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).
Here we report the first utilization
of the novel methane tetra-p-phenylphosphonic acid
(MTPPA) ligand for the preparation of metal complexes with Cu(II).
The hydrothermal and solvothermal reactions of tetratopic MTPPA as
a bridging ligand in conjunction with the square pyramidal {Cu(terpy)}2+ and {Cu2(pbterpy)}4+, (where terpy
= 2,2′:6′,2″-Terpyridine and pbterpy = 4′,4″″-(1,4-Phenylene)bis(2,2′:6′,2″-terpyridine))
as prefixed corner building units have produced one-dimensional [{Cu(terpy)}2(MTPPA-H5) (MTPPA-H6)]·(4.25H2O)(H3O) (1) and two-dimensional [{Cu2(pbterpy)}MTPPA-H4] (2), respectively. The structures
were characterized by single crystal X-ray diffraction and TGA.
We report two novel 3D porous metal‐organophosphonate metal organic frameworks (MOFs) [{Cu(4, 4’‐bpy)0.5(1,4‐NDPA‐H2)] (1), [{Cu2(4,4’‐bpy)0.5}(1,4‐NDPA)] (2) and a non‐porous [{Cu(4, 4’‐bpy)}(2,6‐NDPA‐H2)] (3) constructed using the structurally rigid 1,4‐naphthalenediphosphonic acid (1,4‐NDPA‐H4) and 2,6‐naphthalenediphosphonic acid (2,6‐NDPA‐H4). 1 and 2 exhibit high surface areas obtained using the structurally rigid and short aromatic organophosphonate linkers with copper. The compound 1 has been further analyzed by TGA and Quantum Design PPMS vibrating sample magnetometer.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.