Sekiya Ryo, Nishikiori Shin-ichi
Department of Basic Science, Graduate School of Arts and Sciences, The University of Tokyo, Komaba, Meguro, Tokyo 153-8902, Japan.
Chemistry. 2002 Oct 18;8(20):4803-10. doi: 10.1002/1521-3765(20021018)8:20<4803::AID-CHEM4803>3.0.CO;2-H.
A new host design for an inclusion compound with a preference for large planar aromatic guest molecules has been proposed. Our host design includes a rectangular cavity made using a long and a short building block based on the concept of supramolecular chemistry. The long building block facilitates the inclusion of large guests, and the short building block prevents the formation of an interpenetrated structure, which is often observed in frameworks with large void spaces. The long building block is made when dimers of 4-pyridinecarboxylic acid (isoH) form through hydrogen bonding between the two carboxylic acid moieties. This isoH dimer can link two transition metal centers using the N atoms at both ends to act as a long building block. For the short building block, the thiocyanato ion was used. This makes a bent bridge between two metal centers to form a 1D double-chain [M(SCN)2]infinity complex. From the self-assembly of isoH, SCN- and Ni2+, a 2D network of [Ni(SCN)2(isoH)2]infinity, in which the 1D [Ni(SCN)2]infinity complexes are linked by the isoH dimers, is built up. The rectangular cavity is formed as a mesh within the 2D network. The crystal of our inclusion compound has a layered structure of 2D networks, and a 1D channel-like cavity penetrating the layered 2D networks is formed where guests may be included. Moreover, our host design has the advantage of easy extension of the host structure. Replacement of isoH with another component and use of three components is possible for making the long building block. In the latter case, a linear spacer having two carboxy groups is inserted into the isoH dimer to form a long building block with a trimer structure. Based on our host design, a series of new inclusion compounds were synthesized. The crystal structures of three compounds were determined by single crystal X-ray diffraction. These were a biphenyl inclusion compound [Ni(SCN)2(isoH)2].1/2C12H10 (the basic case), a 9,10-dichloroanthracene inclusion compound [Ni(SCN)2(acrylH)2].1/2C14H8Cl2, where isoH is replaced with 3-(4-pyridinyl)-2-propenoic acid (acrylH), and a perylene inclusion compound [Ni(SCN)2(isoH)2(fumaricH2)].1/2C20H12, whose long building block is a trimer inserted with fumaric acid (fumaricH2) as a linear spacer.
已提出一种用于包合物的新型主体设计,该设计对大型平面芳香客体分子具有偏好性。我们的主体设计包括一个矩形空腔,它是基于超分子化学概念,使用一个长的和一个短的构建单元制成的。长构建单元便于容纳大型客体,短构建单元则可防止形成互穿结构,这种结构在具有大空隙空间的框架中经常出现。长构建单元是由4-吡啶甲酸(isoH)的二聚体通过两个羧酸部分之间的氢键形成的。这种isoH二聚体可以利用两端的N原子连接两个过渡金属中心,从而充当长构建单元。对于短构建单元,使用了硫氰酸根离子。它在两个金属中心之间形成一个弯曲的桥,以形成一维双链[M(SCN)₂]∞配合物。通过isoH、SCN⁻和Ni²⁺的自组装,构建了一个二维网络[Ni(SCN)₂(isoH)₂]∞,其中一维[Ni(SCN)₂]∞配合物由isoH二聚体连接。矩形空腔在二维网络内形成为一个网格。我们包合物的晶体具有二维网络的层状结构,并且形成了一个贯穿层状二维网络的一维通道状空腔,客体可能被包含在其中。此外,我们的主体设计具有易于扩展主体结构的优点。用另一种组分替代isoH以及使用三种组分来制备长构建单元是可行的。在后一种情况下,将具有两个羧基的线性间隔物插入isoH二聚体中,以形成具有三聚体结构的长构建单元。基于我们的主体设计,合成了一系列新的包合物。通过单晶X射线衍射确定了三种化合物晶体结构。它们分别是联苯包合物[Ni(SCN)₂(isoH)₂]·1/2C₁₂H₁₀(基本情况)、9,10-二氯蒽包合物[Ni(SCN)₂(acrylH)₂]·1/2C₁₄H₈Cl₂,其中isoH被3-(4-吡啶基)-2-丙烯酸(acrylH)替代,以及苝包合物[Ni(SCN)₂(isoH)₂(fumaricH₂)]·1/2C₂₀H₁₂,其长构建单元是插入了富马酸(fumaricH₂)作为线性间隔物的三聚体。