五枫藤、小驳骨和川西茶藨的化学成分研究

八月瓜属植物五枫藤(Holboellia latifolia Wall.)和驳骨草属植物小驳骨(Gendarussa vulgaris Nees)均为药用植物, 前者化学成分研究不深入, 后者的化学成分未见报道。川西茶藨(Ribes takare D. Don)为茶藨子属植物, 没有化学成分的报道。本论文对三个植物的化学成分和活性成分进行了研究, 主要通过色谱方法分离得到了48 个化合物, 采用波谱分析或与已知标准品对照等手段鉴定了它们的结构, 其中有1 个新的原小檗碱类化合物和3 个新的联苯类化合物,发现了具有细胞毒活性和α-葡萄糖苷酶抑制活性的化合物。1、从五枫藤地上部分的95%乙醇提取物中分离得到了12 个化合物: 五加苷K (1)、hederagenin 3-O- α-L-rhamnopyranosyl-(1→2)- α-L-arabinopyranoside (2)、β-萘乙酸(3) 、3-O-α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester (4) 、3-O- α-L-rhamnopyranosyl-(1→2)-O- β- D-glucopyranosyl-(1→2)- α-L-arabinopyranosyl oleanolic acid (5) 、3-O-( β-D-glucopyranosiduronic acid)-oleanolic acid 28-O- β-D-glucopyranoside (6)、lup-20(29)-en-3-one (7)、lupeol (8)、β-谷甾醇(9)、齐墩果酸(10)、乌苏酸(11)、β-胡萝卜苷(12)。化合物1 对Lu-06、N-04 和Bre-04 癌细胞株的GI50 分别是0.77µg/mL、1.26 µg/mL 和1.55 µg/mL, 化合物2 对N-04 癌细胞株的GI50 为2.44 µg/mL。2、从小驳骨地上部分的95%乙醇提取物中分离得到了1 个原小檗碱类新化合物13-hydroxyl gusanlung A (25), β-谷甾醇(9)、齐敦果酸(10)、β-胡萝卜苷(12)、棕榈酸(1-)甘油酯(13)、棕榈酸(14)、阿苯哒唑(15)、阿苯哒唑砜(16)、阿苯哒唑亚砜(17)、aurantiamide acetate (18)、华良姜素(19)、芫花素(20)、(-)-丁香树酯醇(21)、gusanlung B (22) 、eupteleasaponinsⅤ acetate (23)、gusanlungA (24)、刺五加苷E (26)、岩白菜素(27)、咖啡酸(28)。化合物25 对肝癌细胞株(HepG2) 的GI50 为2.08 µg/mL。3、从川西茶藨地上部分的95%乙醇提取物中分离鉴定了22 个化合物: β-谷甾醇(9) 、β- 胡萝卜苷(12) 、O-acetyloleanolic aldehyde (29),4,7,8-trimethoxy-2,3-methylenedioxydibenzofuran (30) 、3', 5-dimethoxy-3, 4-methylenedioxybiphenyl (31) 、桦木醇(32) 、6,7-dimethoxy-1-methyl-3,4-dihydroquinolin-2-one (33)、3'-hydroxy-5-methoxy-3,4-methylenedioxybiphenyl (34) 、7-hydroxy-4,8-dimethoxy-2,3-methylenedioxydibenzofuran (35)、桦木醛(36)、没食子酸(37) 、6β- 羟基-4- 烯-3- 酮- 豆甾醇(38) 、5α, 8α-epidioxy-(22E,24R)-ergosta-6, 22-dien-3β-ol (39)、verrucofortine (40)、6-methoxycalpogoniumisoflavone A (41)、2-羟基二苯甲酮(42)、桦木酸(43), 3, 5-二甲氧基苯甲酸-4-O-β-D-吡喃葡萄糖苷(44)、洋芹素(45)、刺槐素(46)、水杨酸(47)、洋芹素-5-O- β-D-葡萄糖苷(48), 化合物30、31 和35 为新的联苯化合物。化合物30的α-葡萄糖苷酶抑制率为10.2% (1.00 mg/mL); 化合物35 的抑制率为17.2% (1.00mg/mL)。4、综述了1960 年以来原小檗碱类化合物药理活性研究进展。 Plants Holboellia latifolia Wall and Gendarussa vulgaris Nees, are used as folkmedicine. Ribes takare D. Don belongs to the genus Ribes. The three plants have notbeen chemically studied in detail. Chemical and bioactive study of three plants led tothe isolation of 48 compounds by chromatography. Their structures were elucidatedon the basis of spectroscopic evidence or comparison with authentic samples. Amongthe 48 componds isolated one protoberberine alkaloid and three biphenyls are newones. Cytotoxic and α-glucosidase inhibitory compounds had been found.1. Twelve compounds were isolated from the 95% ethanol extract of the aerial partof H. latifolia Wall. They were characterized as fellow: eleutheroside K (1),hederagenin-3-O- α-L-rhamnopyranosyl-(1→2)- α-L-arabinopyranoside (2),2-naphthyl acetic acid (3),3-O-α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester (4), 3-O- α-L-rhamnopyranosyl-(1→2)-O- β- D-glucopyranosyl-(1→2)- α-L-arabinopyranosyl oleanolic acid (5),3-O-( β-D-glucopyranosiduronic acid)-oleanolic acid-28-O- β-D-glucopyranoside (6),lup-20(29)-en-3-one (7), lupeol (8), β-sitosterol (9), oleanolic acid (10), ursolicacid (11), and β-daucosterol (12). Compound 1 showed moderate cytotoxicity againstLu-06 (GI50, 0.77 µg/mL), N-04 (GI50, 1.26 µg/mL) and Bre0-4 (GI50=1.55 µg/mL)and compound 2 showed moderate cytotoxicity against N-04 (GI50=2.44 µg/mL).2. A new protoberberine alkaloid, 13-hydroxyl gusanlung A (25), was isolated fromthe aerial part of Gendarussa vulgaris Nees, together with β-sitosterol (9), oleanolicacid (10), β-daucosterol (12), glycerol monopalmitate (13), palmific acid (14),albendazole (15), albendazole sulphone (16), albendazole sufloxide (17), aurantiamideacetate (18), kumatakenin (19), genkwanin (20), (-)-syringaresinol (21), gusanlung B(22), eupteleasaponinsⅤ acetate (23), gusanlung A (24), eleutheroside E (26),bergenin (27) and caffeic acid (28). Compound 25 showed cytotoxicity against HepG2 cells (GI50, 2.08 µg/mL).3. Phytochemical study of the Ribes takare D. Don led to the isolation of three newbiphenyls, 4,7,8-trimethoxy-2,3-methylenedioxydibenzofuran (30), 3', 5-dimethoxy-3,4-methylenedioxybiphenyl (31) and 7-hydroxy-4,8-dimethoxy-2,3-methylenedioxydibenzofuran (35), along with nineteenknown compounds, β-sitosterol (9), β-daucosterol (12), O-acetyloleanolic aldehyde(29), betulin (32), 6,7-dimethoxy-1-methyl-3,4-dihydroquinolin-2-one (33),3'-hydroxy-5-methoxy-3, 4-methylenedioxybiphenyl (34), betulinic aldehyde (36),gallic acid (37), stigmast-4-en-6β-ol-3-one (38), 5α, 8α-epidioxy-(22E, 24R)-ergosta-6,22-dien-3β-ol (39), verrucofortine (40), 6-methoxycalpogonium isoflavone A (41),2-hydroxybenzophenone (42), betulinic acid (43), 3,5-dimethoxygallic acid-4-O- β-D-glucopryranoside (44), apigenin (45), acacetin (46), salicylic acid (47) andapigenin-5-O- β-D-glucopryranoside (48). α-Glucosidase inhibitory rates ofcompound 30 and 35 were respectively 10.2% and 17.2% at a concentration of 1.00 mg/mL).4. Pharmacological activities of protoberberines were summarized.

微生物法生成辅酶Q10的研究

本文根据我们实验室建立的发酵产物中辅酶Q10定性定量检测方法，筛选得到一株可以代谢产生较多辅酶Q10的野生菌株放射形土壤杆菌(Agrobacterium radiobacter No.50)。 为了提高放射形土壤杆菌的辅酶Q10的产量，本实验利用液体培养研究了单因素对菌株辅酶Q10产量的影响，并用正交法确定了最佳液态发酵条件。最佳发酵培养基是：葡萄糖20g,蔗糖40g, 硫酸铵10g,玉米浆30g, 酵母膏3g，K2HPO4 3g,MgSO4.7H2O 1g，蒸馏水1000mL,pH 7.0-7.2。最佳发酵条件是：转接斜面菌种到种子培养基, 转速220r/min、温度28。C培养24h后，转入发酵培养基(250mL三角拼装液量为50mL，pH 7.0), 接种量为10％，转速220r/min、温度28。C，培养120h。在此条件下，菌体湿重约为50g/L，辅酶Q10含量约为20mg/L。 本文以放射形土壤杆菌为出发菌株进行诱变育种，以期获得辅酶Q10高产菌。根据微生物育种原理、参照辅酶Q10的代谢调控机制，以野生型放射形土壤杆菌(Agrobacterium radiobacter No.50)为出发菌株，采用紫外线和亚硝基胍复合诱变技术，依次筛选得到菌体提取物M抗性菌ARM－7、烟草提取物T抗性菌株ARMT-26、Vk3抗性菌株ARMTV-25、链霉素抗性菌株ARMTVS-32，菌株ARMTVS-32产量达到了36.8mg/L，与原始出发菌株相比，产量提高了77％。 研究了茄尼醇、对羟基苯甲酸、橘子皮提取物D、胡萝卜提取物E、烟草提取物对ARMTVS-32合成辅酶Q10的影响，结果表明这些物质对菌体合成辅酶Q10有一定促进作用，添加0.2g/L茄尼醇时，辅酶Q10含量提高了17%，达到了40.7mg/L；添加1.2g/L橘子皮提取物D时，辅酶Q10含量提高了13.8%，达到了39.6mg/L；添加0.5g/L胡萝卜提取物E时，辅酶Q10含量提高了25.3% ，达到了43.6mg/L；添加8g/L烟草提取物时，辅酶Q10含量提高了12.6%，达到了39.2mg/L。 Production of Coenzyme- Q10 (CoQ10) by fermentation is considered as a process with broad prospects.Quantitative Analysis of CoQ10 in the culture of microbe by TLC—UV spectrophotometry was developed, by using this method we got the strain Agrobacterium radiobacter,which was isolated from forest soil of southwest of China. The effect of the single factor on CoQ10-production ability of the strain was examined by liquid cultured, and its best optimum cultivation conditions were established by orthogonal method. The results showed that the optimum fermentation conditions were as following: carbon sources glucose 20g/L,sucrose 40g/L; nitrongen sources (NH4)2SO4 10g/L,maize liquid 30g/L;yeast extract 3g; K2HPO4 3g/L,MgSO4.7H2O 1g/L; initial pH was 7 and volume of medium(medium volume vs flask volume) was 50mL/500mL, incubating for 120h on a rotary shaker at 220 rpm and 28℃.Under these conditions, the biomass and CoQ10 concentration reached 50g/L and 20mg/L respectively. According to the biosynthesis mechanism of CoQ10 and breeding theory, CoQ10 over-production strains were screened by UV--NTG. mutation using Agrobacterium radiobacter No.50 as parent strain. A microbe-juice resistant mutant ARMTVS-32, which also could resist tobacco-juice, VK3 and streptomycin, was screened out from an agar plate. The CoQ10 content of ARMTVS-32 reached 36.8mg/L, which was 77% higher than the initial strain. In addition, We discussed the effects of some organic substrates on the synthesis of CoQ10 in ARMTVS-32. The results showed that solanesol, orange juice D, carrot juice E and tobacco juice could promote the CoQ10 accumulation in the cells. The CoQ10 content of ARMTVS-32 reached 40.7mg/L when added 0.2g/L solanesol,it reached 39.6mg/L when added 1.2g/L orange juice D，it reached 43.6mg/L when added 0.5g/L carrot juice E. it reached 39.2mg/L when added 8g/L tobacco juice.

Multi-strip MRPCs for FOPI

During the last years FOPI has developed a new ToF system as an upgrade of the existing detector based on Multi-strip Multi-gap Resistive Plate Chambers (MMRPCs). The intention is to increase the charged Kaon identification up to a laboratory momentum of 1 GeV/c and to enhance the azimuthal detector granularity. The new ToF barrel has an active area of 5 m(2) with 2400 individual strips (900 x 1.6 mm(2)) [A. Schuttauf, et al., Nucl. Phys. B 158 (2006) 52] which are read out on both sides by a custom designed electronics [M. Ciobanu, et al., IEEE Trans. Nucl. Sci. NS-54 (4) (2007) 1201; K. Koch, et al., IEEE Trans. Nucl. Sci. NS-52(3) (2005) 745]. To reach the envisaged goal a time resolution of 100 ps is needed, at a flight path of 1-1.3 m. Due to the rare production of the K- at SIS energies the efficiency of the MMRPCs has to be above 95%. We report on measurements with the detectors and electronics from the mass production line. For this purpose we used a proton beam at 2.0 and 1.25 GeV, at rates between 0.1 and 5 kHz/cm(2) to determine the timing, efficiency and rate capability of the MMRPCs

重离子束治疗皮肤恶性肿瘤的初步临床结果；Clinical trial of carbon ion radiotherapy for malignant neoplasm of skin

目的:评价重离子束对皮肤恶性肿瘤放射治疗的近期疗效和毒副反应。方法:29例皮肤恶性肿瘤患者分6批接受重离子束放射治疗,其中恶性黑色素瘤13例,皮肤鳞癌及Bowen’s病各6例,基底细胞癌2例,其他皮肤恶性肿瘤2例。照射总剂量(50～70)GyE/(6～12)d,单次剂量5.5～11.67GyE,1f/d,连续治疗。采用RTOG标准和WHO近期疗效标准分别评价毒副反应和近期疗效。结果:截止2009-05,中位随访时间为13.5个月(1～25个月),随访率为100%。29例患者中完全缓解(CR)24例(82.8%),部分缓解(PR)5例(17.2%),有效率(RR)为100%,中位生存时间为22.8个月(95%CI:20.6～24.9)。皮肤反应0度11例(37.9%),Ⅰ度9例(31.0%),Ⅱ度6例(20.7%),Ⅲ度2例(6.9%),Ⅳ度1例(3.4%);血液毒副反应治疗前后无明显改变。结论:重离子束(12C6+)放射治疗皮肤恶性肿瘤近期疗效好,并发症轻,远期疗效、晚期副反应等尚需进一步长期全面的观察和更多的研究提供依据。

黄河源区退化高寒草地土壤种子库:种子萌发的数量和动态

对青藏高原黄河源区不同退化程度高寒草地的土壤种子库土样用土壤分析筛进行浓缩,并以萌发法分析土壤种子库萌发种子数量和动态.结果表明,孔径0.25~2 mm的土壤分析筛分离土样中萌发种子可达萌发种子总量的85%~97%,而小于0.25 mm的土样中未发现种子.因此,用0.25 mm孔径大小的土壤筛对高寒草地土壤种子库土样进行大规模浓缩是一种方便、可靠的方法.4种不同退化程度高寒草地(A:未退化草甸;B:轻度退化草甸;C:中度退化草甸;D:重度退化草甸)的土壤种子库在实验室条件下萌发的种子数量分别为:A 1 194~3 744粒/m2,平均2 421.3粒/m2;B 5 376~1 0912粒/m2,平均7 786.7粒/m2;C 2 304~1 3216粒/m2,平均8 695.5粒/m2;D 4 768~12 352粒/m2,平均8 125.9粒/m2.除样地A外,其它3个样地的可萌发种子数量差异不大.单子叶植物种子在培养到d 10左右开始萌发,双子叶植物在5~7 d内开始萌发,前者3 wk后基本不再萌发,后者5 wk左右停止萌发.4个样地土壤种子库种子萌发主要集中在第2~3周,并表现出近似单峰型格局.图1表3参39

吉林省白城地区干草原栗斑腹的繁殖生态

栗斑腹在吉林省为留鸟 ,一年可繁殖两次 ,其雏鸟为典型的晚成鸟。 4月末开始有求偶追逐和争雌行为 ,5月中旬产卵。雌雄鸟筑巢时间分别是 43 min/d和 3 6min/d(筑巢第 4天 )。平均窝卵数为 5 .0 9± 0 .5 8枚 /巢 (n=3 1 ) ,孵卵前、中、后期雌鸟孵卵占白天活动时间的 3 5 %、74.5 %和 67.6% ,孵化期为 1 2 d,孵化率为 3 6.3 % ,2、8日龄喂雏分别为 4.5次 /h和 9.0次 /h。雏鸟的体重及外部器官的发育除嘴峰外 ,生长曲线均符合 Logistic方程 ,而嘴峰长的生长近似直线 ,栗斑腹雏鸟生长发育体重的生长模型为 :W =1 4.95 /1 +(e- 0 .552 ( t- 3.6 3) ) ,雏鸟 1 1日龄后出飞 ,繁殖成活率为 2 7.7%。

水稻化感品种根分泌物中非酚酸类化感物质的鉴定与抑草活性

水稻化感品种能从根系分泌释放化感作用物质 ,长期以来 ,酚酸类物质被认为是水稻根分泌的主要化感物质 ,但这一结论常常被质疑。利用连续循环和直接树脂吸收两种方法采集典型的水稻化感品种 PI31 2 777幼苗的根分泌物 ,并用液相色谱 /质谱(L C/ MS)联用技术鉴定了根分泌物中的非酚酸类物质。结果显示 ,水稻 PI31 2 777幼苗根系能分泌释放 7-甲氧基羟基肟酸、羟基肟酸、3-异丙基 - 5 -乙酰氧基环己烯酮 - 1、5 ,7,4′-三羟基 - 3′,5′-二甲氧基黄酮、二萜内酯 A和二萜内酯 B6个非酚酸类化合物。经液相色谱 (HPL C)定量分析 ,这些化合物在水稻生长 1 0 d的根分泌物中的浓度为 5～ 1 9μmol/ L。进一步的生测结果显示 ,这些化合物在其释放的浓度范围能对稻田常见的稗草和异型莎草有抑制活性 ,尤其是这些化合物的等摩尔混合物的抑草活性增加 ,同时水稻根分泌物的抑草活性与土壤载体显著相关。表明羟基肟酸、环己烯酮、黄酮和二萜内酯四类非酚酸类物质是水稻的主要化感物质 ,这与近期愈来愈多的研究结果一致

土壤温度和水分对长白山3种温带森林土壤呼吸的影响(英文)

为了研究土壤温度和土壤含水量对阔叶红松林(山地暗棕壤)、云冷杉暗针叶林(山地棕针叶林土壤)和岳桦林(生草森林土)的土壤呼吸的影响,于2001年9月在长白山进行了土壤实验。利用增加土壤样柱的含水量,将土壤含水量分为9%,、21%、30%、37%和43%5个等级,土壤样品分别在0、5、15、25和35 的温度下保持24小时。阔叶红松林土壤在0~35 范围内,土壤呼吸速率与温度呈正相关。在一定的含水量范围内(21%~37%),土壤呼吸随含水量的增加而升高,当含水量超出该范围,土壤呼吸速率则随含水量的变化而降低。土壤温度和水分对土壤呼吸作用存在明显的交互作用。不同森林类型土壤呼吸作用强弱存在显著差异,大小顺序为阔叶红松林>岳桦林>云冷杉暗针叶林.红松阔叶林土壤呼吸作用的最佳条件是土壤温度35 ,含水量37%;云冷杉暗针叶林下的山地棕色针叶土壤呼吸作用的最佳条件是25 ,21%;岳桦林土壤呼吸作用的最佳条件是35 ,含水量37%。但是,由于长白山阔叶红松林,云冷杉林和岳桦林处在不同的海拔带上,同期不同森林类型土壤温度各不相同,相差4~5 ,所以野外所测的同期的山地棕色针叶林土呼吸速率应低于暗棕色森林土呼吸速率,山地生草森林土呼吸速率应高于山地棕色针叶林土的呼吸速率。图2表1参25。

基于ECA规则的企业过程数据集成系统设计与实现

流程企业中的信息主要包括管理数据和过程数据，随着企业信息化进程的推进，实现管理数据和过程数据的集成对提高流程企业生产管理与决策的质量、效益和水平起到越来越重要的作用，为实现流程企业的管控一体化创造了条件。本文在对流程企业的数据集成需求和现有的过程数据集成方法全面分析的基础上，针对现有的过程数据集成方法无法保证数据集成过程的主动性以及数据的时效性问题，提出了基于ECA规则的过程数据集成方法，该方法将具有主动机制的ECA规则引入到数据集成中，通过事件触发规则来完成数据集成任务，保证了数据的时效性和可靠性，具有一定的应用价值。论文主要工作如下： 1．分析了流程企业生产数据的特点和过程数据集成的重要性，总结了现有的解决过程数据集成问题方法的不足，针对已有方法无法保证过程数据集成的主动性和数据的时效性问题，提出了基于ECA规则的过程数据集成方法。 2.分析了流程企业数据集成的具体需求特点，给出了过程数据集成系统中的ECA规则的设计描述。基于实时数据库提供的发布/订阅机制，阐述了系统对规则中主要事件类型产生的捕获处理过程。 3.设计了基于ECA规则的过程数据集成框架，研究了框架中主要模块设计所用到的关键技术，包括复合事件检测机制、规则语法解析和规则调度策略，分析了该框架的特点，说明了系统运行流程。 4．基于上述研究，开发了基于ECA规则的企业过程数据集成系统。该系统已经投入石化和钢铁企业的实际应用中,取得了较好的效果。

基于词汇链与文本切分的更新型多文档摘要技术研究

本文从文本摘要的背景和概念入手，着重介绍了新近出现的两种自动文本摘要类型：查询型摘要和更新型摘要。接着从基于外部特征、基于简单语义分析和基于深度语义分析三个方面详细给出了自动文本摘要技术的主要方法，以及目前国际上普遍采用的三种自动摘要评价方法：ROUGE，Pyramid，BE。本文以基于词汇链的摘要方法为研究重点，在描述词汇链构建算法、词汇链摘要算法及其优化算法的基础上，主要从以下四个方面展开了研究工作： 1) 将用户查询关键词词义序列引入词汇链评分算法，利用词汇链与查询关键词词义序列的语义相似度为词汇链评分，并结合经典的Strongest Chain评分方法以获得能同时满足正确体现原文含义并且符合用户查询的词汇链。 2) 利用词汇链是原始文档含义的中间表示这一特性，通过对来自历史文档和待摘要文档这两方面的词汇链进行相似度计算，实现了历史信息与新信息的分离，并依此生成了更新型摘要。 3) 对旧词汇链结构进行扩展，使之同时包含链成员来源句段，并且通过引入文本切分研究领域的TextTiling算法，对同一条链的链成员来源句段所组成的临时短文进行切分，以切分结果作为摘要候选，实现了句子抽取的摘要生成方法和段落抽取的摘要生成方法的结合，提高了生成摘要的良构性。 4) 依据上述算法改良了原有的自动文本摘要系统，并与跨语言检索系统相结合实现了一个中英跨语言新闻摘要系统。

东北地区热量资源栅格化信息系统的建立和应用

利用东北地区172个气象台站30a(1961年～1990年)的整编温度资料和东北地区500m×500mDEM数据,建立了东北地区温度要素的空间分布模型。结果表明,温度要素的宏观本底值的模拟以三维二次幂级数展开法效果较好,其误差气温多在02℃～04℃,≥10℃初日、终日为11d～20d,≥10℃初终间隔日数为22d～29d,≥10℃积温为56℃·d～89℃·d。3省各温度要素的小地形影响程度不同,文中对小地形影响显著的要素进行了模型修正。利用建立的温度要素空间分布模型,构建了东北地区各温度要素的网格数字专题

Morphology of head-to-tail poly(3-hexylthiophene) single crystals from solution crystallization

Single crystals of head-to-tail poly(3-hexylthiophene)s have been grown through the method of isothermal solution crystallization. Electron diffraction in combination with powder X-ray diffraction revealed the crystal structure, a = 1.52 nm, b = 3.36 nm, c = 1.56 nm and alpha = beta = gamma = 90 degrees.

Crystal structures of EtEDTB center dot 1.4C(2)H(5)OH center dot 5H(2)O and H4EtEDTB(ClO4)(4)center dot C2H5OH (EtEDTB=N, N, N ', N '-tetrakis[2-(1-ethylbenzimidazolyl)methyl]-1,2-ethanediamine)

The crystal structures of EtEDTB.1.4C(2)H(5)OH.5H(2)O 1 and H4EtEDTB(ClO4)(4).C2H5OH 2 (EtEDTB = N, N,N',N'-tetrakis[2-(1-ethylbenzimidazolyl)methyl]-1,2-ethanediamine) have been determined by single-crystal X-ray diffraction method. Compound 1 crystallizes in the space group P(1) over bar with a = 11.489(2), b = 11.866(3), c = 12.002(3) Angstrom, alpha = 97.47(2), beta = 114.564(13), gamma = 114.11(2)degrees, V = 1266.6(5) Angstrom(3), Z = 1, M-r = 847.48, D-c = 1.111 g/cm(3), F(000) = 456 and mu(MoKalpha) = 0.076 mm(-1). A total of 5207 reflections were measured for 1, of which 4323 were independent. The structure of 1 was solved by direct methods and refined by full-matrix least-squares technique to the final R = 0.0706 and wR = 0.1802 for 1318 observed reflections with I > 2sigma(I). In the structure of 1, centrosymmetric EtEDTB molecules are linked by hydrogen bonds through water and ethanol to form 2-dimensional network. Compound 2 crystallizes in the space group C2/c with a = 24.260(5), b = 13.040(3), c = 17.680(4) Angstrom, beta = 97.50(3)degrees, V = 5545.2(2) Angstrom(3), Z = 4, M-r = 1140.80, D-c = 1.366 g/cm(3), F(000) = 2384 and mu(MoKalpha) = 0.289 mm(-1).

Effect of La/Ce ratio on the structure and electrochemical characteristics of La0.7-xCexMg0.3Ni2.8Co0.5 (x=0. 1-0.5) hydrogen storage alloys

The effect of La/Ce ratio on the structure and electrochemical characteristics of the La0.7-xCexMg0.3Ni2.8Co0.5 (x = 0.1, 0.2, 0.3, 0.4, 0.5) alloys has been studied systematically. The result of the Rietveld analyses shows that, except for small amount of impurity phases including LaNi and LaNi2, all these alloys mainly consist of two phases: the La(La, Mg)(2)Ni-9 phase with the rhombohedral PuNi3-type structure and the LaNi5 phase with the hexagonal CaCU5-type structure. The abundance of the La(La, Mg)(2)Ni-9 phase decreases with increasing cerium content whereas the LaNi5 phase increases with increasing Ce content, moreover, both the a and cell volumes of the two phases decrease with the increase of Ce content. The maximum discharge capacity decreases from 367.5 mAh g(-1) (x = 0.1) to 68.3 mAh g(-1) (x = 0.5) but the cycling life gradually improve. As the discharge current density is 1200 mA g(-1), the HRD increases from 55.4% (x = 0.1) to 67.5% (x = 0.3) and then decreases to 52.1% (x = 0.5). The cell volume reduction with increasing x is detrimental to hydrogen diffusion D and accordingly decreases the low temperature dischargeability of the La0.7-xCexMg0.3Ni2.8Co0.5 (x = 0.1-0.5) alloy electrodes.

BaLiF_3∶Ce~(3+)纳米粒子的制备及其光谱特性

BaLiF3属立方钙钛矿型复合氟化物,作为高效闪烁晶体可用于热中子检测[1].由于其能带隙宽,易于实现各种不同价态稀土离子掺杂,可以获得许多可调谐性质,因此它也是比较理想的光学功能材料的基质[2].Ce3+激活的BaLiF3晶体作为紫外发射的短波固体激光材料和光放大材料的研究多有报道[3~5].Ce3+的发射特性强烈依赖于基质晶体结构[6,7].氟化物基质中氧杂质的含量是影响光谱性质的重要因素[8].为了寻找氧含量低、发射波长更短、可调谐范围更宽的激光材料,本工作制备了BaLiF3∶Ce3+纳米晶,获得了一些新的有意义的实验结果.如果将其引入合适的聚合物基体制备出纳米复合体系,有可能为新一代杂化激光材料提供更理想的光学活性组分[9].1实验部分1.1仪器用日本R igaκu D/maxⅡB型X射线衍射仪(XRD)测量样品的晶体结构,辐射源CuKα1(λ=0·154 1 nm);用日本H itachi S-570环境扫描电子显微镜(ESEM)观察样品的形貌和粒径大小;用日立F-4500荧光光谱仪测试样品的激发和发射光谱;用英国VG公司ESCALAB MKⅡX射线电子能谱仪(XPS)检测样品的含氧量.1.2实验过...