Cioffi Carla, Campidelli Stéphane, Sooambar Chloé, Marcaccio Massimo, Marcolongo Gabriele, Meneghetti Moreno, Paolucci Demis, Paolucci Francesco, Ehli Christian, Rahman G M Aminur, Sgobba Vito, Guldi Dirk M, Prato Maurizio
INSTM, Unit of Trieste, Dipartimento di Scienze Farmaceutiche, Università di Trieste, Piazzale Europa 1, I-34127 Trieste, Italy.
J Am Chem Soc. 2007 Apr 4;129(13):3938-45. doi: 10.1021/ja068007p. Epub 2007 Mar 8.
Single-wall carbon nanohorns (SWNHs) are a new class of material that is closely related to single-wall carbon nanotubes. Here, we describe the synthesis and characterization of a series of SWNHs functionalized with ethylene glycol chains and porphyrins. Functionalization of carbon nanohorns has been achieved using two different synthetic protocols: (1) direct attack of a free amino group on the nanohorn sidewalls (nucleophilic addition) and (2) amidation reaction of the carboxylic functions in oxidized nanohorns. The nanohorn derivatives have been characterized by a combination of several techniques, and the electronic properties of the porphyrin/nanohorn assemblies (SWNH/H2P) have been investigated by electrochemistry, spectroelectrochemistry, and a series of steady-state and time-resolved spectroscopy. The cyclic voltammetry curve of nanohorn/porphyrin conjugate 6 showed a continuum of faradic and pseudocapacitive behavior, which is associated with multiple-electron transfers to and from the SWNHs. Superimposed on such a pseudocapacitive current, the curve also displays three discrete reduction peaks at -2.26, -2.57, and -2.84 V and an oxidation peak at 1.12 V (all attributed to the porphyrin moiety). Steady-state and time-resolved fluorescence demonstrated a quenching of the fluorescence of the porphyrin in SWNH/H2P conjugates 5 and 6 compared to the reference free base porphyrin. Transient absorption spectra permitted the electron-transfer process between the porphyrins and the carbon nanostructures to be highlighted.
单壁碳纳米角(SWNHs)是一类与单壁碳纳米管密切相关的新型材料。在此,我们描述了一系列用乙二醇链和卟啉功能化的单壁碳纳米角的合成与表征。碳纳米角的功能化已通过两种不同的合成方案实现:(1)游离氨基对纳米角侧壁的直接进攻(亲核加成)和(2)氧化纳米角中羧基官能团的酰胺化反应。通过多种技术相结合对纳米角衍生物进行了表征,并通过电化学、光谱电化学以及一系列稳态和时间分辨光谱对卟啉/纳米角组装体(SWNH/H2P)的电子性质进行了研究。纳米角/卟啉共轭物6的循环伏安曲线显示出连续的法拉第和赝电容行为,这与SWNHs的多电子转移有关。叠加在这种赝电容电流上,该曲线还在-2.26、-2.57和-2.84 V处显示出三个离散的还原峰以及在1.12 V处显示出一个氧化峰(均归因于卟啉部分)。稳态和时间分辨荧光表明,与参考游离碱卟啉相比,SWNH/H2P共轭物5和6中卟啉的荧光发生了猝灭。瞬态吸收光谱突出了卟啉与碳纳米结构之间的电子转移过程。