Self-templated synthesis of amide catenanes and formation of a catenane coordination polymer
File(s)MS Article Catenanes Lewis Resubmission.pdf (934.23 KB)
Accepted version
Author(s)
Lewis, James EM
Type
Journal Article
Abstract
A self-templation strategy was used to synthesise isophthalamide [2]catenanes of various sizes in up to 51% yield without the need for metal ions as templates or mediators of covalent bond formation. Using this strategy a bis-monodentate catenane was prepared incorporating exohedral pyridine units. Upon complexation of this ligand with AgOTf a one-dimensional coordination polymer was obtained in the solid state in which both macrocycles of the catenane are involved in binding to the metal nodes, resulting in a rare example of a coordination assembly in which mechanical bonds are incorporated into the structure backbone.
Date Issued
2019-03-07
Date Acceptance
2019-02-05
Citation
Organic & Biomolecular Chemistry, 2019, 17 (9), pp.2442-2447
ISSN
1477-0520
Publisher
Royal Society of Chemistry (RSC)
Start Page
2442
End Page
2447
Journal / Book Title
Organic & Biomolecular Chemistry
Volume
17
Issue
9
Copyright Statement
© The Royal Society of Chemistry 2019
Sponsor
The Royal Society
Grant Number
RG170321
Subjects
0304 Medicinal And Biomolecular Chemistry
0305 Organic Chemistry
1115 Pharmacology And Pharmaceutical Sciences
Organic Chemistry
Publication Status
Published
Date Publish Online
2019-02-05