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991.
Fullerene polyhedra of icosahedral symmetry have the midpoints of their 12 pentagonal faces at the vertices of a macroicosahedron and can be characterized by the patterns of their hexagonal faces on the (triangular) macrofaces of this macroicosahedron. The numbers of the vertices in fullerene polyhedra of icosahedral symmetry satisfy the Goldberg equation v=20(h 2+hk+k 2), where h and k are two integers and 0 <hk≥ 0 and define a two-dimensional Goldberg vector G = (h, k). The known tripling (leapfrog), quadrupling (chamfering), and septupling (capra) transformations correspond to the Goldberg vectors (1, 1), (2, 0), and (2, 1), respectively. The tripling and quadrupling transformations applied to the regular dodecahedron generate achiral fullerene polyhedra with the full I h point group. However, the septupling transformation destroys the reflection operations of the underlying icosahedron to generate chiral fullerene polyhedra having only the I icosahedral rotational point group. Generalization of the quadrupling transformation leads to the fundamental homologous series of achiral fullerene polyhedra having 20 n 2 vertices and Goldberg vectors (n, 0). A related homologous series of likewise achiral fullerene polyhedra having 60 n 2 vertices and Goldberg vectors (n, n) is obtained by applying the tripling transformation to regular dodecahedral C20 to give truncated icosahedral C60 followed by the generalized operations (as in the case of quadrupling) for obtaining homologous series of fullerenes. Generalization of the septupling (capra) transformation leads to a homologous series of chiral C20m fullerenes with the I point group and Goldberg vectors G=(h, 1) where m=h 2+h+1.  相似文献   
992.
Spontaneous development of chirality in systems composed of achiral molecules is important for new routes to asymmetric synthesis, chiral superstructures and materials, as well as for the understanding of the mechanisms of emergence of prebiotic chirality. Herein, it is shown that the 4,4′-diphenylbenzil unit is a universal transiently chiral bent building block for the design of multi-chained (polycatenar) rod-like molecules capable of forming a wide variety of helically twisted network structures in the liquid, the liquid crystalline (LC) and the crystalline state. Single polar substituents at the apex of tricatenar molecules support the formation of the achiral (racemic) cubic double network phase with Ia d symmetry and relatively small twist along the networks. The combination of an alkyl chain with fluorine substitution leads to the homogeneously chiral triple network phase with I23 space group, and in addition, provides a mirror symmetry broken liquid. Replacing F by Cl or Br further increases the twist, leading to a short pitch double gyroid Ia d phase, which is achiral again. The effects of the structural variations on the network structures, either leading to achiral phases or chiral conglomerates are analyzed.  相似文献   
993.
    
The crystal structure of C12OH20 (lR-6R-4R-2 R-3,7,7-trimethyl-4-(2-hydroxyethyl) bicyclo [4.1.0] hept-2-ene) has been determined by X-ray diffraction. The compound crystallizes in space group P212121 witha = 5.893(1),b = 22.572(2), c = 26.164(3) ?,V = 3480.3 ?3, Z= 12. The structure was solved by modified direct methods and refined to anR value of 0.081 for 607 unique reflections. Each asymmetric unit has three molecules which are held together through intermolecular hydrogen bonds resulting in a novel spiral-type arrangement of molecules. The six-membered ring has a half-chair conformation. gNCL Communication No. 4305  相似文献   
994.
995.
996.
A modified direct method is developed to find finite symmetry groups of nonlinear mathematical physics systems. Applying the modified direct method to the well-known (2 1)-dimensional asymmetric Nizhnik-Novikov-Vesselov equation and Nizhnik-Novikov-Vesselov equation, both the Lie point symmetry groups and the non-Lie symmetry groups are obtained. The Lie symmetry groups obtained via traditional Lie approaches are only special cases. Furthermore, the expressions of the exact finite transformations of the Lie groups are much simpler than those obtained via the standard approaches.  相似文献   
997.
The new types of conserved quantities, which are directly induced by Lie symmetry of nonholonomie mechanical systems in phase space, are studied. Firstly, the criterion of the weak Lie symmetry and the strong Lie symmetry are given. Secondly, the conditions of existence of the new type of conserved quantities induced by the weak Lie symmetry and the strong Lie symmetry directly are obtained, and their form is presented. Finaily, an Appell-Hamel example is discussed to further illustrate the applications of the results.  相似文献   
998.
总结了近年来对奇特核和极端条件下核物质的研究结果,包括原子核的新有效相互作用、新对称性及奇特性质.在相对论平均场理论中,发现了反核子谱中的自旋对称性,提出了包含微观质心修正的新相互作用PK1,PK1r和PKDD?.这些新相互作用不但可以很好地描述核物质与中子星,还可以很好地给出靠近或远离β稳定线的原子核性质,包括中子滴线核与超核中的晕和巨晕现象.  相似文献   
999.
Lie group technique for solving differential-difference equations is applied to a new (2 1)-dimensional Toda-like lattice. An infinite dimensional Lie algebra and the corresponding commutation relations are obtained.  相似文献   
1000.
单面完整约束力学系统的形式不变性   总被引:7,自引:4,他引:3       下载免费PDF全文
张毅 《物理学报》2004,53(2):331-336
研究单面完整约束力学系统的形式不变性.根据运动微分方程的形式在无限小变换下的不变性,给出了单面完整约束力学系统形式不变性的定义和判据,建立了系统的形式不变性与Noether对称性、Lie对称性之间的关系,并举例说明结果的应用. 关键词: 分析力学 单面约束 形式不变性 Lie对称性 Noether对称性 守恒量  相似文献   
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