Macrospirocyclic oligomers based on carbazole and fluorene

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DOIResolve DOI: http://doi.org/10.1021/ol1025958
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TypeArticle
Journal titleOrganic Letters
ISSN1523-7060
Volume13
Issue2
Pages200203; # of pages: 4
AbstractMonodisperse macrospirocyclic oligomers were prepared using self-condensation of the Friedel-Crafts reaction. Through the C-9s of the central fluorene units of four surrounding oligofluorenes, four carbazole units are connected in a series to form a macrocyclic core. These rodlike oligofluorenes form a rigid three-dimensional structure, affording the resulting macrocyclics a high steric hindrance for close interchain packing. © 2010 American Chemical Society.
Publication date
LanguageEnglish
AffiliationNational Research Council Canada (NRC-CNRC); NRC Institute for Chemical Process and Environmental Technology (ICPET-ITPCE)
Peer reviewedYes
NPARC number21271403
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Record identifier3a5efdcf-a14c-4623-bb9b-3d39fd2c89bd
Record created2014-03-24
Record modified2016-05-09
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