| dc.description |
The organo-templated iron(III) borophosphate (C<sub>4</sub>H<sub>12</sub>N<sub>2</sub>)<sub>3</sub>Fe<sup>III</sup><sub>6</sub>(H<sub>2</sub>O)<sub>4</sub>[B<sub>6</sub>P<sub>12</sub>O<sub>50</sub>(OH)<sub>2</sub>]·2H<sub>2</sub>O was prepared under mild hydrothermal conditions (443 K). The crystal structure was determined from single-crystal X-ray data at 295 K (orthorhombic, Pbca (No. 61), Z=4, a=17.8023(7) Å, b=16.1037(5) Å, c=19.1232(6) Å, V=5482.3(3) Å<sup>3</sup>, R1=0.055, wR2=0.104, 6576 observed reflections with I>2σ(I)) and contains a new type of borophosphate anion: a mixed open- and loop-branched zehner single chain, <sub>∞</sub><sup>1</sup>{[B<sub>6</sub>P<sub>12</sub>O<sub>50</sub>(OH)<sub>2</sub>]<sup>24-</sup>}, built from heptamers [B<sub>2</sub>P<sub>5</sub>O<sub>21</sub>] interconnected by BO<sub>3</sub>(OH) tetrahedra sharing their third oxygen corners with additional (terminal) PO<sub>4</sub> tetrahedra to form open branchings. The mixed open- and loop-branched single chains running along [0 0 1] are interconnected by three crystallographically independent iron coordination octahedra to form a 3D framework structure containing eight-membered ring channels running along [0 1 0] and cages, which are occupied by two crystallographically independent piperazine cations and H<sub>2</sub>O molecules. The displacement parameters of C and N atoms in the piperazine cations are dramatically influenced by the strength of the hydrogen bond reflecting the shape of the cavities. The magnetic investigations indicate the existence of antiferromagnetic interactions as the major components. A narrow hysteresis at low temperatures indicates a weak ferromagnetic component, due to a non-cancellation of spins. |
