1980
DOI: 10.1016/0014-3057(80)90052-x
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Polymerization of butadiene by polybutadienyllithium in the presence of tetrahydrofuran

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Cited by 10 publications
(8 citation statements)
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“…This should lead to the formation of the 1,2‐structure in the penultimate unit of polybutadiene. This theoretical prediction is in complete agreement with our results (Table I) and the literature data 5, 8, 16, 27, 28. In the excited singlet state, butadiene, which becomes an anion‐radical just as in the triplet state, is also closer to the C γ atom than to the terminal C α atom.…”
Section: Resultssupporting
confidence: 93%
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“…This should lead to the formation of the 1,2‐structure in the penultimate unit of polybutadiene. This theoretical prediction is in complete agreement with our results (Table I) and the literature data 5, 8, 16, 27, 28. In the excited singlet state, butadiene, which becomes an anion‐radical just as in the triplet state, is also closer to the C γ atom than to the terminal C α atom.…”
Section: Resultssupporting
confidence: 93%
“…Actually, this state does not exhibit chemical activity in contrast to the electronically excited state (on the complex) in which acts of chemical bond breaking and formation take place 1. In extensive literature on BD polymerization 5–30, such an important characteristic as the content of 1,4‐ cis, 1,4‐ trans, and 1,2 units in its chain depending on polymerization conditions and the nature of the active center (AC) is discussed. According to the data of 1 H and 13 C nuclear magnetic resonance (NMR) spectroscopy 18–23, the structure of the AC terminal unit in both hydrocarbon (HCS) and electron‐donating (EDS) solvents is similar to the π‐allyl structure in which the negative charge is distributed between C α and C γ carbon atoms (Structure 1).…”
Section: Introductionmentioning
confidence: 99%
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