Terminal tungsten pnictide complex formation through pnictaethynolate decarbonylation
Tungsten(IV) tetrakis(2,6-diisopropylphenoxide) (1) has been demonstrated to be a competent platform for decarbonylative formation of anionic terminal pnictide complexes upon treatment with pnictaethynolate anions: cyanate, 2-phosphaethynolate, and 2-arsaethynolate. These transformations constitute...
Main Authors: | Joost, Maximilian G, Transue, Wesley, Cummins, Christopher C |
---|---|
Other Authors: | Massachusetts Institute of Technology. Department of Chemistry |
Format: | Article |
Language: | en_US |
Published: |
Royal Society of Chemistry
2018
|
Online Access: | http://hdl.handle.net/1721.1/117499 https://orcid.org/0000-0001-7445-5663 https://orcid.org/0000-0003-2568-3269 |
Similar Items
-
Diazomethane umpolung atop anthracene: An electrophilic methylene transfer reagent
by: Joost, Maximilian, et al.
Published: (2020) -
An exploding N-isocyanide reagent formally composed of anthracene, dinitrogen and a carbon atom
by: Joost, Maximilian G, et al.
Published: (2018) -
Syntheses and studies of group 6 terminal pnictides, early-metal trimetaphosphate complexes, and a new bis-enamide ligand
by: Clough, Christopher Robert
Published: (2011) -
Decarbonylative Borylation of Amides by Palladium Catalysis
by: Shicheng Shi, et al.
Published: (2019-03-01) -
Phosphinidene Reactivity of a Transient Vanadium P≡N Complex
by: Courtemanche, Marc Andre, et al.
Published: (2018)