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自组装的苝二酰亚胺核三角棱镜作为由“相似相溶”驱动的C和C的缺电子主体。

Self-Assembled Perylene Bisimide-Cored Trigonal Prism as an Electron-Deficient Host for C and C Driven by "Like Dissolves Like".

作者信息

Chang Xingmao, Lin Simin, Wang Gang, Shang Congdi, Wang Zhaolong, Liu Kaiqiang, Fang Yu, Stang Peter J

机构信息

Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education), School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710119, P. R. China.

Department of Chemistry, University of Utah, 315 South 1400 East, Room 2020, Salt Lake City, Utah 84112, United States.

出版信息

J Am Chem Soc. 2020 Sep 16;142(37):15950-15960. doi: 10.1021/jacs.0c06623. Epub 2020 Sep 5.

Abstract

Poor processability of fullerenes is a major remaining drawback for them to be studied monomolecularly and to find real-life applications. One of the strategies to tackle this problem is to encapsulate them within a host, which is however quite often, accompanied by significant alteration of their physical/chemical properties as encountered in chemical modification. To minimize the effect, an electron-deficient entities-based, dissolvable, and fluorescence active supramolecular host was designed and constructed via coordination-driven self-assembly of -tetrapyridyl perylene bisimide (PBI) with -(PEt)Pt(OTf). The trigonal prism possesses a trigonal-prismatic inner cavity with 14.7 Å as the diameter of its inscribed circle. Host-guest chemistry investigations revealed that both C and C could be quantitatively encapsulated by the host in a 1:1 ratio. Further studies demonstrated that the produced host-guest complex is significantly more stable than , allowing complete transformation of the latter to the former and separation of C from its mixture with C. The fullerenes in the inclusion state could rotate freely within the cavity. Electrochemistry and spectroscopy studies disclosed that the encapsulation of the guests shows little effect upon the reduction of the host and its fluorescence properties. Thus, "like dissolves like" is believed to be the main driving force for the formation of the host-guest complexes. Moreover, the host and host-guest complexes can be fabricated into monomolecular membranes using the conventional Langmuir-Blodgett technique. We propose that these unique host-guest complexes could be used as model ensembles for further studies of the physical/chemical properties of fullerenes in both single molecular and 2D membrane states. In addition, their reversible four-electron reduction property may allow them to find applications in photo/electrocatalysis, organic electronics, etc.

摘要

富勒烯较差的可加工性是其进行单分子研究和寻找实际应用的主要遗留缺点。解决这个问题的策略之一是将它们封装在主体中,然而,这通常伴随着它们物理/化学性质的显著改变,就像在化学修饰中遇到的那样。为了将这种影响降至最低,通过配位驱动的四吡啶基苝二酰亚胺(PBI)与二(三乙膦)铂(OTf)的自组装,设计并构建了一种基于缺电子实体、可溶解且具有荧光活性的超分子主体。三角棱柱 具有一个三角棱柱形内腔,其内切圆直径为14.7 Å。主客体化学研究表明,C60和C70都可以以1:1的比例被主体定量封装。进一步的研究表明,生成的主客体复合物 比 稳定得多,能够使后者完全转化为前者,并将C60从其与C70的混合物中分离出来。处于包合状态的富勒烯可以在腔内自由旋转。电化学和光谱研究表明,客体的封装对主体的还原及其荧光性质影响很小。因此,“相似相溶”被认为是形成主客体复合物的主要驱动力。此外,主体和主客体复合物可以使用传统的朗缪尔-布洛杰特技术制成单分子膜。我们提出,这些独特的主客体复合物可以用作模型集合,用于进一步研究单分子和二维膜状态下富勒烯的物理/化学性质。此外,它们可逆的四电子还原性质可能使它们在光/电催化、有机电子等领域找到应用。

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