Directional NâH···O and OâH···O hydrogen bonds reinforced by charge assistance in the presence of anionâcation
interactions have been used to design and synthesise a whole family of new organic-organometallic supramolecular salts. The compounds [C5H16N4]2+[(η5-C5H4COO)2Fe]2â·2C2H5OH, 1, [C5H16N4]2+[(η5-C5H4COOH)(η5-C5H4COO)Fe]2}2â,
2, [C7H20N4]2+[(η5-C5H4COO)2Fe]2â·4H2O, 3, [C7H20N4]2+[(η5-C5H4COOH)(η5-C5H4COO)Fe]2}2â, 4, and [C7H18O2N4]2+[(η5-C5H4COO)2Fe]2â
·4H2O, 5, have been obtained by reacting [(η5-C5H4COOH)2Fe] with the bis-amidines [C5H14N4], [C7H18N4] and [C7H16O2N4]. The self-assembly between singly and doubly deprotonated acids and the protonated cations is controlled by the stoichiometric ratio and by the choice of solvent. The effect of charge assistance on the NâH···O interactions is discussed on the basis of a CSD analysis.
在阴离子-阳离子存在的情况下,通过电荷辅助增强定向 N–H··O 和 O–H···O
氢键
相互作用已被用来设计和合成一系列新型有机-有机
金属超分子盐。化合物 [C5H16N4]2+[(δ5-C5H4COO)2Fe]2â·2C2H5OH, 1, [C5H16N4]2+[(δ5-C5H4COOH)(δ5-C5H4COO)Fe]2 }2-,
2、[C7H20N4]2+[(δ5-C5H4COO)2Fe]2→4H2O, 3、[C7H20N4]2+[(δ5-C5H4COOH)(δ5-C5H4COO)Fe]2 }2−、4 和 [C7H18O2N4]2+[(η5-C5H4COO)2Fe]2−−
·4H2O, 5,通过[(β5-C5H4COOH)2Fe]与双脒[C5H14N4]、[C7H18N4]和[C7H16O2N4]反
应得到。单去质子酸和双去质子酸与质子化阳离子之间的自组装通过
化学计量比和溶剂的选择来控制。基于 C
SD 分析讨论了电荷辅助对 N–H···O 相互作用的影响。