2011
DOI: 10.1016/j.polymer.2011.09.029
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Fluorescent core-sheath fibers by electrospinning of a phenyleneethynylene/poly(styrene-co-maleimide) blend

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Cited by 11 publications
(8 citation statements)
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“…Furthermore, the presence of other functional groups in the molecule susceptible to the hydrolysis conditions must be taken into account. Here, we first prepared step-by-step oligomers having three phenyleneethynylene units and terminated with one ( 9 , Scheme 1 ) or two ( 14 , Scheme 2 ) benzyl-protected carboxylic acids by Pd/Cu cross-coupling [ 26 ] of monomer 5 [ 27 ] with one or two equivalents of 6 to give the bromo-terminated dimer 7 [ 28 ] that was then Pd/Cu cross-coupled with 4 ( Scheme S1 ) to give the carboxylic acid benzyl-protected trimer 8 or the symmetric benzyl-protected terminated oligomer 13 ( Scheme 2 ). After evaluating different methods and conditions to cleave the benzyl group and to carry out the amidation reactions (ESI), the acid groups were deprotected by using KOH and toluene under nitrogen atmosphere in yields higher than 85% and without the detection of any traces of oxidized ethynylene groups.…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, the presence of other functional groups in the molecule susceptible to the hydrolysis conditions must be taken into account. Here, we first prepared step-by-step oligomers having three phenyleneethynylene units and terminated with one ( 9 , Scheme 1 ) or two ( 14 , Scheme 2 ) benzyl-protected carboxylic acids by Pd/Cu cross-coupling [ 26 ] of monomer 5 [ 27 ] with one or two equivalents of 6 to give the bromo-terminated dimer 7 [ 28 ] that was then Pd/Cu cross-coupled with 4 ( Scheme S1 ) to give the carboxylic acid benzyl-protected trimer 8 or the symmetric benzyl-protected terminated oligomer 13 ( Scheme 2 ). After evaluating different methods and conditions to cleave the benzyl group and to carry out the amidation reactions (ESI), the acid groups were deprotected by using KOH and toluene under nitrogen atmosphere in yields higher than 85% and without the detection of any traces of oxidized ethynylene groups.…”
Section: Resultsmentioning
confidence: 99%
“…The synthesized micro/nanofibers with various morphologies including core–sheath, hollow, porous, nanoribbons, and multilayered mates have been produced and shown great potentials in tissue engineering, filtration, textile manufacturing, sensors, electronics, catalysis, energy storage, etc. Despite its advantages such as high surface area/volume ratios, its porosity as well as composition could be manipulated for desired properties and functions . The entangled fibers with heat treatment generate great amount of open pores and large voids for more heavy metal active sites, resulting in enhanced sensing performances …”
Section: Synthesis Methods Of Novel Electrode Materials For Electrochmentioning
confidence: 99%
“…Despite its advantages such as high surface area/volume ratios, its porosity as well as composition could be manipulated for desired properties and functions . The entangled fibers with heat treatment generate great amount of open pores and large voids for more heavy metal active sites, resulting in enhanced sensing performances …”
Section: Synthesis Methods Of Novel Electrode Materials For Electrochmentioning
confidence: 99%
“…Benzyl 4‐Iodobenzoate (2d): 13 Following the general procedure for benzylation under acidic conditions, the title compound was obtained as a colorless crystalline solid (175 mg, 86 %), m.p. 66.4 °C.…”
Section: Methodsmentioning
confidence: 99%