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重要文件

901116

Sigma-Aldrich

反式-双(二环己基苯基膦)(2-甲基苯基)氯化镍(II)

同義詞:

反式-(PCy2Ph)2Ni(o-甲苯基)Cl

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About This Item

經驗公式(希爾表示法):
C43H61ClNiP2
CAS號碼:
分子量::
734.04
分類程式碼代碼:
12352200

形狀

powder or solid

反應適用性

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

mp

174-179 °C

SMILES 字串

Cl[Ni](P(C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H])(C2=C([H])C([H])=C([H])C([H])=C2[H])C3([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C3([H])[H])(P(C4([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C4([H])[H])(C5=C([H])C([H])=C([H

法律資訊

专利申请 PCT/US2014/064565。经麻省理工学院许可销售。

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析證明 (COA)

Lot/Batch Number

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Recent advances in homogeneous nickel catalysis.
Tasker S Z
Nature, 509(7500), 299-299 (2014)
Simplifying nickel (0) catalysis: an air-stable nickel precatalyst for the internally selective benzylation of terminal alkenes.
Standley E A and Jamison T F
Journal of the American Chemical Society, 135(4), 1585-1592 (2013)
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.

文章

The Jamison group has developed a library of bench-stable phosphine-containing nickel(II) precatalysts that are converted into active catalysts in situ.

The Jamison group has developed a library of bench-stable phosphine-containing nickel(II) precatalysts that are converted into active catalysts in situ.

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