Wei Ying, Li Yang, Lin Dongqing, Jin Dong, Du Xue, Zhong Chunxiao, Zhou Ping, Sun Yue, Xie Linghai, Huang Wei
Centre for Molecular Systems and Organic Devices (CMSOD), State Key Laboratory of Organic Electronics and Information Displays & Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, 9 Wenyuan Road, Nanjing 210023, China.
Frontiers Science Center for Flexible Electronics (FSCFE), MIIT Key Laboratory of Flexible Electronics (KLoFE), Northwestern Polytechnical University, Xi'an 710072, China.
Org Biomol Chem. 2021 Dec 8;19(47):10408-10416. doi: 10.1039/d1ob01907d.
Regular or well-defined nanogrids with atomically precise extension sites offer an opportunity for covalent nano-architectures as well as frameworks. Previously, we discovered organic nanogrids based on the 2,7-linkage of fluorene Friedel-Crafts gridization. However, the regularity of nanogrids is not always based on the actual molecular backbone, which leads to ineffective linkage for the more regular complex nanogrids such as nano-windows. Herein, we report the introduction of spirobifluorene, which has more orthogonal shapes, to fix the backbone of nanogridons with regards to the diarylfluorenes. The diamond-type nanogridons (DGs) obtained as a result have the potential feature of cross extension, which is different from their ladder-type counterparts, although they both have four well-defined extension sites. In order to screen efficient monogridon modules, we designed two types of DGs (spiro[fluorene-9,8'-indeno[2,1-]thiophene] (SFIT)-based DGs-1 and spirobifluorene-based DGs-2) and compared their synthetic routes. The results show that the Friedel-Crafts (F-C) gridization of the AB synthon (AB mode) offers DGs-1 in 44-50% yields, while the F-C gridization of A + B synthons (A + B mode) is more efficient and gives DGs-2 in 64% yield. Furthermore, unlike in the AB mode, the dehydroxylated byproduct and linear polymers were not observed in the A + B mode.
具有原子精确延伸位点的规则或定义明确的纳米网格为共价纳米结构以及框架提供了机会。此前,我们基于芴的2,7-键通过傅-克网格化发现了有机纳米网格。然而,纳米网格的规则性并不总是基于实际的分子主链,这导致对于更规则的复杂纳米网格(如纳米窗口)的连接效率低下。在此,我们报道引入具有更多正交形状的螺二芴,以固定二芳基芴类纳米网格单元的主链。由此得到的钻石型纳米网格单元(DGs)具有交叉延伸的潜在特征,这与它们的梯型对应物不同,尽管它们都有四个定义明确的延伸位点。为了筛选高效的单网格单元模块,我们设计了两种类型的DGs(基于螺[芴-9,8'-茚并[2,1-]噻吩](SFIT)的DGs-1和基于螺二芴的DGs-2)并比较了它们的合成路线。结果表明,AB合成子的傅-克(F-C)网格化(AB模式)以44-50%的产率提供DGs-1,而A + B合成子的F-C网格化(A + B模式)效率更高,以64%的产率提供DGs-2。此外,与AB模式不同,在A + B模式中未观察到脱羟基副产物和线性聚合物。