The reactivity of arylisocyanates in supercritical carbon dioxide (scCO(2)) was studied using the easily available complexes CpCo(CO)(2), CpCoPPh3Me2 and Ni(cod)(2) as catalysts. A study of the solubility of the catalysts in scCO(2) was undertaken in all cases. The complex CpCo(CO)(2) is very soluble, 1.7 x 10(-1) mol kg(-1), while CpCoPPh3Me2 has a lower solubility, 7.2 x 10(-3) mol kg(-1), and Ni(cod)(2) is insoluble in scCO(2). For comparison purposes, the reactions were performed in parallel in scCO(2), using toluene as a solvent and just with the neat liquid arylisocyanate. Reactions in scCO(2) either do not take place at all, when CpCo(CO), is used as catalyst, or occur with low yields affording the trimer of the corresponding arylisocyanate when CpCoPPh3Me2 or Ni(cod)(2) act as catalysts. No incorporation of CO2 into the organic substrate was observed. Better conversions to triarylisocyanate were obtained when the reactions were performed by direct mixture of the liquid arylisocyanate ArNCO (Ar = Ph, p-CH3C6H4, p-CH3OC6H4) and the catalyst. Using toluene as a solvent, the yields of the trimers were lower than those obtained in neat arylisocyanate, and in some cases they were not formed at all. For instance in the reaction of CpCo(CO), and tolylisocyanate either under stoichiometric or catalytic conditions the trimer is not obtained, instead the compound H2R3N3C2O2 (R = CH3C6H4), was isolated in low yield. In the reaction of Ni(cod)(2)/PPh3 with phenylisocyanate, the trimer was formed but in low yield. The lower yields of the trimers observed when the reactions were performed in scCO(2) or in toluene, compared to that observed in neat arylisocyanates, indicates that the decrease in reactivity is due to a decrease in concentration. (C) 2001 Elsevier Science B.V. All rights reserved.

New cationic mono-cyclopentadienyl complexes of Co(III) containing mono or bidentate nitrogen donor ligands of general formula [Co(eta (5)-C5H5)(PPh3)L-2][BF4](2) (L = NC-CH3, 2, and NC = Ph, 3) or [Co(eta (5)-C5H5)(PPh3)(L-L)[BF4](2), [L-L = 2,2 ' -bisimidazole (H(2)biim) (4) and dipyridylamine [HN(NC5H5)(2)] (5) have been synthesised by the stoichiometric reaction of the Co(III) complex Co(eta (5)-C5H5)(PPh3)I-2 (1), with Ag[BF4] and the appropriate ligand in CH2Cl2. Under the same conditions and using;trans-azobenzene as a ligand, an orthometalation reaction took placet giving the new compound [Co(eta (5)-C5H5)(PPh3)(kappa -C,kappa -N-C6H4N=NPh)][BF4] (6) in high yield. The structural characterisation of compounds 4 and 6, and of the starting compound Co(eta (5)-C5H5)(PPh3)I-2 (1) was done by single-crystal X-ray diffraction studies. DFT calculations (ADF program) were performed in order to understand the orthometallation reaction. (C) 2001 Elsevier Science B.V. All rights reserved.

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The paper reports on the work on hybrid-{T}refftz finite elements developed by the Structural Analysis Research Group, ICIST, Technical University of Lisbon. A dynamic elastoplastic problem is used to describe the technique used to establish the alternative stress and displacement models of the hybrid-{T}refftz finite element formulations. They are derived using independent time, space and finite element bases, so that the resulting solving systems are symmetric, sparse, naturally $p$-adaptive and particularly well suited to parallel processing. The performance of the hybrid-{T}refftz stress and displacement models is illustrated with a number of representative static and dynamic applications of elastic and elastoplastic structural problems.

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In the recent past, multiple techniques and tools have been proposed and contributed to improve the distributed debugging functionalities, in several distinct aspects, such as handling the non-determinism, allowing cyclic interactive debugging of parallel programs, and providing more user-friendly interfaces. However, most of these tools are tied to a specific programming language and provide rigid graphical user interfaces. So they cannot easily adapt to support distinct abstraction levels or user interfaces. They also don't provide adequate support for cooperation with other tools in a software engineering environment. In this paper we discuss several dimensions which may contribute to develop more flexible distributed debuggers. We describe Fiddle, a distributed debugging tool which aims at overcoming some of the above limitations.

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The practical implantation of the concept of dynamic virtual enterprise is still far from expectations due to a number of factors such as the lack of appropriate interoperable infrastructures and tools, lack of common ontology, and the socio-organizational difficulties. However, the creation of industry clusters supported by advanced information and communication tools can meanwhile provide a basis for the rapid creation of dynamic virtual enterprises in response to the market opportunities. A federated service management approach is introduced in this context and its application to the tourism industry is discussed. Finally, the support for the aggregation of simpler services into value-added services, implemented by distributed business processes within different organizations, is presented.