Homochiral Porous Metal-Organic Frameworks Constructed from a V-Shaped Alanine Derivative Based on Pyridyl-Dicarboxylate

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Abstract

Three novel, homochiral, porous metal-organic frameworks based on the H2PDBAla ligand and different divalent cations (Co(II)) and Cu(II)), namely, [M(PDBAla)(bipy)(H2O)2]·3H2O (M = Co 1 and Cu 2), [Cu(PDBAla)(bpea)]·7H2O (3) (H2PDBAla = pyridine-2,6-dicarbonyl-bis(l-alanine), bipy = 4,4′-bipyridine, bpea = 1,2-bis(4-pyridyl)ethane), have been synthesized and characterized with the assistance of N-donor ligands. The distinctive H2PDBAla ligands are coordinated to divalent metal ions by the different coordination modes, forming various helixes in compounds 1-3. Compounds 1 and 2 are isostructural and feature a 2-fold interpenetrating three-dimensional (3D) framework with the cds topological net built by the combination right-handed helical chains and bipy ligands, whereas a 3D framework with the tcj topological net is observed in compound 3, wherein bpea ligands reinforce the 3D framework constructed by right-handed helical chains. Compounds 1 and 3 display high CO2 absorption capability and superior sorption enthalpies, reflecting the strong affinity of the frameworks for CO2. Moreover, compound 3 exhibits a small enantioselective separation performance for racemic alcohol.

Original languageEnglish
Pages (from-to)2476-2484
Number of pages9
JournalCrystal Growth and Design
Volume19
Issue number4
DOIs
StatePublished - 3 Apr 2019

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