Fliedel, Christophe, Samir Mameri, Samuel Dagorne, and Teresa Aviles. "
{Controlled ring-opening polymerization of trimethylene carbonate and access to PTMC-PLA block copolymers mediated by well-defined N-heterocyclic carbene zinc alkoxides}."
{APPLIED ORGANOMETALLIC CHEMISTRY}. {28} (2014): {504-511}.
Abstract{Four novel Zinc-NHC alkyl/alkoxide/chloride complexes (4, 5, 9 and 9) were readily prepared and fully characterized, including X-ray diffraction crystallography for 5 and 9. The reaction of N-methyl-N-butyl imidazolium chloride (3.HCl) with ZnEt2 (2 equiv.) afforded the corresponding {[}(CNHC)ZnCl(Et)] complex (4) via a protonolysis reaction, as deduced from NMR data. The alcoholysis of 4 with BnOH led to quantitative formation of the dinuclear Zn(II) alkoxide species {[}(CNHC)ZnCl(OBn)]2 (5), as confirmed by X-ray diffraction analysis. The NMR data are in agreement with species 5 retaining its dimeric structure in solution at room temperature. The protonolysis reaction of N-(2,6-diisopropylphenyl)-N-ethyl methyl ether imidazolium chloride (8.HCl) with ZnEt2 (2 equiv.) yielded the {[}(CNHC)ZnCl(Et)] species 9. The latter was found to be reactive with CH2Cl2 in solution and to cleanly convert to the corresponding Zn(II) dichloride {[}(CNHC)ZnCl2]2 (9), whose molecular structure was also elucidated using X-ray diffractometry. Unlike Zn(II)-NHC alkoxide species 1 and 2, which contain a NHC flanked with an additional N-functional group (i.e. thioether and ether, respectively), the Zn(II) alkoxide species 5 incorporates a monodentate NHC ligand. The Zn(II) complexes 1, 2 and 5 were tested in the ring-opening polymerization (ROP) of trimethylene carbonate (TMC). All three species are effective initiators for the controlled ROP of trimethylene carbonate, resulting in the production of narrow disperse PTMC material. Initiator 1 (incorporating a thioether moiety) was found to perform best in the ROP of TMC. Notably, the latter also readily undergoes the sequential ROP of TMC and rac-LA in the presence of a chain-transfer agent, leading to well-defined and high-molecular-weight PTMC/PLA block copolymers. Copyright (c) 2014 John Wiley & Sons, Ltd.}
Maiti, Biplab K., Luisa B. Maia, Kuntal Pal, Bholanath Pakhira, Teresa Aviles, Isabel Moura, Sofia R. Pauleta, Jose L. Nunez, Alberto C. Rizzi, Carlos D. Brondino, Sabyasachi Sarkar, and Jose J. G. Moura. "
{One Electron Reduced Square Planar Bis(benzene-1,2-dithiolato) Copper Dianionic Complex and Redox Switch by O-2/HO-}."
{INORGANIC CHEMISTRY}. {53} (2014): {12799-12808}.
Abstract{The complex {[}Ph4P](2){[}Cu(bdt)(2)] (1(red)) was synthesized by the reaction of {[}Ph4P]2{[}S2MoS2CuCl] with H2bdt (bdt = benzene-1,2-dithiolate) in basic medium. 1(red) is highly susceptible toward dioxygen, affording the one electron oxidized diamagnetic compound {[}Ph4P]{[}Cu(bdt)(2)] (1(ox)). The interconversion between these two oxidation states can be switched by addition of O-2 or base (Et4NOH = tetraethylammonium hydroxide), as demonstrated by cyclic voltammetry and UV-visible and EPR spectroscopies. Thiomolybdates, in free or complex forms with copper ions, play an important role in the stability of 1(red) during its synthesis, since in its absence, 1(ox) is isolated. Both 1(red) and 1(ox) were structurally characterized by X-ray crystallography. EPR experiments showed that 1(red) is a Cu(II)-sulfur complex and revealed strong covalency on the copper-sulfur bonds. DFT calculations confirmed the spin density delocalization over the four sulfur atoms (76%) and copper (24%) atom, suggesting that 1(red) has a ``thiyl radical character{''}. Time dependent DFT calculations identified such ligand to ligand charge transfer transitions. Accordingly, 1(red) is better described by the two isoelectronic structures {[}Cu(I)(bdt(2), 4S(3-{*}))](2-) {[}Cu-II(bdt(2), 4S(4-))](2-). On thermodynamic grounds, oxidation of 1(red) (doublet state) leads to 1(ox) singlet state, {[}Cu-III(bd(t)2, 4S(4-))](1-).}
Silva, João A., João M. Lourenço, and Hervé Paulino. "
Um Mecanismo de Caching para o Protocolo {SCORe}."
Proceedings of INForum Simpósio de Informática. INForum 2014. Porto, Portugal: FEUP Edições, 2014. 260-275.
AbstractOs protocolos de replicação parcial de dados apresentam um grande potencial de escalabilidade. O SCORe é um protocolo para replicação parcial proposto recentemente que faz uso de controlo de concorrência multi-versão. Neste artigo abordamos um dos problemas principais que afeta o desempenho deste tipo de protocolos: a localidade dos dados, i.e., pode-se dar o caso do nó local não ter uma cópia dos dados a que pretende aceder, e nesse caso é necessário realizar uma ou mais operações de leitura remota. Assim, a não ser que se empreguem técnicas para melhorar a localidade no acesso aos dados, o número de operações de leitura remota aumenta com o tamanho do sistema, acabando por afetar o desempenho do mesmo. Nesse sentido, introduzimos um mecanismo de caching que permite replicar cópias de dados remotos de maneira a que seja poss{\'ı}vel servir localmente dados remotos enquanto que se mantém a consistência dos mesmos e a escalabilidade oferecida pelo protocolo. Avaliamos o mecanismo de caching com um benchmark conhecido da literatura e os resultados experimentais mostram resultados animadores com algum aumento no desempenho do sistema e uma redução considerável da quantidade de operações de leitura remota.