2021
DOI: 10.3390/molecules26134067
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Some Novel Cobalt Diphenylphosphine Complexes: Synthesis, Characterization, and Behavior in the Polymerization of 1,3-Butadiene

Abstract: Some novel cobalt diphenylphosphine complexes were synthesized by reacting cobalt(II) chloride with (2-methoxyethyl)diphenylphosphine, (2-methoxyphenyl)diphenylphosphine, and 2-(1,1-dimethylpropyl)-6-(diphenylphosphino)pyridine. Single crystals suitable for X-ray diffraction studies were obtained for the first two complexes, and their crystal structure was determined. The novel compounds were then used in association with methylaluminoxane (MAO) for the polymerization of 1,3-butadiene, and their behavior was c… Show more

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Cited by 3 publications
(3 citation statements)
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“…Obviously, this equilibrium will be more shifted toward MAO as the MAO/Fe ratio increases, and this could account for the 1,2 content decreasing with the increasing MAO/Fe molar ratio. In our opinion, the results obtained in the polymerization of 1,3-butadiene with some cobalt phosphine complexes containing donor heteroatoms within the phosphine structure support this interpretation;…”
Section: Resultsmentioning
confidence: 71%
See 1 more Smart Citation
“…Obviously, this equilibrium will be more shifted toward MAO as the MAO/Fe ratio increases, and this could account for the 1,2 content decreasing with the increasing MAO/Fe molar ratio. In our opinion, the results obtained in the polymerization of 1,3-butadiene with some cobalt phosphine complexes containing donor heteroatoms within the phosphine structure support this interpretation;…”
Section: Resultsmentioning
confidence: 71%
“…Obviously, this equilibrium will be more shifted toward MAO as the MAO/Fe ratio increases, and this could account for the 1,2 content decreasing with the increasing MAO/Fe molar ratio. In our opinion, the results obtained in the polymerization of 1,3-butadiene with some cobalt phosphine complexes containing donor heteroatoms within the phosphine structure support this interpretation; the syndiotacticity shows a significant increase with decreasing the polymerization temperature (cfr. entries 4 and 5 in Table ), and such a behavior was not surprising because it was also detected in the polymerization of 1,3 dienes with several catalysts based on well-defined transition metal complexes with phosphorus and nitrogen ligands; the molecular weight of the resultant polymers is in general very high and the molecular weight distribution quite narrow and unimodal (1.9 < M w / M n < 3.5), suggesting a single site nature of the catalysts. …”
Section: Resultsmentioning
confidence: 71%
“…Moreover, a wide range of ligands has been designed and applied in the catalytic polymerization of conjugated dienes using late transition metal catalysts. 2,12–33…”
Section: Introductionmentioning
confidence: 99%