2000
DOI: 10.1021/ma000346u
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Synthesis and Characterization of New Chiral Side Chain Liquid Crystalline Polyoxetanes

Abstract: Two series of the side chain liquid crystalline polyoxetanes were synthesized via cationic ring-opening polymerization of oxetane monomers bearing pendant mesogenic units including two chiral carbons. The first two polymers have only one pendant group in the repeating unit, whereas the second polymers have two mesogenic groups per repeating unit. The oxetane monomer bearing one mesogenic unit produced high molecular weight polymers, whereas the ones bearing two mesogenic units at the same carbon in the ring pr… Show more

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Cited by 14 publications
(11 citation statements)
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“…The yields of 3,3-bis(tosylmethyl)oxetane reported in Table 3 refer to the pure product after crystallization from a methanol-acetone mixture in a vol/vol 6 : 1 ratio. The 3,3-bis(tosylmethyl) oxetane after crystallization melted in the temperature range of 114-116 8C, which coincides with the literature data [19].…”
Section: 3-bis(azidomethyl)oxetane (Bamo) Synthesis Via Pentaerythrsupporting
confidence: 90%
“…The yields of 3,3-bis(tosylmethyl)oxetane reported in Table 3 refer to the pure product after crystallization from a methanol-acetone mixture in a vol/vol 6 : 1 ratio. The 3,3-bis(tosylmethyl) oxetane after crystallization melted in the temperature range of 114-116 8C, which coincides with the literature data [19].…”
Section: 3-bis(azidomethyl)oxetane (Bamo) Synthesis Via Pentaerythrsupporting
confidence: 90%
“…Oxetane polymerization has also received considerable attention,26–28 but its cationic polymerization again produces low‐molecular‐weight polymers with low yields.…”
Section: Introductionmentioning
confidence: 99%
“…2,7‐Dibromo‐9 H ‐carbazole 1 was synthesized by following the method in the literature. 29 3‐((6‐Bromohexyloxy)methyl)‐3‐methyloxetane 2 was also prepared according to the method in the literature 28. The reaction of 3‐((6‐bromohexyloxy)methyl)‐3‐methyloxetan‐3‐methyloxetane with 2,7‐dibromo‐9 H ‐carbazole yields 2,7‐dibromo‐9‐(6‐((3‐methyloxetan‐3‐yl)methoxy)hexyl)‐9 H ‐carbazole 3 in the presence of sodium hydride.…”
Section: Resultsmentioning
confidence: 99%
“…Compound 1 and 2 were synthesized by following the literature method 28, 29. The synthesis of the polymer 6 (POx‐I) was described in our previous work 22…”
Section: Methodsmentioning
confidence: 99%