Twot rinuclearc opper phosphonate complexes, [Cu 3 (pda) 3 (tBuPO 3 )]·2(Et 3 NH) (1)a nd [Cu 3 (pda) 3 (PhPO 3 )]· 2(Et 3 NH) (2), have been synthesized and investigated by a combination of X-ray crystallography,P XRD, magneto-and electrochemistry,E PR,i ns itu UV-vis spectroelectrochemistry and DLS.T he two complexes feature almosti denticalc rystal structures,t he anions of which are both supported by pda 2À and tBuPO 3 2À /PhPO 3 2À groups, bridging threef ive-coordinated Cu II atoms to form ac rown-like structure. Thisi st he first time that trinuclearc opper phosphonate complexes have been isolated and characterized. Magnetic susceptibility measurements reveal that complexes 1 and 2 both display overall ferromagnetic characters, but with different exchange interactions between the metal ions within the two clusters.T he electrocatalytic activity for water oxidation of the two complexes was preliminarilyi nvestigated, which reveals that both of the two complexes can carry out electrocatalytic water oxidationi naneutral system owing to the introduction of phosphonate ligands into the complexes, with aT OF of about 0.82 s À1 (1)a nd 0.58 s À1 (2), respectively.W e propose that the presence of phosphonatel igands may affect the magnetic property and catalytic activity of the complexes.[a] J.
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