z-logo
open-access-imgOpen Access
Metal and Organic Templates Together Control the Size of Covalent Macrocycles and Cages
Author(s) -
Roy Lavendomme,
Tanya K. Ronson,
Jonathan R. Nitschke
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b06182
Subject(s) - chemistry , covalent bond , template , supramolecular chemistry , imine , palladium , dynamic covalent chemistry , ligand (biochemistry) , metal , self assembly , nuclear magnetic resonance spectroscopy , crystallography , combinatorial chemistry , stereochemistry , polymer chemistry , nanotechnology , catalysis , organic chemistry , crystal structure , biochemistry , materials science , receptor
Covalent macrocycles and three-dimensional cages were prepared by the self-assembly of di- or tritopic anilines and 2,6-diformylpyridine subcomponents around palladium(II) templates. The resulting 2,6-bis(imino)pyridyl-Pd II motif contains a tridentate ligand, leaving a free coordination site on the Pd II centers, which points inward. The binding of ligands to the free coordination sites in these assemblies was found to alter the product stability, and multitopic ligands could be used to control product size. Multitopic ligands also bridged metallomacrocycles to form higher-order supramolecular assemblies, which were characterized via NMR spectroscopy, mass spectrometry, and X-ray crystallography. An efficient method was developed to reduce the imine bonds to secondary amines, leading to fully organic covalent macrocycles and cages that were inaccessible through other means.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom