Reversible guest binding in a non-porous FeII coordination polymer host toggles spin crossover

Anders Lennartson, Peter Southon, Natasha F. Sciortino, Cameron J. Kepert, Cathrine Frandsen, Steen Mørup, Stergios Piligkos, Christine J. McKenzie

30 Citationer (Scopus)

Abstract

Formation of either a dimetallic compound or a 1D coordination polymer of adiponitrile adducts of [Fe(bpte)]2+ (bpte=[1,2-bis(pyridin-2-ylmethyl)thio]ethane) can be controlled by the choice of counteranion. The iron(II) atoms of the bis(adiponitrile)-bridged dimeric complex [Fe2(bpte)22-(NC(CH2)4CN)2](SbF6)4 (2) are low spin at room temperature, as are those in the polymeric adiponitrile-linked acetone solvate polymer {[Fe(bpte)(μ2-NC(CH2)4CN)](BPh4)2 Me2CO} (3Me2CO). On heating 3Me2CO to 80°C, the acetone is abruptly removed with an accompanying purple to dull lavender colour change corresponding to a conversion to a high-spin compound. Cooling reveals that the desolvate 3 shows hysteretic and abrupt spin crossover (SCO) S=0虠S=2 behaviour centred at 205K. Non-porous 3 can reversibly absorb one equivalent of acetone per iron centre to regenerate the same crystalline phase of 3Me2CO concurrently reinstating a low-spin state.

OriginalsprogEngelsk
TidsskriftChemistry: A European Journal
Vol/bind21
Udgave nummer45
Sider (fra-til)16066-16072
Antal sider7
ISSN1521-3765
DOI
StatusUdgivet - 1 nov. 2015

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