Three Cd(II)-based coordination polymers 1− 3 with unique structures and topologies have been successfully constructed under solvothermal conditions by use of a newly designed N-containing rigid triangular ligand tris(4-(4H-1,2,4triazol-4-yl)phenyl)amine (TTPA-4), wherein the structural interpenetration can be modulated by aromatic dicarboxylate coligands including thiophene-2,5-dicarboxylic acid (TDA) and terephthalic acid (TPA). Without using coligands, a noninterpenetrating porous 3-D network of 1 with nia topology was obtained. With the aid of the V-shaped TDA coligand, a 4-fold interpenetrating 3-D network of 2 resulted that is built from (2,3,7)-connecting (4 2 .6)(4 4 .6.8 8 .10 4 .12 4 )-(4) 2 net. In the presence of the linear TPA auxiliary ligand, an 8-fold interpenetrating 3-D network of 3 was produced that is assembled by 3-connecting uninodal srs net. Particularly, compound 1 displays interesting dual function as the result of its unique structural attributes, which not only shows superb sensitivity for nitroaromatics (NACs) with phenolic group but also impressive removal capabilities of toxic Cr 2 O 7 2− oxoanion pollutant from aqueous solution.

An anionic zeolite-like metal-organic framework (AZMOF) with a twisted partially augmented the net, known as the "Moravia" net, [(CH3)2NH2]6[Sr13(O)3()8(OH)2(H2O)16]·xS (, where S represents non-coordinated solvent molecules, and is the abbreviation of benzo-(1,2;3,4;5,6)-tris-(thiophene-2'-carboxylic acid)), has been solvothermally synthesized and characterized, which possesses an anionic framework and nano-sized sodalite cage. Through cation-exchange, is capable of uptaking large organic cationic dyes including Rhodamine B (RB), Basic Red 2 (BR2), Crystal Violet (CV) and Methylene Blue (MB), amongst which the adsorption capability for RB (up to 545 mg g(-1)), and BR2 (up to 675 mg g(-1)) is the highest for reported absorbants to date.

No abstract

No abstract

No abstract