RESUMEN
In this work, eight alkali metal complexes with 1,2-diaza-4-phospholide ligands were prepared and characterized by X-ray single-crystal structural analysis and NMR spectroscopy. Their structures showed varied coordination motifs: (i) a dimeric 1,2-diaza-4-phospholide lithium complex with exo-bidentate bridging coordination (4) consists of two lithium atoms that are linked via two µ2-bridging, κN,κN'-coordinated ligands; (ii) the polymeric chain 1,2-diaza-4-phospholide potassium complex (5) showed an ion-bearing stair-shaped chain structure running through axis a, where the steps are η2 interactions, and there is a transition platform between every two stairs; (iii) the polymeric chain 1,2-diaza-4-phospholide potassium complex (6) also presented a polymeric chain structure in the solid state but displayed a head-to-tail arrangement of two 1,2-diaza-4-phospholides; (iv) in comparison to 6, the 1,2-diaza-4-phospholide sodium complex (7) displayed a tetrameric structure, in which the sodium ions are arranged in a distorted tetrahedral fashion and each of them occupies a vertex of the tetrahedron; (v) the polymeric chain 1,2-diaza-4-phospholide potassium complex (8) presented a solvent-free chain structure, in which potassium ions each is η5-bonded by two 1,2-diaza-4-phospholides and η2-coordinated by another, consisting of a stair-shaped chain structure running through axis a but without significant intermolecular contacts between the adjacent stairs in comparison to that of 5; (vi) the polymeric chain 1,2-diaza-4-phospholide sodium complex (9) presented a solvent-free chain structure, in which sodium ions each is η1(N),η2(N,N),η1(P)-bonded by three 1,2-diaza-4-phospholides, consisting of a chain structure running through axis a; and (vii) the treatment complex 8 with elemental sulphur or selenium in the presence of crown ether gave rare thiophosphonato potassium [η3(S,P,S)-3,5-tBu2dp-(µ-K)(S2)([18]crown-6)] (10) or a selenophosphonato potassium [η3(Se,P,Se)-3,5-tBu2dp-(µ-K)(Se2)([18]crown-6)] (11). Both of the complexes crystallized in the orthorhombic space group Pnma as pale-yellow (or red) crystals. The X-ray diffraction analysis revealed 10 or 11 as a terminal complex with the η1,η1-X,X-coordination mode (X = S and Se). The 1H DOSY NMR spectroscopy study of the species 8 in DMSO-d6 suggested that polymeric complexes (4-9) in the solid state should dissociate into the related monomers in the solutions when the donor solvents were used.
RESUMEN
Bismuth(iii) oxidation of 3,5-di-substituted-1,2,4-triazolato anions afforded a paddlewheel 1,2,4-triazolato dibismuth complex [L2(Bi-Bi)L2] (L = η1,η1-3,5-R2tz, R = Ph (3), iPr (4)) with very short Bi(ii)-Bi(ii) bonds (2.8650(4)-2.8721(3) Å). The reaction involved the intermediates of the organobismuth radical [Bi(R2tz)2]Ë and neutral N-1,2,4-triazolyl radical [3,5-R2tz]Ë. The dimerization of the former produced the corresponding dibismuth complex while the latter was trapped by using spin trap 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) to give the radical adduct of {(3,5-R2tz)(DMPO)}Ë which was unambiguously evidenced by EPR analysis.