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Organogermanium polymers prepared from s ‐indacene and carbodiimide compounds
Author(s) -
Dahrouch Mohamed,
Diaz Enzo,
Gatica Nicolas,
Moreno Yanko,
Chavez Ivonne,
Manriquez Juan Manuel,
Rivière Pierre,
RivièreBaudet Monique,
Gornitzka Heinz,
Castel Annie
Publication year - 2012
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.2867
Subject(s) - chemistry , steric effects , carbodiimide , monomer , polymerization , polymer chemistry , polymer , organic chemistry
The synthesis of bis‐organogermanium compounds including s ‐indacene structure was described and showed the formation of one type of trans isomer characterized by spectroscopic methods. In the same way, the digermyl‐ s ‐indacene dichlorides were prepared and structural characterizations confirmed the unique formation of trans isomers. These digermyl‐ s ‐indacene dichlorides were used as monomers in a polymerization reaction in order to prepare poly(germyl‐ s ‐indacenes) and poly(germyl‐ s ‐indacene carbodiimides). However, only the products obtained from tetraalkyl‐ s ‐indacene reached high molecular weight, probably due to a minor steric hindrance compared to the hexaalkyl‐ s ‐indacene. Thermal degradation only starts from 250°C for poly(germyl‐ s ‐indacene carbodiimides) and from 350°C for poly(germyl‐ s ‐indacenes). The structures of the first digermyl‐ s ‐indacene dichlorides were determined by X‐ray analysis, confirming that the chlorogermyl groups are located in trans positions. Copyright © 2012 John Wiley & Sons, Ltd.

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