Jump to main content
Jump to site search

Issue 46, 2016
Previous Article Next Article

Ring size effect on the solid state assembly of propargyl substituted hexa- and octacyclic peptoids

Author affiliations

Abstract

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.

Graphical abstract: Ring size effect on the solid state assembly of propargyl substituted hexa- and octacyclic peptoids

Back to tab navigation

Supplementary files

Article information


Submitted
18 Aug 2016
Accepted
22 Sep 2016
First published
23 Sep 2016

This article is Open Access

CrystEngComm, 2016,18, 8838-8848
Article type
Paper

Ring size effect on the solid state assembly of propargyl substituted hexa- and octacyclic peptoids

C. Tedesco, A. Meli, E. Macedi, V. Iuliano, A. G. Ricciardulli, F. De Riccardis, G. B. M. Vaughan, V. J. Smith, L. J. Barbour and I. Izzo, CrystEngComm, 2016, 18, 8838
DOI: 10.1039/C6CE01800A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Material from this article can be used in other publications provided that the correct acknowledgement is given with the reproduced material and it is not used for commercial purposes.

Reproduced material should be attributed as follows:

  • For reproduction of material from NJC:
    [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the Centre National de la Recherche Scientifique (CNRS) and the RSC.
  • For reproduction of material from PCCP:
    [Original citation] - Published by the PCCP Owner Societies.
  • For reproduction of material from PPS:
    [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the European Society for Photobiology, the European Photochemistry Association, and RSC.
  • For reproduction of material from all other RSC journals:
    [Original citation] - Published by The Royal Society of Chemistry.

Information about reproducing material from RSC articles with different licences is available on our Permission Requests page.


Social activity

Search articles by author

Spotlight

Advertisements