CN107247042A - With the method for the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5 and iodide ion - Google Patents

With the method for the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5 and iodide ion Download PDF

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CN107247042A
CN107247042A CN201710454120.2A CN201710454120A CN107247042A CN 107247042 A CN107247042 A CN 107247042A CN 201710454120 A CN201710454120 A CN 201710454120A CN 107247042 A CN107247042 A CN 107247042A
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CN107247042B (en
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魏太保
陈进发
韩冰冰
张有明
林奇
姚虹
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Heze Smart New Material Technology Co ltd
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    • 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
    • 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

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Abstract

The method that the present invention relates to the use of the aromatic hydrocarbons indirect of symmetry copolymerization post 5 identification mercury ion and iodide ion, belongs to cation detection technical field.5 benzene ring units of the aromatic hydrocarbons of symmetry copolymerization post 5 provide a good fluorescence signal group, and bromine atoms easily occur nucleophilic substitution with iodide ion and generate new compound(DBP5I), and compound containing iodine easily with mercury ion ligand complex so that DBP5I fluorescent quenching.Therefore, using this property, mercury ion and iodide ion can be recognized indirectly.

Description

With the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5 and iodide ion Method
Technical field
The present invention relates to the method for a kind of aromatic hydrocarbons indirect of use symmetry copolymerization post 5 identification mercury ion and iodide ion, belong to Cation detection technical field.
Background technology
Mercury is applied in industrial chemicals, electrical equipment, silver amalgam and battery by substantial amounts of at present, in its natural state Mercury and the oxide of mercury have very big harmfulness to human body and natural environment.In order to detect and monitor various feelings A kind of mercury under condition, it is necessary to effective method.In the method for various detection mercury ions, fluorescence probe method has highly sensitive Degree, maneuverable feature, are increasingly paid close attention to by people.Up to the present, the fluorescence probe of many mercury ions has been Through being synthesized, but most sensor all contains sulphur atom, and sulphur atom easily forms Hg-S keys with mercury, and causes identification Process is irreversible, it is difficult to circulate.And the sensor of most of sulfur-bearing is all highly susceptible to disturb and influenceed in sulfur-rich environment, It is difficult to the effect for playing detection mercury ion.Therefore being accomplished by a kind of fluorescent optical sensor without element sulphur is used to detect mercury ion.
Iodine is one of important element of synthesized human thyroid hormone, lacks the absorption surplus of iodine and iodine and can all influence body Normal function, or even bring major disease, the abnormal development of such as brain, physique is short and small, physical efficiency is not enough and metabolic disorder. Therefore, the detection of the content of iodine in environment and food is also very necessary.Because iodide ion its own charge density is loose and Itself ionic radius is bigger than normal, therefore iodide ion sensor annoyings many researchers all the time.However, iodide ion easily occurs Nucleophilic substitution, therefore, it can this characteristic using it to detect iodide ion.
Post aromatic hydrocarbons is used as macrocyclic host compound of new generation.Shown in terms of host-guest chemistry very outstanding Effect.Due to containing multiple phenyl ring, therefore show outstanding fluorescence radiation performance.By the modification to post aromatic hydrocarbons structure, permitted The fluorescence chemical sensor of multifunction is developed well.
The content of the invention
The purpose of the present invention is glimmering using symmetry copolymerization 5 aromatic hydrocarbons indirects of post there is provided one kind according to the property of post aromatic hydrocarbons The method that light detects mercury ion and iodide ion.
First, the structure of the aromatic hydrocarbons of symmetry copolymerization post 5
The aromatic hydrocarbons of symmetry copolymerization post 5, labeled as DBP5.5 benzene ring units of the aromatic hydrocarbons of symmetry copolymerization post 5 provide one well Fluorescence signal group, bromine atoms easily occur nucleophilic substitution with iodide ion and generate new compound(DBP5I), and the change containing iodine Compound easily with mercury ion ligand complex so that DBP5I fluorescent quenching.Therefore, using this property, it can recognize indirectly Mercury ion and iodide ion.The structural formula of symmetry post aromatic hydrocarbons is as follows:
2nd, the fluorescence identifying performance of the aromatic hydrocarbons of symmetry copolymerization post 5
1st, to cationic fluorescent recognition performance
0.5mL DBP5 dimethyl sulphoxide solution is pipetted respectively(2×10-3 mol·L-1)With 0.5mL IDimethyl sulfoxide (DMSO) Solution(5×10-3 mol·L-1)DBP5I solution is labeled as in a series of 10 mL colorimetric cylinders, and by the mixed solution.Then Respectively Fe is added in the solution3+, Hg2+, Ca2+, Co2+, Ni2+, Cd2+, Pb2+, Zn2+, Cr3+, Mg2+, Ag+Dimethyl sulfoxide (DMSO) Solution(5×10-4 mol·L-1)0.5 mL, plus distilled water 0.5mL, then be diluted to dimethyl sulfoxide (DMSO) 5mL, now DBP5I Concentration be 2 × 10-4mol·L-1, cation concn is 0.25 times of DBP5I concentration.Placed 1 minute or so after well mixed, Observe response of the acceptor to each cation.
It was found that, in DBP5I solution, it is separately added into after above-mentioned cationic solution, in corresponding ultraviolet spectra, There is absworption peak at 295nm.In its corresponding fluorescence emission spectrum, Hg2+Addition emission peaks of the DBP5I at 328nm is disappeared Lose(Fig. 1), and the addition of remaining cation has no significant effect to the fluorescence spectrum of DBP5I solution.Accordingly, Hg2+Addition make The fluorescent quenching of DBP5I solution, and the addition of remaining cation does not influence on the fluorescence of DBP5I solution.
2nd, the titration experiments of the aromatic hydrocarbons of symmetry copolymerization post 5 and mercury ion
Pipette 2.0mL DBP5I DMSO (aqueous 10%) solution(2.0×10-4mol/L)In quartz cell, with accumulation sample-adding method It is gradually added into Hg2+ Dimethyl sulphoxide solution, survey its fluorescence emission spectrum in 25 DEG C(Fig. 2).Titration experiments explanation, DBP5I's Fluorescence intensity is by Hg2+The influence of concentration, weakens along with the increase of iron concentration.And obtained according to titration experiments DBP5I is to Hg2+The detection of fluorescence spectrum be limited to 3.73 × 10−8mol/L.Thus illustrate, DBP5I can single selective fluorescence Mercury ion is recognized, and it is very high to the detection sensitivity of mercury ion, and therefore, DBP5 has potential in terms of indirect detection mercury ion Application value.
Fig. 3 is the Hg of various concentrations2+(0 ~ 0.08 times)In the presence of DBP5I fitting a straight line figure.Fitting a straight line figure can be clear Clear clear reflection DBP5I fluorescence intensity is in 0 ~ 0.08 times of Hg2+Variation tendency in concentration range.Pass through fitting a straight line figure It can be found that Hg2+In 0 ~ 0.08 times of equivalent, Hg2+Fluorescence intensity with DBP5I is in following linear relationship:
Y=- 2205.4269X+311, R2=0.9936
Y --- the aromatic hydrocarbons+I of symmetry copolymerization post 5-Fluorescence intensity:Unit:a.u.
X——Hg2+Relative concentration, unit:mol/L.
3rd, the cation interference free performance detection of the aromatic hydrocarbons of symmetry copolymerization post 5
In order to determine DBP5I to Hg2+Detection results, we have carried out following test again:Two groups of 10ml colorimetric cylinders are taken to add respectively Enter 0.5mL DBP5 solution and 0.5mL ISolution, then be separately added into the dimethyl sulphoxide solution of the various cations of 0.5mL(4 ×10-3mol·L−1), plus distilled water 0.5mL, 5mL scales are then diluted to dimethyl sulfoxide (DMSO).Add respectively again in another set 0.5mL Hg2+, 0.5mL Fe are separately added into each colorimetric cylinder3+, Ca2+, Co2+, Ni2+, Cd2+, Pb2+, Zn2+, Cr3+, Mg2+, Ag+Dimethyl sulphoxide solution(5×10-4 mol·L-1), plus distilled water 0.5mL, then it is diluted to dimethyl sulfoxide (DMSO) 5mL scales.Observed after above-mentioned solution is well mixed.
Above-mentioned solution left standstill is after 1 minute, and 25 DEG C are surveyed its fluorescence emission spectrum.As a result find, add above-mentioned ten kinds of cations Afterwards, DBP5I fluorescent quenchings at 328nm, this and Hg2+Influence to DBP5I is consistent.So as to illustrate such DBP5 compound Indirect detection Hg2+Do not disturbed by other cations(See Fig. 4).
Experiment shows, in the aqueous DMSO solution of the aromatic hydrocarbons of symmetry copolymerization post 5, and the percentage by volume of water is 5 ~ 15%, symmetrically Property the aromatic hydrocarbons of copolymerization post 5 concentration be 1 × 10-4~4×10-4mol·L-1, the aromatic hydrocarbons+I of symmetry copolymerization post 5Can high sensitivity list One Selective recognition Hg2+, and Hg2+Concentration and BTAP5 fluorescence intensity be in above-mentioned linear relationship.
4、DBP5+Hg2+Research to Anion Recognition performance
0.5 mL DBP5 DMSO solution (2 × 10 is pipetted respectively-3 mol·L-1) in a series of 10 mL colorimetric cylinders, respectively Add 0.5 mL Hg2+DMSO solution (2 × 10-3 mol·L-1) form mixed system DBP5+Hg2+, F is then separately added into again, Cl, Br, I, AcO, H2PO4 , HSO4 , ClO4 , CN、NO3 DMSO solution (4 × 10-3 mol·L-1) 0.5 mL, Plus distilled water 0.5mL, then it is diluted to 5mL with DMSO.Now acceptor DBP5+Hg2+Concentration is 2 × 10-4mol·L-1, anion is dense Spend for 2 times of acceptor density.Observe acceptor DBP5+Hg2+Response to each anion.
As a result find, in fluorescence spectrum, only IAddition cause DBP5+Hg2+Fluorescent quenching of the solution at 328nm (λ ex=295nm), and the addition of other anion, DBP5+Hg2+The fluorescence spectrum of solution does not have any obvious change(Fig. 5), Illustrate DBP5+Hg2+To IVery strong single-minded selectivity is shown, therefore can high selectivity, highly sensitive fluorescence identifying I
5、DBP5+Hg2+With ITitration experiments
Pipette 2.0mL DBP5+Hg2+Solution(2.0×10-4mol/L)In quartz cell, I is gradually added into accumulation sample-adding method's Dimethyl sulphoxide solution, its fluorescence emission spectrum is surveyed in 25 DEG C(Fig. 6).Titration experiments explanation, DBP5+Hg2+Fluorescence intensity by To IThe influence of concentration, increases along with the increase of iodide ion concentration.And obtain DBP5+Hg according to titration experiments2+To IThe detection of fluorescence spectrum be limited to 3.51 × 10−7mol/L.Thus illustrate, DBP5+Hg2+Can single selective fluorescence identifying iodine from Son, and it is very high to the detection sensitivity of iodide ion, therefore, DBP5+Hg2+Have in iodide ion context of detection and potentially apply valency Value.
Fig. 7 is the I of various concentrations(0 ~ 1.2 times)In the presence of DBP5+Hg2+Fitting a straight line figure.Fitting a straight line figure can be clear Clear clear reflection DBP5+Hg2+Fluorescence intensity in 0 ~ 1.2 times of IVariation tendency in concentration range.Pass through fitting a straight line figure It can be found that IIn 0 ~ 1.2 times of equivalent and DBP5+Hg2+Fluorescence intensity be in preferable linear relationship:
Y=- 168.068X+321.191, R2=0.9950
Y——DBP5+Hg2+Fluorescence intensity:Unit:a.u.
X——IRelative concentration, unit:mol/L.
6、DBP5+Hg2+Anion interference free performance detection
In order to determine DBP5+Hg2+To IDetection results, we have carried out following test again:Take two groups of 10ml colorimetric cylinders difference Add the 0.5mL DBP5+Hg2+Solution, then it is separately added into the dimethyl sulphoxide solution of the various anion of 0.5mL(4.0×10- 3mol·L−1), plus distilled water 0.5mL, 5mL scales are then diluted to dimethyl sulfoxide (DMSO).Add 0.5mL in another set respectively again I, 0.5mL F are separately added into each colorimetric cylinder, Cl, Br, AcO, H2PO4 , HSO4 , ClO4 , CN, NO3 Two Methyl sulfoxide solution(4.0×10-3 mol·L-1), plus distilled water 0.5mL, 5mL scales are then diluted to dimethyl sulfoxide (DMSO). Observed after above-mentioned solution is well mixed.
Above-mentioned solution left standstill surveys its fluorescence emission spectrum after 1 minute in 25 DEG C.As a result find, add above-mentioned nine kinds of the moon from After son, DBP5+Hg2+The fluorescent quenching at 328nm, this and ITo DBP5+Hg2+Influence be consistent.So as to illustrate such DBP5+Hg2+Compound test IDo not disturbed by other anion(See Fig. 8).
Experiment shows, in the aqueous DMSO solution of the aromatic hydrocarbons of symmetry copolymerization post 5, and the percentage by volume of water is 5 ~ 15%, symmetrically Property the aromatic hydrocarbons of copolymerization post 5 concentration be 1 × 10-4~4×10-4mol·L-1, the aromatic hydrocarbons+I of symmetry copolymerization post 5Can high sensitivity list One Selective recognition I, and IConcentration and BTAP5+ Hg2+Fluorescence intensity be in above-mentioned linear relationship.
Brief description of the drawings
Fig. 1 is DBP5I(DBP5+I)And fluorescence spectrum when adding 11 kinds of cation(Excitation wavelength:295nm, hair The long 328nm of ejected wave).
Fig. 2 is the Hg of various concentrations2+(0 ~ 0.4 times)In the presence of DBP5I fluorescence spectrum.
Fig. 3 is the Hg of various concentrations2+(0 ~ 0.08 times)In the presence of DBP5I fitting a straight line figure.
Fig. 4 is the interference free performance that DBP5I is recognized to mercury ion;1 ~ 22 represents DBP5I, Hg respectively2+、Fe3+、Ca2+、Co2 +、Ni2+、Cd2+、Pb2+、Zn2+、Cr3+、Mg2+And Ag+
Fig. 5 is DBP5+Hg2+And its fluorescence spectrum when adding 2 times of anion(Excitation wavelength:295nm, transmitted wave It is long:328nm).
Fig. 6 is the I of various concentrationsAcceptor DBP5+Hg in the presence of (0 ~ 2.4 times)2+Fluorescence spectrum.
Fig. 7 is the I of various concentrations(0 ~ 1.2 times)In the presence of DBP5+Hg2+Fitting a straight line figure.
Fig. 8 is DBP5+Hg2+The interference free performance recognized to iodide ion;1 ~ 20 represents DBP5, DBP5+Hg respectively2++I、F、Cl、Br、AcO、H2PO4 、HSO4 、ClO4 、CN、NO3
Embodiment
Below by specific embodiment to the aromatic hydrocarbons of symmetry copolymerization post 5 of the present invention(DBP5)Indirect detects Hg2+、ISide Method is described further.
Embodiment 1, detection Hg2+
Pipette DBP5 DMSO solution(2×10-3 mol·L-1)In a series of 10 mL colorimetric cylinders, I is first separately added into's DMSO solution(5×10-3 mol·L-1);Fe is separately added into again3+, Hg2+, Ca2+, Co2+, Ni2+, Cd2+, Pb2+, Zn2+, Cr3+, Mg2 +, Ag+Dimethyl sulphoxide solution(5×10-4 mol·L-1)If, the fluorescent quenching of solution, that illustrate addition is Hg2+If, The fluorescence of solution does not change, then what explanation was added is other cations.
Embodiment 2,
Detect IIon
Pipette DBP5 DMSO solution(2×10-3 mol·L-1)In a series of 10 mL colorimetric cylinders, Hg is first separately added into2+'s DMSO solution(2×10-3 mol·L-1);It is separately added into F thereto again, Cl, Br, I, AcO, H2PO4 , HSO4 , ClO4 , CN、NO3 Solution(4×10-3 mol·L-1)If, the fluorescent quenching of solution, that illustrate addition is I;If the fluorescence of solution is not Change, then what explanation was added is other anion.

Claims (10)

1. with the method for the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5, it is characterised in that:In a series of symmetry In the aqueous DMSO solution of the aromatic hydrocarbons of copolymerization post 5, I is first added;Cation Fe is separately added into again3+, Hg2+, Ca2+, Co2+, Ni2+, Cd2 +, Pb2+, Zn2+, Cr3+, Mg2+, Ag+Dimethyl sulphoxide solution, if the fluorescent quenching of solution, illustrate add be mercury ion, If the fluorescence of solution does not change, illustrate addition is other cations.
2. as claimed in claim 1 with the method for the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5, its feature exists In:IAddition be 2 ~ 3 times of the aromatic hydrocarbons mole of symmetry copolymerization post 5.
3. as claimed in claim 1 or 2 with the method for the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5, its feature It is:In the aqueous DMSO solution of the aromatic hydrocarbons of symmetry copolymerization post 5, the concentration of the aromatic hydrocarbons of symmetry copolymerization post 5 is 1 × 10-4~4×10-4mol·L-1
4. as claimed in claim 1 or 2 with the method for the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5, its feature It is:
Hg2+With the aromatic hydrocarbons+I of symmetry copolymerization post 5Fluorescence intensity be in following linear relationship:
Y=- 2205.4269X+311, R2=0.9936
Y --- the aromatic hydrocarbons+I of symmetry copolymerization post 5-Fluorescence intensity:Unit:a.u.
X——Hg2+Relative concentration, unit:mol/L.
5. as claimed in claim 1 with the method for the aromatic hydrocarbons indirect fluoroscopic examination mercury ion of symmetry copolymerization post 5, its feature exists In:In the aqueous DMSO solution of the aromatic hydrocarbons of symmetry copolymerization post 5, the percentage by volume of water is 5 ~ 15%.
6. with the method for the aromatic hydrocarbons indirect fluoroscopic examination iodide ion of symmetry copolymerization post 5, it is characterised in that:In a series of symmetry The aqueous DMSO solution of the aromatic hydrocarbons of copolymerization post 5(The percentage by volume of water is 10%), first it is separately added into Hg2+;It is separately added into thereto again F, Cl, Br, I, AcO, H2PO4 , HSO4 , ClO4 , CN, NO3 Solution, if the fluorescent quenching of solution, illustrates what is added It is I;If the fluorescence of solution does not change, illustrate addition is other anion.
7. as claimed in claim 6 with the method for the aromatic hydrocarbons indirect fluoroscopic examination iodide ion of symmetry copolymerization post 5, its feature exists In:Hg2+Addition be 1 ~ 2 times of the aromatic hydrocarbons mole of symmetry copolymerization post 5.
8. the method for the aromatic hydrocarbons indirect fluoroscopic examination iodide ion of symmetry copolymerization post 5, its feature are used as claimed in claims 6 or 7 It is:In the aqueous DMSO solution of the aromatic hydrocarbons of symmetry copolymerization post 5, the concentration of the aromatic hydrocarbons of symmetry copolymerization post 5 is 1 × 10-4~4×10-4 mol·L-1
9. the method for the aromatic hydrocarbons indirect fluoroscopic examination iodide ion of symmetry copolymerization post 5, its feature are used as claimed in claims 6 or 7 It is:IWith the aromatic hydrocarbons+Hg of symmetry copolymerization post 52+Fluorescence intensity be in following linear relationship:
Y=- 168.068X+321.191, R2=0.9950
Y——DBP5+Hg2+Fluorescence intensity:Unit:a.u.
X——IRelative concentration, unit:mol/L.
10. the method for the aromatic hydrocarbons indirect fluoroscopic examination iodide ion of symmetry copolymerization post 5, its feature are used as claimed in claims 6 or 7 It is:In the aqueous DMSO solution of the aromatic hydrocarbons of symmetry copolymerization post 5, the percentage by volume of water is 5 ~ 15%.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107827818A (en) * 2017-11-20 2018-03-23 西北师范大学 The application of gelator and organogel of the one kind based on post [5] aromatic hydrocarbons
CN108088828A (en) * 2017-12-22 2018-05-29 西北师范大学 A kind of twin columns aromatic hydrocarbons mercury ion fluorescent sensor and its preparation and application
CN108640198A (en) * 2018-05-02 2018-10-12 南京工业大学 A method of hexavalent chromium in water body is removed based on absorption method
CN110441279A (en) * 2019-08-29 2019-11-12 云南民族大学 A kind of application of phosphonic acids column [5] aromatic hydrocarbons in identification ferrous ion, copper ion or aluminium ion

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106496121A (en) * 2016-10-19 2017-03-15 西北师范大学 5 aromatic hydrocarbons of post/M-phthalic acid, 1,8 naphthalimide coordination compound and its preparation and application
CN106496186A (en) * 2016-10-19 2017-03-15 西北师范大学 A kind of mercury ion fluorescent sensor and its synthesis and in pure water detect mercury ion application

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106496121A (en) * 2016-10-19 2017-03-15 西北师范大学 5 aromatic hydrocarbons of post/M-phthalic acid, 1,8 naphthalimide coordination compound and its preparation and application
CN106496186A (en) * 2016-10-19 2017-03-15 西北师范大学 A kind of mercury ion fluorescent sensor and its synthesis and in pure water detect mercury ion application

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
TAI-BAO WEI ET AL.: "Novel functionalized pillar[5]arene: synthesis,assembly and application in sequential fluorescent sensing for Fe3+ and F in aqueous media", 《RSC ADVANCES》 *

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CN107827818A (en) * 2017-11-20 2018-03-23 西北师范大学 The application of gelator and organogel of the one kind based on post [5] aromatic hydrocarbons
CN107827818B (en) * 2017-11-20 2021-04-20 西北师范大学 Gel factor based on column [5] arene and application of organogel
CN108088828A (en) * 2017-12-22 2018-05-29 西北师范大学 A kind of twin columns aromatic hydrocarbons mercury ion fluorescent sensor and its preparation and application
CN108088828B (en) * 2017-12-22 2020-07-28 西北师范大学 Double-column aromatic mercury ion fluorescent sensor and preparation and application thereof
CN108640198A (en) * 2018-05-02 2018-10-12 南京工业大学 A method of hexavalent chromium in water body is removed based on absorption method
CN110441279A (en) * 2019-08-29 2019-11-12 云南民族大学 A kind of application of phosphonic acids column [5] aromatic hydrocarbons in identification ferrous ion, copper ion or aluminium ion
CN110441279B (en) * 2019-08-29 2021-10-22 云南民族大学 Application of phosphonic acid column [5] arene in recognition of ferrous ions, copper ions or aluminum ions

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