裂叶荆芥芥穗的化学成分研究

目的：对裂叶荆芥［Schizonepeta mulifida(L.) Briq.］芥穗的化学成分析进行研究。方法：利用溶剂提取和硅胶、聚酰胺、活性炭柱层析进行分离。结果：得到3个化合物，根据化合物的理化性质和光谱数据鉴定其结构。其中1个为已知成分即脱氢枞油烯(dehydrosylvestrene,V),另2个为新成分，分别命名为新壬四酸(neoenneaanetetraoic acid, ）、32亚胺基2N2氮代乙酰胺基丁内酰胺(32imino2N2nitrogen substituted acetamidocyclic buty amide, Ø）。结论：3个化合物均为首次从该植物中分得。另外还得到１个正高级烷烃混合物，经GC2MS分析证明内含十七种正碳烷

Synthesis, crystal structure and properties of (Z)-3-triphenylstannyl-1,1-diphenyl propenol

Five new organotin compounds were synthesized and characterized, X-ray crystal structure analysis of (Z)-3-triphenylstannyl-1,1-diphenyl propenol was performed, The crystal belongs to space group P2(1)/n. The cell parameters are: a = 1.235 7(2) nm, b = 0.987 4(2) nm, c = 2.208 1(4) nm, beta = 95.23(3)degrees, V = 2.683 0(9) nm(3), Z = 4, R = 0.027 9, R-w = 0.064 5. The tin atom of the molecule exists in a distorted tetrahedron, Z isomer of double bond is obtained.

A preliminary study on chemistry of phenoxynaphthacenequinones

A preliminary study on the chemistry of 6-phenoxy-5,12-naphthacenesuinone derivatives was reported, It was found that the main product was 6-(N,N-dimethylamino)-5,12-naphthacenequinone when a reaction of 6-chloro-5,12-naphthacenequinone with 4-hydroxyazobenzenes in DMF was carried out under certain reaction conditions. When the reaction of 6-[4-(4-hydroxyphenyl)isopropyl)phenoxy]-5, 12-naphthacenequinone and epichlorohydrin was carried out in an acetone/DMF(V/V=2/1) mixed solvent and in the presence of K2CO3 and KI, a new phenoxynaphthacenequinone derivative,6,6'-[1-methylethylidenebis(4,1-phenyleneoxy)]bis(5,12-naphthacenequinone), was obtained.

THE SYNTHESES CHARACTERIZATION AND CRYSTAL-STRUCTURE OF RARE-EARTH COMPLEXES WITH L-PROLIN

The complexes of Ln(L-Pro)s(H2O)2(ClO4)3(Ln = Pr, Nd and Er. L-Pro = L-Proline) were synthesized and characterized by elemental analysis, IR. spectra and thermal analysis. The singal crystal Pr2(L-Pro)6(H2O)4(ClO4)6 Was also obtained. The crystal belongs to monoclinic, P2(1), a = 0.9879 (3) nm, b = 2.1883 (4) nm, c = 1.3393 (2)nm, beta = 91.23(2)-degrees, V = 2.895(1) nm3, Z = 2. R = 0.035 for 5032 observed reflections. The coordination polyhedron of Pr(III) ion comprises six oxygen atoms from L-Pro molecules and two water molecules. Each L-Pro molecule coordinates to two Pr(III) ions through its carboxyl group which serves as a bridging bidentate ligand to form onedimensional chain structure.

成键和极化对电子云扩大效应的影响

本文研究了不同晶体中过渡元素的电子云扩大效应参数β(β=1-k·h),发现它与配位体数目N,配位体和全属离子化学健的共价性f_c及配位体的键城极化率d_L有关,给出h参数的表达式:h=(f_c·α_L·N)~(1/2),最后计算了若干晶体的h值和Cr~(3+),Co~(2+),Ni~(2+),Mn~(2+),Ti~(2),V~(2+),Cr~(2+),Fe~(2+)等离子的k值。

稀土与L-脯氨酸配合物的合成、表征及晶体结构

本文合成了通式为Ln(L-Pro)_3(H_2O)_2(ClO_4)_3(Ln=Pr、Nd、Er,L-Pro=L-脯氨酸)的固体配合物.元素分析、红外光谱、热分析对配合物进行了表征.培养了镨脯氨酸配合物的单晶,X射线四圓衍射确定了晶体的结构.晶体属于单斜晶系、空间群P2_1,α=0.9879(3),b=2.1883(4),c=1.3393(2)nm,β=91.23(2)°,V=2.895(1)nm~3,Z=2.晶体中每一个镨原子与来自6个L-脯氨酸羧基上的6个氧原子和2个结晶水分子键合,形成了一个八配位的稍有畸变的三角十二面体.每一个L-脯氨酸分子以羧基双齿方式与两个镨离子配位,形成了一个无限长的链状结构.

EQUATION OF STATE FOR POLYMER SOLIDS

A new equation of state for polymer solids is given by P = B0/4 98[(V0/V)7.14 - (V0/V)2.16 + T/T0] comparison of the equation of state with experimental data is made for six kinds of polymers at different temperatures and pressures. The results obtained shown that the equation is suitable to describe the compression behavior of solid polymers in the region without transition.

CRYSTAL STRUCTURE AND THERMAL ANALYSIS OF ERBIUM COMPLEX WITH BENZENE ACETIC ACID

The crystal structure of erbium (III) complex of benzene acetic acid is reported. The complex crystallizes in the monoclinic space group P2(1)/a with a = 0,9008(3)nm, b=1.4242(5) nm, c=1.8437(7) nm, beta=98.80(3)degrees, V = 2.337(1) nm(3), Z = 4. The mechanism of thermal decomposition of complex has been studied by TG-DTG-DTA. The activation energy for dehydration reaction has been calculated by Freeman Carroll method. The enthalpy change for dehydration and phase change process has been determined.

Er_2((PhCH_2COO)_6)·4H_2O的结构及热分析

用X-射线四圆衍射仪测定了Er_2(PhCH_2COO)_6·4H_2O的晶体结构。配合物属于单斜晶系,空间群为P2_1/α,晶胞参数:α=0.9008(3)nm,b=1.4243(5)nm,c=1.8437(7)nm,β=98.80(3)°,V=2.337(1)nm~3,Z=4.采用TG-DTG-DTA研究了配合物的热分解过程,确定了热分解机理。采用Freeman-Carroll方法计算了配合物脱水过程的活化能和反应级数。用DSC测定了配合物脱水,熔化过程的焓变。

固态高聚物状态方程的研究

本文从理论上导出了一个新的三参数固态高聚物的状态方程p=(B_o/4.98)[(V_o/V)~(7.14)-(V_o/V)~(2.16)+(T/T_o)] 在不发生转变的温度区域内,它适用于描述固态高聚物的压强-体积-温度关系.方程形式简单,物理参数的意义较明确.

1-甲基-1,4,7,10-四氮杂环十二烷镧配合物的合成及晶体结构

合成了1-甲基-1,4,7,10-四氮杂环十二烷(L)配体。在乙腈中培养了La(L)(CH_3CN)-(H_2O)(CF_3SO_3)_3配合物单晶,测定了其红外光谱和质子核磁共振谱。用X射线衍射方法测定了配合物的晶体结构,该晶体属于单斜晶系,P2_1/n空间群,a=0.9700(2)nm,b=1.5966(2)nm,c=1.9085(1)nm,β=104.71(3)°,V=2.8588(50)nm~3。配合物中镧为9配位,其配位多面体为扭曲的单帽四方反棱柱体。

江河源区不同建植年限人工草地土壤微生物及酶活性研究

对江河源区不同建植年限人工草地(2龄、4龄、6龄)土壤养分、微生物数量及酶活性进行研究.结果表明:不同建植年限人工草地土壤养分随着建植年限的增加呈"V"型规律变化,其中人工2龄草地土壤养分含量最高,6龄草地土壤养分含量虽不及2龄草地高,但均明显高于4龄草地.土壤细菌和放线菌数量与土壤养分变化规律一致,真菌数量随建植年限的增加呈降低趋势,土壤脲酶、过氧化氢酶和中性磷酸酶活性与细菌、放线菌和土壤养分变化规律相同.同时,土壤养分、微生物数量和酶活性变化均具有明显的空间层次现象,即随土层的加深呈降低的趋势.经典型相关分析表明,土壤细菌与土壤有机质、全氮、速效钾和pH值之间相关性最好,脲酶和过氧化氢酶活性与土壤有机质、全氮、速效氮、速效钾和pH值之间相关性最好,故土壤微生物数量和酶活性可作为评价土壤肥力的指标.