Novel perylene bisimide dyes bay-functionalized with naphthalimide chromophores have been prepared conveniently by coupling of 1,8-naphthalimide and dibromoperylene bisimides. Their optical properties were investigate...Novel perylene bisimide dyes bay-functionalized with naphthalimide chromophores have been prepared conveniently by coupling of 1,8-naphthalimide and dibromoperylene bisimides. Their optical properties were investigated by UV-vis and fluorescence spectroscopy. The absorption spectra of these compounds showed wide spectral responses from 300 to 700 nm, which would be potentials for application as organic solar cells.展开更多
A novel alkynyl substituted N-aryl-1,8-naphthalimide II (C20H11NO2) was synthesized for the discovery and evaluation of new fluorescence probes, and was characterized by X-ray crystal diffraction. It crystallizes in...A novel alkynyl substituted N-aryl-1,8-naphthalimide II (C20H11NO2) was synthesized for the discovery and evaluation of new fluorescence probes, and was characterized by X-ray crystal diffraction. It crystallizes in monoclinic, space group P21/n with a = 15.898(3), b = 5.0102(10), c = 17.962(4)A, β = 92.97(3)°, V = 1428.7(5) A^3, Z = 4, Mr = 297.30, Dc = 1.382 g/cm^3, F(000) = 616,/J = 0.090 mm^-1, S = 1.011, the final R = 0.0542 and wR = 0.1204 for 1669 observed reflections with I 〉 2σ(I) and 212 variable parameters. Hydrogen-bounding and n-stacking interactions were discussed. The influence of acetylene group on the fluorescence properties was also investigated. In comparison with N-phenyl-1,8-naphthalimide I (C18H11NO2), few new structure characters and fluorescence properties of the title compound have been found.展开更多
White light emitting systems of pure organic materials have attracted extensive research interest due to their better compatibility and functional scalability.The reported organic white light materials are mainly base...White light emitting systems of pure organic materials have attracted extensive research interest due to their better compatibility and functional scalability.The reported organic white light materials are mainly based on the multi-channel emission regulation of the compound itself or the mixing of multicolor luminescence materials,but studies on the dependence between multicolor luminescence and the external environment are lacking,which limits the application of these materials in areas such as identification and sensing.This paper reports that the 4-or 3?hydroxyl-substituted naphthalimides NapH1 and NapH2 form intermolecular hydrogen bonds with adjacent molecules in the environment,and undergo excited-state intermolecular proton transfer under irradiation,resulting in blue-yellow or blue-red dual fluorescence emission,respectively.Since the two compounds have different two-color luminescence channels and the two-color intensity ratio is affected by the environment,and the intermolecular hydrogen bond is determined by the hydrogen bond receptor,polarity,and temperature in the environment,the full spectrum from blue to red light and white light emission can be obtained by adjusting the mixing ratio of the two dyes and the solvent polarity and the ambient temperature.This environmentally sensitive white emission is used to detect the alkalinity of different papers,and the dyed paper can be used as a test strip for acid-base vapor detection.展开更多
A series of compounds 1-11 with different side chains of naphthalimide as fluorescent copper sensors were designed and synthesized. Compounds 1, 9, 10 and 11 presented a high selectivity to Cu2+ in a neutral aqueous e...A series of compounds 1-11 with different side chains of naphthalimide as fluorescent copper sensors were designed and synthesized. Compounds 1, 9, 10 and 11 presented a high selectivity to Cu2+ in a neutral aqueous environment. Here 1, 9 and 10 showed selectivity and affinity to Cu2+ with an association constant of about ~106. It gave somewhat response to Ag+, Co2+, Ni2+ and Fe2+ while 1 detected copper. 9 and 10 displayed better selectivity by changing their hydrophobic side chains to the hydrophilic ones on imide moieties. 11, with one flexible side chain, showed high selectivity and an association constant (Ka = 2.2 × 108), which were much higher than those of 1, 9 and 10. These results indicated that the selectivity and affinity could be improved by changing side chains of naphthalimide. That might provide a novel strategy or method for the development of fluorescent sensors.展开更多
Understanding the physical mechanisms governing aggregation-induced-emission(AIE)and aggrega-tion-caused-quenching plays a vital role in developing functional AIE materials.In this work,tetraphenylethene(TPE,a classic...Understanding the physical mechanisms governing aggregation-induced-emission(AIE)and aggrega-tion-caused-quenching plays a vital role in developing functional AIE materials.In this work,tetraphenylethene(TPE,a classical AiEgen)and naphthalimide(NI,a popular fluorophore with ACQ characteristics)were connected through non-conjugated linkages and conjugated linkages.We showed that the nonconjugated-linkage of TPE to NI fragments leads to substantial PET in molecular aggregates and ACQ.In con trast,the conjugated conn ection between TPE and NI moieties results in the AIE phenomenon by suppressing twisted intramolecular charge transfer.This work provides an important guideline for the rational design of AIE materials.展开更多
A polarity-sensitive fluorescent probe MNP was rationally designed and synthesized with naphthalimide as the fluorophore and maleimide as the receptor for thiols. MNP is weakly fluorescent due to the photoinduced elec...A polarity-sensitive fluorescent probe MNP was rationally designed and synthesized with naphthalimide as the fluorophore and maleimide as the receptor for thiols. MNP is weakly fluorescent due to the photoinduced electron-transfer (PET) from the fluorophore to the receptor, and it displays evidently solvatochromic UV-vis and fluorescence spectra: the emission shifted from 495 nm in n-hexane to 545 nm in phosphate buffer solution. Michael addition reaction between thiols and the maleimide in MNP inhibited the PET process, which led to about eight-fold fluorescence enhancement. In addition, MNP showed highly sensitivity to rnercapto-containing proteins and it could detect as low as 20.4 μg/mL of BSA in PBS. MNP has potential in fluorescent imaging of thiols in living cells.展开更多
Developing the novel fluorescent dyes with a larger Stokes shift is still a challenge in the research of fluorescence probes. In this work, a naphthalimide-modified near-infrared cyanine dye with an emission at 785 nm...Developing the novel fluorescent dyes with a larger Stokes shift is still a challenge in the research of fluorescence probes. In this work, a naphthalimide-modified near-infrared cyanine dye with an emission at 785 nm has been synthesized for lysosome-targeting imaging. This fluorescent dye showed a large Stokes shift(up to 165 nm) and favorable lysosome-targeting property, which facilitated it to be a potential candidate for studying of lysosomal functions. The result also indicated that the probe is a promising contrast agent for in vivo imaging in mouse models.展开更多
A novel hydrophilic copolymer P(NI-HEMA) containing the pendant group of naphthalimide moiety has been prepared. In the aqueous buffer solution, its film on the glass substrate shows an obvious fluorescence change and...A novel hydrophilic copolymer P(NI-HEMA) containing the pendant group of naphthalimide moiety has been prepared. In the aqueous buffer solution, its film on the glass substrate shows an obvious fluorescence change and excellent linear relevance in the pH range of 5.8-8.0. Specifically, using the isobestic point at 406 nm as excitation wavelength can avoid the UV irradiation and the tedious calibration process. The film stability and hydrophilicity of copolymer P(NI-HEMA) were studied. Because of the easy synthesis, low price and high linear relevance to pH, the hydrophilic chemosensor film of P(NI- HEMA) could be potentially applied as a low-cost pH indicator for high-throughput bioprocessing in microreactors.展开更多
Iron is one of the essential trace elements in the human body.It plays an important role in human biology and pathology.Deregulation of iron levels in cells is associated with disease development.In this work,we synth...Iron is one of the essential trace elements in the human body.It plays an important role in human biology and pathology.Deregulation of iron levels in cells is associated with disease development.In this work,we synthesized a novel near-infrared intramolecular charge transfer(ICT)based ratiometric fluorescent probe to detect Fe^(2+),by using naphthalimide and indole moieties as building blocks.Our work showed that the radiometric probe has excellent selectivity,sensitivity and rapid response.Moreover,we could successfully perform real-time monitoring of Fe^(2+) in He La cells and C.elegans.展开更多
Two kinds of fluorescent nano-probes(pH-A and pH-B) with different diameters for the determination of H+concentration, based on photo-induced electron transfer mechanism, were synthesized through click reaction. In...Two kinds of fluorescent nano-probes(pH-A and pH-B) with different diameters for the determination of H+concentration, based on photo-induced electron transfer mechanism, were synthesized through click reaction. In which 1,8-naphthalimide was employed as the fluorophore and N,N-dimethylethylenediamine as the receptor. The effects of particle size and linker length on the photophysical properties of the probe were studied. The results revealed that the nano-probes were more sensitive toward pH with increasing particle size. The fluorescence intensity at 529 nm(I529) of the nano-probe p H-A of 120 nm exhibited good linear relationship with solution's pH in the range of 6–8. The probe p H-A displayed excellent selectivity and competition toward proton over other possible coexisted ions, and it could be applied to detect pH in realistic samples(river water, urine).展开更多
Technical properties of two naphthalimide based disperse dyes on nylon 6 and polyester fibers were investigated in the presence of urea. The two naphthalimide based disperse dyes were synthesized. The dyes were purifi...Technical properties of two naphthalimide based disperse dyes on nylon 6 and polyester fibers were investigated in the presence of urea. The two naphthalimide based disperse dyes were synthesized. The dyes were purified and then fully characterized using 1H-NMR, FTIR and melting point analysis. Dispersion of the dyes was prepared in water and applied on nylon 6 and PET fibers. The dyes offered good build-up properties on the substrates. In order to increase dye adsorption of the substrates, urea was added into the dyebath. By adding urea, the dye adsorption of polyester was increased significantly, while the increase of that of nylon 6 was not marked. The dyes showed good fastness properties on the substrates.展开更多
Two small molecules named PI-DPP and NI-DPP with a DPP core as the central strong acceptor unit and phthalimide/naphthalimide as the terminal weak acceptor were designed and synthesized. The effects of terminal phthal...Two small molecules named PI-DPP and NI-DPP with a DPP core as the central strong acceptor unit and phthalimide/naphthalimide as the terminal weak acceptor were designed and synthesized. The effects of terminal phthalimide/naphthalimide units on the thermal behavior, optical and electrochemical properties, as well as the photovoltaic performance of these two materials were systematically studied. Cyclic voltammetry revealed that the lowest unoccupied molecular orbitals (LUMO) (- -3.6 eV) of both molecules were intermediate to common electron donor (P3HT) and acceptor (PCBM). This indicated that PI-DPP and NI-DPP may uniquely serve as electron donor when blended with PCBM, and as electron acceptor when blended with P3HT, where sufficient driving forces between DPPs and PCBM, as well as between P3HT and DPPs should be created for exciton dissociation. Using as electron donor materials, PI-DPP and NI-DPP devices exhibited low power conversion efficiencies (PCEs) of 0.90% and 0.76% by blending with PCBM, respectively. And a preliminary evaluation of the potential of the NI-DPP as electron acceptor material was carried out using P3HT as a donor material, and P3HT:NI-DPP device showed a PCE of 0.6%, with an open circuit voltage (Voc) of 0.7 V, a short circuit current density (Jsc) of 1.91 mA·cm^-2, and a fill factor (FF) of 45%.展开更多
A nitrone-modified 1,8-naphthalimide was desig ned as a novel bioorthog on alactivated turn-on probe based on strain-promoted alkyne-nitrone cycloadditio n(SPANC).The bioorthog onal cycloadducts were subseque ntly tra...A nitrone-modified 1,8-naphthalimide was desig ned as a novel bioorthog on alactivated turn-on probe based on strain-promoted alkyne-nitrone cycloadditio n(SPANC).The bioorthog onal cycloadducts were subseque ntly tran sformed into fluoresce nt rearra nge-ment products by photo-accelerati on,which exhibited sign ificant fluoresce nee enhan ceme nt,large stokes shift,and high fluores-cence qua ntum yield.DFT calculati ons were performed to elucidate the fluoresce nee OFF-ON mecha nism.This fluoroge nic strategy was successfully applied to labeling of proteins and visualizing mitochondria in live cells in real time.展开更多
The naphthalimide derivative. NA1 was synthesized, which consists of a bis(2-(ethylthio)ethyl)amine group binding cations and naphthalimide unit as chromogenic and fluorogenic signaling subunit. Absorption and emi...The naphthalimide derivative. NA1 was synthesized, which consists of a bis(2-(ethylthio)ethyl)amine group binding cations and naphthalimide unit as chromogenic and fluorogenic signaling subunit. Absorption and emission spectra and the effect of polarity of solvents and pH values were studied. The photo-induced electron transfer (PET) occurred from the donor of bis(2-(ethylthio)ethyl)amine group to the naphthalimide fluorophore. The present study demonstrates that NA1 is a viable candidate as a fluorescent receptor for a new Ag^+ ion sensor. This silver ion chemosensor can discriminate Ag^+ ion well among heavy metal ions by an enhancement of the fluorescence intensity in ethanol-water (1 : 9, V : V). And NA1 is also a pH-sensor because the fluorescence of the compound varies with the pH values.展开更多
Insect chitinolyticβ-N-acetyl-D-hexosaminidase,such as OfHex1 from Ostrinia furnacalis,is a potential target for insecticide design.Among the known OfH ex1 inhibitors,Q2 is of great interest because it is the first n...Insect chitinolyticβ-N-acetyl-D-hexosaminidase,such as OfHex1 from Ostrinia furnacalis,is a potential target for insecticide design.Among the known OfH ex1 inhibitors,Q2 is of great interest because it is the first non-carbohydrate inhibitor.In this study,we designed and synthesized a series of Q2 derivatives by replacing the thiadiazole and naphthalimide groups and changing the linker length.Compound 3 m showed the best inhibitory activity with a Kivalue of 0.34 mmol/L against OfHex1,which is about onequarter that of Q2(K_i=1.4 mmol/L).Compound 6 a showed the best inhibitory activity among the quinoline-containing derivatives(K_i=2.3 mmol/L).Molecular docking indicated that although 3 m,6 a,and Q2 binding the active pocket of OfHex1 in similar mode,compound 3 m engaged better than the other compounds in intermolecular interaction with OfH ex1.展开更多
A ratiometric fluorescent sensor(Hoe-NI) was developed by connecting a nucleus targeted Hoechst unit to a naphthalimide dye via "click chemistry". The sensor achieves high specific nucleus labeling with wash-free ...A ratiometric fluorescent sensor(Hoe-NI) was developed by connecting a nucleus targeted Hoechst unit to a naphthalimide dye via "click chemistry". The sensor achieves high specific nucleus labeling with wash-free staining method in various kinds of living cells. The fluorescence ratio of the two emission bands(450 nm for Hoechst and 505 nm for naphthalimide) is changed sensitively to the variation of DNA concentrations, which provides the quantitative information in the processes of DNA damage induced by hydroxyl radicals and antitumor drug. Therefore, Hoe-NI is a recommendable sensor for the monitoring of nuclear DNA damage that reveals the health status of cells.展开更多
Four 1,8-naphthalimide hydrazone molecules with different electron-donating groups have been applied in the study of linear and nonlinear optical(NLO)properties.These compounds showed strong green emission in solution...Four 1,8-naphthalimide hydrazone molecules with different electron-donating groups have been applied in the study of linear and nonlinear optical(NLO)properties.These compounds showed strong green emission in solution.Their NLO properties such as two-photon absorption(TPA)behavior with femtosecond laser pulses ca.800 nm and excited-state absorption(ESA)behavior with nanosecond laser pulses at 532 nm were investigated.Compound 4 presented the largest two-photon cross section(550 GM)among them due to two factors:the conjugated length of compound 4 is the longest and the electron-donating ability of compound 4 is the strongest.Different from TPA behavior,compound 2 showed the best nonlinear absorption properties at 532 nm and its nonlinear absorption coef-ficient and third-order nonlinear optical susceptibilitiesχ^(3)were up to 1.41×10^(−10) MKS and 4.65×10^(−12) esu,re-spectively.Through the modification of the structure,the nonlinear optical properties of these compounds at differ-ent wavelengths(532 and 800 nm)were well tuned.The great broad-band nonlinear optical properties indicate hy-drazones are good candidates for organic nonlinear optical absorption materials.展开更多
A series of novel naphthalimide derivatives modified by amino acids and their dichloroacetamide derivatives at the 3-position have been synthesized. Their cytotoxic activities were preliminarily evaluated against He/a...A series of novel naphthalimide derivatives modified by amino acids and their dichloroacetamide derivatives at the 3-position have been synthesized. Their cytotoxic activities were preliminarily evaluated against He/a, A549 and K562 cells, which showed that the length of the side chains of the amino acids influenced the cytotoxic activities. Moreover, compound 7d showed a very good cytotoxic activity against A549 cells with an IC50 value of 4.78 μmol L-1, Furthermore, the UV-vis, fluorescence, and circular dichroism (CD) spectroscopies and thermal denaturation experiment indicated that compounds 6a, 6d and 7a, 7d, as DNA intercalators, exhibited binding affinities with calf-thymus DNA (Ct-DNA).展开更多
Herein,two compounds,4-2′-hydroxybenzylidenehydrazinyl-N-butyl-1,8-naphthalimide(BN-1)and 4-benzylidenehydrazinyl-N-butyl-1,8-naphthalimide(BN-2),were synthesized to explore the hydrogen bonding effect on mechanoresp...Herein,two compounds,4-2′-hydroxybenzylidenehydrazinyl-N-butyl-1,8-naphthalimide(BN-1)and 4-benzylidenehydrazinyl-N-butyl-1,8-naphthalimide(BN-2),were synthesized to explore the hydrogen bonding effect on mechanoresponsive luminescent(MRL).The results showed that compound BN-1 exhibited strong emission in solution and solid-state compared with compound BN-2.After grinding,the emission intensity of compound BN-1 sharply decreased by as much as 15 times with an obvious red-shift from 552 nm to 577 nm.The control compound BN-2,by contrast,did not change so much before and after grinding.Single crystal analysis suggests that BN-1 molecule formed strong intramolecular interaction via-N=N⋯H-O hydrogen bond with a distance of 0.2632 nm.An excited-state intramolecular proton transfer(ESIPT)based fluorophore featured this intramolecular hydrogen bond.The intramolecular hydrogen bond as well as other intermolecular interactions can rigidify the molecular conformation of compound BN-1 in solid-state,and thus suppress the nonradiative pathways,resulting in strong emission.These intra-and intermolecular interactions were destroyed by mechanical stimuli,accompanied by molecular conformation change that decreases the luminescence and blocks the ESIPT process.The MRL process was also demonstrated by scanning electron microscopy and powder X-ray diffraction.The molecular stacking mode changed from crystalline to a disordered amorphous state after grinding.展开更多
In this review, we retrospect our progress in biological active naphthalimide and analogues as antitumor agents in the past 20 years. On one hand, various derivations in naphthalimide pharmacophores were developed to ...In this review, we retrospect our progress in biological active naphthalimide and analogues as antitumor agents in the past 20 years. On one hand, various derivations in naphthalimide pharmacophores were developed to enhance their DNA binding affinity and antitumor property thereby. Heterocyclic fused naphthalimides, bis-naphthalimides, non-fused substituted naphthalimides and the carboxamide derivatives were synthesized. For example, thio-heterocyclic fused-naphthalimides were designed and evaluated in comparison with their oxo-heterocyclic fused analogues. Extended or created heterocyclebased skeleton were also developed as antitumor agents. On the other hand, we broaden the design strategy of naphthalimide antitumor agents besides DNA intercalation and topo II poison. We have introduced more drug design methods, such as prodrugs, multitarget drugs, computer-aided drug design,photodynamic therapy. For example, we have got naphthalimide derivatives which inhibited topo II and induced LMP by introducing long alkyl chain and polyamines. Several representative compounds were clarified of their antitumor mechanism of action. In all, our research improves the structure diversity of naphthalimide antitumor agents and distinct variances of antitumor targets and mechanism of action.展开更多
基金This work was supported by National Natural Science Foundation of China and Shanghai Science Committee.
文摘Novel perylene bisimide dyes bay-functionalized with naphthalimide chromophores have been prepared conveniently by coupling of 1,8-naphthalimide and dibromoperylene bisimides. Their optical properties were investigated by UV-vis and fluorescence spectroscopy. The absorption spectra of these compounds showed wide spectral responses from 300 to 700 nm, which would be potentials for application as organic solar cells.
基金supported by Tianjin Municipal Science and Technology Commission (09JCYBJC09200)National Key Basic Research and Development Program of China (973 Program, 2007CB914803)
文摘A novel alkynyl substituted N-aryl-1,8-naphthalimide II (C20H11NO2) was synthesized for the discovery and evaluation of new fluorescence probes, and was characterized by X-ray crystal diffraction. It crystallizes in monoclinic, space group P21/n with a = 15.898(3), b = 5.0102(10), c = 17.962(4)A, β = 92.97(3)°, V = 1428.7(5) A^3, Z = 4, Mr = 297.30, Dc = 1.382 g/cm^3, F(000) = 616,/J = 0.090 mm^-1, S = 1.011, the final R = 0.0542 and wR = 0.1204 for 1669 observed reflections with I 〉 2σ(I) and 212 variable parameters. Hydrogen-bounding and n-stacking interactions were discussed. The influence of acetylene group on the fluorescence properties was also investigated. In comparison with N-phenyl-1,8-naphthalimide I (C18H11NO2), few new structure characters and fluorescence properties of the title compound have been found.
基金the National Natural Science Foundation of China(Nos.22225806,22078314,22278394)Dalian Institute of Chemical Physics(Nos.DICPI202227,DICPI202142).
文摘White light emitting systems of pure organic materials have attracted extensive research interest due to their better compatibility and functional scalability.The reported organic white light materials are mainly based on the multi-channel emission regulation of the compound itself or the mixing of multicolor luminescence materials,but studies on the dependence between multicolor luminescence and the external environment are lacking,which limits the application of these materials in areas such as identification and sensing.This paper reports that the 4-or 3?hydroxyl-substituted naphthalimides NapH1 and NapH2 form intermolecular hydrogen bonds with adjacent molecules in the environment,and undergo excited-state intermolecular proton transfer under irradiation,resulting in blue-yellow or blue-red dual fluorescence emission,respectively.Since the two compounds have different two-color luminescence channels and the two-color intensity ratio is affected by the environment,and the intermolecular hydrogen bond is determined by the hydrogen bond receptor,polarity,and temperature in the environment,the full spectrum from blue to red light and white light emission can be obtained by adjusting the mixing ratio of the two dyes and the solvent polarity and the ambient temperature.This environmentally sensitive white emission is used to detect the alkalinity of different papers,and the dyed paper can be used as a test strip for acid-base vapor detection.
基金Supported by the National Natural Science Foundation of China (Grant No. 20536010)Program of Shanghai Subject Chief Scientist (Grant No. 07XD14009)+2 种基金 Shanghai Leading Academic Discipline Project (Grant No. B507)the National High Technology Research and Development Program of China (Grant No. 2006AA10A201)the 111 Project (Grant No. B07023)
文摘A series of compounds 1-11 with different side chains of naphthalimide as fluorescent copper sensors were designed and synthesized. Compounds 1, 9, 10 and 11 presented a high selectivity to Cu2+ in a neutral aqueous environment. Here 1, 9 and 10 showed selectivity and affinity to Cu2+ with an association constant of about ~106. It gave somewhat response to Ag+, Co2+, Ni2+ and Fe2+ while 1 detected copper. 9 and 10 displayed better selectivity by changing their hydrophobic side chains to the hydrophilic ones on imide moieties. 11, with one flexible side chain, showed high selectivity and an association constant (Ka = 2.2 × 108), which were much higher than those of 1, 9 and 10. These results indicated that the selectivity and affinity could be improved by changing side chains of naphthalimide. That might provide a novel strategy or method for the development of fluorescent sensors.
基金financial support from the National Natural Science Foundation of China (Nos.21676113,21772054)Distinguished Young Scholar Program of Hubei Province (No. 2018CFA079)+5 种基金the 111 Project B17019the Scholar Support Program of CCNU (No.0900-31101090002)the Excellent Doctoral Dissertation Cultivation Grant of CCNU from the colleges’ basic research and operation grant (MOE,No.2019YBZZ029)supported by Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules (No. KLSAOFM2012),Hubei University,Chinasupported by excellent doctorial dissertation cultivation grant of CCNU from the colleges’ basic research and operation of MOE (No.2019YBZZ029)A*STAR under its Advanced Manufacturing and Engineering Program (No.A2083c0051)
文摘Understanding the physical mechanisms governing aggregation-induced-emission(AIE)and aggrega-tion-caused-quenching plays a vital role in developing functional AIE materials.In this work,tetraphenylethene(TPE,a classical AiEgen)and naphthalimide(NI,a popular fluorophore with ACQ characteristics)were connected through non-conjugated linkages and conjugated linkages.We showed that the nonconjugated-linkage of TPE to NI fragments leads to substantial PET in molecular aggregates and ACQ.In con trast,the conjugated conn ection between TPE and NI moieties results in the AIE phenomenon by suppressing twisted intramolecular charge transfer.This work provides an important guideline for the rational design of AIE materials.
基金financially supported by NSFC (Nos.21576085 and 21475044)Shanghai Municipal Natural Science Foundation (No.15ZR1409000)
文摘A polarity-sensitive fluorescent probe MNP was rationally designed and synthesized with naphthalimide as the fluorophore and maleimide as the receptor for thiols. MNP is weakly fluorescent due to the photoinduced electron-transfer (PET) from the fluorophore to the receptor, and it displays evidently solvatochromic UV-vis and fluorescence spectra: the emission shifted from 495 nm in n-hexane to 545 nm in phosphate buffer solution. Michael addition reaction between thiols and the maleimide in MNP inhibited the PET process, which led to about eight-fold fluorescence enhancement. In addition, MNP showed highly sensitivity to rnercapto-containing proteins and it could detect as low as 20.4 μg/mL of BSA in PBS. MNP has potential in fluorescent imaging of thiols in living cells.
基金support from National Natural Science Foundation of China (Nos. 21676113, 21402057, 21472059, 81671803)Youth Chen-Guang Project of Wuhan (2016070204010098)+2 种基金the 111 Project B17019the Ministry Province Jointly Constructed Base for State Key Lab-Shenzhen Key Laboratory of Chemical Biology, Shenzhensupported by Self-determined Research Funds of CCNU from the colleges’ basic research and operation of MOE (No. CCNU16A02004)
文摘Developing the novel fluorescent dyes with a larger Stokes shift is still a challenge in the research of fluorescence probes. In this work, a naphthalimide-modified near-infrared cyanine dye with an emission at 785 nm has been synthesized for lysosome-targeting imaging. This fluorescent dye showed a large Stokes shift(up to 165 nm) and favorable lysosome-targeting property, which facilitated it to be a potential candidate for studying of lysosomal functions. The result also indicated that the probe is a promising contrast agent for in vivo imaging in mouse models.
基金Supported by the National Natural Science Foundation of China (Grant No. 20672036) Program for Shanghai Shuguang Project (Grant No. 07SG34)New Century Excellent Talents in University (Grant No. NCET-06-0418)
文摘A novel hydrophilic copolymer P(NI-HEMA) containing the pendant group of naphthalimide moiety has been prepared. In the aqueous buffer solution, its film on the glass substrate shows an obvious fluorescence change and excellent linear relevance in the pH range of 5.8-8.0. Specifically, using the isobestic point at 406 nm as excitation wavelength can avoid the UV irradiation and the tedious calibration process. The film stability and hydrophilicity of copolymer P(NI-HEMA) were studied. Because of the easy synthesis, low price and high linear relevance to pH, the hydrophilic chemosensor film of P(NI- HEMA) could be potentially applied as a low-cost pH indicator for high-throughput bioprocessing in microreactors.
基金the National Natural Science Foundation of China(Nos.21672185 and 21867019)the"Youth Talent of WanRen Project"Foundation of Yunnan Province of China for the financial support"LianDa Scholar Project"and"Graduate Research and Innovation"Foundation of Yunnan Normal University(No.Ysdyjs2019122)。
文摘Iron is one of the essential trace elements in the human body.It plays an important role in human biology and pathology.Deregulation of iron levels in cells is associated with disease development.In this work,we synthesized a novel near-infrared intramolecular charge transfer(ICT)based ratiometric fluorescent probe to detect Fe^(2+),by using naphthalimide and indole moieties as building blocks.Our work showed that the radiometric probe has excellent selectivity,sensitivity and rapid response.Moreover,we could successfully perform real-time monitoring of Fe^(2+) in He La cells and C.elegans.
基金financial support from the National Natural Science Foundation of China (No. 21576085)
文摘Two kinds of fluorescent nano-probes(pH-A and pH-B) with different diameters for the determination of H+concentration, based on photo-induced electron transfer mechanism, were synthesized through click reaction. In which 1,8-naphthalimide was employed as the fluorophore and N,N-dimethylethylenediamine as the receptor. The effects of particle size and linker length on the photophysical properties of the probe were studied. The results revealed that the nano-probes were more sensitive toward pH with increasing particle size. The fluorescence intensity at 529 nm(I529) of the nano-probe p H-A of 120 nm exhibited good linear relationship with solution's pH in the range of 6–8. The probe p H-A displayed excellent selectivity and competition toward proton over other possible coexisted ions, and it could be applied to detect pH in realistic samples(river water, urine).
文摘Technical properties of two naphthalimide based disperse dyes on nylon 6 and polyester fibers were investigated in the presence of urea. The two naphthalimide based disperse dyes were synthesized. The dyes were purified and then fully characterized using 1H-NMR, FTIR and melting point analysis. Dispersion of the dyes was prepared in water and applied on nylon 6 and PET fibers. The dyes offered good build-up properties on the substrates. In order to increase dye adsorption of the substrates, urea was added into the dyebath. By adding urea, the dye adsorption of polyester was increased significantly, while the increase of that of nylon 6 was not marked. The dyes showed good fastness properties on the substrates.
基金This work was financially supported by the National Natural Science Foundation of China (No. 61204020) and the Innovation Program of Shanghai Municipal Ed- ucation Commission (No. 15ZZ047).
文摘Two small molecules named PI-DPP and NI-DPP with a DPP core as the central strong acceptor unit and phthalimide/naphthalimide as the terminal weak acceptor were designed and synthesized. The effects of terminal phthalimide/naphthalimide units on the thermal behavior, optical and electrochemical properties, as well as the photovoltaic performance of these two materials were systematically studied. Cyclic voltammetry revealed that the lowest unoccupied molecular orbitals (LUMO) (- -3.6 eV) of both molecules were intermediate to common electron donor (P3HT) and acceptor (PCBM). This indicated that PI-DPP and NI-DPP may uniquely serve as electron donor when blended with PCBM, and as electron acceptor when blended with P3HT, where sufficient driving forces between DPPs and PCBM, as well as between P3HT and DPPs should be created for exciton dissociation. Using as electron donor materials, PI-DPP and NI-DPP devices exhibited low power conversion efficiencies (PCEs) of 0.90% and 0.76% by blending with PCBM, respectively. And a preliminary evaluation of the potential of the NI-DPP as electron acceptor material was carried out using P3HT as a donor material, and P3HT:NI-DPP device showed a PCE of 0.6%, with an open circuit voltage (Voc) of 0.7 V, a short circuit current density (Jsc) of 1.91 mA·cm^-2, and a fill factor (FF) of 45%.
基金This work was supported by the Beijing Nova Program(Z201100006820049)the National Natural Science Foundation of China(No.21907109).
文摘A nitrone-modified 1,8-naphthalimide was desig ned as a novel bioorthog on alactivated turn-on probe based on strain-promoted alkyne-nitrone cycloadditio n(SPANC).The bioorthog onal cycloadducts were subseque ntly tran sformed into fluoresce nt rearra nge-ment products by photo-accelerati on,which exhibited sign ificant fluoresce nee enhan ceme nt,large stokes shift,and high fluores-cence qua ntum yield.DFT calculati ons were performed to elucidate the fluoresce nee OFF-ON mecha nism.This fluoroge nic strategy was successfully applied to labeling of proteins and visualizing mitochondria in live cells in real time.
基金Project supported by the National Natural Science Foundation of China (No. 90401026) and the Foundation of Scientific Committee of Shanghai.
文摘The naphthalimide derivative. NA1 was synthesized, which consists of a bis(2-(ethylthio)ethyl)amine group binding cations and naphthalimide unit as chromogenic and fluorogenic signaling subunit. Absorption and emission spectra and the effect of polarity of solvents and pH values were studied. The photo-induced electron transfer (PET) occurred from the donor of bis(2-(ethylthio)ethyl)amine group to the naphthalimide fluorophore. The present study demonstrates that NA1 is a viable candidate as a fluorescent receptor for a new Ag^+ ion sensor. This silver ion chemosensor can discriminate Ag^+ ion well among heavy metal ions by an enhancement of the fluorescence intensity in ethanol-water (1 : 9, V : V). And NA1 is also a pH-sensor because the fluorescence of the compound varies with the pH values.
基金the National Key Research and Development Program of China(Nos.2017YFD0200500,2017YFD0201400,2018YFD0200100)the National Natural Science Foundation of China(No.31871959)for the financial support
文摘Insect chitinolyticβ-N-acetyl-D-hexosaminidase,such as OfHex1 from Ostrinia furnacalis,is a potential target for insecticide design.Among the known OfH ex1 inhibitors,Q2 is of great interest because it is the first non-carbohydrate inhibitor.In this study,we designed and synthesized a series of Q2 derivatives by replacing the thiadiazole and naphthalimide groups and changing the linker length.Compound 3 m showed the best inhibitory activity with a Kivalue of 0.34 mmol/L against OfHex1,which is about onequarter that of Q2(K_i=1.4 mmol/L).Compound 6 a showed the best inhibitory activity among the quinoline-containing derivatives(K_i=2.3 mmol/L).Molecular docking indicated that although 3 m,6 a,and Q2 binding the active pocket of OfHex1 in similar mode,compound 3 m engaged better than the other compounds in intermolecular interaction with OfH ex1.
基金supported by the National Natural Science Foundation of China (Nos. 21376038, 21421005 and 21576040)National Basic Research Program of China (No. 2013CB733702)
文摘A ratiometric fluorescent sensor(Hoe-NI) was developed by connecting a nucleus targeted Hoechst unit to a naphthalimide dye via "click chemistry". The sensor achieves high specific nucleus labeling with wash-free staining method in various kinds of living cells. The fluorescence ratio of the two emission bands(450 nm for Hoechst and 505 nm for naphthalimide) is changed sensitively to the variation of DNA concentrations, which provides the quantitative information in the processes of DNA damage induced by hydroxyl radicals and antitumor drug. Therefore, Hoe-NI is a recommendable sensor for the monitoring of nuclear DNA damage that reveals the health status of cells.
基金The authors thank the National Natural Science Foundation of China(Nos.21071105,20902065 and 21176164).
文摘Four 1,8-naphthalimide hydrazone molecules with different electron-donating groups have been applied in the study of linear and nonlinear optical(NLO)properties.These compounds showed strong green emission in solution.Their NLO properties such as two-photon absorption(TPA)behavior with femtosecond laser pulses ca.800 nm and excited-state absorption(ESA)behavior with nanosecond laser pulses at 532 nm were investigated.Compound 4 presented the largest two-photon cross section(550 GM)among them due to two factors:the conjugated length of compound 4 is the longest and the electron-donating ability of compound 4 is the strongest.Different from TPA behavior,compound 2 showed the best nonlinear absorption properties at 532 nm and its nonlinear absorption coef-ficient and third-order nonlinear optical susceptibilitiesχ^(3)were up to 1.41×10^(−10) MKS and 4.65×10^(−12) esu,re-spectively.Through the modification of the structure,the nonlinear optical properties of these compounds at differ-ent wavelengths(532 and 800 nm)were well tuned.The great broad-band nonlinear optical properties indicate hy-drazones are good candidates for organic nonlinear optical absorption materials.
基金supported by the National Natural Science Foundation of China(Nos.21372059 and 21172051)the Hebei Natural Science Foundation(No.B2012201041)the Foundation of Hebei Education Department(No.YQ2013006)
文摘A series of novel naphthalimide derivatives modified by amino acids and their dichloroacetamide derivatives at the 3-position have been synthesized. Their cytotoxic activities were preliminarily evaluated against He/a, A549 and K562 cells, which showed that the length of the side chains of the amino acids influenced the cytotoxic activities. Moreover, compound 7d showed a very good cytotoxic activity against A549 cells with an IC50 value of 4.78 μmol L-1, Furthermore, the UV-vis, fluorescence, and circular dichroism (CD) spectroscopies and thermal denaturation experiment indicated that compounds 6a, 6d and 7a, 7d, as DNA intercalators, exhibited binding affinities with calf-thymus DNA (Ct-DNA).
基金supported by the National Natural Science Foundation of China(No.21301126)the Natural Science Foundation of Shanxi Province,China(Nos.2013021009-3,201701D221038)the Scientific and Technological Innovation Programs of Higher Education and Institutions in Shanxi Province(STIP),China(No.2017128).
文摘Herein,two compounds,4-2′-hydroxybenzylidenehydrazinyl-N-butyl-1,8-naphthalimide(BN-1)and 4-benzylidenehydrazinyl-N-butyl-1,8-naphthalimide(BN-2),were synthesized to explore the hydrogen bonding effect on mechanoresponsive luminescent(MRL).The results showed that compound BN-1 exhibited strong emission in solution and solid-state compared with compound BN-2.After grinding,the emission intensity of compound BN-1 sharply decreased by as much as 15 times with an obvious red-shift from 552 nm to 577 nm.The control compound BN-2,by contrast,did not change so much before and after grinding.Single crystal analysis suggests that BN-1 molecule formed strong intramolecular interaction via-N=N⋯H-O hydrogen bond with a distance of 0.2632 nm.An excited-state intramolecular proton transfer(ESIPT)based fluorophore featured this intramolecular hydrogen bond.The intramolecular hydrogen bond as well as other intermolecular interactions can rigidify the molecular conformation of compound BN-1 in solid-state,and thus suppress the nonradiative pathways,resulting in strong emission.These intra-and intermolecular interactions were destroyed by mechanical stimuli,accompanied by molecular conformation change that decreases the luminescence and blocks the ESIPT process.The MRL process was also demonstrated by scanning electron microscopy and powder X-ray diffraction.The molecular stacking mode changed from crystalline to a disordered amorphous state after grinding.
基金the financial supports from the National Natural Science Foundation of China(No.20536010)National Key Project for Basic Research(No.2003CB114400)the Program of Shanghai Subject Chief Scientist and the Science and Technology Foundation of Shanghai
文摘In this review, we retrospect our progress in biological active naphthalimide and analogues as antitumor agents in the past 20 years. On one hand, various derivations in naphthalimide pharmacophores were developed to enhance their DNA binding affinity and antitumor property thereby. Heterocyclic fused naphthalimides, bis-naphthalimides, non-fused substituted naphthalimides and the carboxamide derivatives were synthesized. For example, thio-heterocyclic fused-naphthalimides were designed and evaluated in comparison with their oxo-heterocyclic fused analogues. Extended or created heterocyclebased skeleton were also developed as antitumor agents. On the other hand, we broaden the design strategy of naphthalimide antitumor agents besides DNA intercalation and topo II poison. We have introduced more drug design methods, such as prodrugs, multitarget drugs, computer-aided drug design,photodynamic therapy. For example, we have got naphthalimide derivatives which inhibited topo II and induced LMP by introducing long alkyl chain and polyamines. Several representative compounds were clarified of their antitumor mechanism of action. In all, our research improves the structure diversity of naphthalimide antitumor agents and distinct variances of antitumor targets and mechanism of action.