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二硫代氨基甲酸盐作为水溶性量子点的封端配体。

Dithiocarbamates as capping ligands for water-soluble quantum dots.

机构信息

Department of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011-2230, USA.

出版信息

ACS Appl Mater Interfaces. 2010 Nov;2(11):3384-95. doi: 10.1021/am100996g. Epub 2010 Nov 5.

Abstract

We investigated the suitability of dithiocarbamate (DTC) species as capping ligands for colloidal CdSe-ZnS quantum dots (QDs). DTC ligands are generated by reacting carbon disulfide (CS(2)) with primary or secondary amines on appropriate precursor molecules. A biphasic exchange procedure efficiently replaces the existing hydrophobic capping ligands on the QD surface with the newly formed DTCs. The reaction conversion is conveniently monitored by UV-vis absorption spectroscopy. Due to their inherent water solubility and variety of side chain functional groups, we used several amino acids as precursors in this reaction/exchange procedure. The performance of DTC-ligands, as evaluated by the preservation of luminescence and colloidal stability, varied widely among amino precursors. For the best DTC-ligand and QD combinations, the quantum yield of the water-soluble QDs rivaled that of the original hydrophobic-capped QDs dispersed in organic solvents. The mean density of DTC-ligands per nanocrystal was estimated through a mass balance calculation which suggested nearly complete coverage of the available nanocrystal surface. The accessibility of the QD surface was evaluated by self-assembly of His-tagged dye-labeled proteins and peptides using fluorescence resonance energy transfer. DTC-capped QDs were also exposed to cell cultures to evaluate their stability and potential use for biological applications. In general, DTC-capped CdSe-ZnS QDs have many advantages over other water-soluble QD formulations and provide a flexible chemistry for controlling the QD surface functionalization. Despite previous literature reports of DTC-stabilized nanocrystals, this study is the first formal investigation of a biphasic exchange method for generating biocompatible core-shell QDs.

摘要

我们研究了二硫代氨基甲酸盐 (DTC) 作为胶体 CdSe-ZnS 量子点 (QD) 盖帽配体的适用性。DTC 配体是通过将二硫化碳 (CS(2)) 与适当前体分子上的伯胺或仲胺反应生成的。两相交换程序有效地将 QD 表面上现有的疏水性盖帽配体用新形成的 DTC 取代。反应转化率可以通过紫外-可见吸收光谱方便地监测。由于其固有的水溶性和各种侧链官能团,我们在该反应/交换程序中使用了几种氨基酸作为前体。通过发光和胶体稳定性的保留来评估 DTC 配体的性能,氨基酸前体之间差异很大。对于最佳的 DTC-配体和 QD 组合,水溶性 QD 的量子产率可与分散在有机溶剂中的原始疏水性盖帽 QD 相媲美。通过质量平衡计算估计了每个纳米晶体的 DTC 配体的平均密度,这表明纳米晶体表面的可用位置几乎完全被覆盖。通过使用荧光共振能量转移进行 His 标记的染料标记蛋白和肽的自组装来评估 QD 表面的可及性。还将 DTC 封端的 QD 暴露于细胞培养物中,以评估它们的稳定性和在生物应用中的潜在用途。总的来说,与其他水溶性 QD 制剂相比,DTC 封端的 CdSe-ZnS QD 具有许多优势,并为控制 QD 表面功能化提供了灵活的化学方法。尽管以前有关于 DTC 稳定的纳米晶体的文献报道,但这项研究是首次对生成生物相容的核壳 QD 的两相交换方法进行的正式研究。

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