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The effects of the composition of catalyst (the structure and amount of bident ligand and strong acid, the cocatalytic activity of Cu〓, the roles of methanol and phenol etc.) and the copolymerization condition (the reaction time, temperature, amount of ST and CO, the structure and amount of dilution reagent etc.) on catalytic activity were studied in detail. Also the optimum copolymerization condition was chosen.

深入考察了催化体系组成(含氮双齿配体的结构与用量、强酸的结构与用量、铜盐的助催化作用、醇类与酚类化合物的作用等)和沉淀共聚反应条件(共聚反应的温度与时间、稀释剂结构与用量、苯乙烯与一氧化碳量等)对该共聚反应的催化活性的影响,优化共聚反应的聚合条件。

The oxidant 〓 plays indirect role in dissolving gold, and mainly controls the mix potential of Au in the alkaline thiourea solution. In which the "mix potential"is the decisive factor affecting the dissolution of gold. The reaction driving force is enough to have formamidine disulfide oxidize Au to Au〓 at the potential of about 0.4V. And then thiourea molecular complexes with Au〓 ion soon, which causes the fast dissolution of gold in the alkaline thiourea media. The dissolved weight of gold in 0.25 M thiourea solution with 0.05M Na〓SO〓 and 0.1M 〓 of pH 12. 5 by air at the temperature of 303K is 7. 8mg·cm〓 within 1hr.

在碱性硫脲溶金过程不起直接作用,而是通过S〓O〓来控制二硫甲脒有效形成的金在溶液中的混合电位;&混合电位&是影响碱性硫脲溶液溶金与否的决定性因素,在0.4V左右,有足够的推动力致使二硫甲脒氧化Au成Au〓,随后硫脲与Au〓络合形成稳定的络离子Au〓,从而使金快速溶解;温度为303K、pH为12.5时,在含0.05MNa〓SO〓、0.1M 〓及0.25M硫脲的溶液中,鼓入空气,金的溶解量在1hr内为7.8mg·cm〓;铜只有微量溶解,银、镍、铁则几乎不溶解。

In order to get the information of interaction between metal complex and DNA and select metal complexes which can cleave DNA effectively, twenty seven transition metal complexes containing O/N coordinate atoms have been synthesized in this thesis. We report the synthesis, crystal structure and properties of the complexes. One of the complexes is the first μ〓-oxalato tetranuclear Cu complex, in which there is ferromagnetic interaction between the copper atoms bridged by oxalate ions. Two trinuclear copper complexes containing partial cubane Cu〓O〓 cores have been synthesized and discussed the magnetic properties.

为了解金属配合物与DNA的相互作用及筛选能有效切割DNA的金属配合物,为无机药物合成及应用提供基础信息,本文利用十个含N、O原子的多齿配体设计合成了二十七个未见文献报道的过渡金属配合物,并解析了它们的晶体结构:其中包括首例μ〓-草酸根的四核铜配合物;合成了两个具有μ〓-OH〓三核缺角立方烷结构的Cu配合物;以HCBP衍生物为配体合成了七个过渡金属配合物;以SCN〓、N〓,C〓O〓等为桥联配体,以dmpyen为端基配体合成了十一个配合物。

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