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1 References  













(2,4,6-Trimethylphenyl)gold






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From Wikipedia, the free encyclopedia
  

(2,4,6-Trimethylphenyl)gold
Crystal structure of (2,4,6-trimethylphenyl)gold

Pentameric form

Names
IUPAC name

(2,4,6-Trimethylphenyl)gold

Other names

Mesitylgold; Mesitylgold(I); (2,4,6-Trimethylphenyl)gold(I)

Identifiers

CAS Number
  • 89340-02-3 pentamer checkY

    • 3D model (JSmol)
  • Interactive image
    • ChemSpider

    PubChem CID

    CompTox Dashboard (EPA)

    • InChI=1S/C9H11.Au/c1-7-4-8(2)6-9(3)5-7;/h4-5H,1-3H3; checkY

      Key: VUMCLWYYCJSHBH-UHFFFAOYSA-N checkY

    • Cc1cc(C)c([Au])c(C)c1

    • CC1=CC(C)=C([Au])C(C)=C1

    Properties

    Chemical formula

    		 AuC
    9    H
    11
    Molar mass 316.15 g mol−1

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    (2,4,6-Trimethylphenyl)gold is a member of a special group of compounds where an aryl carbon atom acts as a bridge between two gold atoms. This compound is formed in a reaction between Au(CO)Cl and the Grignard reagent mesitylmagnesium bromide.[1] It crystallizes as a cyclical pentamer.[1]

    References

    [edit]
    1. ^ a b Gambarotta, Sandro; Floriani, Carlo; Chiesi-Villa, Angiola; Guastini, Carlo (1983). "A homoleptic arylgold(I) complex: Synthesis and structure of pentanuclear mesitylgold(I)". Journal of the Chemical Society, Chemical Communications (22): 1304. doi:10.1039/C39830001304.
    Stub icon

    This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

  • t
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    • Retrieved from "https://en.wikipedia.org/w/index.php?title=(2,4,6-Trimethylphenyl)gold&oldid=1089503653"
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    ●This page was last edited on 24 May 2022, at 05:42 (UTC).
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