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Ferrocenylborane polymers

Borylated ferrocenes have been exploited by Wagner as building blocks for the assembly of macrocycles and coordination polymers (Scheme 15). Treatment of the diborylated ferrocene l,L-fc(BMe2)2 with the bifunctional aromatic amines pyrazine and 4,4 -bipyridine, respectively, led to spontaneous and reversible formation of (89) and related ferrocenylborane polymers.The polymeric nature of... [Pg.496]

Scheme 15 Coordination polymers and macrocycles from ferrocenylboranes... Scheme 15 Coordination polymers and macrocycles from ferrocenylboranes...
Scheme 12 shows the thermally initiated ROP of boron bridge containing [l]ferrocenophanes. Due to the high strain of these molecules from the large ring tilts, the ROP reaction was able to proceed at temperatures of 180-200°C. All the poly(ferrocenylboranes) formed were found to be insoluble except for polymer 42c. [Pg.17]


See other pages where Ferrocenylborane polymers is mentioned: [Pg.557]    [Pg.497]    [Pg.557]    [Pg.497]    [Pg.36]    [Pg.495]    [Pg.63]    [Pg.494]   


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