CN109320454A - 一种双组分超分子有机凝胶及其金属凝胶的制备和应用 - Google Patents
一种双组分超分子有机凝胶及其金属凝胶的制备和应用 Download PDFInfo
- Publication number
- CN109320454A CN109320454A CN201811443350.XA CN201811443350A CN109320454A CN 109320454 A CN109320454 A CN 109320454A CN 201811443350 A CN201811443350 A CN 201811443350A CN 109320454 A CN109320454 A CN 109320454A
- Authority
- CN
- China
- Prior art keywords
- organogel
- component
- fluorescence
- component supramolecular
- supramolecular organogel
- 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
Links
- 239000002184 metal Substances 0.000 title claims abstract description 28
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title description 5
- 238000007306 functionalization reaction Methods 0.000 claims abstract description 18
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000001514 detection method Methods 0.000 claims abstract description 12
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 claims abstract description 10
- 150000004753 Schiff bases Chemical class 0.000 claims abstract description 10
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 claims abstract description 10
- 235000004237 Crocus Nutrition 0.000 claims abstract description 9
- 241000596148 Crocus Species 0.000 claims abstract description 9
- 239000002262 Schiff base Substances 0.000 claims abstract description 9
- 229960004979 fampridine Drugs 0.000 claims abstract description 9
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- DNJIKASUTWZIMI-UHFFFAOYSA-N iron;perchloric acid;hydrate Chemical compound O.[Fe].OCl(=O)(=O)=O DNJIKASUTWZIMI-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000010791 quenching Methods 0.000 claims abstract description 5
- 230000002776 aggregation Effects 0.000 claims abstract description 4
- 238000004220 aggregation Methods 0.000 claims abstract description 4
- 230000000171 quenching effect Effects 0.000 claims abstract description 4
- 238000001816 cooling Methods 0.000 claims abstract 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 18
- 239000007864 aqueous solution Substances 0.000 claims description 12
- 230000015572 biosynthetic process Effects 0.000 claims description 9
- 238000003786 synthesis reaction Methods 0.000 claims description 9
- 230000008859 change Effects 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- 150000002500 ions Chemical class 0.000 claims description 5
- 229910001914 chlorine tetroxide Inorganic materials 0.000 claims description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Chemical compound [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 claims 1
- ZMYGBKXROOQLMY-UHFFFAOYSA-N N=NC=NN.N=NC=NN.C1=CC=CC2=CC=CC=C12 Chemical compound N=NC=NN.N=NC=NN.C1=CC=CC2=CC=CC=C12 ZMYGBKXROOQLMY-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000003949 imides Chemical class 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 abstract description 5
- 150000001450 anions Chemical class 0.000 abstract description 3
- 125000002091 cationic group Chemical class 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 description 31
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 150000001768 cations Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 238000004448 titration Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N CHCl3 Substances ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- -1 iron ion Chemical class 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 208000018737 Parkinson disease Diseases 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000003927 aminopyridines Chemical class 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- 230000003851 biochemical process Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000012921 fluorescence analysis Methods 0.000 description 1
- 238000002189 fluorescence spectrum Methods 0.000 description 1
- GFAUNYMRSKVDJL-UHFFFAOYSA-N formyl chloride Chemical compound ClC=O GFAUNYMRSKVDJL-UHFFFAOYSA-N 0.000 description 1
- 231100000753 hepatic injury Toxicity 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000005298 paramagnetic effect Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000001338 self-assembly Methods 0.000 description 1
- 238000011896 sensitive detection Methods 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/14—Aza-phenalenes, e.g. 1,8-naphthalimide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0052—Preparation of gels
- B01J13/0065—Preparation of gels containing an organic phase
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/02—Iron compounds
- C07F15/025—Iron compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/008—Supramolecular polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N21/643—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" non-biological material
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/187—Metal complexes of the iron group metals, i.e. Fe, Co or Ni
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
- G01N2021/6432—Quenching
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Immunology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Dispersion Chemistry (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Pathology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Abstract
本发明公开了一种双组分超分子有机凝胶因子,是将含西弗碱功能化的萘二甲酰亚胺与4‑氨基吡啶功能化的均苯三甲酰氯,在加热下充分溶解到DMSO‑H2O中,得透明溶液;冷却至室温,形成稳定的具有橘黄色聚集态荧光的双组分超分子有机凝胶MQ。向MQ中分别加入一系列阳离子溶液,只有Fe3+的加入使其荧光猝灭,因此MQ能专一选择性荧光识别Fe3+。将双组分超分子有机凝胶与六水合高氯酸铁加热溶解于DMSO‑H2O中,冷却后形成金属凝胶,当向金属凝胶中分别加入一系列阴离子,只有H2PO4 ‑的加入能使金属凝胶的荧光打开,且荧光由黑色变为橘黄色,从而实现了对H2PO4 ‑的超灵敏检测。
Description
技术领域
本发明涉及一种由西弗碱功能化的萘二甲酰亚胺与4-氨基吡啶功能化的均苯三甲酰氯凝胶因子通过氢键、π-π作用形成具有强荧光的双组份超分子有机凝胶;本发明同时还涉及基于该超分子有机凝胶的金属凝胶在选择性荧光识Fe3+、H2PO4 -的应用,属于超分子有机凝胶领域。
背景技术
超分子有机凝胶是一种低分子量的有机化合物(凝胶因子)在有机溶剂中通过氢键、范德华力、π-π堆积作用及亲水-疏水作用等分子间弱相互作用自组装形成的超分子(软)材料。这种材料同时具有固体材料和液体材料特有的优点:超分子有机凝胶分子保持自己的化学性质,可以进行其在溶液中的一些反应,同时该凝胶材料又具有类似于固体的稳定,如易于保存等优点,因此,在超分子软材料领域具有广泛的应用。
最近几年,为金属离子在环境中寻找超灵敏检测分离的离子响应材料已经变得十分重要。到目前为止,有多种方法用来检测不同离子在环境中的存在,如原子吸收光谱法、荧光分析法等。但是这些方法操作起来比较复杂,而且设备价格昂贵,不宜大量投入实际应用中。因此,研究新的方法以实现在环境中有效地检测且分离不同离子仍然是一个具有挑战性的问题。具有刺激响应的超分子有机凝胶作为一种新兴的功能和智能材料,由于它本身具有的特殊性质和很好的应用前景,已经越来越被人们的关注。
Fe3+在细胞水平的许多生化过程中起着关键的作用,人体中缺少Fe3+会导致贫血、肝损伤、帕金森病和癌症等疾病,同时,Fe3+由于具有顺磁性的本质,导致它成为一种荧光猝灭剂,这就使人们很难研究出一种连续可逆的荧光传感器来检测分离Fe3+。H2PO4 -不仅在各种环境和生物学的应用中起着至关重要的作用,而且在信息传输和能量储存方面也扮演着重要的角色。
发明内容
本发明的目的是提供一种由含西弗碱功能化的萘二甲酰亚胺与4-氨基吡啶功能化的均苯三甲酰氯凝胶因子通过氢键、π-π作用形成具有强荧光的双组份超分子有机凝胶及其制备方法;
本发明的另一目的是提供一种该双组分超分子有机凝胶在单一选择性荧光识别铁离子(Fe3+)和连续识别磷酸二氢根(H2PO4 -)的应用。
一、双组分超分子有机凝胶
本发明的双组分超分子有机凝胶,是将含西弗碱功能化的萘二甲酰亚胺凝胶因子(标记为M)与4-氨基吡啶功能化的均苯三甲酰氯凝胶因子(标记为Q),在加热下按30~35mg/mL的质量体积比充分溶解到DMSO-H2O中得到透明溶液;冷却至室温形成稳定的双组分超分子有机凝胶(标记为MQ)。DMSO-H2O中,DMSO与H2O的体积比为3:1~1:1。
其中,西弗碱功能化的萘二甲酰亚胺的结构式为:
4-氨基吡啶功能化的均苯三甲酰氯的结构式为:
MQ的结构式为:
实验表明,该双组分超分子有机凝胶MQ具有良好的稳定性,放置一周后双组分超分子有机凝胶MQ的形态保持不变。双组分超分子有机凝胶MQ的转溶温度为75~80℃。
图1为MQ在成凝胶过程中荧光强度随温度的变化(λex=415 nm);图1的结果显示,双组分超分子有机凝胶MQ在溶胶状态下荧光较弱(MQ-Sol);随着温度的降低,溶胶转化成凝胶,并产生强烈的橘黄色的聚集态荧光(MQ-Gel)。
二、双组分超分子有机凝胶MQ对阳离子的识别实验
1、MQ对Fe3+的荧光响应
在白色点滴板上分别取13份少量(约0.02g)的双组分超分子有机凝胶MQ,分别在这些双组分超分子有机凝胶上加入20μL的不同阳离子(C =0.1moL/L,Mg2+,Ca2+,Cr3+,Fe3+,Co2+,Ni2+,Cu2+,Zn2+,Ag+,Cd2+,Hg2+,Pb2+)的水溶液。然后在紫外灯下观察该双组分超分子有机凝胶的荧光变化。结果显示,超分子有机凝胶MQ在遇到Fe3+水溶液时荧光猝灭,而在遇到含其他阳离子的水溶液时,超分子有机凝胶MQ的荧光未猝灭且颜色不变(如图2所示)。因此,该双组分超分子有机凝胶MQ能专一选择性荧光识别Fe3+。同时,当在双组分超分子有机凝胶MQ中加入含Fe3+的固体待测样品时,它可以直接溶解待测样品而实现对铁离子的检测,这将简化样品的检测过程。因此,该材料的使用将大大简化铁离子的检测方法并降低检测成本。
2、双组分超分子有机凝胶MQ对Fe3+的荧光滴定实验
在微量荧光比色池中配制一份体积为250μL(凝胶浓度为30mg/mL)的双组分超分子有机凝胶MQ,向MQ中加入不同当量Fe3+的水溶液(C =0.1moL/L),测双组分超分子有机凝胶荧光强度的变化。随着Fe3+的逐渐加入,530nm处的荧光逐渐减弱并最终趋于稳定(如图3所示);并且MQ对Fe3+的荧光光谱检测限为6.10×10-8M(如图4所示)。该检测限很低,达到了超灵敏检测的水平。说明MQ在环境中可以超灵敏检测Fe3+。
三、双组分超分子金属有机凝胶对磷酸二氢根的识别实验
1、双组分超分子金属有机凝胶的制备
将双组分超分子有机凝胶MQ与六水合高氯酸铁(超分子有机凝胶MQ与六水合高氯酸铁的摩尔比为1:1.5)一同加热溶解于DMSO-H2O中,冷却至室温后,形成了稳定的超分子金属有机凝胶,标记为MQ+Fe3+。DMSO-H2O中,DMSO与H2O的体积比为3:1~2:1。。双组分超分子有机凝胶MQ与六水合高氯酸铁按30~35mg/mL的质量体积比溶解于DMSO-H2O中。实验表明,该超分子金属有机凝胶MQ+Fe3+具有良好的稳定性,放置一周后其形态保持不变。
2、双组分超分子金属有机凝胶(MQ+Fe3+)对磷酸二氢根的识别实验
MQ+Fe3+对H2PO4 -的荧光响应实验:在白色点滴板上分别取14份少量(约0.02g)的双组分超分子金属有机凝胶MQ+Fe3+,然后在其基础之上分别加入20μL的各种阴离子(F-,Cl-,Br-,I-,N3 -,S2-,OH-,CN-, SCN-,H2PO4 -,AcO-,HSO4 -,ClO4 -,C=0.1mol/L),然后在紫外灯下观察该双组分超分子金属有机凝胶的荧光变化。结果发现,该超分子金属有机凝胶MQ+Fe3+只有在遇到H2PO4 -水溶液时荧光打开,在415nm的激发波下,荧光颜色由黑色为橘黄色,表明Fe3+被H2PO4 -竞争络合掉,从而使得超分子有机凝胶MQ+Fe3+的荧光颜色由黑色为橘黄色(如图5所示)。因此,该超分子金属有机凝胶MQ+Fe3+在水溶液中能荧光识别H2PO4 -。
MQ+Fe3+对H2PO4 -的滴定实验
在微量荧光比色池中配制一份体积为250μL(凝胶浓度为30mg/mL)的MQ+Fe3+,向其中加入不同当量H2PO4 -的水溶液(C=0.1moL/L),测双组分超分子有机凝胶荧光强度的变化。随着H2PO4 -的逐渐加入,530nm处的荧光逐渐增强并最后趋于稳定,并且MQ+Fe3+对H2PO4 -的荧光光谱检测限为1.56×10-7M(见图6、图7),说明MQ+Fe3+在环境中可以超灵敏检测H2PO4 -。
四、MQ对Fe3+和H2PO4 -的连续性识别机理
对于MQ对Fe3+和H2PO4 -的连续性识别机理,我们通过IR、XRD、SEM等进行了研究。IR表明(图8),M形成MQ后,-NH2、-NH、-C=O伸缩振动峰向低波数方向移动,说明有氢键作用。XRD表明(图9),2𝜽=23.434℃,d=3.794Å,说明存在π-π作用。SEM表明(图10),RQ形貌呈现螺旋状。IR表明,当向MQ中加入Fe3+会导致-NH2、-NH、-C=O伸缩振动峰向低波数移动(图11);XRD表明(图12),π-π作用减弱。SEM表明(图13),MQ+ Fe3+形貌呈现块状,进一步说明,Fe3+在其中发生配位、形成阳离子π作用。IR表明,再向MQ+Fe3+中加入H2PO4 -会导致-NH2、-NH、-C=O伸缩振动峰移向低波数的位置;在XRD中,2𝜽=23.142℃,d=3.840Å,说明存在π-π作用再次出现;在MQ+Fe3+中加入H2PO4 -形貌又呈现螺旋状(如图14所示)。
综上所述,双组分超分子有机凝胶MQ超灵敏识别过程是通过新型的配位作用与阳离子π竞争实现的。当向MQ中加入Fe3+,由于Fe3+能与MQ产生阳离子π作用、配位作用;导致MQ的荧光猝灭;当向荧光猝灭的双组分超分子金属有机凝胶MQ+Fe3+中加入H2PO4 -时,由于H2PO4 -与Fe3+络合使MQ之间的螺旋结构再次恢复,导致荧光回到原来的现象,从而实现了对Fe3+和H2PO4 -连续可逆超灵敏检测。
附图说明
图1为MQ在成凝胶过程中荧光强度随温度的变化(λex=415 nm);
图2为MQ对阳离子的全扫描图;
图3为MQ对Fe3+的荧光滴定(λex=415nm);
图4MQ对Fe3+的拟合曲线;
图5为MQ+Fe3+对H2PO4 -的阴离子的全扫描图;
图6为MQ+Fe3+对H2PO4 -的荧光滴定(λex=415 nm);
图7为MQ+Fe3+对H2PO4 -的拟合曲线;
图8为M、Q、MQ的红外光谱图;
图9为M、Q、MQ的XRD图;
图10为MQ的SEM图;
图11为MQ、MQ+Fe3+、MQ+Fe3++H2PO4 -的红外光谱图;
图12为MQ、MQ+Fe3+、MQ+Fe3++H2PO4 -的XRD图;
图13为MQ+Fe3+的SEM图;
图14为MQ+Fe3++H2PO4 -的SEM图。
具体实施方式
下面通过具体实施例对本发明双组分超分子有机凝胶因子MQ的合成,以及单一性选择识别Fe3+与H2PO4 -的方法作进一步说明。
实施例1、双组分超分子有机凝胶MQ的合成
(1)基于西弗碱功能化的萘二甲酰亚胺凝胶因子M的合成:向100mL圆底烧瓶中分别加入对苯二胺(1.08 g,10~10.5mmol),1,8-萘二甲酸酐(1.98g,10~10.5mmol)和100 mL乙醇,在80 ℃加热回流搅拌24h。反应结束后抽滤,用热的乙醇淋洗,抽滤烘干,得到黄色粉末中间体;然后,100mL圆底烧瓶中分别取黄色粉末中间体(1.45g,5~5.5mmol)、2-羟基萘甲醛(0.88g,5~5.5mmol)、1.5mL的冰CH3COOH和60mL乙醇,在80℃加热回流搅拌24h,反应结束后抽滤,用热的乙醇淋洗,抽滤烘干,得到黄色粉末M,产率为:90%;
(2)4-氨基吡啶功能化的均苯三甲酰氯凝胶因子Q的合成:向100 mL圆底烧瓶中加入4-氨基吡啶(0.75 g,8.0~8.05mmol)与CHCl3(40 mL),在恒压漏斗中加入均苯三甲酰氯(0.52g,5.0 ~5.05mmol)与CHCl3(40 mL),使其慢慢滴入圆底烧瓶内,过夜;抽滤得到白色固体Q,产率为:80%;
(3)双组分超分子有机凝胶(MQ)的合成:称取MQ(0.005g),加入到100μL的DMSO与60μL的H2O中,在加热下使其充分溶解,得透明溶液;冷却至室温时,溶液形成稳定的双组分超分子有机凝胶MQ。MQ在溶胶状态下荧光较弱(MQ-Sol);随着温度的降低,溶胶转化成凝胶,并产生强烈的橘黄色的聚集态荧光(MQ-Gel)。
实施例2、MQ识别实验Fe3+
在白色点滴板上分别取13份少量(约0.02g)的有机凝胶MQ,分别在其上加入20μL的不同阳离子(C=0.1moL/L,Mg2+,Ca2+,Cr3+,Fe3+,Co2+,Ni2+,Cu2+,Zn2+,Ag+,Cd2+,Hg2+,Pb2+)的水溶液。在紫外灯下观察其荧光颜色变化,如果有机凝胶MQ的荧光颜色由橘黄色变为黑色,则说明加入的是Fe3+溶液,若MQ的荧光颜色不变,则说明加入的是其他阳离子的水溶液。
实施例3、双组分超分子金属有机凝胶(MQ+Fe3+)的制备及识别H2PO4 -
先称取双组分超分子金属有机凝胶MQ(0.005g),再称取六水合高氯酸铁(0.0158g)一同加入到100μL的DMSO与60μL的H2O中,加热使其溶解,冷却至室温后,形成了稳定的双组分超分子金属有机凝胶(MQ+Fe3+)。
在上述黑色的超分子金属有机凝胶MQ-Fe3+中,分别加入20μL的各种阴离子(F-,Cl-,Br-,I-,N3 -,S2-,OH-,CN-, SCN-,H2PO4 -,AcO-,HSO4 -,ClO4 -,C=0.1mol/L),若超分子金属有机凝胶MQ-Fe3+的荧光打开,且荧光由黑色变为橘黄色,说明加入的是H2PO4 -的水溶液;若发现双组分超分子金属有机凝胶的荧光未打开,说明加入的不是H2PO4 -的水溶液。
Claims (10)
1.一种双组分超分子有机凝胶,其结构式如下:
。
2.如权利要求1所述一种双组分超分子有机凝胶的合成,是将含西弗碱功能化的萘二甲酰亚胺与4-氨基吡啶功能化的均苯三甲酰氯,在加热下充分溶解到DMSO-H2O中,得透明溶液;冷却至室温,形成稳定的具有橘黄色聚集态荧光的双组分超分子有机凝胶。
3.如权利要求2所述一种双组分超分子有机凝胶的合成,其特征在于:所述西弗碱功能化的萘二甲酰亚胺的结构式为:
4-氨基吡啶功能化的均苯三甲酰氯的结构式为:
。
4.如权利要求2所述一种双组分超分子有机凝胶的合成,其特征在于:西弗碱功能化的萘二甲酰亚胺与4-氨基吡啶功能化的均苯三甲酰氯的摩尔比为3:1。
5.如权利要求2所述一种双组分超分子有机凝胶的合成,其特征在于:DMSO-H2O中,DMSO与H2O的体积比为3:1~2:1。
6.如权利要求1所述一种双组分超分子有机凝胶,其特征在于:西弗碱功能化的萘二甲酰亚胺与4-氨基吡啶功能化的均苯三甲酰氯按30~35mg/mL的质量体积比溶解于DMSO-H2O中。
7.如权利要求1所述一种双组分超分子有机凝胶用于单一选择性荧光识别Fe3+,其特征在于:在双组分超分子有机凝胶上分别加入Fe3+,Hg2+,Ag+,Ca2+,Cu2+,Co2+,Ni2+,Cd2+,Pb2+,Zn2+,Cr3+,Mg2+的水溶液,只有Fe3+的加入能使双组分超分子有机凝胶的荧光猝灭,而其他阳离子的加入均不能使双组分超分子有机凝胶的荧光发生变化。
8.一种基于如权利要求1所述双组分超分子有机凝胶的超分子金属有机凝胶,是将双组分超分子有机凝胶与六水合高氯酸铁以1:1~1:2的摩尔比,加热溶解于DMSO-H2O中,冷却至室温后,形成了稳定的金属双组分超分子有机凝胶。
9.如权利要求8所述超分子金属有机凝胶,其特征在于:DMSO-H2O中,DMSO与H2O的体积比为3:1~2:1;双组分超分子有机凝胶与六水合高氯酸铁按30~35mg/mL的质量体积比溶解于DMSO-H2O中。
10.如权利要求9所述超分子有机金属凝胶在检测H2PO4 -的应用,其特征在于:分别在超分子金属有机凝胶上加入F-,Cl-,Br-,I-,N3 -,S2-,OH-,CN-, SCN-,H2PO4 -,AcO-,HSO4 -,ClO4 -的水溶液,只有H2PO4 -的加入能使超分子金属有机凝胶的荧光打开,且荧光由黑色变为橘黄色。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811443350.XA CN109320454B (zh) | 2018-11-29 | 2018-11-29 | 一种双组分超分子有机凝胶及其金属凝胶的制备和应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811443350.XA CN109320454B (zh) | 2018-11-29 | 2018-11-29 | 一种双组分超分子有机凝胶及其金属凝胶的制备和应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN109320454A true CN109320454A (zh) | 2019-02-12 |
CN109320454B CN109320454B (zh) | 2021-07-09 |
Family
ID=65258935
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201811443350.XA Expired - Fee Related CN109320454B (zh) | 2018-11-29 | 2018-11-29 | 一种双组分超分子有机凝胶及其金属凝胶的制备和应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109320454B (zh) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110015989A (zh) * | 2019-04-16 | 2019-07-16 | 西北师范大学 | 4-氨基吡啶功能化的均苯三甲酰亚胺在检测硝酸根离子的应用 |
CN110041251A (zh) * | 2019-04-16 | 2019-07-23 | 西北师范大学 | 4-氨基吡啶功能化均苯三甲酰亚胺在检测甲醛和3-氟苯甲醛的应用 |
CN110054586A (zh) * | 2019-04-16 | 2019-07-26 | 西北师范大学 | 一种稀土金属配合物凝胶的制备及其在检测组氨酸的应用 |
CN110354068A (zh) * | 2019-06-26 | 2019-10-22 | 南昌大学 | 一种以熊果酸/齐墩果酸为原料的超分子水凝胶、制备方法及应用 |
CN116284836A (zh) * | 2023-05-22 | 2023-06-23 | 暨南大学 | 一种金属凝胶及其制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108658804A (zh) * | 2018-05-04 | 2018-10-16 | 西北师范大学 | 一种基于三柱[5]芳烃的超分子凝胶因子及其有机凝胶的制备和应用 |
CN108772027A (zh) * | 2018-06-20 | 2018-11-09 | 西北师范大学 | 一种超分子有机凝胶及其金属凝胶的制备和应用 |
-
2018
- 2018-11-29 CN CN201811443350.XA patent/CN109320454B/zh not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108658804A (zh) * | 2018-05-04 | 2018-10-16 | 西北师范大学 | 一种基于三柱[5]芳烃的超分子凝胶因子及其有机凝胶的制备和应用 |
CN108772027A (zh) * | 2018-06-20 | 2018-11-09 | 西北师范大学 | 一种超分子有机凝胶及其金属凝胶的制备和应用 |
Non-Patent Citations (2)
Title |
---|
苏婷,等: "双组分超分子凝胶的研究进展", 《现代化工》 * |
贺有周,等: "超分子凝胶可视化选择性识别有机小分子的研究进展", 《化学研究与应用》 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110015989A (zh) * | 2019-04-16 | 2019-07-16 | 西北师范大学 | 4-氨基吡啶功能化的均苯三甲酰亚胺在检测硝酸根离子的应用 |
CN110041251A (zh) * | 2019-04-16 | 2019-07-23 | 西北师范大学 | 4-氨基吡啶功能化均苯三甲酰亚胺在检测甲醛和3-氟苯甲醛的应用 |
CN110054586A (zh) * | 2019-04-16 | 2019-07-26 | 西北师范大学 | 一种稀土金属配合物凝胶的制备及其在检测组氨酸的应用 |
CN110015989B (zh) * | 2019-04-16 | 2021-07-16 | 西北师范大学 | 4-氨基吡啶功能化的均苯三甲酰亚胺在检测硝酸根离子的应用 |
CN110041251B (zh) * | 2019-04-16 | 2021-07-20 | 西北师范大学 | 4-氨基吡啶功能化均苯三甲酰亚胺在检测甲醛和3-氟苯甲醛的应用 |
CN110054586B (zh) * | 2019-04-16 | 2021-09-28 | 西北师范大学 | 一种稀土金属配合物凝胶的制备及其在检测组氨酸的应用 |
CN110354068A (zh) * | 2019-06-26 | 2019-10-22 | 南昌大学 | 一种以熊果酸/齐墩果酸为原料的超分子水凝胶、制备方法及应用 |
CN116284836A (zh) * | 2023-05-22 | 2023-06-23 | 暨南大学 | 一种金属凝胶及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN109320454B (zh) | 2021-07-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109320454A (zh) | 一种双组分超分子有机凝胶及其金属凝胶的制备和应用 | |
She et al. | Design strategy and recent progress of fluorescent probe for noble metal ions (Ag, Au, Pd, and Pt) | |
Guo et al. | Multifunctional Ln-MOF luminescent probe displaying superior capabilities for highly selective sensing of Fe3+ and Al3+ ions and nitrotoluene | |
Xu et al. | Eu (III) functionalized Zr-based metal-organic framework as excellent fluorescent probe for Cd2+ detection in aqueous environment | |
Yan et al. | Carbon dots as nanosensor for sensitive and selective detection of Hg2+ and l-cysteine by means of fluorescence “Off–On” switching | |
CN109536160A (zh) | 一种基于均苯三甲酰氯的三足准轮烷超分子凝胶及其金属凝胶的制备和应用 | |
Xiong et al. | Two new quinoline-based regenerable fluorescent probes with AIE characteristics for selective recognition of Cu 2+ in aqueous solution and test strips | |
Steed | Coordination and organometallic compounds as anion receptors and sensors | |
Peralta-Domínguez et al. | A Schiff base derivative from cinnamaldehyde for colorimetric detection of Ni2+ in water | |
Li et al. | A highly selective and reversible water-soluble polymer based-colorimetric chemosensor for rapid detection of Cu 2+ in pure aqueous solution | |
Luo et al. | A Eu3+ post-functionalized metal-organic framework as fluorescent probe for highly selective sensing of Cu2+ in aqueous media | |
Sutar et al. | Coordination polymer gels with modular nanomorphologies, tunable emissions, and stimuli-responsive behavior based on an amphiphilic tripodal gelator | |
Ju et al. | A Salen-based covalent organic polymer as highly selective and sensitive fluorescent sensor for detection of Al3+, Fe3+ and Cu2+ ions | |
Niamsa et al. | Hybrid organic–inorganic nanomaterial sensors for selective detection of Au 3+ using rhodamine-based modified polyacrylic acid (PAA)-coated FeNPs | |
Nagarajan et al. | Recent advancements in the role of N-Heterocyclic receptors on heavy metal ion sensing | |
Li et al. | A novel reversible colorimetric chemosensor for the detection of Cu 2+ based on a water-soluble polymer containing rhodamine receptor pendants | |
Yu et al. | A novel colorimetric and fluorescent probe for detecting fluoride anions: from water and toothpaste samples | |
CN110240683A (zh) | 一种共价有机框架材料及其制备方法和在荧光传感器中的应用 | |
Saini et al. | Naphthalimide-based organic nanoparticles for aluminium recognition in acidic soil and aqueous media | |
Chopra et al. | Selective chemosensing of spermidine based on fluorescent organic nanoparticles in aqueous media via a Fe 3+ displacement assay | |
CN103241776B (zh) | 四氧化三铁纳米复合颗粒及其制备方法和用途 | |
CN109265398B (zh) | 一种超分子有机凝胶及其荧光识别汞离子的应用 | |
Xiu et al. | Naphthalene-grafted MOF as a unique fluorescent sensor for “turn-off” detection for Fe3+ and “turn-on” detection for ClO4-in different solvents with high selectivity and sensitivity | |
Mahajan et al. | A nano sensor for sensitive and selective detection of Cu2+ based on fluorescein: Cell imaging and drinking water analysis | |
Tian et al. | A quinoline group modified Fe3O4@ SiO2 nanoparticles for sequential detection of Zn2+ and hydrogen sulfide in aqueous solution and its logic behavior |
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 | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20210709 Termination date: 20211129 |