Organoselenium chemistry-based polymer synthesis
文献情報
Qilong Li, Yuanyuan Zhang, Zijun Chen, Xiangqiang Pan, Zhengbiao Zhang, Jian Zhu
Due to their unique properties, selenium-containing polymers have become one of the research focuses of polymer materials in recent years. First, selenium can transform among various states of selenoxide, selenone, and selenium free radicals, and then be restored under these conditions, which endows these polymers with multiresponsive behaviors, including responses to redox changes, light, radiation, etc. Second, these polymers show characteristic properties. Selenium-containing polymers exhibit unique multiple optical–electrical characteristics, including high photoconductivity, anisotropic thermoconductivity, high piezoelectric and thermoelectric responses, and a high refractive index. Based on these various properties, selenium-containing polymers are regarded as excellent functional polymer materials. Therefore, it is meaningful to synthesize selenium-containing polymers with various structures. This paper principally gives a summary of the organic reactions of organoselenium compounds and reviews the research on the synthesis of selenium-containing polymers via different methods, such as the use of selenium-containing monomers and their polymerization, selenium-containing initiators for polymerization, selenium-containing mediators for controlled polymerization and selenium-containing molecules for the postmodification of polymers. Moreover, applications of selenium-containing polymers are described, including their use as intrinsic high refractive index polymeric materials, oxidative- and reductive-responsive materials, dynamic exchanging polymers, selective metal adsorbents, and catalysts.
関連文献
Observation of partial reduction of manganese in the lithium rich layered oxides, 0.4Li2MnO3–0.6LiNi1/3Co1/3Mn1/3O2, during the first charge
Hyung Cheoul Shim, Donghan Kim, Dongwook Shin, Seungmin Hyun, Chang-Su Woo, Taehwan Yu, Jae-Pyoung Ahn
DOI: 10.1039/C6CP07574F
Charge ordering and scattering pre-peaks in ionic liquids and alcohols
DOI: 10.1039/C6CP07834F
Energetics and structural characterization of the “DFG-flip” conformational transition of B-RAF kinase: a SITS molecular dynamics study
Qiang Shao, Zhijian Xu, Jinan Wang, Jiye Shi, Weiliang Zhu
DOI: 10.1039/C6CP06624K
Internal dynamics in helical molecules studied by X-ray diffraction, NMR spectroscopy and DFT calculations
Martin Dračínský, Jan Storch, Vladimír Církva, Ivana Císařová, Jan Sýkora
DOI: 10.1039/C6CP07552E
New insight into the roles of oxygen vacancies in hematite for solar water splitting
Xin Zhao, Jianyong Feng, Shi Chen, Yizhong Huang, Tze Chien Sum, Zhong Chen
DOI: 10.1039/C6CP06410H
Unravelling the early photochemical behavior of (8-substituted-7-hydroxyquinolinyl)methyl acetates through electronic structure theory and ultrafast transient absorption spectroscopy
Jan-Michael Mewes, Kyle T. Harris, David Lee Phillips, Andreas Dreuw
DOI: 10.1039/C6CP05499D
Dynamic phase change and local structures in IL-containing mixtures: classical MD simulations and experiments
Yang Wu, Xia Wang, Qiaozhen Liu, Dawei Fang, Xuefei Jiang, Wei Guan
DOI: 10.1039/C6CP06300D
Jahn–Teller effect in LiMn2O4: influence on charge ordering, magnetoresistance and battery performance
K. Ragavendran, H. Xia, P. Mandal, A. K. Arof
DOI: 10.1039/C6CP07289E
Hysteresis phenomena in perovskite solar cells: the many and varied effects of ionic accumulation
Daniel A. Jacobs, Yiliang Wu, Heping Shen, Chog Barugkin, Fiona J. Beck, Thomas P. White, Klaus Weber, Kylie R. Catchpole
DOI: 10.1039/C6CP06989D
Sizing and Eddy currents in magnetic core nanoparticles: an optical extinction approach
Luis J. Mendoza Herrera, Ignacio J. Bruvera
DOI: 10.1039/C6CP08260B
こちらもおすすめ
4'-ブロモビフェニル-3-メトークシーディ.ActionBarはどのように保存すればよいですか?
4'-ブロモビフェニル-3-メトークシーディ.ActionBarは、冷暗所で、直射日光を避け、密栓の容器に保存し、遠隔場所に保管してください。温度は常温(0〜2...
2-異丙基フェニルヒドラジン塩酸塩とは何ですか?
2-異丙基フェニルヒドラジン塩酸塩は、CAS番号58928-82-8を有する化合物で、構造式はC11H14N2HClです。これは塩基性化合物であり、水に溶けやす...
5-(4-クロロフェニル)-4H-1,2,4-三氮唑-3-アミンを取り扱う際の実験室安全事項は何ですか?
5-(4-クロロフェニル)-4H-1,2,4-三氮唑-3-アミンは取り扱いに注意が必要です。PPEとして防塵マスク、ゴーグル、手袋を使用し、ドラフトチャンバーを...
去甲基雷贝拉唑硫醚はどのように合成されますか?
去甲基雷贝拉唑硫醚は、ベンジミダゾール硫化物と3-メチル-4-ピリジノールの反応によって合成されます。具体的には、2-チオキシドベンジミダゾールと3-メチル-4...
2-ブロモ-5-フロロ-N-(2-フェノールメチル)ベンゼンウレアは安全ですか?
2-ブロモ-5-フロロ-N-(2-フェノールメチル)ベンゼンウレアは、毒性や刺激性の実験データに基づき、適切な取扱いと防護措置を講じることで安全に使用できます。...
対甲苯磺酸酯-四聚乙二醇-四氢吡喃醚の物理化学的性質は何ですか?
対甲苯磺酸酯-四聚乙二醇-四氢吡喃醚のCAS番号は86259-89-4です。この化合物は無色の液体で、分子量は約724.8です。高濃度では溶血性が報告されており...
2-(3-(二氟甲基)-4-氟苯基)-4,4,5,5-四甲基-1,3,2-二噁硼戊環はどのように保存すればよいですか?
2-(3-(二氟甲基)-4-氟苯基)-4,4,5,5-四甲基-1,3,2-二噁硼戊環は、室温で暗い場所に保管し、直射日光から遠ざけ、容器は密閉状態で保存してくだ...
6-アミノ-5-クロロ-2-シクロプロピルピリミジンカルボン酸の代替品はありますか?
この化合物の代替品には、ピロリミジン酸やその類似物、またピロリミジンカルボン酸の他の異性体があります。これらの代替品は、特定の化学反応や目的に応じて選択すること...
5-クロロベンゾ[1,3]二オキセイン-4-アミンに適用される法規ガイドラインは何ですか?
5-クロロベンゾ[1,3]二オキセイン-4-アミンはCAS番号379228-45-2に該当します。この化合物はGHS分類でH314(接触により急性毒性がある)と...
掲載誌
Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry












![(1R)-N-((1R)-1-Phenylethyl)-1-[4-(tert-butyldimethylsilyloxymethyl)cyclohexyl]ethan-1-amine structure (1R)-N-((1R)-1-Phenylethyl)-1-[4-(tert-butyldimethylsilyloxymethyl)cyclohexyl]ethan-1-amine structure](https://static.chemtradehub.com/structs/672/672314-45-3-47ef.webp)
![(1S)-1,5-Anhydro-2-O-alpha-L-arabinopyranosyl-1-[5-hydroxy-7-({6-O-[3-(4-hydroxy-3-methoxyphenyl)propanoyl]-beta-D-glucopyranosyl}oxy)-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-6-yl]-D-glucitol structure (1S)-1,5-Anhydro-2-O-alpha-L-arabinopyranosyl-1-[5-hydroxy-7-({6-O-[3-(4-hydroxy-3-methoxyphenyl)propanoyl]-beta-D-glucopyranosyl}oxy)-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-6-yl]-D-glucitol structure](https://static.chemtradehub.com/structs/225/2252345-81-4-bcff.webp)
![{3-[Bis(4-hydroxyphenyl)methyl]-1-[2-(dimethylamino)ethyl]-1H-indol-2-yl}[4-(2-chlorophenyl)-1-piperazinyl]methanone structure {3-[Bis(4-hydroxyphenyl)methyl]-1-[2-(dimethylamino)ethyl]-1H-indol-2-yl}[4-(2-chlorophenyl)-1-piperazinyl]methanone structure](https://static.chemtradehub.com/structs/170/170365-25-0-e4d7.webp)