首页> 美国卫生研究院文献>Chemical Science >Diphosphine-protected ultrasmall gold nanoclusters: opened icosahedral Au13 and heart-shaped Au8 clusters
【2h】

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

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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 AuI precursor (Au2(dppm)2Cl2; dppm = Ph2PCH2PPh2) with or without a S2– releasing reagent, we enriched our knowledge of the members in the families of Au13 and Au8 by the structural determinations of two new dppm-protected gold nanoclusters, [Au13(dppm)6]5+ (>SD/Au1) and [Au8(dppm)4S2]2+ (>SD/Au2), respectively. Within >SD/Au1, the Au13 kernel significantly deviates from the ideal Ih icosahedron by the elongation of three surface Au–Au bonds to ∼3.5 Å, giving it C3 symmetry, whereas >SD/Au2 has a novel heart-shaped C2 symmetric Au8S2 core (central Au4 tetrahedron + two Au2S units) protected by four μ2-dppm ligands in the outer shell. Of note, >SD/Au1 represents a rare Au13 nanocluster with an opened icosahedral geometry, and >SD/Au2 shows a new edge-shared “core + 4exo” 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 Au13 and Au8 nanoclusters can be ascribed to 8- and 2-electron superatoms with 1S21P6 and 1S2 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 AuI 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,通过在有或没有S 2-释放试剂的情况下还原二膦Au I 前体(Au2(dppm)2Cl2; dppm = Ph2PCH2PPh2),我们丰富了对通过两个新的受dppm保护的金纳米簇[Au13(dppm)6] 5 + (> SD / Au1 )的结构测定来确定Au13和Au8家族的成员[Au8(dppm)4S2] 2 + (> SD / Au2 )。在> SD / Au1 中,Au13核通过三个表面Au–Au键延伸至〜3.5Å而显着偏离理想的Ih二十面体,使其具有C3对称性,而> SD / Au2 < / strong>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)被外壳中的四个μ 2 -dppm配体保护。值得注意的是,> SD / Au1 代表稀有的Au 13 纳米团簇,具有开放的二十面体几何形状,而> SD / Au2 显示了一个新的边缘共享“ core + 4exo”结构类型,以前从未观察到。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具有1S 2 的8和2电子超原子。 sup> 1P 6 和1S 2 配置。有趣的是,簇> SD / Au2 表现出亮黄色发光,最大发射波长为591 nm,冷却至93 K时略有变色移至581 nm。我们的发现不仅丰富了由二膦保护的超小分子家族金纳米团簇,但也证明了从简单的Au I 前体向Au纳米团簇转变过程中金核的丰富变化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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