Varghese Eldhose V, Liu Yi-Hung, Chen Hsing-Yin, Li Chien-Hung, Chen Chia-Hsiang
Department of Medicinal and Applied Chemistry, Kaohsiung Medical University 80708 Kaohsiung Taiwan
Department of Chemistry, National Taiwan University 10617 Taipei Taiwan.
Chem Sci. 2025 May 6. doi: 10.1039/d5sc02827b.
The conformation of nanographene plays a pivotal role in determining its electronic, mechanical, and optical properties. Analyzing the conformation of nanographene is crucial because of its significant implications in various scientific and technological domains. In this work, we examined the changes in the structural conformation of nanographene upon coordination with a metal. We synthesized a series of nitrogen-doped nanographenes (2, 3, and 4) that differed by one C-C bond and their corresponding nanographene-Re complexes (2Re, 3Re, and 4Re). The conformations of the metal complexes were thoroughly analyzed using various spectroscopic techniques. A comparison of the X-ray crystal structures of nanographene before and after rhenium coordination revealed that rhenium coordination induced conformational changes in the nanographene moiety. Additionally, we assessed the catalytic activity of the nanographene-Re complexes toward the electrocatalytic hydrogen evolution reaction (HER). In the presence of a small amount of weak acid (1.5 mM acetic acid), the nanographene-Re complex exhibited hydrogen production at a low overpotential of 133 mV.
纳米石墨烯的构象在决定其电学、力学和光学性质方面起着关键作用。分析纳米石墨烯的构象至关重要,因为它在各种科学和技术领域都有重大影响。在这项工作中,我们研究了纳米石墨烯与金属配位后结构构象的变化。我们合成了一系列相差一个C-C键的氮掺杂纳米石墨烯(2、3和4)及其相应的纳米石墨烯-铼配合物(2Re、3Re和4Re)。使用各种光谱技术对金属配合物的构象进行了全面分析。铼配位前后纳米石墨烯的X射线晶体结构比较表明,铼配位诱导了纳米石墨烯部分的构象变化。此外,我们评估了纳米石墨烯-铼配合物对电催化析氢反应(HER)的催化活性。在少量弱酸(1.5 mM乙酸)存在下,纳米石墨烯-铼配合物在133 mV的低过电位下表现出产氢。