Department of Chemistry , Indian Institute of Technology Madras , Chennai 600036 , India.
Inorg Chem. 2018 May 7;57(9):5145-5158. doi: 10.1021/acs.inorgchem.8b00213. Epub 2018 Apr 24.
A series of self-assembled binuclear complexes (1-4) of PdL'L composition are prepared by combination of selected cis-protected palladium(II) component cis-PdL' with equimolar amount of the nonchelating bidentate ligand 1,3-bis((pyridine-4-yl)methyl)urea, L. The cis-protecting unit L' crafted in the complexes Pd(L')(L), 1-4, are ethylenediamine (en), tetramethylethylenediamine (tmeda), 2,2'-bipyridine (bpy), and 1,10-phenanthroline (phen), respectively. Complexation of palladium(II) with the ligand L, however, resulted in the self-assembled trinuclear complex Pd(L), 5, of PdL composition. A few other mononuclear complexes relevant to this work are the homoleptic (6-9) and the heteroleptic (10-12) of PdL' composition, where the term L' in the formula stands for en, tmeda, bpy, and phen. The two units of L' in the complexes 6-12 are en-en, tmeda-tmeda, bpy-bpy, phen-phen, en-tmeda, en-bpy, and en-phen, respectively. Keeping in mind the recombination of fragments in biomolecular systems, it was considered to study the recombination of fragments among assorted self-assembled coordination complexes. In this context, the complexes 1-12 are employed. The recombination was planned on the basis of information already coded in the complexes that we realized from our experience. Designated complexes from this list are subjected to deliberate circumstances, whereupon remarkable "molecular recombination" processes ensued. For instance, combination of Pd(en)(L), 1 with Pd(tmeda), 7 at 1:2 molar ratio produced Pd(tmeda)(L), 2 and concomitant Pd(en)(tmeda), 10 at 1:2 molar ratio. A number of reorganization reactions are studied through selective combinations of two types of complexes from the pool of 1-12. The detailed finding is described in the article so as to conceptualize molecular recombination and other related dynamic processes in self-assembled coordination complexes of a chosen family. Crystal structures of a few complexes (2, 4, and 5) and intermolecular interactions in the crystal packing with particular reference to π-π interactions in 4 are also discussed.
一系列钯配合物(1-4)通过顺式保护的钯(II)配合物 cis-PdL'与等摩尔量的非螯合双齿配体 1,3-双((吡啶-4-基)甲基)脲 L 的组合制备而成。配合物Pd(L')(L)3,1-4 中的顺式保护单元 L'分别为乙二胺(en)、四甲基乙二胺(tmeda)、2,2'-联吡啶(bpy)和 1,10-菲啰啉(phen)。然而,钯(II)与配体 L 的络合导致形成了钯配合物Pd(L)3,5 的三聚体。这项工作还涉及到几个其他单核配合物,包括钯配合物Pd(L')3,6-9 和钯配合物Pd(L')3,10-12,其中公式中的 L'表示 en、tmeda、bpy 和 phen。配合物 6-12 中的两个 L'单元分别为 en-en、tmeda-tmeda、bpy-bpy、phen-phen、en-tmeda、en-bpy 和 en-phen。考虑到生物分子系统中碎片的重组,我们认为有必要研究各种自组装配合物中碎片的重组。在这种情况下,使用了配合物 1-12。重组是基于我们从经验中意识到的配合物中已经编码的信息来计划的。从这个列表中指定的配合物受到故意的情况的影响,随之而来的是显著的“分子重组”过程。例如,将Pd(en)(L)3,1 与Pd(tmeda)3,7 以 1:2 的摩尔比组合,生成Pd(tmeda)(L)3,2 和相应的Pd(en)(tmeda)3,10 以 1:2 的摩尔比。通过从 1-12 中选择两种类型的配合物进行有选择的组合,研究了许多重排反应。详细的发现描述在文章中,以便在所选家族的自组装配位配合物中概念化分子重组和其他相关的动态过程。还讨论了一些配合物(2、4 和 5)的晶体结构以及晶体堆积中的分子间相互作用,特别是 4 中的π-π相互作用。