Novel supramolecular artificial light-harvesting systems based on AIE-active macrocycles for efficient white-light photocatalysis in water†

IF 7.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jun-Cheng Yang, Ke Chen, Guo-Ling Zhang, Chunxuan Qi, Hai-Tao Feng and Ben Zhong Tang
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Abstract

Constructing supramolecular artificial light-harvesting systems (ALHSs) based on the Förster resonance energy transfer (FRET) mechanism provides an optimal platform for understanding natural photosynthesis and simulating natural light-harvesting systems. In the present work, rigid macrocycle K-1 with a nonplanar conformation and aggregation-induced emission (AIE) properties was selected as an energy donor in ALHSs, while the non-cyclic AIEgen K-2 was used for a comparative study. In aqueous solution, an efficient one-step energy-transfer process was established between blue-emitting K-1 and an acceptor (namely PBTB) with orange fluorescence to afford a high energy-transfer efficiency (ΦET) of up to 82.6%. Notably, bright white light emission can be readily realized. Moreover, the triad FRET system was fabricated through energy transfer from the AIEgens to PBTB, then further transferring the captured energy to the final red-emitting acceptor (namely as Z1), achieving an efficient two-step sequential energy transfer. When the ratio of K-1/PBTB/Z1 assemblies reached 1000 : 40 : 14, the optimal ΦET was 66.4%. More importantly, it was found that the ALHS based on macrocycle K-1 showed much higher photocatalytic activity for the cross-dehydrogenative coupling (CDC) reaction. Therefore, the flexibility of this novel supramolecular strategy renders the macrocyclic AIEgen a promising candidate to construct efficient ALHSs for photocatalysis.

Abstract Image

基于aie活性大环的新型超分子人工光收集系统在水中的高效白光催化。
构建基于Förster共振能量转移(FRET)机制的超分子人工捕光系统(alhs)为理解自然光合作用和模拟自然捕光系统提供了最佳平台。本研究选择具有非平面构象和聚集诱导发射(AIE)性质的刚性大环K-1作为alhs的能量供体,并采用非环AIEgen K-2进行比较研究。在水溶液中,蓝光K-1与具有橙色荧光的受体(即PBTB)之间建立了高效的一步能量转移过程,能量转移效率(Φ ET)高达82.6%。值得注意的是,可以很容易地实现明亮的白光发射。此外,通过将能量从AIEgens转移到PBTB,然后将捕获的能量进一步转移到最终的发红受体(即Z1),制备了三元FRET系统,实现了高效的两步顺序能量转移。当K-1/PBTB/Z1组合的比例达到1000:40:14时,最优Φ ET为66.4%。更重要的是,发现基于K-1大环的ALHS对交叉脱氢偶联(CDC)反应具有更高的光催化活性。因此,这种新型超分子策略的灵活性使大环AIEgen成为构建高效光催化alhs的有希望的候选者。
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来源期刊
Chemical Science
Chemical Science CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
4.80%
发文量
1352
审稿时长
2.1 months
期刊介绍: Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.
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