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Single crystal-to-single crystal transformation – from two distinct to three distinct spin crossover centers in 2D coordination polymer [Fe(bbtr)3](CF3SO3)2
Autorzy
Rok wydania
2022
Czasopismo
Numer woluminu
51
Strony
958-968
DOI
10.1039/d1dt03578a
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
1,4-di(1,2,3-triazol-1-yl)butane (bbtr) forms two-dimensional (2D) coordination polymer (1) in the reaction with iron(II) triflate. In the crystal lattice there are two crystallographically unique iron(II) ions surrounded octahedrally by 1,2,3-triazole ring coordinated through nitrogen atoms N3. Single crystal X-ray diffraction studies revealed that spin crossover for each crystallographically independent iron(II) ions proceeds at different temperatures (T1/2(Fe1) = 201 K; T1/2(Fe2) = 216 K), while the magnetic measurements showed that there is one step, complete thermally induced spin crossover (T1/2 = 205 K). The complex 1 undergoes, with time, single crystal-to-single crystal transformation (SCSC) to the converted system (1c) from R-3 to P63 space group, accompanied by significant changes of the lattice parameters c (shortening of approx. 1/3) and consequently unit cell volume. Structural transformation is associated with rebuilding polymeric layer as well as anions network which is reflected in results of Mössbauer studies. In polymorphic system (1c) there are three crystallographically independent iron(II) ions. Results of temperature dependence of magnetic susceptibility indicated complete, one step spin crossover very similar to 1, however, single crystal X-ray diffraction studies of 1c revealed that spin crossover for each crystallographically independent iron(II) ions occurs in different manner revealing three elementary stages (T1/2(Fe1) = 200 K; T1/2(Fe2) = 212 K, T1/2(Fe3) = 214 K).
Adres publiczny
http://dx.doi.org/10.1039/D1DT03578A
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