Ghosh Goutam, Paul Mithun, Sakurai Tsuneaki, Matsuda Wakana, Seki Shu, Ghosh Suhrit
Polymer Science Unit, Indian Association for the Cultivation of Science, 700032, Kolkata, India.
Department of Organic Chemistry, Indian Association for the Cultivation of Science, 700032, Kolkata, India.
Chemistry. 2018 Feb 6;24(8):1938-1946. doi: 10.1002/chem.201704825. Epub 2018 Jan 4.
Herein, the self-assembly of a few 1,3-dihydroxyl functionalized naphthalene diimide (NDI) derivatives has been reported with particular emphasis on the impact of chirality on gelation and the effect of self-assembly on charge-carrier mobility. A nonconventional gelator (R)-NDI, devoid of any long alkyl chains, exhibited spontaneous gelation in tetra-chloroethylene (TCE). Based on X-ray crystallography and powder X-ray diffraction studies, it was established that a ladder-like hydrogen-bonded chain formation between the 1,3-dihydroxyl group leads to the fibrillar structures with preferential helicity. Likewise the (S)-isomer also exhibited identical gelation and mesoscopic structure but produced fibrils with the opposite handedness. Intriguingly, an equimolar mixture of the (R)- and (S)-isomers did not show any gelation ability, rather a macroscopic precipitation was observed and, in sharp contrast to the individual isomers, the morphology of the mixture showed ill-defined near spherical agglomerates. Differential scanning calorimetry (DSC) studies revealed an identical crystallization peak for the supramolecular polymer produced from the enantiopure gelators ((R)- or (S)-isomer), which was absent in their equimolar mixture. However, mixtures of the two isomers with enantiomeric excess retrieved the gelation ability and preferential helicity demonstrating that chiral amplification is operative in the present system through the so-called "majority rule" effect. Chirality induction was also realized by the "sergeant and soldier" principle in the supramolecular assembly of an achiral NDI gelator in the presence of either the (R)- or (S)-isomer as the chiral dopant. However, the strong helical bias induced by the chiral gelator was found to be opposite in nature compared to that found in the self-assembly of the pure chiral gelator that has been rarely reported in the literature. Flash-photolysis time-resolved microwave conductivity (FP-TRMC) measurements indicated the strong positive impact of the gelation on the electrical conductivity.
本文报道了几种1,3 - 二羟基官能化萘二亚胺(NDI)衍生物的自组装,特别强调了手性对凝胶化的影响以及自组装对电荷载流子迁移率的影响。一种不含任何长烷基链的非常规凝胶剂(R)-NDI在四氯乙烯(TCE)中表现出自发凝胶化。基于X射线晶体学和粉末X射线衍射研究,确定1,3 - 二羟基之间形成的梯状氢键链导致具有优先螺旋性的纤维状结构。同样,(S)-异构体也表现出相同的凝胶化和介观结构,但产生了相反手性的纤维。有趣的是,(R)-和(S)-异构体的等摩尔混合物没有显示出任何凝胶化能力,而是观察到宏观沉淀,并且与单个异构体形成鲜明对比的是,混合物的形态显示出不明确的近球形团聚体。差示扫描量热法(DSC)研究表明,由对映体纯凝胶剂((R)-或(S)-异构体)产生的超分子聚合物具有相同的结晶峰,而在它们的等摩尔混合物中不存在该峰。然而,两种异构体的对映体过量混合物恢复了凝胶化能力和优先螺旋性,表明在手性放大通过所谓的“多数规则”效应在本系统中起作用。在手性NDI凝胶剂与作为手性掺杂剂的(R)-或(S)-异构体存在下的超分子组装中,也通过“士兵与长官”原理实现了手性诱导。然而,发现手性凝胶剂诱导的强螺旋偏向在性质上与纯手性凝胶剂自组装中发现的相反,这在文献中很少报道。闪光光解时间分辨微波电导率(FP - TRMC)测量表明凝胶化对电导率有强烈的正向影响。