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101.
WANG Jingping ZHAO Junwei & NIU Jingyang Institute of Molecule Crystal Engineering School of Chemistry Chemical Engineering Henan University Kaifeng China 《中国科学B辑(英文版)》2005,(4)
Polyoxometalate chemistry is a very important re- search field in modern inorganic chemistry. Poly- oxometalates have attracted extensive interest owingto their unique physical-chemical and unusual topo- logical properties as well as their great potential… 相似文献
102.
报道了以Nd∶LiYF(Nd∶LYF)为增益介质、用硅酸镓镧(La3Ga5SiO14,LGS)晶体进行电光调Q的非稳腔调Q激光器的脉冲特性。Nd∶LiYF的两端按σ偏振1.053μm光的布儒斯特角切割,不需另加起偏镜,实现了单一偏振光振荡。LGS晶体电光Q开关插入损耗小(2%),抗光伤阈值高(950MW/cm2),与DKDP相比,具有不潮解等优点。当抽运能量为120J、重复率3Hz时,单脉冲输出能量为275mJ,脉冲宽度为8ns,动静比为76%,输出能量不稳定度小于3%,偏振度大于99%,光束发散角为0.7mrad。文中还对本激光器偏振特性、非稳腔设计、LiYF导热性能和热透镜效应补偿进行了分析,对LGS电光调Q开关工作性能、工作方式以及存在的问题也进行了分析。 相似文献
103.
本文采用提拉法生长了硼酸钙氧钆GdCa4O(BO3)3(简称GdCOB)晶体,测定了晶体在不同几何配置下的拉曼光谱,并与三硼酸钙氧钇YCa4O(BO3)3(简称YCOB)晶体进行了比较,讨论了稀土元素对拉曼光谱的影响。由于钆和钇原子半径的差别和镧系稀土元素的晶场效应,使GdCOB晶体的部分拉曼谱线存在红移,从拉曼光谱随方向的变化可知晶体有很强的各向异性;从拉曼光谱的强度可知晶体有较强的非线性光学性质。实验可知其非线性光学特性主要来自硼氧三角形而不是氧八面体的畸变。 相似文献
104.
研究了Ce∶KNSBN光折变类光纤在泵浦光和信号光夹角分别为小角度和大角度两种情况下简并四波混频的基本特性 .当夹角较大时 ,在光折变类光纤内部形成了两个四波混频作用区域 ,获得了比小角度情况提高 4倍的大相位共轭反射率 .给出了Ce∶KNSBN光折变类光纤中 ,在入射夹角分别为小角度和大角度两种情况下 ,相位共轭光反射率分别随信号光光强、两束泵浦光光强比变化的实验结果 ,并用理论公式进行了拟合 ,理论分析和实验结果相符 .还研究了Ce∶KNSBN光折变类光纤四波混频光栅模式和相位共轭光时间响应特性 .光折变类光纤的相位共轭响应时间较快 ,可为秒量级 . 相似文献
105.
106.
HIGH CONVERSION EFFICIENCY TANDEM KTP FREQUENCY DOUBLER 总被引:2,自引:0,他引:2
Xueiju SHEN Chunming LIU ^Optical Teaching Eesearching Section Ordnance Engineering Academy Shijiazhuaug ChinaZhongshu SHAO Enquan LIUCrystal Materials Besearch Institute Shandong University Jinan China 《Chinese Journal of Lasers》1992,1(1):61-65
The two-piece tandem KTP frequency doubler with mutually perpendi-oular KZ planes has been studied both theoretically and experimentally.Its conversionefficiency of second harmonic generation(SHG)exceeds 80% and the dynamic range ismuch greater than that of monolithic KTP doubler at the laser power used in theexperiments.The experimental result shows that this doubler has excellent performancesand the second harmonic beam is elliptically polarized. 相似文献
107.
108.
Electrons are transferred in collisions between potassium atoms and CH(3)NO(2) molecules that have been oriented in space prior to collision. The electron transfer produces K(+) ions, parent negative ions CH(3)NO(2)(-), and the fragment ions e(-), NO(2)(-), and O(-) in amounts that depend on the energy. The positive and negative ions are detected in coincidence by separate time-of-flight mass spectrometers at various collision energies for both CH(3)-end attack and NO(2)-end attack. The steric asymmetry for electrons and CH(3)NO(2)(-) is essentially zero, but the steric asymmetry for NO(2)(-) shows that NO(2)(-) is formed mainly in CH(3)-end collisions. There is evidence that the electrons and NO(2)(-) have the same transient precursor, despite having different steric asymmetries. It appears likely that the precursor is formed by electron transfer mainly in collisions normal to the molecular axis leading to near zero steric asymmetry for the electron. This transient precursor can also eject an NO(2)(-) ion, which is more likely to be removed as KNO(2) salt when K(+) ions are near the NO(2) end of the molecule, with the result that CH(3)-end collisions seem to produce more NO(2)(-). 相似文献
109.
Sie Tiong Ha Teck Ming Koh Guan Yeow Yeap Hong Cheu Lin Jun Kit Beh Yip Foo Win Peng Lim Boey 《中国化学快报》2009,20(9):1081-1084
A homologous series of Schiff base esters,6-methoxy-2-(2-hydroxy-4-alkanoyloxybenzylidenamino)benzothiazoles,comprising a benzothiazole moiety as the core was synthesized.All the members of this series exhibited an enantiotropic nematic phase. The azomethine linkage along with the lateral hydroxyl and terminal methoxyl groups were found to exert an effect on the mesomorphic properties. 相似文献
110.
The cyanocarbons tetracyanoethylene (TCNE) and tetracyanoquinodimethane (TCNQ) are important electron acceptors used in organic electronic applications. A common approach to enhancing their performance is by structural modification with previous studies focusing on substituting the cyano ligands or annular moiety. In this work, we assess the effect of hypovalent substitution, swapping carbon for silicon, on the potential energy surfaces and adiabatic electron affinities (AEAs). Si-substitution generally enhances AEA, and in the case of TCNQ stabilizes an open-shell singlet diradical state. Such findings may find value in the design of new materials based on the cyanocarbon platform.
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