《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.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

<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.     

《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(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

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.[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.     

《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.     

《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.     

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 antitumor activities of a new series of 4,5-dihydro-1H-thiochromeno[4,3-d]pyrimidine derivatives

A new series of 4,5-dihydro-1H-thiochromeno[4,3-d]pyrimidine derivatives have been designed and synthesized.The antitumor activities of the target compounds have been evaluated in vitro against two human cancer cell lines including A549 (human alveolar adenocarcinoma cell) and H460 (human lung cancer) by MTT assay.Most of the target compounds exhibited significant antitumor activities against A549 and H460 cancer cell lines.The most potent compound 4-(benzo[d][1,3]dioxol5-yl)-8,9-difluoro-2-(4-methylpiperazin-1-yl)-4,5-dihydro-1H-thiochromeno[4,3-d]pyrimidine (CH05) (IC50=0.44 M,3.07 M) was 2.0 and 8.4 times more active than gefitinib (IC50=0.89 M,16.81 M) against A549 and H460 cell lines,respectively.     

Syntheses,Structures and Properties of a Series of Polymeric Oxohaloplumbates

A series of polymeric oxyhaloplumbates [Pb3 I2(μ4-O)L]n(1, H_2L = ethylene glycol) and [Pb8 M(μ3-O)2 X8(XH)L3]n {X = Br, M = Mn(2 a), Co(2 b); X = I, M = Mn(2 c), Co(2 d)} have been synthesized under solvothermal conditions and structurally characterized. 1 consists of an infinite [Pb3 I2(μ4-O)L]n ribbon built up through the linkage of [PbI2] units and [Pb2(μ4-O)L]n chains to give a new type of 1-D oxoiodoplumbate [Pb3 I2(μ4-O)L]n decorated by deprotonated ethylene glycols. 2 a～d are isostructural and exhibit 3-D heterometallic frameworks constructed by the combination of infinite [Pb2 X9] chains and heptanuclear heterometallic [Pb6 M(μ3-O)2 L3] clusters. The present oxohaloplumbates exhibit wide-band-gap semiconducting properties with absorption band edges in the range of 2.21～2.71 eV. The magnetic properties of 2 a～d have also been studied.     

ENHANCEMENT OF THE SALT EFFECT ON THE CONFORMATION OF M. L. DNA MOLECULES BY METHYLATION

Methylated Micrococcus luteus DNA (M. L. DNA) in which the DNA methylation level was 2.39% was prepared by using Hhal DNA methylase. (The natural M. L. DNA is completely unmethylated.) The [θ]_(275) value of M. L. DNA was decreased and the —[θ]_(220-250) value was increased with increasing concentration of MgC1_2. The UV spectra of M. L. DNA at different concentration of MgCl_2 showed that a hypochromisity happens at 260nm with increasing concentration of MgC1_2. The heat-releasing of M. L. DNA also increased with increasing concentration of MgC1_2. A11 these results showed that the M. L. DNA molecules tend to shrink in space, The difference between methylated DNA and unmethylated DNA was compared. The sensitivity of methylated DNA to MgC1_2 is 40—70 fold higher than that of the unmethylated M. L. DNA.     

Hydrothermal Synthesis of Nanorods and Nanowires of Mg/Al Layered Double Hydroxides

Layered double hydroxides (LDHs) are a class of synthetic anion clays, characterized by the formula[MⅡ1-xMⅢx (OH)2]x (An- )x/n·yH2O (where M =metal and A = anion, usually carbonate)[1-3]. A large number of LDHs with a wide variety of M Ⅱ-M Ⅲ cation pairs including M Ⅰ-M Ⅲ ( e. g. , Li-Al ) and M Ⅱ-MⅣ( e. g. , Co-Ti) have been reported. Thus the identities of the cations(MⅠ , MⅡ , MⅢ and MⅣ) and the interlayer anion (An-) together with the value of the stoichiometric coefficient (x) may vary widely, giving rise to a large class of isostructural materials.