2018
DOI: 10.1016/j.bios.2018.01.035
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Chirality detection of amino acid enantiomers by organic electrochemical transistor

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Cited by 81 publications
(39 citation statements)
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“…Owing to the separable structure of the OECT devices, the gate electrode and channel can be fabricated individually and conveniently. Zhang et al [54] fabricated the OECT-based amino acid sensors in two steps. Firstly, the Au gate electrode was modified with L-Trp molecularly imprinted polymer (MIP) by cyclic voltammetry on an electrochemical workstation.…”
Section: Gate Surface As Sensing Interfacementioning
confidence: 99%
“…Owing to the separable structure of the OECT devices, the gate electrode and channel can be fabricated individually and conveniently. Zhang et al [54] fabricated the OECT-based amino acid sensors in two steps. Firstly, the Au gate electrode was modified with L-Trp molecularly imprinted polymer (MIP) by cyclic voltammetry on an electrochemical workstation.…”
Section: Gate Surface As Sensing Interfacementioning
confidence: 99%
“…Such difficult goals can be achieved through a nanoarchitectonics approach, namely molecular imprinting [103–105]. Qiu and co-workers developed sensors for chirality detection of amino acid guests using an organic electrochemical transistor with a poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT/PSS) system modified with molecularly imprinted polymer films [106]. The selectivity factor of ʟ-tryptophan over ᴅ-tryptophan and that of ʟ-tyrosine over ᴅ-tyrosine were 11.6 and 14.5, respectively.…”
Section: Reviewmentioning
confidence: 99%
“…Figure 3 (top) also includes the three cases of functionalization on the second cyclopentadienyl ring. While the presence of trialkylsilyl groups in 1' position (8,9) is practically unperceivable in respect to the parent case, consistent with a Hammett constant close to zero, a styrene group (7) results in a more positive reduction peak and a more negative oxidation peak (i. e. both easier oxidation and reduction), which can be justified in terms of a mesomeric effect as a result of extended conjugation, possibly also via π stacking. This might also explain the double peak system (see SI.2), which might account for two near-equivalent redox centers (i. e. the two styrene-cyclopentadienyl moieties) reciprocally interacting, although the presence of the electron attracting phosphane sulfide on one of the conjugated systems may also contribute to the potential difference.…”
Section: Reductionmentioning
confidence: 73%