Six coordination polymers based on 9,10-di(pyridine-4-yl)-anthracene(DPA)and 1,6-di(1H-imidazol-1-yl)pyrene(DIP)were obtained by solvothermal reactions.{[Zn(DPA)Cl_(2)]·DMF·2H_(2)O}n(1)and{[Zn_(1.5)(DPA)_(1....Six coordination polymers based on 9,10-di(pyridine-4-yl)-anthracene(DPA)and 1,6-di(1H-imidazol-1-yl)pyrene(DIP)were obtained by solvothermal reactions.{[Zn(DPA)Cl_(2)]·DMF·2H_(2)O}n(1)and{[Zn_(1.5)(DPA)_(1.5)Cl_(3)]·5H_(2)O}n(2)are framework isomers,which both contain zigzag chains formed by DPA,Zn^(2+),and Cl-.The zigzag chains in 1 are further assembled by C—H…Cl interactions into layers,and these layers exhibit two different orientations,displaying a rare 2D to 3D interpenetration mode.The zigzag chains in 2 are parallelly arranged.{[Zn_(3)(DPA)_(3)Br_(6)]·2DMF·_(1.5)H_(2)O}n(3)is isostructural to 2.3 was obtained using ZnBr_(2)instead of ZnCl_(2).[M(DPA)(formate)_(2)(H_(2)O)_(2)]n[M=Co(4),Cu(5)]are isostructural,contain chain structures formed by DPA,Cu^(2+)/Co^(2+),and for-mate ions,which were formed in situ in the solvothermal reaction.{[Zn(DIP)_(2)Cl]ClO_(4)}n(6)contains a layer structure formed by DIP and Zn^(2+).Free DPA and DIP ligands exhibited high fluorescence at room temperature,and coordina-tion polymers 3 and 6 displayed enhanced fluorescent emissions.展开更多
We report five coordination polymers(CPs)based on fluorescent ligands[1,6-di(1H-imidazol-1-yl)pyrene(dip),9,10-di(1H-imidazol-1-yl)anthracene(dia)]and anionic ligands[cyclohexane-1,4-dicarboxylic acid(H_(2)cda),campho...We report five coordination polymers(CPs)based on fluorescent ligands[1,6-di(1H-imidazol-1-yl)pyrene(dip),9,10-di(1H-imidazol-1-yl)anthracene(dia)]and anionic ligands[cyclohexane-1,4-dicarboxylic acid(H_(2)cda),camphoric acid(H_(2)cpa)].In[Cd(dip)(cda)]·4H_(2)O}_(n)(1),the Cd^(2+)ions,acting as tetrahedral nodes,are linked by dipand cda^(2-)ligands with four Cd^(2+)ions into five-fold interpenetrating network array of topology of dia.In{[Cd(dip)(cpa)]·4H_(2)O}_(n)(2),the Cd^(2+)ions,acting as a 4-connector,are linked by cpa^(2-)and dip ligands into a 3D framework ofcds topology.In{[Ni(dia)_(2)Cl_(2)]·DMF}_(n)(3),the Ni^(2+)ion is linked by four dia ligands into a layer structure,and 1Dchannels of a cross-section of 1.35 nm×0.96 nm are formed.In{[Cd(dia)_(2)(H_(2)O)_(2)](NO_(3))_(2)·2DMSO}n(4),the dia ligandsconnected Cd^(2+)ions into a 2D layer,and 1D channels are formed between adjacent layers with a cross-section of0.87 nm×0.43 nm.In[Zn(dip)Cl_(2)]_(n)(5),the Zn^(2+)ion is linked by dip ligands into an infinite 1D chain.The infrared,thermal gravimetric,and fluorescent emission data were collected and analyzed for these coordination polymers.CCDC:2356055,1;2440075,2;2356057,3;2356057,4;2356059,5.展开更多
The synergistic effect of Se with Fe can enhance the catalytic activities of the system for oxidation reactions.Based on this principle,a series of Se/Fe materials have been invented to develop the heterogeneous catal...The synergistic effect of Se with Fe can enhance the catalytic activities of the system for oxidation reactions.Based on this principle,a series of Se/Fe materials have been invented to develop the heterogeneous catalysts with industrial application potential.However,the present methods suffer from the tedious procedures,the high reaction temperature,and the low synthetic efficiency.In this paper,we report the synthesis of Se/Fe materials just by precipitating Fe(NO_(3))_(3)with the in situ prepared aqueous NaSe/NaSeO_(3)under mild conditions.The concise method may resolve the issues hindering the large-scale applications of Se/Fe materials.展开更多
Synthesizing highly efficient,low-toxicity catalysts for the remediation of polycyclic aromatic hydrocarbons(PAHs)contaminated soils is crucial.Nanoscale zero-valent iron(n-ZVI)is widely used in the treatment of pollut...Synthesizing highly efficient,low-toxicity catalysts for the remediation of polycyclic aromatic hydrocarbons(PAHs)contaminated soils is crucial.Nanoscale zero-valent iron(n-ZVI)is widely used in the treatment of pollutants due to its high catalytic activity.However,n-ZVI is prone to aggregation and passivation.Therefore,to design an environmentally friendly,efficient,and practical catalyst material,this study designed a nanoscale zero-valent iron-loaded biochar(BC)polyacrylic acid(PAA)composite materials.Biochar and polyacrylic acid can prevent the ag-gregation of zero-valent iron and provide a large number of functional groups.The iron on the carrier is uniformly distributed,exposing active sites and activating persulfate to remove anthracene(ANT)pollutants from the soil.The BC/PAA/Fe0 system can achieve an anthracene degradation efficiency of 93.7%in soil,and the degradation efficiency of anthracene remains around 90%under both acidic and alkaline con-$$ditions.Free radical capture experiments indicate that the degradation of anthracene proceeds through the radical pathways SO4,$OH,O2 and the non-radical pathway 1O2.In addition,possible degradation pathways for anthracene have been proposed.Plant planting experiments have shown that the catalyst designed in this study has low toxicity and has excellent application prospects in thefield of soil remediation.展开更多
Metal-organic frameworks(MOFs)containing face-to-faceπ-πinteracting anthracene groups are promising photoresponsive materials because of their rich photophysical properties and their ability to undergo reversible[4+...Metal-organic frameworks(MOFs)containing face-to-faceπ-πinteracting anthracene groups are promising photoresponsive materials because of their rich photophysical properties and their ability to undergo reversible[4+4]photocycloaddition reaction,but it is extremely challenging to obtain such materials.Herein,we propose a generalized method to accomplish photoresponsive MOFs by introducing anthracene pairs into the framework of the dianthracene-phosphonate-based MOFs by controlling the synthesis temperature.Compounds Dy_(2)(ampH)_(2x)(amp2H_(2))_(3-x)(H_(2)O)_(6)·4H_(2)O[x=0.01,Dy-70;x=0.02,Dy-80;x=0.037,Dy-90;amp_(2)H_(4)=pre-photodimerized 9-anthracenemethylphosphonic acid(amp H_(2))]were obtained by the reaction of DyCl_(3)and amp_(2)H_(4)in water at 70,80,and 90℃,respectively.They all show excimer emission of paired anthracenes at ca.555 nm.Detailed studies of Dy-90 have shown that it undergoes a reversible photodimerization reaction under 365 nm and then 280 nm illumination,accompanied by luminescence changes.This property further enables Dy-90 to be used for optical anti-counterfeiting.展开更多
MoS_2 samples with controllable morphologies and structures were synthesized using surfactantassisted hydrothermal processes.The effects of surfactants（PEG,PVP,P123,SDS,AOT,and CTAB）on the morphologies and structure...MoS_2 samples with controllable morphologies and structures were synthesized using surfactantassisted hydrothermal processes.The effects of surfactants（PEG,PVP,P123,SDS,AOT,and CTAB）on the morphologies and structures of MoS_2 samples were investigated.The results revealed that spherical,bulk-like,and flower-like MoS_2 particles assembled by NH4~＋-intercalated MoS_2 nano-sheets were synthesized.The morphologies of the MoS_2 samples and their structures（including the slab length and the number of stacked layers） of MoS_2 nano-sheets in these samples could be controlled by adjusting the surfactants.Mono-dispersed spherical MoS_2 particles could be synthesized with PEG via the creation of MoS_2 nano-sheets with slab lengths shorter than 15 nm and fewer than six stacked layers.Possible formation mechanisms of these MoS_2 samples created via surfactant-assisted hydrothermal processes are proposed.Further,the catalytic activities of MoS_2 samples for anthracene hydrogenation were evaluated in a slurry-bed reactor.The catalyst synthesized with the surfactant PEG exhibited the highest catalytic hydrogenation activity.Compared with the other catalysts,it had a smaller particle size,mono-dispersed spherical morphology,shorter slab length,and fewer stacked layers;these were all beneficial to exposing its active edges.This work provides an efficient approach to synthesize transition metal sulfides with controllable morphologies and structures.展开更多
Interlayer energy transfer between 2, 3-naphtho-10-hexadecylaza-15-crown-5 (NC16) and N-[1-(9-methoxyanthryl)]decylaza-15-crown-5 (A10C) within multilayer Langmuir-Blodgett films has been studied by steady-state fluor...Interlayer energy transfer between 2, 3-naphtho-10-hexadecylaza-15-crown-5 (NC16) and N-[1-(9-methoxyanthryl)]decylaza-15-crown-5 (A10C) within multilayer Langmuir-Blodgett films has been studied by steady-state fluorescence spectra. The donor and acceptor could be separated precisely by inserting stearic acid (SA) spacers. The efficiency of the energy transfer increases with the decrease in the donor-acceptor distance by a quadratic manner, suggesting the donor excitations are delocalized in the layer.展开更多
Polycyclic aromatic hydrocarbons(PAHs) are common contaminants in a municipal solid waste(MSW) composting site.Knowledge of changes in microbial structure is useful to identify particular PAH degraders.However,the mic...Polycyclic aromatic hydrocarbons(PAHs) are common contaminants in a municipal solid waste(MSW) composting site.Knowledge of changes in microbial structure is useful to identify particular PAH degraders.However,the microbial community in the MSW composting soil and its change associated with prolonged exposure to PAHs and subsequent biodegradation remain largely unknown.In this study,anthracene was selected as a model compound.The bacterial community structure was investigated using terminal restriction fragment length polymorphism(TRFLP) and 16S rRNA gene clone library analysis.The two bimolecular tools revealed a large shift of bacterial community structure after anthracene amendment and subsequent biodegradation.Genera Methylophilus,Mesorhizobium,and Terrimonas had potential links to anthracene biodegradation,suggesting a consortium playing an active role.展开更多
Ultrasonic-assisted extraction(UAE)combined with medium pressure liquid chromatography(MPLC)was designed for carbazole separation from anthracene slag(AS).The effects of liquid/solid ratio,temperature,and extraction t...Ultrasonic-assisted extraction(UAE)combined with medium pressure liquid chromatography(MPLC)was designed for carbazole separation from anthracene slag(AS).The effects of liquid/solid ratio,temperature,and extraction times on carbazole separation were investigated.When using CC14 and ethyl acetate as extraction solvents and combining with MPLC,carbazole recovery and purity are 75.1%and 95.4%,respectively.The mechanism for carbazole separation were presumed by examining intermolecular interactions such as N-H…π,π-π,and C-Cl…πinteractions.These results demonstrate that UAE/MPLC has a considerable potential as a green and promising strategy for separating and purifying carbazole and other chemicals from AS.展开更多
The photo-induced electron transfer reactions of anthracene with N,N -diethylaniline(DEA) and phenothiazine(PTZ) occur in the membrane phase of a Triton X-100/ n -C 10 H 21 OH(1-decanol)/H 2O microemulsion. DEA and PT...The photo-induced electron transfer reactions of anthracene with N,N -diethylaniline(DEA) and phenothiazine(PTZ) occur in the membrane phase of a Triton X-100/ n -C 10 H 21 OH(1-decanol)/H 2O microemulsion. DEA and PTZ exist in the membrane phase of the microemulsion. Anthracene exists in the oil continuous phase of the W/O microemulsion and in the oil core and membrane phase of the O/W microemulsion.展开更多
The reactions of gas-phase anthracene and suspended anthracene particles with O3 and O3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol （SOA） formations from gas-phase reac...The reactions of gas-phase anthracene and suspended anthracene particles with O3 and O3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol （SOA） formations from gas-phase reactions of anthracene with O3 and O3-NO were observed. Meanwhile, the size distributions and mass concentrations of SOA were monitored with a scanning mobility particle sizer （SMPS） during the formation processes. The rapid exponential growths of SOA reveal that the atmospheric lifetimes of gas-phase anthracene towards O3 and O3-NO are less than 20.5 and 4.34 hr, respectively. The particulate oxidation products from homogeneous and heterogeneous reactions were analyzed with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer （VUV-ATOFMS）. Gas chromatograph/mass spectrometer （GC/MS） analyses of oxidation products of anthracene were carried out for assigning the time-of-flight （TOF） mass spectra of products from homogeneous and heterogeneous reactions. Anthrone, anthraquinone, 9,10- dihydroxyanthracene, and 1,9,10-trihydroxyanthracene were the ozonation products of anthracene, while anthrone, anthraquinone, 9-nitroanthracene, and 1,8-dihydroxyanthraquinone were the main products of anthracene with O3-NO.展开更多
Surfactants, such as non-ionic Surfynol 485 （ethoxylated 2,4,7,9-tetramethyl-5-decyne-4,7-diol）, have been applied to accelerate removal of polycyclic aromatic hydrocarbons from soil. This study investigated the dis...Surfactants, such as non-ionic Surfynol 485 （ethoxylated 2,4,7,9-tetramethyl-5-decyne-4,7-diol）, have been applied to accelerate removal of polycyclic aromatic hydrocarbons from soil. This study investigated the dissipation of anthracene, and carbon （C） and nitrogen （N） mineralization in soil amended with non-ionic Surfynol 485 at different rates. Soil samples of a Typic Fragiudept taken from Otumba, Mexico were spiked with anthracene at a final concentration of 520 mg kg^-1 dry soil using acetone as solvent, amended with 0.0, 24.9, 49.8 or 124.4 g kg^-1 soil of the surfactant and incubated in the laboratory. The soil not amended with anthracene, acetone and the surfactant was used as a control. Dynamics of C and N and the concentration of anthracene were monitored for 56 d. After 56 d of incubation, 38% of the anthracene was removed from the unamended soil, and 47%, 55% and 66% of the anthracene were removed when 24.9, 49.8 and 124.4 g kg^-1 of the surfactant were applied, respectively. Application of acetone, anthracene or surfactant increased the emission of CO2, but decreased the mineral N compared to the unamended control. Applying the surfactant to the acetone or anthracene-amended soil reduced emission of CO2, but increased the mineral N at the lower application rates of the surfactant. It was found that the application of the non-ionic surfactant increased the bioavailability of anthracene and thus its removal from soil, increased C mineralization, but decreased N miaeralization. Consequently, the application of non-ionic surfactant could be easily used to accelerate the removal of pollutants from hydrocarbon-contaminated soils, but mineral N in the soil would decrease, which might inhibit plant growth.展开更多
Two species of marine phytoplankton, Platymonas helgolandica var. tsingtaoensis and Heterosigma akashiwo, were cul- tivated in bi-algal cultures to investigate the effect of anthracene （ANT） on the interaction betwe...Two species of marine phytoplankton, Platymonas helgolandica var. tsingtaoensis and Heterosigma akashiwo, were cul- tivated in bi-algal cultures to investigate the effect of anthracene （ANT） on the interaction between them. Without ANT, H. akashiwo out-competed P. helgolandica at low initial biomass ratios （P. helgolandica （P）： H. akashiwo （H） = 1：4 and 1 ： 1）, but not at the highest （P：H=4：I）. This observation was consistent with the description in Lotka-Volterra two species competition model. It was found that P. helgolandica was excluded at low initial biomass ratios, while the unstable equilibrium between two species was predicted at the highest. For both species, carrying capacity and maximal specific growth rate decreased in bi-algal cultures compared to those in monocultures. H. akashiwo exhibited a higher sensitivity to ANT than P helgolandica. This resulted markedly in a reduced cell den- sity of H. akashiwo but an increased cell density ofP. helgolandica. Carrying capacity ofP. helgolandica was consistently higher in bi-algal cultures with ANT than those without ANT, suggesting that ANT, through the elimination of H. akashiwo, generated the dominance of P helgolandica independently of initial biomass ratios. This study showed a density-dependent effect of harmful alga （H. akashiwo） on dietary alga （P helgolandica）, and indicated that ocean pollutant ANT could induce the succession of marine phytoplankton.展开更多
Carbazole is an irreplaceable basic organic chemical raw material and intermediate in industry.The separation of carbazole from anthracene oil by environmental benign solvents is important but still a challenge in che...Carbazole is an irreplaceable basic organic chemical raw material and intermediate in industry.The separation of carbazole from anthracene oil by environmental benign solvents is important but still a challenge in chemical engineering.Deep eutectic solvents (DESs) as a sustainable green separation solvent have been proposed for the separation of carbazole from model anthracene oil.In this research,three quaternary ammonium-based DESs were prepared using ethylene glycol (EG) as hydrogen bond donor and tetrabutylammonium chloride (TBAC),tetrabutylammonium bromide or choline chloride as hydrogen bond acceptors.To explore their extraction performance of carbazole,the conductor-like screening model for real solvents (COSMO-RS) model was used to predict the activity coefficient at infinite dilution (γ^(∞)) of carbazole in DESs,and the result indicated TBAC:EG (1:2) had the stronger extraction ability for carbazole due to the higher capacity at infinite dilution (C^(∞)) value.Then,the separation performance of these three DESs was evaluated by experiments,and the experimental results were in good agreement with the COSMO-RS prediction results.The TBAC:EG (1:2) was determined as the most promising solvent.Additionally,the extraction conditions of TBAC:EG (1:2) were optimized,and the extraction efficiency,distribution coefficient and selectivity of carbazole could reach up to 85.74%,30.18 and 66.10%,respectively.Moreover,the TBAC:EG (1:2) could be recycled by using environmentally friendly water as antisolvent.In addition,the separation performance of TBAC:EG (1:2) was also evaluated by real crude anthracene,the carbazole was obtained with purity and yield of 85.32%,60.27%,respectively.Lastly,the extraction mechanism was elucidated byσ-profiles and interaction energy analysis.Theoretical calculation results showed that the main driving force for the extraction process was the hydrogen bonding ((N–H...Cl) and van der Waals interactions (C–H...O and C–H...π),which corresponding to the blue and green isosurfaces in IGMH analysis.This work presented a novel method for separating carbazole from crude anthracene oil,and will provide an important reference for the separation of other high value-added products from coal tar.展开更多
Microporous hypercross-linked conjugated quinonoid chromophores represent a novel class of amorphous polymers, synthesized by the reaction of anthracene with dimethoxy methane in the presence of FeCl3 catalyst. Their ...Microporous hypercross-linked conjugated quinonoid chromophores represent a novel class of amorphous polymers, synthesized by the reaction of anthracene with dimethoxy methane in the presence of FeCl3 catalyst. Their N2 adsorption isotherms confirm their microporous nature. Diffuse reflectance UV-Visible（DRS UV-Vis） spectroscopy confirms their matrix built with the conjugated quinonoids by their broad light absorption characteristics extending from 1000 nm to 200 nm with the absorbance maximum close to 400 nm. The catalyst cross-linked anthracene with ―CH2― bridges and subsequently dehydrogenating them to form quinonoids. Their Fourier transform infrared（FTIR） spectra showed their characteristic quinonoid vibrations between 1600 and 1700 cm-1. The synthesis of polymers was carried out at 30, 40, 50, 60, 70 and 80 ℃, but the quinonoid content of the polymer obtained at 80 ℃ was higher than that of the others. Their scanning electron microscopy（SEM） images showed microspheres of 1 to 5 μm size built with tiny particles. Their surfaces were not smooth. The polymer synthesized at 80 ℃ showed 5.1 wt% CO2 sorption at 25 ℃ and 0.1 MPa, but when it was recross-linked, the CO2 sorption increased to 8 wt%. Hence, hypercross-linked conjugated quinonoid chromophores of anthracene are good for sorption of CO2.展开更多
This study presents a facile strategy for the formation of highly substituted butterfly 1,4-adducts/9,10-adducts via the Diels-Alder reaction of benzyne intermediates.The method achieves very good to excellent yields ...This study presents a facile strategy for the formation of highly substituted butterfly 1,4-adducts/9,10-adducts via the Diels-Alder reaction of benzyne intermediates.The method achieves very good to excellent yields of the respective anthracene derivative s under mild conditions.This practical protocol is compatible with a variety of sensitive functional groups and provides access to difunctionalized bridge 1,4-adducts/9,10-adducts.展开更多
In situ formation of composite micro-mesoporous dendritic fibrous nano-silica(DFNS) and Al-DFNS was prepared using a cetylpyridinium bromide(CPB) template synthetic system. Dealumination is induced by impregnation of ...In situ formation of composite micro-mesoporous dendritic fibrous nano-silica(DFNS) and Al-DFNS was prepared using a cetylpyridinium bromide(CPB) template synthetic system. Dealumination is induced by impregnation of zirconium with flux followed by a sulfuric acid treatment. This procedure results in a series of highly uniform nano-spheres, which exhibit stronger acid property than that of Al-MCM-41. In the selective alkylation of anthracene with tert–amyl alcohol, SO_(4)^(2-)modified Zr-contained dealuminated Al-DFNS(SZ-De Al-DFNS) shows great catalytic activity and higher conversion(60.8%). The DFNS samples were characterized with XRD, SEM, TEM, NH_(3)-TPD and other techniques. The results reveal that DFNSs consist of center-radial micro-mesopores and that the acid contribution of SZ-De Al-DFNS is much broader,as compared with amorphous aluminosilicate.展开更多
Objective: To establish a mouse model of skin squamous cell carcinoma induced by high dose 7, 12-dimethyl-benzodiazepine [a] anthracene, and to provide experimental basis for the prevention and treatment of skin squam...Objective: To establish a mouse model of skin squamous cell carcinoma induced by high dose 7, 12-dimethyl-benzodiazepine [a] anthracene, and to provide experimental basis for the prevention and treatment of skin squamous cell carcinoma. Methods: 36 BALB/c mice were randomly divided into 3 groups, respectively is: the high dose group (group A), low dose group (group B), and blank control group (group c), recorded in the process of building body weight in mice, and skin changes back, local skin tissue for building after HE staining of PCNA immunohistochemical staining, and the expression of PCNA positive staining level as reflected in mice skin squamous cell carcinoma of the malignant indicators, using the Image Pro Plus calculation PCNA staining of integral optical density (IOD) and positive area, and the results were statistically analyzed. Results: at 12 weeks, there were statistically significant differences in tumor number and tumor volume between group A and group B (P<0.05), and the tumor bearing rate was up to 83.3% and 66.7%, and the incidence of SCC was up to 75% and 33.3%. Immunohistochemical analysis showed statistical differences in IOD and positive area of mice in groups A, B and C (P<0.01). Conclusion: compared with the mouse model of skin squamous cell carcinoma established by the traditional two-stage protocol, this model has the characteristics of shorter experimental period, higher tumor formation rate and easier operation, providing a reliable experimental basis for the study of skin squamous cell carcinoma.展开更多
To harvest the sun light and to promote the amount of energy stored,a new binary compound which links a sensitizer(electron donor), anthracene,and substrate(electron acceptor),norbornadiene,in a non- conjugated manner...To harvest the sun light and to promote the amount of energy stored,a new binary compound which links a sensitizer(electron donor), anthracene,and substrate(electron acceptor),norbornadiene,in a non- conjugated manner without increase in molecular weight was synthesized.The inter-and intramolecular photosensitized isomerization and the mechanism were studied.展开更多
Aggregation-induced emission-active 4-（3,4,5-bis（octyloxy）phenyl-9-anthracene acylhydrazone （AHP- T8） has been designed and synthesized, and the photo-responsive properties of organogel and xerogel irradiated by ...Aggregation-induced emission-active 4-（3,4,5-bis（octyloxy）phenyl-9-anthracene acylhydrazone （AHP- T8） has been designed and synthesized, and the photo-responsive properties of organogel and xerogel irradiated by visible light were investigated systematically. AHP-T8 can form thermo-reversible gels in some of the tested solvents. The enhanced fluorescence emission has been observed after gelation although the dilute solution of AHP-T8 was almost non-fluorescent. When the organogel was exposed under visible light, the gel-sol phase transition occurred, and the corresponding morphology, fluorescence intensity, intermolecular hydrogen bonding and the structure all changed. In addition, the xerogel is more sensitive to visible light than that of organogel. The photoresponsive behaviour of AHP-T8 upon irradiation by visible light was demonstrated to be due to the E-Z isomerizations of -C=N-group. rather than the photodimerization of anthracene groups展开更多
文摘Six coordination polymers based on 9,10-di(pyridine-4-yl)-anthracene(DPA)and 1,6-di(1H-imidazol-1-yl)pyrene(DIP)were obtained by solvothermal reactions.{[Zn(DPA)Cl_(2)]·DMF·2H_(2)O}n(1)and{[Zn_(1.5)(DPA)_(1.5)Cl_(3)]·5H_(2)O}n(2)are framework isomers,which both contain zigzag chains formed by DPA,Zn^(2+),and Cl-.The zigzag chains in 1 are further assembled by C—H…Cl interactions into layers,and these layers exhibit two different orientations,displaying a rare 2D to 3D interpenetration mode.The zigzag chains in 2 are parallelly arranged.{[Zn_(3)(DPA)_(3)Br_(6)]·2DMF·_(1.5)H_(2)O}n(3)is isostructural to 2.3 was obtained using ZnBr_(2)instead of ZnCl_(2).[M(DPA)(formate)_(2)(H_(2)O)_(2)]n[M=Co(4),Cu(5)]are isostructural,contain chain structures formed by DPA,Cu^(2+)/Co^(2+),and for-mate ions,which were formed in situ in the solvothermal reaction.{[Zn(DIP)_(2)Cl]ClO_(4)}n(6)contains a layer structure formed by DIP and Zn^(2+).Free DPA and DIP ligands exhibited high fluorescence at room temperature,and coordina-tion polymers 3 and 6 displayed enhanced fluorescent emissions.
文摘We report five coordination polymers(CPs)based on fluorescent ligands[1,6-di(1H-imidazol-1-yl)pyrene(dip),9,10-di(1H-imidazol-1-yl)anthracene(dia)]and anionic ligands[cyclohexane-1,4-dicarboxylic acid(H_(2)cda),camphoric acid(H_(2)cpa)].In[Cd(dip)(cda)]·4H_(2)O}_(n)(1),the Cd^(2+)ions,acting as tetrahedral nodes,are linked by dipand cda^(2-)ligands with four Cd^(2+)ions into five-fold interpenetrating network array of topology of dia.In{[Cd(dip)(cpa)]·4H_(2)O}_(n)(2),the Cd^(2+)ions,acting as a 4-connector,are linked by cpa^(2-)and dip ligands into a 3D framework ofcds topology.In{[Ni(dia)_(2)Cl_(2)]·DMF}_(n)(3),the Ni^(2+)ion is linked by four dia ligands into a layer structure,and 1Dchannels of a cross-section of 1.35 nm×0.96 nm are formed.In{[Cd(dia)_(2)(H_(2)O)_(2)](NO_(3))_(2)·2DMSO}n(4),the dia ligandsconnected Cd^(2+)ions into a 2D layer,and 1D channels are formed between adjacent layers with a cross-section of0.87 nm×0.43 nm.In[Zn(dip)Cl_(2)]_(n)(5),the Zn^(2+)ion is linked by dip ligands into an infinite 1D chain.The infrared,thermal gravimetric,and fluorescent emission data were collected and analyzed for these coordination polymers.CCDC:2356055,1;2440075,2;2356057,3;2356057,4;2356059,5.
基金the Jiangsu Provincial Six Talent Peaks Project(No.XCL-090)the Cooperation Project of Yangzhou City with Yangzhou University(No.YZ2023209)+1 种基金Jiaxing Key Laboratory for Creation of Animal Models&Synthesis of Lead Compounds of New Drug(No.jxsz21006)the Priority Academic Program Development of Jiangsu Higher Education Institutions for support。
文摘The synergistic effect of Se with Fe can enhance the catalytic activities of the system for oxidation reactions.Based on this principle,a series of Se/Fe materials have been invented to develop the heterogeneous catalysts with industrial application potential.However,the present methods suffer from the tedious procedures,the high reaction temperature,and the low synthetic efficiency.In this paper,we report the synthesis of Se/Fe materials just by precipitating Fe(NO_(3))_(3)with the in situ prepared aqueous NaSe/NaSeO_(3)under mild conditions.The concise method may resolve the issues hindering the large-scale applications of Se/Fe materials.
基金support provided by the National Natural Science Foundation of China(22478267,22438009,U24A20535)Basic Research Program of Jiangsu province(BK20243002)+1 种基金Prospective Application Research Project of Suzhou(SYC2022042)the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD).
文摘Synthesizing highly efficient,low-toxicity catalysts for the remediation of polycyclic aromatic hydrocarbons(PAHs)contaminated soils is crucial.Nanoscale zero-valent iron(n-ZVI)is widely used in the treatment of pollutants due to its high catalytic activity.However,n-ZVI is prone to aggregation and passivation.Therefore,to design an environmentally friendly,efficient,and practical catalyst material,this study designed a nanoscale zero-valent iron-loaded biochar(BC)polyacrylic acid(PAA)composite materials.Biochar and polyacrylic acid can prevent the ag-gregation of zero-valent iron and provide a large number of functional groups.The iron on the carrier is uniformly distributed,exposing active sites and activating persulfate to remove anthracene(ANT)pollutants from the soil.The BC/PAA/Fe0 system can achieve an anthracene degradation efficiency of 93.7%in soil,and the degradation efficiency of anthracene remains around 90%under both acidic and alkaline con-$$ditions.Free radical capture experiments indicate that the degradation of anthracene proceeds through the radical pathways SO4,$OH,O2 and the non-radical pathway 1O2.In addition,possible degradation pathways for anthracene have been proposed.Plant planting experiments have shown that the catalyst designed in this study has low toxicity and has excellent application prospects in thefield of soil remediation.
基金supported by grants from the National Natural Science Foundation of China(Nos.22273037,21731003)。
文摘Metal-organic frameworks(MOFs)containing face-to-faceπ-πinteracting anthracene groups are promising photoresponsive materials because of their rich photophysical properties and their ability to undergo reversible[4+4]photocycloaddition reaction,but it is extremely challenging to obtain such materials.Herein,we propose a generalized method to accomplish photoresponsive MOFs by introducing anthracene pairs into the framework of the dianthracene-phosphonate-based MOFs by controlling the synthesis temperature.Compounds Dy_(2)(ampH)_(2x)(amp2H_(2))_(3-x)(H_(2)O)_(6)·4H_(2)O[x=0.01,Dy-70;x=0.02,Dy-80;x=0.037,Dy-90;amp_(2)H_(4)=pre-photodimerized 9-anthracenemethylphosphonic acid(amp H_(2))]were obtained by the reaction of DyCl_(3)and amp_(2)H_(4)in water at 70,80,and 90℃,respectively.They all show excimer emission of paired anthracenes at ca.555 nm.Detailed studies of Dy-90 have shown that it undergoes a reversible photodimerization reaction under 365 nm and then 280 nm illumination,accompanied by luminescence changes.This property further enables Dy-90 to be used for optical anti-counterfeiting.
基金supported by the National Natural Science Foundation of China(21303186)the Strategic Priority Research Program of the Chinese Academy of Sciences(XDA07020300)~~
文摘MoS_2 samples with controllable morphologies and structures were synthesized using surfactantassisted hydrothermal processes.The effects of surfactants（PEG,PVP,P123,SDS,AOT,and CTAB）on the morphologies and structures of MoS_2 samples were investigated.The results revealed that spherical,bulk-like,and flower-like MoS_2 particles assembled by NH4~＋-intercalated MoS_2 nano-sheets were synthesized.The morphologies of the MoS_2 samples and their structures（including the slab length and the number of stacked layers） of MoS_2 nano-sheets in these samples could be controlled by adjusting the surfactants.Mono-dispersed spherical MoS_2 particles could be synthesized with PEG via the creation of MoS_2 nano-sheets with slab lengths shorter than 15 nm and fewer than six stacked layers.Possible formation mechanisms of these MoS_2 samples created via surfactant-assisted hydrothermal processes are proposed.Further,the catalytic activities of MoS_2 samples for anthracene hydrogenation were evaluated in a slurry-bed reactor.The catalyst synthesized with the surfactant PEG exhibited the highest catalytic hydrogenation activity.Compared with the other catalysts,it had a smaller particle size,mono-dispersed spherical morphology,shorter slab length,and fewer stacked layers;these were all beneficial to exposing its active edges.This work provides an efficient approach to synthesize transition metal sulfides with controllable morphologies and structures.
基金Financial support fron he National Key Project on Fundamental Research and Development(Grant No.G2000078104 and G2000077502)the National Natural Science Foundation of China is grateful
文摘Interlayer energy transfer between 2, 3-naphtho-10-hexadecylaza-15-crown-5 (NC16) and N-[1-(9-methoxyanthryl)]decylaza-15-crown-5 (A10C) within multilayer Langmuir-Blodgett films has been studied by steady-state fluorescence spectra. The donor and acceptor could be separated precisely by inserting stearic acid (SA) spacers. The efficiency of the energy transfer increases with the decrease in the donor-acceptor distance by a quadratic manner, suggesting the donor excitations are delocalized in the layer.
基金Project (No. 50979002) supported by the National Natural Science Foundation of China
文摘Polycyclic aromatic hydrocarbons(PAHs) are common contaminants in a municipal solid waste(MSW) composting site.Knowledge of changes in microbial structure is useful to identify particular PAH degraders.However,the microbial community in the MSW composting soil and its change associated with prolonged exposure to PAHs and subsequent biodegradation remain largely unknown.In this study,anthracene was selected as a model compound.The bacterial community structure was investigated using terminal restriction fragment length polymorphism(TRFLP) and 16S rRNA gene clone library analysis.The two bimolecular tools revealed a large shift of bacterial community structure after anthracene amendment and subsequent biodegradation.Genera Methylophilus,Mesorhizobium,and Terrimonas had potential links to anthracene biodegradation,suggesting a consortium playing an active role.
基金Supported by the Key Project of Joint Fund for the research on Coal-Based Low Carbon Technology from National Natural Science Foundation of China and the Government of Shanxi(U1610223)Coal-based Key Scientific and Technological Projects of Shanxi Province(MJH2014-15)the National Key Research and Development Program of China(2018YFB0604602).
文摘Ultrasonic-assisted extraction(UAE)combined with medium pressure liquid chromatography(MPLC)was designed for carbazole separation from anthracene slag(AS).The effects of liquid/solid ratio,temperature,and extraction times on carbazole separation were investigated.When using CC14 and ethyl acetate as extraction solvents and combining with MPLC,carbazole recovery and purity are 75.1%and 95.4%,respectively.The mechanism for carbazole separation were presumed by examining intermolecular interactions such as N-H…π,π-π,and C-Cl…πinteractions.These results demonstrate that UAE/MPLC has a considerable potential as a green and promising strategy for separating and purifying carbazole and other chemicals from AS.
基金Supported by the National Natural Science Foundation of China( No.2 0 0 730 38,2 0 2 330 10 )
文摘The photo-induced electron transfer reactions of anthracene with N,N -diethylaniline(DEA) and phenothiazine(PTZ) occur in the membrane phase of a Triton X-100/ n -C 10 H 21 OH(1-decanol)/H 2O microemulsion. DEA and PTZ exist in the membrane phase of the microemulsion. Anthracene exists in the oil continuous phase of the W/O microemulsion and in the oil core and membrane phase of the O/W microemulsion.
基金supported by the funding for Creative Research Groups of China (No. 50921064)the China Postdoctoral Science Foundation Funded Project (No. 2011M500433)the President Fund of GUCAS (No. Y25102GN00)
文摘The reactions of gas-phase anthracene and suspended anthracene particles with O3 and O3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol （SOA） formations from gas-phase reactions of anthracene with O3 and O3-NO were observed. Meanwhile, the size distributions and mass concentrations of SOA were monitored with a scanning mobility particle sizer （SMPS） during the formation processes. The rapid exponential growths of SOA reveal that the atmospheric lifetimes of gas-phase anthracene towards O3 and O3-NO are less than 20.5 and 4.34 hr, respectively. The particulate oxidation products from homogeneous and heterogeneous reactions were analyzed with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer （VUV-ATOFMS）. Gas chromatograph/mass spectrometer （GC/MS） analyses of oxidation products of anthracene were carried out for assigning the time-of-flight （TOF） mass spectra of products from homogeneous and heterogeneous reactions. Anthrone, anthraquinone, 9,10- dihydroxyanthracene, and 1,9,10-trihydroxyanthracene were the ozonation products of anthracene, while anthrone, anthraquinone, 9-nitroanthracene, and 1,8-dihydroxyanthraquinone were the main products of anthracene with O3-NO.
基金Supported by Cinvestav,M'exico,Consejo Nacional de Ciencia y Tecnología(CONACy T),Mexico and Sistema Nacional de Investigadores(SNI),Mexico
文摘Surfactants, such as non-ionic Surfynol 485 （ethoxylated 2,4,7,9-tetramethyl-5-decyne-4,7-diol）, have been applied to accelerate removal of polycyclic aromatic hydrocarbons from soil. This study investigated the dissipation of anthracene, and carbon （C） and nitrogen （N） mineralization in soil amended with non-ionic Surfynol 485 at different rates. Soil samples of a Typic Fragiudept taken from Otumba, Mexico were spiked with anthracene at a final concentration of 520 mg kg^-1 dry soil using acetone as solvent, amended with 0.0, 24.9, 49.8 or 124.4 g kg^-1 soil of the surfactant and incubated in the laboratory. The soil not amended with anthracene, acetone and the surfactant was used as a control. Dynamics of C and N and the concentration of anthracene were monitored for 56 d. After 56 d of incubation, 38% of the anthracene was removed from the unamended soil, and 47%, 55% and 66% of the anthracene were removed when 24.9, 49.8 and 124.4 g kg^-1 of the surfactant were applied, respectively. Application of acetone, anthracene or surfactant increased the emission of CO2, but decreased the mineral N compared to the unamended control. Applying the surfactant to the acetone or anthracene-amended soil reduced emission of CO2, but increased the mineral N at the lower application rates of the surfactant. It was found that the application of the non-ionic surfactant increased the bioavailability of anthracene and thus its removal from soil, increased C mineralization, but decreased N miaeralization. Consequently, the application of non-ionic surfactant could be easily used to accelerate the removal of pollutants from hydrocarbon-contaminated soils, but mineral N in the soil would decrease, which might inhibit plant growth.
基金supported by the Ocean Public Welfare Scientific Research Projects, State Oceanic Administration People’s Republic of China (Grant Nos. 200905020, 2010225007, and 201305009)the National Natural Science Foundation of China (Grant No. 31070458)
文摘Two species of marine phytoplankton, Platymonas helgolandica var. tsingtaoensis and Heterosigma akashiwo, were cul- tivated in bi-algal cultures to investigate the effect of anthracene （ANT） on the interaction between them. Without ANT, H. akashiwo out-competed P. helgolandica at low initial biomass ratios （P. helgolandica （P）： H. akashiwo （H） = 1：4 and 1 ： 1）, but not at the highest （P：H=4：I）. This observation was consistent with the description in Lotka-Volterra two species competition model. It was found that P. helgolandica was excluded at low initial biomass ratios, while the unstable equilibrium between two species was predicted at the highest. For both species, carrying capacity and maximal specific growth rate decreased in bi-algal cultures compared to those in monocultures. H. akashiwo exhibited a higher sensitivity to ANT than P helgolandica. This resulted markedly in a reduced cell den- sity of H. akashiwo but an increased cell density ofP. helgolandica. Carrying capacity ofP. helgolandica was consistently higher in bi-algal cultures with ANT than those without ANT, suggesting that ANT, through the elimination of H. akashiwo, generated the dominance of P helgolandica independently of initial biomass ratios. This study showed a density-dependent effect of harmful alga （H. akashiwo） on dietary alga （P helgolandica）, and indicated that ocean pollutant ANT could induce the succession of marine phytoplankton.
基金financially supported by Shanxi Province Natural Science Foundation of China(20210302123167)NSFC-Shanxi joint fund for coal-based low carbon(U1610223)Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering(2021SX-TD006).
文摘Carbazole is an irreplaceable basic organic chemical raw material and intermediate in industry.The separation of carbazole from anthracene oil by environmental benign solvents is important but still a challenge in chemical engineering.Deep eutectic solvents (DESs) as a sustainable green separation solvent have been proposed for the separation of carbazole from model anthracene oil.In this research,three quaternary ammonium-based DESs were prepared using ethylene glycol (EG) as hydrogen bond donor and tetrabutylammonium chloride (TBAC),tetrabutylammonium bromide or choline chloride as hydrogen bond acceptors.To explore their extraction performance of carbazole,the conductor-like screening model for real solvents (COSMO-RS) model was used to predict the activity coefficient at infinite dilution (γ^(∞)) of carbazole in DESs,and the result indicated TBAC:EG (1:2) had the stronger extraction ability for carbazole due to the higher capacity at infinite dilution (C^(∞)) value.Then,the separation performance of these three DESs was evaluated by experiments,and the experimental results were in good agreement with the COSMO-RS prediction results.The TBAC:EG (1:2) was determined as the most promising solvent.Additionally,the extraction conditions of TBAC:EG (1:2) were optimized,and the extraction efficiency,distribution coefficient and selectivity of carbazole could reach up to 85.74%,30.18 and 66.10%,respectively.Moreover,the TBAC:EG (1:2) could be recycled by using environmentally friendly water as antisolvent.In addition,the separation performance of TBAC:EG (1:2) was also evaluated by real crude anthracene,the carbazole was obtained with purity and yield of 85.32%,60.27%,respectively.Lastly,the extraction mechanism was elucidated byσ-profiles and interaction energy analysis.Theoretical calculation results showed that the main driving force for the extraction process was the hydrogen bonding ((N–H...Cl) and van der Waals interactions (C–H...O and C–H...π),which corresponding to the blue and green isosurfaces in IGMH analysis.This work presented a novel method for separating carbazole from crude anthracene oil,and will provide an important reference for the separation of other high value-added products from coal tar.
基金financially supported by the Korea CCS R&D Centrefunded by the Ministry of Education,Science and Technology of the Korean Government
文摘Microporous hypercross-linked conjugated quinonoid chromophores represent a novel class of amorphous polymers, synthesized by the reaction of anthracene with dimethoxy methane in the presence of FeCl3 catalyst. Their N2 adsorption isotherms confirm their microporous nature. Diffuse reflectance UV-Visible（DRS UV-Vis） spectroscopy confirms their matrix built with the conjugated quinonoids by their broad light absorption characteristics extending from 1000 nm to 200 nm with the absorbance maximum close to 400 nm. The catalyst cross-linked anthracene with ―CH2― bridges and subsequently dehydrogenating them to form quinonoids. Their Fourier transform infrared（FTIR） spectra showed their characteristic quinonoid vibrations between 1600 and 1700 cm-1. The synthesis of polymers was carried out at 30, 40, 50, 60, 70 and 80 ℃, but the quinonoid content of the polymer obtained at 80 ℃ was higher than that of the others. Their scanning electron microscopy（SEM） images showed microspheres of 1 to 5 μm size built with tiny particles. Their surfaces were not smooth. The polymer synthesized at 80 ℃ showed 5.1 wt% CO2 sorption at 25 ℃ and 0.1 MPa, but when it was recross-linked, the CO2 sorption increased to 8 wt%. Hence, hypercross-linked conjugated quinonoid chromophores of anthracene are good for sorption of CO2.
基金the National Natural Science Foundation of China(Nos.21572002,21272005)The Research Culture Funds of Anhui Normal UniversityDepartment of Human Resources of Anhui Province for financial support。
文摘This study presents a facile strategy for the formation of highly substituted butterfly 1,4-adducts/9,10-adducts via the Diels-Alder reaction of benzyne intermediates.The method achieves very good to excellent yields of the respective anthracene derivative s under mild conditions.This practical protocol is compatible with a variety of sensitive functional groups and provides access to difunctionalized bridge 1,4-adducts/9,10-adducts.
基金supported by the Zhejiang Provincial Key Laboratory of Advanced Chemical Engineering Manufacture Technology (No. 2017E10001)。
文摘In situ formation of composite micro-mesoporous dendritic fibrous nano-silica(DFNS) and Al-DFNS was prepared using a cetylpyridinium bromide(CPB) template synthetic system. Dealumination is induced by impregnation of zirconium with flux followed by a sulfuric acid treatment. This procedure results in a series of highly uniform nano-spheres, which exhibit stronger acid property than that of Al-MCM-41. In the selective alkylation of anthracene with tert–amyl alcohol, SO_(4)^(2-)modified Zr-contained dealuminated Al-DFNS(SZ-De Al-DFNS) shows great catalytic activity and higher conversion(60.8%). The DFNS samples were characterized with XRD, SEM, TEM, NH_(3)-TPD and other techniques. The results reveal that DFNSs consist of center-radial micro-mesopores and that the acid contribution of SZ-De Al-DFNS is much broader,as compared with amorphous aluminosilicate.
基金Beijing University of Chemical Technology-China-Japan Friendship Hospital Joint Fund (PYBZ1710)
文摘Objective: To establish a mouse model of skin squamous cell carcinoma induced by high dose 7, 12-dimethyl-benzodiazepine [a] anthracene, and to provide experimental basis for the prevention and treatment of skin squamous cell carcinoma. Methods: 36 BALB/c mice were randomly divided into 3 groups, respectively is: the high dose group (group A), low dose group (group B), and blank control group (group c), recorded in the process of building body weight in mice, and skin changes back, local skin tissue for building after HE staining of PCNA immunohistochemical staining, and the expression of PCNA positive staining level as reflected in mice skin squamous cell carcinoma of the malignant indicators, using the Image Pro Plus calculation PCNA staining of integral optical density (IOD) and positive area, and the results were statistically analyzed. Results: at 12 weeks, there were statistically significant differences in tumor number and tumor volume between group A and group B (P<0.05), and the tumor bearing rate was up to 83.3% and 66.7%, and the incidence of SCC was up to 75% and 33.3%. Immunohistochemical analysis showed statistical differences in IOD and positive area of mice in groups A, B and C (P<0.01). Conclusion: compared with the mouse model of skin squamous cell carcinoma established by the traditional two-stage protocol, this model has the characteristics of shorter experimental period, higher tumor formation rate and easier operation, providing a reliable experimental basis for the study of skin squamous cell carcinoma.
文摘To harvest the sun light and to promote the amount of energy stored,a new binary compound which links a sensitizer(electron donor), anthracene,and substrate(electron acceptor),norbornadiene,in a non- conjugated manner without increase in molecular weight was synthesized.The inter-and intramolecular photosensitized isomerization and the mechanism were studied.
基金supported by the Natural Science Foundation of Jilin Province(No. 20170101112JC)Project 985-Automotive Engineering of Jilin University
文摘Aggregation-induced emission-active 4-（3,4,5-bis（octyloxy）phenyl-9-anthracene acylhydrazone （AHP- T8） has been designed and synthesized, and the photo-responsive properties of organogel and xerogel irradiated by visible light were investigated systematically. AHP-T8 can form thermo-reversible gels in some of the tested solvents. The enhanced fluorescence emission has been observed after gelation although the dilute solution of AHP-T8 was almost non-fluorescent. When the organogel was exposed under visible light, the gel-sol phase transition occurred, and the corresponding morphology, fluorescence intensity, intermolecular hydrogen bonding and the structure all changed. In addition, the xerogel is more sensitive to visible light than that of organogel. The photoresponsive behaviour of AHP-T8 upon irradiation by visible light was demonstrated to be due to the E-Z isomerizations of -C=N-group. rather than the photodimerization of anthracene groups
