Comment on "Insight into the reversible structural crystalline-state transformation from MIL-53(Al) to MIL-68.Al)" by A. Perea-Cachero, E. Romero, C. Tellez and J. Coronas, CrystEngComm, 2018, 20, 402
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Kriesten, Martin
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Friedrich Alexander Univ Erlangen Nurnberg, Erlangen Catalysis Resource Ctr ECRC, Egerlandstr 3, D-91058 Erlangen, GermanyFriedrich Alexander Univ Erlangen Nurnberg, Erlangen Catalysis Resource Ctr ECRC, Egerlandstr 3, D-91058 Erlangen, Germany
Kriesten, Martin
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Hoffmann, Kilian
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Friedrich Alexander Univ Erlangen Nurnberg, Erlangen Catalysis Resource Ctr ECRC, Egerlandstr 3, D-91058 Erlangen, GermanyFriedrich Alexander Univ Erlangen Nurnberg, Erlangen Catalysis Resource Ctr ECRC, Egerlandstr 3, D-91058 Erlangen, Germany
Hoffmann, Kilian
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Hartmann, Martin
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Friedrich Alexander Univ Erlangen Nurnberg, Erlangen Catalysis Resource Ctr ECRC, Egerlandstr 3, D-91058 Erlangen, GermanyFriedrich Alexander Univ Erlangen Nurnberg, Erlangen Catalysis Resource Ctr ECRC, Egerlandstr 3, D-91058 Erlangen, Germany
Hartmann, Martin
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[1] Friedrich Alexander Univ Erlangen Nurnberg, Erlangen Catalysis Resource Ctr ECRC, Egerlandstr 3, D-91058 Erlangen, Germany
In a recently published communication (CrystEngComm, 2018, 20, 402-406), Perea-Cachero et al. stated that the topologically isomeric metal-organic frameworks MIL-53(Al) and MIL-68(Al) could be reversibly transformed into each other. However, the suggested synthesis procedure for MIL-68 indeed resulted in MIL-53 with DMF entrapped inside of the pores. The collected PXRD pattern of MIL-53DMF was then inadvertently assigned to the MIL-68 structure.