IDEAS home Printed from https://ideas.repec.org/a/zib/zbacmy/v8y2024i1p13-18.html
   My bibliography  Save this article

Synthesis And Structural Elucidation Of Symmetrical Tetrakis-Imidazolium Dinuclear Silver(I) Di-N-Heterocyclic Carbene Complex

Author

Listed:
  • Muhammad Zulhelmi Nazri

    (Innovation Centre in Agritechnology for Advanced Bioprocessing (ICA), Universiti Teknologi Malaysia (Pagoh Campus), Eduhub Pagoh 84600 Pagoh, Johor, Malaysia)

  • Mohd Rizal Razali

    (School of Chemical Sciences, Universiti Sains Malaysia 11800 Minden, Penang, Malaysia)

Abstract

This brief report outlines the synthesis and analysis of symmetrical dinuclear Ag(I) di-N-heterocyclic carbene (NHC) complexes, primarily derived from tetrakis-benzimidazolium salts. The symmetrical tetrakis-imidazolium salt was synthesized by reacting 1,2,4,5-tetrakis(bromomethyl)benzene with the imidazole moiety of 1‧Br. These salts were then transformed into their respective complexes through an in-situ deprotonation reaction with Ag2O, utilizing different salt-to-metal molar ratios, resulting in the establishment of dinuclear Ag(I) di-NHC complexes designated as Ag1. The structures of both the tetrakis-imidazolium (1‧Br) salts and the Ag(I) di-NHC complex Ag1 were determined using a combination of spectroscopic techniques (FTIR, 1H- and 13C-NMR), CHN elemental analysis, and single crystal X-ray diffraction. The single crystal X-ray diffraction analysis of the macrocyclic complex Ag1 suggests a crystalline structure resembling a cylinder.

Suggested Citation

  • Muhammad Zulhelmi Nazri & Mohd Rizal Razali, 2024. "Synthesis And Structural Elucidation Of Symmetrical Tetrakis-Imidazolium Dinuclear Silver(I) Di-N-Heterocyclic Carbene Complex," Acta Chemica Malaysia (ACMY), Zibeline International Publishing, vol. 8(1), pages 13-18, March.
  • Handle: RePEc:zib:zbacmy:v:8:y:2024:i:1:p:13-18
    DOI: 10.26480/acmy.01.2024.13.18
    as

    Download full text from publisher

    File URL: https://www.actachemicamalaysia.com/archives/1acmy2024/1acmy2024-13-18.pdf
    Download Restriction: no

    File URL: https://libkey.io/10.26480/acmy.01.2024.13.18?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:zib:zbacmy:v:8:y:2024:i:1:p:13-18. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Zibeline International Publishing The email address of this maintainer does not seem to be valid anymore. Please ask Zibeline International Publishing to update the entry or send us the correct address (email available below). General contact details of provider: https://www.actachemicamalaysia.com/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.