901126
trans-Bis(tribenzylphosphine)(2-methylphenyl)nickel(II) chloride
95%
Synonym(s):
trans-(PBn3)2Ni(o-tolyl)Cl
About This Item
Recommended Products
Assay
95%
form
powder or solid
reaction suitability
reaction type: Cross Couplings
reagent type: catalyst
mp
200-205 °C
SMILES string
Cl[Ni](C1=C(C)C=CC=C1)(P(CC2=CC=CC=C2)(CC3=CC=CC=C3)CC4=CC=CC=C4)P(CC5=CC=CC=C5)(CC6=CC=CC=C6)CC7=CC=CC=C7
Application
Other Notes
Legal Information
related product
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Articles
The Jamison group has developed a library of bench-stable phosphine-containing nickel(II) precatalysts that are converted into active catalysts in situ.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Related Content
Research in the Jamison group is centered on the development of new reactions and technologies for organic synthesis. Towards these themes, the group has pioneered a number of air-stable nickel precatalysts supported by phosphines and N-heterocyclic carbenes that are readily converted to the active catalyst in situ.
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