...
首页> 外文期刊>Chemical science >Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au13 and heart-shaped Au8 clusters
【24h】

Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au13 and heart-shaped Au8 clusters

机译:受二膦保护的超小金纳米簇:开放的二十面体Au13和心形Au8簇

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Due to distinctive quantum confinement effects, ultrasmall gold nanoparticles usually exhibit interesting electronic structure and molecular-like properties. However, the lack of atomically-precise structural information makes the understanding of them almost impossible, such as understanding the relationships between their compositions and unique properties. Herein, by reducing a diphosphine Au ~(I) precursor (Au _(2) (dppm) _(2) Cl _(2) ; dppm = Ph _(2) PCH _(2) PPh _(2) ) with or without a S ~(2?) releasing reagent, we enriched our knowledge of the members in the families of Au _(13) and Au _(8) by the structural determinations of two new dppm-protected gold nanoclusters, [Au _(13) (dppm) _(6) ] ~(5+) ( SD/Au1 ) and [Au _(8) (dppm) _(4) S _(2) ] ~(2+) ( SD/Au2 ), respectively. Within SD/Au1 , the Au _(13) kernel significantly deviates from the ideal I _(h) icosahedron by the elongation of three surface Au–Au bonds to ~3.5 ?, giving it C _(3) symmetry, whereas SD/Au2 has a novel heart-shaped C _(2) symmetric Au _(8) S _(2) core (central Au _(4) tetrahedron + two Au _(2) S units) protected by four μ _(2) -dppm ligands in the outer shell. Of note, SD/Au1 represents a rare Au _(13) nanocluster with an opened icosahedral geometry, and SD/Au2 shows a new edge-shared “core + 4 exo ” structure type that has never been observed before. The electronic structures and optical absorption spectra of these systems are correlated with time-dependent density functional theory (TDDFT) calculations. Based on the spherical jellium model, the stability of the Au _(13) and Au _(8) nanoclusters can be ascribed to 8- and 2-electron superatoms with 1S ~(2) 1P ~(6) and 1S ~(2) configurations, respectively. Interestingly, the cluster SD/Au2 exhibits bright yellow luminescence with an emission maximum at 591 nm that slightly hypsochromically shifts to 581 nm upon cooling to 93 K. Our findings not only enrich the family of diphosphine-protected ultrasmall gold nanoclusters, but also demonstrate the rich variations of gold kernels during the transformation from a simple Au ~(I) precursor to Au nanoclusters.
机译:由于独特的量子限制效应,超小金纳米粒子通常表现出令人感兴趣的电子结构和分子状特性。但是,由于缺乏原子级精确的结构信息,因此几乎无法理解它们,例如了解它们的成分与独特性质之间的关系。在此,通过还原二膦Au〜(I)前体(Au _(2)(dppm)_(2)Cl _(2); dppm = Ph _(2)PCH _(2)PPh _(2))或不使用S〜(2?)脱模剂,通过两个新的dppm保护的金纳米簇[Au _]的结构测定,我们丰富了Au _(13)和Au _(8)家族成员的知识。 (13)(dppm)_(6)]〜(5+)(SD / Au1)和[Au _(8)(dppm)_(4)S _(2)]〜(2+)(SD / Au2 ), 分别。在SD / Au1中,Au _(13)核通过三个表面Au–Au键伸长至〜3.5?显着偏离理想的I _(h)二十面体,使其具有C _(3)对称性,而SD / Au2具有新颖的心形C _(2)对称Au _(8)S _(2)核(中心Au _(4)四面体+两个Au _(2)S单元),受四个μ_(2)保护-dppm配体在外壳中。值得注意的是,SD / Au1代表稀有的Au _(13)纳米簇,具有开放的二十面体几何形状,并且SD / Au2显示了从未见过的新的边缘共享的“核+ 4 exo”结构类型。这些系统的电子结构和光吸收光谱与时变密度泛函理论(TDDFT)计算相关。基于球形胶体模型,Au _(13)和Au _(8)纳米团簇的稳定性可以归因于1S〜(2)1P〜(6)和1S〜(2)的8和2电子超原子)配置。有趣的是,簇SD / Au2表现出亮黄色发光,最大发射峰在591 nm处,冷却至93 K时略有色移移至581 nm。我们的发现不仅丰富了由二膦保护的超小型金纳米团簇,而且还证明了从简单的Au〜(I)前体到Au纳米团簇的转变过程中,金粒的丰富变化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号