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71.
If G is a p-solvable finite group with a p-complement H and φ ∈ IBr(G), then P. Fong showed that there exists α ∈ Irr(H) such that αG=Φφ. In this note we prove that α can be chosen such that the field of values index
divides φ (1)p.
Received: 6 May 2005 相似文献
72.
73.
74.
Corinne Boudon Jean-Paul Gisselbrecht Maurice Gross Lyle Isaacs Harry L. Anderson Rüdiger Faust Franois Diederich 《Helvetica chimica acta》1995,78(5):1334-1344
The first systematic electrochemical study by cyclic voltammetry (CV) and rotating-disk electrode (RDE) of the changes in redox properties of covalent fullerene derivatives ( 2 – 11 ) as a function of increasing number of addends is reported. Dialkynylmethanofullerenes 2 – 4 undergo multiple, fullerene-centered reduction steps at slightly more negative potentials than C60 ( 1 ; see Table and Fig. 1). The two C-spheres in the dumbbell-shaped dimeric fullerene derivative 4 show independent, identical redox characteristics. This highlights the insulating character of the sp3-C-atoms in methanofullerenes which prevent through-bond communication of substituent effects from the methano bridge to the fullerene sphere. In the series of mono- through hexakis-adducts 5 – 11 , formed by tether-directed remote functionalization, reductions become increasingly difficult and more irreversible with increasing number of addends (see Table and Fig. 2). Whereas, in 0.1M Bu4NPF6/CH2Cl2, the first reduction of mono-adduct 5 occurs reversibly at ?1.06 V vs. the ferrocene/ferricinium couple (Fc/Fc+), hexakis-adduct 11 is reduced irreversibly only at ? 1.87 V. Hence, with incremental functionalization of the fullerene, the LUMO of the remaining conjugated framework is raised in energy. Reduction potentials are also dependent on the relative spatial disposition of the addends on the surface of the fullerene sphere. Observed UV/VIS spectral changes and changes in the chemical reactivity along the series 5 – 11 are in accord with the results of electrochemical measurements. Further, with increasing number of addends, the oxidation of derivatives 5 – 11 becomes more reversible. Whereas oxidations are increasingly facilitated upon going from mono-adduct 5 (+1.22 V) to tris-adduct 7 (+0.90 V), they occur at nearly the same potential (+0.95 to +0.99 V) in the higher adducts 8 – 11 . This indicates that the oxidations occur in these compounds at a common sub-structural element, for which a ‘cubic’ cyclophane is proposed (see Fig. 3). This sub-structure is fully developed in hexakis-adduct 11 . 相似文献
75.
I. Martin Isaacs 《Mathematische Zeitschrift》1983,182(2):205-221
76.
The crystal structures of T?3PSe4 and T?3AsS4 have been determined by x-ray diffraction techniques. These isomorphous materials are layered, with orthorhombic Pcmn symmetry. Ultrasonic measurements have shown that the shear mode velocity is anomalously low for both materials. Measurements at high pressure on T?3PSe4 have shown that the anomalous shear velocity softens to zero at 1.40 ± 0.01 GPa, indicating a second- order structural transition at that pressure. 相似文献
77.
I. M. Isaacs 《Proceedings of the American Mathematical Society》2001,129(10):2853-2859
A group is said to be capable if it is isomorphic to the central factor group for some group . It is shown in this paper that if is finite and capable, then the index of the center in is bounded above by some function of the order of the derived subgroup . If is cyclic and its elements of order are central, then, in fact, .
78.
Let G be a finite group and suppose that G = AB, where A andB are abelian subgroups. By a theorem of Ito, the derived subgroupG' is known to be abelian. If either of the subgroups A or Bis cyclic, then more can be said. The paper shows, for example,that G'/(G'A) is isomorphic to a subgroup of B in this case. 相似文献
79.
Suppose that we are given a set of powers of a prime and that . A technique is presented that enables the construction of a -group of specified nilpotence class such that its set of irreducible character degrees is exactly . If , then this can be done for and if , then the only requirement is .
80.