901169
trans-Bis(methyldiphenylphosphine)(2-methylphenyl)nickel(II) chloride
Synonym(s):
trans-(PPh2Me)2Ni(o-tolyl)Cl
About This Item
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form
powder or solid
reaction suitability
core: nickel
reaction type: Cross Couplings
reagent type: catalyst
mp
152-157 °C
SMILES string
Cl[Ni](PC([H])([H])[H])(P(C1=C([H])C([H])=C([H])C([H])=C1[H])(C2=C([H])C([H])=C([H])C([H])=C2[H])C([H])([H])[H])C3=C(C([H])([H])[H])C([H])=C([H])C([H])=C3[H].[H]C4=C(C5=C([H])C([H])=C([H])C([H])=C5[H])C([H])=C([H])C([H])=C4[H]
Application
Other Notes
Legal Information
related product
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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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.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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