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Phenylphosphine

Index Phenylphosphine

Phenylphosphine is an organophosphorus compound with the chemical formula C6H5PH2. [1]

12 relations: Air-free technique, Allyl group, Aniline, Chemische Berichte, Coordination complex, Dichlorophenylphosphine, Grignard reaction, Journal of Polymer Science Part A, Ligand, Organophosphorus compound, Phosphinidene, Reformatsky reaction.

Air-free technique

Air-free techniques refer to a range of manipulations in the chemistry laboratory for the handling of compounds that are air-sensitive.

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Allyl group

An allyl group is a substituent with the structural formula H2C.

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Aniline

Aniline is an organic compound with the formula C6H5NH2.

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Chemische Berichte

Chemische Berichte (usually abbreviated as Ber. or Chem. Ber.) was a German-language scientific journal of all disciplines of chemistry founded in 1868.

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Coordination complex

In chemistry, a coordination complex consists of a central atom or ion, which is usually metallic and is called the coordination centre, and a surrounding array of bound molecules or ions, that are in turn known as ligands or complexing agents.

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Dichlorophenylphosphine

Dichlorophenylphosphine is an organophosphorus compound with the formula C6H5PCl2.

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Grignard reaction

The Grignard reaction (pronounced) is an organometallic chemical reaction in which alkyl, vinyl, or aryl-magnesium halides (Grignard reagents) add to a carbonyl group in an aldehyde or ketone.

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Journal of Polymer Science Part A

The Journal of Polymer Science, Part A: Polymer Chemistry is a peer-reviewed scientific journal covering polymer science.

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Ligand

In coordination chemistry, a ligand is an ion or molecule (functional group) that binds to a central metal atom to form a coordination complex.

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Organophosphorus compound

Organophosphorus compounds are organic compounds containing phosphorus.

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Phosphinidene

In chemistry phosphinidenes (IUPAC: phosphanylidenes, or in older chemistry phosphinediyls) are the phosphorus analogs of carbenes and nitrenes, having the general structure RP:.

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Reformatsky reaction

The Reformatsky reaction (sometimes spelled Reformatskii reaction) is an organic reaction which condenses aldehydes or ketones, with α-halo esters, using a metallic zinc to form β-hydroxy-esters: The organozinc reagent, also called a 'Reformatsky enolate', is prepared by treating an alpha-halo ester with zinc dust.

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Redirects here:

C6H7P, Fenylfosfin, Monophenylphosphine, Phosphaniline.

References

[1] https://en.wikipedia.org/wiki/Phenylphosphine

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