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Pentakis trimethyl phosphite nickel II Bis tetraphenylborate

The reaction is carried out at room temperature in a hood. A 500-mL filter flask is equipped with a stirring bar coated with Teflon, and a slow stream of [Pg.76]

The yellow powder is fairly stable in air, but solutions are less stable. The compound is soluble in acetone and dichloromethane, insoluble in hydrocarbons, tetrahydrofuran and alcohols. The complex displays a 31P 1H nmr spectrum that is a single line in fast exchange and an A2B3 spin system in slow exchange.48 [Pg.77]

PdCl2 + 5P(OCH3)3 + 2Na[BPh4]---- [Pd[P(OCH3)3]s] [BPhJj +2 NaCl [Pg.77]

The platinum complex is reasonably air stable, but the palladium complex is moderately air sensitive, turning to a black powder overnight if stored in air. Their solubilities are similar to those of the nickel analogue. There is a tendency for both the palladium and platinum complexes to lose a phosphite ligand on recrystallization. [Pg.78]

Recrystallization in the presence of a slight excess of phosphite can make purification more straightforward. [Pg.78]


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2.3.4.5.6- pentakis

Bis ]nickel

Bis tetraphenylborate

Bis- phosphite

II) Tetraphenylborate

Nickel pentakis

Nickel(II)

Tetraphenylborate

Tetraphenylborates

Trimethyl phosphite

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