Braiding structures on formal Poisson groups and classical solutions of the QYBE

If is a quasitriangular Lie bialgebra, the formal Poisson group can be given a braiding structure. This was achieved by Weinstein and Xu using purely geometrical means, and independently by the authors by means of quantum groups. In this paper we compare these two approaches. First, we show that the braidings they produce share several similar properties (in particular, the construction is functorial); secondly, in the simplest case (G=SL₂) they do coincide. The question then rises of whether they are always the same this is positively answered in a separate paper.     

Bundles, Handcuffs, and Local Freedom

We answer a question of J. Anderson's by producing infinitely many commensurability classes of fibered hyperbolic 3-manifolds whose fundamental groups contain subgroups that are locally free and not free. These manifolds are obtained by performing 0–surgery on a collection of knots with the same properties.     

Recognition of subgroups of direct products of hyperbolic groups

We give examples of direct products of three hyperbolic groups in which there cannot exist an algorithm to decide which finitely presented subgroups are isomorphic.

     

Algebraization of Spectral Problems in the Bargmann—Fock Representation

Examples of quasi-exactly solvable hamiltonians in the Bargmann—Fock representation are given. The existence of an invariant subspace is studied as a result of hidden symmetry of the spectral problem.     

On Two Theorems of Finite Solvable Groups

For a finite group G, let T（G） denote a set of primes such that a prime p belongs to T（G） if and only if p is a divisor of the index of some maximal subgroup of G. It is proved that if G satisfies any one of the following conditions： （1） G has a p-complement for each p∈T（G）; （2）│T（G）│= 2： （3） the normalizer of a Sylow p-subgroup of G has prime power index for each odd prime p∈T（G）; then G either is solvable or G/Sol（G）≌PSL（2, 7） where Sol（G） is the largest solvable normal subgroup of G.     

Sugar conjugates of fulvestrant (ICI 182,780): efficient general procedures for glycosylation of the fulvestrant core

We have prepared glucose and cellobiose conjugates at the phenolic 3- and hydroxylic 17-positions of the pure anti-estrogenic compound fulvestrant (ICI 182,780), which has recently been approved in the USA for the treatment of advanced postmenopausal breast cancer. Glycosylation at the 17-position was achieved most effectively using pivaloyl protection of the sugar imidates employed, which we found suppressed the competing transacylation reaction and led to improved yields of the product glycosides.     

Central quotients of biautomatic groups

The quotient of a biautomatic group by a subgroup of the center is shown to be biautomatic. The main tool used is the Neumann-Shapiro triangulation of S ^n-1, associated to a biautomatic structure on . Among other applications, a question of Gersten and Short is settled by showing that direct factors of biautomatic groups are biautomatic. Received: October 4, 1994     

关于(QU)型模糊拓扑群的直积

研究(QU)型模糊拓扑群族直积,证明了任意(QU)型模糊拓扑群族的直积仍是(QU)型模糊拓扑群;研究了(QU)型模糊拓扑群族直积的模糊单位元之重域基的结构,得到了(QU)型模糊拓扑群族直积的一些重要性质.     

子群次正规性对有限群可解性的影响

考查了次正规子群对有限群结构的影响,得到有限群可解的若干充分条件和超可解的一个充分条件.     

Synthesis of new thermosetting poly(2,6‐dimethyl‐1,4‐phenylene oxide)s containing epoxide pendant groups

A new class of thermosetting poly(2,6‐dimethyl‐1,4‐phenylene oxide)s containing pendant epoxide groups were synthesized and characterized. These new epoxy polymers were prepared through the bromination of poly(2,6‐dimethyl‐1,4‐phenylene oxide) in halogenated aromatic hydrocarbons followed by a Wittig reaction to yield vinyl‐substituted polymer derivatives. The treatment of the vinyl‐substituted polymers with m‐chloroperbenzoic acid led to the formation of epoxidized poly(2,6‐dimethyl‐1,4‐phenylene oxide) with variable pendant ratios, and the structures and properties were studied with nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and gel permeation chromatography. The ratios of pendant functional groups were tailored for the polymer properties, and the results showed that the glass‐transition temperatures increased as the benzylic protons were replaced by bromo‐, vinyl‐, or epoxide‐functional groups, whereas the thermal stability decreased in comparison with the original polymer. Within a molar fraction of 20–50%, the degree of functionalization had little effect on the glass‐transition temperature; however, it correlated inversely with the thermal stability of each functionalized polymer. The thermal curing behavior of the epoxide‐functionalized polymer was enhanced by the increment of the pendant functionality, which resulted in a significant increase in the glass‐transition temperature as well as the thermal stability after the curing reaction. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5875–5886, 2006