2012
DOI: 10.1016/j.electacta.2011.12.097
|View full text |Cite
|
Sign up to set email alerts
|

Novel ferrocene derivatized poly(2,5-dithienylpyrrole)s: Optoelectronic properties, electrochemical copolymerization

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

0
29
0

Year Published

2012
2012
2023
2023

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 58 publications
(29 citation statements)
references
References 41 publications
0
29
0
Order By: Relevance
“…1 ν = 3285, 2949, 1713, 1698, 1586, 1552, 1503, 1454, 1379 The obtained solution was added to a solution of benzyl alcohol (3.75 mL, 36.2 mmol) in mesitylene (6 mL) at 130°C, stirred for 5 min and then allowed to cool to room temp.…”
Section: Compoundmentioning
confidence: 99%
See 2 more Smart Citations
“…1 ν = 3285, 2949, 1713, 1698, 1586, 1552, 1503, 1454, 1379 The obtained solution was added to a solution of benzyl alcohol (3.75 mL, 36.2 mmol) in mesitylene (6 mL) at 130°C, stirred for 5 min and then allowed to cool to room temp.…”
Section: Compoundmentioning
confidence: 99%
“…1 ν = 3277, 2957, 1764, 1698, 1639, 1612, 1513, 1463, 1377, 1348, 1303, 1243, 1220, 1200, 1173, 1112, 1061, 1028 The obtained solution was dried, and the crude solid was dissolved in THF (2 mL) and transferred to a www.eurjoc.org microwave vessel.…”
Section: Compound 23mentioning
confidence: 99%
See 1 more Smart Citation
“…The monomer 2,5-di(2-thienyl)pyrroles (SNS) consists of thiophene and pyrrole rings interconnected by their α-positions; the high reactivity of a pyrrole system creates the possibility of introducing a substituent into the β-position of the pyrrole ring even with the free α-positions of thiophene rings, making possible further modification to properties [27]. In recent years, a number of SNS derivatives have been synthesized with substituted branched alkyl [4], ferrocene [28], phenyl derivatives [29], aryl derivatives [30], and anthraquinone [31]. The oxidation potentials of SNS derivatives are quite low (about 0.7 V vs Ag/Ag + ) due to the conjugation of SNS in the aromatic system and the presence of electron donating atoms (S and N) in the main chain [32].…”
Section: Introductionmentioning
confidence: 99%
“…Electrochemical properties of copolymers of EDOT have z E-mail: toppare@metu.edu.tr been also widely studied previously. [16][17][18] However, to the best of our knowledge, use of a novel BIMN for that matter has not yet been reported.…”
mentioning
confidence: 99%