Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pentacarbonylchlororhenium

After solvent is removed under continuous vacuum (0.1 mm) at room temperature, the crude, slightly brownish residue is transferred to a sub-limator and sublimed at 80-45° and 0.1 mm. Yield 1.10 g [94.1%, based on Re2(CO)io] [Checkers yield 85%]. [Pg.161]


The reaction of bromopentacarbonylmanganese(I) and of pentacarbonylchlororhenium(I) with bis[trimethylstannyl] tellurium produced dimeric carbonyl complexes with two trimethylstannyltelluro groups bridging the metal centers5. [Pg.18]


See other pages where Pentacarbonylchlororhenium is mentioned: [Pg.43]    [Pg.44]    [Pg.259]    [Pg.43]    [Pg.44]    [Pg.161]    [Pg.161]    [Pg.161]    [Pg.161]    [Pg.43]    [Pg.44]    [Pg.259]    [Pg.43]    [Pg.44]    [Pg.161]    [Pg.161]    [Pg.161]    [Pg.161]   


SEARCH



Pentacarbonylchlororhenium (Alternate Procedure)

© 2024 chempedia.info