Multiphonon vibrational relaxation in liquids: should it lead to an exponential-gap law?

The profound differences between solids and liquids notwithstanding, high-frequency vibrational energy relaxation in liquids seems to be well described by assuming that the excess energy is being transferred into discrete overtones of some fundamental intermolecular vibrations-precisely the way it is in crystalline solids. In a solid-state context, this kind of analysis can be used to justify the observation that relaxation rates fall off exponentially with the energy being transferred. Liquids, however, have a substantial degree of disorder, causing their relevant intermolecular spectra to have correspondingly diffuse band edges and large bandwidths. It is therefore not at all obvious what should become of this exponential-gap-law phenomenology. We show in this paper how near exponential-gap-law behavior can still be derived for vibrational energy relaxation in liquids. To do so, we take advantage of the simple dynamics that the high-frequency relaxation has when it is launched from an individual instantaneous configuration. Interestingly, the physically relevant region turns out not to be true asymptotic limit of our formalism, but for realistic liquid parameters the behavior in the physical regime differs only slightly from an exact exponential-gap law and is strikingly independent of the details of the intermolecular spectra.     

The stereoselective synthesis of novel macrolide antibacterial agents via an intramolecular 1,3-dipolar cycloaddition of azomethine ylide

An intramolecular 1,3-dipolar cycloaddition of azomethine ylide, generated in situ via the reaction of C12-glycinate derivative of macrolide with formaldehyde, provided a novel tricyclic macrolide. The high stereoselectivity of this [2+3] reaction was achieved by introducing a suitable directing group at C-6 position of macrolide.     

邻苯二酚紫退色光度法测定微量锰(Ⅱ)

在硫酸介质中．高锰酸根氧化邻苯二酚紫使其退色，退色程度在一定范围内与高锰酸根加入量成良好的线性关系。据此建立了一种测定微量锰（Ⅱ）的新方法。最大吸收波长λmax＝550nm，表观摩尔吸光系数ε＝4．2×104L·mol-1·cm－1·。锰（Ⅱ）量在0－0．8mg／L范围内符合比耳定律．方法应用于求和面粉中微量锰（Ⅱ）的测定，结果满意。     

乙醇酸和DL─乳酸交替共聚物的合成和表征

乙醇酸和ＤＬ－乳酸交替共聚物具有不同于其无规共聚物的理化性能和生物降解性。以ＤＬ－３－甲基－１，４－二烷－２，５－二酮为单体，通过在辛酸亚锡引发下的本体开环聚合，合成了该交替共聚物，并进行了结构表征。     

交联网络和浓溶液中高分子链运动的NMR研究Ⅲ.质子自旋-晶格弛豫时间与凝胶和浓溶液体系中高分子链段的运动

用自旋－晶格弛豫时间（Ｔ１）研究了溶胀的交联聚丙烯酰胺－丙烯酸网络和线型聚苯乙烯溶液中质子的弛豫行为。交联网络中，随着交联度增大，Ｔ１ＣＨ／Ｔ１ＣＨ２的值由１．１７逐渐趋近于１；而线型聚苯乙烯溶液中，Ｔ１ＣＨ／Ｔ１ＣＨ２的值由最稀浓度下的１．７过渡到１。说明在交联网络中，交联度很低时，链段的运动已经相当受约束；但交联度很大时，充分溶胀的交联网络中链段运动仍有一定自由度。而在线型高分子浓溶液中，链段的运动严重受阻，导致自旋扩散效应非常完全，彻底平均掉了各质子间Ｔ１时间的差异。     

Fission barriers for Na N 2+ cluster dissociation

The competition experimentally observed between asymmetric fission and neutral monomer evaporation as dissociation channels of excited doubly charged sodium clusters has been investigated by means of an axially symmetric, fully selfconsistent Kohn-Sham method. Ellipsoidal equilibrium configurations for parent and daughter clusters have been considered using a deformed jellium model.This paper was originally submitted in connection with the 2nd. Int. Conference on Atomic and Nuclear Clusters held in Santorini from 28. June–2. July 1993 and is published here as a regular article after an independent refereeing procedure according to the standards of Z. Phys. D     

用共振电离飞行时间质谱仪分析土壤中超痕量气态金

采用激光共振电离飞行时间质谱技术（简称ＲＩＳ－ＴＯＦ技术）对土壤中超痕量气态金的含量进行了分析研究。ＲＩＳ－ＴＯＦ谱仪具有极高的灵敏度和很强的选择性，避免了对样品的预富集过程。本文给出了该谱仪对金元素的检测限和６５个土壤中气态金样品的分析结果，以及用中子活化法随机抽样检查的结果。     

精制煤液化中油加氢裂化制取喷气燃料的研究

在实验室固定床反应装置上,选用Mo-Ni-P/Si-Al工业催化剂,对精煤液化中油进行了加氢裂化制取喷气燃料的实验。考察了反应温度、空速对芳烃加氢转化及产品馏分分布的影响。通过加氢裂化,降低了油品芳烃含量,提高了喷气燃料馏分的收率。在总压为15MPa,反应温度为350—360℃,空速为0.8—1.0h~(-1)条件下,获得了芳烃含量低于10w%的低结晶点的优质喷气燃料产品。并对煤液化中油制取的喷气燃料的组成和性质进行了分析和评价。     

基于交叉共轭结构的功能材料

近年来,人们对交叉共轭体系的制备、性能以及理论研究方面产生了极大的兴趣。本文综述了近期国内外在交叉共轭体系研究方面取得的一些最新进展,重点介绍了其在自组装、有机电致发光和离子检测等方面的最新发展动态。最后还对本课题组在交叉型p-n双嵌段寡聚物方面的研究作了详细的介绍,并对一些热点问题作了展望。