Four-connected metal-organic frameworks constructed by tetracarboxylate acid-based ligands

Libo Sun, Qinhe Pan, Zhiqiang Liang*, Jihong Yu

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Citations (Scopus)

Abstract

Three tetracarboxylate acid ligands, 5,5′-(1H-1,2,3-triazole-1,4-diyl)diisophthalic acid (H4TADIP), 5-(bis(4-carboxybenzyl)amino)isophthalic acid (H4BCBAIP), and 5-(3,5-dicarboxybenzyloxy)isophthalic acid (H4DBIP) have been reacted with Mn(ii), Co(ii) and In(iii) salts to construct four new metal-organic frameworks, [Mn2(TADIP)(DMF)3]·2DMF·3H2O (1), [Co2(TADIP)(DEF)3]·0.5DEF (2), [Mn2(BCBAIP)(DMF)3]·7.5DMF (3), and (Me2NH2)[In(DBIP)]·3DMF·7H2O (4) under solvothermal conditions. Due to the rotation ability of these ligands that exhibit a quadrangle or tetrahedral geometry, these compounds show diverse three-dimensional four-connected topologies. Compound 1 is composed of binuclear Mn(ii) units and quadrangle type ligand H4TADIP with pts topology, while compound 2 possesses a zeolitic abw topology constructed from the 4-connected tetrahedral type ligand H4TADIP and binuclear Co(ii) units. Compound 3 is a 3D structure possessing a zeolitic sod topology from the coordination of binuclear Mn(ii) units with the tetrahedral type ligand H4BCBAIP. Compound 4 is an anionic framework constructed from tetrahedral type ligand H4DBIP and In(iii) ions that has a topology of unc. Variable temperature magnetic susceptibility measurements show that compound 1 exhibits antiferromagnetic behavior. The selective dye-adsorption and luminescent properties of compound 4 have been studied in detail.

Original languageEnglish
Pages (from-to)478-486
Number of pages9
JournalInorganic Chemistry Frontiers
Volume1
Issue number6
DOIs
Publication statusPublished - Jun 2014
Externally publishedYes

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