A one-pot approach using recyclable template to prepare dual-responsive yolk–shell or Janus-like nanoparticles
文献情報
Shuai Long, Chunyang Chen, Jun Luo, Haiyan Dong, Limin Wu, Daoyong Chen
Herein, we report a one-pot approach using polymeric micelles as the recyclable template to prepare hybrid yolk–shell or Janus-like nanoparticles (NPs). The micelles were formed by a block copolymer PEG-b-P4VP (EV) in a methanol/water (1/9, v/v) mixture with PEG as the shell and P4VP as the core. In the mixture of the micelles with AIBN (azobiisobutyronitrile), HAuCl4, NIPAM (N-isopropylacrylamide) and MBA (N,N′-methylenebisacrylamide), hybrid NPs could be obtained by simply heating the mixture at 76 °C. At this temperature, AIBN that was largely localized within the hydrophobic P4VP core decomposed into radicals, which reduced HAuCl4 to form Au NPs within the core and initiated the copolymerization of NIPAM and MBA at the core–shell interface to form a poly (NIPAM-co-MBA) network (PNM) to cover the core. The micelle template was conveniently removed from the hybrid NPs by decreasing the pH value of the medium to 3.0. At a low pH, the P4VP block chains were fully protonated; thus, EV becomes highly hydrophilic and soluble in the medium. Moreover, the micelle template dissociated and then gradually diffused into the bulk solution phase as individual EV chains. After the removal of the micelle template, Au@void@PNM yolk–shell NPs were formed. However, when the EV micelles (with the core being slightly noncovalently crosslinked) were used as the template, the same process resulted in the Janus-like NPs; moreover, the micelles were recyclable. After the yolk–shell or Janus NPs were separated by centrifugation, the micelles were recovered in the supernatant and then used again as a template for additional cycles of the yolk–shell or Janus-like NPs preparation and the same results were obtained. Both the yolk–shell and the Janus NPs were easily redispersible in water, and they were confirmed to have both thermal sensitivity and photo sensitivity. We believe that the facile and cost-effective preparation of the yolk–shell NPs (with dual sensitivities) and the Janus NPs (with a relatively high structural regularity) by localizing the chemical reactions within different nanodomains of the micelles should generate considerable interest in the fields of polymer chemistry and soft materials.
関連文献
Redox processes in sodium vanadium phosphate cathodes – insights from operando magnetometry
Gregor Klinser, Roman Zettl, Heinz Krenn, Roland Würschum
DOI: 10.1039/C9CP04045E
Growth of well-ordered iron sulfide thin films
Earl Matthew Davis, Giulia Berti, Helmut Kuhlenbeck, Vedran Vonk, Hans-Joachim Freund
DOI: 10.1039/C9CP04157E
Quantification of protein aggregation rates and quenching effects of amylin–inhibitor complexes
Suparna Khatun, Anurag Singh, Debabrata Mandal, Amar Nath Gupta
DOI: 10.1039/C9CP03238J
Potential molecular semiconductor devices: cyclo-Cn (n = 10 and 14) with higher stabilities and aromaticities than acknowledged cyclo-C18
Mengyang Li, Zhibin Gao, Yanbo Han, Yaoxiao Zhao, Kun Yuan, Shigeru Nagase, Masahiro Ehara, Xiang Zhao
DOI: 10.1039/D0CP00167H
Dichlorine peroxide (ClOOCl), chloryl chloride (ClCl(O)O) and chlorine chlorite (ClOClO): very accurate ab initio structures and actinic degradation
Najoua Derbel, Thibaud Cours, Alexander Alijah
DOI: 10.1039/C9CP06875A
Molecular and electronic structure of an azidocobalt(iii) complex derived from X-ray crystallography, linear spectroscopy and quantum chemical calculations
Luis I. Domenianni, Reinhold Fligg, Annett Schäfermeier, Steffen Straub, Julia Beerhues, Biprajit Sarkar, Peter Vöhringer
DOI: 10.1039/C9CP04350K
Why does the presence of silicon atoms improve the emission properties of biphenyl derivatives? – Verification of various hypotheses by experiment and theory
Karolina Rachuta, Jacek Koput, Gordon L. Hug, Mariusz Majchrzak
DOI: 10.1039/C9CP03749G
Comment on “Atmospheric oxidation reactions of imidazole initiated by hydroxyl radicals: kinetics and mechanism of reactions and atmospheric implications” by Safaei et al., Phys. Chem. Chem. Phys., 2019, 21, 8445
Lam K. Huynh
DOI: 10.1039/C9CP02187F
Porosity controls the catalytic activity of platinum nanoparticles
Wenmiao Yu, Christopher Batchelor-McAuley, Xin Chang, Neil P. Young, Richard G. Compton
DOI: 10.1039/C9CP03887F
Dynamic nuclear polarization with photo-excited triplet electrons using 6,13-diphenylpentacene
Hiroshi Nonaka, Shinsuke Sando
DOI: 10.1039/C9CP00977A
こちらもおすすめ
H-Leu-Ser-Lys-Leu-OH trifluoroacetate saltに適用される法規ガイドラインは何ですか?
CAS番号162559-45-7のH-Leu-Ser-Lys-Leu-OH trifluoroacetate saltは、GHS( Chemicals Clas...
Trimethyltin Chlorideの物理化学的性質は何ですか?
CAS番号1066-45-1のトリメチルチリドは、白色結晶性粉末で、分子量は297.77です。この化合物は水にわずかに溶けますが、酢酸、エタノール、ジエチルエー...
ニコール酸化物水和物の主な用途は何ですか?
ニコール酸化物水和物は、主に金属分離、研磨剤、酸化剤、染料製造の原料として利用されます。また、電気化学製品、触媒、分析化学の分野でも広く使用されています。
(2,3-二甲基-2H-吲唑-6-基)boronic acidを取り扱う際の実験室安全事項は何ですか?
(2,3-二甲基-2H-吲唑-6-基)boronic acidを取り扱う際は、PPE(防護服、ゴーグル、マスク、手袋)を使用する必要があります。ドラフトチャンバ...
4-ブロモ-1-メトキシ-2-(2-メトキシエトオキシ)ベンゼンは安全ですか?
4-ブロモ-1-メトキシ-2-(2-メトキシエトオキシ)ベンゼンは一般的に安全とは言えません。取扱いには注意が必要で、直接的な皮膚接触や吸入は避けてください。
4,4-双(5-甲基-2-苯并噁唑基)二苯乙烯はどの業界で使用されていますか?
4,4-双(5-甲基-2-苯并噁唑基)二苯乙烯は医薬業界、ポリマー業界、センサー業界、半導体業界で使用されています。特に、光触媒や蛍光材料として利用されています...
2,3,5,6-四氯-4-ピリジンスチオールを取り扱う際の実験室安全事項は何ですか?
2,3,5,6-四氯-4-ピリジンスチオールは非常に毒性があり、皮膚や粘膜に刺激を与える可能性があります。取り扱う際には、ゴーグル、ゴム手袋、防塵マスクを着用し...
TG 4-155はどのように合成されますか?
TG 4-155は、2-(2-メチル-1H-インドン-1-イル)エチルアミドと3,4,5-トリメトキシフェノールを反応させ、選択性的に合成できます。一般的には、...
エチルヒドロキシキニリン-6-カルボキシ酸は適用される法規ガイドラインは何ですか?
エチルヒドロキシキニリン-6-カルボキシ酸のCAS番号1261631-01-9は、GHS分類の第2クラスの腐食物質(皮膚に強い腐食性)に分類されます。また、EU...
掲載誌
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.











![3-[7-Amino-3-(3-pyridinyl)pyrazolo[1,5-a]pyrimidin-6-yl]phenol structure 3-[7-Amino-3-(3-pyridinyl)pyrazolo[1,5-a]pyrimidin-6-yl]phenol structure](https://static.chemtradehub.com/structs/861/861249-77-6-025b.webp)
![2-Bromo-7-chloro-4H-pyrrolo[2,3-b]pyrazine structure 2-Bromo-7-chloro-4H-pyrrolo[2,3-b]pyrazine structure](https://static.chemtradehub.com/structs/115/1150617-58-5-0b0a.webp)

![methyl 6-amino-1H-pyrrolo[2,3-b]pyridine-4-carboxylate structure methyl 6-amino-1H-pyrrolo[2,3-b]pyridine-4-carboxylate structure](https://static.chemtradehub.com/structs/119/1190315-60-6-9d9a.webp)