Effect of Linker Substituent on Layers Arrangement, Stability, and Sorption of Zn-Isophthalate/Acylhydrazone Frameworks

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Kornel Roztocki - , Jagiellonian University in Kraków (Author)
  • Damian Jȩdrzejowski - , Jagiellonian University in Kraków (Author)
  • Maciej Hodorowicz - , Jagiellonian University in Kraków (Author)
  • Irena Senkovska - , Chair of Inorganic Chemistry I (Author)
  • Stefan Kaskel - , Chair of Inorganic Chemistry I (Author)
  • Dariusz Matoga - , Jagiellonian University in Kraków (Author)

Abstract

A series of mixed-linker metal-organic frameworks [Zn2(Xiso)2(pcih)2]n containing substituted isophthalate linkers (Xiso2- X = OH or CH3 or NH2 or H) and 4-pyridinecarbaldehyde isonicotinoyl hydrazone pillars (pcih) have been prepared by using both solution and mechanochemical methods. Single-crystal X-ray diffraction reveals their interdigitated two-dimensional structures with different arrangements of layers, dependent on hydrogen bonding and CH···π interactions involving the substituents and/or linkers. These supramolecular interactions are responsible for the formation of interlayer pores of various volumes, shapes, and dimensionality. All materials exhibit selective gas adsorption of CO2 over N2 with diverse profiles. Polar groups (OH and NH2) of the isophthalate linkers increase chemical affinity to carbon dioxide as well as hydrolytic and thermal stability of the frameworks.

Details

Original languageEnglish
Pages (from-to)488-497
Number of pages10
JournalCrystal Growth and Design
Volume18
Issue number1
Publication statusPublished - 3 Jan 2018
Peer-reviewedYes