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Architectural Control in the Transition‐Metal‐Catalyzed Ring‐Opening Polymerization of Silicon‐Bridged [1]Ferrocenophanes
Author(s) -
GómezElipe Paloma,
Macdonald Peter M.,
Manners Ian
Publication year - 1997
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199707621
Subject(s) - silicon , transition metal , catalysis , polymerization , ring (chemistry) , polymer chemistry , ring opening polymerization , materials science , chemistry , organic chemistry , polymer , composite material
Regioregular poly(ferrocenylsilane)s 1 , end‐group‐functionalized polymers of controlled molecular weight, and novel graft copolymers 2 are accessible by transition‐metal‐catalyzed ring‐opening polymerization of strained ferrocenophanes at ambient temperature.

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