Banach空间中一类强非线性发展方程的反周期解

本文讨论一类强非线性发展方程的反周期解的存在性。针对一大类既含有单调非线性算子又含有非单调非线性算子的发展方程。我们巧妙地结合单调算子理论与Leray-Schauder不动点理论，证明了其反周期解的存在性。最后，举例说明理论结果在2m阶拟线性抛物型方向的时间反周期问题中的应用。     

全球化与儒家文化--一种可能的前景

加入WTO后，中国全球化的进程进一步加快，儒家文化也面临着新的挑战，社群主义对全球化市场资本主义的批判撼动了全球化的理性市场法则在精神向度上的根基，揭露了它们的先天不足，西方国家理论界对现代市场资本主义的自我批判的反省与儒家文化主张的从社会关系，人群网络中建立和发展自我价值的思路有一定的相似性，我们可从中发掘出儒家文化对全球化的意义，随着全球化的进一步深入，儒学将发展出具有普遍意义的价值。     

英汉语比较研究综述

对我国英汉语比较研究进行了综合性论述,其中包括研究的性质、范围与方法,研究的历史与现状及研究的宗旨与目的。文章坚持使用的术语是“比较”而不是“对比”,旨在倡导研究方法上从“重异”转移到“异同并重”或“重同”,因为这是人类思维本质的共同点所规定的。从近百年的英汉语比较研究的历史中,文章归纳出十个研究目的;一、促进对外汉语教学;二、促进现代汉语研究;三、深化英语教学改革;四、深化汉语教学改革;五、为翻译学建设打基础;六、革新英汉、汉英词典编纂工作;七、革新现代汉语词典编纂工作;八、深化对语言本质的认识;九、促进英汉语类型学研究;十、进一步认识语言与思维及文化的关系。     

21世纪中国跨国公司发展战略

随着改革开放的深入发展，利用外资逐年增多，国际跨国公司的触角日益伸到我国，我国企业也逐步国际化，中国经济与世界经济的相互依存度越来越高，中国企业的跨国经营从无到有日益发展，在国民经济中发挥着越来越重要的作用。本文将对我国跨国公司的产生、发展进行研究，重点探讨在21世纪中国作为WTO成员，如何面对发展中的困难和问题以及发展中的途径。     

田径运动肌肉损伤及康复对策研究

在田径教学、训练与比赛中,由于没有完全遵循人体运动的生理规律和调控生物节律,不能使机体的工作运行保持在良好的竞技状态,导致各种各样的运动创伤,严重地影响教学、训练与运动成绩的提高.文章从运动医学理论对田径运动中肌肉损伤的原因进行分析,寻找科学的田径运动损伤康复手段。     

咪唑季铵盐棉纤维制备及其对DOSO_3~-吸附性能研究

本文用20%的NaOH溶液对棉纤维的预处理、醚化、接枝合成工艺进行了优化;在不同条件下,研究了咪唑季铵盐棉纤维对DOSO~-_3的吸附性能.结果表明,用NaOH预处理棉纤维后,在适当的条件下醚化棉纤维素,再用氢氧化钠作催化剂,按3 g环氧基纤维素醚与10 mL甲基咪唑配比接枝,得到白色味唑季铵盐纤维素.用咪唑季铵盐棉纤维对DOSO~-_3进行吸附,吸附率可达91.8%,吸附效果令人满意.     

电子商务的应用及对企业的影响

简述了电子商务理论的演变过程及电子商务的应用形式,包括电子数据交换、网上营销、网络银行等。探讨了电子商务的应用使企业面临的历史变革,指出作为21世纪的一种基本商务形式,电子商务已经成为具有敏锐战略眼光企业家的选择。     

Cr3+：MgAl2O4晶体EPR参量及其电子精细光谱的研究

考虑了SS(Spin-Spin)作用和SOO(Spin-Other-Orbit)作用，采用完全对角化方法，结合自旋Hamiltonian理论，研究了Cr³⁺∶MgAl₂O₄晶体EPR参量及其吸收光谱，理论与实验符合甚好. 在此基础上，进一步研究了⁴A₂(3d³)离子EPR参量的微观起源. 研究表明，EPR参量起源于四种微观机制：(1) SO(Spin-Orbit) 耦合机制；(2) SS耦合机制；(3)SOO耦合机制；(4) SO～SS～SOO总联合作用机制. 在这些机制中，SO机制是最主要的.     

The Crystal Structure of N-Benzoyl-N''-(2-hydroxyethyl)-thiourea

Thiourea compounds are excellent agents of bioactive substance. A number of biological activities are associated with substituted thiourea derivatives. A survey of literature reveals that some work has been reported on benzoylthiourea, which has found plenty of applications as a facile and simple ligand in determination of trances of the transition metal and as an available starting material in preparation of a wide variety of metal complexes. In recent years,N-benzoyl-N'-(2-hydroxyethyl)-thiourea has attracted considerable attention as selective reagents for the liquid-liquid extraction and preconcentration of platinum group metals and its antifungle activity.As a part of our works in studying coordination behaviours of N-benzoyl-N'-(2-hydroxyethyl)-thiourea and its bioactivity, in view of these observations and in continuation of our previous works on it, the present work was reported on the crystal structure of N-benzoyl-N'-( 2-hydroxyethyl)-thiourea.The crystals structure in the monoclinic system and space group of P21/c of N-benzoyl-N'-(2-hydroxyethyl)- thiourea (C10H12N2O2S) was determined from single-crystal X-ray diffraction analysis, a = 17.083 (3) A, b = 4.5490 (10) A, c = 14.279 (3)A, a = 90.00°, a = 102.44(3)°, a = 90.00 °, Ⅴ = 1083.6 (4)A3, Z = 4, Dc = 1.375 Mg/m3, i (Mo Ka)= 0.280 mm-1, F(000) =472. The final R and u R are 0.0399 and 0.0881 for 783 observed reflections [Ⅰ＞26(Ⅰ)].Fig. 1 shows the molecular crystal structure of N-benzoyl-N'-(2-hydroxyethyl)thiourea indicating that the carbonyl and thiocarbonyl moieties are pointing in approximate opposite directions. The six atoms in the ring structure hydrogen bonded are almost in one plane. The N(2)-H proton pendant arm extends to the carbonyl oxygen atom, forms hydrogen bond between them.The existence of hydrogen bond in benzoyl-thiourea molecular six-membered ring structure has significant implications on coordination properties, suggest the possibility of intramolecular hydrogen bond controlled coordination behaviors of these potentially bidentate ligands. In the coordination compound reported by Bourne et al.,cis-bis(N-benzoyl-N'-propylthiourea)dichloroplatinum(Ⅱ), the two ligand molecules bind to Pt(Ⅱ)via the sulfur atoms only, the carbonyl oxygen atom being locked into hydrogen bond similar to that in the free ligands.     

Synthesis under Micromave Irradition and Crystal Structure of 4''-Acetylbenzo-15 -crown-5thiosemicarbazone

The title compound is a bifunctional receptors including a thiourea group and a crown ether ring. Due to many possible potentials as a new class of reagents for membrane transports,ion-selective electrodes as well as reaction catalysts, the design and synthesis of bifunctional receptors for simultaneous binding of cations and anions is of ongoning interest in srprarnolecular chemistry1-5. In bifunctional receptors, the binding sites for anions and cations are covalently linked so as to exhibit allosteric or cooperative complexation where the binding affinity for anions(cations)is modified as a result of the cation(anion) complexation.Literature[6] reported that the ability of the thiourea group to bind anions is significantly enhanced when Na+ is bound to the crown moiety. To date, however only a few receptors of this class have been reported.6-8In this paper, we report an improved procedure under microwave irradiation that gives higher yields of title compound and needs fewer reaction times than traditional method.The structure of this compound was determined by IR ,element analysis and X-ray analysis.Scheme 1 The reaction equationThe crystal belongs to triclinic crystal system, P-1 space group, a=0.9547(0)nm, b=1.3637(3)nm,c=1.6029(3)nm, α =75.33(3) , β =83.62(3) , γ =70.99(3) ,Z=4,Dc=1.335g/cm3,F(000)=816,R1= 0.0557 ,wR2=0.1281. It is assembled into a three-dimensionalsupramolecule by intermolecular hydrogen bonds.