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Key Documents

205796

Sigma-Aldrich

Potassium tetrachloropalladate(II)

98%

Synonyme(s) :

Potassium palladium(II) chloride

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About This Item

Formule linéaire :
K2PdCl4
Numéro CAS:
Poids moléculaire :
326.43
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352302
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Niveau de qualité

Pureté

98%

Forme

crystals

Pf

105 °C (dec.) (lit.)

Densité

2.67 g/mL at 25 °C (lit.)

Chaîne SMILES 

[K+].[K+].Cl[Pd--](Cl)(Cl)Cl

InChI

1S/4ClH.2K.Pd/h4*1H;;;/q;;;;2*+1;+2/p-4

Clé InChI

LGCKLDWLSVFMGL-UHFFFAOYSA-J

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Description générale

Potassium tetrachloropalladate(II) is a dark brown crystalline solid widely used as a Pd source in the field of catalysis, nanomaterial synthesis, and electronics.

Application

Potassium tetrachloropalladate(II) can be used:
  • As a precursor to synthesize Pd nanoparticles for catalytic degradation of organic pollutants and Pd-GO electrocatalyst in formic acid and ethanol oxidation.
  • To synthesize Pd–Pt alloy nanocrystals (NCs) with hollow structures by a galvanic replacement method with uniform Pd octahedral and cubic NCs as sacrificial templates. The hollow NCs exhibited higher ORR activities.
  • To synthesize immobilized Pd catalysts, a versatile method involves the layer-by-layer deposition of PAA and PEI-Pd(II) on alumina, followed by the reduction of Pd2+. This approach offers several benefits, including the stabilization of particles through the polyelectrolyte matrix, introduction of selectivity, and a significant reduction in undesired isomerization. Expanding the application of polyelectrolyte films holds promise for further enhancing selectivity in hydrogenation and other reactions.
  • To fabricate conductive and porous metal-organic frameworks(MOFs) for gas sensing applications and also to synthesize bimetallic Pd/SnO2 nanoparticles on metal organic framework (MOF) as an electrocatalyst for ethanol oxidation.
  • To prepare rigid macrocyclic pincer catalysts possessing polyaromatic ligands with enhanced catalytic activity.

Caractéristiques et avantages

Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar. Reacts with bis(dithiolates) to metal-bis(dithiolates) with applications in laser Q-switch materials, optical CD recording media, bar code material and superconductivity.

Pictogrammes

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Mention d'avertissement

Warning

Mentions de danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Consulter la Bibliothèque de documents

Mathis, M. et al.
Chemistry of Materials, 10, 3568-3568 (1998)
B L Iverson et al.
Nucleic acids research, 15(19), 7823-7830 (1987-10-12)
Reaction of DNA with K2PdCl4 at pH 2.0 followed by a piperidine workup produces specific cleavage at adenine (A) residues. Product analysis revealed the K2PdCl4 reaction involves selective depurination at adenine, affording an excision reaction analogous to the other chemical
A water-based synthesis of octahedral, decahedral, and icosahedral Pd nanocrystals.
Byungkwon Lim et al.
Angewandte Chemie (International ed. in English), 46(48), 9279-9282 (2007-10-31)
V A Tomilets et al.
Farmakologiia i toksikologiia, 44(1), 77-80 (1981-01-01)
A scheme has been devised that makes it possible to assess a specific mechanism of action of any histamine-releasing agent. The scheme suggests a switch off of different stages of histamine secretion--interaction of a histamine liberator with surface cell receptors
Can reliable information sources be trusted?
Malin Engfeldt et al.
Contact dermatitis, 65(6), 364-367 (2011-11-15)

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