Palladium black

Palladium black is a coarse, sponge-like form of elemental palladium which offers a large surface area for catalytic activity. It is used in organic synthesis as a catalyst for hydrogenation reactions.[1]

Palladium black
Names
IUPAC name
Palladium
Other names
Palladium black
Identifiers
3D model (JSmol)
EC Number
  • 231-115-6
UNII
Properties
Pd
Molar mass 106.42
Appearance Black powder
Solubility Organic Solvents
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

The term palladium black is also used colloquially to refer to a black precipitate of elemental palladium, which forms via decomposition of various palladium complexes[2].

Preparation

Palladium black is typically prepared from palladium(II) chloride or palladium(II)-ammonium chloride.[1] The palladium chloride process entails the formation of palladium hydroxide using lithium hydroxide followed by reduction under hydrogen gas[3] while the palladium(II)-ammonium chloride route employs a solution formic acid followed by the precipitation of the catalyst using potassium hydroxide.[4]

gollark: Intellectual property law means that you can't, say, freely give someone else a binary I give you. It doesn't mean you have the source code to it so you can make changes, and it doesn't mean I can't make it only work on one computer (based on windows's "hardware ID" or whatever).
gollark: Nope.
gollark: I don't think you can do much about this outside of... I don't know, banning all SaaS and mandating open source code.
gollark: This is also not entirely related to DRMy things.
gollark: Just use osmarkscalculator™, coming 2026 when I work out how computer algebra systems work.

See also

References

  1. Nishimura, Shigeo (2001). Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis (1st ed.). New York: Wiley-Interscience. pp. 34–35. ISBN 9780471396987.
  2. Iwasawa, Tetsuo; Tokunaga, Makoto; Obora, Yasushi; Tsuji, Yasushi (2004-06-01). "Homogeneous Palladium Catalyst Suppressing Pd Black Formation in Air Oxidation of Alcohols". Journal of the American Chemical Society. 126 (21): 6554–6555. doi:10.1021/ja031936l. ISSN 0002-7863. PMID 15161274.
  3. Nishimura, Shigeo; Itaya, Takashi; Shiota, Michio (1967). "Reactions of cycloalkanones in the presence of platinum-metal catalysts and hydrogen". Chemical Communications (London) (9): 422–423. doi:10.1039/C19670000422.
  4. Zelinsky, N.; Glinka, N. (1911). "Über gleichzeitige Reduktions- und Oxydationskatalyse" (PDF). Berichte der Deutschen Chemischen Gesellschaft. 44 (3): 2305–2311. doi:10.1002/cber.19110440347.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.