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1.
Paul阱中共面两离子系统的能量本征态   总被引:3,自引:0,他引:3       下载免费PDF全文
邬云文  海文华 《物理学报》2006,55(7):3315-3321
通过对Paul阱中共面两离子体系的研究,考虑共面两离子在Paul阱中库仑关联,得到了两离子系统Schrdinger方程的精确解;椐方程的精确解,分析了质心能级简并情况,计算了两离子的平衡距离和低能级的几个态函数,设计程序作出了质心径向概率分布图. 关键词: Paul阱 两离子 共面 量子逻辑操作  相似文献   
2.
1IntroductionShadowmoireinterferometryisawholefieldnoncontact3Dmeasurementtechnique.ItisfirstappliedbyH.Takasaki[1]in1970.In...  相似文献   
3.
文章首先把双星运动看做二体问题,研究以一个星体为参照系,另一个星体的轨迹为圆锥曲线,以系统的质心为参照系,每一个星体的轨迹也是圆锥曲线,然后提出了行星与恒星之间也是双星现象,地球与月球之间也是双星现象,解释了困扰物理学与天文学多年的行星运行轨道的共面性、公转的同向性难题,指出了研究行星运行轨道时惯性质量应当用折合质量计算。  相似文献   
4.
《中国化学快报》2020,31(11):2985-2987
Polymorphism makes it possible to clarify the relationship between emission property and crystal structure. However, based on the exact molecular conformation in tetraphenylethene polymorphisms, it is still challenging to evaluate the difference of intramolecular coplanarity without the support of calculation because of the complex combination of four different torsion angles between four peripheral benzenes and the central ethylene plane. Here, by using a di-formyl-functionalized tetraphenylethene derivative, two ideal polymorphisms with a consistent trend of the corresponding torsion angles have been obtained. For the first time, we explicitly demonstrated that intramolecular coplanarity is the underlying cause of the polymorphism-dependent emission of tetraphenylethene derivatives.  相似文献   
5.
1 Introduction  Intheearly 1970s ,PhilipsCo .Ltd .(Netherlands)broughtforthanovelmounttechnology—SMT (SurfaceMountTechnology ) ,whichistostickcomponentsandsolderingpasteonaprintedboardwithoutperforation .SMT basedintegratedcircuitchip ,namelySMIC ,includingBGA(Bal…  相似文献   
6.
A novel poly(aryleneethynylene), in which the main chain and the tetrathiafulvalene (TTF) side chains are coplanar, has been prepared and characterized. The polymer can self‐assemble in tetrahydrofuran (THF) and the π‐extended coplanar backbones adopt good face‐to‐face stacking, which is confirmed by X‐ray diffraction (XRD) analysis. Cyclic voltammetry has revealed that the polymer has reversible electroactive properties. The optical bandgap deduced by UV‐vis absorption spectroscopy and the electrochemical bandgap are 2.03 and 2.14 eV. The conductivities of the powder and the realigning solid of the polymer are 6 × 10−8 and 4 × 10−6 S cm−1.

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7.
Crystal structures of 5-(5-methylthien-2-yl)-2-deoxyuridine (I), 5-(5-thien-2-yl)-2-deoxyuridine (II) and 5-(5-bromothien-2-yl)-2-deoxyuridine (III) have been obtained from data collected on a four-circle Enraf-Nonius diffractometer (CAD-4 system). Space group, unit/cell parameters and finalR indices are:I, monoclinic,P21,a=9.105(2),b=20.819(2),c=7.932(2) Å, =98.79(2)°,R=5.7%;II, monoclinic,P21,a=8.720(4),b=20.793(4),c=7.884(4) Å, =95.06(2)°,R=5.8%;III, monoclinic,P21,a=9.260(2),b=41.655(7),c=7.926(2) Å, =97.996(13)°,R=9.4%. Structural properties of the title compounds are compared with those of 5-(5-chlorothien-2-yl)-2-deoxyuridine (IV) previously reported in order to explain their affinity for HSV-1 thymidine kinase and their eventual interaction with viral DNA polymerase. The main structural features observed are the coplanarity of the uracil and thienyl cycles stabilized by a S–O intramolecular interaction and the formation of dimeric intermolecular H bonds between two uracil moieties.  相似文献   
8.
Polymorphism makes it possible to clarify the relationship between emission property and crystal structure. However, based on the exact molecular conformation in tetraphenylethene polymorphisms, it is still challenging to evaluate the difference of intramolecular coplanarity without the support of calculation because of the complex combination of four different torsion angles between four peripheral benzenes and the central ethylene plane. Here, by using a di-formyl-functionalized tetraphenylethene derivative, two ideal polymorphisms with a consistent trend of the corresponding torsion angles have been obtained. For the first time, we explicitly demonstrated that intramolecular coplanarity is the underlying cause of the polymorphism-dependent emission of tetraphenylethene derivatives.  相似文献   
9.
A series of acceptor-donor-acceptor alternative small molecules were synthesized containing electron-donating central building moieties of phenothiazine, 2,7-carbazole and thieno[3,4-b]thiophene and electron-accepting moie- ties of tetrazine on both sides. The various conformations of the central blocks, with the coplanarity in an order of phenothiazine〈2,7-carbazole〈thieno[3,4-b]thiophene, have an obvious influence on the optical, electrochemical property and the crystallinity of small molecule. In addition, the blend films between small molecule and (6,6)-phenyl-C6rbutyric acid methyl ester offered significantly various morphologies, changing from uniform sur- face to interpenetrated networks. As a result, the bulk heterojunction photovoltaic devices based on the three small molecules provided varied performance, and the highest coplanar molecule based device exhibited the best photo- voltaic performance.  相似文献   
10.
In this paper, a successful application of line-structured laser sensor, involved in SMIC chip lead coplanarity measurement, is presented. With the experimental measurement system and its corresponding mathematics model, a contact-datum-plane assessment of SMIC chip lead coplanarity is developed to provide method for on-line measurement.  相似文献   
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