2015
DOI: 10.1007/s00289-015-1448-7
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis, characterization, and optical properties of new pyridine- and thiophene-based copolymer bearing bulky naphthyl group

Abstract: A new copolymer was synthesized via reaction of new pyridine-containing dibromo compound, 2,6-bis(4-bromophenyl)-4-(naphthalen-1-yl) pyridine, with thiophene-based diboronic ester via Suzuki cross-coupling reactions. 2,6-Bis(4-bromophenyl)-4-(naphthalen-1-yl) pyridine was synthesized starting from condensation reactions of 4-bromoacetophenone and 1-naphthaldehyde. The synthesized monomer and polymer were characterized by FT-IR and NMR spectroscopy. The physical properties of the polymer, including solubility a… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 35 publications
0
2
0
Order By: Relevance
“…Furthermore, a trans configuration is indicated by the coupling constant between 13.0 and 17.0 hertz. In the IR spectrum, the carbonyl group of simple aliphatic ketones normally has a strong absorption band in the range of 1720-1708 cm ‑1 . However, for chalcone, the conjugation of CO will shift the frequency to the lower region due to the delocalization of π electrons ( I , II ), , as illustrated in Scheme . In this case, the conjugation of CO with α or β will give rise to absorption in the region 1700-1675 cm ‑1 , whereas CC will give rise to absorption at 1644-1617 cm ‑1 .…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, a trans configuration is indicated by the coupling constant between 13.0 and 17.0 hertz. In the IR spectrum, the carbonyl group of simple aliphatic ketones normally has a strong absorption band in the range of 1720-1708 cm ‑1 . However, for chalcone, the conjugation of CO will shift the frequency to the lower region due to the delocalization of π electrons ( I , II ), , as illustrated in Scheme . In this case, the conjugation of CO with α or β will give rise to absorption in the region 1700-1675 cm ‑1 , whereas CC will give rise to absorption at 1644-1617 cm ‑1 .…”
Section: Resultsmentioning
confidence: 99%
“…[ 31 ] Other promising approaches include the synthesis of various types of composites and copolymers. [ 9 ] Copolymers of aniline, such as butyl thioaniline [ 32 ] and pyridine‐thiophene based copolymer [ 33 ] are reported and show a noticeable decrease in band gap or increase in conductivity when compared to their respective homopolymers. [ 34 ] PANI and polythiophene both are well established as conducting polymers and are extensively studied.…”
Section: Introductionmentioning
confidence: 99%