Tripodal imidazole frameworks: Reversible vapour sorption both with and without significant structural changes
Date
2011
Authors
Willans C.E.
French S.
Anderson K.M.
Barbour L.J.
Gertenbach J.-A.
Lloyd G.O.
Dyer R.J.
Junk P.C.
Steed J.W.
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Abstract
A series of tripodal imidazole frameworks (TIFs) are reported based on a tripodal, cavity-containing tris(imidazole) derivative. In the case of [Co 3Cl6(1)2]·n(solvent) (TIF-1) which possesses a doubly interpenetrated framework structure, the material exhibits rigid, permanent porosity and selectively absorbs CO2. The non-interpenetrated [Co(1)2(H2O)2]Cl 2·4H2O (TIF-2) also absorbs gases and vapours fully reversibly exhibiting a reversible phase change in the process and considerable conditioning and hysteresis. The very highly hydrated [Co(1) 2]Cl2·22H2O (TIF-3) irreversibly dehydrates to the layered structure [Co(1)2]Cl2· H2O (TIF-4). A nickel analogue [Ni(1)2]Cl 2·22H2O (TIF-5) closely related to TIF-3 is also reported along with two isostructural, non-porous materials [MCl2(1)] (M = Mn, TIF-6; M = Cd, TIF-7) based on d5 and d10 Mn(II) and Cd(II). Some of the materials may be prepared by mechanochemical as well as solution based methods. We liken TIF-1 to a gas cylinder, TIF-2 to a sponge and TIF-3 to a fragile soda can that is crushed on emptying to give TIF-4. © 2011 The Royal Society of Chemistry.
Description
Keywords
Interpenetrated frameworks, Isostructural, Layered Structures, Mechanochemicals, Phase Change, Structural change, Gas cylinders, Manganese compounds, Porous materials, Sorption, Manganese
Citation
Dalton Transactions
40
3
40
3