1,720,998 research outputs found
Chemical reactivity in ionic liquids: Nitroso group transfer from N-nitrososulfonamide
Get PDFNitroso group trnsfer in ionic liquids exhibits good correlation with the polarity parameters of the ionic liquid, showing that the amine nucleophililicity in no increased on going from water to the ionic liquidFil: Adam, Claudia Guadalupe. Universidad Nacional del Litoral. Instituto de Química Aplicada del Litoral. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Química Aplicada del Litoral.; ArgentinaFil: García-Río, Luis. Universidad de Santiago de Compostela; EspañaFil: Godoy, Ana. Universidad de Santiago de Compostela; EspañaFil: Leis, J. Ramón. Universidad de Santiago de Compostela; Españ
Going Beyond Counting First Authors in Author Co-citation Analysis
Get PDFThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Nitroso Group Transfer in S -Nitrosocysteine: Evidence of a New Decomposition Pathway for Nitrosothiols
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The rate of S-nitrosocysteine decomposition in a pH range between 0.7 S-nitrosocysteine, which proceeds via an intramolecular nitroso group transfer producing a primary N-nitrosamine that decomposes rapidly to give the corresponding diazonium salt. The nitroso group transfer reaction occurs intermolecularly for the decomposition pathway exhibiting a quadratic dependence on cysteine concentration. Both nitroso group transfer pathways are subject to acid catalysis by cysteine. Kinetic results indicate that the extent of S‚‚‚NO bond cleavage in the transition state is ahead of protonation of the AH‚‚‚S sulfur atom. The results obtained show the existence of a new decomposition pathway for the S-nitrosocysteine where NO is not released, and hence, it has a significant biological impact due to the potential use of nitrosothiols as NO donors.
Fil: Adam, Claudia Guadalupe. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina. Universidad de Santiago de Compostela; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; ArgentinaFil: García Río, Luis. Universidad de Santiago de Compostela; EspañaFil: Leis, José Ramón. Universidad de Santiago de Compostela; EspañaFil: Ribeiro, Lara. Universidad de Santiago de Compostela; Españ
Variations on the Author
Get PDF“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
Get PDFWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Characterization of reverse micelles formulated with the ionic-liquid-like surfactant Bmim-AOT and comparison with the traditional Na-AOT: Dynamic light scattering, 1H NMR spectroscopy, and hydrolysis reaction of carbonate as a probe
Get PDFThe present study investigated how the presence of butylmethylimidazolium cation (bmim+) alters the interfacial properties of reverse micelles (RMs) created with the ionic liquid-like surfactant 1-butyl-3-methylimidazolium 1,4-bis-2-ethylhexylsulfosuccinate (bmim-AOT), in comparison to sodium 1,4-bis-2-ethylhexylsulfosuccinate (Na-AOT) RMs, employing dynamic light scattering (DLS) and 1H NMR techniques. Moreover, through the hydrolysis reaction of bis(4-nitrophenyl)carbonate inside both RMs as reaction probe, interfacial properties changes were explored in more detail. The kinetic solvent isotope effect was also analyzed. Micellar systems were formed using n-heptane as external nonpolar solvent and water as the polar component. According to the DLS studies, water is encapsulated inside the organized media; however, a different tendency is observed depending on the cationic component of the surfactant. For Na-AOT system, the results suggest that the micellar shapes are probably spherical, while in the case of bmim-AOT, a transition from ellipsoidal to spherical micelles could be occurring when water is added. 1H NMR data show that water is structured differently when Na+ cation is replaced by bmim+ in bmim-AOT RMs, the interaction of water with the surfactant is weaker and the water hydrogen-bonding network is less disturbed than in Na-AOT RMs. Kinetic studies reveal that the hydrolysis reaction in bmim-AOT RMs was much more favorable in comparison to Na-AOT RMs. In addition, when water content decreases in bmim-AOT RMs, the hydrolysis reaction rate increases and the solvent isotope effect remains constant, while for Na-AOT solutions, both the reaction rate and the solvent isotope effect decrease. Our results indicate that bmim+ cation would be located in the surfactant layer in such a way the negative charge density in the interface is less than that in Na-AOT RMs, and the reaction is more favorable. Additionally, as 1H NMR studies reveal, the interfacial water molecules would be more available in bmim-AOT RMs to participate in the nucleophilic attack. Therefore, the present study evidences how the replacement of Na+ counterion by bmim+ alters the composition of the interface of AOT RMs.Fil: Dib, Nahir. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Falcone, Ruben Dario. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Acuña, Angel. Universidad de Santiago de Compostela; EspañaFil: García-Río, Luis. Universidad de Santiago de Compostela; Españ
The ionic liquid-surfactant bmim-AOT and nontoxic lipophilic solvents as components of reverse micelles alternative to the traditional systems. A study by 1H NMR spectroscopy
No full textAqueous reverse micelles (RMs) of the ionic liquid-surfactant 1-butyl-3-methylimidazolium 1,4-bis-2-ethylhexylsulfosuccinate (bmim-AOT) in the biocompatible nonpolar solvents isopropyl myristate (IPM) and methyl laurate (ML) were formulated and characterized by DLS and 1H NMR techniques; the goal is to develop less toxic and more environmentally friendly reverse micellar systems than traditional RMs formed by organic solvents such as n-heptane (n-Hp). The interfacial composition of these new micellar systems was compared with water/bmim-AOT/n-Hp RMs, analyzing the effect of changing the conventional external nonpolar solvent n-Hp for the biocompatible solvents IPM and ML. Also, they were compared with the RMs of the traditional surfactant sodium 1,4-bis-2-ethylhexylsulfosuccinate (Na-AOT) in IPM and ML to analyze the role of the bmim+ counterion compared to Na+ in the interfacial properties of the generated RMs. The results indicate that both ML and IPM can be used as nonpolar solvents to prepare RMs using bmim-AOT as surfactant. In comparison to n-Hp, IPM and ML penetrate more to the micellar interface, therefore, the ester group of the biocompatible solvent located at the micellar interface interacts with the bmim+ cation. As a consequence of this fact, the bmim+-AOT− interaction decreases when IPM or ML are used as the external solvent instead of n-Hp. In the Na-AOT/IPM and Na-AOT/ML systems, the dissimilar penetration of the external solvent makes the interfacial properties of both RMs clearly different. Interestingly, in the bmim-AOT/biocompatible solvent systems, the micellar interface properties are strongly governed by the bmim+ counterion, finding similar behavior if the external biocompatible solvent is IPM or ML.Fil: Dib, Nahir. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Falcone, Ruben Dario. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Acuña, Angel. Universidad de Santiago de Compostela; EspañaFil: García-Río, Luis. Universidad de Santiago de Compostela; Españ
Dispelling the Myths Behind First-author Citation Counts
Get PDFWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
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