2015
DOI: 10.1016/j.carbon.2015.06.016
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Graphene chemically synthesized from benzene at liquid–liquid interfaces

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Cited by 31 publications
(17 citation statements)
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References 37 publications
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“…Among the many approaches leading to nanographenes, the benzene ring seems to be an ideal candidate for the bottom‐up synthesis of such structures . Zarabin and co‐workers attempted the construction of nanographene sheets from benzene at a liquid–liquid interface. According to their strategy, a single benzene ring should undergo FeCl 3 ‐mediated oxidative coupling to give oligo(paraphenylene) and/or poly(paraphenylene).…”
Section: Intermolecular Oxidative Aromatic Couplingmentioning
confidence: 99%
See 1 more Smart Citation
“…Among the many approaches leading to nanographenes, the benzene ring seems to be an ideal candidate for the bottom‐up synthesis of such structures . Zarabin and co‐workers attempted the construction of nanographene sheets from benzene at a liquid–liquid interface. According to their strategy, a single benzene ring should undergo FeCl 3 ‐mediated oxidative coupling to give oligo(paraphenylene) and/or poly(paraphenylene).…”
Section: Intermolecular Oxidative Aromatic Couplingmentioning
confidence: 99%
“…Among the many approaches leading to nanographenes,the benzene ring seems to be an ideal candidate for the bottom-up synthesis of such structures. [5,6,35,36] Zarabin and co-workers attempted [37] the construction of nanographene sheets from benzene at al iquid-liquid interface.A ccording to their strategy,asingle benzene ring should undergo FeCl 3 -mediated oxidative coupling to give oligo(paraphenylene) and/or poly(paraphenylene). Thep oly(paraphenylene) fractions should spontaneously migrate to the water-benzene interface, where the second polymerization step that creates lateral chains occurs.I nt he final step,as eries of intramolecular oxidative coupling processes between adjacent phenyl rings within the branched polymer takes place.T he proposed method allows the preparation of large graphene nanosheets with asurface area of about 800 nm 2 .…”
Section: Oxidative Homocoupling Of Arenes and Heteroarenesmentioning
confidence: 99%
“…The simultaneous formation of a 2D morphology and a hierarchical porous architecture is attributed to a combined self‐templating effect from PDAA as well as the etching by KOH. As shown in Figure f, the numerous phenyl and trizaine rings in our PDAA resin allows its facile conversion into sp 2 hexagonal carbon rings and carbon rings with nitrogen dopants, which is related to oxidative dehydrogenation (Scholl reaction) of the precursor . Carbonization of PDAA leads to the formation of these graphitic layers embedded in amorphous and defective carbons, for example the carbons derived from the hemiaminal units.…”
mentioning
confidence: 97%
“…In addition, the method employed to process the material for the application is a key step, where thick films can damage the performance of the device, blocking the access of the inner electroactive sites and avoiding the use of high charge-discharge currents. Our research group developed a very effective route to deposit thin, transparent and homogeneous films of different unprocessable materials, as carbon nanotubes 23 24 , graphene 24 25 26 , metallic nanoparticles and different kind of nanocomposites 25 26 27 28 29 , in which the film is stabilized at a liquid-liquid interface, and easily deposited over different kind of ordinary substrates.…”
mentioning
confidence: 99%