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Diffraction Analysis. (diffraction + analysis)

Distribution by Scientific Domains
Chemistry100%

Kinds of Diffraction Analysis.

  • x-ray diffraction analysis.
    		•

    Selected Abstracts

    Unprecedented Rearrangement of Molybdenum(VI) Oxide to (,2 -Oxido)bis[dioxidomolybdenum(VI)] Hexamolybdate

    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 25 2007
    María R. Pedrosa
    Abstract MoO2(acac)2 reacts with water, amides, sulfoxides, and phosphane oxides in aqueous methanol, under mild conditions, to afford a new family of molybdates of composition [Mo2O5L6][Mo6O19] (L = H2O, dimethylformamide, dimethylacetamide, dimethyl sulfoxide, dibutyl sulfoxide, tributylphosphane oxide, triphenylphosphane oxide, hexamethylphosphoramide). The crystal and molecular structures of the two first structurally characterized (,2 -oxido)bis[dioxidomolybdenum(VI)] hexamolybdates were established by X-ray diffraction analysis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source]

    An Unusual Reaction of (,-Dimethylaminoethoxy)triethyltin with Phenyltin Trichloride.

    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 21 2006
    Aryl; X, Symmetrical Dimers [R2SnXY], The First X-ray Structural Evidence of the Existence of Complexes R2SnXY·R2SnXY (R = Alkyl, Y = Hal, Y) Both as Unsymmetrical Adducts [R2SnX2·R2SnY2]
    Abstract The substituent exchange reaction of PhSnCl3 with [Et3Sn(OCH2CH2NMe2)] gives rise unexpectedly to the unsymmetrical adduct [Ph2SnCl2·Ph2Sn(OCH2CH2NMe2)2] (2). It has been unambiguously proved for the first time that compounds of the RSnX3 type are able to undergo the hydrocarbon substituent redistribution reaction. The analogous tin complexes [Et2SnCl2·Et2Sn(OMe)2] (5) and [Bu2Sn(OAc)2·Bu2Sn(OMe)2] (6), which have ligands other than ,-dimethylaminoethoxy and could be considered as "organotin analogs of Grignard reagents" have symmetrical dimeric structures, i.e., can be formulated as [Bu2Sn(OMe)(OAc)]2 and [Et2Sn(OMe)Cl]2, respectively. Both types of structures, viz., unsymmetrical adduct (2) and symmetrical dimer (5, 6), have been characterized by X-ray diffraction analysis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source]

    The Synthesis and Characterisation of Bis(phosphane)-Linked (6 - p -Cymene)ruthenium(II),Borane Compounds

    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 23 2005
    Adrian B. Chaplin
    Abstract The reaction of [(,6 - p -cymene)RuCl2]2 with some bis(phosphane) ligands (dppm, dppe, dppv, dppa, dpp14b, dppf) has been investigated. In general mixtures of products were obtained, although the pendant phosphane complexes [(,6 - p -cymene)RuCl2(,1 -dppv)] and [(,6 - p -cymene)RuCl2(,1 -dppa)] were isolated and characterized in the solid state by X-ray diffraction. The later complex was obtained in lower yield and undergoes an equilibration reaction resulting in the formation of a dimeric species, where the dppa bridges two ruthenium centres, and uncoordinated phosphane; the bridging species was also structurally characterised in the solid state. In contrast, the reaction of [(,6 - p -cymene)RuCl2(PPh3)] with dppa in the presence of [NH4]PF6 results in the formation of [(,6 - p -cymene)RuCl(PPh3)(,1 -dppa)]PF6, which is stable in solution. A series of linked ruthenium,borane complexes, viz. [(,6 - p -cymene)RuCl2(,1 -phosphane-BH3)] (phosphane = dppm, dppe, dppv, dppa, dpp14b, dppf) and [(,6 - p -cymene)RuCl(PPh3)(,1 -dppa-BH3)]PF6 have been prepared from isolated pendant phosphane complexes, those generated in situ, or from a preformed phosphane,borane adduct. The solid-state structures of [(,6 - p -cymene)RuCl2(,1 -dppm-BH3)], [(,6 - p -cymene)RuCl2(,1 -dppe-BH3)] and [(,6 - p -cymene)RuCl2(,1 -dppv-BH3)] have been determined by X-ray diffraction analysis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source]

    Synthesis of novel substituted pyridine derivatives from 3,5-diacetyl-2,6-dimethylpyridine

    HETEROATOM CHEMISTRY, Issue 3 2009
    Jun Zhang
    A series of novel (1-acetyl-5-aryl-4,5-dihydro)-1H-pyrazole substituted pyridine derivatives and poly substituted [2,3,-bipyridine]-5-carbonitrile derivatives were synthesized from 3,5-diacetyl-2,6-dimethylpyridine. The structures of two typical 3,5-bis[1-acetyl-5-(4-chlorophenyl)-4,5-dihydro-1H-pyrazol-3-yl]-2,6-dimethylpyridines [3b(1) and 3b(2)] were confirmed by X-ray diffraction analysis. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:123,130, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20522 [source]