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   <subfield code="a">Two Borate Supramolecular Frameworks Based on B4O5(OH)4 Cluster Units</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Guang Huang, Rui Pan, Huan He, Bai-Feng Yang, Guo-Yu Yang]</subfield>
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   <subfield code="a">Two new tetraborates, namely [Li(H2O)4]2[Cu(H2O)6][Cu(H2O)5]2[B4O5(OH)4]4·4H2O (1) and [Cu(en)2(H2O)2][Cu(en)2(B(OH)3)2][B4O5(OH)4]2·H2O (2) have been made under solvothermal conditions and characterized by FT-IR spectroscopy, powder X-ray diffraction, single crystal X-ray diffraction and thermogravimetric analysis, respectively. 1: triclinic, Pī, a=7.0400(2)Å, b=7.8779(3)Å, c=25.8958(11)Å, α=90.827(3)º, β=95.985(3)º, γ=105.816(3)º, Z=1. 2: monoclinic, P2/c, a=12.5723(6)Å, b=9.1508(5)Å, c=15.9800(6)Å, β=94.742(4)º, Z=2. In structure 1, the B4O5(OH)4 clusters join together via H-bonding interactions to produce 3-D supramolecular framework with three types of channels located by the Cu(H2O)6, Cu(H2O)5 and Li(H2O)4 polyhedra, respectively. While in 2, the B4O5(OH)4 clusters link each other to form 2-D layers and then further pillared by Cu(en)2(B(OH)3)2 complexes via H-bonding interactions, resulting in 3-D supramolecular framework with hexagonal and rectangle channels, in which the rectangle channels are filled by Cu(H2O)2(en)2 complexes.</subfield>
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