![]() 2 h yielded the tetrakis(ph0sphine) complex Reaction of RuC13-3H,0 with an excess (5-7 molar equivalents) of PPh,H or PPhH, in degassed, refluxing EtOH under Structure of trans-*0.5CHC13by Stephenson Have been reported previously by Sanders,6 and the crystal The syntheses of trans- and related complexes Single-crystal structure determinations on trans- and trans-[OsC12(PPh,H),J~CH,C12 Now report the synthesis and redox studies of Īnd, (M = Ru or Os, R = Ph or C6Hll). Studies were intended to establish the susceptibility of PR,HĪnd PRH, complexes to spontaneous deprotonation we haveĮxtended this work to ruthenium and osmium complexes. Of Pd" and Pt" undergo spontaneous deprotonation to give the Solution over very long period^.^ In contrast, PPh,H complexes NMR spectroscopy to be stable with respect to deprotonation in We have recently reported the complex cations (M = Pd or Pt) which were shown by multinuclear Recently reported the first example of an agostic Pd Poorly studied,-* and early studies indicated that upon coordination the P-H bonds become unstable to deprotonation Good yields initially with the PH groups intact, therebyĪllowing controlled deprotonation and further reaction.ĭespite the vast literature describing tertiary phosphine (PR,)Ĭo-ordination, PRH, and PR,H ligation have been relatively The PH groups, it is essential that they can be synthesised in To be useful for further functionalisation, such as alkylation, at Order for these primary and secondary phosphine complexes In their template syntheses of tetraphosphine macrocycles. Offer the possibility of further functionalisation following coordination, as shown for example by Stelzer and co-workers ' Our interest arises from the fact that they Primary and secondary phosphines (PRH, and PR,H) with We have been investigating the co-ordination chemistry of Reversible oxidation in each case, which is assigned to a M"-M"' redox couple. With the exception of (irreversible),Ĭyclic voltammetric studies on the complexes trans- and trans- show a The crystal-structure determination of trans- *CH,CI, showed two independent half Octahedral arrangement seen in trans- compared to trans- ~0.5CHC13. The lower steric demands of the PPhH, ligands compared to PPh,H are reflected in the more regular It confirms a transĪrrangement of the CI- ligands with the Ru" occupying a crystallographic inversion centre with four The crystal structure of trans- has been determined. Prolonged standing of trans in CH,CI, solution led to partial isomerisation to the cis isomer a s confirmed by 31PN M R Species exist a s trans isomers in solution and the integrity of the PH functions. Ultraviolet-visible and 31P N M R spectroscopic studies confirm that these In degassed refluxing EtOH solution (or EtOH-water for 0 s ) gave and in Reaction of RuCI3.3H,O or, with 5-7 molar equivalents of PR,H ( R = Ph or C,H,) or PPhH, Roche Research Centre, Welwyn Garden City AL7 3AY, UK S i m p s o dĪ Department of Chemistry, The University of Edinburgh, West Mains Road, Edinburgh EH9 3JJ, UKĭepartment of Chemistry, The University of Southampton, Highfield, Southampton SO9 5NH, U K Single-crystal Structures of trans- andĪlexander J. Synthesis and Redox Studies on Ruthenium and OsmiumĬomplexes with Primary and Secondary Phosphines. Downloaded by State University of New York at Stony Brook on 06:32:32. There is now a public Git repository at Bitbucket: pyDM3reader where one may find the latest stable and development versions.View Article Online / Journal Homepage / Table of Contents for this issue Dependencies : Python Imaging Library, NumPy.Plt.matshow(dm3f.imagedata, vmin=dm3f.cuts, vmax=dm3f.cuts) Use in your own script would typically require lines such as: import dm3_lib as dm3 It may also extract and dump all metadata (« Tags ») and pass thumbnail and image data as PIL Images or Numpy arrays, as well as save the thumbnail view in a PNG file. It now allows to extract various metadata (specimen, operator, HV, MAG, etc.) from GATAN DigitalMicrograph DM3 or DM4 files. This module was initially meant to be called by a script indexing electron microscope images into a database. This Python module is a transposition and adaptation of the DM3_Reader ImageJ plug-in by Greg Jefferis. Il permet d’extraire les données et méta-données des fichiers DM3 (et DM4) produits par le logiciel DigitalMicrograph de GATAN. Ce module Python est une adaptation du plug-in DM3_Reader (développé par Greg Jefferis) pour ImageJ.
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