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Sigma-Aldrich

Gold(III) chloride

99%

Sinónimos:

Trichlorogold

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About This Item

Fórmula lineal:
AuCl3
Número de CAS:
13453-07-1
Peso molecular:
303.33
EC Number:
236-623-1
MDL number:
MFCD00014172
UNSPSC Code:
12352302
PubChem Substance ID:
24860214
NACRES:
NA.23

assay

99%

form

powder

reaction suitability

reagent type: catalyst
core: gold

SMILES string

Cl[Au](Cl)Cl

InChI

1S/Au.3ClH/h;3*1H/q+3;;;/p-3

InChI key

RJHLTVSLYWWTEF-UHFFFAOYSA-K

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General description

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.

Application

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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)
Ligand-induced gold nanocrystal superlattice formation in colloidal solution.
Lin XM, et al.
Chemistry of Materials, 11(2), 198-202 (1999)
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
Vanajakshi Gudla et al.
The Journal of organic chemistry, 76(24), 9919-9933 (2011-10-28)
An intramolecular approach to generate compounds containing an arylnaphthalene lignan scaffold in high yields is presented. It involves a sequential intramolecular electrophilic attack of carbonyl on arylalkyne followed by benzannulation catalyzed by gold salt. AuCl(3) in combination with AgSbF(6) works
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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