Origin of the oscillator strength of the triplet state of a trion in a magnetic field

The dynamics of the spin-triplet trion state, under high magnetic field in a GaAs/AlGaAs quantum well, are studied using time resolved spectroscopy. The oscillator strength of the triplet transition is shown to rise with increasing electron density, in good agreement with a theoretical model where the trion interacts with excess electrons in the quantum well. This analysis suggests that the spin-triplet trion state, which is expected to be an optically "dark" state, is experimentally observable due to the interactions with the excess electrons, demonstrating that X- cannot be regarded as an isolated three particle complex.     

Kondo effect in a quantum antidot

We report Kondo-like behavior in a quantum antidot (a submicron depleted region in a two-dimensional electron gas) in the quantum-Hall regime. When both spins of the lowest Landau level are present all around the antidot, the resonances between extended edge states via antidot bound states show an abnormal feature in alternate Coulomb-blockaded regions. The feature becomes suppressed when the temperature or source-drain bias is raised as for Kondo resonances in quantum dots. Although the exact mechanism is unknown, Kondo-like correlated tunneling may arise from a Skyrmion-type edge reconstruction. This observation demonstrates the generality of the Kondo phenomenon.     

Maximal non- hamilton-laceable graphs

For bipartite graphs the property of being Hamilton laceable is analogous to the property of being Hamilton connected for simple graphs. in this paper it is proven that all of the graphs obtained by deleting fewer than m ? 1 edges from either of the complete bipartite graphs K_{m, m} or K_{m, m+1} are Hamilton laceable. It is also proven that the deletion of m ? 1 edges results in a non-Hamiltonlaceable graph if and only if the graph is either the complement of the star K_1,m?1 in K_{m, m} or K_{m, m+1} or else the complement in K_3,3 of a pair of nonadjacent edges.     

Shock wave interaction with laser-generated single bubbles

The interaction of a lithotripter shock wave (LSW) with laser-generated single vapor bubbles in water is investigated using high-speed photography and pressure measurement via a fiber-optic probe hydrophone. The interaction leads to nonspherical collapse of the bubble with secondary shock wave emission and microjet formation along the LSW propagation direction. The maximum pressure amplification is produced during the collapse phase of the bubble oscillation when the compressive pulse duration of the LSW matches with the forced collapse time of the bubble.     

An ESR study of some group IVB free radical adducts of diethylketomalonate

The formation of the compound RSnX(acac)₂ (acac = 2,4-pentanedionato) by reaction of bis(2,4-pentanedionato)tin(II) on a halide RX with R = CH₃, C₂H₅, C₄H₉, C₆H₅, CH₂I, (C₆H₅)₃SnCH₂, (C₂H₅)₃SnCH₂ and X = I, Br has been studied by polarography. At 25°C, it is in fact an equilibrium whose constant has been measured. The intermediate formation of the ion-pair [RSn(acac)₂⁺X^?] has allowed us to explain the experimental results.     

Synthesis and characterization of near‐monodisperse electron acceptor homopolymers of 2‐[(3,5‐dinitrobenzoyl)oxy]ethyl methacrylate

Homopolymers of 2‐(trimethylsiloxy)ethyl methacrylate of degrees of polymerization from 5 to 50 were synthesized by group transfer polymerization in tetrahydrofuran (THF) using 1‐methoxy‐1‐(trimethylsiloxy)‐2‐methyl propene as the initiator and tetrabutylammonium bibenzoate as the catalyst. These polymers were first converted to poly[2‐(hydroxy)ethyl methacrylate]s by removal of the trimethylsilyl‐protecting groups by acidic hydrolysis, and subsequently transformed to poly{2‐[(3,5‐dinitrobenzoyl)oxy]ethyl methacrylate}s by reaction with 3,5‐dinitrobenzoyl chloride in the presence of triethylamine. Gel permeation chromatography in THF and proton nuclear magnetic resonance (¹H NMR) spectroscopy in CDCl₃ and d₆ dimethyl sulfoxide were used to characterize the polymers in terms of their molecular weight and composition. The molecular weights were found to be close to the values expected from the polymerization stoichiometry and the molecular weight distributions were narrow, with polydispersity indices around 1.1. The hydrolysis and reesterification steps were found to be almost quantitative for all polymers. Differential scanning calorimetry and thermal gravimetric analysis were also employed to measure the glass transition temperatures (T_g 's) and decomposition temperatures, which were determined to be approximately 80 and 320 °C, respectively. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 1457–1465, 2000     

DIBAL-mediated reductive transformation of trans-dimethyl tartrate acetonide into ε-hydroxy α,β-unsaturated ester and its derivatives

Stepwise, selective DIBAL reduction of the acetonide diester derived from tartaric acid followed by the Horner-Emmons reaction effectively provided desymmetrized hydroxy mono-olefination products in a one-pot operation.     

Synthesis,structure and magnetic properties of unsymmetrical dodecanuclear Mn–Ln clusters

Reaction of manganese acetate and lanthanide nitrates in the presence of excess of PhCOOH affords highly asymmetric dodecanuclear mixed-metal [Mn₁₀Ln₂(OH)(O)₈(PhCOOH)(PhCOO)₁₉] (Ln = Pr^III (1), Nd^III (2)) clusters. The similar reaction, but with only 2 equiv. of PhCOOH resulted in the compounds with higher nuclearity [Mn₁₁Eu₄(O)₈(OH)₈(PhCOO)₁₈(NO₃)₂(H₂O)₆]NO₃ · 4CH₃CN (3). Variable-temperature solid-state magnetic susceptibility of 1 and 2 in the temperature range 1.8–300 K were carried out, and for both complexes antiferromagnetic exchange interactions between the metal centers were observed, giving an estimated S = 17/2 ground state. AC magnetic susceptibility data have revealed out-of-phase signals, which suggest that these complexes exhibit a slow relaxation of magnetization as observed in single-molecule magnets.