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Author

D. Dodd

Bio: D. Dodd is an academic researcher. The author has contributed to research in topics: Cobalt. The author has an hindex of 1, co-authored 1 publications receiving 147 citations.
Topics: Cobalt

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Journal ArticleDOI
TL;DR: In this paper, a synthese presentant les structures cristallines et moleculaires de molecules contenant la moitie Co(DH) 2, ou DH est le monoanion de la dimethylglyoxime.

326 citations

Journal ArticleDOI
TL;DR: In this paper, the authors summarized the advances in understanding and synthetic scope of CMRP since its discovery and discussed the cobalt-carbon bond formation by dual contribution of reversible termination and degenerative chain transfer, as well as the impact of additives able to coordinate the metal.

323 citations

Journal ArticleDOI
TL;DR: It is proposed that the polymerization is controlled by the reversible homolytic cleavage of an organocobalt(III) dormant species in the presence of ED and the faster polymerization after the induction period in the absence of ED is due to a degenerative transfer process with the radicals produced by the continuous decomposition of the excess initiator.
Abstract: The molecular structure of bis(acetylacetonate)cobalt(II) ([Co-(acac) 2 ]) in solution and in the presence of the electron donors (ED) pyridine (py), NEt 3 , and vinyl acetate (VOAc) was investigated using 1 HNMR spectroscopy in C 6 D 6 . The extent of formation of ligand adducts, [Co(acac) 2 (ED) x ], varies in the order py > NEt 3 > VOAc (no interaction). Density functional theory (DFT) calculations on a model system agree with Co-ED bond strengths decreasing in the same order. The effect of electron donors on the [Co(acac) 2 ]-mediated radical polymerization of VOAc was examined at 30°C by the addition of excess py or NEt 3 to the complex in the molar ratio [VOAc] 0 /[Co] 0 /[V-70] 0 / [py or NEt 3 ] 0 =500:1:1:30 (V-70=2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile)). As previously reported by R. Jerome et al., the polymerization showed long induction periods in the absence of ED. However, a controlled polymerization without an induction period took place in the presence of ED, though the level of control was poorer. The effective polymerization rate decreased in the order py> NEt 3 . A similar behavior was found when these electron donors were added to an ongoing [Co(acac) 2 ]-mediated radical polymerization of VOAc. On the basis of the NMR and DFT studies, it is proposed that the polymerization is controlled by the reversible homolytic cleavage of an organocobalt(III) dormant species in the presence of ED. Conversely, the faster polymerization after the induction period in the absence of ED is due to a degenerative transfer process with the radicals produced by the continuous decomposition of the excess initiator. Complementary experiments provide additional results in agreement with this interpretation.

133 citations

Book
20 Nov 2012

123 citations