Examples of 'triphenylphosphine' in a sentence

Meaning of "triphenylphosphine"

'Triphenylphosphine' is a noun referring to a type of organophosphorus compound in chemistry, often used as a ligand in coordination chemistry
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  • The aromatic compound (C₆H₅)₃P, that is used in the synthesis of organic and organometallic compounds

How to use "triphenylphosphine" in a sentence

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triphenylphosphine
The triphenylphosphine oxide precipitate is removed by filtration.
Examples of appropriate reactants are triphenylphosphine and tributylphosphine.
Triphenylphosphine can be obtained as a commercially available product.
The product was contaminated with some triphenylphosphine.
In this case triphenylphosphine on solid support was used.
Most preferably the phosphine ligand is triphenylphosphine.
The triphenylphosphine oxide is filtered off.
The product was isolated with residual triphenylphosphine.
By the reaction of triphenylphosphine and carbontetrabromide.
The phosphine may be a trialkylphosphine or a triarylphosphine such as triphenylphosphine.
Phosphine and phosphoramide include triphenylphosphine and hexamethylphosphoramide.
The triphenylphosphine oxide was filtered off.
Acetonitrile was added until some triphenylphosphine oxide was precipitated.
It is advantageous to use a phosphine and more particularly triphenylphosphine.
The solid triphenylphosphine oxide so formed was filtered off.

See also

Suitable phosphine derivatives include triphenylphosphine and tributylphosphine.
Additional triphenylphosphine was added until the solution became colorless.
Preferably equimolar amounts of triphenylphosphine and bromine are used.
The triorganophosphine compound used as the catalyst is triphenylphosphine.
A single crystal of triphenylphosphine oxide was added.
Triethylamine and of a triarylphosphine such as triphenylphosphine.
The majority of triphenylphosphine oxide was crystallized by the addition of heptane.
Examples of phosphine reagents include triphenylphosphine and tributylphosphine.
Additional triphenylphosphine was added until the yellow color disappeared.
Bismaleimides are generally catalyzed with triphenylphosphine and imidazoles.
The triphenylphosphine complexes are preferred.
The currently preferred phosphine oxide is triphenylphosphine oxide.
The solution is chilled and triphenylphosphine followed by carbontetrabromide are added.
The organophosphorus compounds are exemplified by triphenylphosphine.
The triphenylphosphine oxide was filtered off and is concentrated in vacuo.
Reducing agents include sulfur dioxide and triphenylphosphine.
Particular mention is made of triphenylphosphine oxide and methyldiphenylphosphine oxide.
The product was contaminated by some triphenylphosphine.
A small amount of additional triphenylphosphine was added to clear the solution.
The trisubstitiuted phosphine is preferably triphenylphosphine.
Triphenylphosphine dichloride is usually prepared fresh by the addition of chlorine to triphenylphosphine.
Suitable trialkylphosphines are tributylphosphine and triphenylphosphine.
Tetrakis triphenylphosphine palladium.
A preferred unsupported triorganophosphine oxide catalyst is triphenylphosphine oxide.
Triphenylphosphine is particularly preferred.
The phosphine is for example triphenylphosphine.
Preferably triphenylphosphine is used because this compound is generally readily available.
Suitable reducing agents include triphenylphosphine.
Filtered off triphenylphosphine oxide precipitate and concentrated filtrate to an oil.
Among the most preferred materials are triphenylphosphine and triphenylphosphite.
Via an iodation reaction followed by nucleophilic substitution with triphenylphosphine.
Peroxides were determined by adding a triphenylphosphine solution in acetone to the reaction sample.
The preferable catalyst among these is palladium acetate or triphenylphosphine.
The solution was seeded with triphenylphosphine oxide and cooled in ice.
Preferred dehydrating agent is diethyl azocarboxylate in combination with triphenylphosphine.

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