Methoxy-functionalized N-heterocyclic carbenes

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Nelson, David J. and Collado, Alba and Manzini, Simone and Meiries, Sebastien and Slawin, Alexandra M Z and Cordes, David B. and Nolan, Steven P. (2014) Methoxy-functionalized N-heterocyclic carbenes. Organometallics, 33 (8). pp. 2048-2058. ISSN 0276-7333 (https://doi.org/10.1021/om5001919)

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Abstract

The effect of methoxy functionalization of three N-heterocyclic carbene ligands was assessed using a variety of methods. The steric environment of each carbene has been assessed in various coordination environments. The electronic properties, specifically the electron-donating character and π-accepting ability, have been evaluated using nickel and iridium complexes and selenium adducts, respectively. Comparisons with the parent systems have been made with respect to both electronic and steric properties. The carbenes IPr OMe, SIPrOMe, and IPrOMe have been found to be more electron donating than the parent systems IPr, SIPr, and IPr* and only slightly less π accepting, yet they exhibit similar steric properties.

ORCID iDs

Nelson, David J. ORCID logoORCID: https://orcid.org/0000-0002-9461-5182, Collado, Alba, Manzini, Simone, Meiries, Sebastien, Slawin, Alexandra M Z, Cordes, David B. and Nolan, Steven P.;
  • Item type:Article
    ID code:48360
    Dates:
    Date
    Event
    28 April 2014
    Published
    Subjects:Science > Chemistry
    Department:UNSPECIFIED
    Depositing user: Pure Administrator
    Date deposited:30 May 2014 09:09
    Last modified:01 Dec 2024 23:11
    Related URLs:
    URI:https://strathprints.strath.ac.uk/id/eprint/48360
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