“光催化产氢和CO2还原专刊”前言（英文）

Jointly hosted by Wuhan University of Technology,Changsha University and Kent State University,the 3rd International Workshop on Graphene and C3N4-based Photocatalysts(IWGCP3)was held at Wuhan University of Technology,Wuhan,China on March 23-26,2019.This workshop was sponsored by National Natural Science Foundation of China(NSFC),Wuhan University of Technology,Changsha University,Beijing Perfectlight and others.Over 300 colleagues from all over the world participated in this workshop,which featured 8 plenary lectures,12 keynote lectures,22 invited lectures,13 oral lectures and 157 posters.Top ten posters enjoyed recognition by the scientific committee during the workshop.     

第一届华人光催化材料学术研讨会专刊前言（英文）

正The Chinese Symposium on Photocatalytic Materials (CSPM)was held at the Wuhan University of Technology, Wuhan, China onJuly26-29,2018.TheCSPMsymposiumwasjointly organizedbyWuhanUniversityofTechnology,Fuzhou UniversityandXuchangUniversity,andwassupportedby National Natural Science Foundation of China (NSFC), Wuhan UniversityofTechnology,FuzhouUniversity,Xuchang University,BeijingPerfectlightandothers.Morethan320colleagues from four continents (Asia, America, Australia and Europe)participatedinthissymposium,andpresented10plenary lectures, 13 keynote lectures, 35 invited lectures, 8 oral lectures and 144 posters. 10 best posters were selected.     

Preface

This issue is devoted to the pubication of the invited and plenary lectures presented in the FourthInernational Symposium for Chinese Organic Chemists(ISCOC96 HK)on April5～8,1996 hosted bythe Chinese University of Hong Kong.The biennial ISCOC Symposium series was launched inShanghaiin 1990 with the inaugural meeting geld at the Shanghai Institute of Organic Chemistry aftera protracted preparatory period;this was followed by the second and third symposia held in Beijing and     

Preface: Celebrating the 100th anniversary of chemical sciences in Nanjing University

正The School of Chemistry and Chemical Engineering of Nanjing University was found in 1920, and it is one of the earliest departments of chemistry in China. Afterwards, the primeval National Central University’s Chemistry Discipline united with Jinling University’s Chemistry Discipline to form the Department of Chemistry of Nanjing University.     

Preface to Special Issue on the International Symposium on Environmental Catalysis (ISEC 2016)

With a growing awareness of pollution and increasing demands for environmental protection, a great deal of effort is being put into the development of catalysts with improved activity for the abatement of pollutants, which are mainly emitted by industrial plants and transport vehicles. Therefore, we organized the International Symposium on Environmental Catalysis (ISEC 2016), one of the post-Satellite Symposia of the 16th International Congress on Catalysis (ICC16), which took place between the 9th and 11th July 2016 at the South-Central University for Nationalities, Wuhan, China. Our objectives were the following: to provide an international forum for the exchange of information, to identify technical problems, and to establish direction for future research by appraising recent technology trends and theoretical investigations into environmental issues.     

Fabrication of high-performance non-doped OLEDs by combining aggregation-induced emission and thermally activated delayed fluorescence

正Undoubtedly,the realization of"one stone and two birds"is ideal,which is also applicable to the molecular design in the pursuit of excellent performance.Recently,this standpoint has been confirmed again by an interesting story written from the lab of Zujin Zhao,Shi-Jian Su,and BenZhong Tang,at South China University of Technology and the Hong Kong University of Science and Technology,in the design of DBT-BZ-DMAC(Figure 1)[1].Despite its simple structure,DBT-BZ-DMAC exhibits wonderful characteristics,     

Preface for the Special Column of the INRET 2006

I would like to take this opportunity to thank the editorial board of Journal of Natural Gas Chemistry for allowing me to write a preface for this special column. The articles appearing in this section are specially selected from the First International Conference on Natural Resources Engineering and Technology 2006 （INRET 2006）. In line with the theme of JNGC, the selected articles are focused on natural gas or low hydrocarbon conversions to important chemicals, fuels and materials. The conference was held on July 24-25, 2006 in Marriott Putrajaya, Malaysia. It was organized by the Chemical and Biotechnology （ChemBio） Focus Group, under the Research Management Centre, Universiti Teknologi Malaysia.     

Preface: celebrating the 60th anniversary of the University of Science and Technology of China

正The University of Science and Technology of China(USTC)is a prominent institution with an excellent reputation for education and innovation that resonates across the world.The university holds a special place in history.It was established by the Chinese Academy of Sciences(CAS)in1958 to meet China’s science and technology needs and increase the country’s international competitiveness.Throughout its history we have focused on frontier areas of science and technology and educated top leaders in science and technology for China and the world.     

Influence and Characterization of Acidity on Fine Silicon Powder Immobilized Photocatalyst

TiO2 photocatalyst was supported with tetrabutyl titanate sol as precursor and fine silicon powder obtained from ferroalloys factory as carder to discuss the influence of pH value of gel precursor on microstructure and activity of photocatalyst in the process of synthesizing nano-TiO2 by using sol-gel method, the purpose of which is to provide fundamental data for the recycle of photocatalytic material. Under the irradiation of ultraviolet light, the photocatalytic degradation rate of methyl orange solution was used to characterize the photocatalytic activity of the sample. The specific surface area of the sample was tested by N2 desorption method, crystal form of TiO2 was analyzed by X-ray powder diffraction, and the microtopography of the sample was observed by scanning electron microscopy. The experimental results showed that the acidity of gel precursor could greatly affect the specific surface area and photocatalytic activity of the photocatalyst, and the optimum pH value of the precursor was determined as 2.0, and at this time the specific surface area of photocatalyst could reach 34.0 m^2/g. In the sample, the proporticn of anatase to rutile is 7：3, which makes l0 mg·L^-1 methyl orange solution fade after irradiation by 15W ultraviolet light for 24 h, and the degradation rate might be up to 98.1%.     

Good Memories of Prof.Yingyan Jiang and International Conference on Fine Chemistry and Functional Polymers:Fruitful Discussions Resulted in Excellent Findings

正About 15years have passed since I first attended the International Conference on Fine Chemistry and Functional Polymers(FCFP).One day,I was asked by Prof.Inomata of Kanazawa University to attend the conference,and after a while Prof.Jiang sent me a kind invitation letter.This is the beginning of my first trip to China.Prof.Takemoto of Osaka University was also very active to     

Sc2MgGa2 and Y2MgGa2

Scandium magnesium gallide, Sc₂MgGa₂, and yttrium magnesium gallide, Y₂MgGa₂, were synthesized from the corresponding elements by heating under an argon atmosphere in an induction furnace. These intermetallic compounds crystallize in the tetragonal Mo₂FeB₂‐type structure. All three crystallographically unique atoms occupy special positions and the site symmetries of (Sc/Y, Ga) and Mg are m2m and 4/m, respectively. The coordinations around Sc/Y, Mg and Ga are pentagonal (Sc/Y), tetragonal (Mg) and triangular (Ga) prisms, with four (Mg) or three (Ga) additional capping atoms leading to the coordination numbers [10], [8+4] and [6+3], respectively. The crystal structure of Sc₂MgGa₂ was determined from single‐crystal diffraction intensities and the isostructural Y₂MgGa₂ was identified from powder diffraction data.     

The alkali hypophosphites KH2PO2, RbH2PO2 and CsH2PO2

The structures of the hypophosphites KH₂PO₂ (potassium hypophosphite), RbH₂PO₂ (rubidium hypophosphite) and CsH₂PO₂ (caesium hypophosphite) have been determined by single‐crystal X‐ray diffraction. The structures consist of layers of alkali cations and hypophosphite anions, with the latter bridging four cations within the same layer. The Rb and Cs hypophosphites are isomorphous.     

Electrochemical study of (NEt4)2Cl2FeS2MoS2 and (NEt4)2Cl2FeS2MoS2FeCl2

Summary The ability of [MoS₄]^2–, anions to be used as ligands for transition metal ions has been widely demonstrated, especially with Fe²⁺. The present study has been restricted to linear complexes such as (NEt₄)₂ [Cl₂FeS₂MoS₂] and (NEt₄)₂[Cl₂FeS₂MoS₂FeCl₂]. Their electrochemical properties are described: upon electrochemical reduction, these compounds yield MoS₂, as a black precipitate, and an iron complex in solution, assumed to be [SFeCl₂]^2–. The electrochemical reduction goes through two electron transfers, coupled with the breakdown of the molecular skeleton: a DISPl and an ECE mechanism. Depending on the solvent, the following equilibrium may be observed: [Cl₄Fe₂MoS₄]^2–[Cl₂FeMoS₄]^2–+FeCl₂. The equilibrium constant, K_D, was evaluated by differential pulse polarography. K_D is tightly related to the donor number of the solvent.     

Zur Kenntnis der Dialkalimetalldichalkogenide β-Na2S2, K2S2, α-Rb2S2, β-Rb2S2, K2Se2, Rb2Se2, α-K2Te2, β-K2Te2 und Rb2Te2

On Dialkali Metal Dichalcogenides β-Na₂S₂, K₂S₂, α-Rb₂S₂, β-Rb₂S₂, K₂Se₂, Rb₂Se₂, α-K₂Te₂, β-K₂Te₂ and Rb₂Te₂ The first presentation of pure samples of α- and β-Rb₂S₂, α- and β-K₂Te₂, and Rb₂Te₂ is described. Using single crystals of K₂S₂ and K₂Se₂, received by ammonothermal synthesis, the structure of the Na₂O₂ type and by using single crystals of β-Na₂S₂ and β-K₂Te₂ the Li₂O₂ type structure will be refined. By combined investigations with temperature-dependent Guinier-, neutron diffraction-, thermal analysis, and Raman-spectroscopy the nature of the monotropic phase transition from the Na₂O₂ type to the Li₂O₂ type will be explained by means of the examples α-/β-Na₂S₂ and α-/β-K₂Te₂. A further case of dimorphic condition as well as the monotropic phase transition of α- and β-Rb₂S₂ is presented. The existing areas of the structure fields of the dialkali metal dichalcogenides are limited by the model of the polar covalence.     

Formal [(2+2)+2] and [(2+2)+(2+2)] nonconjugated dienediyne cascade cycloadditions

[reaction: see text] Fluoranthene 2 and heptacycle 3 are easily accessible from the reaction of diyne 1 and norbornadiene (NBD) in the presence of the rhodium catalyst. The unusual [(2+2)+(2+2)] adduct 3 was confirmed by the X-ray crystal structure analysis.     

Crystal Structures of [Bu2Sn(O2PPh2)2], [Ph2Sn(O2PPh2)2], and [PhClSn(O2PPh2)OMe]2. Raman Spectra of [Ph2Sn(O2PPh2)2] and [PhClSn(O2PPh2)OMe]2

[(n‐Bu)₂Sn(O₂PPh₂)₂] ( 1 ), and [Ph₂Sn(O₂PPh₂)₂] ( 2 ) have been synthesized by the reactions of R₂SnCl₂ (R=n‐Bu, Ph) with HO₂PPh₂ in Methanol. From the reaction of Ph₂SnCl₂ with diphenylphosphinic acid a third product [PhClSn(O₂PPh₂)OMe]₂ ( 3 ) could be isolated. X‐ray diffraction studies show 1 to crystallize in the monoclinic space group P2₁/c with a = 1303.7(1) pm, b = 2286.9(2) pm, c = 1063.1(1) pm, β = 94.383(6)°, and Z = 4. 2 crystallizes triclinic in the space group , the cell parameters being a = 1293.2(2) pm, b = 1478.5(4) pm, c = 1507.2(3) pm, α = 98.86(3)°, β = 109.63(2)°, γ = 114.88(2)°, and Z = 2. Both compounds form arrays of eight‐membered rings (SnOPO)₂ linked at the tin atoms to form chains of infinite length. The dimer 3 consists of a like ring, in which the tin atoms are bridged by methoxo groups. It crystallizes triclinic in space group with a = 946.4(1) pm, b = 963.7(1) pm, c = 1174.2(1) pm, α = 82.495(6)°, β = 66.451(6)°, γ = 74.922(6)°, and Z = 1 for the dimer. The Raman spectra of 2 and 3 are given and discussed.     

The bivalent metal hypophosphites Sr(H2PO2)2, Pb(H2PO2)2 and Ba(H2PO2)2

The structures of isomorphous monoclinic strontium and lead bis­(di­hydrogenphosphate), Sr(H₂PO₂)₂ and Pb(H₂PO₂)₂, and orthorhombic barium bis­(di­hydrogen­phos­phate), Ba(H₂PO₂)₂, consist of layers of hypophosphite anions and metal cations exhibiting square antiprismatic coordination by O atoms. The Sr and Pb atoms are located on sites with point symmetry 2, and the Ba atoms are on sites with point symmetry 222. Within the layers, each anion bridges four metal cations.     

Syntheses,Spectroscopic Studies,and Crystal Structures of Me2Sn(O2PPh2)2, Ph2Pb(O2PMe2)2, and Ph2Pb(O2PPh2)2

Me₂Sn(O₂PPh₂)₂ ( 1 ), Ph₂Pb(O₂PMe₂)₂ ( 2 ), and Ph₂Pb(O₂PPh₂)₂ ( 3 ) have been synthesized by the reactions of Me₂SnCl₂ or Ph₃PbCl with the corresponding diorganophosphinic acid in methanol. X‐ray diffraction studies show that the diorganophosphinate groups behave as double bridges between the metal atoms leading to polymeric ring‐chain structures with M₂O₄P₂ (M = Pb, Sn) eight‐membered rings. The organic groups bonded to the metal atoms are in trans‐position in the resulting octahedral arrangement around the metal atoms. The IR and the mass spectra were reported and discussed.