Verma Parul, Rahimi Faruk Ahamed, Samanta Debabrata, Kundu Arup, Dasgupta Jyotishman, Maji Tapas Kumar
Molecular Materials Laboratory, School of Advanced Materials (SAMat), Chemistry and Physics of Materials Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India.
Department of Chemical Sciences, Tata Institute of Fundamental Research (TIFR), Mumbai, 400005, India.
Angew Chem Int Ed Engl. 2022 Apr 11;61(16):e202116094. doi: 10.1002/anie.202116094. Epub 2022 Feb 21.
The self-assembly of a well-defined and astutely designed, low-molecular weight gelator (LMWG) based linker with a suitable metal ion is a promising method for preparing photocatalytically active coordination polymer gels. Here, we report the design, synthesis, and gelation behaviour of a tetrapodal LMWG based on a porphyrin core connected to four terpyridine units (TPY-POR) through amide linkages. The self-assembly of TPY-POR LMWG with Ru ions results in a Ru-TPY-POR coordination polymer gel (CPG), with a nanoscroll morphology. Ru-TPY-POR CPG exhibits efficient CO photoreduction to CO (3.5 mmol g h ) with >99 % selectivity in the presence of triethylamine (TEA) as a sacrificial electron donor. Interestingly, in the presence of 1-benzyl-1,4-dihydronicotinamide (BNAH) with TEA as the sacrificial electron donor, the 8e /8H photoreduction of CO to CH is realized with >95 % selectivity (6.7 mmol g h ). In CPG, porphyrin acts as a photosensitizer and covalently attached [Ru(TPY) ] acts as a catalytic center as demonstrated by femtosecond transient absorption (TA) spectroscopy. Further, combining information from the in situ DRIFT spectroscopy and DFT calculation, a possible reaction mechanism for CO reduction to CO and CH was outlined.
将定义明确且设计精巧的低分子量凝胶剂(LMWG)基连接体与合适的金属离子进行自组装,是制备具有光催化活性的配位聚合物凝胶的一种很有前景的方法。在此,我们报告了一种基于卟啉核心的四足LMWG的设计、合成及凝胶化行为,该卟啉核心通过酰胺键连接到四个三联吡啶单元(TPY-POR)。TPY-POR LMWG与Ru离子的自组装产生了具有纳米卷轴形态的Ru-TPY-POR配位聚合物凝胶(CPG)。在作为牺牲电子供体的三乙胺(TEA)存在下,Ru-TPY-POR CPG能高效地将CO光还原为CO(3.5 mmol g h ),选择性>99%。有趣的是,在以TEA作为牺牲电子供体且存在1-苄基-1,4-二氢烟酰胺(BNAH)的情况下,能以>95%的选择性(6.7 mmol g h )实现CO到CH的8e /8H光还原。在CPG中,卟啉作为光敏剂,共价连接的[Ru(TPY) ]作为催化中心,这已通过飞秒瞬态吸收(TA)光谱得到证明。此外,结合原位漫反射红外傅里叶变换光谱(DRIFT)和密度泛函理论(DFT)计算的信息,概述了CO还原为CO和CH的可能反应机理。