Brownian confinement and pinning in a Poissonian potential. II

Summary We continue our study ofd-dimensional Brownian motion in a soft repulsive Poissonian potential over a long time interval [0,t]. We prove here a pinning effect: for typical configuratons, with probability tending to 1 ast tends to , the particle gets trapped close to locations of near minima of certain variational problems. These locations lie at distances growing almost linearly witht from the origin, and the particle gets pinned within distance smaller than any positive power oft of one such location. In dimension 1, we can push further our estimates and show that in a suitable sense, the particle gets trapped with high probability, within time t and within distance (logt)²⁺ from a suitable location at distance of ordert/(logt)³ from the origin.This article was processed by the author using the LATEX style filepljour1m from Springer-Verlag     

Zero cycles on conic fibrations and a conjecture of Bloch

Let X be a smooth projective surface over a number field k. Let (CH₀(X)) denote the Chow group of zero-cyles modulo rational equivalence on X. Let CH₀(X) be the subgroup of CH ₀(X) consisting of classes which vanish when going over to an arbitrary completion of k. Bloch put forward a conjecture asserting that this group is isomorphic to the Tate-Shafarevich group of a certain Galois module atttached to X. In this paper, we disprove this general conjecture. We produce a conic bundle X over an elliptic curve, for which the group (CH₀(X) is not zero, but the Galois-theoretic Tate-Shafarevich group vanishes.     

A perturbation bound for the generalized polar decomposition

LetA be anm×n complex matrix. A decompositionA=QH is termed ageneralized polar decomposition ofA ifQ is anm×n subunitary matrix (sometimes also called a partial isometry) andH a positive semidefinite Hermitian matrix. It was proved that a nonzero matrixA ^m×n has a unique generalized polar decompositionA=QH with the property (Q ^H )=(H), whereQ ^H denotes the conjugate transpose ofQ and (H) the column space ofH. The main result of this note is a perturbation bound forQ whenA is perturbed.     

First synthesis of 1,9-dideoxyforskolin from ptychantin A

1,9-Dideoxyforskolin 2 has been synthesized starting from ptychantin A 3.     

Counterexamples in optimal quadrature

It is widely believed that order of exactness is a good measure of the quality of an algorithm for numerical quadrature. We show that this is not the case, by exhibiting a situation in which the optimal algorithm does not even integrate constants exactly. We also show that there are situations in which the penalty for using equidistant nodes is unbounded. Finally, we show that the complexity of obtaining an -approximation can be an arbitrary function of , i.e., there is no hardest quadrature problem.     

The erdös-dushnik-miller theorem for topological graphs and orders

A topological graph is a graph G=(V, E) on a topological space V such that the edge set E is a closed subset of the product space V x V. If the graph contains no infinite independent set then, by a well-known theorem of Erdös, Dushnik and Miller, for any infinite set LV, there is a subset LL of the same oardinality |L| = |L| such that the restriction G L is a complete graph. We investigate the question of whether the same conclusion holds if we weaken the hypothesis and assume only that some dense subset AV does not contain an infinite independent set. If the cofinality cf (|L|)>|A|, then there is an L as before, but if cf (|L|)<-|A|, then some additional hypothesis seems to be required. We prove that, if the graph GA is a comparability graph and A is a dense subset, then for any set LV such that cf (|L|)>, there is a subset LL of size |L|=|L| such that GL is complete. The condition cf (|L|)> is needed.Research supported by NSERC grant #A5198.     

苯胺气相N－烷基化反应研究Ⅱ．苯胺和乙醇常压催化合成N－乙基苯胺的工业应用

苯胺气相Ｎ－烷基化反应研究Ⅱ．苯胺和乙醇常压催化合成Ｎ－乙基苯胺的工业应用陈骏如，李瑞祥，韩银仙，李贤均（四川大学化学系成都６１００６４）Ｎ－乙基苯胺是制造染料、塑料、炸药和医药等许多化工产品的重要中间体，其合成方法过去多采用无机酸催化剂，如Ｈ＿２Ｓ...     

σ,π-acetylido complexes via P---C bond cleavage of phosphinoacetylenes: X-ray structure of Fe2(CO)6(CCPh)(PPh2)

Solutions of Co^II salts of organic acids in primary amines absorb molecular oxygen rapidly and irreversibly forming μ-dioxygen—cobalt complexes. Thermolysis leads to a homopolar cleavage of the OO bond with subsequent radical reactions involving ligand amine. After thermolysis the capacity of oxygen uptake is reestablished (catalysis).     

Concerted cycloaddition of chlorosulfonyl isocyanate to α-pinene stepwise rearrangement of the β-lactam cycloadduct to a γ-lactam

Chlorosulfonyl isocyanate adds to α-pinene in concerted fashion to give the unrearranged N-chlorosulfonyl-β-lactam 2 (75%). Thermolysis of cycloadduct 2 affords the rearranged N-chlorosulfonyl-γ-lactam 6 (60%) via a sequence of transient carbonium ions (45). Reductive hydrolysis of 2 and 6 gave, respectively, the NH-β-lactam 3 (70%) and the NH-γ-lactam 7 (70%). Proof of structure of the rearranged γ-lactams 6 and 7 are provided, respectively, by X-ray crystallographic analysis and the application of the Eu(dpm)₃ NMR shift reagent.     

Reaction of η5-cyclopentadienylbis(triphenylphosphine)cobalt(I) with alkadiynes. Preparation and reactions of bicyclic cobalt metallocycles and a stable trimethylsilyl-substituted mono-complexed alkadiyne. Comments on the mechanism of cobalt-catalyzed alkyne cooligomerization

Reactions of η⁵-cyclopentadienylbis(triphenylphosphine)cobalt(I) (5) with several 2,n-alkadiynes (2) were investigated. Each of these reactions leads initially to a material in which one of the acetylene functional groups is π-coordinated to cobalt; this complex then undergoes conversion to a metallocycle. In cases where the two acetylene functions are connected by three- and four-carbon bridges (2b, 2c), metallocycles formed by intramolecular reaction of two acetylene functions in the same molecule may be isolated. In cases where the acetylene functions are joined by larger or smaller bridges, the reactions are more complex, and both inter- and intramolecular metallocycles are formed. Reactions of 5 with 1,8-bis(trimethylsilyl)-1,7-octadiyne (16) gives an isolable crystalline mono-acetylene complex (17), this material is stable in the solid state but undergoes conversion to metallocycle (18) in benzene solution. The relationship of these results to the mechanism of the CpCo(CO)₂-catalyzed benzocycloalkene synthesis is discussed; it is suggested that intramolecular metallocycles are intermediates in reactions leading to benzocyclopentanes and -cyclohexenes, but intermolecular metallocycles are probably involved in reactions leading to benzocyclobutenes.