Luan Thanh Nguyen, Hai Le Tran, Tam Hoang Luu, Duong Le Thanh, Cam Hong Thi Nguyen, Thao Phuong Le Nguyen, Tam Huu Nguyen, Chau Duc Tran, Le-Thu T. Nguyen, Quoc Thiet Nguyen, Mai Ha Hoang, Ha Tran Nguyen
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The chemical structure of the diblock polymer was confirmed via <sup>1</sup>H NMR and FTIR spectroscopies. In addition, its optical and thermal properties were also investigated via differential scanning calorimetry (DSC), UV–Vis and photoluminescence spectroscopies. The influence of solvent polarity on the conformational states and optical properties of the regioregular P3HT chains was examined.</p><h3>Graphical abstract</h3><p>Multi-responsive conjugated rod-coil block copolymers have attracted due to their response to external signals, resulting in structure, shape, and property changes in the coil segments. This class of copolymers combines the tunable structural control and photophysical properties of conjugated rods with the self-assembly behavior and physical properties of block copolymers. The morphologies of block copolymers have been extensively researched, attracting fundamental and application-oriented interests. The diblock copolymers with hydrophilic and hydrophobic segments exhibit distinct natures that give rise to unique phase behaviors in nanometer dimensions, leading to a broad range of applications, including data recording, optical switching, drug delivery systems, and sensors. In this research, a rod-coil diblock copolymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) which was synthesized by a combination of the Kumada catalyst-transfer polymerization and ATRP polymerization of co-monomers including 2-(dimethylamino)ethyl methacrylate (DMAEMA), 1-pyrenylmethyl methacrylate (PyMA) and methacrylate spirooxazine (MSp). The synthesized diblock polymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) reveals a controlled molecular weight of 15200 g/mol with a dispersity index of 1.16. The chemical structure of the diblock copolymer was confirmed via 1H NMR and FTIR spectroscopies. In addition, its optical and thermal properties were also investigated through differential scanning calorimetry (DSC) and UV-Vis spectroscopies.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":688,"journal":{"name":"Macromolecular Research","volume":"32 10","pages":"959 - 970"},"PeriodicalIF":2.8000,"publicationDate":"2024-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Controlled synthesis and optical investigation of conjugated rod-coil diblock copolymer based on poly(3-hexylthiophene) and poly(2-(dimethylamino)ethyl methacrylate-random-1-pyrenylmethyl methacrylate-random-methacrylate spirooxazine)\",\"authors\":\"Luan Thanh Nguyen, Hai Le Tran, Tam Hoang Luu, Duong Le Thanh, Cam Hong Thi Nguyen, Thao Phuong Le Nguyen, Tam Huu Nguyen, Chau Duc Tran, Le-Thu T. 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The influence of solvent polarity on the conformational states and optical properties of the regioregular P3HT chains was examined.</p><h3>Graphical abstract</h3><p>Multi-responsive conjugated rod-coil block copolymers have attracted due to their response to external signals, resulting in structure, shape, and property changes in the coil segments. This class of copolymers combines the tunable structural control and photophysical properties of conjugated rods with the self-assembly behavior and physical properties of block copolymers. The morphologies of block copolymers have been extensively researched, attracting fundamental and application-oriented interests. The diblock copolymers with hydrophilic and hydrophobic segments exhibit distinct natures that give rise to unique phase behaviors in nanometer dimensions, leading to a broad range of applications, including data recording, optical switching, drug delivery systems, and sensors. In this research, a rod-coil diblock copolymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) which was synthesized by a combination of the Kumada catalyst-transfer polymerization and ATRP polymerization of co-monomers including 2-(dimethylamino)ethyl methacrylate (DMAEMA), 1-pyrenylmethyl methacrylate (PyMA) and methacrylate spirooxazine (MSp). The synthesized diblock polymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) reveals a controlled molecular weight of 15200 g/mol with a dispersity index of 1.16. The chemical structure of the diblock copolymer was confirmed via 1H NMR and FTIR spectroscopies. 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Controlled synthesis and optical investigation of conjugated rod-coil diblock copolymer based on poly(3-hexylthiophene) and poly(2-(dimethylamino)ethyl methacrylate-random-1-pyrenylmethyl methacrylate-random-methacrylate spirooxazine)
This research presents a conjugated rod–coil diblock copolymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) which was synthesized by a combination of the Kumada catalyst-transfer polymerization and ATRP method of co-monomers including 2-(dimethylamino)ethyl methacrylate (DMAEMA), 1-pyrenylmethyl methacrylate (PyMA) and methacrylate spirooxazine (MSp). The synthesized copolymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) revealed a controlled molecular weight of 12,200 g/mol with a dispersity index of 1.16. The chemical structure of the diblock polymer was confirmed via 1H NMR and FTIR spectroscopies. In addition, its optical and thermal properties were also investigated via differential scanning calorimetry (DSC), UV–Vis and photoluminescence spectroscopies. The influence of solvent polarity on the conformational states and optical properties of the regioregular P3HT chains was examined.
Graphical abstract
Multi-responsive conjugated rod-coil block copolymers have attracted due to their response to external signals, resulting in structure, shape, and property changes in the coil segments. This class of copolymers combines the tunable structural control and photophysical properties of conjugated rods with the self-assembly behavior and physical properties of block copolymers. The morphologies of block copolymers have been extensively researched, attracting fundamental and application-oriented interests. The diblock copolymers with hydrophilic and hydrophobic segments exhibit distinct natures that give rise to unique phase behaviors in nanometer dimensions, leading to a broad range of applications, including data recording, optical switching, drug delivery systems, and sensors. In this research, a rod-coil diblock copolymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) which was synthesized by a combination of the Kumada catalyst-transfer polymerization and ATRP polymerization of co-monomers including 2-(dimethylamino)ethyl methacrylate (DMAEMA), 1-pyrenylmethyl methacrylate (PyMA) and methacrylate spirooxazine (MSp). The synthesized diblock polymer P3HT-b-P(DMAEMA-r-PyMA-r-MSp) reveals a controlled molecular weight of 15200 g/mol with a dispersity index of 1.16. The chemical structure of the diblock copolymer was confirmed via 1H NMR and FTIR spectroscopies. In addition, its optical and thermal properties were also investigated through differential scanning calorimetry (DSC) and UV-Vis spectroscopies.
期刊介绍:
Original research on all aspects of polymer science, engineering and technology, including nanotechnology
Presents original research articles on all aspects of polymer science, engineering and technology
Coverage extends to such topics as nanotechnology, biotechnology and information technology
The English-language journal of the Polymer Society of Korea
Macromolecular Research is a scientific journal published monthly by the Polymer Society of Korea. Macromolecular Research publishes original researches on all aspects of polymer science, engineering, and technology as well as new emerging technologies using polymeric materials including nanotechnology, biotechnology, and information technology in forms of Articles, Communications, Notes, Reviews, and Feature articles.