Journal
CRYSTENGCOMM
Volume 18, Issue 46, Pages 8838-8848Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ce01800a
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Funding
- People Programme (Marie Curie Actions) of the European Union's Seventh Framework Programme/under REA [PIRSES-GA-2012-319011]
- University of Salerno (FARB)
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The investigation of the solid state assembly of propargyl substituted hexa- and octacyclic peptoids highlights the effect of ring size in determining the packing arrangement of the macrocycles. A layered arrangement is obtained in the case of the hexacyclic peptoid 1 and a tubular arrangement in the case of the octacyclic peptoid 2. Guest molecules either intercalate between the layers as in 1 or are located within the peptoid nanotube as in 2.
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