In order to investigate detonation propagation characteristics of different charge patterns,the detonation velocities of superposition strip shaped charges made up of a detonating cord and explosives were measured by...In order to investigate detonation propagation characteristics of different charge patterns,the detonation velocities of superposition strip shaped charges made up of a detonating cord and explosives were measured by a detonation velocity measuring instrument under conditions of different ignition.The experimental results and theoretical analysis show that the maximum detonation propagation velocity depends on the explosive materials with the maximum velocity among all the explosive materials.Using detonating cord in a superposition charge can shorten detonation propagation time and improve the efficiency of explosive energy.The measurement method of detonation propagation velocity and experimental results are presented and investigated.展开更多
Reactive fragment enhances lethality by incorporating the defeat mechanisms of kinetic energy and chemical energy into a unitary damage unit. Combined studies on the behavior of reactive fragment initiating covered ex...Reactive fragment enhances lethality by incorporating the defeat mechanisms of kinetic energy and chemical energy into a unitary damage unit. Combined studies on the behavior of reactive fragment initiating covered explosive are performed theoretically and experimentally. The results in- dicate that the response of the covered explosive subjected to reactive fragment is not consistent with the classical shock initiation model. When impacting and penetrating into the covered explosive, the reactive fragment releases great amounts of thermo-chemical energy up to 5. 68 times of its kinetic energy into the explosive due to violent chemical reactions. This impact-induced chemical energy re- lease behavior of the reactive fragment significantly enhances the initiation capability and damage effects on the covered explosive.展开更多
Heterocyclic skeleton(Azoles)and different energetic groups containing high performing explosives are highly emerged in recent years to meet the challenging requirements of energetic materials in both military and civ...Heterocyclic skeleton(Azoles)and different energetic groups containing high performing explosives are highly emerged in recent years to meet the challenging requirements of energetic materials in both military and civilian applications with improved performance.For this purpose tetrazole(Azole)is identified as an attractive heterocyclic backbone with energetic functional groups nitro(-NO_(2)),nitrato(-ONO_(2)),nitrimino(-NNO_(2)),and nitramino(eNHeNO_(2))to replace the traditionally used high performing explosives.The tetrazole based compounds having these energetic functional groups demonstrated advanced energetic performance(detonation velocity and pressure),densities,and heat of formation(HOF)and became a potential replacement of traditional energetic compounds such as RDX.This review presents a summary of the recently reported nitro-tetrazole energetic compounds containing poly-nitro,di/mono-nitro,nitrato/nitramino/nitrimino,bridged/bis/di tetrazole and nitro functional groups,describing their preparation methods,advance energetic properties,and further applications as highperforming explosives,especially those reported in the last decade.This review aims to provide a fresh concept for designing nitro-tetrazole based high performing explosives together with major challenges and perspectives.展开更多
Ti1Al2O3 Functionally Gradient Material (FGM) was prepared by an explosive compaction/SHS process. Ten sheets of the compounding powder were laminated and pressed to get a green body of FGM. It was then compacted expl...Ti1Al2O3 Functionally Gradient Material (FGM) was prepared by an explosive compaction/SHS process. Ten sheets of the compounding powder were laminated and pressed to get a green body of FGM. It was then compacted explosively By burying the explosive compaction body into a stoichiometric Al/TiO2 mixture and igniting the combustion of the stoichiometric Al/TiO2 mixture, the SHS reaction of the explosive compaction body was initiated by the heat released from the combustion of the stoichiometric Al/TiO2 mixture. In this way, Ti/Al2O3 FGM was synthesized. The adiabatic temperatures of each gradient layer were calculated when the preheating temperatures were 298 K and 1173 K, respectively The microstructure, composition and properties of Ti/Al2O3 FGM and the reaction mechanism of each gradient layer were studied. It was found that Ti/Al2O3 FGM prepared by the explosive compaction/SHS process had a high density and a high microhardness. Its structure, composition and properties showed apparent gradient distribution. The structure of the standard stoichiometric ratio gradient layer of FGM was a network structure. Its reaction mode could be described as follows: Al powder melted first, then the molten Al penetrated into the TiO2 zone and reacted with TiO2, and big pores were left in the original positions of Al powder. The reaction of gradient layers with the addition of Al3O3 as diluents was similar to that of the standard stoichiometric ratio gradient layer, so were their structure and composition. However, the reaction of gradient layers with the addition of Ti as diluents was more complex and the composition deviated slightly from the designed one展开更多
Reactive Materials(RMs),a new material with structural and energy release characteristics under shockinduced chemical reactions,are promising in extensive applications in national defense and military fields.They can ...Reactive Materials(RMs),a new material with structural and energy release characteristics under shockinduced chemical reactions,are promising in extensive applications in national defense and military fields.They can increase the lethality of warheads due to their dual functionality.This paper focuses on the energy release characteristics of RM casings prepared by alloy melting and casting process under explosive loading.Explosion experiments of RM and conventional 2A12 aluminum alloy casings were conducted in free field to capture the explosive fireballs,temperature distribution,peak overpressure of the air shock wave and the fracture morphology of fragments of reactive material(RM)warhead casings by using high-speed camera,infrared thermal imager temperature and peak overpressure testing and scanning electron microscope.Results showed that an increase of both the fireball temperature and air shock wave were observed in all RM casings compared to conventional 2A12 aluminum ally casings.The RM casings can improve the peak overpressure of the air shock wave under explosion loading,though the results are different with different charge ratios.According to the energy release characteristics of the RM,increasing the thickness of RM casings will increase the peak overpressure of the near-field air shock wave,while reducing the thickness will increase the peak overpressure of the far-field air shock wave.展开更多
A water-stable zinc-organic framework, Zn(bpda)(hip)·(DMF)(H2O)(1, H2bpda = N4,N4’-di(pyridin-4-yl)biphenyl-4,4’-dicarboxamide, H2 hip = 5-hydroxyisophthalic acid), has been synthesized via solvothermal reactio...A water-stable zinc-organic framework, Zn(bpda)(hip)·(DMF)(H2O)(1, H2bpda = N4,N4’-di(pyridin-4-yl)biphenyl-4,4’-dicarboxamide, H2 hip = 5-hydroxyisophthalic acid), has been synthesized via solvothermal reactions. Compound 1 exhibits strong fluorescence emission in water and can be used to detect various nitroaromatic explosives and antibiotics by means of fluorescence quenching in aqueous solution.展开更多
Comprehensive Summary Fluorescent silk has potential application in many fields such as bioimaging,tissue engineering scaffolds,luminescent marks,and dazzling fabrics.Among the methods to endow natural silk with fluor...Comprehensive Summary Fluorescent silk has potential application in many fields such as bioimaging,tissue engineering scaffolds,luminescent marks,and dazzling fabrics.Among the methods to endow natural silk with fluorescent properties,feeding silkworms with fluorescent additives is facile,low-cost and environment friendly,which has the prospect of large-scale production.In this paper,we reviewed the research progress for this aim in the past ten years,and summarized the unified characteristics for the substances that can enter the silk gland by digestive tract of silkworms.The advantages and disadvantages of various fluorescent materials for this application are compared in detail.And the future research directions are suggested to overcome the shortcomings of the present research.展开更多
Anovel metal-organic framework{[In_(3)(TATAT)_(2)]·3CH_(3)NH_(3)·7NMF·8H_(2)O}[JLU-MOF101,H_(6)TATAT=5,5′,5″-(1,3,5-triazine-2,4,6-triyl)tris-(azanediyl)triisophthalate,NMF=N-methyl-formamide]with cor...Anovel metal-organic framework{[In_(3)(TATAT)_(2)]·3CH_(3)NH_(3)·7NMF·8H_(2)O}[JLU-MOF101,H_(6)TATAT=5,5′,5″-(1,3,5-triazine-2,4,6-triyl)tris-(azanediyl)triisophthalate,NMF=N-methyl-formamide]with cor topology has been synthesized under solvothermal conditions.The framework of JLU-MOF101 is constructed by{In(COO)_(4)}-nodes and a hexacarboxylic organic ligand.JLU-MOF101 exhibits excellent fluorescence properties in N,N-dimethylformamide(DMF)solution,and its emission spectrum can be greatly overlapped with the ultraviolet absorption spectra of trinitrophenol(TNP)and 2,4-dinitrophenol(2,4-DNP).As a result,JLU-MOF101 exhibits excellent performance of fluorescence quenching for TNP and 2,4-DNP.In addition,we demonstrate the selective detection capability of JLU-MOF101 through a large number of anti-interference tests.展开更多
The identification and detection of various types of explosives are essential for human health and environmental monitoring.Array-based sensing approach offers significant advantages in detecting multi-analytes simult...The identification and detection of various types of explosives are essential for human health and environmental monitoring.Array-based sensing approach offers significant advantages in detecting multi-analytes simultaneously,thereby holding great potential in identifying multiple explosives.Here,we report a tri-channel fluorescence array composed of three distinct fluorescence probes based on gold nanoclusters and nicotinamide adenine dinucleotide with well-separated emission colors.Through the specific interactions of explosives with different fluorescent probes and the yielded response patterns,seven explosives can be successfully distinguished with 100%accuracy.In particular,the sensor array exhibits excellent performance in the quantitative analysis of individual explosive and the differentiation of multiple explosive mixtures.To facilitate the field detection towards practical application,the tri-channel fluorescence array was further integrated with polymer hydrogels.The fabricated portable hydrogel-based array sensors can not only visually identify seven different explosives by their distinct fluorescence color change,but also enable quantitative detection based on linear discriminant analysis(LDA)together with a smartphone.This study illustrates the great potential of hydrogel-based fluorescence sensor array as robust sensors for explosives,which also holds significant promise for the development of portable explosive devices towards practical application.展开更多
Nitrate explosive is hard to detect due to lack of aromatic ring and weak interaction with fluorescence probe.More challenging is even to differentiate the dinitrates with multiple nitrate explosives based on photo in...Nitrate explosive is hard to detect due to lack of aromatic ring and weak interaction with fluorescence probe.More challenging is even to differentiate the dinitrates with multiple nitrate explosives based on photo induced electron transfer or aggregation caused fluorescence change mechanism.A highly selective dinitrate explosive probe was designed based on a new strategy-stepwise aggregation of multiple anchored fluorene dimer 8Py-2 F.Compared with its monomer counterpart 2Py-F,8Py-2 F showed a selective and stepwise fluorescence quenching to dinitrate explosives-ethylene glycol(EGDN)and triethylene glycol dinitrate(TEGDN).The limits of detection(LODs)are 2.72μM for TEGDN and 0.46μM for EGDN,which is three orders of magnitude lower than those of 2Py-F.The stepwise quenching process is well matched with the stepwise aggregation process as evidence by scanning electron microscopy(SEM).Nuclear magnetic resonance(NMR)and quantum chemical calculation proved the interaction force between the dinitrate and 8Py-2 F is hydron bonding interaction,and interaction distance is far less than that of the multiple nitrates coming from the flexibility of the chain and steric hinderance,which resulted in a self-adaptive interaction and higher selectivity.The new strategy is beneficial for the differentiation of the chemicals with similar energy level which is difficult to realize via other method,and the new method provides fluorometric probe for dinitrate explosive detection and makes it an ideal candidate for chemical detection and analysis in public safety and environmental monitoring.展开更多
Two novel thieno-[3,4-b]-pyrazine-based molecules, TP-E and TP-O, were designed and synthesized for potential application as red fluorescent emitters. The bulky tetraphenylethylene groups were attached at the peripher...Two novel thieno-[3,4-b]-pyrazine-based molecules, TP-E and TP-O, were designed and synthesized for potential application as red fluorescent emitters. The bulky tetraphenylethylene groups were attached at the periphery of the thieno-[3,4-b]-pyrazine core to form the non-planar molecules, as efficient solid- state emitting materials. The peripheral groups were grafted to the emissive core through either a conjugated acetylene bond, or a non-conjugated ether bond. These molecules exhibit strnng red fluorescence in both dilute solutions and in thin films with large Stokes shifts of over 100 nm. The cyclic voltammetry measurements showed the reversible oxidation and reduction behavior for both compounds. All these properties indicate the two compounds are possible functional materials for use in ontoelectronic devices.展开更多
Fluorescent materials have received more and more attention in the past few decades because of their great potentials in the fields of luminescent devices,sensing,data storage,bioimaging,and other optical applications...Fluorescent materials have received more and more attention in the past few decades because of their great potentials in the fields of luminescent devices,sensing,data storage,bioimaging,and other optical applications.Fluorescent materials comprising organic molecules are of broad interest owing to their highly tunable emission.Initial studies on organic fluorescent materials were mainly focused on the design and covalent modification of fluorophores in order to improve their photophysical properties at the molecular level,whereas in recent decades,many studies have revealed that the intermolecular or intramolecular noncovalent interactions also play a crucial role in luminescence.For example,the modulation of noncovalent interactions in aggregates and selfassemblies was proven to be capable of adjusting aggregation-induced emission(AIE)-active fluorophores by the restriction of intramolecular motions(RIM).In addition,in the crystalline state,intermolecular noncovalent interactions are able to promote phosphorescence by decreasing nonradiative decays.Introducing supramolecular macrocycles into organic fluorescent materials is an intriguing prospect because multiple noncovalent interactions are incorporated.On one hand,the photophysical properties of fluorophores can be changed upon inclusion within the macrocycles,providing unforeseen luminescence.On the other hand,the dynamic and reversible features of host−guest recognition endow the materials with controllability and stimuli-responsiveness,which is beneficial to the fabrication of smart materials.Among numerous supramolecular macrocycles,pillararenes are promising candidates that can be included in fluorescent materials.The advantages of pillararenes are their easy functionalization and planar chirality.After modification with proper substituents,pillararene derivatives possess high solubility and stability in both organic and aqueous media,and reversible guest binding remains.Such features make pillararenes versatile hosts in different environments.Additionally,pillararenes are planar chiral,and the interconversion between enantiomers can be adjusted with different-sized substituents and external stimuli,which are favorable to the construction of chiroptical materials.In this Account,we summarize research progress in the field of pillararene-based luminescent materials,which mainly includes the contributions made by our group.Using pillararenes as building blocks can facilitate the fabrication of high-performance fluorescent materials,in solution or the solid state,with different functions and mechanisms.Therefore,we categorize pillararene-based luminescent materials as those in solution or in the solid state.The applications and the advantages of pillararenes are discussed in detail.For example,in the solid state,pillararene-based host−guest complexation is capable of minimizing the aggregation-caused quenching(ACQ)of fluorophores.This broadens the application of fluorophores in crystalline materials.In solution,the host−guest complexes of pillararenes and fluorophores can self-assemble into well-defined nanostructures,which not only adjust the photophysical properties but also enable functions such as bioimaging.The remaining challenges and future perspectives are outlined at the end.It is expected that this Account will inspire new researchers in different fields and offer new opportunities for the construction of novel luminescent materials with pillararenes and other macrocycles.展开更多
Self-assembly ofπ-conjugated compounds into supramolecular polymers has received considerable attention because of their intrinsic scientific interests and technological applications.As compared toπ-conjugated rods,...Self-assembly ofπ-conjugated compounds into supramolecular polymers has received considerable attention because of their intrinsic scientific interests and technological applications.As compared toπ-conjugated rods,discotics,and macrocycles,propeller-shapedπ-conjugated molecules have been less exploited to form long-range-ordered supramolecular polymers.Herein a novel type of supramolecular polymers has been constructed on the basis of propeller-shaped triphenylamine cyanostilbenes.The designed compound adopts nucleation-elongation cooperative mechanism for the supramolecular polymerization process,because of the participation of three-fold hydrogen bonds between the neighbouring monomers.The supramolecular polymeric state displays amplified chirality and enhanced emission than those in the monomeric state.The resulting supramolecular polymers exhibit severe emission quenching upon addition of 2,6-dinitrotoluene,ascribed to photoinduced electron transfer from the triphenylamine cyanostilbenes to the explosive analyte.The current study proves the feasibility to supramolecular polymerize propeller-likeπ-conjugated molecules,serving as a promising type of explosive sensor owing to their guest encapsulation and signal amplification capabilities.展开更多
A novel polymeric reaction monomer (NPRM) for preparing highly fluorescent rare earth polymer materials was synthesized via interface and coordinating reaction. The composition and structure of the NPRM and intermedia...A novel polymeric reaction monomer (NPRM) for preparing highly fluorescent rare earth polymer materials was synthesized via interface and coordinating reaction. The composition and structure of the NPRM and intermediate product (ligand) were characterized through the Fourier transform infrared spectroscopy (FT-IR), carbon-nuclear magnetic resonance spectrum (13CNMR), Mass spectra (MS), and element analysis data. The results showed that the composition and structure of NPRM agreed with that of anticipated product. The NPRM was composed of two important sections. Section 1 was able to provide excellent fluorescent properties for final rare earth polymer material through the effect energy transfer between ligand and rare earth ion; Section 2 would endow with the NPRM excellent polymeric active and form highly fluorescent rare earth polymer material. Fluorescent properties of the NPRM were also researched via a CARY ECLIPSE fluorescent spectrometer. The results showed that the NPRM possessed excellent luminescent properties. The corresponding emission peaks based on the 5D0→7F1(601.6 nm), 5D0→7F2(625.0 nm), 5D0→7F3(660.5 nm) and 5D0→7F4(706.3 nm) transitions for Eu3+ were observed. The strongest emission peak was at 625 nm, which belonged to 5D0→7F2 transition.展开更多
文摘In order to investigate detonation propagation characteristics of different charge patterns,the detonation velocities of superposition strip shaped charges made up of a detonating cord and explosives were measured by a detonation velocity measuring instrument under conditions of different ignition.The experimental results and theoretical analysis show that the maximum detonation propagation velocity depends on the explosive materials with the maximum velocity among all the explosive materials.Using detonating cord in a superposition charge can shorten detonation propagation time and improve the efficiency of explosive energy.The measurement method of detonation propagation velocity and experimental results are presented and investigated.
基金Supported by the National Innovation Funds(7130619)
文摘Reactive fragment enhances lethality by incorporating the defeat mechanisms of kinetic energy and chemical energy into a unitary damage unit. Combined studies on the behavior of reactive fragment initiating covered explosive are performed theoretically and experimentally. The results in- dicate that the response of the covered explosive subjected to reactive fragment is not consistent with the classical shock initiation model. When impacting and penetrating into the covered explosive, the reactive fragment releases great amounts of thermo-chemical energy up to 5. 68 times of its kinetic energy into the explosive due to violent chemical reactions. This impact-induced chemical energy re- lease behavior of the reactive fragment significantly enhances the initiation capability and damage effects on the covered explosive.
基金We are thankful to the NSAF(U1830134),NSFC(21905023 and 21911530096)for their generous financial support.
文摘Heterocyclic skeleton(Azoles)and different energetic groups containing high performing explosives are highly emerged in recent years to meet the challenging requirements of energetic materials in both military and civilian applications with improved performance.For this purpose tetrazole(Azole)is identified as an attractive heterocyclic backbone with energetic functional groups nitro(-NO_(2)),nitrato(-ONO_(2)),nitrimino(-NNO_(2)),and nitramino(eNHeNO_(2))to replace the traditionally used high performing explosives.The tetrazole based compounds having these energetic functional groups demonstrated advanced energetic performance(detonation velocity and pressure),densities,and heat of formation(HOF)and became a potential replacement of traditional energetic compounds such as RDX.This review presents a summary of the recently reported nitro-tetrazole energetic compounds containing poly-nitro,di/mono-nitro,nitrato/nitramino/nitrimino,bridged/bis/di tetrazole and nitro functional groups,describing their preparation methods,advance energetic properties,and further applications as highperforming explosives,especially those reported in the last decade.This review aims to provide a fresh concept for designing nitro-tetrazole based high performing explosives together with major challenges and perspectives.
文摘Ti1Al2O3 Functionally Gradient Material (FGM) was prepared by an explosive compaction/SHS process. Ten sheets of the compounding powder were laminated and pressed to get a green body of FGM. It was then compacted explosively By burying the explosive compaction body into a stoichiometric Al/TiO2 mixture and igniting the combustion of the stoichiometric Al/TiO2 mixture, the SHS reaction of the explosive compaction body was initiated by the heat released from the combustion of the stoichiometric Al/TiO2 mixture. In this way, Ti/Al2O3 FGM was synthesized. The adiabatic temperatures of each gradient layer were calculated when the preheating temperatures were 298 K and 1173 K, respectively The microstructure, composition and properties of Ti/Al2O3 FGM and the reaction mechanism of each gradient layer were studied. It was found that Ti/Al2O3 FGM prepared by the explosive compaction/SHS process had a high density and a high microhardness. Its structure, composition and properties showed apparent gradient distribution. The structure of the standard stoichiometric ratio gradient layer of FGM was a network structure. Its reaction mode could be described as follows: Al powder melted first, then the molten Al penetrated into the TiO2 zone and reacted with TiO2, and big pores were left in the original positions of Al powder. The reaction of gradient layers with the addition of Al3O3 as diluents was similar to that of the standard stoichiometric ratio gradient layer, so were their structure and composition. However, the reaction of gradient layers with the addition of Ti as diluents was more complex and the composition deviated slightly from the designed one
基金the Fundamental Research Funds for the Central Universities(No.30920021108)Open Foundation of Hypervelocity Impact Research Center of CARDC(20200106).
文摘Reactive Materials(RMs),a new material with structural and energy release characteristics under shockinduced chemical reactions,are promising in extensive applications in national defense and military fields.They can increase the lethality of warheads due to their dual functionality.This paper focuses on the energy release characteristics of RM casings prepared by alloy melting and casting process under explosive loading.Explosion experiments of RM and conventional 2A12 aluminum alloy casings were conducted in free field to capture the explosive fireballs,temperature distribution,peak overpressure of the air shock wave and the fracture morphology of fragments of reactive material(RM)warhead casings by using high-speed camera,infrared thermal imager temperature and peak overpressure testing and scanning electron microscope.Results showed that an increase of both the fireball temperature and air shock wave were observed in all RM casings compared to conventional 2A12 aluminum ally casings.The RM casings can improve the peak overpressure of the air shock wave under explosion loading,though the results are different with different charge ratios.According to the energy release characteristics of the RM,increasing the thickness of RM casings will increase the peak overpressure of the near-field air shock wave,while reducing the thickness will increase the peak overpressure of the far-field air shock wave.
基金financially supported by the National Natural Science Foundation of China(No.21801111)Key Scientific Research Projects of Higher Education of He’nan Province(19A150034)
文摘A water-stable zinc-organic framework, Zn(bpda)(hip)·(DMF)(H2O)(1, H2bpda = N4,N4’-di(pyridin-4-yl)biphenyl-4,4’-dicarboxamide, H2 hip = 5-hydroxyisophthalic acid), has been synthesized via solvothermal reactions. Compound 1 exhibits strong fluorescence emission in water and can be used to detect various nitroaromatic explosives and antibiotics by means of fluorescence quenching in aqueous solution.
基金by the National Natural Science Foundation of China(21975048,21771039)the Shanghai Science and Technology Committee(19Dz2270100).
文摘Comprehensive Summary Fluorescent silk has potential application in many fields such as bioimaging,tissue engineering scaffolds,luminescent marks,and dazzling fabrics.Among the methods to endow natural silk with fluorescent properties,feeding silkworms with fluorescent additives is facile,low-cost and environment friendly,which has the prospect of large-scale production.In this paper,we reviewed the research progress for this aim in the past ten years,and summarized the unified characteristics for the substances that can enter the silk gland by digestive tract of silkworms.The advantages and disadvantages of various fluorescent materials for this application are compared in detail.And the future research directions are suggested to overcome the shortcomings of the present research.
基金supported by the National Natural Science Foundation of China(Nos.22171100,22288101)and the“111”Project of China(No.B17020).
文摘Anovel metal-organic framework{[In_(3)(TATAT)_(2)]·3CH_(3)NH_(3)·7NMF·8H_(2)O}[JLU-MOF101,H_(6)TATAT=5,5′,5″-(1,3,5-triazine-2,4,6-triyl)tris-(azanediyl)triisophthalate,NMF=N-methyl-formamide]with cor topology has been synthesized under solvothermal conditions.The framework of JLU-MOF101 is constructed by{In(COO)_(4)}-nodes and a hexacarboxylic organic ligand.JLU-MOF101 exhibits excellent fluorescence properties in N,N-dimethylformamide(DMF)solution,and its emission spectrum can be greatly overlapped with the ultraviolet absorption spectra of trinitrophenol(TNP)and 2,4-dinitrophenol(2,4-DNP).As a result,JLU-MOF101 exhibits excellent performance of fluorescence quenching for TNP and 2,4-DNP.In addition,we demonstrate the selective detection capability of JLU-MOF101 through a large number of anti-interference tests.
基金supported by the National Natural Science Foundation of China(Nos.21705129 and 22274131)Shaanxi Fundamental Science Research Project for Chemistry&Biology(No.22JHQ071).
文摘The identification and detection of various types of explosives are essential for human health and environmental monitoring.Array-based sensing approach offers significant advantages in detecting multi-analytes simultaneously,thereby holding great potential in identifying multiple explosives.Here,we report a tri-channel fluorescence array composed of three distinct fluorescence probes based on gold nanoclusters and nicotinamide adenine dinucleotide with well-separated emission colors.Through the specific interactions of explosives with different fluorescent probes and the yielded response patterns,seven explosives can be successfully distinguished with 100%accuracy.In particular,the sensor array exhibits excellent performance in the quantitative analysis of individual explosive and the differentiation of multiple explosive mixtures.To facilitate the field detection towards practical application,the tri-channel fluorescence array was further integrated with polymer hydrogels.The fabricated portable hydrogel-based array sensors can not only visually identify seven different explosives by their distinct fluorescence color change,but also enable quantitative detection based on linear discriminant analysis(LDA)together with a smartphone.This study illustrates the great potential of hydrogel-based fluorescence sensor array as robust sensors for explosives,which also holds significant promise for the development of portable explosive devices towards practical application.
基金supported by the research program from the Ministry of Science and Technology(2017YFC0821100)the National Natural Science Foundation of China(61731016,61771460)a grant from the Youth Innovation Promotion Association CAS(2015190)
文摘Nitrate explosive is hard to detect due to lack of aromatic ring and weak interaction with fluorescence probe.More challenging is even to differentiate the dinitrates with multiple nitrate explosives based on photo induced electron transfer or aggregation caused fluorescence change mechanism.A highly selective dinitrate explosive probe was designed based on a new strategy-stepwise aggregation of multiple anchored fluorene dimer 8Py-2 F.Compared with its monomer counterpart 2Py-F,8Py-2 F showed a selective and stepwise fluorescence quenching to dinitrate explosives-ethylene glycol(EGDN)and triethylene glycol dinitrate(TEGDN).The limits of detection(LODs)are 2.72μM for TEGDN and 0.46μM for EGDN,which is three orders of magnitude lower than those of 2Py-F.The stepwise quenching process is well matched with the stepwise aggregation process as evidence by scanning electron microscopy(SEM).Nuclear magnetic resonance(NMR)and quantum chemical calculation proved the interaction force between the dinitrate and 8Py-2 F is hydron bonding interaction,and interaction distance is far less than that of the multiple nitrates coming from the flexibility of the chain and steric hinderance,which resulted in a self-adaptive interaction and higher selectivity.The new strategy is beneficial for the differentiation of the chemicals with similar energy level which is difficult to realize via other method,and the new method provides fluorometric probe for dinitrate explosive detection and makes it an ideal candidate for chemical detection and analysis in public safety and environmental monitoring.
基金the National Natural Science Foundation of China(Nos.21274016 and 21072026)Fundamental Research Funds for the Central Universities(No.DUT13LK06)for financial support to this work
文摘Two novel thieno-[3,4-b]-pyrazine-based molecules, TP-E and TP-O, were designed and synthesized for potential application as red fluorescent emitters. The bulky tetraphenylethylene groups were attached at the periphery of the thieno-[3,4-b]-pyrazine core to form the non-planar molecules, as efficient solid- state emitting materials. The peripheral groups were grafted to the emissive core through either a conjugated acetylene bond, or a non-conjugated ether bond. These molecules exhibit strnng red fluorescence in both dilute solutions and in thin films with large Stokes shifts of over 100 nm. The cyclic voltammetry measurements showed the reversible oxidation and reduction behavior for both compounds. All these properties indicate the two compounds are possible functional materials for use in ontoelectronic devices.
基金supported by the National Key Research and Development Program of China(2021YFA0910100)the National Natural Science Foundation of China(22035006)+1 种基金the Zhejiang Provincial Natural Science Foundation of China(LD21B020001)the Starry Night Science Fund of Zhejiang University Shanghai Institute for Advanced Study(SN-ZJU-SIAS-006).
文摘Fluorescent materials have received more and more attention in the past few decades because of their great potentials in the fields of luminescent devices,sensing,data storage,bioimaging,and other optical applications.Fluorescent materials comprising organic molecules are of broad interest owing to their highly tunable emission.Initial studies on organic fluorescent materials were mainly focused on the design and covalent modification of fluorophores in order to improve their photophysical properties at the molecular level,whereas in recent decades,many studies have revealed that the intermolecular or intramolecular noncovalent interactions also play a crucial role in luminescence.For example,the modulation of noncovalent interactions in aggregates and selfassemblies was proven to be capable of adjusting aggregation-induced emission(AIE)-active fluorophores by the restriction of intramolecular motions(RIM).In addition,in the crystalline state,intermolecular noncovalent interactions are able to promote phosphorescence by decreasing nonradiative decays.Introducing supramolecular macrocycles into organic fluorescent materials is an intriguing prospect because multiple noncovalent interactions are incorporated.On one hand,the photophysical properties of fluorophores can be changed upon inclusion within the macrocycles,providing unforeseen luminescence.On the other hand,the dynamic and reversible features of host−guest recognition endow the materials with controllability and stimuli-responsiveness,which is beneficial to the fabrication of smart materials.Among numerous supramolecular macrocycles,pillararenes are promising candidates that can be included in fluorescent materials.The advantages of pillararenes are their easy functionalization and planar chirality.After modification with proper substituents,pillararene derivatives possess high solubility and stability in both organic and aqueous media,and reversible guest binding remains.Such features make pillararenes versatile hosts in different environments.Additionally,pillararenes are planar chiral,and the interconversion between enantiomers can be adjusted with different-sized substituents and external stimuli,which are favorable to the construction of chiroptical materials.In this Account,we summarize research progress in the field of pillararene-based luminescent materials,which mainly includes the contributions made by our group.Using pillararenes as building blocks can facilitate the fabrication of high-performance fluorescent materials,in solution or the solid state,with different functions and mechanisms.Therefore,we categorize pillararene-based luminescent materials as those in solution or in the solid state.The applications and the advantages of pillararenes are discussed in detail.For example,in the solid state,pillararene-based host−guest complexation is capable of minimizing the aggregation-caused quenching(ACQ)of fluorophores.This broadens the application of fluorophores in crystalline materials.In solution,the host−guest complexes of pillararenes and fluorophores can self-assemble into well-defined nanostructures,which not only adjust the photophysical properties but also enable functions such as bioimaging.The remaining challenges and future perspectives are outlined at the end.It is expected that this Account will inspire new researchers in different fields and offer new opportunities for the construction of novel luminescent materials with pillararenes and other macrocycles.
基金the National Natural Science Foundation of China(Nos.21922110 and 21871245)the Collaborative Innovation Program of Hefei Science Center,CAS(No.2022HSC-CIP014)the Fundamental Research Funds for the Central Universities(No.WK3450000005).
文摘Self-assembly ofπ-conjugated compounds into supramolecular polymers has received considerable attention because of their intrinsic scientific interests and technological applications.As compared toπ-conjugated rods,discotics,and macrocycles,propeller-shapedπ-conjugated molecules have been less exploited to form long-range-ordered supramolecular polymers.Herein a novel type of supramolecular polymers has been constructed on the basis of propeller-shaped triphenylamine cyanostilbenes.The designed compound adopts nucleation-elongation cooperative mechanism for the supramolecular polymerization process,because of the participation of three-fold hydrogen bonds between the neighbouring monomers.The supramolecular polymeric state displays amplified chirality and enhanced emission than those in the monomeric state.The resulting supramolecular polymers exhibit severe emission quenching upon addition of 2,6-dinitrotoluene,ascribed to photoinduced electron transfer from the triphenylamine cyanostilbenes to the explosive analyte.The current study proves the feasibility to supramolecular polymerize propeller-likeπ-conjugated molecules,serving as a promising type of explosive sensor owing to their guest encapsulation and signal amplification capabilities.
基金the Development Programof Science &Technology of Tianjin (06TXTJJC14400)
文摘A novel polymeric reaction monomer (NPRM) for preparing highly fluorescent rare earth polymer materials was synthesized via interface and coordinating reaction. The composition and structure of the NPRM and intermediate product (ligand) were characterized through the Fourier transform infrared spectroscopy (FT-IR), carbon-nuclear magnetic resonance spectrum (13CNMR), Mass spectra (MS), and element analysis data. The results showed that the composition and structure of NPRM agreed with that of anticipated product. The NPRM was composed of two important sections. Section 1 was able to provide excellent fluorescent properties for final rare earth polymer material through the effect energy transfer between ligand and rare earth ion; Section 2 would endow with the NPRM excellent polymeric active and form highly fluorescent rare earth polymer material. Fluorescent properties of the NPRM were also researched via a CARY ECLIPSE fluorescent spectrometer. The results showed that the NPRM possessed excellent luminescent properties. The corresponding emission peaks based on the 5D0→7F1(601.6 nm), 5D0→7F2(625.0 nm), 5D0→7F3(660.5 nm) and 5D0→7F4(706.3 nm) transitions for Eu3+ were observed. The strongest emission peak was at 625 nm, which belonged to 5D0→7F2 transition.