整立电杆三点吊最优吊点的研究分析

根据输电线路中杆塔施工的实际工程需要,主要研究分析了整立电杆三点吊最优吊点的确定方法,建立了整体电杆三点吊的数学模型,编制了微机软件,解决了整体电杆三点吊方案设计中的难题。     

Host dependent thermal stability and frequency upconversion of Er^3＋-doped heavy metal oxyfluoride germanate glasses

The upconversion properties of Er^3＋-doped heavy metal oxyfluoride germanate glasses under 975 nm excitation have been investigated. The intense green （551 and 529 nm） and relatively weak red （657 nm） emissions corresponding to the transitions ^4S3/2→^4I15/2, ^2H11/2→^4 I15/2 and ^4F9/2 →^4I15/2, respectively, were simultaneously observed at room temperature. The content of PbF2 has an important influence on the upconversion luminescence emission. With increasing content of PbF2, the intensities of green （529 nm） and red （657 nm） emissions increase slightly, while the green emission （551 nm） increases markedly. These results suggest that PbF2 has an influence on the green （551 nm） emission more than on the green （529 nm） and red （657 nm） emissions.     

Spectroscopic properties of neodymium-doped tellurite glass fiber

Nd~(3+)-doped tellurite glass and a single mode tellurite glass fiber with a core diameter of 8 μm were prepared in this work. The 1.33-μm emission from the ~4F_(3/2)→~4I_(13/2) transition of Nd~(3+) with a spectral bandwidth of 55 nm in tellurite glass fiber is observed. The lifetime of 164 μs of ~4F_(3/2) level and quantum efficiency of about 100% are obtained.     

一种新的含吡唑啉酮氨基硫脲化合物的晶体结构及其光致变色性质

A new photochromic organic compound of thiosemicarbazone, 4-（p-bromo-α-methylaminothiocarbonyl hydrazonobenzal）-2,5-dihydro-3-mcthyl-5-oxo-1-phcnyl pyrazolc, was synthesized and characterized by elemental analyses, IR, ^1H NMR spectra, and X-ray single-crystal diffraction analysis. The compound exhibited an interesting photochromism in the solid state when irradiated by ultraviolet light at 365 nm. The photochromic kinetics was studied by the time-dependent powder UV-Vis reflectance spectra. The intcrmolecular and intramolecular hydrogcn-bonding interactions may be responsible for the photochromic phenomenon.     

类氢氖在高温高密度等离子体中的光谱漂移

 采用离子球模型，通过自洽求解Poisson方程和Dirac方程，得到氖的类氢离子低能级组态的能级能量随等离子体电子温度和电子密度的变化关系，进一步研究了等离子体电子温度和电子密度对光谱漂移的影响。结果表明：光谱漂移随着等离子体电子密度的增大而增大，随着电子温度的升高而减小；谱线精细结构分裂随着电子密度的增大而减小，随着电子温度的升高而增大。等离子体对束缚电子的屏蔽是决定光谱漂移的主要原因。这些变化规律不仅对等离子体光谱模拟结果产生影响，而且使实验上观测光谱的相对或绝对漂移成为可能，从而为高密度等离子体诊断的新方法提供了理论依据。     

Lanthanide Complexes for Oligomerization of Phenyl Isocyanate

IntroductionThestudyonthereactivitiesoflanthanidecomplexesto wardisocyanateshasattractedmuchattention .Ithasbeenre portedthatlanthanidealkoxides,1anddivalentdiaza pentadi enyllanthanidecomplexes2 canbeusedasthesinglecompo nentinitiatorsforisocyanatespolymerization .Recentlyourre searchgrouphasalsofoundthatlanthanoceneamide ,3diva lentaryloxideofsamarium4 ,5anddivalentsamarocene6 areallactivefortheoligomerizationofphenylisocyanate,andtheactivespeciesforthesethreesystemswereallsuccessfullyisolat…     

Amplified spontaneous emission properties of a single mode Er3+-doped tellurite fiber

Spectral characteristics of the amplified spontaneous emission(ASE)from a novel single mode Er3+ doped tellurite fiber with D-type cladding is reported in this letter.When pumped at 980 nm,an ASE source that has nearly a 100-nm flat FWHM bandwidth is obtained with a fiber length of 30-60 cm. Variation of ASE spectra with pump powers and fiber lengths are measured.Output power up to 2.0 mW is obtained with a launched pump power of 660 mW.     

一类反应扩散系统的分歧与斑图

本文研究了一类发生在密闭容器中的不可激活的高次自催化反应扩散系统．在适当的条件下,用渐进近似的方法讨论了系统平衡态的稳定范围;用多重尺度的方法证明了当扩散系数λ充分小时,系统出现两种类型的斑图,一类是由Hopf分歧引出的驻波斑图;另一类是由 Pitchfork分歧引出的定波斑图．进一步还讨论了,在分歧点附近,对于大于空间或等于空间波数的小扰动,斑图是局部稳定的,而小于自身空间波数的小扰动,斑图是不稳定的．     

The First Intramolecular Charge Transfer Transition Based on 2-Ureido-4[1H]-pyrimidinone Binding Module

The first intramolecular charge transfer transition based on 2-ureido-4[1H]-pyrimidinone binding module was reported.     

钌亚丙二烯基配合物与肼的反应性质:丙烯腈配合物的生成（英文）

以双齿P,N-配体8-(二苯基膦基)喹啉(DPPQ)为支撑配体的钌亚丙二烯基配合物[RuCl(=C=C=CR_2)(DPPQ)_2]-[BPh_4](3a:R=苯基;3b:CR_2=FN=亚芴基)可由双核钌配合物[Ru(μ-Cl)(DPPQ)_2]_2[BPh_4]_2(1)分别与过量的1,1-二苯基炔丙醇(2a)或9-乙炔-9-芴醇(2b)反应得到.配合物3易与肼在室温下反应生成丙烯腈的钌配合物[RuCl(N≡C—CH=CR)2)(DPPQ))2][BPh)4](4a:R=苯基;4b:CR)2=FN=亚芴基),该反应涉及肼对亚丙二烯基配体α-碳原子的分子间亲核进攻,是首例肼对金属亚丙二烯基加成生成丙烯腈的反应.配合物4与过量的丙炔醇2反应可释放出3,3-二苯基丙烯腈(5a)或3-芴基丙烯腈(5b),并再生亚丙二烯基配合物3.此外,初步考察了配合物1对端基炔丙醇与肼反应生成丙烯腈的催化活性,结果表明该催化反应的确可以进行,但是得到的丙烯腈产物的产率不高.尽管结果不是很理想,但是这些研究表明可望发展端基炔丙醇与肼经由过渡金属亚丙二烯基中间体转化为丙烯腈的新催化反应.