二价稀土金属有机配合物的合成及反应

本文将试图对二价的铕、镱、和钐的有机配合物的合成,结构及反应性能作了较为全面的综述。     

芳烃金属配合物在有机合成中的应用

本文讨论了芳烃金属配合物中的芳香部份在与金属配合后性质上的变化,以及这些变化后的性质在有机合成中的应用。     

碱土金属邻苯二甲酸盐的振动光谱

测定了CaPHT·H2O和两种CaPHT的晶体结构, 其空间群分别属于P21/c(C2h^5,Z=4), P21/m(C2h^2, Z=8)和P2/m(C2h^1, Z=6), 研究CaPHT·H2O、CaPHT(A)、CaPHT(B)、MgPHT、SrPHT和BaPHT的IR及CaPHT·H2O的拉曼光谱, 讨论了固体样品中PHT与碱土金属离子的配位结构及其对光谱的影响。     

1-氨基环丙烷-1-羧酸的合成: 新型植物生长调节剂

本文报道了合成1-氨基环丙烷-1-羧酸的简便而价廉的方法,即乙酰乙酸乙酯法和α-氰乙酸乙酯法;并测定了产品的结构。     

Clathrate formation in water-cyclic ether systems at high pressures

Experimental data on the investigation of the water-trimethyleneoxide system,P, t, x phase diagram (up to 6 kbar) are presented. The results are compared with those on water systems with ethyleneoxide, 1,3- and 1,4-dioxane, 1,3-dioxolane and tetrahydrofuran, on the basis of which a summarizedP, t, x diagram is plotted for water-cyclic ether systems. It is shown that in all the systems in which a cubic structure II hydrate forms at 1 bar, it eventually turns to cubic structure I under pressure. The nature of high pressure hydrates is discussed.Dedicated to the memory of D. W. Davidson.     

12,14-二羟基紫韧革烯的分离和结构测定

由紫韧革菌(Stereum purpureum)代谢产物中分离出一个新的三环倍半萜烯醇(sterpurenol), 12,14-二羟基紫韧革烯。用二维核磁共振确定了它具有紫韧革烯(sterpurene,1)的骨架及它的整个分子结构。     

Iodination of alcohols using triphenylphosphine/iodine under solvent-free conditions using microwave irradiation

A straightforward and effective procedure for the conversion of benzylic, allylic and aliphatic alcohols to the corresponding iodides using Ph₃P/I₂ under solvent-free conditions using microwave irradiation is reported.     

铜催化下格氏试剂与α,ω-二溴代烷的偶合反应

七十年代发展了铜催化下格氏试剂与卤代物、磺酸酯、酰卤的选择性交叉偶合反应,以后对这类反应并未深入研究。我们以几种铜     

双核钴配合物(ROCH2C≡CCH2OR)Co2(CO)6的合成

Co_2(CO)_3中两个桥连的羰基很容易被一个炔键取代,生成羰基配合物(ROCH_2C)_2Co_2(CO)_6。此类配合物既可以催化炔烃三聚成苯,也可以作为炔烃的保护基团,还可以用它进行其它的合成。为此,我们用下述反应合成了这类配合物:     

Adducts of Rh2[MTPA]4 with some phosphine chalcogenides: nature of binding and ligand exchange

Adducts of four phosphine chalcogenides with the chiral dirhodium complex ([Rh-Rh]) were investigated by variable-temperature 1H and 31P NMR spectroscopy in order to compare their properties as axial ligands. Whereas the selenide (1) and the sulfide (2) are strong ligands with electrostatic attraction and, in addition, a significant orbital (HOMO-LUMO) interaction, the phosphine oxide compounds (P=O) bind primarily via electrostatic attraction and are relatively weak donors. Moreover, the overall bond strength in these adducts depends on steric congestion around the P=O group.