Communications 2-Fluoro-5-[trans-4-(fmns-4"-pentylcyclohexyl)-cyclohexyl]pyrimidine CCM-5-F: 2-Dimethylamino-5-[tru~,~-4'-(trun.~-4"-pentylcyclohexyl)-cyclohexyllpyrimidine (30.2 g, 85 mmol) was dissolved in 300 ml toluene and at 0 "C methyltrifluoromethylsulfonate (16.4 g, 100 mmol) in 40 ml of tol
The mechanism of initiation in the free radical polymerization of N-vinylcarbazole and N-vinylpyrrolidone
β Scribed by S. Bottle; W.K. Busfield; I.D. Jenkins; S. Thang; E. Rizzardo; D.H. Solomon
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 359 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
The reactions of N-vinylcarbazole and of N-vinylpyrrolidone with benzoyl peroxide and with di-t-butyl peroxalate in the presence of the nitroxide scavenger l,l,3,3-tetramethyl-l,3-dihydroisoindol-2yloxyl are reported. Use of di-t-butyl peroxalate leads to the expected radical intermediates which are efficiently scavenged by the nitroxide. When benzoyl peroxide is used as initiator however, both ionic and radical processes are involved. The importance of electron-transfer processes is discussed.
π SIMILAR VOLUMES
Two possible crosslinking mechanisms of PNVF gels. Scheme 1. Polymerization of NVF and hydrolysis of PNVF to PVAm.
In order to obtain more detailed information on the mechanism of the polymerization of N-vinylcarbazole (N-VC) in the presence of carbon black, a comparison of the rates of conversion under various conditions was made and the following results were obtained. The phenolic hydroxyl groups on the surfa
The polymerization of a mixture of N-vinylcarbazole (NVC) and pyrrole (PY) by 0-chloranil in toluene yields an insoluble black polymer P(PY-NVC) which exhibits properties distinct from PPY or PNVC. The inclusion of either monomer moieties in P(PY-NVC) has been endorsed by IR spectroscopy. Kinetics o
Conductimetry was used for monitoring the radical polymerization of a weak electrolyte (acrylic acid) in aqueous solution and for determination of the kinetic parameters of the reaction (reaction order with respect to monomer, activation energy). The results obtained were consistent with those deter