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TELOMERIZATION

Telomerization

Chemical reaction producing oligomers with two distinct end groups

(synthesis) Telomerization (dimerization) IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025). Online version: (2006–) "telomerization".

Telomerization

Oligomer

Molecule composed of copies of a small unit

macromolecular complexes through a finite degree of polymerization. Telomerization is an oligomerization carried out under conditions that result in chain

Oligomer

Fluorotelomer

Fluorinated oligomer of limited size produced by radical polymerization reaction

Fluorotelomers are fluorocarbon-based oligomers, or telomers, synthesized by telomerization. Some fluorotelomers and fluorotelomer-based compounds are a source

Fluorotelomer

Telomerization (dimerization)

The telomerization is the linear dimerization of 1,3-dienes with simultaneous addition of a nucleophile in a catalytic reaction. The reaction was independently

Telomerization (dimerization)

Telomerization_(dimerization)

6:2-Fluorotelomersulfonic acid

Chemical compound

also called H4PFOS. 6:2-Fluorotelomersulfonic acid is produced via telomerization. In addition, it is also formed, for example, from some perfluorocarboxybetaines

6:2-Fluorotelomersulfonic acid

6:2-Fluorotelomersulfonic_acid

Telomer

Topics referred to by the same term

Telomer may refer to: telomerization, in polymer science, which results in an extremely small polymer—one whose degree of polymerization is generally between

Telomer

Benzimidazole

Chemical compound

Frisch; M. Beller; D. Rottger; M. Malaun; B. Bildstein (2002). "Efficient telomerization of 1,3-butadiene with alcohols in the presence of in situ generated

Benzimidazole

Perfluorooctanoic acid

Perfluorinated carboxylic acid

acids. The telomerization synthesis of PFOA was pioneered by DuPont, and is not well suited to the laboratory. PFOA formed by telomerization is completely

Perfluorooctanoic acid

Perfluorooctanoic_acid

Butadiene

Chemical compound

Butadiene is also a precursor to 1-octene via palladium-catalyzed telomerization with methanol. This reaction produces 1-methoxy-2,7-octadiene as an

Butadiene

1-Octene

Chemical compound

aromatic hydrocarbons. Another route to 1-octene involves butadiene telomerization of butadiene. This technology was commercialized by Dow in a facility

1-Octene

Carboalkoxylation

Process for converting alkenes to esters

and adhesives. Carboalkoxylation has been incorporated into various telomerization schemes. For example carboalkoxylation has been coupled with the dimerization

Carboalkoxylation

Fisher-Porter tube

Glass pressure vessel

Kunihiko Takabe; Takashi Yamada; Takao Katagiri; Juntaro Tanaka (1989). "Telomerization of Isoprene with Dialkylamine: N,N-Diethylnerylamine". Org. Synth. 67:

Fisher-Porter tube

Fisher-Porter_tube

Yves Chauvin

French chemist and Nobel Prize laureate

(1971). "Catalysis of olefin transformations by tungsten complexes. II. Telomerization of cyclic olefins in the presence of acyclic olefins". Makromol. Chem

Yves Chauvin

Yves_Chauvin

Surflon S-111

fluorotelomer olefins. Fluorotelomer olefins are synthesized using a telomerization of tetrafluoroethylene taxogens (monomers), followed by an ethylene

Surflon S-111

Surflon_S-111

Free-radical addition

Organic addition reaction which involves free radicals

they catalyze polymerization instead. In thermal silane additions, telomerization usually proceeds to about 6 units. In the case of silicon, germanium

Free-radical addition

Free-radical_addition

Alexander Nesmeyanov

Soviet chemist and academician

field of radical telomerization and rearrangement radicals. In addition to studies of already known reactions, thermal telomerization of ethylene and propylene

Alexander Nesmeyanov

Alexander_Nesmeyanov

Perfluorodecanoic acid

Chemical compound

main synthesis road for perfluorodecanoic acid used commercially is telomerization. Since PFDA has an even number of carbons, the starting material should

Perfluorodecanoic acid

Perfluorodecanoic_acid

TPPTS

Chemical compound

Rhône-Poulenc process. hydrocyanation of olefins and dienes with Ni(0) TPPTS. telomerization of butadiene to 2.7 octadiene -1-ol with Pd(0) TPPTS. The Rh(I) TPPTS

TPPTS

Silacyclobutane

Chemical compound

ISSN 0366-7022. Nametkin, N. S.; Vdovin, V. M.; Grinberg, P. L. (June 1964). "Telomerization of silicacyclobutanes". Bulletin of the Academy of Sciences, USSR Division

Silacyclobutane

Radical polymerization

Polymerization process involving free radicals as repeating units

small polymers are formed with chain lengths of 2-5 repeating units (telomerization). The Mayo equation estimates the influence of chain transfer on chain

Radical polymerization

Radical_polymerization

Telomere (disambiguation)

Topics referred to by the same term

resolvase, an enzyme found in bacteria which contain linear plasmids. Telomerization This disambiguation page lists articles associated with the title Telomere

Telomere (disambiguation)

Telomere_(disambiguation)

1,1,1,3,3,3-Hexachloropropane

Chloroalkane

1021/ci960024i Teruzo Asahara, Manabu Senō, and Cheng-Ching Wu (1969): "Telomerization of ethylene with carbon tetrachloride initiated by amine-cupric chloride

1,1,1,3,3,3-Hexachloropropane

Thermoresponsive polymers in chromatography

methacrylate copolymer). The polymers were synthesized using radical telomerization with varying BMA content. Where pure PNIPAAm was unable to resolve hydrophobic

Thermoresponsive polymers in chromatography

Thermoresponsive_polymers_in_chromatography