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901165

Sigma-Aldrich

trans-Bis(tricyclohexylphosphine)(2-methylphenyl)nickel(II) chloride

≥95%

Sinônimo(s):

trans-(PCy3)2Ni(o-tolyl)Cl

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About This Item

Fórmula empírica (Notação de Hill):
C43H73ClNiP2
Número CAS:
Peso molecular:
746.13
Código UNSPSC:
12352200

Ensaio

≥95%

forma

powder or solid

adequação da reação

core: nickel
reaction type: Cross Couplings
reagent type: catalyst

pf

>300 °C

cadeia de caracteres SMILES

Cl[Ni](C1=C(C)C=CC=C1)(P(C2CCCCC2)(C3CCCCC3)C4CCCCC4)P(C5CCCCC5)(C6CCCCC6)C7CCCCC7

Aplicação

The following Ni-complex is an air-stable precatalyst for various Ni-catalyzed reactions which normally require Ni(cod)2, however, this precatalyst will not require any glovebox or schlenk techniques that must be followed with Ni(cod)2. Rates are enhanced and selectivity is maintained when compared to the same reaction with Ni(cod)2.

Informações legais

Patent application PCT/US2014/064565. Sold under license from the Massachusetts Institute of Technology.

Código de classe de armazenamento

4.1B - Flammable solid hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Recent advances in homogeneous nickel catalysis.
Tasker S Z, et al.
Nature, 509(7500), 299-299 (2014)
Sarah Z Tasker et al.
Nature, 509(7500), 299-309 (2014-05-16)
Tremendous advances have been made in nickel catalysis over the past decade. Several key properties of nickel, such as facile oxidative addition and ready access to multiple oxidation states, have allowed the development of a broad range of innovative reactions.

Artigos

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.

Conteúdo relacionado

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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