Evidence map›Paper›PMID 36614403›Full record

ArticleMaterials (Basel, Switzerland)2022

Preparation and Electrochromic Properties of Benzodithiophene-Isoindigo Conjugated Polymers with Oligoethylene Glycol Side Chains.

Qilin Wang, Yuehui Zhai, Danming Chao, Zheng Chen, Zhenhua Jiang

Abstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Qilin WangEngineering Research Center of Special Engineering Plastics, Ministry of Education, National and Local Joint Engineering Laboratory for Synthetic Technology of High Performance Polymer, College of Chemistry, Jilin University, Changchun 130012, China.
Yuehui ZhaiSchool of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, China.
Danming ChaoEngineering Research Center of Special Engineering Plastics, Ministry of Education, National and Local Joint Engineering Laboratory for Synthetic Technology of High Performance Polymer, College of Chemistry, Jilin University, Changchun 130012, China.
Zheng ChenEngineering Research Center of Special Engineering Plastics, Ministry of Education, National and Local Joint Engineering Laboratory for Synthetic Technology of High Performance Polymer, College of Chemistry, Jilin University, Changchun 130012, China.
Zhenhua JiangEngineering Research Center of Special Engineering Plastics, Ministry of Education, National and Local Joint Engineering Laboratory for Synthetic Technology of High Performance Polymer, College of Chemistry, Jilin University, Changchun 130012, China.

Funding

Cross Discipline Training Program for young teachers and students of Jilin University No. 415010300062Jilin Province Science and Technology Department No. 20200404177YY
6 · The paper itself

Abstract

Functional polymers featuring good processability in non-halogenated, benzene-free green solvents are highly desired due to health and environmental concerns. Herein, a series of novel D-A type conjugated polymers, PBDT-IIDs, are designed and successfully prepared by "green" functionalization of the polymers with highly hydrophilic, highly polar, highly flexible, and biocompatible oligoethylene glycol (OEG) side chains in order to improve the processability. These series polymers are named PBDT-IID2, PBDT-IID3, and PBDT-IID4, respectively, according to the number of oxygen atoms in the side chain. After confirmation by structural characterization, the basic properties of PBDT-IIDs are also investigated. With the increase in the OEG side chain length, the polymer PBDT-IID4 not only has good solubility in the halogen solvent chlorobenzene, but also exhibits excellent solubility in the green halogen-free solvent methyltetrahydrofuran (Me-THF). As a result, the green solvent Me-THF can also be applied to prepare PBDT-IIDs' electrochromic active layers, except for chlorobenzene and toluene. The electrochromism of PBDT IIDs under both positive and negative voltages has a practical application potential. The several controllable switches between dark green and khaki (0-0.6 V) are expected to show great potential in the field of military camouflage. Furthermore, according to the principle of red, green, and blue (RGB) mixing, light blue-green in the reduced state (-1.6 V) can be used in the preparation of complementary ECDs to provide one of the three primary colors (green).

Indexed as

benzodithiophene-isoindigoelectrochromismgreen solventoligoethylene glycol (OEG)

Identifiers

PMID36614403
PMCPMC9821313

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.