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Molybdenocene dichloride

Molecular recognition, in Rh Cp complexes, 7, 155 Molecular weight, in alkene living polymerizations, 11, 715 Moller-Plesset calculations, as perturbation method, 1, 646 Molten salts, and ionic liquids, 1, 848 Molybdacarboranes, synthesis, 3, 216 Molybdenocene dichloride, bioorganometallic chemistry,... [Pg.146]

Compared to molybdenocene dichloride, the thiol derivatives are stable in water at physiological pH, and in tests on V79 Chinese hamster lung, human breast MCF7, and ovarian 2008 cell lines, they are not cycotoxic. The... [Pg.450]

Figure 6 Examples of molybdenocene dichloride thiol derivatives of biological relevance prepared in water under facile conditions. Figure 6 Examples of molybdenocene dichloride thiol derivatives of biological relevance prepared in water under facile conditions.
Significant antiviral ejfectivity was shown in vitro for titanocene dichloride (I) against numerous DNA and RNA viruses in the extracellular phase Typical examples of viruses, which were inhibited by direct contact with I and lost infectivity up to 100%, were orthopoxvirus (vaccinia) and herpes virus (pseudorabies) as DNA viruses, and rhabdovirus (vesicular stomatitis), paramyxovirus (Newcastle disease) and diverse orthomyxoviruses (e.g. influenza A and B) as RNA viruses. A comparable antiviral effect against herpes viruses was detectable after application of the ferricenium salt whereas, on the other hand, vanadocene dichloride (11) and molybdenocene dichloride (V) failed to show antiviral activity under the same experimental conditions. [Pg.142]

The first reported pesticide hydrolyses by an organometallic complex, which are the paraoxon and parathion hydrolysis by the aqueous molybdenocene dichloride (CP2M0CI2), have been reported. The synthesis and structural characterisation of a new one-to-one charge-transfer salt ferromagnet which is constructed from decamethylchromocene and dimethylcyanofumarate have been... [Pg.400]

For titanocene dichloride (I) and molybdenocene dichlotide (V), concentrations of 5 X 10 and 10" mol/1, respectively, i.e., 100-fold higher concentrations than for II, were required to induce equivalent effects in vitro (Fig. 7). [Pg.120]


See other pages where Molybdenocene dichloride is mentioned: [Pg.62]    [Pg.450]    [Pg.451]    [Pg.62]    [Pg.450]    [Pg.451]    [Pg.221]   
See also in sourсe #XX -- [ Pg.125 ]

See also in sourсe #XX -- [ Pg.144 ]




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Molybdenocene

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