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POLYFERROCENES

Polyferrocenes

nearly a half-century of research, polyferrocenes still have no commercial applications. The simplest notional polyferrocene is poly(1,1′‑ferrocenylene), corresponding

Polyferrocenes

Vinylferrocene

Chemical compound

As the ferrocene analogue of styrene, it is the precursor to some polyferrocenes. It is an orange, air-stable oily solid that is soluble in nonpolar

Vinylferrocene

Inorganic polymer

Polymer whose backbone does not contain carbon

include materials with transition metals in the backbone. Examples are Polyferrocenes, Krogmann's salt and Magnus's green salt. Inorganic polymers are formed

Inorganic polymer

Inorganic_polymer

Ferrocenophanes

be prepared. Ferrocenophanes undergo ring-opening polymerization to polyferrocenes. Rolf Gleiter, Henning Hopf: Modern Cyclophane Chemistry, Wiley-VCH

Ferrocenophanes

Ferrocene

Organometallic compound: Fe(II) sandwiched between two cyclopentadienyl rings

polystyrene (the phenyl groups are replaced with ferrocenyl groups). Another polyferrocene which can be formed is poly(2-(methacryloyloxy)ethyl ferrocenecarboxylate)

Ferrocene

High-refractive-index polymer

Polymer with refractive index > 1.50

ability and relatively low optical dispersion. Polyferrocenylsilanes and polyferrocenes containing phosphorus spacers and phenyl side chains show unusually

High-refractive-index polymer

High-refractive-index_polymer