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Triphenylphosphine

Index Triphenylphosphine

Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C6H5)3 - often abbreviated to PPh3 or Ph3P. [1]

79 relations: Alcohol, Aldehyde, Alkene, Alkyne, Amine oxide, Ammonium chloride, Aromatic sulfonation, Azide, Benzene, Carbon monoxide, Chlorobenzene, Chlorodiphenylphosphine, Diethyl ether, Diisopropyl azodicarboxylate, Dimethyl sulfide, Dimethyl sulfoxide, Diphenylphosphine, Ethanol, Geoffrey Wilkinson, Haloalkane, Heck reaction, Homogeneous catalysis, Hydroformylation, Inorganic Syntheses, Isopropyl alcohol, Ketone, Ligand cone angle, Lithium, Lithium diphenylphosphide, Menshutkin reaction, Methyl iodide, Organic compound, Organic synthesis, Organometallic chemistry, Organometallics, Organophosphorus compound, Oxidative addition, Ozonide, Phenyl group, Phenyllithium, Phenylmagnesium bromide, Phosphine, Phosphonium, Phosphorus, Phosphorus trichloride, Phosphorus-31 nuclear magnetic resonance, Polysulfide, Potassium selenocyanate, Reagent, Recrystallization (chemistry), ..., Relative permittivity, Selenium, Staudinger reaction, Stryker's reagent, Sulfur, Suzuki reaction, Tetrahydrofuran, Tetrakis(triphenylphosphine)palladium(0), Thioether, Thiol, TPPTS, Transition metal, Transition metal hydride, Trimethylphosphine, Triphenylamine, Triphenylarsine, Triphenylphosphine dichloride, Triphenylphosphine oxide, Triphenylphosphine phenylimide, Triphenylphosphine selenide, Triphenylphosphine sulfide, Triplet state, Vaska's complex, Walter Reppe, Wilkinson's catalyst, Wittig reaction, Ylide, 1,2-Bis(diphenylphosphino)ethane, 1,2-Dibromoethane. Expand index (29 more) »

Alcohol

In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a carbon.

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Aldehyde

An aldehyde or alkanal is an organic compound containing a functional group with the structure −CHO, consisting of a carbonyl center (a carbon double-bonded to oxygen) with the carbon atom also bonded to hydrogen and to an R group, which is any generic alkyl or side chain.

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Alkene

In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.

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Alkyne

In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond.

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Amine oxide

An amine oxide, also known as amine-N-oxide and N-oxide, is a chemical compound that contains the functional group R3N+−O−, an N−O coordinate covalent bond with three additional hydrogen and/or hydrocarbon side chains attached to N. Sometimes it is written as R3N→O or, wrongly, as R3N.

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Ammonium chloride

Ammonium chloride is an inorganic compound with the formula NH4Cl and a white crystalline salt that is highly soluble in water.

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Aromatic sulfonation

Aromatic sulfonation is an organic reaction in which a hydrogen atom on an arene is replaced by a sulfonic acid functional group in an electrophilic aromatic substitution.

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Azide

Azide is the anion with the formula N. It is the conjugate base of hydrazoic acid (HN3).

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Benzene

Benzene is an important organic chemical compound with the chemical formula C6H6.

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Carbon monoxide

Carbon monoxide (CO) is a colorless, odorless, and tasteless gas that is slightly less dense than air.

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Chlorobenzene

Chlorobenzene is an aromatic organic compound with the chemical formula C6H5Cl.

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Chlorodiphenylphosphine

Chlorodiphenylphosphine is an organophosphorus compound with the formula (C6H5)2PCl, abbreviated Ph2PCl.

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Diethyl ether

Diethyl ether, or simply ether, is an organic compound in the ether class with the formula, sometimes abbreviated as (see Pseudoelement symbols).

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Diisopropyl azodicarboxylate

Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid.

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Dimethyl sulfide

Dimethyl sulfide (DMS) or methylthiomethane is an organosulfur compound with the formula (CH3)2S.

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Dimethyl sulfoxide

Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH3)2SO.

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Diphenylphosphine

Diphenylphosphine, also known as diphenylphosphane, is an organophosphorus compound with the formula (C6H5)2PH.

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Ethanol

Ethanol, also called alcohol, ethyl alcohol, grain alcohol, and drinking alcohol, is a chemical compound, a simple alcohol with the chemical formula.

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Geoffrey Wilkinson

Sir Geoffrey Wilkinson FRS (14 July 1921 – 26 September 1996) was a Nobel laureate English chemist who pioneered inorganic chemistry and homogeneous transition metal catalysis.

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Haloalkane

The haloalkanes (also known as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens.

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Heck reaction

The Heck reaction (also called the Mizoroki-Heck reaction) is the chemical reaction of an unsaturated halide (or triflate) with an alkene in the presence of a base and a palladium catalyst (or palladium nanomaterial-based catalyst) to form a substituted alkene.

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Homogeneous catalysis

In chemistry, homogeneous catalysis is catalysis in a solution by a soluble catalyst.

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Hydroformylation

Hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes from alkenes.

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Inorganic Syntheses

Inorganic Syntheses is a book series which aims to publish "detailed and foolproof" procedures for the synthesis of inorganic compounds.

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Isopropyl alcohol

Isopropyl alcohol (IUPAC name propan-2-ol; commonly called isopropanol) is a compound with the chemical formula C3H8O.

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Ketone

In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.

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Ligand cone angle

thumb The ligand cone angle (a common example being the Tolman cone angle or θ) is a measure of the size of a ligand.

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Lithium

Lithium (from lit) is a chemical element with symbol Li and atomic number 3.

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Lithium diphenylphosphide

Lithium diphenylphosphide contains lithium and the organophosphorus anion with the formula (C6H5)2Li.

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Menshutkin reaction

In organic chemistry, the Menshutkin reaction converts a tertiary amine into a quaternary ammonium salt by reaction with an alkyl halide.

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Methyl iodide

Methyl iodide, also called iodomethane, and commonly abbreviated "MeI", is the chemical compound with the formula CH3I.

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Organic compound

In chemistry, an organic compound is generally any chemical compound that contains carbon.

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Organic synthesis

Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.

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Organometallic chemistry

Organometallic chemistry is the study of organometallic compounds, chemical compounds containing at least one chemical bond between a carbon atom of an organic molecule and a metal, including alkaline, alkaline earth, and transition metals, and sometimes broadened to include metalloids like boron, silicon, and tin, as well.

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Organometallics

Organometallics is a biweekly journal published by the American Chemical Society.

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Organophosphorus compound

Organophosphorus compounds are organic compounds containing phosphorus.

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Oxidative addition

Oxidative addition and reductive elimination are two important and related classes of reactions in organometallic chemistry.

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Ozonide

Ozonide is the unstable, reactive polyatomic anion analog of ozone or any of several classes of organic organic peroxide compounds similar formed by the reaction of ozone with an unsaturated compound.

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Phenyl group

In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C6H5.

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Phenyllithium

Phenyllithium or lithobenzene is an organometallic agent with the empirical formula C6H5Li.

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Phenylmagnesium bromide

Phenylmagnesium bromide, with the simplified formula, is a magnesium-containing organometallic compound.

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Phosphine

Phosphine (IUPAC name: phosphane) is the compound with the chemical formula PH3.

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Phosphonium

The phosphonium (more obscurely: phosphinium) cation describes polyatomic cations with the chemical formula.

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Phosphorus

Phosphorus is a chemical element with symbol P and atomic number 15.

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Phosphorus trichloride

Phosphorus trichloride is a chemical compound of phosphorus and chlorine, having the chemical formula PCl3.

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Phosphorus-31 nuclear magnetic resonance

Phosphorus-31 NMR spectroscopy is an analytical chemistry technique that uses nuclear magnetic resonance (NMR) to study chemical compounds that contain phosphorus.

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Polysulfide

Polysulfides are a class of chemical compounds containing chains of sulfur atoms.

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Potassium selenocyanate

Potassium selenocyanate is the inorganic compound with the formula KSeCN.

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Reagent

A reagent is a substance or compound added to a system to cause a chemical reaction, or added to test if a reaction occurs.

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Recrystallization (chemistry)

In chemistry, recrystallization is a technique used to purify chemicals.

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Relative permittivity

The relative permittivity of a material is its (absolute) permittivity expressed as a ratio relative to the permittivity of vacuum.

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Selenium

Selenium is a chemical element with symbol Se and atomic number 34.

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Staudinger reaction

The Staudinger reaction is a chemical reaction of an azide with a phosphine or phosphite produces an iminophosphorane.

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Stryker's reagent

Stryker's reagent (6), also known as the Osborn complex, is a hexameric copper hydride ligated with triphenylphosphine.

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Sulfur

Sulfur or sulphur is a chemical element with symbol S and atomic number 16.

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Suzuki reaction

The Suzuki reaction is an organic reaction, classified as a coupling reaction, where the coupling partners are a boronic acid and an organohalide catalyzed by a palladium(0) complex.

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Tetrahydrofuran

Tetrahydrofuran (THF) is an organic compound with the formula (CH2)4O.

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Tetrakis(triphenylphosphine)palladium(0)

Tetrakis(triphenylphosphine)palladium(0) (sometimes called quatrotriphenylphosphine) is the chemical compound Pd4, often abbreviated Pd(PPh3)4, or rarely PdP4.

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Thioether

A thioether is a functional group in organosulfur chemistry with the connectivity C–S–C as shown on right.

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Thiol

Thiol is an organosulfur compound that contains a carbon-bonded sulfhydryl (R–SH) group (where R represents an alkyl or other organic substituent).

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TPPTS

3,3′,3″-Phosphanetriyltris(benzenesulfonic acid) trisodium salt (abbreviated TPPTS when isolated and tppts as a ligand), is an organic compound that is also known as sodium triphenylphosphine trisulfonate.

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Transition metal

In chemistry, the term transition metal (or transition element) has three possible meanings.

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Transition metal hydride

Transition metal hydrides are chemical compounds containing a transition metal bonded to hydrogen.

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Trimethylphosphine

Trimethylphosphine is the organophosphorus compound with the formula P(CH3)3, commonly abbreviated as PMe3.

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Triphenylamine

Triphenylamine is an organic compound with formula (C6H5)3N.

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Triphenylarsine

Triphenylarsine is the chemical compound with the formula As(C6H5)3.

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Triphenylphosphine dichloride

Triphenylphosphine dichloride, Ph3PCl2, is a chlorinating agent widely used in organic chemistry.

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Triphenylphosphine oxide

Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C6H5)3, also written as Ph3PO or PPh3O (Ph.

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Triphenylphosphine phenylimide

Triphenylphosphine phenylimide is the organophosphorus compound with the formula Ph3P.

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Triphenylphosphine selenide

Triphenylphosphine selenide is a organophosphorus compound with the formula (C6H5)3PSe.

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Triphenylphosphine sulfide

Triphenylphosphine sulfide (IUPAC name: triphenyl-λ5-phosphanethione) is the organophosphorus compound with the formula (C6H5)3PS, usually written Ph3PS (where Ph.

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Triplet state

In quantum mechanics, a triplet is a quantum state of a system with a spin of quantum number s.

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Vaska's complex

Vaska's complex is the trivial name for the chemical compound trans-carbonylchlorobis(triphenylphosphine)iridium(I), which has the formula IrCl(CO)2.

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Walter Reppe

Walter Julius Reppe (29 July 1892 in Göringen – 26 July 1969 in Heidelberg) was a German chemist.

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Wilkinson's catalyst

Wilkinson's catalyst, is the common name for chloridotris(triphenylphosphane)rhodium(I), a coordination complex of rhodium with the formula RhCl(PPh3)3 (Ph.

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Wittig reaction

The Wittig reaction or Wittig olefination is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide.

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Ylide

A ylide or ylid is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached to a heteroatom with a formal positive charge (usually nitrogen, phosphorus or sulfur), and in which both atoms have full octets of electrons.

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1,2-Bis(diphenylphosphino)ethane

1,2-Bis(diphenylphosphino)ethane (dppe) is an organophosphorus compound with the formula (Ph2PCH2)2 (Ph.

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1,2-Dibromoethane

1,2-Dibromoethane, also known as ethylene dibromide (EDB), is the organobromine compound with the chemical formula (CH2Br)2.

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Redirects here:

C18H15P, PPh3, Ph3P, Triphenyl phosphine, Triphenylphosphane.

References

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

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