1,721,037 research outputs found
Recent Advances in Gold(III) Chemistry: Structure, Bonding, Reactivity, and Role in Homogeneous Catalysis
Over the past decade the organometallic chemistry of gold(III) has seen remarkable advances. This includes the synthesis of the first examples of several compound classes that have long been hypothesized as being part of catalytic cycles, such as gold(III) alkene, alkyne, CO and hydride complexes, and important catalysis-relevant reaction steps have at last been demonstrated for gold, like migratory insertion and β-H elimination reactions. Also, reaction pathways that were already known, for example the generation of gold(III) intermediates by oxidative addition and their reductive elimination, are much better understood. A deeper understanding of fundamental organometallic reactivity of gold(III) has revealed unexpected mechanistic avenues, which can open when the barriers for reactions that for other metals would be regarded as "standard" are too high. This review summarizes and evaluates these developments, together with applications of gold(III) in synthesis and catalysis, with emphasis on the mechanistic insight gained in these investigations
Pincer complexes of gold: An overview of synthesis, reactivity, photoluminescence, and biological applications
This chapter discusses the structures, reactivity patterns, and applications of gold(III) pincer complexes, organized according to ligand types: (1) neutral heteroatom pincers type N^N^N; (2) anionic heteroatom pincers N(-)^N^N(-) and E(-)^N^E(-) (E=O, S); (3) neutral C-based pincers C^N^N; (4) monoanionic C-based pincers C(-)^N^N, C^N(-)^C, and N^C(-)^N; and (5) dianionic C-based ligands C(-)^N^C(-) and C(-)^C(-)^N, with emphasis on the more recent literature. The ability of pincer complexes to stabilize previously unknown compounds, such as gold(III) hydrides, alkene, CO, and CO2 complexes is discussed, followed by a discussion on their photophysical properties and the applications as luminescent compounds and a survey of their biological and medicinal activity, especially their role as cytotoxic agents in anticancer studies
Carbon-sulfur bond formation by reductive elimination of gold(iii) thiolates
Whereas the reaction of the gold(iii) pincer complex (C^N^C)AuCl with 1-adamantyl thiol (AdSH) in the presence of base affords (C^N^C)AuSAd, the same reaction in the absence of base leads to formation of aryl thioethers as the products of reductive elimination of the Au-C and Au-S ligands (C^N^C = dianion of 2-6-diphenylpyridine or 2-6-diphenylpyrazine). Although high chemical stability is usually taken as a characteristic of pincer complexes, results show that thiols are capable of cleaving one of the pincer Au-C bonds. This reaction is not simply a function of S-H acidity, since no cleavage takes place with other more acidic X-H compounds, such as carbazole, amides, phenols and malonates. The reductive C-S elimination follows a second-order rate law, -d[1a]/dt = k[1a][AdSH]. Reductive elimination is enabled by displacement of the N-donor by thiol; this provides the conformational flexibility necessary for C-S bond formation to occur. Alternatively, reductive C-S bond formation can be induced by reaction of pre-formed thiolates (C^N^C)AuSR with a strong Brønsted acid, followed by addition of SMe2 as base. On the other hand, treatment of (C^N^C)AuR (R = Me, aryl, alkynyl) with thiols under similar conditions leads to selective C-C rather than C-S bond formation. The reaction of (C^N^C)AuSAd with H+ in the absence of a donor ligand affords the thiolato-bridged complex [{(C^N-CH)Au(μ-SAd)}2]2+ which was crystallographically characterised
Going Beyond Counting First Authors in Author Co-citation Analysis
The 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
Variations on the Author
“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
We 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
Heterolytic bond activation at gold: Evidence for gold(III) H-B, H-Si complexes, H-H and H-C cleavage
The coordinatively unsaturated gold(III) chelate complex [(C^N-CH)Au(C6F5)]+ (1+) reacts with main group hydrides H-BPin and H-SiEt3 in dichloromethane solution at 70 °C to form the corresponding σ-complexes, which were spectroscopically characterized (C^N-CH = 2-(C6H3But)-6-(C6H4But)-pyridine anion; Pin = OCMe2CMe2O). In the presence of an external base such as diethyl ether, heterolytic cleavage of the silane H-Si bond leads to the gold hydrides [{(C^N-CH)AuC6F5}2(μ-H)]+ (2+) and (C^N-CH)AuH(C6F5) (5), together with spectroscopically detected [Et3Si-OEt2]+. The activation of dihydrogen also involves heterolytic H-H bond cleavage but requires a higher temperature ( 20 °C). H2 activation proceeds in two mechanistically distinct steps: the first leading to 2 plus [H(OEt2)2]+, the second to protonation of one of the C^N pyridine ligands and reductive elimination of C6F5H. By comparison, formation of gold hydrides by cleavage of suitably activated C-H bonds is very much more facile; e.g. the reaction of 1·OEt2 with Hantzsch ester is essentially instantaneous and quantitative at 30 °C. This is the first experimental observation of species involved in the initial steps of gold catalyzed hydroboration, hydrosilylation and hydrogenation and the first demonstration of the ability of organic C-H bonds to act as hydride donors towards gold
Dispelling the Myths Behind First-author Citation Counts
We 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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