Gomes, Ana Sofia, and José Júlio Alferes. "
A procedure for an event-condition-transaction language."
Web Reasoning and Rule Systems - 9th International Conference, RR 2015, Proceedings. Vol. 9209. Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics), 9209. Springer-Verlag, 2015. 113-129.
AbstractEvent-Condition-Action languages are the commonly accepted para- digm to express and model the behavior of reactive systems. While numerous Event-Condition-Action languages have been proposed in the literature, differing e.g. on the expressivity of the language and on its operational behavior, existing Event-Condition-Action languages do not generally support the action compo- nent to be formulated as a transaction. In this paper, sustaining that it is important to execute transactions in reactive languages, we propose an Event-Condition- Transaction language, based on an extension of Transaction Logic. This exten- sion, called Transaction Logic with Events (T Rev ), combines reasoning about the execution of transactions with the ability to detect complex events. An impor- tant characteristic of T Rev is that it takes a choice function as a parameter of the theory, leaving open the behavioral decisions of the logic, and thereby allowing it to be suitable for a wide-spectrum of application scenarios like Semantic Web, multi-agent systems, databases, etc. We start by showing how T Rev can be used as an Event-Condition-Action language where actions are considered as transac- tions, and how to differently instantiate this choice function to achieve different operational behaviors. Then, based on a particular operational instantiation of the logic, we present a procedure that is sound and complete w.r.t. the semantics and that is able to execute T Rev programs
Coelho, Helena, T. Matsushita, G. Artigas, H. Hinou, FJ Cañada, R. Lo-Man, C. Leclerc, E. J. Cabrita, J. Jiménez-Barbero, S. - I. Nishimura, F. Garcia-Martín, and F. Marcelo. "
The Quest for Anticancer Vaccines: Deciphering the Fine-Epitope Specificity of Cancer-Related Monoclonal Antibodies by Combining Microarray Screening and Saturation Transfer Difference NMR."
J. Am. Chem. Soc.. 137 (2015): 12438-12441.
Gonçalves, L., Z. Santos, Miguel Amado, I. Craveiro, J. Cabral, Lapão L.V., A. P. Delgado, A. Correia, D. Alves, and R. Simões. "
Urban Planning and Health Inequities: looking in a small-scale in a City of Cape Verde."
PLOSone. 23/11/2015.DOI: 10.1371/journal.pone.0142955 (2015).
Fliedel, Christophe, Vitor Rosa, Filipa M. Alves, Ana. M. Martins, Teresa Aviles, and Samuel Dagorne. "
{P,O-Phosphinophenolate zinc(II) species: synthesis, structure and use in the ring-opening polymerization (ROP) of lactide, epsilon-caprolactone and trimethylene carbonate}."
{DALTON TRANSACTIONS}. {44} (2015): {12376-12387}.
Abstract{The P, O-type phosphinophenol proligands (1 center dot H, 2-PPh2-4-Me-6-Me-C6H2OH; 2 center dot H, 2-PPh2-4-Me-6-Bu-t-C6H2OH) readily react with one equiv. of ZnEt2 to afford in high yields the corresponding Zn(II)ethyl dimers of the type {[}(kappa(2)-P, O) Zn-Et](2) (3 and 4) with two mu-O-Ph bridging oxygens connecting the two Zn(II) centers, as determined by X-ray diffraction (XRD) studies in the case of 3. Based on diffusion-ordered NMR spectroscopy (DOSY), both species 3 and 4 retain their dimeric structures in solution. The alcoholysis reaction of Zn(II) alkyls 3 and 4 with BnOH led to the high yield formation of the corresponding Zn(II) benzyloxide species {[}(kappa(2)-P, O) Zn-OBn](2) (5 and 6), isolated in a pure form as colorless solids. The centrosymmetric and dimeric nature of Zn(II) alkoxides 5 and 6 in solution was deduced from DOSY NMR experiments and multinuclear NMR data. Though the heteroleptic species 5 is stable in solution, its analogue 6 is instable in CH2Cl2 solution at room temperature to slowly decompose to the corresponding homoleptic species 8 via the transient formation of (kappa(2)-P, O)(2)Zn-2(mu-OBn)(mu-kappa(1):kappa(1)-P, O) (6'). Crystallization of compound 6 led to crystals of 6', as established by XRD analysis. The reaction of ZnEt2 with two equiv. of 1 center dot H and 2 center dot H allowed access to the corresponding homoleptic species of the type {[}Zn(P, O)(2)] (7 and 8). All gathered data are consistent with compound 7 being a dinuclear species in the solid state and in solution. Data for species 8, which bears a sterically demanding P, O-ligand, are consistent with a mononuclear species in solution. The Zn(II) alkoxide species 5 and the {[}Zn(P, O)(2)]-type compounds 7 and 8 were evaluated as initiators of the ring-opening polymerization (ROP) of lactide (LA), epsilon-caprolactone (epsilon-CL) and trimethylene carbonate (TMC). Species 5 is a well-behaved ROP initiator for the homo-, co- and terpolymerization of all three monomers with the production of narrow disperse materials under living and immortal conditions. Though species 7 and 8 are ROP inactive on their own, they readily polymerize LA in the presence of a nucleophile such as BnOH to produce narrow disperse PLA, presumably via an activated-monomer ROP mechanism.}
Kauf, Thomas, Vitor Rosa, Christophe Fliedel, Roberto Pattacini, Naina Deibel, Teresa Aviles, Biprajit Sarkar, and Pierre Braunstein. "
{Reactivity of TCNE and TCNQ derivatives of quinonoid zwitterions with Cu(I)}."
{DALTON TRANSACTIONS}. {44} (2015): {5441-5450}.
Abstract{The reactions of TCNE- and TCNQ-functionalized (TCNE: tetracyanoethylene and TCNQ: 7,7', 8,8'-tetra-cyanoquinodimethane) zwitterionic benzoquinonemonoimines with a Cu(I)-BIAN complex (BIAN = bis-(o, o'-bisisopropylphenyl)acenaphthenequinonediimine) have been investigated and found to follow a diversity of interesting patterns. The complexes {[}Cu(BIAN)(NCMe)(L2)]BF4 (2) and {[}Cu(BIAN)(L2)(2)]BF4 (4) were obtained by reacting {[}Cu(BIAN)(NCMe) 2] BF4 (1) with one and two equivalents of L2, respectively. Following similar procedures, the complexes {[}Cu(BIAN)(NCMe)(L3)] BF4 (6) and {[}Cu(BIAN)(L3)(2)]BF4 (7) were obtained by reaction of 1 with L3. The reaction of 2 with 0.5 equiv. of 4,4'-bipyridine afforded {[}\{Cu(BIAN)-(L2)\}(2)(mu-4,4'-bipyridine)](BF4)(2) (3). The complexes were characterized by multinuclear NMR, IR and UV-Vis spectroscopic techniques, mass spectrometry, cyclic voltammetry and elemental analysis. The molecular structures of complexes 3 center dot 4CH(2)Cl(2) and 4 center dot CH2Cl2 were determined by single crystal X-ray diffraction. An unexpected coordination polymer {[}Cu(L2(-))(2)](infinity) (5) was also structurally characterized, which contains Cu(II) centres chelated by two N, O-bound ligands resulting from the monodeprotonation of L2.}