A 1D double-zigzag framework, {[Zn(paps)2(H2O)2](ClO4)2}n (1; paps=N,N'-bis(pyridylcarbonyl)-4,4'-diaminodiphenyl thioether), was synthesized by the reaction of Zn(ClO4)2 with paps. However, a similar reaction, except that dry solvents were used, led to the formation of a novel 2D polyrotaxane framework, [Zn(paps)2(ClO4)2]n (2). This difference relies on the fact that water coordinates to the ZnII ion in 1, but ClO4- ion coordination is found in 2. Notably, the structures can be interconverted by heating and grinding in the presence of moisture, and such a structural transformation can also be proven experimentally by powder and single-crystal X-ray diffraction studies. The related N,N'-bis- (pyridylcarbonyl)-4,4'-diaminodiphenyl ether (papo) and N,N'-(methylenedi-para-phenylene)bispyridine-4-carboxamide (papc) ligands were reacted with ZnII ions as well. When a similar reaction was performed with dry solvents, except that papo was used instead of paps, the product mixture contained mononuclear [Zn(papo)(CH3OH)4](ClO4)2 (5) and the polyrotaxane [Zn(papo)2(ClO4)2]n (4). From the powder XRD data, grinding this mixture in the presence of moisture resulted in total conversion to the pure double-zigzag {[Zn(papo)2(H2O)2](ClO4)2}n (3) immediately. Upon heating 3, the polyrotaxane framework of 4 was recovered. The double-zigzag {[Zn(papc)2(H2O)2](ClO4)2}n (6) and polyrotaxane [Zn(papc)2(ClO4)2]n (7) were synthesized in a similar reaction. Although upon heating the double-zigzag 6 undergoes structural transformation to give the polyrotaxane 7, grinding solid 7 in the presence of moisture does not lead to the formation of 6. Significantly, the bright emissions for double-zigzag frameworks of 1 and 3 and weak ones for polyrotaxane frameworks of 2 and 4 also show interesting mechanochromic luminescence.
