Four new coordination polymers (CPs) have been prepared and evaluated for their efficacy in adsorbing hydrogen sulfide. The reactions of the structurally flexible assembling dithione ligand, , with different silver(I) salts lead to four new metal-organic coordination architectures (CPs , , , and ) exhibiting either one- or two-dimensional networks. CP , 2D-[(AgCl)], exhibits a linear series of rhomboid (S)Ag(μ-Cl)Ag(S) secondary building units (SBUs) where S is one of the thione functions of , altogether forming a 2D-network. CP , 2D-[(AgI)], is built upon parallel staircase-shaped 1D-[Ag(μ-I)] SBUs bridged by S atoms of that form a 2D-grid. CP V, 2D-[(Ag)(NO)], presents parallel 1D-folded S-shaped [Ag] chains linked by strong argentophilic Ag···Ag interactions, forming a 2D-scaffolding. CP , 1D-[(Ag)(CrO)], shows 1D-zigzag [{Ag(η-μ,η-μ,μ-)}] chains accompanied by CrO counteranions. The adsorption isotherms of HS gas by these new CPs were examined and compared to those of related CPs [(AgBr)] (), [(AgCN)] (), [(Ag)(CFSO)] (), and [(Ag)(NO)(ClO)] (). Among the tested polymers, the 3D-CP featuring cyanide anions exhibits the highest adsorption capacity of the CPs studied in this work. In order to determine the reason for this marked difference, density functional theory (DFT) computations were used. All in all, it turns out that the electrostatic interactions (CN···H-SH) are significantly stronger than the O···H-SH ones. This investigation provides a valuable conceptual tool for other designs of CPs and MOFs having the purpose of capturing toxic gases.

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http://dx.doi.org/10.1021/acsami.4c02350DOI Listing

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