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   <subfield code="a">Two New Borates Made of [B5O6(OH)4]− and [B5O10(OH)]6− Clusters, Accompanying a Novel In Situ Organic Reaction</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 pentaborate clusters, [MPD][B5O6(OH)4] (1, MPD=2-methyl-1,4,5,6-tetrahydropyrimidine-3-ium) and SrB5O8(OH) H2O (2), have been hydro(solvo)thermally synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis, powder X-ray diffraction and single-crystal X-ray structural analysis, respectively. Crystal data for 1: monoclinic, P21/c, a=9.3384(3)Å, b=17.3774(5)Å, c=9.1886(3)Å, β=93.172(3)°, Z=4. Crystal data for 2: triclinic, P-1, a=6.6406(6)Å, b=6.6784(8)Å, c=10.2162(15)Å, α=98.905(11)°, β=92.237(9)°, γ=119.446(11)°, Z=2. In compound 1, all the terminal O atoms of [B5O6(OH)4]− clusters are hydroxyl groups, which hinder the further connection of the [B5O6(OH)4]− clusters, only forming 3-D supramolecular frameworks via extensive hydrogen-bonding interactions. In compound 2, the [B5O10(OH)]6− clusters link each other to form a 2-D layer, which are further extended to 3-D supramolecular frameworks via extensive hydrogen-bonding interactions. Interestingly, a novel in situ organic reaction between 1,3-diaminoprapane and CH3COO− group has been observed during the formation of compound 1.</subfield>
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