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单壁碳纳米管局部掺杂位点化学反应驱动的近红外光致发光多步波长转换。

Multistep Wavelength Switching of Near-Infrared Photoluminescence Driven by Chemical Reactions at Local Doped Sites of Single-Walled Carbon Nanotubes.

机构信息

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

International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, 819-0395, Japan.

出版信息

Chemistry. 2018 Dec 20;24(72):19162-19165. doi: 10.1002/chem.201805342. Epub 2018 Dec 4.

Abstract

Local chemical functionalization is used for defect doping of single-walled carbon nanotubes (SWNTs), to develop near-infrared photoluminescence (NIR PL) properties. We report the multistep wavelength shifting of the NIR PL of SWNTs through chemical reactions at local doped sites tethered to an arylaldehyde group. The PL wavelength of the doped SWNTs is modulated based on imine chemistry. This involves the imine formation of aldehyde groups with added arylamines, imine dissociation reaction, exchange reaction of bound arylamines in the imine, and the Kabachnik-Fields reaction of imine groups using diisopropyl phosphite. Using doped sites as a localized chemical reaction platform can exploit the versatile molecularly driven functionality of carbon nanotubes and related nanomaterials.

摘要

通过在与芳醛基团相连的局部掺杂位点进行化学反应,实现了单壁碳纳米管(SWNTs)的近红外光致发光(NIR PL)性能的局域化学功能化和缺陷掺杂。我们报告了通过与外加芳胺发生席夫碱反应、亚胺的解反应、亚胺中结合的芳胺的交换反应以及用二异丙基亚膦酸进行亚胺基团的Kabachnik-Fields 反应,实现了 SWNTs 的 NIR PL 的多步波长移动。该方法基于亚胺化学,调节了掺杂 SWNTs 的 PL 波长。这种方法可以利用碳纳米管和相关纳米材料的多功能分子驱动功能,将掺杂位点作为局部化学反应平台。

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