禄春安息香种子和攀援孔药花全草的化学成分研究

本文对禄春安息香（Styrax macranthus）种子和攀援孔药花（Porandra scandens）全草的化学成分进行了研究，共获得30个化合物，其中2个为新化合物。 从禄春安息香种子95%乙醇提取物中分离并鉴定了12个化合物，其中2个新化合物鉴定为3-[7-methoxy-2-(3,4-methylenedioxy phenyl) benzofuran-5-yl] propyl 3-[7-methoxy-2-(3,4-methylenedioxyphenyl)benzofuran-5-yl] propanoate (1) 和去甲氧基-egonol-龙胆双糖甙 (2)；已知化合物分别为2-(3,4-二氧亚甲基苯基)-5-甲酰基-7-甲氧基-苯并呋喃 (3)、egonol (4)、去甲氧基-egonol (5)、去甲基-egonol (6)、egonol-葡萄糖甙 (7)、egonol-龙胆双糖甙 (8)、egonol-龙胆三糖甙 (9)、豆甾醇 (10)、二十四烷酸 1-甘油酯 (11) 和胡萝卜甙 (12)。生物活性测试发现，化合物2具有促进雌激素E2合成的作用。 从攀援孔药花全草95%乙醇提取物中分离并鉴定了19个化合物：(2S,3S,4R)-2-[(2R)-2-羟基-二十一烷酰基氨基]-二十一烷-1,3,4-三醇 (13)、(2S,3S,4R)–2–二十四烷酰基氨基-十八烷-1,3,4-三醇 (14)、胡萝卜甙 (12)、β-谷甾醇 (15)、(20S,22E,24R)-5α,8α-表二氧-麦角甾-6,22-二烯-3β-醇 (16)、6β-羟基-豆甾-4-烯-3-酮 (17)、十六烷酸 1-甘油酯 (18)、桦木酸 (19)、大黄素 (20)、二十二烷酸 1-甘油酯 (21)、对羟基苯甲醛 (22)、十七烷酸 1-甘油酯 (23)、金色酰胺醇乙酸酯(24)、十九烷酸 1-甘油酯 (25)、棕榈酸 (26)、(E)-p-香豆酸 (27)、(22E,24S)-24-麦角甾醇-7,22-二烯-3β,5α,6β-三醇 (28)、2-去氧-β-蜕皮激素 (29)和auranamide (30)。 综述了近十年来发现的2－芳基苯并呋喃类新木脂素的结构特征、来源、生物活性和化学全合成。 Phytochemical investigation on the seeds of Styrax macranthus and the whole plants of Porandra scandens led to the isolation of thirty compounds, two of which were new ones. Two new 2-aryl benzofuran derivatives, 3-[7-methoxy-2-(3,4-methylenedioxy phenyl) benzofuran-5-yl]propyl 3-[7-methoxy-2-(3,4-methylenedioxyphenyl)benzo furan-5-yl]propanoate (1) and demethoxy egonol gentiobioside (2), were isolated from the 95% aqueous ethanolic extract of the seeds of Styrax macranthus, together with 7-methoxy-2-(3,4-methylenedioxyphenyl) benzofuran-5-carbaldehyde (3), egonol (4), demethoxy egonol (5), demethyl egonol (6), egonol glucoside (7), egonol gentiobioside (8), egonol gentiotrioside (9), stigmasterol (10), 2,3-dihydroxypropyl tetracosoate (11), and daucosterol (12). In vitro test, compound 2 promote the synthesis of estrogen E2. Nineteen compounds were isolated from the 95% aqueous ethanolic extract of the whole plant of Porandra scandens for the first time. Their structures were identified as (2S,3S,4R)-2-[(2R)-2-hydroxy-heneicosanoylamino]-1,3,4- heneicosanetriol (13), (2S,3S,4R)-2-tetracosanoylamino-1,3,4-octadecanetriol (14), daucosterol (15), β-sitosterol (12), (20S,22E,24R)-5α,8α-epidioxy-ergosta-6,22-diene- 3β-ol (16), 6β-hydroxylstigmast-4-en-3-one (17), 1-glycerol-1-hexadecoate (18), betulinic acid (19), emodin (20), 1-glycerol-1-docosoate (21), p-hydroxybenzaldehyde (22), 1-glycerol-1-heptadecoate (23), aurantiamide acetate (24), 1-glycerol-1- nonadecoate (25), palmatic acid (26), (E)-p-coumaric acid (27), (22E,24S)- 24-metbylcbolesta-7,22-diene-3β,5α,6β-triol (28), 2-deoxycrustecdysone (29), and auranamide (30). The characteristic, natural resource, bioactivity, and the total synthesis of 2-aryl benzofurans were reviewed.

唐古特瑞香和大果大戟的化学成分研究

本学位论文由两部分共3章组成。第一部分分别报道2种藏药唐古特瑞香和大果大戟化学成分的研究成果，从2种药用植物共分离鉴定了60个不同的化合物，其中12个为新结构，特别有意义的是发现了2个具有同一新骨架的二萜化合物。第二部分概述了大戟科植物多环二萜的研究进展。 第一部分包括第1和2章。在这2章中分别报道了唐古特瑞香（Daphne tangutica Maxim）和大果大戟（Euphorbia wallichii Hook. f. Fl）化学成分的分离纯化与结构鉴定。实验采用正、反相硅胶柱层析、薄层制备及HPLC等分离方法，从唐古特瑞香的根皮中共分离出32个化合物，通过红外、质谱及核磁共振等波谱方法鉴定了其中的31个，结构类型分别属于瑞香二萜类、木脂素类、香豆素类、苯丙素类及甾体类，其中有三个新的瑞香二萜型化合物，经波谱分析将它们的结构分别鉴定为1,2a-二氢-20-棕榈酰瑞香毒素、1,2a-二氢-5b-羟基-6a,7a-环氧-树脂大戟醇-14-苯甲酸酯及1,2b-二氢-5b-羟基-6a,7a-环氧-树脂大戟醇-14-苯甲酸酯，另外还有13个已知化合物为首次从该植物中分离得到。从大果大戟的根部共分离出33个化合物，鉴定了其中的30个，其主要成分为种类丰富的二萜，包括巨大戟烷型、续随子烷型、对映－阿替生烷型、对映－贝壳杉烷型、对映－松香烷型、ent-trachylobane型、对映－异海松烷型及一新骨架五环二萜ent-wallichane型，另外还有香豆素、甾体、三萜和一些简单的小分子化合物。其中新化合物有9个，经波谱分析将它们的结构分别鉴定为5-O-(2E,4E,6E)-癸三烯酰基-3,20-O-二乙酰基巨大戟醇、5-O-(2E,4Z)-癸二烯酰基-3-O-乙酰基-20-去氧巨大戟醇、3-O-(2E,4Z)-癸二烯酰基-5b,6b-氧-交京大戟醇、7-苯甲酰氧基-3,5,15-三乙酰基-续随子醇、ent-trachylobane-3-one-17-oic-acid、3α-羟基-对映-阿替斯-16-烯-14-酮、3α,6-二羟基-对映-异海松-7-烯-2,15-二酮、wallichanol A 和 wallichanol B，其中，wallichanol A 和 wallichanol B属于一新骨架类型的五环二萜。除此以外，另有13个已知化合物为首次从该植物中分离得到。 第2部分即第3章，首次概述了大戟属植物中多环二萜的化学和药理研究进展。 This dissertation is composed by two parts. The first part reports the phytochemical investigation of two Tibetan medicine plants, Daphne tangutica Maxim and Euphorbia wallichii Hook. f. Fl. Sixty different compounds including ten new compounds and two novel diterpenoids possessing a new carbon skeleton were isolated and identified. The second part is a review about the progress of studies on the polycyclic diterpeniods of the plant family of Euphorbia. The first part consists two chapters, which expatiate on the isolation and identification of chemical constituents from D. tangutica and E. wallichii. Thirty-one compounds were isolated from the root barks of D. tangutica by methods of column chromatography (silica gel, including reversed phase), preparative TLC and HPLC, and their structure were identified as nine daphnane diterpenes, six lignans, nine cumarin derivatives, five phenylpropanoid derivatives, a steroids and a benzoate on the basis of spectroscopic methods including IR, MS and NMR. Among them, three are new diterpenes with skeleton of daphnane and the structure were determined as 1,a-dihydro-20-palimoyl-daphnetoxin, 1,2a-dihydro-5b- hydroxy-6a,7a-epoxy-resiniferonol-14-benzoate and 1,2b-dihydro-5b-hydroxy- 6a,7a-epoxy-resiniferonol-14-benzoate. In addition, thirteen known ones were isolated from this plant for the first time. Isolation of the roots of E. wallichii yielded thirty compounds, twenty-four of them were elucidated as diterpenoids, which belong to different skeleton types of ingenol, lathyrane, ent-atisane, ent-kaurane, ent-abietane, ent-trachylobane, ent-isopimarane and a new pentacyclic skeleton ent-wallichane respectively. The remains including a cumarine, a triterpenoid, a steroid and three compounds with small molecule. Nine new compounds were characterized as 5-O-deca-2E,4E,6E- trienoyl-3,20-O-diacetylingenol, 5-O-deca-2E,4Z-dienoyl-3-O-acetyl-20- deoxyingenol, 3-O-deca-2E,4Z-dienoyl-jolkinol-5b,6b-oxide, 7-benzoyl-3,5,15- triacetyl-7-hydroxylathyrol, ent-trachylobane-3-one-17-oic-acid, 3α-hydroxy-ent- atis-16-en-14-one, 3α,6-dihydroxy-ent-isopimarane-7-en-2,15-dione, wallichanol A and wallichanol B, respectively, by means of comprehensive spectroscopic analysis. Among them, wallichanol A and wallichanol B were two notable novel pentacyclic diterpenoids processing a new rearranged carbon skeleton. And more, thirteen ones were firstly reported from this plant. The third chapter summarizes the research development on chemistry and pharmacology of polycyclic diterpenes from the plant family of Euphorbia for the first time.

中药射干的化学成分研究

本学位论文由4章组成。第一章是论文的主体，报道了中药射干的化学成分研究。第二章是中药射干代用品川射干的化学成分研究，并附带报道了西番莲化学成分的研究结果。第三章是射干、川射干及西番莲提取物化学成分串联质谱分析的报道。第四章为综述，概述了射干及鸢尾属植物的化学成分和药理研究进展。 在第一和二章中分别报道了射干（Belamcanda chinensis (L.) DC.）、川射干 （Iris tectorum Maxim.）及西番莲（Passiflora incarnate L.）化学成分的分离纯化与结构鉴定。采用正、反相硅胶柱层析、凝胶柱层析、薄层制备及HPLC等各种分离方法，从三种药用植物中共分离出68个不同的化合物，其中61个的结构得 得以鉴定，另外4个化合物的结构正在鉴定中，3个由于量少且有点杂质未作进一步的鉴定。 中药射干（Rhizoma Belamcandae）为射干植物的干燥根茎，从中共分离出53个化合物，通过红外、质谱及核磁共振等波谱方法鉴定了包括12个新化合物在内的48个，结构类型分别属于iridal型三萜及其新颖的二聚体、异黄酮、黄酮及黄酮醇、香豆素、甾体、芳香酸和脂肪酸及其甘油酯等。新化合物中有两个异黄酮类化合物，其结构分别鉴定为5,7,8,4′-四羟基-6-甲氧基异黄酮和5,6-二羟基-4′-甲氧基异黄酮-7-O-β-D-吡喃葡萄糖苷；八个新的iridal型三萜化合物分别鉴定为鸢尾烯（L）、16-甲氧基鸢尾烯、16-去羟基鸢尾烯、2-(E)-16-去羟基鸢尾烯、16-去羟基鸢尾烯B、3-乙酰基-16-去羟基鸢尾烯、iristectoroneL和iristectoroneM；两个结构骨架新颖的双三萜，分别命名为射干素A和射干素B，其分离纯化的困难以及结构的新颖和复杂突显出该论文的科学意义。除这些新化合物外，还有9个已知化合物为首次从中药射干中分离得到。此外，从中药射干的代用品川射干中分离得到7个已知化合物，主要是黄酮类成分及iridal型三萜化合物，其中1个三萜化合物为从射干中分离鉴定的新成分。另外还从西番莲中分离出8个化合物，鉴定了其中的6个，主要为黄酮碳苷。 第三章是关于射干、川射干及西番莲提取物化学成分的ESI-MS-MS分析，在初步探讨了从这些植物中分离鉴定出的一些异黄酮及黄酮碳苷的质谱裂解规律基础上，通过质谱和串联质谱分析，定性和半定量地检测了射干和川射干中主要的异黄酮成分以及西番莲中的黄酮碳苷成分，为这些药材品质的快速鉴定提供了一种简便方法。 第四章概述了射干及鸢尾属药用植物的化学和药理研究进展，特别是对其中异黄酮及三萜类成分的研究进展进行了深入系统的综述。 This dissertation is composed by four chapters. The first and second chapter reports the phytochemical investigation of three medicine plants, Belamcanda chinensis (L.)DC., Iris tectorum Maxim. and Passiflora incarnate L. Sixty eight different compounds were isolated and sixty one of them were identified. The third chapter described rapid ESI-MS-MS analysis of B. chinensis, I. tectorum, and P. incarnate. The forth part is a review about the progress of studies on the chemical constituents from Belamcanda chinensis and Iris species. Fifty-three compounds were isolated from Rhizoma Belamcandae, the rhizomes of B. chinensis by the methods of column chromatography (normal and reversed phase silica gel, Sephadex LH-20), preparative TLC and HPLC. On the basis of spectroscopic methods including IR, ESI-MS, 1-D and 2-D NMR, forty eight of them were identified as seventeen flavonoids, seventeen tritepenoids, one cumarin, five steroids and some benzene derivative etc. Among them, the structures of twelve new compounds were elucidated as 6-methoxy-5,7,8,4′-tetrahydryoxyisoflavoe, 4′-methoxy-5,6-dihydroxyisoflavone-7-O-β-D-glucopyranoside, iristectorene L, 16-methoxyisoiridogermanal, 16-dehydroxyisoiridogermanal, 2-(E)-16-dehydroxy isoiridogermanal, 16-dehydroxyiristectorene B, 3-acetyl-16-dehydroxyisoiridoger- manal, iristectorone L, iristectorone M, belamcandene A and belamcandene B. Last two new compounds are dimer of triterpenoids with a novel carbon skeleton. Beside the new compounds, nine known ones were isolated from this plant for the first time. Isolation of I. tectorum yielded seven compounds. On the basis of spectroscopic methods including ESI-MS, NMR and the comparison with authentic samples, three of them were determined as isoflavone, two of them were triterpenoids, and other two were β-sitosterol and apocynin. All of them are known compounds except one of iridal type triterpenoid, 16-dehydroxyiristectorene B, which also obtained from B. chinensis as a new compound. Isolation of P. incarnate yielded eight compounds. Six of them were determined on the basis of spectroscopic methods including ESI-MS, NMR and the comparison with authentic samples. Four of them are flavone-C-gluconside, and two are steroids. The third chapter describes the tandem mass spectrometry (ESI-MS-MS) analysis of the isoflavonoids from B. chinensis and I. tectorum, as well as C-glycosyl-flavonoide from P. incarnate, in order to explore the rapid methodology of validating the quality of the herbs. In addition, the fractionation rules of some iosflavonoids and C-glycosyl-flavonoids were discussed. The fourth chapter summarizes the research development on chemistry and pharmacology of medicine plants of B.chinensis and Iris species.

一种多阳极横向场电离室

描述了一种将用于兰州放射性束流线较重离子鉴别的多阳极横向场电离室。对其性能进行了初步测试,得到该电离室有较长的坪区和较好的能量分辨。在10~4Pa的P10工作气体(10％CH_4+90％Ar)下,坪区长度为700V。对~(244)Cm α放射源,在第4片阳极对应的灵敏区域能量损失为1.30MeV,能量分辨41.1keV,相对能量分辨约3.16％。

中子星物质中的K介子凝聚

用密度相关的相对论平均场理论计算了中子星物质中的K介子凝聚 ,结果表明中子星物质发生K介子凝聚的临界密度约为 2 .75 ρ0 .中子星物质URCA过程发生的临界密度在考虑DB核物质中核子自能动量修正时为 ρρ0≈ 3.16,在不考虑DB核物质中核子自能动量修正时为 ρρ0≈ 2 .2 5 ,并进一步计算了密度相关的相对论平均场理论两种参数形式对中子星物质状态方程的影响 .

枸杞体细胞胚发生中对痕量金属离子吸收的动态研究

以药用植物宁夏枸杞 (LyciumbarbarumL .)愈伤组织为材料 ,离体培养诱导体细胞胚发生。采用多重示踪技术和γ射线能谱分析法研究枸杞体细胞胚发生中对多种痕量金属离子的吸收动态。结果表明 :( 1)体胚发生中对多种痕量金属离子的吸收呈选择性。对多重示踪剂溶液中的 2 3种核素 ,只吸收了其中的 16种 (Mn_5 2、Zn_65、Co_5 6、Co_60、As_74、Se_75、mTc_95、Rh_99、V_4 8、Rb_83、Rb_84、Sr_85、Y_87、Y_88、Zr_88和Zr_89) ,而对另 7种未吸收 (Be_7、Tc_96、Ru_97、mRh_10 1、Sc_4 6、Ga_67和Cr_5 1)。 ( 2 )吸收呈动态变化 ,在同一发育期对不同的金属离子吸收率不同 ,如第 10天 ,大部分金属离子的吸收率在 5 % /g左右 ,而Se_75、Rb_83、Sr_85和Zr_89的则是 10 %～ 3 0 % /g ;在不同发育期对同一种金属离子的吸收率不同 ,如对Se_75的吸收总体呈上升趋势。第 5天达第 1峰值 14 % /g。随后缓慢下降 ,基本稳定 ,第 15天后急剧上升 ,至第 2 0天达第 2个峰值 2 0 % /g ;随着胚性细胞的分化与分裂 ,吸收既存在一致性 ,也存在非一致性。Se_75、Rb_83、Sr_85、Co_5 6和V_4 8等核素的吸收趋势相似 ,基本上呈上升曲线。而Mn_5 2的吸收趋势则类似正态分布曲线。

用于RIBLL和CSR的气体探测的研制

气体探测器是历史最悠久的核探测器之一气体探测器具有成本低廉、制备简单、性能可靠和使用方便等特点。而且气体探测器的形状和尺寸可任意设计，厚度可随气体气压的变化而改变，适合做大面积位置灵敏、大立本角探测和有较宽的动态测量范围。所以气体探测器在各自的应用范围内发挥着巨大的作用。在兰州放射性束流线（RIBLL）上开展次级束实验的过程中，束流的定位和发散度测定都是非常重要的。我们研制了两种高性能的双维位置灵勘平行板雪崩计数器（PPAC），一种为传统的三个极板结构，另外一种为五个极板的多极结构，分别适用于较重粒子和轻粒子的位置测量。对于五个极板的多极结构的探测器，灵敏面积为100mm×100mm，采用电荷分除法读出位置，我们用3组分α源测试，工作气体选用异丁烷。测试在6.5mb气压下，位置分辨为0.55mm（FWHM），探测效率大于99.2％，位置离散小于士0.2mm。一系列的性能指标都达到了同类探测器的最好水平。该探测器和以前研制的三极板PPAC的性能均已满足RIBLL的要求，将会用作RIBLL重要的束诊元件和位置探测器。同时改进后还能在即将建成的兰州重离子加速器冷却存储环（HIRFL-CSR）上的束流诊断过程中发挥重要的作用。同时，为在RIBLL上开展超重元素和超重核素的合成实验研制了一种多阳极横向场气体电离室（MAIC）。在100mbP10气体下，对应第四块大灵敏区域，5.806MeV~(244)Cm的α粒子的能量损失为1.30MeV，得出该探测器的能量分辨为41.1keV（FwHM），相对分辨为3.16％。该探测器适合于较重粒子的鉴别，性能指标已经满足RIBLL鉴glI灼子的要求。

不同土壤水分条件下北方稻田耗水规律研究

采用田测法研究不同土壤水分条件下稻田需水规律 .试验采用淹灌、湿润灌和间歇灌 3种灌水处理 .结果表明 ,在整个生育期内由田测法测得的淹灌、湿润灌和间歇灌 3种处理的蒸散量分别为 889.1、6 35 .9和 775 .9mm ,蒸散速率分别为 6 .9、4 .9和 6 .0mm·d-1.与淹灌处理相比 ,湿润灌和间歇灌处理分别节水 2 8.5 %和 12 .7% .在充分供水的情况下 ,由Penman法计算的潜在蒸散值分别比田测法小 2 9.30 % .淹灌、湿润灌和间歇灌 3种处理的生物产量分别为 16 4 38.2 2、15 887.94和 15 75 7.88kg·hm-2 ,经济产量分别为 80 14 .0 1、782 8.91和 785 3.93kg·hm-2 .统计分析结果表明 ,3种处理间的产量差别不显著 .淹灌、湿润灌和间歇灌 3种处理的水分利用效率 (WUE)分别为 9.0 1、12 .31和 10 .12kg·hm-2 ·mm-1,淹灌的WUE分别比湿润灌和间歇灌减少 2 6 .8%和 11.0 % .对比分析结果表明 ,湿润灌的节水效果最好

海洋胶红酵母、光合细菌、生化黄腐酸在海参育苗和养成中的应用效果

用二氧化氯(含量≥8%)日投量1g/m3水体两天处理一次水质,海洋胶红酵母(浓度为1×1010cfu/mL)日投量1～10mL/m3水体、光合细菌(浓度为2×1010cfu/mL)日投量1～10mL/m3水体、生化黄腐酸(含量≥60%)日投量5～10g/m3水体在海参育苗中应用。试验结果表明:与用恩诺沙星日投量1g/m3水体、EDTA螯合剂日投量2g/m3水体,及常规投饵方式进行比较,海参幼体烂边病发病率从20.0%降低到10.0%,烂胃病发病率从23.0%降低到10.0%。在海参养殖中应用海洋胶红酵母、光合细菌(球形红假单胞菌),可提高成参产量14.3%～16.4%。海洋胶红酵母、光合细菌和生化黄腐酸在海参育苗和养成中应用具有广阔前景。

黄土丘陵区林-草景观边界土壤表层大型动物多样性研究

文章通过对黄土高原丘陵区刺槐林-草地复合系统景观边界上3种景观位置的土壤表层大型动物调查、分析,结果表明:复合系统共有大型土壤动物16类,隶属于3门6纲;林缘处是土壤表层大型动物多样性最高的地方,这里土壤动物群落较复杂,类群数较多,分布均匀;草地是土壤表层大型动物多样性最低的地方,这里土壤动物群落较单一,土壤动物类群数偏少,个体数偏多,分布的均匀性较差,优势类群表现突出;林地的土壤表层大型动物多样性介于二者之间。林缘与林地内土壤动物的分布特征相似性较大,林缘与草地内土壤动物的分布特征相似性较小。

21世纪中国经济发展面临的严峻挑战

一、面临的形势在人类文明的车轮辗过数千年后,现已跨入崭新的时代之际,人类的前景却越来越暗淡,环顾当今世界,人口爆炸、粮食紧缺、生态破坏、环境污染、经济危机等社会问题,一个又一个的危机,不仅使人类已有的文明成果黯然失色,而且使人类的未来也越来越充满艰险。英国著名的生态学家爱德华·戈德把全球的生态环境恶化喻为第三次世界大战。他说,由于这场大战,“大自然在崩溃,在衰亡,其速度之快,以致如果让这种趋势继续发展,自然界将很快失去供养人类生存的能力”。这似乎是危言耸听,但严峻的现实却必须引起人们的高度警惕。生态环境的严重破坏,无论是大气污染、温室效应、全球气候变暖和酸雨等,还是各类人为灾害均大大制约着经济的发展。所以人口———环境———经济如何协调发展,是一个全球性的重大课题。80年代以来,联合国许多国际组织,以及绝大多数国家和政府,对此有一种危机感、紧迫感,并做过许多研究和分析,制定相应的政策保护环境。联合国粮农组织将1989年世界粮食日主题定为“粮食与环境”;世界卫生组织将1990年世界卫生日主题定为“环境与健康”;联合国教科文组织将90年代列为“国际环境教育10年”,1992年6月在巴西召开的联合国环境与发展大会,...

Spatio-temporal changes in annual accumulated temperature in China and the effects on cropping systems, 1980s to 2000

Change in thermal conditions can substantially affect crop growth, cropping systems, agricultural production and land use. In the present study, we used annual accumulated temperatures > 10 degrees C (AAT10) as an indicator to investigate the spatio-temporal changes in thermal conditions across China from the late 1980s to 2000, with a spatial resolution of 1 x 1 km. We also investigated the effects of the spatio-temporal changes on cultivated land use and cropping systems. We found that AAT10 has increased on a national scale since the late 1980s, Particularly, 3.16 x 10(5) km(2) of land moved from the spring wheat zone (AAT10: 1600 to 3400 degrees C) to the winter wheat zone (AAT10: 3400 to 4500 degrees C). Changes in thermal conditions had large influences on cultivated land area and cropping systems. The areas of cultivated land have increased in regions with increasing AAT10, and the cropping rotation index has increased since the late 1980s. Single cropping was replaced by 3 crops in 2 years in many regions, and areas of winter wheat cultivation were shifted northward in some areas, such as in the eastern Inner Mongolia Autonomous Region and in western Liaoning and Jilin Provinces.

Synthesis, molecular structures, and norbornene addition polymerization activity of the neutral nickel catalysts supported by beta-diketiminato [N, N], ketiminato [N, O], and Schiff-Base [N, O] ligands

A series of neutral nickel complexes [Ni(Ph)(PPh3)(N, O)] with Schiff-base ligands (N, O) [N, O = 5-Me-3-tert-Bu-(Ar-N=CH)C6H2O (1, Ar = 2,6-Me2C6H3; 2, Ar = 2,6-i-Pr2C6H3)], [Ni(Ph)(PPh3)(N,O)1, with beta-ketiminato ligands (N, O) [N, O = CH3COCHC=(CH3)N-Ar (3, Ar = 2,6-Me2C6H3; 4, Ar = 2,6-i-Pr2C6H3)] and [Ni(N, N)(PPh3)], and with beta-diketiminato ligands (N, N) [5, N, N = [2,6-i-Pr-2(C6H3)N=C(CH3)](2)CH] have been synthesized and characterized. The molecular structures of complexes 1, 4, and 5 have been confirmed by X-ray single-crystal analyses. Although their ligands have similar structures, complex 4 possesses a structure similar to that of four-coordination nickel with complex 1, while complex 5 reveals a rare three-coordination nickel geometry. These compounds show high catalytic activities of up to 3.16 x 10(7) g PNB mol(-1) Ni h(-1) for the addition polymerization of norbornene in the presence of modified methylaluminoxane (MMAO) as cocatalyst. Catalytic activities, polymer yield, molecular weights, and molecular weight distributions of polyborbornene have been investigated under various reaction conditions.

仲辛基苯氧乙酸萃取铜(Ⅱ)、钴(Ⅱ)、镍(Ⅱ)的机理

采用溶剂萃取法 ,研究了一种新型萃取剂———仲辛基苯氧乙酸 (CA -12 )氨化后从盐酸介质中萃取Cu(Ⅱ )、Co(Ⅱ )、Ni(Ⅱ )的机理。确定了萃取反应的机理、萃合物的组成及萃取反应的平衡常数。并经红外光谱确证了氨皂化的CA -12从盐酸介质中萃取Cu(Ⅱ )、Co(Ⅱ )、Ni(Ⅱ )的机理