2014
DOI: 10.1021/ma5021402
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New Fullerene-Based Polymers and Their Electrical Memory Characteristics

Abstract: Covalent incorporations into polymers of fullerene were achieved via the Cu(I)-catalyzed azide−alkyne click polymerizations of a fullerene derivative monomer functionalized with 5-(trimethylsilyl)pent-4-yn-1-yl groups and a comonomer functionalized with azidomethyl groups, producing the novel fullerene polymers P1-C 60 and P2-C 60 . Despite their extremely high fullerene loading levels, the polymers were soluble in common organic solvents and exhibited no aggregation of fullerene units in films. Moreover, devi… Show more

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Cited by 36 publications
(27 citation statements)
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“…Moreover, their superior flexibility, toughness, dimensional stability and device properties can be easily tuned by tailoring their chemical structures during synthesis. [14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31] However, the realization of high-density polymeric memory devices in a low-cost manner is highly constrained by the fact that the majority of reported polymeric memory materials will readily degrade or dissolve upon exposure to the solvents or wet chemicals used in multilayer device fabrication processes. [21][22][23][24][25] Although some of these materials have high dimensional and mechanical stability, their film forms are not sufficiently resilient to survive the device fabrication process.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, their superior flexibility, toughness, dimensional stability and device properties can be easily tuned by tailoring their chemical structures during synthesis. [14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31] However, the realization of high-density polymeric memory devices in a low-cost manner is highly constrained by the fact that the majority of reported polymeric memory materials will readily degrade or dissolve upon exposure to the solvents or wet chemicals used in multilayer device fabrication processes. [21][22][23][24][25] Although some of these materials have high dimensional and mechanical stability, their film forms are not sufficiently resilient to survive the device fabrication process.…”
Section: Introductionmentioning
confidence: 99%
“…[16][17][18][19] Thus far, numerous electrical memory polymers composed either of fully π-conjugated backbones [17][18][19][21][22][23][24][25] or of nonconjugated backbones bearing only electron-donor units or both electron-donor and -acceptor units as parts of the backbone and/or side groups have been reported. [18][19][20][26][27][28][29] In particular, the majority of the nonconjugated polymers have been synthesized with carbazole, triphenylamine, fluorine and their derivatives. [18][19][20][26][27][28][29] Moreover, they are known to mainly exhibit p-type electrical memory characteristics.…”
Section: Introductionmentioning
confidence: 99%
“…[18][19][20][26][27][28][29] In particular, the majority of the nonconjugated polymers have been synthesized with carbazole, triphenylamine, fluorine and their derivatives. [18][19][20][26][27][28][29] Moreover, they are known to mainly exhibit p-type electrical memory characteristics. In contrast, n-type memory polymers have rarely been reported.…”
Section: Introductionmentioning
confidence: 99%
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“…While there has been considerable interest in the research community that incorporate fullerene C 60 into -conjugated polymeric systems for nearly a decade (some containing transition metal chromophores) [18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35], these systems use relatively complicated structures that do not facilitate efficient electronic communication between the two moieties [36,37]. In contrast, our relatively simple synthetic strategy provides a more robust connection between the subunits and presumably more efficient electronic interactions.…”
Section: Introductionmentioning
confidence: 99%