A new polynuclear copper(II) complex [Cu 7 (OH) 6 Cl 2 -(pn) 6 (H 2 O) 2 ](C(CN) 3 ) 4 Cl 2 with hydroxo-bridging ligands has been prepared; the centrosymmetric cluster cation can be described as two Cu 4 O 3 Cl distorted cubane units sharing one copper cation.Various multinuclear copper(II) complexes have been reported in the last decade with a great number of simple and sophisticated bridging ligands; 1-5 however, some nuclearities remain comparatively scarce. In the case of tetranuclear complexes with Cu 4 O 4 cubane-like clusters some examples have been thoroughly described, 2 but to date little is known about clusters involving more than four metal centres. 3,4 Concerning the heptanuclear copper(II) clusters, as far as we are aware, only one example of the dicubane-like type has been described. 5 Here we report the structure and preliminary magnetic studies of a novel vertex sharing dicubane-like heptanuclear copper(II) cluster [Cu 7 (OH) 6 Cl 2 (pn) 6 (H 2 O) 2 ]-(tcm) 4 Cl 2 (1) [pn = 1,3-diaminopropane; tcm 2 = C(CN) 3 2 = tricyanomethanide] with chloro-and hydroxo-bridging ligands.1.00 mL (12 mmol) of 1,3-diaminopropane (pn) was slowly added to a warm aqueous solution of CuCl 2 ·2H 2 O (12 mmol) and then an aqueous solution of sodium hydroxide (12 mmol) was added. To the resulting clear solution were immediately and consecutively added concentrated aqueous solutions of CuCl 2 ·2H 2 O (2 mmol) and potassium tricyanomethanide (8 mmol). Slow evaporation gave prismatic blue crystals of [Cu 7 (OH) 6 Cl 2 (pn) 6 (H 2 O) 2 ](tcm) 4 Cl 2 (yield 1.28 g, 42%) suitable for crystallography. ‡ The structure of 1 is unique and consists of a centrosymmetric hydroxo-bridged heptanuclear copper(II) cation (Fig. 1) which can be described as two Cu 4 O 3 Cl distorted cubanes which share one copper cation (Cu1) ( Fig. 1 and 2). The four crystallographically independent Cu(II) centres differ markedly in their co-ordination geometry.The central atom (Cu1) presents a strongly elongated octahedral coordination which involves a CuO 4 equatorial plane with essentially equivalent Cu-O bonds [see Fig. 2(a)] and two semicoordinated Cl anions in axial positions (Cu…Cl = 3.029(2) Å). The Cu2 and Cu3 cations have distorted square pyramidal CuO 2 N 2 Cl environments. In both cases, the basal planes are occupied by two hydroxo bridging ligands (O1 and O3 for Cu2; O2 and O3 for Cu3) and two nitrogen atoms of the chelating pn ligand (Cu-O range 1.977-2.016 Å and Cu-N range 1.975-2.021 Å). Both pyramids share a strongly elongated axial position filled by the bridging Cl1 atom (Cu2-Cl1 = 2.654(2) Å and Cu3-Cl1 = 2.679(2) Å) (Fig. 1). The co-ordination † Electronic supplementary information (ESI) available: detailed synthesis and X-ray crystallography of 1. See http://www.rsc.org/suppdata/cc/b1/ b105231b/