1,2,4,5-Benzenetetrasulfonic acid and 1,4-benzenedisulfonic acid as sulfo analogues of pyromellitic and terephthalic acids for building coordination polymers of manganese

摘要

The new polysulfonic acids H4B4S (1,2,4,5-benzenetetrasulfonic acid) and H2BDS (1,4-benzenedisulfonic acid) were used for the preparation of five manganese coordination polymers. The reactions of H4B4S and MnCO3 were performed in dimethylformamide (DMF) or N-methylpyrrolidone (NMP) as solvent in sealed glass ampoules at elevated temperatures. Two benzenetetrasulfonates could be obtained, [NH2(CH3)(2)](2){Mn(B4S)(DMF)(2)} (I) (P2(1)/c, Z = 2, a = 942.02(5) pm, b = 1684.86(6) pm, c = 918.45(5) pm, beta = 97.746(6)degrees, R-1; wR(2) (I-o > 2 sigma(I-o)) = 0.0357; 0.0771) and [HNMP](2){Mn(B4S)(NMP)(2)} (II) (P2(1)/c, Z = 2, a = 931.7(1) pm, b = 1049.2(1) pm, c = 1944.9(1) pm, beta = 113.529(3)degrees, R-1; wR(2) (I-o > 2 sigma(I-o)) = 0.0470; 0.0952). Both compounds exhibit anionic chains according to (1)(infinity){Mn(B4S)(2/2)(L)(2)}(2)- (L = DMF, NMP). The Mn2+ ions are in octahedral coordination of oxygen atoms. The charge of the anionic chains is either compensated by dimethylammonium cations, [NH2(CH3)(2+)], or by protonated NMP molecules, HNMP+. Solvothermal reactions of H2BDS and MnCO3 in the solvents DMF, NMP and dimethylacetamide (DMA), respectively, yielded the disulfonates Mn(BDS)(DMF)(2) (III) (P (1) over bar, Z = 1, a = 514.3(1) pm, b = 926.2(1) pm, c = 940.2(1) pm, alpha = 93.552(8)degrees, beta = 99.993(7)degrees, gamma = 99.237(7)degrees, R-1; wR(2) (I-o > 2 sigma(I-o)) = 0.0290; 0.0637), Mn(BDS)(DMA)(2) (IV) (P (1) over bar, Z = 2, a = 936.00(4) pm, b = 984.94(4) pm, c = 1034.75(5) pm, alpha = 81.606(2)degrees, beta = 88.941(2)degrees, gamma = 82.364(2)degrees, R-1; wR(2) (I-o > 2 sigma(I-o)) = 0.0387; 0.1046) and Mn(BDS)(NMP)(2) (V) (P (1) over bar, Z = 2, a = 962.97(3) pm, b = 976.76(3) pm, c = 1034.23(3) pm, alpha = 89.371(1)degrees, beta = 78.839(1)degrees, gamma = 87.604(2)degrees, R-1; wR(2) (I-o > 2 sigma(I-o)) = 0.0243; 0.0713). In the crystal structures of the three compounds, the octahedrally coordinated Mn2+ ions are linked by the disulfonate ions to layers according to (2)(infinity){Mn(BDS)(4/4)(L)(2)} (L = DMF, DMA, NMP). The thermal analysis of all compounds shows that they can be desolvated completely and that the remaining solvent-free sulfonates exhibit decomposition temperatures up to 500 degrees C that is exceptionally high when compared to the respective carboxylates. Temperature-dependent magnetic susceptibility measurements of [NH2(CH3)(2)](2){Mn(B4S)(DMF)(2)} show paramagnetic behavior of the Mn2+ ions.