《影像科学与光化学》参考文献格式要求

<正>一.专著作者(全部).书名.版本(第1版不著录).出版地点:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.[2]Forster T W.In:Rurton M,Kirby-Smith J S,Magee J I,eds.Comparative Effects of Radiation[M].Vol.30,3rd ed.New York and London:Wiley,1960.300.[3]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.     

《影像科学与光化学》参考文献格式要求

<正>一.专著作者(全部).书名.版本(第1版不著录).出版地点:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.[2]Forster T W.In:Rurton M,Kirby-Smith J S,Magee J I,eds.Comparative Effects of Radiation[M].Vol.30,3rd ed.New York and London:Wiley,1960.300.[3]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.     

《影像科学与光化学》参考文献格式要求

<正>一.专著作者(全部).书名.版本(第1版不著录).出版地点:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.[2]Forster T W.In:Rurton M,Kirby-Smith J S,Magee J I,eds.Comparative Effects of Radiation[M].Vol.30,3rd ed.New York and London:Wiley,1960.300.[3]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.     

《影像科学与光化学》参考文献格式要求

<正>一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M〗.北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.     

《影像科学与光化学》参考文献格式要求

正一.专著作者(全部).书名.版本(第1版不著录).出版地点:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.[2]Forster T W.In:Rurton M,Kirby-Smith J S,Magee J I,eds.Comparative Effects of Radiation[M].Vol.30,3rd ed.New York and London:Wiley,1960,300.[3]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001,316-319.     

《影像科学与光化学》参考文献格式要求

正一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.     

《影像科学与光化学》参考文献格式要求

<正>一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M〗.北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.二.期刊作者.文章题名[J].刊名,出版年,卷号(期号):起止页码.示例:     

《影像科学与光化学》参考文献格式要求

<正>一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1] Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M〗.北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.     

《影像科学与光化学》参考文献格式要求

一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1] Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.二.期刊作者.文章题名[J].刊名,出版年,卷号(期号):起止页码.示例:[1] Kobayashi C A N,Leite A L,Silva T L,et al.Proteomic analysisof urine in rats chronically exposed to fluoride[J].     

《影像科学与光化学》参考文献格式要求

一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.Wang D H,Jiang L.Theory and Application of UV-curing Material[M].Beijing:Science Press,2001.316-319.二.期刊作者.文章题名[J].刊名,出版年,卷号(期号):起止页码.示例:[1]Kobayashi C A N,Leite A L,Silva T L,et al.Proteomic analysisof urine in rats chronically exposed to fluoride[J].Journal of Biochemical and Molecular Toxicology,2011,25(1):8-14.     

《影像科学与光化学》参考文献格式要求

正一.专著作者(全部).书名.版本(第1版不著录).出版地点:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.[2]Forster T W.In:Rurton M,Kirby-Smith J S,Magee J I,eds.Comparative Effects of Radiation[M].Vol.30,3rd ed.New York and London:Wiley,1960.300.[3]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.     

《影像科学与光化学》参考文献格式要求

一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.二.期刊作者.文章题名[J].     

《影像科学与光化学》参考文献格式要求

一.专著作者.书名[M].版本(第1版不著录).出版地:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.25-32.[2]王德海,江棂.紫外光固化材料理论与应用[M].北京:科学出版社,2001.316-319.     

《影像科学与光化学》参考文献格式要求

<正>一.专著作者(全部).书名.版本(第1版不著录).出版地点:出版单位,出版年.起止页码.示例:[1]Griffiths L.Colour and Constitution of Organic Molecules[M].London:Academic Press,1976.[2]Forster T W.In:Rurton M,Kirby-Smith J S,Magee J I,eds.Comparative Effects of Radiation[M].Vol.30,3rd ed.New York and London:Wiley,1960.300.     

PHOTOINDUCED CHARGE TRANSFER REACTION OF BENZOPHENONE WITH AMINE IN VESICLES

Photoinduced charge transfer reaction of benzophenone(BP) with, minewas carried out in the vesicles of dicetyldimethylammonium bromide (DCDAB)over wide ranges of amine concentration (0. 01～4. 0M). Linear plots of φ~(-1) vs.[TEA]~(-1) at low concentration of amine (<0.02M) and Φ~(-1) vs. [TEA]~(-2) at highconcentration were obtained. Kinetic data demonstrate that the electrontransfer is promoted significantly by DCDAB vesicles and proton transferbecomes more efficient at high Rmlne concentrations, leading to a decrease ofKd/Kr and increase of Kh/Ke. The kinetic expressions of photoreaction of BPbound to DCDAB bilayer are developed.     

Theoretical Studies on the M-M Bonding in Complexes [M2Cl4L2] and [M2Cl7L]- （M = Mo, Re; L = Ph2Ppy, （Ph2P）2py）

The structures of complexes [MⅡ2Cl4L2] and [MⅢ2Cl7L]- (M = Mo, Re; L = Ph2Ppy, (Ph2P)2py) were calculated by using density functional theory (DFT) PBE0 method. Based on the optimized geometries, the natural bond orbital (NBO) analyses were carried out to study the nature of Re-Re and Mo-Mo bonds. The conclusions are as follows: the M-M distances in two-Ph2Ppy or (Ph2P)2py complexes [MⅡ2Cl4L2] are shorter than those in mono-Ph2Ppy or (Ph2P)2py complexes [MⅢ2Cl7L]- due to the double bridged N-C-P interactions. For singlet of all complexes, there is ReⅢ-ReⅢ or MoⅡ-MoⅡ quadruply bond in complex [Re2Cl7L]- or [Mo2Cl4L2], while only ReⅡ-ReⅡ or MoⅢ-MoⅢ triply bond in complex [Re2Cl4L2] or [Mo2Cl7L]-. The most stable spin state of 2 and 6, triplet, only contains triple ReⅢ-ReⅢ bond. Because the LPCl → BD*Re-Re delocalizations weaken the Re-Re bond, the distance of ReⅢ-ReⅢ quadruple bonds in [Re2Cl7L]- is slightly longer than that of ReⅡ-ReⅡ triple bonds in [Re2Cl4L2]. Moreover, due to the delocalizations from the lone pair electrons of the remaining P' atom to the M-M antibonding orbitals, the M-M distance in (Ph2P)2py complexes is slightly longer than that in Ph2Ppy complexes.     

Synthesis and Characterization of Two Novel High Valent Dinuclear Complexes with a Triphenolate Ligand Bearing Functional Groups

Two novel high valent complexes [M2(III, III)L(p--OAc)2].PF6 (M=Mn, Fe; 9) were prepared, where L was the tri-anion of 2,6-bis{[(2-hydroxy-3-(morpholin-4-yl methyl)-5-tertbutyl benzyl)(pyridyl-2-methyl)amino]methyl}-4-methyl phenol which contained additional phenolic, tert-butyl and morpholin-4-yl methyl groups compared to its parent [Mn2(Ⅱ, Ⅱ)(bpmp)(μ-OAc)2]-ClO4 (10). These improvements decreased the difference between the new model and (Mn)4 cluster (OEC in nature).     

《燃料化学学报》参考文献著录格式

参考文献是科技论文的一个重要组成部分,是进行引文统计分析的重要信息源之一。参考文献的质量与数量是评价论文质量和水平的重要指标。参考文献著录的完整性、准确性直接影响统计结果及期刊的文献计量学指标。作者在投稿时不应忽视参考文献特有的价值和作用。因此本刊要求作者必须严格按照下列要求准确、完整地著录参考文献。 各类参考文献格式如下： (1)期刊文章[序号]作者(只列3人,其余用"等").文章题名[J].刊名,出版年,卷(期)：起止页码.例：[2]金显贺,王显长,王忠东,等.一种用于在线检测局部放电的数字滤波技术[J].清华大学学报(自然科学版),1993,33(4)：62～67. (2)专著(书籍)、论文集[序号]作者.书或文集名[M或C].版本(第1版不注).出版地：出版者,出版年.起止页码.例：[1]徐如人,庞文琴,屠昆岗,等.沸石分子筛的结构与合成[M].吉林：吉林大学出版社,1987.131～161. (3)学位论文、报告[序号]作者.论文或报告题名[D或R].保存地点：保存单位,年份.例：[6]张筑生.微分半动力系统的不变集[D].北京：北京大学数学研究所,1983. (4)专著、论文集中的析出文献[序号]作者.析出文献题名[A].见(英文用In)：主编.专著或文集名[M或C].出版地：出版者,出版年.析出文献起止页码.例：[5]陈俊武.流化催化裂化反应工程[A].见：侯祥麟主编.中国炼油技术新进展[M].北京：中国石化出版社,1998.18～26. (5)专利[序号]发明人.专利题名[P].专利国别：专利号,出版日期.例：[3]姜锡洲.一种温热外敷药制备方案[P].中国专利：881056073,1989-07-26. (6)国际、国家标准[序号]标准编号,标准名称[S].例：[4]GB/T 16159-1996,汉语拼音正词法基本规则[S]. (7)电子文献[序号]主要责任者.电子文献题名[电子文献及载体类型标识].电子文献的出处或可获得地址,发表或更新日期/引用日期(任选).例：[7]万锦堃.中国大学学报论文文摘(1983～1993).英文版[DB/CD].北京：中国大百科全书出版社,1996. [8]王明亮.关于中国学术期刊标准化数据库系统工程的进展[EB/OL].http：∥www.cajcd.edu.cn/pub/wml.txt/980810-2.html,1998-08-16/1998-10-04. (8)各种未定义类型的文献[序号]主要责任者.文献题名[Z].出版地：出版者,出版年.     

Synthesis, Crystal Structure and Property of a Series of Supramolecular Polymers Based on Novel 3,5-Dimethyl- 2,6-bis（3-（pyrid-2-yl）-1,2,4-triazolyl）pyridine Ligand

Solvothermal reactions of 3,5-dimethyl-2,6-bis(3-(pyrid-2-yl)-1,2,4-triazolyl) pyridine (L), 1,4-benzendicarboxylic acid (H2bdc), and transitional metal cations of MII (M = Mn, Co, Cd) in the presence of oxalic acid (H2ox) afford three novel supramolecular polymers (CPs), namely, {[M2(ox)(L)2][bdc][M2(Hox)2(OH)2(H2O)4].3H2O}n (M=Mn for 1, Co for 2, Cd for 3). Single-crystal X-ray diffraction analysis reveals that complexes 1-3 are isostructural and the 3D supramolecular structure was connected through non-covalent interactions. With the help of H2ox, the L ligands cheated with center atoms forming a butterfly [M2(ox)(L)2]2+ building block. The bdc2- ligand linked with the unprecedented [M2(Hox)2(OH)2(H2O)4] units through strong O-H…O hydrogen bonds forming a zigzag chain, which are further connected through π…π interactions between L and bdc2- ligands to form a 3D supramolecular structure. Moreover, elemental analyses, IR, thermogravimetric, PXRD and luminescence have been investigated.     

Synthesis of Novel Discotic C60-triphenylene Derivative by 1, 3-Dipolar Cycloaddition

1 IntroductionFullerene has received considerable attention and a great researching interest due to its unique structure and interesting properties[1-3].Many functional groups have been introduced,often region-or stereo-selectively,for tuning the physical properties of C60 and for constructing supramolecular architectures[4-6].Among all kinds of C60 derivatives,the diseotic molecule-substituted C60 derivatives show interesting properties,especially,liquid crystal properties.Up to now,few C60 derivatives with discotic-molecular groups and their liquid crystal properties have been studied.In 1996,Deschenaux et al.[7]reported the first mesomorphic C60-ferrocene derivative.Tian et al.[8]synthesized a C60-perylene derivative in 2004.Nakanishi et al.[9]prepared a series of uncommon liquid C60derivatives with 2,4,6-tris(alkyloxy)benzal groups in 2006.Lately,Geerts et al.[10]described the synthesis of mesogenic phthalocyanine-C60.