Correction: A cobalt arylphosphonate MOF - superior stability, sorption and magnetism.

Correction for 'A cobalt arylphosphonate MOF - superior stability, sorption and magnetism' by Yunus Zorlu et al., Chem. Commun.

A cobalt arylphosphonate MOF - superior stability, sorption and magnetism.

We report a novel metal-organic framework (MOF) based on a cobalt arylphosphonate, namely, [Co2(H4-MTPPA)]·3NMP·H2O (1·3NMP·H2O), which was prepared solvothermically from the tetrahedral linker tetraphenylmethane tetrakis-4-phosphonic acid (H8-MTPPA) and CoSO4·7H2O in N-methyl-2-pyrrolidone (NMP). Compound 1 has the highest porosity (BET surface area of 1034 m2 g-1) ever reported for a MOF based on an aryl phosphonic acid linker. The indigo blue crystals of 1·3NMP·H2O are composed of edge-shared eight-membered Co2P2O4 rings, and are thermally very stable up to 500 °C.

The use of sea shell (Donax trunculus) powder to remove Sr(II) ions from aqueous solutions.

This study aimed to investigate and explore the possibility of using ground sea shell powder (Donax trunculus) (SSP) for sorption of Sr(II) ions from aqueous solutions. The maximum removal of Sr(II) removal in SSP was 60% at initial Sr(II) concentration of 25 mg/L, at pH 6.0, contact time 120 min, temperature 25 °C and volume/mass ratio equivalent to 500.

A potential Cu/V-organophosphonate platform for tailored void spaces via terpyridine mold casting.

The reaction of appropriate copper and vanadium salts with tetratopic methane tetra-p-phenylphosphonic acid (MTPPA) in the presence of 2,2':6':2''-terpyridine (terpy) yielded the three-dimensional bimetallic copper vanadium phosphonate framework [{Cu(terpy)}Cu(VO)(MTPPA-H)]·4HO (1). Terpy has no net contribution to the three-dimensional structure providing a potential platform for void space formation via mold-casting. The structure was characterized by single-crystal X-ray diffraction and thermogravimetric analysis (TGA).