Citation

BibTex format

@article{Inkpen:2016:10.1038/nchem.2553,
author = {Inkpen, MS and Scheerer, S and Linseis, M and White, AJP and Winter, RF and Albrecht, T and Long, NJ},
doi = {10.1038/nchem.2553},
journal = {Nature Chemistry},
pages = {825--830},
title = {Oligomeric ferrocene rings},
url = {http://dx.doi.org/10.1038/nchem.2553},
volume = {8},
year = {2016}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Cyclic oligomers comprising strongly interacting redox-active monomer units represent an unknown, yet highly desirable class of nanoscale materials. Here we describe the synthesis and properties of the first family of molecules belonging to this compound category—differently sized rings comprising only 1,1′-disubstituted ferrocene units (cyclo[n], n = 5–7, 9). Due to the close proximity and connectivity of centres (covalent Cp–Cp linkages; Cp = cyclopentadienyl) solution voltammograms exhibit well-resolved, separated 1e– waves. Theoretical interrogations into correlations based on ring size and charge state are facilitated using values of the equilibrium potentials of these transitions, as well as their relative spacing. As the interaction free energies between the redox centres scale linearly with overall ring charge and in conjunction with fast intramolecular electron transfer (∼107s−1), these molecules can be considered as uniformly charged nanorings (diameter ∼1–2nm).
AU - Inkpen,MS
AU - Scheerer,S
AU - Linseis,M
AU - White,AJP
AU - Winter,RF
AU - Albrecht,T
AU - Long,NJ
DO - 10.1038/nchem.2553
EP - 830
PY - 2016///
SN - 1755-4330
SP - 825
TI - Oligomeric ferrocene rings
T2 - Nature Chemistry
UR - http://dx.doi.org/10.1038/nchem.2553
UR - http://hdl.handle.net/10044/1/37075
VL - 8
ER -