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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
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
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
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)
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
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
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
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
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
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
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
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
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
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
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
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)
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
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
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
fluorotelomer olefins. Fluorotelomer olefins are synthesized using a telomerization of tetrafluoroethylene taxogens (monomers), followed by an ethylene
Surflon_S-111
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
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
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
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Son of saint, Lord of earth
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