Preparation method and application of ratiometric fluorescent probe

Also Published As

Publication number Publication date
CN113666966B (en) 2023-07-25

Similar Documents

Publication Publication Date Title
CN110240683A (en) A kind of covalent organic frame material and preparation method thereof and the application in fluorescent optical sensor
CN112209871B (en) Zinc ion fluorescent probe based on tetraphenylethylene and preparation method and application thereof
CN111393461B (en) Palladium ion fluorescent probe compound based on BODIPY and synthetic method thereof
CN110283586B (en) Near-infrared fluorescent dye and preparation method thereof
CN113666966B (en) Synthesis and application of fluorescent probe for detecting trace water in dimethyl sulfoxide
CN109060733A (en) iron ion molecular fluorescence sensor and preparation method thereof
CN113214144B (en) Metal organic framework material based on dipole organic ligand, synthetic method and application thereof
CN107759504B (en) Dual-phase organic fluorescent material with strong fluorescence in solid and liquid states and preparation method thereof
CN111533692B (en) Fluorescent molecular probe for detecting mercury ions and preparation method and application thereof
CN103012375B (en) Pyridyl triazole methyl substituted acridine derivative, preparation method and application thereof
CN114605398A (en) Pyrrole compound with organic amine compound fluorescence recognition performance and preparation method thereof
Kou et al. Coumarin functionalized cellulose-based fluorescent probe for detection of hydrazine and its applications in environmental analysis
CN113880851A (en) Trifluorene bridged hexaimidazole macrocyclic compound and preparation method and application thereof
CN113121566B (en) Pyrene derivative fluorescent molecule and preparation method and application thereof
CN112341453A (en) Fluorescent probe based on coumarin and preparation method and application thereof
CN114230495B (en) Hydrogenated nitrosyl donor and preparation method thereof
Huang et al. A 3D europium-organic-framework from phenyl imidazole dicarboxylate showing high sensitivity in detection of nitrobenzene
CN115594856B (en) Preparation method and application of ratio fluorescent probe
CN105384744B (en) Four (trifluoro ethoxy) phthalocyanine europium complexes and its preparation method and application
CN113999203B (en) Near infrared fluorescent dye and method for detecting SO (SO) 32- /HSO 3- The above application
CN116003390B (en) Indole-benzimidazole derivative fluorescent probe and preparation method and application thereof
CN115521293B (en) Hydrazide luminescent dye, and preparation method and application thereof
CN114702953B (en) Fluorescent probe based on lanthanide ion hybridization covalent organic framework material and preparation method and application thereof
CN115745965B (en) Fluorescent molecule and preparation method and application thereof
CN116082186B (en) Preparation method and application of novel fluorescent probe molecule based on perylene

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant