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Synthesis from nonconjugated polymers

A. Synthesis and Properties of Polymers from Nonconjugated Diynes. 983... [Pg.946]

Ho, S. C. H. Wu, M. M. Xiong, Y. Novel cyclopolymerization polymers from nonconjugated dienes and 1-alkenes. PCT International Patent Application WO 95/06669 (Mobil Oil Corp.), March 9,1995. Hustad, P. D. Coates, G W. Insertion/isomerization polymerization of 1,5-hexadiene synthesis of functional propylene copolymers and block copolymers. J. Am. Chem. Soc. 2062,124, 11578-11579. Hustad, P. D. Tian, J. Coates, G. W. Mechanism of propylene insertion using bis(phenoxyimine)-based titanium catalysts an unusual secondary insertion of propylene in a group IV catalyst system. J. Am. Chem. Soc. 2002,124,3614-3621. [Pg.506]

Figure 13 shows the irreversible conversion of a nonconjugated poly (p-phenylene pentadienylene) to a lithiun-doped conjugated derivative which has a semiconducting level of conductivity (0.1 to 1.0 S/cm) (29). Obviously, the neutral conjugated derivative of poly (p-phenylene pentadienylene) can then be reversibly generated from the n-type doped material by electrochemical undoping or by p-type compensation. A very similar synthetic method for the conversion of poly(acetylene-co-1,3-butadiene) to polyacetylene has been reported (30), Figure 14. This synthesis of polyacetylene from a nonconjugated precursor polymer containing isolated CH2 units in an otherwise conjugated chain is to be contrasted with the early approach of Marvel et al (6) in which an all-sp3 carbon chain was employed. Figure 13 shows the irreversible conversion of a nonconjugated poly (p-phenylene pentadienylene) to a lithiun-doped conjugated derivative which has a semiconducting level of conductivity (0.1 to 1.0 S/cm) (29). Obviously, the neutral conjugated derivative of poly (p-phenylene pentadienylene) can then be reversibly generated from the n-type doped material by electrochemical undoping or by p-type compensation. A very similar synthetic method for the conversion of poly(acetylene-co-1,3-butadiene) to polyacetylene has been reported (30), Figure 14. This synthesis of polyacetylene from a nonconjugated precursor polymer containing isolated CH2 units in an otherwise conjugated chain is to be contrasted with the early approach of Marvel et al (6) in which an all-sp3 carbon chain was employed.

See other pages where Synthesis from nonconjugated polymers is mentioned: [Pg.194]    [Pg.42]    [Pg.143]    [Pg.73]    [Pg.42]    [Pg.444]    [Pg.447]    [Pg.64]    [Pg.693]    [Pg.79]    [Pg.79]    [Pg.947]    [Pg.79]    [Pg.624]    [Pg.4226]    [Pg.497]    [Pg.339]    [Pg.1366]    [Pg.952]   
See also in sourсe #XX -- [ Pg.444 ]




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Polymers nonconjugated

Synthesis from nonconjugated

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