安定なテトラフェニルエチレンベースの電荷支援水素結合有機構造体によるAl3+イオンのターンオン蛍光センシング
Yingjia Deng1, Yijin Wang1, Xiangyu Gao1
1State Key Laboratory of Porous Materials for Separation and Conversion, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, College of Smart Materials and Future Energy, Fudan University, 2005 Songhu Road, Shanghai 200438, China.
Abstract:
The development of stable and sensitive fluorescent sensors for metal ion detection remains a challenge in materials chemistry. Although hydrogen-bonded organic frameworks (HOFs) have shown great potential in luminescent applications, their practical use is often limited by structural instability. In this work, we present a novel charge-assisted HOF, termed FDU-HOF-21 ([H(NH2Bpy)]2(TPE)), constructed from a tetraphenylethylene (TPE)-based carboxylic acid ligand (H4TCPE) and 2,2'-bipyridine-5,5'-diamine (NH2Bpy). Single-crystal X-ray diffraction (SCXRD) reveals a stable three-dimensional framework stabilized by an extensive hydrogen-bonding network and reinforced by charge-assisted hydrogen bonds (CAHBs), and it exhibits exceptional stability across various solvents and pH conditions. Moreover, FDU-HOF-21 serves as a highly sensitive and selective fluorescent turn-on sensor for Al3+ ions, with a lowest limit of detection (LOD) of 1.7 × 10-6 M. Characterization and time-dependent density functional theory (TDDFT) calculations reveal that the fluorescence enhancement originates from the suppression of non-radiative decay likely due to the reduction in intermolecular charge transfer (Inter-CT) during the emission process, coupled with the restricted intramolecular rotation upon Al3+ chelation.
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Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.


