The crystal engineering of 3d-metal with two tetrazole-phenyl-carboxylate linkers and multiple post-synthetic metal exchange

Ligand with mixed-groups contributes to the construction of special structure motif with novel properties, yet it is challenging to understand and regulate the competitive coordination of different functional groups toward metal ions. Herein, the crystal engineering for MOF construction from two linear di-topic linkers of 4-(1H-tetrazol-5-yl)benzoic acid (H 2 tzba) and the longer 4′-(1H-tetrazol-5-yl)-[1,1′-biphenyl]-4-carboxylic acid (H 2 tzbba) featuring dual groups of phenyl-carboxylate and tetrazole, with three typical 3d metal ions (Mn 2+ , Fe 2+ and Zn 2+ ) were investigated. A series of five new MOFs, that are [Mn 3 (tzba) 3 (dmf) 4 ]·11dmf ( 1 , dmf = N ,N-Dimethylformamide), [Mn(tzba)(H 2 O)] ( 2 ), [Zn 2 (tzba) 2 (dmf)]·0.5dmf ( 3 ), [Fe 2 (tzba) 2 (dmf)]·0.5dmf ( 4 ) and [Zn 2 (tzbbz)(gac)(dmf) 2 ]·1.5dmf ( 5 ), were synthesized under solvothermal reactions. The modified solvent template and temperature effects lead to 3D framework of 1 (dmf solution under 433 K) with [Mn 3 (tz) 3 (COO) 3 ] nodes and 1D hexagonal channels, while the 2 (water solution under 373 K) posssesses compact pillared-layer motif from [Mn 2 (tz) 2 ] nodes. Under changed metal salt reactents but same solvent of dmf, the generated 3 and 4 have isoreticular and porous pillared-layer structure constituted of [M 2 (COO) 2 ] nodes. The use of tzbba coupled with a crucial auxiliary ligand of glycollic acid, leads to 5 as porous pillared-layer MOFs with 1D rounded channels. The porous flexible skeleton of 1 constructed from [Mn 3 ] node with four coordinated dmf facilitates post-synthetic metal exchange of the Mn 2+ by radius similar metal ions following priority of Cu 2+ < Zn 2+ < Ni 2+ < Co 2+ , with maximum exchange percentage ranging from 17 % to 69 %. Time dependent ICP-AES analysis revealed the quite wide feasible solvents for post-synthetic metal exchange, as well as the fine control on substituting degree based on soaking temperature and time. Particularly, the compatible introduce of four different metal ions support the potential of preparing bi-, tri-, tetra- and penta- metal MOF crystals, that can not be obtained by traditional solvothermal reactions.