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Merck

334049

Sigma-Aldrich

氯化金 (III)

99%

别名:

Trichlorogold

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About This Item

线性分子式:
AuCl3
CAS号:
分子量:
303.33
EC號碼:
MDL號碼:
分類程式碼代碼:
12352302
PubChem物質ID:
NACRES:
NA.23

一般說明

Gold(III) chloride is a Lewis acid with monoclinic structure. It is a hygroscopic and light-sensitive solid. It is frequently utilized to dope organic conducting compounds, to boost their conductivity. It also serves as a catalyst in organic synthesis and a precursor to synthesize gold nanoparticles for various electrochemical applications.

應用

Gold(III) chloride can be used:
  • As a dopant to fabricate graphene protection layer between PEDOT:PSS and ITO for perovskite solar cells. It helps to enhance the photoconversion efficiency by protection ITO and collecting holes.
  • To fabricate flexible and transparent electrodes for OLEDs. It fills the defects in graphene and improves current efficiency without affecting the transmittance.
  • As a precursor for green synthesis of gold nanoparticles.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Ligand-induced gold nanocrystal superlattice formation in colloidal solution.
Lin XM, et al.
Chemistry of Materials, 11(2), 198-202 (1999)
A comparative study of galvanic replacement reactions involving Ag nanocubes and AuCl2? or AuCl4?
Au L, et al.
Advanced Materials, 20(13), 2517-2517 (2008)
Synthesis and optical properties of cubic gold nanoframes
Au L, et al.
Nano Research, 1(6), 441-449 (2008)
Ahmed A Elzatahry et al.
International journal of nanomedicine, 7, 2829-2832 (2012-06-30)
This report concerns nanofiber composites that incorporate N-heterocyclic carbenes and the use of such composites for testing antimicrobial and antifungal activities. The nanofiber composites were produced by electrospinning mixtures of the gold chloride or gold acetate complexes of a bis(imino)acenaphthene
Zhi-Xiong Ma et al.
Organic letters, 14(22), 5736-5739 (2012-11-06)
An imino-Nazarov cyclization using α-aryl-substituted allenamides is described. This gold(I)-catalyzed cascade is efficient and regioselective in constructing a diverse array of synthetically useful aromatic-ring fused cyclopentenamides. The success in this transformation represents a solution to the challenge in establishing an

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