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Propadiene, 1,2-

This monomer will polymerize to crystalline or amorphous polymers by various coordination catalysts. Kinetic studies have been reported for polymerization initiated by rhodium complexes of the compositions. [Pg.228]

The experimental findings were as follows for polymerization conducted in ethanol solution [290]. [Pg.228]

Results were not presented in a form such that reaction rate coefficients could be calculated. [Pg.229]

Polymerization was dependent on the ability of the solvent to produce a monomolecular catalyst species, but not to form too strong a complex with the solvent. Thus polymerization occurred in ethanol but not in strong donors such as dimethyl sulphoxide or hexamethyl phosphoramide. The results were interpreted by the following mechanism  [Pg.229]

Displacement of carbon monoxide from the complexes by other ligands. [Pg.229]


L,2-propadiene, allene, CH2=C = CH2, CjH4. Colourless gas prepared by the electrolysis of potassium itaeonate, or by the action of zinc and alcohol on 1,3-dibromopropane. It is easily isomerized to propyne (methylacetyl-ene), and is produced as a mixture with this substance from some reactions. [Pg.328]

The recent discovery that propadiene can be converted into a lithio compound, which is stable enough at low temperature to allow functionalization, has made it an important starting compound for the synthesis of derivatives. A fortunate circumstance is that allene can be obtained in > 30% yield in an extremely simple... [Pg.118]

Addition of arylhydroxylamines to electrophilic allenes such as methyl propadienoate or l-methancsulfonyl-l,2-propadiene is another route to 0-vinyl derivatives[2]. The addition step is carried out by forming the salt of the hydroxylamine using NaH and the addition is catalysed with LiO CCFj. The intermediate adducts are cyclized by warming in formic acid. Yields are typically 80% or better. [Pg.70]

Cumulated dienes are those m which one carbon atom is common to two carbon-carbon double bonds The simplest cumulated diene is 1 2 propadiene also called allene and compounds of this class are generally referred to as allenes... [Pg.398]

Propadiene (H2C=C=CH2) also called allene, is the simplest cumulated diene The two tt bonds m an allene share an sp hybridized carbon and are at right angles to each other Certain allenes such as 2 3 pentadiene (CH3CH=C=CHCH3) possess a chirality axis and are chiral... [Pg.417]

The gases leaving the purification system are scmbbed with water to recover solvent and a continuous small purge of solvent gets rid of polymers. The acetylene purity resulting from this system is 99%. The main impurities in the acetylene are carbon dioxide, propadiene, and a very small amount of... [Pg.390]

The overhead of the depropanizer is sent to the propylene fractionator. The methylacetylene (MA) and propadiene (PD) are usually hydrogenated before entering the tower. An MAPD converter is similar to an acetylene converter, but operates at a lower temperature and in the Hquid phase. Due to recent advances in catalysis, the hydrogenation is performed at low temperatures (50—90°C) in trickle bed reactors (69). Ordy rarely are methylacetylene and propadiene recovered. [Pg.441]

Chemical Designations - Synonyms Allene-methylacetylene mixture MAPP gas Methylacetylene-allene mixture Propadiene-methylacetylene mixture Chemical Formula. CH3C=CH+CH2=C=CHj Ohservahle Characteristics - Physical State (as shipped) Liquefied compressed gas Color. Colorless Odor Offensive, like acetylene. [Pg.250]

One approach is to uses solvent extraction with dimethyl formamide (DMF) to remove Cj acetylene and a C, acetylene-propadiene mixture from their steam cracked ethylene and propylene streams. The simple acetylene is sold as welding gas, and the C, stream is sold as starting material for chemical synthesis. [Pg.110]


See other pages where Propadiene, 1,2- is mentioned: [Pg.1237]    [Pg.22]    [Pg.22]    [Pg.71]    [Pg.162]    [Pg.420]    [Pg.421]    [Pg.423]    [Pg.143]    [Pg.197]    [Pg.398]    [Pg.398]    [Pg.412]    [Pg.524]    [Pg.572]    [Pg.606]    [Pg.686]    [Pg.818]    [Pg.1203]    [Pg.172]    [Pg.173]    [Pg.390]    [Pg.252]    [Pg.252]    [Pg.126]    [Pg.348]    [Pg.105]    [Pg.164]    [Pg.368]    [Pg.368]    [Pg.379]    [Pg.242]    [Pg.250]    [Pg.250]    [Pg.250]    [Pg.104]    [Pg.89]    [Pg.339]    [Pg.345]    [Pg.398]   


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1,2-Propadiene, reactions

1,2-Propadienes. cycloaddition

1,3 -dicyclopropyl-1,2-propadiene

1,3-Substituted propadienes

1- -1,2-propadiene, metallation

Allene: 1,2-Propadiene

Hydrogenation of Propadiene

Methyl Acetylene-propadiene Mixture

Methylacetylene + propadiene

Methylacetylene-propadiene Mixture

Propadien

Propadien

Propadiene Compounds

Propadiene acidity

Propadiene hydrogenation

Propadiene, polymerization

Propadiene, selective hydrogenation

Propadiene-methyl acetylene

Propadienes—

Propadienes—

Propyne-propadiene mixture

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