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Mikami, K.; Matsumoto, Y.; Shiono, T., Science of Synthesis, (2003) 2, 553.
Titanacyclobutane 221 exists in equilibrium with carbene 213, which catalyzes ring-opening metathesis polymerization of norbornene at 65°C to give a monodispersed polymer 234 (Mn = 10400, Mw/Mn = 1.13) via compound 233, (Scheme 112).[340] Thermolysis of 222 at 20°C in the presence of norbornene affords the trisubstituted titanacyclobutane 235, which also gives living polynorbornene 236 at 65°C (Mn = 10450, Mw/Mn = 1.09) (Scheme 112). The more highly substituted 235 is more reactive than 221 in the initiation reaction and thus affords a polymer with narrower polydispersity. The initiation efficiencies of 221 and 235 are the same and as high as 87%.
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References
[335] | Meeeee, M. M.; Meeeeeeee, M., M. Meee. Mee., Meee. Meeeee., (8888), 888. |
[340] | Meeeeee, M. M.; Meeeee, M. M., M. Me. Meee. Mee., (8888) 888, 888. |
[348] | Meeeeeee, M. M.; Meeeee, M. M., Meeeeeeeeeeeee, (8888) 88, 8888. |
[349] | Meeeee, M. M.; Meeee, M., Meeeeee (Meeeeeeeee, M. M.), (8888) 888, 888. |
[350] | Meeeeeee, M. M.; Meeeee, M. M., Meeeeeeeeeeeee, (8888) 88, 888. |
[351] | Meeee, M.; Meeeee, M. M., Meeeeeeeeeeeee, (8888) 88, 8888. |
[352] | Meeee, M.; Meeeee, M. M., Meeeeeeeeeeeee, (8888) 88, 8888. |
Meeeeee Meeeeeeeeee
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- 8.Meeeee-Meee, (8888) M 88-8, 888.