2004
DOI: 10.1080/00914030490472908
|View full text |Cite
|
Sign up to set email alerts
|

Polyfuran and Co-Polymers: A Chemical Synthesis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
17
0

Year Published

2009
2009
2024
2024

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 33 publications
(17 citation statements)
references
References 18 publications
0
17
0
Order By: Relevance
“…Conducting polymers (CPs), such as polypyrrole (PPy), polyaniline (PANI) and polythiophene (PTh) and their derivatives [11], have been considered as promising candidates because of their high theoretical specific capacitances, low cost, facile synthesis, fast charge/discharge electron-transfer kinetics, and high conductivity in the doped state [12]. The reasons accounting for this phenomenon are probably the susceptibility of the furan on the side reactions during the polymerization and low stability of the resulting polymers [23][24][25][26]. The reasons accounting for this phenomenon are probably the susceptibility of the furan on the side reactions during the polymerization and low stability of the resulting polymers [23][24][25][26].…”
Section: Introductionmentioning
confidence: 99%
“…Conducting polymers (CPs), such as polypyrrole (PPy), polyaniline (PANI) and polythiophene (PTh) and their derivatives [11], have been considered as promising candidates because of their high theoretical specific capacitances, low cost, facile synthesis, fast charge/discharge electron-transfer kinetics, and high conductivity in the doped state [12]. The reasons accounting for this phenomenon are probably the susceptibility of the furan on the side reactions during the polymerization and low stability of the resulting polymers [23][24][25][26]. The reasons accounting for this phenomenon are probably the susceptibility of the furan on the side reactions during the polymerization and low stability of the resulting polymers [23][24][25][26].…”
Section: Introductionmentioning
confidence: 99%
“…But they lack processability to form fibres or filaments due to their inherent structural intractability and stiffness that comes from conjugation along molecular chain [2,3]. Among these conductive polymers, polypyrrole (PPy) has low cost, good environmental stability, and satisfactory electrical conductivity in doped condition [4][5][6][7]. Textile materials are insulator but strong, light-weight, and flexible.…”
Section: Introductionmentioning
confidence: 99%
“…Corma and co-workers further exemplified the "oligomerization" of MF with a number of biomass-derived aldehydes and ketones; notably, aldehydes (e.g., pentanal) exhibited higher reaction rates than ketones (e.g., 2-pentanone) [2]. Besides the acid-catalyzed oligomerization, the polymerization of furans with oxidizing agents has been investigated [4][5][6]. During this reaction, the furan rings do not open and the furan chain (polyfuran) is dehydrogenated.…”
Section: Introductionmentioning
confidence: 97%