首页> 外文期刊>European Journal of Chemistry >Crystal structure of 4-(dimethylamino)pyridin-l-ium-2,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,4-bis(olate) 4-dimethylaminopyridine (2:1) water undeca-solvate
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Crystal structure of 4-(dimethylamino)pyridin-l-ium-2,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,4-bis(olate) 4-dimethylaminopyridine (2:1) water undeca-solvate

机译:4-(二甲基氨基)吡啶-1-Ium-2,5-二氯-3,6-二氧基碳酸-1,4-二烯-1,4-双(olate)4-二甲基氨基吡啶(2:1)水未鳕鱼的晶体结构 -Solvate.

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The structure of the title compound, 4-(dimethylamino)pyridin-l-ium-2,5-dichloro-3,6-dioxocyclohexa-l,4-diene-l,4-fcis(olate) 4-dimethylaminopyridine water undeca-solvate, C_(57)H_(87)Cl5N_(12)O_(21), obtained from interaction between chloranilic acid (caH2), and dimethyl aminopyridine (DMAP) has been determined by single crystal X-ray diffraction. The title compound, (DMAPH)5(ca)2.5-(DMAP)-llH20, crystallized in the triclinic crystal system with space group, P1 (no. 2], a = 13.3824[15) A, b = 13.4515(17) A, c = 19.048(2) A, a = 86.014(4)°, β = 88.821(4)°, y= 86.367(4)°, V= 3413.3(7) A3, Z = 2, T= 100(2) K, u(MoKa) = 0.294 mm~1, Dcalc = 1.414 g/cm~3, 59413 reflections measured (3.76° < 20 s 56°), 16405 unique (R_(int) = 0.0517, R_(_igma) = 0.0589) which were used in all calculations. The final R1 was 0.0460 (1 >2σ(1)) and wR2 was 0.1271 (all data). Using supramolecular chemistry principles, proton donors (chloranilic acid) and acceptor (DMAP) were combined to generate a multicomponent hydrogen-bonded system. Due to the presence of protonated bases (DMAPH+), the dominant interactions are the N+-H-0 hydrogen bonds, whereas the negative charges of an acceptor from the chloranilate dianion (ca~2) are delocalized. Additionally, three sets of water clusters in the title compound were identified, namely a cyclic pentamer, a linear, and an acute-shaped trimer water cluster. It was further observed that strong hydrogen bond interactions occurred between the solvated aqua molecule(s) acting as a proton donor and the neutral DMAP acting as a proton acceptor. The crystal packing is further stabilized by O-H-Cl and C-H--C1 weak halogen interactions. The lattice metric strength is further held by observed π-π stacking interactions (centroid-centroid) with inter centroid distances between sets of the DMAPH rings of 3.624(3), 3.642(4), 3.739(3), 3.863(3) and 3.898(3) A, respectively.
机译:标题化合物的结构,4-(二甲基氨基)吡啶-1-Ium-2,5-二氯-3,6-二氧基碳酸o-1,4-二烯-1,4-FCIS(olate)4-二甲基氨基吡啶水未溃疡 - 通过单晶X射线衍射确定从氯酸(CaH 2)和二甲基氨基吡啶(DMAP)之间的相互作用获得的C_(57)H_(87)Cl 5N_(12)O_(21)。标题化合物,(DMAph)5(CA)2.5-(DMAP)-LLH20,在具有空间组的三级晶体系统中结晶,P1(NO.2],A = 13.3824 [15)A,B = 13.4515(17) A,C = 19.048(2)A,A = 86.014(4)°,β= 88.821(4)°,Y = 86.367(4)°,V = 3413.3(7)A3,Z = 2,T = 100( 2)k,u(moka)= 0.294 mm〜1,dcalc = 1.414g / cm〜3,59413测量的反射(3.76°<20 s 56°),16405独特(r_(int)= 0.0517,r _(_ igma) = 0.0589)用于所有计算。最终R1为0.0460(1>2σ(1)),WR2为0.1271(所有数据)。使用超分子化学原理,合并质子供体(氯酸)和受体(DMAP)以产生多组分的氢键体系。由于质子化碱基(Dmaph +)的存在,所显性的相互作用是N + -H-0氢键,而来自氯酸酯脱膜(Ca〜2)的受体的负电荷被划分。另外,鉴定了标题化合物中的三组水簇,即环状五聚体,线性和急性形状三聚体水簇。进一步观察到,在用作质子供体和作为质子受体的中性DMAP之间的溶剂化的AQUA分子之间发生强氢键相互作用。通过O-H-Cl和C-H-C1弱卤素相互作用进一步稳定晶体包装。通过观察到3.624(3),3.642(4),3.739(3),3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.863(3)和3.898(3)A分别。

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