Excited-State Dynamics of a Novel Bisimide-C60 Complex

The excited-state dynamics of a bisimide derivative (ZI) and a novel Z1-C60 complex (PSF) has been investigated by means of steady state optical spectroscopies and femtosecond time-resolved absorption spectroscopies. The lifetime of the singlet excited state of Z1 shortens drastically from 2.4 ns to 1.7ps upon going from Z1 to PSF, a significant kinetics change is in coincidence with the complete fluorescence quench caused by the C^60 attachment.Highly efficient Zl-to-C60 excitation energy transfer which is governed by the mechanism of Z1-C60 electron exchange has been verified for the PSF complex.     

Dynamics of Genuine Three-Qubit Entanglement in Ising Spin Systems

We investigate the dynamics of genuine three-qubit entanglement in the Ising model of three spins. A scheme is presented for generating the genuine three-qubit entanglement by the nearest-neighbour couplings. The effect of magnetic fields on the dynamics of genuine three-qubit entanglement is also discussed.     

Formation of three-body entanglement via a vacuum optical cavity induction in Tavis-Cummings model

After briefly introducing Akhtarshenas, concurrence vector and subvector for describing many-body entanglement, we investigate the entanglement formation for a system which contains three bodies, i.e. two identical atoms and a single- model cavity field, in the Tavis-Cummings model by calculating the concurrences. The results show that the coupling strength between two atoms, the decay cavity and the atomic spontaneous emission can change the entanglement of formation according to different modes： these factors destroy periodicity and symmetry of all concurrences, and that the coupling strength of two atoms does not change the peak value of concurrence （C）, but the strength of decay cavity and the atomic spontaneous emission decline in the peak value of concurrence （C） and the latter is more serious than the former under the same strengths. The concurrence vector and subvector are a useful measure of entanglement for a pure state of the many-body system, in that it can give novel pictures about the entanglements for the entire system and between its inner bodies.     

C60的[3＋2]环加成反应

综述了Ｃ６０的［３＋２］环加成反应的研究进展。包括Ｃ６０与亚胺叶立德、重氮化合物、叠氮化合物、氧化腈、腈亚胺、ｃｉｓ－ＨＯＣＨ２ＣＨ＝ＣＨＣＨ２ＯＣＯ２Ｅｔ、１，８－二碘萘、环丙烯酮缩醛和Ｐｙｒａｚｏｌｉｄｉｎｉｕｍ叶立德发生的［３＋２］环加成反应。     

二维高分子——新碳同素异形体石墨炔研究

二维平面网络结构的石墨炔具有大的共轭体系、宽面间距、优良的化学稳定性和半导体性能.石墨炔特殊的电子结构和孔洞结构使其在信息技术、电子、能源、催化以及光电等领域具有潜在、重要的应用前景.自2010年被成功合成后,吸引了来自化学、物理、材料、电子、微电子和半导体领域的科学家,对其诱人的半导体、微纳电子、光学、储能、催化和机械性能进行了探索.本文总结了二维高分子石墨炔的研究进展,重点描述了石墨炔潜在性质和性能的理论预测,以及石墨炔的合成及其在电子、光伏、储能和催化领域的应用等.     

1,3-Dipolar cycloaddition reaction of two different azomethine ylides to C70

1,3-Dipolar cycloaddition to Cyo of an azomethine ylide,which was generated in situ from refluxing a mixture of cyclohexanone and DL-valine in chlorobenzene under N2 afforded a monoadduct and a bisadduct.Even for longer reaction time,however,only monoadduct was obtained from the reaction of C70 with an azomethine ylide generated from refluxing a mixture of 2-undecanone and 2-aminoisobutyric acid in chlorobenzene under N2 The electrochemical properties of all the products were studied by cyclic voltammetry.     

聚(苯乙烯-丙烯酸)载体铁邻菲啰啉(5-硝基邻菲啰啉)配合物的合成及其对丁二烯聚合的催化活性

合成了不同邻菲啰啉(phen)含量的聚(苯乙烯-丙烯酸)载体铁邻菲啰啉配合物(SAAC·Fe·phen)和不同5-硝基邻菲啰啉(Nphen)含量的聚(苯乙烯-丙烯酸)载体铁5-硝基邻菲啰啉配合物(SAAC·Fe·Nphen)。元素分析和红外结果证明SAAC·Fe·phen具有下面的结构:SAAC·Fe·phen-(i-Bu)_3Al二元体系的催化效率是SAAC·Fe-phen-(i-Bu)_3Al三元体系的2倍,是小分子铁的400倍。在SAAC·Fe·phen和SAAC·Fe·Nphen体系中,当phen(或N pnen)/Fe的摩尔比为0.7左右时催化活性最高。催化活性随着Al/Fe摩尔比的增大而升高,但当Al/Fe摩尔比大于70以上活性趋于恒定,和小分子铁催化荆相比这种高分子铁催化剂可以提高聚合温度。     

聚合物载体-稀土金属配合物的研究ⅩⅦ聚(苯乙烯-4-乙烯基吡啶)钕配合物在丁二烯聚合中的催化行为

聚合物载体－稀土金属配合物的研究．聚（苯乙烯－４－乙烯基吡啶）钕配合物在丁二烯聚合中的催化行为李晓莉于广谦＊李玉良（中国科学院长春应用化学研究所长春１３００２２）关键词苯乙烯，乙烯基吡啶，共聚物，钕配合物，丁二烯聚合１９９６－０４－１１收稿，１９９６...