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吸附表面活性剂在芳基重氮盐与单壁碳纳米管反应中的作用。

Role of adsorbed surfactant in the reaction of aryl diazonium salts with single-walled carbon nanotubes.

机构信息

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

Langmuir. 2012 Jan 17;28(2):1309-21. doi: 10.1021/la204067d. Epub 2012 Jan 3.

Abstract

Because covalent chemistry can diminish the optical and electronic properties of single-walled carbon nanotubes (SWCNTs), there is significant interest in developing methods of controllably functionalizing the nanotube sidewall. To date, most attempts at obtaining such control have focused on reaction stoichiometry or strength of oxidative treatment. Here, we examine the role of surfactants in the chemical modification of single-walled carbon nanotubes with aryl diazonium salts. The adsorbed surfactant layer is shown to affect the diazonium derivatization of carbon nanotubes in several ways, including electrostatic attraction or repulsion, steric exclusion, and direct chemical modification of the diazonium reactant. Electrostatic effects are most pronounced in the cases of anionic sodium dodecyl sulfate and cationic cetyltrimethylammonium bromide, where differences in surfactant charge can significantly affect the ability of the diazonium ion to access the SWCNT surface. For bile salt surfactants, with the exception of sodium cholate, we find that the surfactant wraps tightly enough such that exclusion effects are dominant. Here, sodium taurocholate exhibits almost no reactivity under the explored reaction conditions, while for sodium deoxycholate and sodium taurodeoxycholate, we show that the greatest extent of reaction is observed among a small population of nanotube species, with diameters between 0.88 and 0.92 nm. The anomalous reaction of nanotubes in this diameter range seems to imply that the surfactant is less effective at coating these species, resulting in a reduced surface coverage on the nanotube. Contrary to the other bile salts studied, sodium cholate enables high selectivity toward metallic species and small band gap semiconductors, which is attributed to surfactant-diazonium coupling to form highly reactive diazoesters. Further, it is found that the rigidity of anionic surfactants can significantly influence the ability of the surfactant layer to stabilize the diazonium ion near the nanotube surface. Such Coulombic and surfactant packing effects offer promise toward employing surfactants to controllably functionalize carbon nanotubes.

摘要

由于共价化学会降低单壁碳纳米管(SWCNT)的光学和电子性能,因此人们非常关注开发可控功能化纳米管侧壁的方法。迄今为止,大多数获得这种控制的尝试都集中在反应化学计量或氧化处理的强度上。在这里,我们研究了表面活性剂在芳基重氮盐与单壁碳纳米管的化学修饰中的作用。吸附的表面活性剂层以多种方式影响碳纳米管的重氮衍生化,包括静电吸引或排斥、空间排斥和重氮反应物的直接化学修饰。静电效应在阴离子十二烷基硫酸钠和阳离子十六烷基三甲基溴化铵的情况下最为明显,其中表面活性剂电荷的差异会显著影响重氮离子接近 SWCNT 表面的能力。对于胆盐表面活性剂,除了胆酸钠之外,我们发现表面活性剂包裹得足够紧,以至于排斥效应占主导地位。在这里,牛磺胆酸钠在探索的反应条件下几乎没有反应性,而对于脱氧胆酸钠和牛磺脱氧胆酸钠,我们表明,反应程度最大的是一小部分纳米管物种,直径在 0.88 到 0.92nm 之间。这种直径范围内的纳米管异常反应似乎表明表面活性剂在这些物种上的涂层效果较差,导致纳米管表面的覆盖度降低。与研究的其他胆盐不同,胆酸钠能够实现对金属物种和小带隙半导体的高选择性,这归因于表面活性剂-重氮结合形成高反应性的重氮酯。此外,还发现阴离子表面活性剂的刚性可以显著影响表面活性剂层在纳米管表面附近稳定重氮离子的能力。这种库仑和表面活性剂堆积效应为利用表面活性剂可控地功能化碳纳米管提供了希望。

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