Berrettini Mia G, Braun Gary, Hu Jerry G, Strouse Geoffrey F
Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306-4390, USA.
J Am Chem Soc. 2004 Jun 9;126(22):7063-70. doi: 10.1021/ja037228h.
Solid-state NMR analysis on wurtzite 2-nm hexadecylamine-capped CdSe nanocrystals (CdSe-HDA) provides evidence of discrete nanoparticle reconstruction within the Se sublattice of the nanomaterial. The cadmium and selenium atoms are probed with (1)H-(113)Cd and (1)H-(77)Se cross-polarization magic angle spinning (MAS) experiments, which demonstrate five ordered selenium sites in the nanoparticle that can be assigned to contributions arising from different surface sites and a selenium site one layer down from the surface. Intriguingly, in these materials both HDA and thiophenol are observed to selectively bind to specific sites on the nanoparticle surface. 2D heteronuclear chemical shift correlation (HETCOR) experiments provide evidence for thiophenol selectively binding at surface vacancies. Analysis of the NMR provides a model of a 2-nm CdSe-HDA molecular surface.
对纤锌矿型2纳米十六烷基胺包覆的CdSe纳米晶体(CdSe-HDA)进行的固态核磁共振分析,为纳米材料硒亚晶格内离散纳米颗粒的重构提供了证据。通过¹H-¹¹³Cd和¹H-⁷⁷Se交叉极化魔角旋转(MAS)实验对镉和硒原子进行探测,结果表明纳米颗粒中有五个有序的硒位点,这些位点可归因于不同表面位点以及从表面向下一层的一个硒位点的贡献。有趣的是,在这些材料中,观察到HDA和苯硫酚都选择性地结合到纳米颗粒表面的特定位点。二维异核化学位移相关(HETCOR)实验为苯硫酚选择性结合在表面空位提供了证据。核磁共振分析提供了一个2纳米CdSe-HDA分子表面的模型。