The separation of aromatic/aliphatic hydrocarbon mixtures is a significant process in chemical industry, but challenged in some cases. Compared with conventional separation technologies, pervaporation is quite promisi...The separation of aromatic/aliphatic hydrocarbon mixtures is a significant process in chemical industry, but challenged in some cases. Compared with conventional separation technologies, pervaporation is quite promising in terms of its economical, energy-saving, and eco-friendly advantages. However, this technique has not been used in industry for separating aromatic/aliphatic mixtures yet. One of the main reasons is that the separation performance of existed pervaporation membranes is unsatisfactory. Membrane material is an important factor that affects the separation performance. This review provides an overview on the advances in studying membrane materials for the pervaporation separation of aromatic/aliphatic mixtures over the past decade. Explored pristine polymers and their hybrid materials(as hybrid membranes) are summarized to highlight their nature and separation performance. We anticipate that this review could provide some guidance in the development of new materials for the aromatic/aliphatic pervaporation separation.展开更多
The separation of aromatic/aliphatic hydrocarbon mixtures is crucial in the petrochemical industry.Pervaporation is regarded as a promising approach for the separation of aromatic compounds from alkanes. Developing me...The separation of aromatic/aliphatic hydrocarbon mixtures is crucial in the petrochemical industry.Pervaporation is regarded as a promising approach for the separation of aromatic compounds from alkanes. Developing membrane materials with efficient separation performance is still the main task since the membrane should provide chemical stability, high permeation flux, and selectivity. In this study, the hyperbranched polymer(HBP) was deposited on the outer surface of a polyvinylidene fluoride(PVDF)hollow-fiber ultrafiltration membrane by a facile dip-coating method. The dip-coating rate, HBP concentration, and thermal cross-linking temperature were regulated to optimize the membrane structure.The obtained HBP/PVDF hollow-fiber-composite membrane had a good separation performance for aromatic/aliphatic hydrocarbon mixtures. For the 50%/50%(mass) toluene/n-heptane mixture, the permeation flux of optimized composite membranes could reach 1766 g·m^(-2)·h^(-1), with a separation factor of 4.1 at 60℃. Therefore, the HBP/PVDF hollow-fiber-composite membrane has great application prospects in the pervaporation separation of aromatic/aliphatic hydrocarbon mixtures.展开更多
The development of efficient photocatalysts for crucial organic transformation,such as aerobic oxidation,remains challenging.Although powdered porous materials offer abundant accessible active sites,their application ...The development of efficient photocatalysts for crucial organic transformation,such as aerobic oxidation,remains challenging.Although powdered porous materials offer abundant accessible active sites,their application in liquid-phase catalysis is often limited by insufficient light absorption and inevitable charge recombination,which are inherent drawbacks of conventional heterogeneous catalysts.Here,through rational design and nanoscale-engineering of porous aromatic frameworks(PAFs)comprising porphyrin and porous organic cage,a quasi-homogeneous porous photocatalyst with high catalytic activity and controllable dimension was developed.The interface-directed growth in oil-in-water emulsion shaped the morphology of photoactive PAFs from powders to nanoflakes,which facilitated the light absorbance and catalyst-substrate interaction.Compared with PAF powders,PAF nanoflakes exhibited superior photocatalytic activity for aerobic oxidation.For mustard gas simulant(2-chloroethyl ethyl sulfide,CEES),PAF nanoflakes exhibited ultrafast detoxification rates in room air with a half-life(t_(1/2))as fast as 26s,which even exceeded other catalysts in pure oxygen.It also completely catalyzed the aerobic oxidation of thioether within 15 min,which is almost the fastest rate among any reported organic photocatalysts.Furthermore,the efficient catalytic performance under mild conditions caused by improved light enrichment,surface charge transfer and carrier lifetime was elucidated.展开更多
Redox-active porous aromatic frameworks(PAFs)have emerged as hopeful candidates for sodium-ion batteries(SIBs)in view of their porous structures,chemical stability and tunable architectures.Herein,we successfully synt...Redox-active porous aromatic frameworks(PAFs)have emerged as hopeful candidates for sodium-ion batteries(SIBs)in view of their porous structures,chemical stability and tunable architectures.Herein,we successfully synthesized two redox-active PAFs(PAF-305 and PAF-306)with different nitrogen-containing motifs,and demonstrated their application as cathode materials for SIBs.Density functional theory(DFT)calculations reveal that nitrogen-rich PAF-305 exhibits a lower lowest unoccupied molecular orbital(LUMO)energy level(-3.35 eV)and a narrower energy gap(E_(g))(2.40 eV)compared with nitrogen-poor PAF-306.As expected,PAF-305 displays outstanding electrochemical performance,comprising a high reversible capacity of 145.2 mAh g^(-1)at 0.05 A g^(-1)and satisfactory cycling stability with 92% capacity retention over 1000 cycles at 0.2 A g^(-1).Remarkably,PAF-305 maintains robust electrochemical properties across a wide temperature range(-20℃ to 50℃).Through a combination of experimental characterizations and theoretical calculations,the sodium-ion storage mechanism of PAF-305 is elucidated.This study not only provides a promising strategy for exploring other redox-active organic units in the design of novel PAFs,but also expands the potential applications of PAFs in energy storage systems.展开更多
In situ melt polycondensation was proposed to prepare biodegradable aliphatic-aromatic copolyesters/nano-SiO2 hybrids based on terephthalic acid （TPA）, poly（L-lactic acid） oligomer （OLLA）, 1,4-butanediol （BDO）...In situ melt polycondensation was proposed to prepare biodegradable aliphatic-aromatic copolyesters/nano-SiO2 hybrids based on terephthalic acid （TPA）, poly（L-lactic acid） oligomer （OLLA）, 1,4-butanediol （BDO） and nano-SiO2. TEM and FT-IR characterizations confirmed that TPA, OLLA and BDO copolymerized to obtain biodegradable copolyesters, poly（butylene terepbthalate-co-lactate） （PBTL）, and the abundant hydroxyl groups on the surface of nano-SiO2 provided potential sites for in situ grafting with the simultaneous resulted PBTL. The nano-SiO2 particles were chemically wrapped with PBTL to form PBTL/nano- SiO2 hybrids. Due to the good dispersion and interfacial adhesion of nano-SiO2 particles with the copolyester matrix, the tensile strength and the Young＇s modulus increased from 5.4 and 5.6 MPa for neat PBTL to 16 and 390 MPa for PBTL/nano-SiO2 hybrids with 5 wt.% nano-SiO2, respectively. The mechanical properties of PBTL/nano-SiO2 hybrids were substantially improved.展开更多
Straightforward etherification of benzyl alcohols （1） via intermolecular dehydration can be efficiently catalyzed by sodium bisulfite under solvent-free conditions. In the presence of 0.3 mol% or 0.6 mol% amount of ...Straightforward etherification of benzyl alcohols （1） via intermolecular dehydration can be efficiently catalyzed by sodium bisulfite under solvent-free conditions. In the presence of 0.3 mol% or 0.6 mol% amount of sodium bisulfite, symmetric and unsymmetric ethers are prepared from the corresponding alcohols in high yields （up to 95%）. Etherification of benzhydryl alcohols is also discussed.展开更多
Biodegradable aliphatic/aromatic copolyesters, poly（butylene terephthalate-co-lactate） （PBTL） were prepared via direct melt polycondensation of terephthalic acid （TPA）, 1,4-butanediol （BDO） and poly（L-lactic ...Biodegradable aliphatic/aromatic copolyesters, poly（butylene terephthalate-co-lactate） （PBTL） were prepared via direct melt polycondensation of terephthalic acid （TPA）, 1,4-butanediol （BDO） and poly（L-lactic acid） oligomer （OLLA）. The effects of polymerization time and temperature, as well as aliphatic/aromatic moiety ratio on the physical and thermal properties were investigated. The largest molecular weight of the copolyesters was up to 64100 with molecular weight distribution index of 2.09 when the polycondensation was carried out at 230℃ for 6 h. DSC, XRD, DMA and TGA analysis clearly indicated that the degree of crystallinity, glass-transition temperature, melting point, decomposition temperature, tensile strength, elongation and Young＇s modulus were influenced by the ratio between TPA and OLLA in the final copolyesters. Hydrolytic degradation results demonstrated that the incorporation of biodegradable lactate moieties into the aromatic polyester could efficiently improve hydrolytic degradability of the copolymer even though it still had many aromatic units in the main chains.展开更多
The separation of aromatics from aliphatics is essential for achieving maximum exploitation of oil resources in the petrochemical industry.In this study,a series of metal chloride-based ionic liquids were prepared and...The separation of aromatics from aliphatics is essential for achieving maximum exploitation of oil resources in the petrochemical industry.In this study,a series of metal chloride-based ionic liquids were prepared and their performances in the separation of 1,2,3,4-tetrahydronaphthalene(tetralin)/dodecane and tetralin/decalin systems were studied.Among these ionic liquids,1-ethyl-3-methylimidazolium tetrachloroferrate([EMIM][FeCl_(4)])with the highest selectivity was used as the extractant.Density functional theory calculations showed that[EMIM][FeCl_(4)]interacted more strongly with tetralin than with dodecane and decalin.Energy decomposition analysis of[EMIM][FeCl_(4)]-tetralin indicated that electrostatics and dispersion played essential roles,and induction cannot be neglected.The van der Waals forces was a main effect in[EMIM][FeCl_(4)]-tetralin by independent gradient model analysis.The tetralin distribution coefficient and selectivity were 0.8 and 110,respectively,with 10%(mol)tetralin in the initial tetralin/dodecane system,and 0.67 and 19.5,respectively,with 10%(mol)tetralin in the initial tetralin/decalin system.The selectivity increased with decreasing alkyl chain length of the extractant.The influence of the extraction temperature,extractant dosage,and initial concentrations of the system components on the separation performance were studied.Recycling experiments showed that the regenerated[EMIM][FeCl_(4)]could be used repeatedly.展开更多
A series of biodegradable aliphatic-aromatic copolyesters, poly(butylene terephthalate-co-butylene adipate-co- ethylene terephthalate-co-ethylene adipate) (PBATE), were synthesized from terephthalic acid (PTA), adipic...A series of biodegradable aliphatic-aromatic copolyesters, poly(butylene terephthalate-co-butylene adipate-co- ethylene terephthalate-co-ethylene adipate) (PBATE), were synthesized from terephthalic acid (PTA), adipic acid (AA), 1,4-butanediol (BG) and ethylene glycol (EG) through direct esterification and polycondensation. The sequence structure and crystallinity of the copolyester were investigated by 1H NMR spectroscopy and the wide-angle X-ray diffractometry (WAXD). The analytical results showed that the PBATE copolyester was a random copolymer and the composition of PBATE copolyester was almost consistent with the feed molar ratios. The crystal structure of PBATE copolyester belonged to the triclinic crystalline system; The variation in melting point of the synthesized PBATE copolyester agreed well with the estimation obtained by the Flory equation and was applicable to the random copolymer.展开更多
A series organosoluble and heterocyclic poly（ether-amide）s （PEA）s were synthesized from a new diamine containing pyridine moiety and four aliphatic-aromatic dicarboxylic acids by direct polycondensation reactions....A series organosoluble and heterocyclic poly（ether-amide）s （PEA）s were synthesized from a new diamine containing pyridine moiety and four aliphatic-aromatic dicarboxylic acids by direct polycondensation reactions. Dicarboxilic acids 4a-4d containing ether groups were synthesized in two step reactions. At first, dialdehydes 3a-3d were synthesized from four dibromo alkanes la-ld and 4-hydroxybenzaldehyde 2, then dicarboxilic acids 4a-4d were synthesized from dialdehydes 3a-3d and malonic acid in a solvent free reaction. On the other hand, the new diamine 8 containing pyridine ring was synthesized in two step reactions. The structures of synthesized monomers and polymers were proven by FTIR, NMR spectroscopy and elemental analysis. Also all of the above polymers were fully characterized by inherent viscosity, solubility tests, gel permeation chromatography （GPC）, differential scanning calorimetry （DSC） and thermogravimetric analysis （TGA）. The resulted PEAs have shown good inherent viscosities, solubility and thermal properties.展开更多
P450 enzymes-catalyzed aromatic hydroxylation plays an important role in detoxification,biosynthesis,and potential carcinogenic effect of aromatic compounds.Though it has been explored for decades,the actual process o...P450 enzymes-catalyzed aromatic hydroxylation plays an important role in detoxification,biosynthesis,and potential carcinogenic effect of aromatic compounds.Though it has been explored for decades,the actual process of aromatic hydroxylation and mechanism of regioselectivity catalyzed by cytochrome P450 monooxygenases remained ambiguous.Here,we have resolved these issues.With a stable chiral organofluorine probe,and especially with X-ray data of two isolated arene oxides derivatives,we demonstrate that an arene oxide pathway is definitely involved in P450-catalyzed aromatic hydroxylation.By the capture,isolation,identification and reactivity exploration of the arene 1,2-oxide and arene 2,3-oxide intermediates,together with advanced QM calculations,the mechanism of how two intermediates go to the same product has been elucidated.In addition to the model substrate,we also confirmed that an arene oxide intermediate is involved in the P450-catalyzed hydroxylation pathway of a natural product derivative methyl cinnamate,which indicates that this intermediate appears to be universal in P450-catalyzed aromatic hydroxylation.Our work not only provides the most direct evidence for the arene oxide pathway and new insights into the regioselectivity involved in P450-catalyzed aromatic hydroxylation,but also supplies a new synthetic approach to achieve the dearomatization of aromatic compounds.展开更多
Particulate matter(PM)can cause adverse health effects by overproducing reactive oxygen species(ROS).Although the ability of PM to induce ROS generation depends on its composi-tion and environmental factors.This study...Particulate matter(PM)can cause adverse health effects by overproducing reactive oxygen species(ROS).Although the ability of PM to induce ROS generation depends on its composi-tion and environmental factors.This study explores how photo-oxidation affects ROS gen-eration from aromatic compounds(ACs,including catechol(CAT),phthalic acid(PA),and 4,4-oxydibenzoic acid(4,4-OBA))and their mixtures with transition metals(TMs,includ-ing Fe(II),Mn(II),and Cu(II))using Fourier-transform infrared(FTIR)and Ultraviolet-visible spectroscopy(UV-Vis).Results showed that photo-oxidation facilitated ROS generation from ACs.CAT-Fe(II)/Cu(II)showed synergistic effects,but 4,4-OBA-Fe(II)/Cu(II)showed antag-onistic effects.ACs-Mn(II)and PA-Fe(II)/Cu(II)exhibited synergistic effects first and then showed antagonistic effects.The different interactions were due to complexation between ACs and TMs.The photo-oxidized ACs-TMs significantly enhanced ROS generation com-pared with ACs-TMs.The study suggested the photo-oxidation mechanism involved that the transfer ofπ-electrons from the ground to an excited state in benzene rings and func-tional groups,leading to the breakage and formation of chemical bonds or easierπ-electron transfer from ACs to TMs.The former could generate ROS directly or produce polymers that promoted ROS generation,while the latter promoted ROS generation by transferringπ-electrons to dissolved oxygen quickly.Our study revealed that both interactions among components and photo-oxidation significantly influenced ROS generation.Future studies should integrate broader atmospheric factors and PM components to fully assess oxidative potential and health impacts.展开更多
The associations of polycyclic aromatic hydrocarbon(PAH)exposure with serum uric acid(SUA)or hyperuricemia have been rarely assessed.We aimed to investigate the relationships between urinary PAH metabolites and SUA or...The associations of polycyclic aromatic hydrocarbon(PAH)exposure with serum uric acid(SUA)or hyperuricemia have been rarely assessed.We aimed to investigate the relationships between urinary PAH metabolites and SUA or hyperuricemia among US adults and to explore the mediating role of systemic inflammation in the associations.A total of 10,307 US adults were conducted to assess the associations of seven urinary hydroxy–PAH with SUA and hyperuricemia and evaluate the role of C-reactive protein(CRP),a biomarker of systemic inflammation,in such associations.Results showed that each 1-unit increase in ln-transformed 2-hydroxynaphthalene(2-OHNa),1-hydroxyphenanthrene(1-OHPh),2&3-hydroxyphenanthrene(2&3-OHPh)and total hydroxyphenanthrene(OHPh)was associated with a 1.68(95%confidence interval(CI):0.19 to 3.17),2.46(0.78 to 4.13),3.34(1.59 to 5.09),and 2.99(1.23 to 4.75)μmol/L increase in SUA,and a 8%(odds ratio(OR):1.08,1.02 to 1.15),9%(OR:1.09,1.02 to 1.18),13%(OR:1.13,1.05 to 1.22),and 12%(OR:1.12,95%CI:1.03,1.21)increase in hyperuricemia,respectively.Co-exposure of seven PAHs was positively associated with SUA and hyperuricemia,with 2&3-OHPh showing the highest weight(components weights:0.83 and 0.78,respectively).The CRP mediated 11.47%and 10.44%of the associations ofΣOHPh and 2&3-OHPh with SUA and mediated 8.60%and 8.62%in associations ofΣOHPh and 2&3-OHPh with hyperuricemia,respectively.In conclusion,internal levels of PAH metabolites were associated with elevated SUA levels and the increased risk of hyperuricemia among US adults,and CRP played a mediating role in the associations.展开更多
Novel benzo-bridged hexaphyrin(2.1.2.1.2.1)and its copper complex were synthesized.Single-crystal structures showed typical figure-of-eight Huckel topologies.NMR,NICS,HOMA,ACID,and EDDB analysis supported their non-ar...Novel benzo-bridged hexaphyrin(2.1.2.1.2.1)and its copper complex were synthesized.Single-crystal structures showed typical figure-of-eight Huckel topologies.NMR,NICS,HOMA,ACID,and EDDB analysis supported their non-aromatic properties owning to the strong local aromatic benzo rings cutting the global aromatic ring of the benzo-bridged figure-of-eight hexaphyrin(2.1.2.1.2.1).The redox properties and degenerate HOMOs and LUMOs levels indicate multielectron donating and accepting abilities.展开更多
The asymmetric alternating copolymerization of meso-epoxide and cyclic anhydrides provides an efficient access to enantiopure polyesters.Contrary to the extensive investigation of the stereochemistry resulting from ep...The asymmetric alternating copolymerization of meso-epoxide and cyclic anhydrides provides an efficient access to enantiopure polyesters.Contrary to the extensive investigation of the stereochemistry resulting from epoxide building block,the chirality from anhydride and the configurational match with epoxide remain elusive.Herein,we discover that the bimetallic chromium catalysts have led to an obvious enhancement in terms of reactivity and enantioselectivity for the asymmetric copolymerization of meso-epoxide with various non-symmetric chiral anhydrides.Up to 97%ee was obtained during the asymmetric copolymerization of cyclohexene oxide(CHO)with(R)-methylsuccinic anhydride(R-MSA),and three-or four-carbon chiral centers were simultaneously installed in the aliphatic polyester backbone.In particular,the different combinations of stereochemistry in epoxide and anhydride building blocks considerably affect the thermal properties and crystalline behaviors of the resulting polyesters.This study uncovers an interesting method for regulating polymer crystallinity via matching the chirality of different monomers.展开更多
Understanding microbial responses to polycyclic aromatic hydrocarbon(PAH)pollution is crucial for assessing the current status of PAH contamination in polar regions.In this study,intertidal and marine sediments were e...Understanding microbial responses to polycyclic aromatic hydrocarbon(PAH)pollution is crucial for assessing the current status of PAH contamination in polar regions.In this study,intertidal and marine sediments were enriched with a mixture of PAHs(naphthalene,phenanthrene,fluorene,pyrene,and fluoranthene).Isolation of culturable bacteria,high-throughput sequencing,and functional prediction were combined to systematically analyze bacterial structural and predicted functional responses to PAH exposure.High-throughput sequencing results showed that the relative abundance of Proteobacteria was significantly increased after enrichment,and Pseudomonas and Acinetobacter were identified as dominant genera under PAH exposure.These findings were consistent with the 19 potential PAH-degrading strains(mainly Pseudomonas)that were successfully isolated from enrichment cultures.Distinct bacterial taxa between enriched marine and intertidal sediments indicated the existence of distinct PAH-degrading groups.PICRUSt2-based functional predictions suggested higher predicted abundances of PAH-degradation pathways in polar sediments,likely through the preferential degradation of parent PAH compounds in response to elevated concentrations.This study provides valuable data on microbial responses to PAH pollution in polar regions and offers new insights for evaluating ecological hazards induced by PAHs.展开更多
Objective To investigate the association of various polycyclic aromatic hydrocarbon(PAH)metabolites with diverse subtypes of cardiovascular disease(CVD)risk.Methods A novel predicting risk of cardiovascular disease EV...Objective To investigate the association of various polycyclic aromatic hydrocarbon(PAH)metabolites with diverse subtypes of cardiovascular disease(CVD)risk.Methods A novel predicting risk of cardiovascular disease EVENTs PREVENT equation was used to estimate the 10-year diverse subtypes of CVD risk,and their associations with PAH metabolites were analyzed using multiple logistic regression models,the weighted quantile sum(WQS)model,the quantile g-computation(qgcomp)model,and a stratified analysis of subgroups.Results For this study,six thousand seven hundred and forty-five participants were selected,and significant positive associations were observed between PAHs,naphthalene(NAP),and fluorene(FLU),and the risks of total CVD,atherosclerotic cardiovascular disease(ASCVD),and heart failure(HF).NAP and FLU were the primary contributors to the effects of PAH mixtures,and their associations with total CVD,ASCVD,and HF risk were significant in younger participants(30≤age<50 years);however,the associations of phenanthrene(PHEN)with ASCVD,HF,coronary heart disease(CHD),and stroke were dominant in aging participants(age≥50 years).Notably,pyrene(PYR)was negatively associated with the risk of ASCVD,HF,CHD,and stroke.Similarly,negative associations of PYR with the four CVD subtypes were noticeable in aging participants.Conclusion Different PAHs metabolites had different impacts on each CVD subtype among different age groups.Notably,the protective effects of PYR on ASCVD,HF,CHD,and stroke were noticeable in aging individuals.展开更多
Organic compounds are important contributors to the optical properties and health effects of combustion-derived particles.However,the connection between optical properties and toxicity of combustion particles remains ...Organic compounds are important contributors to the optical properties and health effects of combustion-derived particles.However,the connection between optical properties and toxicity of combustion particles remains a matter of little concern.In this study,combustion particles were collected from 11 primary sources,including biomass burning,coal combustion,and vehicle exhaust.The extractable organic matter(EOM)in bituminous coal combustion particles shows the highest light-absorption,fluorescence properties,and toxicity among samples.Parallel factor(PARAFAC)analysis combined excitation−emission matrix(EEM)spectroscopy resolved 4 types of basic chromophore components in EOM.Fourier transform ion cyclotron resonance mass spectrometry(FT-ICR MS)analysis further resolved∼800 molecules,predominantly aromatics(84%±4.6%),which showed positive correlations with the light-absorption,fluorescence properties and toxicity of EOM(p<0.05).Aromatics are inferred to be the intrinsic link between the optical properties and toxicity of EOM in combustion particles.Additionally,the benzene poly(carboxylic acid)s(BPCAs)method,which could identify and quantify fused benzene rings in EOM,further indicates the high condensation degree of aromatics is closely correlated with the lightabsorption,fluorescence properties of EOM.However,the toxicity of EOM may depend on the bay or fjord region of aromatics.These findings provide valuable insights into the light-absorption,fluorescence properties and toxicity of EOM in combustion particles.展开更多
Dion-Jacobson (DJ) phase hybrid perovskites have been proven to improve the photovoltaic performance of the devices due to its unique structure.At present,some DJ hybrid perovskites have been reported and used for pho...Dion-Jacobson (DJ) phase hybrid perovskites have been proven to improve the photovoltaic performance of the devices due to its unique structure.At present,some DJ hybrid perovskites have been reported and used for photodetection filed,but most of them are based on lead-bromide systems,which is not conducive to construct broadband photodetection devices due to the limitation of intrinsic absorption.Herein,we constructed a bilayered DJ hybrid perovskite (3AMPY)(EA)Pb_(2)I_(7)(3AMPY^(2+)is 3-(aminomethyl)pyridinium,EA^(+)is ethylammonium) using an aromatic spacer,which exhibit large current on/off ratios of 10~4under 520 and 637 nm illumination.In particular,the single crystal device based on (3AMPY)(EA)Pb_(2)I_(7)shows a distinguished detectivity of 7.4×10^(12)Jones and a high responsivity of 0.89A/W under 637 nm illumination.Such finding not only enriches the quantities of DJ hybrid perovskites,but also provides useful assistance for constructing high-performance optoelectronic device in the future.展开更多
Donor-acceptor(D-A)compounds are particularly important in optoelectronic and biological applications.However,they are normally synthesized in the presence of transition metal catalysts.Herein,we report a metal-free m...Donor-acceptor(D-A)compounds are particularly important in optoelectronic and biological applications.However,they are normally synthesized in the presence of transition metal catalysts.Herein,we report a metal-free method by a complexmediated nucleophilic aromatic substitution of aryl nitriles with amines.The method can lead to rich D-A type aggregation-induced emission luminogens(AIEgens)with tunable properties.They emit from deep-blue to yellow-green and possess high photoluminescence quantum yields up to 70.5%in the aggregate state.Interestingly,the suppression of intramolecular flapping is proved to play an indispensable role in the AIE behavior,which is different from the mechanism met in other AIEgens.Moreover,the biocompatible AIEgens possess specific staining of lipid droplets in HeLa cells and the superiority of identifying fatty liver over traditional Oil Red O staining is exhibited.展开更多
基金Supported by the National Natural Science Foundation of China(21406006,21576003)the Science and Technology Program of Beijing Municipal Education Commission(KM201510005010)+1 种基金the Importation and Development of High-Caliber Talents Project of Beijing Municipal Institutions(CIT&TCD20150309)the China Postdoctoral Science Foundation funded project(2015M580954)
文摘The separation of aromatic/aliphatic hydrocarbon mixtures is a significant process in chemical industry, but challenged in some cases. Compared with conventional separation technologies, pervaporation is quite promising in terms of its economical, energy-saving, and eco-friendly advantages. However, this technique has not been used in industry for separating aromatic/aliphatic mixtures yet. One of the main reasons is that the separation performance of existed pervaporation membranes is unsatisfactory. Membrane material is an important factor that affects the separation performance. This review provides an overview on the advances in studying membrane materials for the pervaporation separation of aromatic/aliphatic mixtures over the past decade. Explored pristine polymers and their hybrid materials(as hybrid membranes) are summarized to highlight their nature and separation performance. We anticipate that this review could provide some guidance in the development of new materials for the aromatic/aliphatic pervaporation separation.
基金financially supported by the National Natural Science Foundation of China (22178008, 22125801)Petrochina (2022DJ6004)。
文摘The separation of aromatic/aliphatic hydrocarbon mixtures is crucial in the petrochemical industry.Pervaporation is regarded as a promising approach for the separation of aromatic compounds from alkanes. Developing membrane materials with efficient separation performance is still the main task since the membrane should provide chemical stability, high permeation flux, and selectivity. In this study, the hyperbranched polymer(HBP) was deposited on the outer surface of a polyvinylidene fluoride(PVDF)hollow-fiber ultrafiltration membrane by a facile dip-coating method. The dip-coating rate, HBP concentration, and thermal cross-linking temperature were regulated to optimize the membrane structure.The obtained HBP/PVDF hollow-fiber-composite membrane had a good separation performance for aromatic/aliphatic hydrocarbon mixtures. For the 50%/50%(mass) toluene/n-heptane mixture, the permeation flux of optimized composite membranes could reach 1766 g·m^(-2)·h^(-1), with a separation factor of 4.1 at 60℃. Therefore, the HBP/PVDF hollow-fiber-composite membrane has great application prospects in the pervaporation separation of aromatic/aliphatic hydrocarbon mixtures.
基金supported by the National Natural Science Foundation of China(22075040,U21A20330,22131004)the National Key R&D Program of China(2022YFB3805900)+2 种基金the Jilin Provincial Scientific and Technological Development Program(20240602105RC)the Innovation Platform for Academicians of Hainan Provincethe Specific Research Fund of the Innovation Platform for Academicians of Hainan Province(YSPTZX202321)。
文摘The development of efficient photocatalysts for crucial organic transformation,such as aerobic oxidation,remains challenging.Although powdered porous materials offer abundant accessible active sites,their application in liquid-phase catalysis is often limited by insufficient light absorption and inevitable charge recombination,which are inherent drawbacks of conventional heterogeneous catalysts.Here,through rational design and nanoscale-engineering of porous aromatic frameworks(PAFs)comprising porphyrin and porous organic cage,a quasi-homogeneous porous photocatalyst with high catalytic activity and controllable dimension was developed.The interface-directed growth in oil-in-water emulsion shaped the morphology of photoactive PAFs from powders to nanoflakes,which facilitated the light absorbance and catalyst-substrate interaction.Compared with PAF powders,PAF nanoflakes exhibited superior photocatalytic activity for aerobic oxidation.For mustard gas simulant(2-chloroethyl ethyl sulfide,CEES),PAF nanoflakes exhibited ultrafast detoxification rates in room air with a half-life(t_(1/2))as fast as 26s,which even exceeded other catalysts in pure oxygen.It also completely catalyzed the aerobic oxidation of thioether within 15 min,which is almost the fastest rate among any reported organic photocatalysts.Furthermore,the efficient catalytic performance under mild conditions caused by improved light enrichment,surface charge transfer and carrier lifetime was elucidated.
基金supported by the Science&Technology Department of Jilin Province(20230508057RC)。
文摘Redox-active porous aromatic frameworks(PAFs)have emerged as hopeful candidates for sodium-ion batteries(SIBs)in view of their porous structures,chemical stability and tunable architectures.Herein,we successfully synthesized two redox-active PAFs(PAF-305 and PAF-306)with different nitrogen-containing motifs,and demonstrated their application as cathode materials for SIBs.Density functional theory(DFT)calculations reveal that nitrogen-rich PAF-305 exhibits a lower lowest unoccupied molecular orbital(LUMO)energy level(-3.35 eV)and a narrower energy gap(E_(g))(2.40 eV)compared with nitrogen-poor PAF-306.As expected,PAF-305 displays outstanding electrochemical performance,comprising a high reversible capacity of 145.2 mAh g^(-1)at 0.05 A g^(-1)and satisfactory cycling stability with 92% capacity retention over 1000 cycles at 0.2 A g^(-1).Remarkably,PAF-305 maintains robust electrochemical properties across a wide temperature range(-20℃ to 50℃).Through a combination of experimental characterizations and theoretical calculations,the sodium-ion storage mechanism of PAF-305 is elucidated.This study not only provides a promising strategy for exploring other redox-active organic units in the design of novel PAFs,but also expands the potential applications of PAFs in energy storage systems.
基金support from the Natural Science Foundation of Ningbo(No.2007A610030)Science and Technology Department of Zhejiang Province(No.2008C11092-2)
文摘In situ melt polycondensation was proposed to prepare biodegradable aliphatic-aromatic copolyesters/nano-SiO2 hybrids based on terephthalic acid （TPA）, poly（L-lactic acid） oligomer （OLLA）, 1,4-butanediol （BDO） and nano-SiO2. TEM and FT-IR characterizations confirmed that TPA, OLLA and BDO copolymerized to obtain biodegradable copolyesters, poly（butylene terepbthalate-co-lactate） （PBTL）, and the abundant hydroxyl groups on the surface of nano-SiO2 provided potential sites for in situ grafting with the simultaneous resulted PBTL. The nano-SiO2 particles were chemically wrapped with PBTL to form PBTL/nano- SiO2 hybrids. Due to the good dispersion and interfacial adhesion of nano-SiO2 particles with the copolyester matrix, the tensile strength and the Young＇s modulus increased from 5.4 and 5.6 MPa for neat PBTL to 16 and 390 MPa for PBTL/nano-SiO2 hybrids with 5 wt.% nano-SiO2, respectively. The mechanical properties of PBTL/nano-SiO2 hybrids were substantially improved.
文摘Straightforward etherification of benzyl alcohols （1） via intermolecular dehydration can be efficiently catalyzed by sodium bisulfite under solvent-free conditions. In the presence of 0.3 mol% or 0.6 mol% amount of sodium bisulfite, symmetric and unsymmetric ethers are prepared from the corresponding alcohols in high yields （up to 95%）. Etherification of benzhydryl alcohols is also discussed.
基金supported by the Natural Science Foundation of Ningbo(No.2007A610030)Scientific Special Fund of Zhejiang Province(No.2008C11092-2)
文摘Biodegradable aliphatic/aromatic copolyesters, poly（butylene terephthalate-co-lactate） （PBTL） were prepared via direct melt polycondensation of terephthalic acid （TPA）, 1,4-butanediol （BDO） and poly（L-lactic acid） oligomer （OLLA）. The effects of polymerization time and temperature, as well as aliphatic/aromatic moiety ratio on the physical and thermal properties were investigated. The largest molecular weight of the copolyesters was up to 64100 with molecular weight distribution index of 2.09 when the polycondensation was carried out at 230℃ for 6 h. DSC, XRD, DMA and TGA analysis clearly indicated that the degree of crystallinity, glass-transition temperature, melting point, decomposition temperature, tensile strength, elongation and Young＇s modulus were influenced by the ratio between TPA and OLLA in the final copolyesters. Hydrolytic degradation results demonstrated that the incorporation of biodegradable lactate moieties into the aromatic polyester could efficiently improve hydrolytic degradability of the copolymer even though it still had many aromatic units in the main chains.
基金supported by the National Natural Science Foundation of China(22125802,22078010).
文摘The separation of aromatics from aliphatics is essential for achieving maximum exploitation of oil resources in the petrochemical industry.In this study,a series of metal chloride-based ionic liquids were prepared and their performances in the separation of 1,2,3,4-tetrahydronaphthalene(tetralin)/dodecane and tetralin/decalin systems were studied.Among these ionic liquids,1-ethyl-3-methylimidazolium tetrachloroferrate([EMIM][FeCl_(4)])with the highest selectivity was used as the extractant.Density functional theory calculations showed that[EMIM][FeCl_(4)]interacted more strongly with tetralin than with dodecane and decalin.Energy decomposition analysis of[EMIM][FeCl_(4)]-tetralin indicated that electrostatics and dispersion played essential roles,and induction cannot be neglected.The van der Waals forces was a main effect in[EMIM][FeCl_(4)]-tetralin by independent gradient model analysis.The tetralin distribution coefficient and selectivity were 0.8 and 110,respectively,with 10%(mol)tetralin in the initial tetralin/dodecane system,and 0.67 and 19.5,respectively,with 10%(mol)tetralin in the initial tetralin/decalin system.The selectivity increased with decreasing alkyl chain length of the extractant.The influence of the extraction temperature,extractant dosage,and initial concentrations of the system components on the separation performance were studied.Recycling experiments showed that the regenerated[EMIM][FeCl_(4)]could be used repeatedly.
文摘A series of biodegradable aliphatic-aromatic copolyesters, poly(butylene terephthalate-co-butylene adipate-co- ethylene terephthalate-co-ethylene adipate) (PBATE), were synthesized from terephthalic acid (PTA), adipic acid (AA), 1,4-butanediol (BG) and ethylene glycol (EG) through direct esterification and polycondensation. The sequence structure and crystallinity of the copolyester were investigated by 1H NMR spectroscopy and the wide-angle X-ray diffractometry (WAXD). The analytical results showed that the PBATE copolyester was a random copolymer and the composition of PBATE copolyester was almost consistent with the feed molar ratios. The crystal structure of PBATE copolyester belonged to the triclinic crystalline system; The variation in melting point of the synthesized PBATE copolyester agreed well with the estimation obtained by the Flory equation and was applicable to the random copolymer.
文摘A series organosoluble and heterocyclic poly（ether-amide）s （PEA）s were synthesized from a new diamine containing pyridine moiety and four aliphatic-aromatic dicarboxylic acids by direct polycondensation reactions. Dicarboxilic acids 4a-4d containing ether groups were synthesized in two step reactions. At first, dialdehydes 3a-3d were synthesized from four dibromo alkanes la-ld and 4-hydroxybenzaldehyde 2, then dicarboxilic acids 4a-4d were synthesized from dialdehydes 3a-3d and malonic acid in a solvent free reaction. On the other hand, the new diamine 8 containing pyridine ring was synthesized in two step reactions. The structures of synthesized monomers and polymers were proven by FTIR, NMR spectroscopy and elemental analysis. Also all of the above polymers were fully characterized by inherent viscosity, solubility tests, gel permeation chromatography （GPC）, differential scanning calorimetry （DSC） and thermogravimetric analysis （TGA）. The resulted PEAs have shown good inherent viscosities, solubility and thermal properties.
文摘P450 enzymes-catalyzed aromatic hydroxylation plays an important role in detoxification,biosynthesis,and potential carcinogenic effect of aromatic compounds.Though it has been explored for decades,the actual process of aromatic hydroxylation and mechanism of regioselectivity catalyzed by cytochrome P450 monooxygenases remained ambiguous.Here,we have resolved these issues.With a stable chiral organofluorine probe,and especially with X-ray data of two isolated arene oxides derivatives,we demonstrate that an arene oxide pathway is definitely involved in P450-catalyzed aromatic hydroxylation.By the capture,isolation,identification and reactivity exploration of the arene 1,2-oxide and arene 2,3-oxide intermediates,together with advanced QM calculations,the mechanism of how two intermediates go to the same product has been elucidated.In addition to the model substrate,we also confirmed that an arene oxide intermediate is involved in the P450-catalyzed hydroxylation pathway of a natural product derivative methyl cinnamate,which indicates that this intermediate appears to be universal in P450-catalyzed aromatic hydroxylation.Our work not only provides the most direct evidence for the arene oxide pathway and new insights into the regioselectivity involved in P450-catalyzed aromatic hydroxylation,but also supplies a new synthetic approach to achieve the dearomatization of aromatic compounds.
基金supported by the Weiqiao-UCAS Special Projects on Low-Carbon Technology Development(No.GYY-DTFZ-2022-007)the Fundamental Research Funds for the Central Universities(No.E0E48927×2)the National Natural Science Foundation of China(No.21677145).
文摘Particulate matter(PM)can cause adverse health effects by overproducing reactive oxygen species(ROS).Although the ability of PM to induce ROS generation depends on its composi-tion and environmental factors.This study explores how photo-oxidation affects ROS gen-eration from aromatic compounds(ACs,including catechol(CAT),phthalic acid(PA),and 4,4-oxydibenzoic acid(4,4-OBA))and their mixtures with transition metals(TMs,includ-ing Fe(II),Mn(II),and Cu(II))using Fourier-transform infrared(FTIR)and Ultraviolet-visible spectroscopy(UV-Vis).Results showed that photo-oxidation facilitated ROS generation from ACs.CAT-Fe(II)/Cu(II)showed synergistic effects,but 4,4-OBA-Fe(II)/Cu(II)showed antag-onistic effects.ACs-Mn(II)and PA-Fe(II)/Cu(II)exhibited synergistic effects first and then showed antagonistic effects.The different interactions were due to complexation between ACs and TMs.The photo-oxidized ACs-TMs significantly enhanced ROS generation com-pared with ACs-TMs.The study suggested the photo-oxidation mechanism involved that the transfer ofπ-electrons from the ground to an excited state in benzene rings and func-tional groups,leading to the breakage and formation of chemical bonds or easierπ-electron transfer from ACs to TMs.The former could generate ROS directly or produce polymers that promoted ROS generation,while the latter promoted ROS generation by transferringπ-electrons to dissolved oxygen quickly.Our study revealed that both interactions among components and photo-oxidation significantly influenced ROS generation.Future studies should integrate broader atmospheric factors and PM components to fully assess oxidative potential and health impacts.
基金supported by the Key Program of National Natural Science Foundation of China(No.82241088)the Natural Science Foundation of Hubei Province(No.2022CFB813).
文摘The associations of polycyclic aromatic hydrocarbon(PAH)exposure with serum uric acid(SUA)or hyperuricemia have been rarely assessed.We aimed to investigate the relationships between urinary PAH metabolites and SUA or hyperuricemia among US adults and to explore the mediating role of systemic inflammation in the associations.A total of 10,307 US adults were conducted to assess the associations of seven urinary hydroxy–PAH with SUA and hyperuricemia and evaluate the role of C-reactive protein(CRP),a biomarker of systemic inflammation,in such associations.Results showed that each 1-unit increase in ln-transformed 2-hydroxynaphthalene(2-OHNa),1-hydroxyphenanthrene(1-OHPh),2&3-hydroxyphenanthrene(2&3-OHPh)and total hydroxyphenanthrene(OHPh)was associated with a 1.68(95%confidence interval(CI):0.19 to 3.17),2.46(0.78 to 4.13),3.34(1.59 to 5.09),and 2.99(1.23 to 4.75)μmol/L increase in SUA,and a 8%(odds ratio(OR):1.08,1.02 to 1.15),9%(OR:1.09,1.02 to 1.18),13%(OR:1.13,1.05 to 1.22),and 12%(OR:1.12,95%CI:1.03,1.21)increase in hyperuricemia,respectively.Co-exposure of seven PAHs was positively associated with SUA and hyperuricemia,with 2&3-OHPh showing the highest weight(components weights:0.83 and 0.78,respectively).The CRP mediated 11.47%and 10.44%of the associations ofΣOHPh and 2&3-OHPh with SUA and mediated 8.60%and 8.62%in associations ofΣOHPh and 2&3-OHPh with hyperuricemia,respectively.In conclusion,internal levels of PAH metabolites were associated with elevated SUA levels and the increased risk of hyperuricemia among US adults,and CRP played a mediating role in the associations.
基金partly supported by the National Natural Science Foundation of China(No.22301108)the Project Startup Foundation for Distinguished Scholars of Jiangsu University(Nos.4111310026 and 5501310014).
文摘Novel benzo-bridged hexaphyrin(2.1.2.1.2.1)and its copper complex were synthesized.Single-crystal structures showed typical figure-of-eight Huckel topologies.NMR,NICS,HOMA,ACID,and EDDB analysis supported their non-aromatic properties owning to the strong local aromatic benzo rings cutting the global aromatic ring of the benzo-bridged figure-of-eight hexaphyrin(2.1.2.1.2.1).The redox properties and degenerate HOMOs and LUMOs levels indicate multielectron donating and accepting abilities.
基金financially supported by the National Natural Science Foundation of China(Nos.22071016 and 21920102006)。
文摘The asymmetric alternating copolymerization of meso-epoxide and cyclic anhydrides provides an efficient access to enantiopure polyesters.Contrary to the extensive investigation of the stereochemistry resulting from epoxide building block,the chirality from anhydride and the configurational match with epoxide remain elusive.Herein,we discover that the bimetallic chromium catalysts have led to an obvious enhancement in terms of reactivity and enantioselectivity for the asymmetric copolymerization of meso-epoxide with various non-symmetric chiral anhydrides.Up to 97%ee was obtained during the asymmetric copolymerization of cyclohexene oxide(CHO)with(R)-methylsuccinic anhydride(R-MSA),and three-or four-carbon chiral centers were simultaneously installed in the aliphatic polyester backbone.In particular,the different combinations of stereochemistry in epoxide and anhydride building blocks considerably affect the thermal properties and crystalline behaviors of the resulting polyesters.This study uncovers an interesting method for regulating polymer crystallinity via matching the chirality of different monomers.
基金supported by the project from the National Natural Science Foundation of China(Grant no.42230411)the Science&Technology Innovation Project of Laoshan Laboratory(Grant no.LSKJ202203206)。
文摘Understanding microbial responses to polycyclic aromatic hydrocarbon(PAH)pollution is crucial for assessing the current status of PAH contamination in polar regions.In this study,intertidal and marine sediments were enriched with a mixture of PAHs(naphthalene,phenanthrene,fluorene,pyrene,and fluoranthene).Isolation of culturable bacteria,high-throughput sequencing,and functional prediction were combined to systematically analyze bacterial structural and predicted functional responses to PAH exposure.High-throughput sequencing results showed that the relative abundance of Proteobacteria was significantly increased after enrichment,and Pseudomonas and Acinetobacter were identified as dominant genera under PAH exposure.These findings were consistent with the 19 potential PAH-degrading strains(mainly Pseudomonas)that were successfully isolated from enrichment cultures.Distinct bacterial taxa between enriched marine and intertidal sediments indicated the existence of distinct PAH-degrading groups.PICRUSt2-based functional predictions suggested higher predicted abundances of PAH-degradation pathways in polar sediments,likely through the preferential degradation of parent PAH compounds in response to elevated concentrations.This study provides valuable data on microbial responses to PAH pollution in polar regions and offers new insights for evaluating ecological hazards induced by PAHs.
基金the technology projects entrusted by enterprises and institutions(2022KJ000803)the Beijing Natural Science Foundation(No.7242184)the project that Study on the role of ASGR1 in regulating chaperone mediated autophagy involved in methyl tert-butyl ether–induced hepatic lipotoxicity(XSKY2024).
文摘Objective To investigate the association of various polycyclic aromatic hydrocarbon(PAH)metabolites with diverse subtypes of cardiovascular disease(CVD)risk.Methods A novel predicting risk of cardiovascular disease EVENTs PREVENT equation was used to estimate the 10-year diverse subtypes of CVD risk,and their associations with PAH metabolites were analyzed using multiple logistic regression models,the weighted quantile sum(WQS)model,the quantile g-computation(qgcomp)model,and a stratified analysis of subgroups.Results For this study,six thousand seven hundred and forty-five participants were selected,and significant positive associations were observed between PAHs,naphthalene(NAP),and fluorene(FLU),and the risks of total CVD,atherosclerotic cardiovascular disease(ASCVD),and heart failure(HF).NAP and FLU were the primary contributors to the effects of PAH mixtures,and their associations with total CVD,ASCVD,and HF risk were significant in younger participants(30≤age<50 years);however,the associations of phenanthrene(PHEN)with ASCVD,HF,coronary heart disease(CHD),and stroke were dominant in aging participants(age≥50 years).Notably,pyrene(PYR)was negatively associated with the risk of ASCVD,HF,CHD,and stroke.Similarly,negative associations of PYR with the four CVD subtypes were noticeable in aging participants.Conclusion Different PAHs metabolites had different impacts on each CVD subtype among different age groups.Notably,the protective effects of PYR on ASCVD,HF,CHD,and stroke were noticeable in aging individuals.
基金supported by the National Natural Science Foundation of China(No.42030715 and 42192511)the Alliance of International Science Organizations(ANSO-CRKP-2021-05)+1 种基金the Basic and Applied Basic Research Foundation of Guangdong Province(2023B0303000007,2023B1515020067 and 2022A1515011271)the Youth Innovation Promotion Association of the Chinese Academy of Sciences(2022359).
文摘Organic compounds are important contributors to the optical properties and health effects of combustion-derived particles.However,the connection between optical properties and toxicity of combustion particles remains a matter of little concern.In this study,combustion particles were collected from 11 primary sources,including biomass burning,coal combustion,and vehicle exhaust.The extractable organic matter(EOM)in bituminous coal combustion particles shows the highest light-absorption,fluorescence properties,and toxicity among samples.Parallel factor(PARAFAC)analysis combined excitation−emission matrix(EEM)spectroscopy resolved 4 types of basic chromophore components in EOM.Fourier transform ion cyclotron resonance mass spectrometry(FT-ICR MS)analysis further resolved∼800 molecules,predominantly aromatics(84%±4.6%),which showed positive correlations with the light-absorption,fluorescence properties and toxicity of EOM(p<0.05).Aromatics are inferred to be the intrinsic link between the optical properties and toxicity of EOM in combustion particles.Additionally,the benzene poly(carboxylic acid)s(BPCAs)method,which could identify and quantify fused benzene rings in EOM,further indicates the high condensation degree of aromatics is closely correlated with the lightabsorption,fluorescence properties of EOM.However,the toxicity of EOM may depend on the bay or fjord region of aromatics.These findings provide valuable insights into the light-absorption,fluorescence properties and toxicity of EOM in combustion particles.
基金financially supported by the National Natural Science Foundation of China(Nos.22005183 and 22275117)the Program of State Key Laboratory of Quantum Optics and Quantum Optics Devices(No.KF202204)。
文摘Dion-Jacobson (DJ) phase hybrid perovskites have been proven to improve the photovoltaic performance of the devices due to its unique structure.At present,some DJ hybrid perovskites have been reported and used for photodetection filed,but most of them are based on lead-bromide systems,which is not conducive to construct broadband photodetection devices due to the limitation of intrinsic absorption.Herein,we constructed a bilayered DJ hybrid perovskite (3AMPY)(EA)Pb_(2)I_(7)(3AMPY^(2+)is 3-(aminomethyl)pyridinium,EA^(+)is ethylammonium) using an aromatic spacer,which exhibit large current on/off ratios of 10~4under 520 and 637 nm illumination.In particular,the single crystal device based on (3AMPY)(EA)Pb_(2)I_(7)shows a distinguished detectivity of 7.4×10^(12)Jones and a high responsivity of 0.89A/W under 637 nm illumination.Such finding not only enriches the quantities of DJ hybrid perovskites,but also provides useful assistance for constructing high-performance optoelectronic device in the future.
基金supported by the National Natural Science Foundation of China(22275072 and 62105184)the Natural Science Foundation of Guangdong Province(2020A1515010622)+1 种基金the Project of Science and Technology of Guangzhou(2024A04J3712)the Teli Young Scholar Program of Beijing Institute of Technology.
文摘Donor-acceptor(D-A)compounds are particularly important in optoelectronic and biological applications.However,they are normally synthesized in the presence of transition metal catalysts.Herein,we report a metal-free method by a complexmediated nucleophilic aromatic substitution of aryl nitriles with amines.The method can lead to rich D-A type aggregation-induced emission luminogens(AIEgens)with tunable properties.They emit from deep-blue to yellow-green and possess high photoluminescence quantum yields up to 70.5%in the aggregate state.Interestingly,the suppression of intramolecular flapping is proved to play an indispensable role in the AIE behavior,which is different from the mechanism met in other AIEgens.Moreover,the biocompatible AIEgens possess specific staining of lipid droplets in HeLa cells and the superiority of identifying fatty liver over traditional Oil Red O staining is exhibited.
