强大的,高度发光的Au13超原子受到N-异环碳素的保护
Mina R Narouz1, Shinjiro Takano2, Paul A Lummis1
1Department of Chemistry , Queen's University , Chernoff Hall, Kingston , Ontario K7L 3N6 , Canada.
Journal of the American Chemical Society
|September 10, 2019
概括
由N-异环碳酸 (NHC) 稳定的新金超原子纳米集群表现出增强的光发光. 这些NHC-Au集群表现出高稳定性和广泛的能量差距,超过之前的配体保护的金纳米集群.
科学领域:
- 无机化学
- 纳米技术
- 材料科学
背景情况:
- 由于其独特的特性,金纳米集群对各种应用具有前景.
- 黄金纳米集群的稳定通常涉及可以影响其电子和光学特性的配体.
- N-异环碳素 (NHC) 为金属复合物提供强大的稳定性.
研究的目的:
- 通过N-异环碳素 (NHCs) 和化物稳定新型金超原子纳米集群的合成和特征.
- 研究这些新开发的NHC-Au纳米集群的结构,光学和电子特性.
- 将这些NHC稳定集群的性能与现有的配体保护的金纳米集群进行比较.
主要方法:
- 精确定义的NHC-Au-Cl复合物的合成.
- 减少前体复合物以形成金超原子纳米集群.
- 用X射线结晶学进行结构阐明.
- 光发光光谱测定量子产量
- 电子结构的密度功能理论 (DFT) 分析.
主要成果:
- 已经成功合成了具有icosahedral Au13核心的金超原子纳米集群.
- 集群由9个NHC和3个化物稳定,具有显著的CH-π和π-π相互作用.
- 观察到异常高的光发光量子产量,高达16.0%.
- DFT分析显示了一个8电子超原子配置,具有2 eV的HOMO-LUMO能量差距.
- 与素稳定黄金集群相比,表现出高稳定性.
结论:
- NHC连接物为金超原子纳米集群提供有效的稳定性,从而提高性能.
- 独特的结构特征和电子配置有助于卓越的光发光和稳定性.
- 这些NHC-Au纳米集群代表了联体保护黄金纳米集群领域的重大进步.
相关概念视频
12:19Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
8.9K
We describe a protocol to photogenerate N-heterocyclic carbenes (NHCs) by UV irradiation of a 2-isopropylthioxanthone/imidazolium tetraphenylborate salt system. Methods to characterize the photoreleased NHC and elucidate the photochemical mechanism are proposed. The protocols for ring-opening metathesis photopolymerization in solution and miniemulsion illustrate the potential of this 2-component NHC photogenerating...
8.9K
19:58Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions
10.2K
Detailed and generalized protocols are presented for the synthesis and subsequent purification of four palladium N-heterocyclic carbene complexes from benzimidazolium salts. The complexes were tested for catalytic activity in arylation and Suzuki-Miyaura reactions. For each reaction investigated, at least one of the four complexes successfully catalyzed the...
10.2K
10:44Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
11.5K
We present protocols for the isolation of stable heterocyclic carbenes. The synthesis of a cyclic (alkyl)(amino) carbene (CAAC) and an N-heterocyclic carbene (NHC) is demonstrated using filter cannulas and Schlenk technique. We furthermore present the synthesis of the related oxygen-sensitive, electron-rich mixed “Wanzlick dimer” and the reduced stable organic...
11.5K
Basicity of Heterocyclic Aromatic Amines
6.9K
Heterocyclic amines, where the N atom is a part of an alicyclic system, are similar in basicity to alkylamines. Interestingly, the heterocyclic amine having a nitrogen atom as part of an aromatic ring has much less basicity than its corresponding alicyclic counterpart. For this reason, as presented in Figure 1, piperidine (pKb = 2.8) is significantly more basic than pyridine (pKb = 8.8).
6.9K
04:00Luminescence-Based Assay to Assess Neurotoxicity of Test Compounds on Neurons
601
In this video, we describe a luminescence-based method to assess the neurotoxicity of neurite outgrowth-promoting small molecule compounds on the viability of hNPC-derived neurons. The assay measures intracellular ATP level, an indicator of cell viability, to evaluate neurotoxicity following test compound...
601
Nomenclature of Aryl and Heterocyclic Amines
3.1K
The simplest aromatic amine is phenylamine, which contains an –NH2 functionality directly attached to an aromatic ring. The name aniline is designated for this skeleton. As shown in Figure 1, the common names of the functionalized anilines involve prefixes ortho-, meta-, and para- to indicate the substitution position. Different functionalized aniline derivatives also have notable trivial names.
3.1K


