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使用长烷基链苯重氮化合物分离半导体单壁碳纳米管。

Separation of semiconducting single-walled carbon nanotubes by using a long-alkyl-chain benzenediazonium compound.

作者信息

Toyoda Shouhei, Yamaguchi Yoshifumi, Hiwatashi Masataka, Tomonari Yasuhiko, Murakami Hiroto, Nakashima Naotoshi

机构信息

Department of Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395, Japan.

出版信息

Chem Asian J. 2007 Jan 8;2(1):145-9. doi: 10.1002/asia.200600279.

Abstract

We designed and synthesized 4-dodecyloxybenzenediazonium tetrafluoroborate (1), which preferentially reacts with metallic single-walled carbon nanotubes (SWNTs) by kinetic control. We first determined the suitable experimental conditions for the preferential reaction of 1 with individually dissolved SWNTs by monitoring the decrease in absorbance for the metallic SWNT in the range of 400-650 nm in the absorption spectrum of the SWNTs. The reacted SWNTs were thoroughly rinsed with THF to obtain THF-insoluble SWNTs. The Raman spectrum of the THF-insoluble SWNTs showed a strong peak near 180 cm(-1), which corresponds to a semiconducting breathing band. The metallic breathing bands (approximately 220 cm(-1)) and Breit-Wingner-Fano (BWF) modes (1520 cm(-1)) corresponding to the metallic SWNTs were much weaker than those of the pristine SWNTs. We also confirmed that metallic peaks in the range of 400-650 nm in the absorption spectrum of THF-insoluble SWNTs that were individually dissolved in an aqueous micelle of sodium cholate were almost nondetectable. All the results indicate that the THF-insoluble SWNTs are semiconducting.

摘要

我们设计并合成了四氟硼酸4-十二烷氧基苯重氮盐(1),它通过动力学控制优先与金属性单壁碳纳米管(SWNTs)发生反应。我们首先通过监测单壁碳纳米管吸收光谱中400 - 650 nm范围内金属性单壁碳纳米管吸光度的下降,确定了1与单独溶解的单壁碳纳米管优先反应的合适实验条件。将反应后的单壁碳纳米管用四氢呋喃(THF)彻底冲洗,以获得不溶于四氢呋喃的单壁碳纳米管。不溶于四氢呋喃的单壁碳纳米管的拉曼光谱在180 cm⁻¹附近显示出一个强峰,这对应于一个半导体呼吸带。与金属性单壁碳纳米管对应的金属呼吸带(约220 cm⁻¹)和布赖特 - 维格纳 - 法诺(BWF)模式(1520 cm⁻¹)比原始单壁碳纳米管的要弱得多。我们还证实,单独溶解在胆酸钠水胶束中的不溶于四氢呋喃的单壁碳纳米管的吸收光谱在400 - 650 nm范围内的金属峰几乎检测不到。所有结果表明,不溶于四氢呋喃的单壁碳纳米管是半导体性的。

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