Coordination pyramid inversion, angular cluster core and homochiral single-stranded helix formation in polynuclear Mn(ii) assemblies supported by a bicompartmental salen-type ligand based on an o-xylylenediamine platform

IF 2.4 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
CrystEngComm Pub Date : 2026-04-14 DOI:10.1039/D6CE00172F
Ilia D. Shutilov, Pavel A. Volodin, Lyubov V. Frantsuzova, Aidar T. Gubaidullin, Alexander S. Ovsyannikov, Svetlana E. Solovieva and Igor S. Antipin
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引用次数: 0

Abstract

Although salen-type compartmental ligands have a rich history, these fascinating compounds still attract considerable attention due to the wide potential applications that their complexes can exhibit. By varying the flexibility of the spacer group, connecting two NO-chelating salicylideneamine moieties, and adjusting the type of anchored additional binding sites or co-ligands used, the formation of 3d metal clusters with the desired nuclearity can be achieved. In this work, we report the synthesis of two new binuclear {MnII2} (1-Mn2Cl3 and 1-Mn2Cl2) clusters and one angular (pseudo-linear) trinuclear {MnII3} (12-Mn3Cl2) cluster, supported by an o-xylylenediamine Schiff base derivative, bearing o-methoxy-substituted salicylideneamine units and acting as a bicompartmental ligand. The structures of prepared Mn-based complexes were established by single crystal X-ray diffraction (SCXRD), revealing the role of o-xylylenediamine platform on the diversity of observed coordination motifs. For the first time, in the case of {MnII2} clusters, displaying a similar coordination motif, it was established that the Mn atom, accommodated within the N2O2 coordination pocket, can adopt two different orientations of the MnN2O2Cl coordination pyramid relative to the o-xylylene spacer group. Additionally, the simultaneous effect of H-bonding, electrostatic and CH/π interactions between the anionic 1-Mn2Cl3 cluster and the NHEt3 cation species leads to the formation of helices, stacked in a homochiral crystal with the polar chiral P41 space group, which is reported for the first time for complexes based on salen-type ligands. Finally, the formation of the trinuclear complex 12-Mn3Cl2, exhibiting an unusual angular motif of the cluster core, stabilized by the ligand structure and intramolecular CH/π-bonding, is observed.

Abstract Image

基于邻二甲二胺平台的双室salen型配体支持的多核Mn(ii)组合中的配位金字塔反转、角簇核和同手性单链螺旋形成
尽管salen型区室配体具有丰富的历史,但由于其配合物具有广泛的潜在应用前景,这些迷人的化合物仍然引起了相当大的关注。通过改变间隔基团的柔韧性,连接两个no螯合水杨柳二胺基团,以及调整锚定的附加结合位点或所使用的共配体的类型,可以形成具有所需核的3d金属簇。在这项工作中,我们报道了两个新的双核{MnII2} (1-Mn2Cl3和1-Mn2Cl2)簇和一个角(伪线性)三核{MnII3} (12-Mn3Cl2)簇的合成,由邻二甲二胺希夫碱衍生物支撑,含有邻甲氧基取代水杨基胺单元,并作为双室配体。通过单晶x射线衍射(SCXRD)对所制备的锰基配合物的结构进行了表征,揭示了邻二甲二胺平台对所观察到的配位基的多样性的作用。在{MnII2}簇中,首次建立了具有相似配位基序的Mn原子在N2O2配位袋内相对于邻二甲苯间隔基团可以采用两种不同取向的MnN2O2Cl配位金字塔。此外,阴离子1-Mn2Cl3簇和NHEt3阳离子之间的h键、静电和CH/π相互作用的同时作用导致螺旋形成,并与极性手性P41空间基团堆叠在同手性晶体中,这是基于salen型配体的配合物首次报道。最后,观察到12-Mn3Cl2三核配合物的形成,该配合物具有独特的簇核角基序,由配体结构和分子内CH/π键稳定。
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来源期刊
CrystEngComm
CrystEngComm 化学-化学综合
CiteScore
5.50
自引率
9.70%
发文量
747
审稿时长
1.7 months
期刊介绍: Design and understanding of solid-state and crystalline materials
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