1988
DOI: 10.1016/0022-0728(88)87036-0
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Quinone molecular films derived from aminoquinones

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Cited by 20 publications
(4 citation statements)
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“…The spectrum of the monomer presents a maximum at 425 nm, which shifts towards 535 nm for the polymer, indicating that the conjugation length is increased. This absorption band probably corresponds to the quinone moiety [25].…”
Section: Electrosynthesis Of Pjug Filmsmentioning
confidence: 95%
“…The spectrum of the monomer presents a maximum at 425 nm, which shifts towards 535 nm for the polymer, indicating that the conjugation length is increased. This absorption band probably corresponds to the quinone moiety [25].…”
Section: Electrosynthesis Of Pjug Filmsmentioning
confidence: 95%
“…This redox couple can be suitably used for the cathode material of lithium secondary batteries with high energy density [4][5][6][7][8]. Recently, Gall et al [9] have reported that a poly(quinone) derivative of poly(2,5-dihydroxy-1,4-benzoquinone-3,6-methylene) (PDBM) composited with 40% acetylene black (AB) demonstrates reversible redox cycle-ability with a specific capacity of 120-130 mAh g -PDBM quinone moieties but does not rise in the energy density.…”
Section: Introductionmentioning
confidence: 99%
“…Other polymers were also used, and more particularly polyquinones, which present particular redox properties. For example, a series of aminonaphthoquinones and aminoanthraquinones were originally developed in the 80’s and 90’s for electrocatalytic purposes or energy storage [ 31 , 32 , 33 , 34 , 35 , 36 , 37 ]. More recently, other polyquinone films were developed to be used as transducers in biosensors [ 38 , 39 ].…”
Section: General Introductionmentioning
confidence: 99%