IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v10y2019i1d10.1038_s41467-018-07957-6.html
   My bibliography  Save this article

Halogen-bonded cocrystallization with phosphorus, arsenic and antimony acceptors

Author

Listed:
  • Katarina Lisac

    (University of Zagreb)

  • Filip Topić

    (McGill University)

  • Mihails Arhangelskis

    (McGill University)

  • Sara Cepić

    (University of Zagreb)

  • Patrick A. Julien

    (McGill University)

  • Christopher W. Nickels

    (McGill University)

  • Andrew J. Morris

    (University of Birmingham, Edgbaston)

  • Tomislav Friščić

    (McGill University)

  • Dominik Cinčić

    (University of Zagreb)

Abstract

The formation of non-covalent directional interactions, such as hydrogen or halogen bonds, is a central concept of materials design, which hinges on using small compact atoms of the 2nd period, notably nitrogen and oxygen, as acceptors. Heavier atoms are much less prominent in that context, and mostly limited to sulfur. Here, we report the experimental observation and theoretical study of halogen bonds to phosphorus, arsenic and antimony in the solid state. Combining 1,3,5-trifluoro-2,4,6-triiodobenzene with triphenylphosphine, -arsine, and -stibine provides cocrystals based on I···P, I···As and I···Sb halogen bonds. The demonstration that increasingly metallic pnictogens form halogen bonds sufficiently strong to enable cocrystal formation is an advance in supramolecular chemistry which opens up opportunities in materials science, as shown by colossal thermal expansion of the cocrystal involving I···Sb halogen bonds.

Suggested Citation

  • Katarina Lisac & Filip Topić & Mihails Arhangelskis & Sara Cepić & Patrick A. Julien & Christopher W. Nickels & Andrew J. Morris & Tomislav Friščić & Dominik Cinčić, 2019. "Halogen-bonded cocrystallization with phosphorus, arsenic and antimony acceptors," Nature Communications, Nature, vol. 10(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-018-07957-6
    DOI: 10.1038/s41467-018-07957-6
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-018-07957-6
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-018-07957-6?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
    ---><---

    More about this item

    Statistics

    Access and download statistics

    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:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-018-07957-6. 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: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.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.