Loading…
Guest-dependent single-ion magnet behaviour in a cobalt() metal-organic framework
Single-ion magnets (SIMs) are the smallest possible magnetic devices for potential applications in quantum computing and high-density information storage. Both, their addressing in surfaces and their organization in metal-organic frameworks (MOFs) are thus current challenges in molecular chemistry....
Saved in:
Published in: | Chemical science (Cambridge) 2016-03, Vol.7 (3), p.2286-2293 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Single-ion magnets (SIMs) are the smallest possible magnetic devices for potential applications in quantum computing and high-density information storage. Both, their addressing in surfaces and their organization in metal-organic frameworks (MOFs) are thus current challenges in molecular chemistry. Here we report a two-dimensional 2D MOF with a square grid topology built from cobalt(
ii
) SIMs as nodes and long rod-like aromatic bipyridine ligands as linkers, and exhibiting large square channels capable to host a large number of different guest molecules. The organization of the cobalt(
ii
) nodes in the square layers improves the magnetic properties by minimizing the intermolecular interactions between the cobalt(
ii
) centres. Moreover, the SIM behaviour was found to be dependent on the nature of the aromatic guest molecules. The whole process could be followed by single-crystal X-ray diffraction, providing comprehensive evidence of the putative role of the solvent guest molecules that leave a "fingerprint" on the 2D structures and thus, on the cobalt environment.
Such exciting properties as porosity and single-ion magnetic behavior are merged into a single unique material which affords the first in-depth study of guest-dependent SIM behavior in a MOF. |
---|---|
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/c5sc04461h |