A σ-Donor with a Planar Six-π-Electron B2N2C2 Framework: Anionic N-Heterocyclic Carbene or Heterocyclic Terphenyl Anion?
Forster, T., Krahulic, K., Tuononen, H., McDonald, R., Parvez, M., & Roesler, R. (2006). A σ-Donor with a Planar Six-π-Electron B2N2C2 Framework: Anionic N-Heterocyclic Carbene or Heterocyclic Terphenyl Anion?. Angewandte Chemie, International Edition, 45(38), 6356-6359. https://doi.org/10.1002/anie.200601229
Julkaistu sarjassa
Angewandte Chemie, International EditionPäivämäärä
2006Tekijänoikeudet
© 2006 Wiley-VCH Verlag GmbH & Co. This is a final draft version of an article whose final and definitive form has been published by Wiley. Published in this repository with the kind permission of the publisher.
NB! The anionic ligand 2 was synthesized through deprotonation of a planar, formally zwitterionic diazadiborine precursor, isolated as a lithium salt, and structurally characterized. According to experimental evidence and theoretical calculations, 2 can be considered as an intermediate between two classical classes of ligands: N-heterocyclic carbenes 1 and terphenyls 3.
Julkaisija
WileyISSN Hae Julkaisufoorumista
1433-7851Julkaisu tutkimustietojärjestelmässä
https://converis.jyu.fi/converis/portal/detail/Publication/16479167