Highly efficient hydrogen-bonding catalysis of the Diels-Alder reaction of 3-vinylindoles and methyleneindolinones provides carbazolespirooxindole skeletons

Carbazolespirooxindole derivatives were synthesized in a high-yielding, atypically rapid, stereocontrolled Diels-Alder reaction catalyzed by a C(2)-symmetric bisthiourea organocatalyst. Simple precursors and mild conditions were used to construct carbazolespirooxindole derivatives with high enantiopurity and structural diversity under H-bonding catalysis. The practical approach recycles the organocatalyst and solvent. This simple and efficient operational procedure will allow diversity-oriented syntheses of this intriguing class of compounds.     

Elucidating the nature and reactivity of Ti ions incorporated in the framework of AlPO-5 molecular sieves. New evidence from 31P HYSCORE spectroscopy

The incorporation of Ti ions within the framework of aluminophosphate zeotype AlPO-5 and their chemical reactivity is studied by means of CW-EPR, HYSCORE, and UV-vis spectroscopies. Upon reduction, Ti(3+) ions are formed, which exhibit large (31)P hyperfine couplings, providing direct evidence for framework substitution of reducible Ti ions at Al sites.     

Structural and spectroscopic investigation of ZnS nanoparticles grown in quaternary reverse micelles

ZnS nanoparticles were synthesized in four component "water in oil" microemulsions formed by a cationic surfactant (cetyltrimethylammonium bromide, CTAB), a cosurfactant (pentanol or butanol), n-hexane and water. The effect of various parameters (nature of cosurfactant, water/surfactant W(0), and alcohol/surfactant P(0)) on the formation and stability of ZnS nanoparticles was investigated thoroughly. UV-Vis spectroscopy was employed to directly follow the formation of ZnS systems in the microemulsions. Thus, particle size was estimated from the position of the first excitonic transition by employing an approximate finite-depth equation and an empirical correlation, giving average diameters in the ranges 2.3-2.5 and 3.0-3.5nm, respectively. Stable ZnS nanoparticles were obtained by employing low water and high cosurfactant amounts. This suggests that at high concentration the cosurfactant molecules act as capping agents on the surface of the inverse micelles, while low water amounts are needful to obtain water droplets with a radius close to that of the interfacial film spontaneous curvature. HRTEM analysis showed that the samples are formed by a few crystalline ZnS nanoparticles of spherical shape, embedded in and amorphous organic matrix, with a coherent scattering domain between 2 and 4nm.     

Hetero-Diels-Alder reaction of phosphinyl and phosphonyl nitroso alkenes with conjugated dienes: an aza-Cope rearrangement

Phosphorylated nitroso alkenes react with cyclic dienes such as cyclopentadiene or cyclohexadiene to afford hetero Diels-Alder-type cycloadducts where the nitroso alkene participates as dienophile component and the cyclic olefin acts as the 4π-electron (diene) system. Subsequent aza-Cope rearrangement affords highly functionalized 5,6-dihydro-4H-1,2-oxazines. Conversely, the reaction of TMS-substituted cyclopentadiene (dienophile) with nitroso alkenes as heterodienes leads directly to bicyclic 1,2-oxazines. Theoretical studies are in agreement with the experimental results and with the new aza-Cope rearrangement proposed.     

A rapid and economical method for profiling feature heights during microfabrication

Quality control is an important and integral part to any microfabrication process. While the widths of features often can be easily assessed by light microscopy, the heights of the fabricated structures are more difficult to determine. Here, we present a rapid, accurate, and low-cost method to measure the heights of microfabricated structures during and after the fabrication process. This technique is based on white-light interferometry, which offers accuracy on the submicrometre scale.     

Integral Representation Results for Energies Defined on Stochastic Lattices and Application to Nonlinear Elasticity

This article is devoted to the study of the asymptotic behavior of a class of energies defined on stochastic lattices. Under polynomial growth assumptions, we prove that the energy functionals F_e{F_\varepsilon} stored in the deformation of an e{{\varepsilon}}-scaling of a stochastic lattice Γ-converge to a continuous energy functional when e{{\varepsilon}} goes to zero. In particular, the limiting energy functional is of integral type, and deterministic if the lattice is ergodic. We also generalize, to systems and nonlinear settings, well-known results on stochastic homogenization of discrete elliptic equations. As an application of the main result, we prove the convergence of a discrete model for rubber towards the nonlinear theory of continuum mechanics. We finally address some mechanical properties of the limiting models, such as frame-invariance, isotropy and natural states.     

Rare earth doped cobalt ferrite thin films deposited by PLD

CoFe₂O₄ thin films with preferential texture structure, small grain size, and perpendicular magnetic anisotropy can be obtained by the pulsed laser deposition (PLD) technique. In this work, we studied the influence of the Fe³⁺ ions substitution by three elements from lanthanide group (Dy, La, and Gd) on the structural properties of the thin films. The samples were deposited by Nd:YAG laser (λ=532 nm, 10 ns) ablation of CoFe_1.8RE_0.2O₄, (RE=Dy, La, Gd) targets at various substrate temperatures ranging from room temperature to 600 °C. The microstructure and chemical composition of the thin films were investigated by Raman spectroscopy, XRD, SEM-EDS, and ToF-SIMS. The XRD patterns and Raman spectra of the thin films indicated the formation of a single spinel structure. Thus, the desired substitution of the iron ions in the spinel lattice with the RE elements was achieved in the thin films, although in the bulk material, their presence determined the formation of a residual phase with a perovskite-type structure.     

Complexity theory and collaboration: An agent-based simulator for a space mission design team

In this paper, we investigate how complexity theory can benefit collaboration by applying an agent-based computer simulation approach to a new form of synchronous real-time collaborative engineering design. Fieldwork was conducted with a space mission design team during their actual design sessions, to collect data on their group conversations, team interdependencies, and error monitoring and recovery practices. Based on the fieldwork analysis, an agent-based simulator was constructed. The simulation shows how error recovery and monitoring is affected by the number of small group, or sidebar, conversations, and consequent noise in the room environment. This simulation shows that it is possible to create a virtual environment with cooperating agents interacting in a dynamic environment. This simulation approach is useful for identifying the best scenarios and eliminating potential catastrophic combinations of parameters and values, where error recovery and workload in collaborative engineering design could be significantly impacted. This approach is also useful for defining strategies for integrating solutions into organizations. Narjès Bellamine-Ben Saoud is an Associate Professor at the University of Tunis and Researcher at RIADI-GDL Laboratory, Tunisia. After Computer Science engineering diploma (1993) of the ENSEEIHT of Toulouse, France, she received her PhD (1996), on groupware design applied to the study of cooperation within a space project, from the University of Toulouse I, France. Her main research interests concern studying complex systems particularly by modeling and simulating collaborative and socio-technical systems; developing Computer Supported Collaborative Learning in tunisian primary schools; and Software Engineering. Her current reserach projects include modeling and simulation of emergency rescue activities for large-scale accidents, modeling of epidemics and study of malaria, simulation of collabration artifacts. Gloria Mark is an Associate Professor in the Department of Informatics, University of California, Irvine. Dr. Mark received her Ph.D. in Psychology from Columbia University in 1991. Prior to UCI, she was a Research Scientist at the GMD, in Bonn, Germany, a visiting research scientist at the Boeing Company, and a research scientist at the Electronic Data Systems Center for Advanced Research. Dr. Mark’s research focuses on the design and evaluation of collaborative systems. Her current projects include studying worklife in the network-centric organization, multi-tasking of information workers, nomad workers, and a work in a large-scale medical collaboratory. Dr. Mark is widely published in the fields of CSCW and HCI, is currently the program co-chair for the ACM CSCW’06 conference and is on the editorial board of Computer Supported Cooperative Work: The Journal of Collaborative Computing, and e-Service Qu@rterly.     

THE RELATIVE EFFICIENCY OF DIFFERENT STANDARDS WHEN FIRMS VARY

Pollution standards in practice take many forms, such as measuring pollution per unit of output rather than just restricting pollution. This paper uses simulations to provide some evidence on the effects of these two forms of standards when firms vary. For the cases studied, it shows that a pollution standard can lead to higher profits, but a pollution-per-output standard leads to higher output and lower price; the overall efficiency effects are therefore ambiguous.     

Surface green function matching approach to the surface dynamics of ionic crystals: I. Equivalence with the invariant green function method

The surface Green function matching (SGFM) method is shown to be equivalent to the Green function method in its translationally and rotationally invariant formulation (IGF). Such equivalence between matching and invariance conditions makes the SGFM method easily applicable to the surface dynamics of ionic crystals, due to the existing possibility of deriving an effective short-range perturbation from the invariance conditions. An application to the inelastic scattering of He from LiF(001) in the eikonal approximation is presented.