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从硫-胺溶液到金属硫化物纳米晶体:深入探究油胺-硫黑箱。

From sulfur-amine solutions to metal sulfide nanocrystals: peering into the oleylamine-sulfur black box.

机构信息

Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada.

出版信息

J Am Chem Soc. 2011 Apr 6;133(13):5036-41. doi: 10.1021/ja1109997. Epub 2011 Mar 8.

Abstract

In this Article, we present our findings on the formation of metal sulfide nanocrystals from sulfur-alkylamine solutions. By pulsed field gradient diffusion NMR along with the standard toolbox of 1D and 2D NMR, we determined that sulfur-amine solutions used as a sulfur precursor exist as alkylammonium polysulfides at low temperatures. Upon heating to temperatures used in nanocrystal synthesis, the polysulfide ions react with excess amine to generate H(2)S, which combines with the metal precursor to form metal sulfide. Four different reaction pathways were found, each of which produced H(2)S and the byproducts identified in this Article. Thioamides were identified as an intermediate and were shown to exhibit much more rapid kinetics than sulfur-alkylamine solutions at low temperatures in the synthesis of metal sulfide nanocrystals.

摘要

在本文中,我们展示了我们关于从硫-烷基胺溶液中形成金属硫化物纳米晶体的研究结果。通过脉冲场梯度扩散 NMR 以及 1D 和 2D NMR 的标准工具包,我们确定用作硫前体的硫-胺溶液在低温下作为烷基多硫化物存在。当加热到纳米晶体合成中使用的温度时,多硫化物离子与过量的胺反应生成 H(2)S,它与金属前体结合形成金属硫化物。发现了四种不同的反应途径,每种途径都生成了 H(2)S 和本文中鉴定的副产物。硫代酰胺被鉴定为中间体,并在金属硫化物纳米晶体合成中在低温下显示出比硫-烷基胺溶液更快的动力学。

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