Download Comprehensive Coordination Chemistry II: From Biology to by Jon A. MacCleverty, Thomas J. Meyer, E. C. Constable, J. R. PDF

By Jon A. MacCleverty, Thomas J. Meyer, E. C. Constable, J. R. Dilworth

This quantity offers a survey of vital advancements within the chemistry of teams 7 and eight ofthe transition metals because the e-book of entire Coordination Chemistry (CCC) in 1987. the cloth for every aspect is equipped by way of oxidation kingdom of the steel and likewise by way of thenature of the ligands concerned, with extra sections protecting particular beneficial properties of the coordinationchemistry and functions of the complexes.

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Extra resources for Comprehensive Coordination Chemistry II: From Biology to Nanotechnology, Volume 5: Transition Metal Groups 7 and 8

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NH N O N N Py 3-Me-Py NH HIm O acac N 3,5-iPr2pzH F F F F O O F O Hdpm O F N N OH hfacac R OH Hhmp OH OH N SH CO2H H3C CO2H N N CO2– thiosal CO2H CO2H H2phth Himac HO2C CO2H CO2H H2edt sal S– SH SH CO2– H2Lc SH H2tdt O– CH OH R = H: H2spa R = OMe: H23-OMe-spa O OH O CO2H HO2C CO2H N H2mpdp Hhqn N CO2H O O H2XDK Figure 16 H4Ct 36 Manganese N N N 4,4'-bpy N N N 4,4'-Me2bpy bpe N N N N N N N bmpe N N N N ttco H N N N N N N N P N TMIMA N O– N N N TMIP ppam N N N N N N N H N NH2 N N H2N dien bpia bpmpa N N N N N N N N N N N O– BBAE bbpmax Figure 17 The chemistry of manganese(III) is dominated by dinuclear, trinuclear, and tetranuclear complexes and the core types observed are shown in Figures 20–22.

94 A˚). 8 A˚. These distances closely resemble those found by EXAFS measurements of the S2 state of the PSII active site185 making it a potential structural model. 9 A˚) over the equatorial counterparts. There are three -carboxylates (Me, Ph, p-OMe-Ph, p-Me-Ph) that bridge adjacent MnIII–MnIV pairs along with three chelating dbmÀ that coordinate each MnIII ion. The unique 3 site is occupied by variety of oxygen donor ligands like acetate, benzoate, methoxide, phenoxide, hydroxide, and nitrate.

209 These molecules possess the useful property of retaining their magnetization in the absence of an applied magnetic field, a classical property of a magnet. 210–212 This results in a significantly high barrier (Ueff = S2D) for the relaxation of the magnetization that can be estimated from the Arrhenius relation. 214 The family of Mn12 complexes is now known to exist in three oxidation state levels. The neutral form of the complex [Mn4IVMn8III] (Mn12) has a central [MnIV4O4] cuboidal unit surrounded by a noncoplanar ring of eight MnIII ions (Figure 11).

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