Repulsive Gravitation in the Kerr-Newman Field

It is shown that uncharged test particles, released from rest at infinity in the Kerr-Newman field, stop and rebound when the radial coordinate r takes the value r₀ = Q²/(2M). This expression corresponds to the position of a stationary source of the Kerr-Newman field found by the author. It represents the surface of a massive oblate ellipsoid of revolution undergoing rigid rotation. Besides, the magnitude of r₀ guarantees that no violation of causality occurs throughout spacetime. Although the test particles' angular momenta are always zero, they acquire a rotational motion as a consequence of the dragging of inertial frames.     

含1, 6-二(4'-吡啶基)-2, 5-二氮杂己烷的一维链状和二维网状 银(I)超分子配 合物的合成与结构

本文报道了一种新型四齿配体L：1,6-二(4'-吡啶基)-2,5-二氮杂己烷的合成,及其与银(I)的超分子配合物的一维链状和二维网状的结构。     

阴离子型表面活性剂所组成微乳液的异常流变性

对以正十六烷、油酸钾、正己醇和水所组成的微乳液进行研究,对其流变性和机理作了探讨.微乳液粘度和水油比变化的关系可用相转化来说明.层形结构区显示出有高粘度特征,并具有明显的负触变性现象.对此进行了讨论,并研究了pH值和盐类的影响.     

溶液中某些镉(II)的混合配体配合物的稳定性研究: 关于混合配体配合物相对稳定性定量表征的讨论

本文用pH电位法研究了在70%(v/v)乙醇-水溶液中Cd(II)与维生素D3(VD3)和乙二胺(en)或2,2'-联吡啶(bipy)在37±0.1℃和离子强度为0.10(KNO3)条件下, 三元混配配合物的稳定性。结果表明, 上述混合配位体系均形成稳定的1:1:1型混配配合物, 且△logK值均为较大的正值(分别为+1.06和+1.54), 但相应的logX值却并不很大(分别为2.18和2.83)。从统计效应和配合物分子内的配体间疏水相互作用, 讨论了造成这种反应常结果的可能原因, 并针对如何判断三元混配配合物相对稳定性高低等问题提出了作者的见解。     

单硼五元杂环配体(C~4BH~5)过渡金属夹心高聚物的理论研究

用一维自洽场晶体轨道法探讨了过渡金属夹心高聚物[(C~4BH~5)M]~n(M=Cr,Mn,Fe,Co,Ni)的一维链结构和电子结构.计算表明,堆积单元(C~4BH~5)M中价电子数为奇数的高聚物结构会发生Peierls畸变,而价电子数为偶数的将取规则结构,由能带结构得到, [(C~4BH~5)Mn]~n的前线能带出现交叉,可能会发生进一步的结构畸变,但也有可能保持非满状态,成为异体.[(C~4BH~5)Ni]~n可能是不稳定的.其余三个高聚物为半导体或绝缘体,这系列高聚物电荷载流子通路主要依赖于金属d轨道重叠.     

内酯型冠醚的电子电离和场解吸质谱

本文报道了十四个内酯型(包括脂肪和芳香类)冠醚的EIMS行为,借助于精确质量测定、联动扫描、去焦技术以及同位素氘标记,对它们的碎裂方式作了详尽的总结和讨论,对于其中十个化合物的FD谱图特点也作了相应的归纳。     

应用快速介吸化学电离质谱法测定热不稳定有机化合物

中图分类号:     

场解吸质谱 I: 环化核苷酸类

In this paper, nineteen FD mass spectra of cyclic nucletides are repoted. The results indicated that only (M+ + H) peak presents in the spectra of cy-AMP, cy-CMP and cy-UMP. The derivatives of cy-AMP (except 7) have M+, (M+ + H) peaks, and the main fragments corresponding to (B + 1), (T + 1) peaks as shown in Fig. 1 in the Chinese Text. The adenosine 3', 5'-cyclic phosphite and its derivatives with P(III) are somewhat different as compared with P(Ve. In some cases neither M+ nor (M+ + H) is present in their spectra, but there are some characteristic peaks. Their fragmentation process has been shown in Fig. 2 in the Chinese Text.     

单取代苯的多重散射Xα研究

多重散射Xα方法讨论了氟苯、苯胺、硝基苯和苯腈的电离能、π轨道的电荷分布、π轨道的系数及等值图形. 表明多重散射Xα方法的波函数和电荷分布在描述取代苯活化位置方面存在某种局限性, 讨论了改善的可能途径.     

A New Look at the Ashtekar–Magnon Energy Condition

In 1975, Ashtekar and Magnon showed that anenergy condition selects a unique quantization procedurefor hypersurface orthogonal observers in general, curvedspacetimes. We generalize this result in two important ways, by eliminating the need toassume a particular form for the (quantum) Hamiltonian,and by considering the surprisingly nontrivial extensionto non-minimal coupling, for which the classical Hamiltonian differs from the classical energycalculated from the stress-energy tensor.