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Metal Chemistry (metal + chemistry)
Selected AbstractsLandmarks in Organo-Transition Metal Chemistry.ANGEWANDTE CHEMIE, Issue 41 2009A Personal View. Springer Verlag, Heidelberg 2009. 354,S., gebunden ,,85.55.,ISBN 978-0387098470 [source] Integration of magnetism and heavy metal chemistry of soils to quantify the environmental pollution in Kathmandu, NepalISLAND ARC, Issue 4 2005Pitambar Gautam Abstract Soil profiles of the Kathmandu urban area exhibit significant variations in magnetic susceptibility (,) and saturation isothermal remanence (SIRM), which can be used to discriminate environmental pollution. Magnetic susceptibility can be used to delineate soil intervals by depth into normal (< 10,7 m3/kg), moderately enhanced (10,7,< 10,6 m3/kg) and highly enhanced (, 10,6 m3/kg). Soils far from roads and industrial sites commonly fall into the ,normal' category. Close to a road corridor, soils at depths of several centimeters have the highest ,, which remains high within the upper 20 cm interval, and decreases with depth through ,moderately magnetic' to ,normal' at approximately 30,40 cm. Soils in the upper parts of profiles in urban recreational parks have moderate ,. Soil SIRM has three components of distinct median acquisition fields (B1/2): soft (30,50 mT, magnetite-like phase), intermediate (120,180 mT, probably maghemite or soft coercivity hematite) and hard (550,600 mT, hematite). Close to the daylight surface, SIRM is dominated by a soft component, implying that urban pollution results in enrichment by a magnetite-like phase. Atomic absorption spectrometry of soils from several profiles for heavy metals reveals remarkable variability (ratio of maximum to minimum contents) of Cu (16.3), Zn (14.8) and Pb (9.3). At Rani Pokhari, several metals are well correlated with ,, as shown by a linear relationship between the logarithmic values. At Ratna Park, however, both , and SIRM show significant positive correlation with Zn, Pb and Cu, but poor and even negative correlation with Fe (Mn), Cr, Ni and Co. Such differences result from a variety of geogenic, pedogenic, biogenic and man-made factors, which vary in time and space. Nevertheless, for soil profiles affected by pollution (basically traffic-related), , exhibits a significant linear relationship with a pollution index based on the contents of some urban elements (Cu, Pb, Zn), and therefore it serves as an effective parameter for quantifying the urban pollution. [source] Hani Amouri and Michel Gruselle Chirality in transition metal chemistry: molecules, supramolecular assemblies and Materials Wiley, 2008, 260 pp. £37.50/,46.90 0470060549 ISBN-13 9780470060544APPLIED ORGANOMETALLIC CHEMISTRY, Issue 5 2009Nick Fletcher No abstract is available for this article. [source] The Diversity of Difluoroacetylene Coordination Modes Obtained by Coupling Fluorocarbyne Ligands on Binuclear Manganese Carbonyl SitesCHEMISTRY - A EUROPEAN JOURNAL, Issue 22 2009Xian-mei Liu Abstract One Mn or two? The fluorocarbyne manganese carbonyl complexes [Mn(CF)(CO)n] (n=3,,4) and [Mn2(CF)2(CO)n] (n=4,7; see picture) have been investigated by density functional theory. In mononuclear complexes the CF ligand behaves very much like the NO ligand in terms of ,-acceptor strength. In binuclear complexes the two CF ligands couple in many of the low-energy structures to form a bridging C2F2 ligand derived from difluoroacetylene. Recent work has shown that the fluorocarbyne ligand CF, isoelectronic with the NO ligand, can be generated by the defluorination of CF3 metal complexes, as illustrated by the 2006 synthesis by Hughes et,al. of [C5H5Mo(CF)(CO)2] in good yield by the defluorination of [C5H5Mo(CF3)(CO)3]. The fluorocarbyne ligand has now been investigated as a ligand in the manganese carbonyl complexes [Mn(CF)(CO)n] (n=3,,4) and [Mn2(CF)2(CO)n] (n=4,7) by using density functional theory. In mononuclear complexes, such as [Mn(CF)(CO)4], the CF ligand behaves very much like the NO ligand in terms of ,-acceptor strength. However, in the binuclear complexes the two CF ligands couple in many of the low-energy structures to form a bridging C2F2 ligand derived, at least formally, from difluoroacetylene, FCCF. The geometries of such [Mn2(C2F2)(CO)n] complexes suggest several different bonding modes of the bridging C2F2 unit. These include bonding through the orthogonal ,,bonds of FCCF, similar to the well-known [R2C2Co2(CO)6] complexes, or bonding of the C2F2 unit as a symmetrical or unsymmetrical biscarbene. This research suggests that fluorocarbyne metal chemistry can serve as a means for obtaining a variety of difluoroacetylene metal complexes, thereby avoiding the need for synthesizing and handling the very unstable difluoroacetylene. [source] | ||||||||||