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   <subfield code="a">Preparation and Reactivity of 4,4′-diaminostilbene-2,2′disulphonate</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Natalie Rader, Heather Nees, Paul Szalay, Matthias Zeller, Allen Hunter]</subfield>
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   <subfield code="a">The precursor compound 4,4′-diaminostilbene-2,2′disulphonic acid DAS-(SO3H)2 was successfully deprotonated through reactions with (n-Bu4N)(OH) and NaOH to produce the corresponding salts sodium 4,4′-diaminostilbene-2,2′disulphonate Na2(DAS-(SO3)2) (1) and tetrabutylammonium 4,4′-diaminostilbene-2,2′disulphonate (n-Bu4N)2(DAS-(SO3)2) (2). The structure of (n-Bu4N)2(DAS-(SO3)2) (2) was confirmed through the use of single crystal X-ray diffraction. Compound (2) crystallizes in the monoclinic space group P21/n with the lattice parameters of a=10.0645(6), b=14.2573(9), c=17.6053(11), and β=94.3160(10). The reaction of Cu2+(aq) with (n-Bu4N)2(DAS-(SO3)2) resulted in the crystallization of the molecular organocopper cluster, [CuDAS-(SO3)2]2·3H2O (3), that resembles a molecular parallelogram as revealed by single crystal X-ray diffraction. Compound (3) crystallizes in the monoclinic space group P21/n with the lattice parameters of a=8.8647(6), b=10.5247(7), c=21.2265(14), and β=93.1730(10). Within the structure of (3) each [DAS-(SO3)2]2− ligand is shown to bind two copper atoms through interactions with three of the five available metal binding sites.</subfield>
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