2011
DOI: 10.1016/j.reactfunctpolym.2011.02.008
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Synthesis of a novel fluorescent and ion sensitive monomer bearing quinoxaline moieties and its electropolymerization

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Cited by 22 publications
(4 citation statements)
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“…The energy difference between these two levels is the band gap (Eg) and can be estimated from the onset of lower energy end of this band. The band gap (Eg) of P(EE-Q) was found to be 1.75 eV which is lower than its analogue P(TT-Q) and indicates that EDOT is a stronger donor group than thiophene [19,27]. Upon electrochemical oxidation, the P(EE-Q) film shows a simultaneous decrease in the absorbance at 530 nm, which is accompanied with a color change from brownish red to green.…”
Section: Electro-optical Properties Of P(ee-q)mentioning
confidence: 95%
See 1 more Smart Citation
“…The energy difference between these two levels is the band gap (Eg) and can be estimated from the onset of lower energy end of this band. The band gap (Eg) of P(EE-Q) was found to be 1.75 eV which is lower than its analogue P(TT-Q) and indicates that EDOT is a stronger donor group than thiophene [19,27]. Upon electrochemical oxidation, the P(EE-Q) film shows a simultaneous decrease in the absorbance at 530 nm, which is accompanied with a color change from brownish red to green.…”
Section: Electro-optical Properties Of P(ee-q)mentioning
confidence: 95%
“…There are also several reports on their use as metal chelators [17,18]. Recently, we have synthesized a series of new fluorescent monomers based on terthienyl systems bearing pendant quinoxaline moieties and found that 4-((2,5-dithiophen-2-yl)thiophen-3-yl)pyrrolo[1,2-a]quinoxaline (TT-Q) monomer and its polymer exhibit high sensitivity towards Fe 3+ ions [19]. Moreover, it was found that the polymer obtained on the basis of donor-acceptor approach exhibits reversible electrochromic response with high coloration efficiency.…”
Section: Introductionmentioning
confidence: 99%
“…C4‐alkenyl substituted pyrrolo[1,2‐ a ]quinoxalines such as III could be used as antileishmanial agents [1c] . Polymerization of the thiophene‐substituted pyrrolo[1,2‐ a ]quinoxaline IV afforded a promising sensor toward detection of Fe [3+] ion [1d] . Reduced forms of pyrrolo/indolo [1,2‐ a ]quinoxalines such as V (as Sirtuin 6 activator) and VI (as anti‐metastatic agent) were included in bio‐related studies [1e,f] .…”
Section: Introduction Of Pyrrolo/indolo [12‐a]quinoxalinesmentioning
confidence: 99%
“…On the other hand, compounds containing a pyrrolo[1,2- a ]quinoxaline subunit display a wide spectrum of biological profiles as antagonists [ 26 27 ], PARP-1 inhibitors [ 28 ], anticancer agents [ 29 – 30 ], anti-HIV agents [ 31 ], and antimalarial agents [ 32 33 ]. These molecules are also important intermediates for the construction of 5-HT 3 receptor agonists [ 34 35 ] and are useful as fluorescent materials for various applications [ 36 37 ].…”
Section: Introductionmentioning
confidence: 99%