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61.
ZHAO Bao-xiang SCHAUDT Marco BLECHERT Siegfried 《高等学校化学研究》2007,23(1):22-30
IntroductionThe discovery of stable and defined carbenecomplexes of molybdenum and ruthenium as efficientprecatalysts for olefin metathesis has made this transfor-mation one of the most important C—C bond formingreactions[1—11]. Specifically, ring-closi… 相似文献
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Bridged 2,3-naphthalocyaninatoruthenium oligomers {[MacRu(L)] n } were synthesized and characterized using solid-state methods. For comparison, soluble t-butyl substituted phthalocyaninatoruthenium oligomers were prepared and their chain length examined by 1H NMR spectroscopy. The powder conductivities of all bridged compounds ([MacRu(L)] n ) were measured and the dependence of the conductivities on the bridging ligands is discussed. 相似文献
64.
Polymeric dispersions with a concentric core-shell structure of the latex particles were obtained by a two-stage emulsion polymerization technique. Conditions for the formation of shells on polymeric seeds are discussed. SANS and SAXS investigations were carried out in order to verify the core-shell structure of the particles. DSC and IR measurements indicate the existence of an interfacial layer between core and shell polymers. The results are transferred to emulsion polymers containing inorganic filler particles. 相似文献
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The crystal structures of pyrene and substituted and complexed derivatives of pyrene have been investigated by X-ray and neutron diffraction. The geometry of the pyrene skeleton has been determined experimentally with high accuracy and calculated by quantum chemical methods. In the cases reported in the literature and cited here the pyrene skeleton has the molecular symmetry mmm or mm2 with values for the bond lengths of the six symmetrically independent bondsa, b, c, d, e, f differing significantly in the limits of error. Mean values of a number of experimental and theoretical bond lengths are given and can be considered as standard values for the mm2 symmetric pyrene skeleton. In the case of substitution of the pyrene in 3-position with a polar heterocyclic molecule of the azomethine-imine type the mm2 symmetry vanishes, a C–H ... N intramolecular hydrogen bond arises and the directly neighbouring pyrene units are not packed parallel with their planes to each other, but they are considerably tilted. Relatively narrow intermolekular C-C contacts, 3.314 and 3.368 Å, have been observed. The conclusion is drawn that the asymmetry of the pyrene molecule and a tilt of directly neighbouring pyrene units in the crystal packing can be induced by substitution e. g. with suitable polar heterocycles.
Juli 1985. 相似文献
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Siegfried Blechert 《Nachrichten aus der Chemie》1979,27(6):321-322
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