| Abstract: | Multifunctional 2‐amino‐5‐sulfobenzoic acid (H2afsb) can exhibit a variety of roles during the construction of supramolecular coordination polymers. The pendant carboxylic acid, sulfonic acid and amino groups could not only play a role in directing bonding but could also have the potential to act as hydrogen‐bond donors and acceptors, resulting in extended high‐dimensional supramolecular networks. Two new CuII coordination compounds, namely catena‐poly[[[diaquacopper(II)]‐μ‐1,6‐bis(1H‐1,2,4‐triazol‐1‐yl)hexane‐κ2N4:N4′] bis(3‐amino‐4‐carboxybenzenesulfonate) dihydrate], {[Cu(C10H16N6)2(H2O)2](C7H6NO5S)2·2H2O}n or {[Cu(bth)2(H2O)2](Hafsb)2·2H2O}n, (1), and bis(μ‐2‐amino‐5‐sulfonatobenzoato‐κ2O1:O1′)bis{μ‐1,2‐bis[(1H‐imidazol‐1‐yl)methyl]benzene‐κ2N3:N3′}bis[aquacopper(II)] trihydrate, [Cu2(C7H5NO5S)2(C14H14N4)2(H2O)2]·3H2O or [Cu2(afsb)2(obix)2(H2O)2]·3H2O, (2), have been obtained through the assembly between H2afsb and the CuII ion in the presence of the flexible N‐donor ligands 1,6‐bis(1H‐1,2,4‐triazol‐1‐yl)hexane (bth) and 1,2‐bis[(1H‐1,2,4‐triazol‐1‐yl)methyl]benzene (obix), respectively. Compound (1) consists of a cationic coordination polymeric chain and 3‐amino‐4‐carboxybenzenesulfonate (Hafsb−) anions. Compound (2) exhibits an asymmetric dinuclear structure. There are hydrogen‐bonded networks within the lattices of (1) and (2). Interestingly, both (1) and (2) exhibit reversible dehydration–rehydration behaviour. |
