2000
DOI: 10.1002/1099-0518(20000701)38:13<2293::aid-pola10>3.0.co;2-m
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Addition polymers of aldehydes

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Cited by 49 publications
(37 citation statements)
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“…1(B)]. In contrast, the amount of copolymers increased with FeCl 3 and GaCl 3 . GaCl 3 showed the highest catalytic activity among the three metal halides for copolymerization, reaching 70% monomer conversion in 1 h [ Fig.…”
Section: Copolymerization Of Bza With Ibve Using Various Lewis Acidsmentioning
confidence: 90%
See 1 more Smart Citation
“…1(B)]. In contrast, the amount of copolymers increased with FeCl 3 and GaCl 3 . GaCl 3 showed the highest catalytic activity among the three metal halides for copolymerization, reaching 70% monomer conversion in 1 h [ Fig.…”
Section: Copolymerization Of Bza With Ibve Using Various Lewis Acidsmentioning
confidence: 90%
“…Such well-controlled reaction has not been achieved using other initiators (cationogens) including an adduct of IBVE with acetic acid and a trimethylsilyl iodide, even when combined with GaCl 3 . The better control with EtSO 3 H/GaCl 3 is likely attributed to rapid addition of EtSO 3 H with IBVE 42 and subsequent efficient ionization of the resulting adduct by GaCl 3 . 43 The efficient initiation from vinyl ether cations is most likely to promote copolymerization, as discussed earlier.…”
Section: Controlled Copolymerization Using Ethanesulfonic Acid As An mentioning
confidence: 99%
“…The isoselective polymerization of acetaldehyde has been achieved using initiators such as zinc and aluminum alkyls, Grignard reagents, and lithium alkoxides [Kubisa et al, 1980;Pasquon et al, 1989;Pregaglia and Binaghi, 1967;Tani, 1973;Vogl, 2000]. The isoselectivity is high in some systems with isotactic indices of 80-90%.…”
Section: -13 Aldehydesmentioning
confidence: 99%
“…The product is optically inactive since there is an equal probability of propagating via right-and left-handed helices. Polymerization of the bulky monomer chloral yields an optically active product when one uses a chiral initiator, e.g., lithium salts of methyl (þ)-or (À)-mandelate or (R)-or (S)octanoate [Corley et al, 1988;Jaycox and Vogl, 1990;Qin et al, 1995;Vogl, 2000]. The chiral initiator forces propagation to proceed to form an excess of one of the two enantiomeric helices.…”
Section: -14b Chiral Conformationmentioning
confidence: 99%
“…These latter techniques also have produced many beautiful objects. 42 During this period I became interested also in the art and theater of Japan (Kabuki and Noh). Since I have lived mostly in Kyoto, the old capital and the cultural center of Japan, I have been exposed to many scrolls and screens, in temples and other places, and have become fascinated with the block prints of 19th century Japan (Hokusai, Hiroshige, and Shiganobu) and, most important, with Japanese lacquerware and the interiors and the inner sancta of temples.…”
Section: Oriental Lacquerwarementioning
confidence: 99%