Taborowska Patrycja, Dzienia Andrzej, Janas Dawid
Department of Chemistry, Silesian University of Technology B. Krzywoustego 4 44-100 Gliwice Poland
Chem Sci. 2024 Dec 11;16(3):1374-1389. doi: 10.1039/d4sc04785k. eCollection 2025 Jan 15.
Harnessing the unique optical properties of chirality-enriched single-walled carbon nanotubes (SWCNTs) is the key to unlocking the application of SWCNTs in photonics. Recently, it has been discovered that chemical modification of SWCNTs greatly increases their potential in this context. Despite the dynamic progress in this area, the mechanism of the chemical modification of SWCNTs and the impact of the reaction conditions on the properties of the obtained functional nanomaterials remain unclear. In this study, we demonstrate how the reaction environment influences the observed fluorescence pattern of SWCNTs after modification with benzoyloxy radicals generated . The obtained results reveal that each diacyl peroxide molecule can generate either one or two radicals by two different mechanisms, , induced or spontaneous decomposition. Through proper selection of the reactant concentration, process temperature, and solvent, we were able to activate one or both radical decay pathways. In addition, the choice of a solvent, such as tetrahydrofuran or acetonitrile, allowed drastic changes in the functionalization process. Consequently, the SWCNT surface was grafted with functional groups C-C bonds using radicals derived from the solvent molecules instead of attaching an aromatic moiety from the reactant present in the system through the expected C-O linkage. Verification of the structure of the chemically bound functional groups through hydrolysis opens the route to further modification of SWCNT surfaces using the labile ester connection. By gaining a better understanding of the emergence and behavior of the generated radicals, we demonstrate the possibility of controlling the density of introduced defects, as well as the selectivity of the functionalization process. The identification of the underlying chemical pathways responsible for the functionalization of SWCNTs paves the way for the design of precise methods of SWCNT modification to adjust their photonic characteristics for specific applications.
利用富含手性的单壁碳纳米管(SWCNT)独特的光学性质是开启SWCNT在光子学领域应用的关键。最近,人们发现SWCNT的化学修饰在这方面极大地提升了它们的潜力。尽管该领域取得了动态进展,但SWCNT化学修饰的机制以及反应条件对所得功能纳米材料性质的影响仍不明确。在本研究中,我们展示了反应环境如何影响用生成的苯甲酰氧基自由基修饰后SWCNT的荧光图案。所得结果表明,每个二酰基过氧化物分子可通过两种不同机制产生一个或两个自由基,即诱导分解或自发分解。通过适当选择反应物浓度、工艺温度和溶剂,我们能够激活一种或两种自由基衰减途径。此外,选择诸如四氢呋喃或乙腈等溶剂会使功能化过程发生剧烈变化。因此,SWCNT表面是用源自溶剂分子的自由基接枝官能团C-C键,而不是通过预期的C-O键连接从体系中存在的反应物连接一个芳香部分。通过水解对化学结合官能团结构的验证为使用不稳定酯连接进一步修饰SWCNT表面开辟了道路。通过更好地理解生成自由基的出现和行为,我们证明了控制引入缺陷密度以及功能化过程选择性的可能性。确定负责SWCNT功能化的潜在化学途径为设计精确的SWCNT修饰方法以针对特定应用调整其光子特性铺平了道路。