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| 1 | Porous coordination polymers based on three planar rigid ligands显示文摘During the last two decades,porous coordination polymers(PCPs),usually called as metal-organic frameworks(MOFs),have been developed rapidly due to their versatile structural diversities and potential physical and chemical functions.This article provides a short review of recent advances in the design and constructions of porous coordination polymers based on three planar rigid ligands,including imidazole-4,5-dicarboxlate(H3IDC),1H-tetrazole(HTz),as well as 1H-tetrazole-5-carboxylate(H2Tzc).Their preparations,crystal structures,and desirable properties have been reviewed. | ZHONG DiChang LU TongBu | 2011 | Science China Chemistry2011，54，9： | 12 |
| 2 | Single titanium-oxide species implanted in 2D g-CsN4 matrix as a highly efficient visible-light CO2 reduction photocatalyst显示文摘A visible-light-response, efficie nt and robust photo-catalyst for CO2 reduction is highly desirable. Herein, we demonstrate that single titanium-oxide species impla nted in two-dime nsion al (2D) graphitic carb on n itride (g-C3N4) matrix (2D TiO-CN) can efficie ntly photo-catalyze the reduction of CO2 to CO under the irradiation of visible light. The synergistic interaction between single titanium oxide species and g-C3N4 in 2D TiO-CN not only enhances the separation of photo-excited charges, but also results in visible light response of single titanium-oxide species, realizing high activity of CO2 photo-reduction with extremely high CO generation rate of 283.9 pmol·h^-1·g^-1, 5.7, 6.8 and 292.2 times larger than those of TQ2/CN hybrid material, CN and commercial TiO2, respectively. Time-resolved fluoresce nee and electron spin resonance spectroscopy revealed the catalytic mechanism of the fabricated 2D TiO-CN photocatalysts for CO2 reduction. | Shangfeng Tang Xuepeng Yin Guanyu Wang Xiuli Lu Tongbu Lu | 2019 | Nano Research2019，12，2： | 8 |
| 3 | Direct imaging and determination of the crystal structure of six-layered graphdiyne显示文摘自从它的发现,因为它在由一根电子横梁的照耀下面是太精细的,很少层 graphdiyne 的水晶结构的直接成像和决心证明了困难。在这个工作,六分层的 graphdiyne nanosheet 的水晶结构被低电压的传播电子显微镜学(TEM ) 直接用低当前的密度观察。高分辨率的 TEM (HRTEM ) 模拟,电子精力损失光谱学,和电子衍射的联合使用表明同样综合的 nanosheet 是有 2.19 nm 的厚度的水晶的 graphdiyne (相应于六层的厚度) 并且叠的显示出的 ABC。因此,这个工作为存在和很少层 graphdiyne 的水晶结构提供直接证据,它是对 graphene 补足的二维的碳材料的一种新类型。 | Chao Li Xiuli Lu Yingying Han Shangfeng Tang Yi Ding Ruirui Liu Haihong Bao Yuliang Li Jun Luo Tongbu Lu | 2018 | Nano Research2018，11，3： | 5 |
| 4 | Synthesis and structures of two supramolecular complexes constructed via hydrogen bond linking显示文摘Two supramolecular complexes,[Ni(rac-L)]3[CrO4]2[ClO4]2-4H2O (1) and [meso-H2L]0.5[VO3]-0.16H2O (2) (L= 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetra-decane),have been prepared in an aqueous solu-tion,and detected by elemental analysis,IR,TG,and single crystal X-ray diffraction analyses. Com-pound 1 shows a one-dimensional hexagonal prism formed by the hydrogen bonding interactions between the secondary amines of rac-L and CrO42-anion/water molecules. Compound 2 displays a three-dimensional structure constructed by the hydrogen bond linking the helical chains of [VO3]nn-to the secondary amines of meso-L to generate 1D hexagon-shaped channels,and the channels are oc-cupied by guest water molecules. | OU GuangChuan JIANG Long FENG XiaoLong LU TongBu | 2009 | Science China Chemistry2009，52，4： | 4 |
| 5 | Acetate-assistant efficient cation-exchange of halide perovskite nanocrystals to boost the photocatalytic CO_(2) reduction显示文摘The judicious implantation of active metal cations into the surface of semiconductor nanocrystal(NC)through cation-exchange is one of the facile and viable strategies to enhance the activity of catalysts for photocatalytic CO_(2)reduction,by shortening the transfer pathway of photogenerated carriers and increasing the active sites simultaneously.However,cation-exchange is hard to achieve for halide perovskite NCs owing to the stable octahedron of[PbX6]4−with strong interaction between halogen and lead.Herein,we report a facile method to overcome this obstacle by replacing partial Br−with acetate(Ac−)to generate CsPbBr_(3) NC(coded as CsPbBr_(3−x)Ac_(x)).A small amount of Ac−instead of Br−does not change the crystal structure of halide perovskite.Owing to the weaker interaction between acetate and lead in comparison with bromide,the corresponding octahedron structure containing acetate in CsPbBr_(3−x)Ac_(x) can be easily opened to realize efficient cation-exchange with Ni^(2+) ions.The resulting high loading amount of Ni^(2+) as active site endows CsPbBr_(3−x)Ac_(x) with an improved performance for photocatalytic CO_(2)reduction under visible light irradiation,exhibiting a significantly increased CO yield of 44.09μmol·g^(−1)·h^(−1),which is over 8 and 3 times higher than those of traditional pristine CsPbBr_(3) and nickel doped CsPbBr_(3) NC,respectively.This work provides a critical solution for the efficient metal doping of low-cost halide perovskite NCs to enhance their photocatalytic activity,promoting their practical applications in the field of photocatalysis. | Jialin Cheng Yanfei Mu Liyuan Wu Zhaolei Liu Ke Su Guangxing Dong Min Zhang Tongbu Lu | 2022 | Nano Research2022，15，3： | 3 |
| 6 | DNA-binding and cleavage studies of macrocyclic copper ( Ⅱ ) complexes 显示文摘 | Liu Jie Zhang Tixiang Lu Tongbu | 2002 | J Inorg Biochem2002，91，1： | 1 |
| 7 | Low-loading gold in situ doped with sulfur by biomolecule-assisted approach for promoted electrochemical carbon dioxide reduction显示文摘For electrochemical carbon dioxide reduction(CO_(2)RR),CO_(2)-to-CO conversion is considered an ideal route towards carbon neutrality for practical applications.Gold(Au)is known as a promising catalyst with high selectivity for CO;however,it suffers from high cost and low mass-specific activity.In this study,we design and prepare a catalyst featuring uniform S-doped Au nanoparticles on N-doped carbon support(denoted as S-Au/NC)by an in situ synthesis strategy using biomolecules.The S-Au/NC displays high activity and selectivity for CO in CO_(2)RR with a Au loading as low as 0.4 wt.%.The Faradaic efficiency of CO(FECO)for S-Au/NC is above 95%at−0.75 V(vs.RHE);by contrast,the FECO of Au/NC(without S)is only 58%.The Tafel slope is 77.4 mV·dec−1,revealing a favorable kinetics process.Furthermore,S-Au/NC exhibits an excellent long-term stability for CO_(2)RR.Density functional theory(DFT)calculations reveal that the S dopant can boost the activity by reducing the free energy change of the potential-limiting step(formation of the*COOH intermediate).This work not only demonstrates a model catalyst featuring significantly reduced use of noble metals,but also establishes an in situ synthesis strategy for preparing high-performance catalysts. | Meijie Tan Xiaoqian Han Sen Ru Chao Zhang Zhouru Ji Zhaolin Shi Guomeng Qiao Yunying Wang Ruixue Cui Qiquan Luo Jiqing Jiao Yaguang Li Tongbu Lu | 2023 | Nano Research2023，16，2： | 1 |
| 8 | Two stable 3D metal-organic frameworks constructed by nanoscale cages via sharing the single-layer walls 显示文摘 | Lu Wenguan Su Chengyong Lu Tongbu | 2006 | J Am Chem Soc2006，128，1： | 1 |
| 9 | Iron sites on defective BiOBr nanosheets:Tailoring the molecular oxygen activation for enhanced photocatalytic organic synthesis显示文摘Sunlight-driven activation of molecular oxygen(O_(2))for organic oxidation reactions offers an appealing strategy to cut down the reliance on fossil fuels in chemical industry,yet it remains a great challenge to simultaneously tailor the charge kinetics and promote reactant chemisorption on semiconductor catalysts for enhanced photocatalytic performance.Herein,we report iron sites immobilized on defective BiOBr nanosheets as an efficient and selective photocatalyst for activation of O_(2) to singlet oxygen(^(1)O_(2)).These Fe^(3+) species anchored by oxygen vacancies can not only facilitate the separation and migration of photogenerated charge carrier,but also serve as active sites for effective adsorption of 02.Moreover,low-temperature phosphorescence spectra combined with X-ray photoelectron spectroscopy(XPS)and electronic paramagnetic resonance(EPR)spectra under illumination reveal that the Fe species can boost the quantum yield of excited triplet state and accelerate the energy transfer from excited triplet state to adsorbed O2 via a chemical loop of Fe^(3+)/Fe^(2+),thereby achieving highly efficient and selective generation of ^(1)O_(2).As a result,the versatile iron sites on defective BiOBr nanosheets contributes to near-unity conversion rate and selectivity in both aerobic oxidative coupling of amines to imines and sulfoxidation of organic sulfides.This work highlights the significant role of metal sites anchored on semiconductors in regulating the charge/energy transfer during the heterogeneous photocatalytic process,and provides a new angle for designing high-performance photocatalysts. | Xinhui Ye Yu Li Peipei Luo Bingcai He Xinxing Cao Tongbu Lu | 2022 | Nano Research2022，15，2： | 1 |
| 10 | The production of glucose oxidase using the waste myceliums of Aspergillus niger and the effects of metal ions on the activity of glucose oxidase显示文摘 | Tongbu Lu Xinyu Peng Huiying Yang Liangnian Ji | 1996 | Enzyme and Microbial Technology1996，，5： | 1 |
| 11 | Co-POM@MOF-derivatives with trace cobalt content for highly efficient oxygen reduction显示文摘A simple and effective method for constructing highly efficient oxygen reduction catalysts with trace amount of isolated cobalt was firstly developed by the pyrolysis of Co-centered polyoxometalate@metalorganic framework (Co-POM@MOF).The Co-centered polyoxometalate ([Co W_(12)O_(40)]^(6-)) was confined in the well-defined void space of ZIF-8 to achieve homogeneous dispersion of polyoxoanions,where the isolated Co centers were well surrounded by the W-O shell and ZIF-8 framework.The Co-POM@MOF-derived N-doping porous carbon (Co-W-NC) with trace cobalt content was facilely prepared by the pyrolysis of the Co-POM@MOF under Ar atmosphere.The single dispersion of polyoxoanions in the metal-organic framework with complete separation of Co center surrounding by W-O shell and ZIF-8 framework ensures the uniform dispersion of Co atoms,confirmed by the Fourier transform extended X-ray absorption fine structure measurement.The Co-W-NC composite catalysts exhibit high performance for oxygen reduction reactions with a half-wave potential of 0.835 V in 0.1 mol/L KOH solution with excellent durability,which is much superior to that of the control samples derived from the[PW_(12)O_(40)]@ZIF-8,and the commercial Pt/C.This work highlights a new insight for constructing highly efficient catalysts via the introduction of metal-centered polyoxometalate into metal-organic framework following the high temperature treatment process. | Yitao Song Yewang Peng Shuang Yao Peng Zhang Yujie Wang Jianmin Gu Tongbu Lu Zhiming Zhang | 2022 | Chinese Chemical Letters2022，33，2： | 1 |
| 12 | Homogeneous Electrocatalytic Water Oxidation by a Rigid Macrocyclic Copper(Ⅱ) Complex显示文摘 | Jiawei Wang Haihua Huang Tongbu Lu | 2017 | Chinese Journal of Chemistry2017，35，5： | 0 |
| 13 | Three-dimensional Pyrenyl Graphdiyne Supported Pd Nanoparticle as an Efficient and Easily Recyclable Catalyst for Reduction of 4-Nitrophenol显示文摘The fabrication of highly active and easily recyclable Pd-based catalyst is meaningful for their practical application.Herein,a Pd-based dip-catalyst(Pd@Pyr-GDY)is fabricated on graphdiyne(Pyr-GDY)grown on copper foam,and applied in the reduction of nitroarenes.Specially,the as-formed Pd@Pyr-GDY shows good catalytic performance toward the reduction of 4-nitrophenol(4-NP)to 4-aminophenol(4-AP)by NaBH4 with a rate constant k value of 3.84 min^(−1),which is 12-fold higher than that of the commercial Pd/C.More importantly,Pd@Pyr-GDY could be easily and rapidly recovery from the reaction medium and no distinct inactivation was found after six cycles of the reaction.This work presents an easy way to design an efficient and easily recyclable Pd-based catalyst for practical use. | RONG Xin LU Xiuli LU Tongbu | 2021 | Chemical Research in Chinese Universities2021，37，6： | 0 |
| 14 | Enhancing photocatalytic performance of metal-organic frameworks for CO_(2) reduction by a bimetallic strategy显示文摘Metal-organic frameworks(MOFs) as a type of crystalline heterogeneous catalysts have shown potential application in photocatalytic CO_(2)reduction.However,MOF catalysts with high efficiency and selectivity are still in pursuit.Herein,by a bimetallic strategy,the catalytic performance of a Co-MOF for photocatalytic CO_(2)reduction was enhanced.Specifically,the Co-MOF based on 4,5-dicarboxylic acid(H;IDC) and4,4’-bipydine(4,4’-bpy) can catalyze CO;reduction to CO,with high efficiency but relatively low selectivity.After replacement of 2/3 Co(Ⅱ) with Ni(Ⅱ) within Co-MOF,the resulted isostructural Co_(1)Ni_(2)-MOF not only retains high efficiency for photocatalytic CO_(2)reduction,but also shows enhanced CO selectivity.The CO evolution rate reaches 1160 μmol g^(-1)h^(-1)and the CO selectivity reaches as high as 94.6%.The enhanced photocatalytic CO_(2)reduction performance is supported by theoretical calculation results.This case demonstrates that bimetallic strategy is an effective mean to optimize the catalytic performance of MOF catalysts for photochemical CO_(2)reduction. | Jihong Zhang Yuchen Wang Hongjuan Wang Dichang Zhong Tongbu Lu | 2022 | Chinese Chemical Letters2022，33，4： | 0 |
| 15 | Engineering Coordination Environment of Cobalt Center in Molecular Catalysts for Improved Photocatalytic CO_(2) Reduction显示文摘The creation of effective and inexpensive catalysts is essential for photocatalytic CO_(2) reduction.Homogeneous molecular catalysts,possessing definite crystal structures,are desirable to study the relationship between catalytic performance and coordination microenvironment around catalytic center.In this report,we elaborately developed three Co(II)-based molecular catalysts with different coordination microenvironments for CO_(2) reduction,named[CoN_(3)O]ClO_(4),[CoN_(4)]ClO_(4),and[CoN_(3)S]ClO_(4),respectively.The optimal[CoN_(3)O]ClO_(4) photocatalyst has a maximum TON of 5652 in photocatalytic reduced CO_(2) reduction,which is 1.28 and 1.65 times greater than that of[CoN_(4)]ClO_(4) and[CoN_(3)S]ClO_(4),respectively.The high electronegativity of oxygen in L1(N,N-bis(2-pyridylmethyl)-N-(2-hydroxybenzyl)amine)provides the Co(II)catalytic centers with low reduction potentials and a more stable*COOH intermediate,which facilitates the CO_(2)-to-CO conversion and accounts for the high photocatalytic activity of[CoN_(3)O]ClO_(4).This work provides researchers new insights in development of catalysts for photocatalytic CO_(2) reduction. | Yuchen Wang Jihong Zhang Wei Yang Weixue Tao Keying Tao Jihua Deng Wenjie Shi Dichang Zhong Tongbu Lu | 2023 | Chinese Journal of Chemistry2023，41，23： | 0 |
| 16 | New Crystalline Forms of Mebendazole with n-Alkyl Carboxylic Acids Neutral and Ionic Status显示文摘mebendazole 的水晶的形式的结构的信息,反寄生的药,被限制,尽管这药的三种多态的形式被报导了。现在的工作与一系列n烷基调查 mebendazole 的不同水晶的形式的结构和性质羧基的酸包括 trifluroacetic 酸( 1 ),蚁的酸( 2 ),醋酸( 3 ), propanoic 酸( 4 ), butanoic 酸( 5 ),颉草的酸( 6 )和 hexanoic 酸( 7 )。这些混合物被 thermogravimetric 分析和单个水晶的 X 光检查衍射分析描绘。R22 (8 ) 结构的主题在所有七个产品被检测,它被一双 NH 形成 ?? O/OH ?? 在 mebendazole 和羧基的酸之间的 N 氢契约。, 37 处于良好的竟技状态 1 和 2 被发现是中立 solvate 的形式,质子转移从羧基的酸被观察到 mebendazole。 | Jiamei Chen Tongbu Lu | 2013 | Chinese Journal of Chemistry2013，31，5： | 0 |
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