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Titel
s-Block metal complexes of superbulky (BuSi)N: a new weakly coordinating anion?
Ist Teil von
  • Chemical science (Cambridge), 2024-03, Vol.15 (12), p.4386-4395
Erscheinungsjahr
2024
Link zum Volltext
Quelle
EZB Free E-Journals
Beschreibungen/Notizen
  • Sterically hindered amide anions have found widespread application as deprotonation agents or as ligands to stabilize metals in unusual coordination geometries or oxidation states. The use of bulky amides has also been advantageous in catalyst design. Herein we present s-block metal chemistry with one of the bulkiest known amide ligands: ( t Bu 3 Si) 2 N − (abbreviated: t Bu N − ). The parent amine ( t Bu NH), introduced earlier by Wiberg, is extremely resistant to deprotonation (even with n BuLi/KO t Bu superbases) but can be deprotonated slowly with a blue Cs + /e − electride formed by addition of Cs 0 to THF. ( t Bu N)Cs crystallized as a separated ion-pair, even without cocrystallized solvent. As salt-metathesis reactions with ( t Bu N)Cs are sluggish and incomplete, it has only limited use as an amide transfer reagent. However, ball-milling with LiI led to quantitative formation of ( t Bu N)Li and CsI. Structural characterization shows that ( t Bu N)Li is a monomeric contact ion-pair with a relatively short N-Li bond, an unusual T-shaped coordination geometry around N and extremely short Li Me anagostic interactions. Crystal structures are compared with Li and Cs complexes of less bulky amide ligands (iPr 3 Si) 2 N − ( iPr N − ) and (Me 3 Si) 2 N − ( Me N − ). DFT calculations show trends in the geometries and electron distributions of amide ligands of increasing steric bulk ( Me N − < iPr N − < t Bu N − ) and confirm that t Bu N − is a rare example of a halogen-free weakly coordinating anion. The extremely challenging deprotonation of the amine ( t Bu 3 Si) 2 NH led to a range of s-block metal complexes with superbulky ( t Bu 3 Si) 2 N − . Depending on metal and solvent, ( t Bu 3 Si) 2 N − can be classified as a halogen-free weakly coordinating anion.
Sprache
Identifikatoren
ISSN: 2041-6520
eISSN: 2041-6539
DOI: 10.1039/d3sc06896j
Titel-ID: cdi_rsc_primary_d3sc06896j
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