学院简介

深圳大学高等研究院是深圳大学于2014年成立的一个包含本科与研究生培养、侧重跨学科教学与学术研究的校内综合办学单位。作为深圳大学内部探索全面改革创新的学术特区,高等研究院与香港和海外著名高校合作,借鉴国内外研究型大学通行的管理模式,引进具有一流视野的资深教授和发展潜力的青年教师,营造与国际接轨的学术氛围和培养环境,开展卓越的教学、研究和管理工作。

人员信息

陈友根

博士,助理教授

邮箱:chenyg@szu.edu.cn

通讯地址:深圳大学行政办公楼341


教育背景:

2012,日本北海道大学,高分子化学,博士

2010,日本北海道大学,高分子化学,硕士

2007,哈尔滨工程大学,化学工程与工艺,学士


工作经历:

2013.12—2015.12,北海道大学,助理教授

2012.11—2013.11,苏黎世联邦理工学院 (ETH Zürich),博士后

2011.07—2011.10,国立台湾大学 (NTU),访问研究员

2010.04—2013.03,日本学术振兴会 (JSPS),特别研究员兼任


学术兼职:

北海道大学工学研究院 特聘教员 (2016.04-)


所获奖项:

2017年深圳市海外高层次人才计划:孔雀计划C类

2016年北海道大学教学研究校长奖


研究兴趣:

主要从事于聚合物的可控合成,聚合物结构-性能关系的解析,以及新型聚合方法的开发。近年来主要关注于应用有机小分子催化剂合成无金属残留的绿色聚合物材料,以实现所得高分子在光电、生物、以及环境友好型材料等领域的应用;并为聚合物材料的工业化生产提供实用的解决手段。除此之外,也关注于各种对温度,pH,手性等外部刺激产生高敏性感应的高分子材料的开发与应用。已在高分子相关领域发表SCI论文50余篇。课题组接受材料方向推免研究生,并长期招收博士后,欢迎化学、催化、高分子相关专业的博士毕业生申请。

1. 基于有机催化的新型聚合方法的开发;

2. 有机催化基团转移聚合方法的研究与应用;

3. 有机催化开环聚合方法的开发与应用;

4. 对外部刺激产生高敏应答性高分子材料的开发与应用


科研项目:

1,深圳科技创新委员会基础研究项目面上项目,JCYJ20190808154011907,环状聚酯的新型合成方法及其物性研究,2020-2022,40万,主持,在研。

2,深圳科技创新委员会基础研究项目学科布局,JCYJ20180507182227257,基20180286 微塑料与内分泌干扰物对海洋贝类联合毒性效应研究,2019-2021,100万,参与,在研。

3,国家自然科学基金青年项目,21604057,基于有机分子催化基团转移聚合的丙烯酸类聚合物末端官能化的基础性研究及其拓展,2017-2019,20万,主持,已结题。

4,深圳科技创新委员会基础研究项目,JCYJ20160422154131724,基于有机催化基团转移聚合的新型表面涂覆技术的研究,2017-2018,30万,主持,已结题。


发表论文:

1. Q. Jia, Z.-C. Yan, Y. Li, J. Liu, Y. Ding, Y. Liu, J. Li, Y.-G. Chen*, Synthesis of well-defined di- and triblock acrylic copolymers consisting of hard poly(dicyclopentanyl acrylate) and soft poly(alkyl acrylate) segments by organocatalyzed group transfer polymerization and their glass transition behavior. Polym. Chem., 2021, 12, xxxx-xxxx. Accepted.

2. Y. Liu, Q. Jia, Y. Ding, Y.-G. Chen*, Synthesis of polyacrylate-based polyurethane by organocatalyzed group transfer polymerization and polyaddition, Macromol. Chem. Phys., 2020, https://doi.org/10.1002/macp.202000217.

3. 陈友根*, 丁远生. 有机催化基团转移聚合的研究进展.化学学报, 2020, 78, 733-745.

4. M. W. Ali, Z. Muhammad, Q. Jia, L. W. Li*, M. Saleem, M. Siddiq, Y.-G. Chen*. Synthesis of cyclic poly(2-ethyl-2-oxazoline) with degradable disulfide bond. Polym. Chem., 2020, 11, 4164–4171.

5. M. Saleem, R. Sidra, Y.-G. Chen*. Silk fibroin/hydroxyapatite scaffold: a highly compatible material in bone regeneration, Sci. Technol. Adv. Mater., 2020, 21, 242-266.

6. Y. Huang, Y. Liu, M. Saleem, Q. Jia, Y. Ding, Y.-G. Chen*. A facile end-functionalization of polystyrene by ATRP and click chemistry: chain endeffect on the glass transition temperature, React. Funct. Polym., 2020, 148, doi: 10.1016/j.reactfunctpolym.2020.104566.

7. J. Deng, M. Saleem, Q. Jia, Y. Ding, Y. Liu, Y.-G. Chen*. Synthesis, surface wettability, and thermal property of poly(ε-caprolactone)-based polyurethane bearing triethylene glycol monomethyl as side chain, React. Funct. Polym., 2020, 148, doi.org/10.1016/j.reactfunctpolym.2020.104506.

8. J. Li, S. Kikuchi, S.-i. Sato, Y.-G. Chen, L. Xu, B. Song, Q. Duan, Y. Wang, T. Kakuchi*, X. Shen*. Core-First Synthesis and Thermoresponsive Property of Three , Four , and Six-Arm Star-Shaped Poly(N,N diethylacrylamide)s and Their Block Copolymers with Poly(N,N dimethylacrylamide). Macromolecules 2019, 52, 19, 7207-7217.

9.Y.-G. Chen*, Q. Jia, Y. Ding, S.-I. Sato, L. Xu, C. Zang, X. Shen, and T. Kakuchi*. B(C6F5)3-catalyzed group transfer polymerization of acrylates using hydrosilane: polymerization mechanism, applicable monomers, and synthesis of well-defined acrylate polymers, Macromolecules 2019, 51, 844-856.

10. F.-C. Liang, Y.-H. Huang, C.-C. Kuo, C.-J. Cho, S.-P. Rwei, Q. Jia, Y. Ding, Y.-G. Chen*, R. Borsali. Thermally deposited silk fibroin as the gate dielectric layer in organic thin film transistors based on conjugated polymer. React. Funct. Polym., 2018, 131, 386-377.

11.陳友根、沈賢徳、覚知豊次. 有機分子触媒を用いたグループトランスファー重合の新展開.日本接着学会誌 , 2017, 53, 432-440.

12. J.-T. Wang, K. Saito, H.-C. Wu, H.-S. Sun, C.-C. Hung, Y.-G. Chen, T. Isono, T. Kakuchi, T. Satoh, W.-C. Chen. High performance strechable resistive memories using donor-acceptor block copolymers with fluorene rods and pendent isoindigo coils. NPG Asia Materials, 2016, 8, e298; doi:10.1038/am.2016.112.

13. S. Kikuchi, Y.-G. Chen, E. Ichinohe, K. Kitano, T. Satoh, S. Sato, T. Kakuchi, Synthesis and thermoresponsive property of linear, cyclic, and star-shaped poly(N,N-diethylacrylamide)s using B(C6F5)3-catalyzed group transfer polymerization as facile end-functionalization method, Macromolecules 2016, 49, 4828-4838.

14. N. Xue, X. Qiu, Y.-G. Chen, T. Satoh,T. Kakuchi,F.-M. Winnik, Effect of chain architecture on the phase transitions of star and cyclic poly(N-isopropylacrylamide) in water, J. Polym. Sci., Part B: Polym. Phys., 2016, 54, 2059-2068.

15. L. Hong, J. He, Y.-G. Chen, T. Kakuchi, Synthesis of ABB’ and ABC star copolymers via a combination of NMRP and ROP reaction, Polym. Chem., 2016, 7, 3599-3607.

16.Y.-G. Chen, T. Kakuchi, Organocatalyzed group transfer polymerization. Chem. Rec., 2016, 16, 2161-2183.

17. S. Kikuchi, Y.-G. Chen, K. Kitano, T. Satoh, T. Kakuchi, B(C6F5)3-catalyzed group transfer polymerization of N,N-disubstituted acrylamide using hydrosilane: effect of hydrosilane and monomer structures, polymerization mechanism, and synthesis of -end-functionalized polyacrylamides. Macromolecules 2016, 49, 3049-3060.

18. J.-T. Wang, S. Takashima, H.-C. Wu, Y.-C. Chiu, Y.-G. Chen, T. Isono, T. Kakuchi, T. Satoh, W.-C. Chen. Donor-acceptor poly(3-hexylthiophene)-block-pendent poly(isoindigo) with dual roles of charge transporting and storage layer for high-performance transistor-type memory applications. Adv. Funct. Mater., 2016, 26, 2695-2705.

19. H.-S. Sun, Y.-G. Chen, W.-Y. Lee, T. Isono, T. Satoh, T. Kakuchi, W.-C. Chen. Synthesis, morphology, and electrical memory application of oligosaccharide-based block copolymers with π-conjugated pyrene moieties and their supramolecules. Polym. Chem., 2016, 7, 1249-1263.

20.Y.-G. Chen, K. Fuchise, T. Satoh, T. Kakuchi, Anionic polymerization: Principles, Practice,Strength, Consequences, and Applications, 2-11. Group Transfer Polymerization of Acrylic Monomers, Springer, 2015, 451-494.

21. S. Kikuchi, Y.-G. Chen, K. Kitano, K. Takada, T. Satoh, T. Kakuchi, Organic acids as efficient catalysts for group transfer polymerization of N,N-disubstituted acrylamide with silyl ketene acetal: polymerization mechanism and synthesis of diblock copolymers. Polym. Chem., 2015, 6, 6845-6856.

22. O.-T. Eric, Y.-G. Chen, K. Takada, S.-I. Sato, T. Satoh, T. Kakuchi, Synthesis of AB block and A2B2 and A3B3 miktoarm star-shaped copolymers using ω-end-functionalized poly(methyl methacrylate) with a hydroxyl group prepared by organocatalyzed group transfer polymerization. Polym. Chem., 2015, 6, 7841-7850.

23. H.-S. Sun, Y.-C. Chiu, W.-Y. Lee, Y.-G. Chen, A. Hirao, T. Satoh, T. Kakuchi, W.-C. Chen, Synthesis of oligosaccharide-based block copolymers with pendent π-conjugated oligofluorenemoieties and their electrical device applications. Macromolecules, 2015, 48, 3907–3917.

24.Y.-G. Chen, K. Kitano, S. Tsuchida, S. Kikuchi, K. Takada, T. Satoh, T. Kakuchi, B(C6F5)3-catalyzed group transfer polymerization of alkyl methacrylates with dimethylphenylsilane through in situ formation of silyl ketene acetal by B(C6F5)3-catalyzed 1,4-hydrosilylation of methacrylate monomer. Polym. Chem., 2015, 6, 3502-3511.

25.Y.-G. Chen, N. Xiao, M. Fukuoka, K. Yoshida, Q. Duan, T. Satoh, T. Kakuchi. Synthesis and thermoresponsive properties of four-arm star-shaped poly(N-isopropylacrylamide)s bearing covalent and non-covalent cores. Polym. Chem., 2015, 6, 3608-3616.

26. J.-Z. Wang, Y.-C. Chiu, H.-S. Sun, K. Yoshida, Y.-G. Chen, T. Satoh, T. Kakuchi. W.-C. Chen. Synthesis of multifunctional poly(1-pyrenemethyl methacrylate)-b-poly(N-isopropylacrylamide)-b-poly(N-methylolacrylamide)s and their electrospun nanofibers for metal ion sensory applications. Polym. Chem., 2015, 6, 2327-2336.

27. K. Takada, T. Ito, K. Kitano, S. Tsuchida, Y. Takagi, Y.-G. Chen, T. Satoh, T. Kakuchi. Synthesis of homopolymers, diblock copolymers, and multiblock polymers by organocatalyzed group transfer polymerization of various acrylate monomers. Macromolecules 2015, 48, 511-519.

28.Y.-G. Chen*, K. Takada, N. Kubota, O. T. Eric, T. Ito, T. Isono, T. Satoh, T, Kakuchi. Synthesis of end-functionalized poly(methyl methacrylate) by organocatalyzed group transfer polymerization using functional silyl ketene acetals and α-phenylacrylates. Polym. Chem., 2015, 6,1830-1837.

29. K. Fuchise, S. Tsuchida, K. Takada, Y.-G, Chen, T. Satoh, T. Kakuchi, B(C6F5)3-catalyzed group transfer polymerization of n-butyl acrylate with hydrosilane through in situ formation of initiator by 1,4-hydrosilylation of n-butyl acrylate. ACS Macro Lett., 2014, 6, 1015-1019.

30. T. Isono, Y. Kondo, S. Ozawa, Y.-G. Chen, R. Sakai, S.-I. Sato, K. Tajima, T. Kakuchi, T. Satoh, Stereoblock-like brush copolymers consisting of poly(L-lactide) and poly(D-lactide) side chains along poly(norbornene) backbone: synthesis, stereocomplex formation, and structure–property relationship. Macromolecules 2014, 47, 7118-7128.

31. Y.-C. Chiu, Z.-Y. Chen, Y.-G. Chen, T. Satoh, T. Kakuchi, W.-C. Chen, High-performance nonvolatile organic transistor memory devices using the electrets of semiconducting blends. ACS Appl. Mater. & Interfaces, 2014, 6, 12780-12788.

32. T. Kenji, K. Fuchise, N. Kubota, T. Ito, Y.-G. Chen, T. Satoh, T. Kakuchi, Synthesis of α-, ω-, and α,ω-end-functionalized poly(n-butyl acrylate)s by organocatalytic group transfer polymerization using functional initiator and terminator. Macromolecules 2014, 47, 5514-5525.

33. S. Kikuchi, Y.-G. Chen, K. Fuchise, K. Takada, J. Kitakado, S. Sato, T. Satoh, T, Kakuchi. Thermoresponsive properties of 3-, 4-, 6-, and 12-armed star-shaped poly[2-(dimethylamino)ethyl methacrylate]s prepared by core-first group transfer polymerization. Polym. Chem., 2014, 5, 4701-4709.

34. T. Isono, Y. Satoh, K. Miyachi, Y.-G. Chen, S. Sato, K. Tajima, T. Satoh, T, Kakuchi. Synthesis of linear, cyclic, figure-eight-shaped, and tadpole-shaped amphiphilic block copolyethers via t-Bu-P4-catalyzed ring-opening polymerization of hydrophilic and hydrophobic glycidylethers. Macromolecules 2014, 47, 2853–2863.

35.Y.-G. Chen, N. Xiao, T. Satoh, T, Kakuchi. Synthesis of 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, and 12-armed star-shaped poly(styrene oxide) Ru(II) complexes by a click-to-chelate approach. Polym. Chem., 2014, 5, 4993-5001.

36.Y.-G. Chen, M. Li, P. Payamyar, Z.-K. Zheng, J. Sakamoto, A. D. Schlüter. Room temperature synthesis of a covalent monolayer sheet at air/water interface using a shape-persistent photoreactive amphiphilic monomer. ACS Macro Lett., 2014, 3, 153-158.

37. K. Fuchise, Y.-G. Chen, T. Satoh, T. Kakuchi. Recent progress in organocatalytic group transfer polymerization. Polym. Chem., 2013, 4, 4278-4291.

38. Y.-C. Chiu, C.-L. Liu, W.-Y. Lee, Y.-G. Chen, T. Kakuchi, W.-C. Chen, Multilevel nonvolatile transistor memories using a star-shaped poly((4-diphenylamino)benzyl methacrylate) gate electret. NPG Asia Materials, 2012, 4, e35; doi:10.1038/am.2012.64.

39.Y.-G. Chen, K. Takada, K. Fuchise, T. Satoh, T. Kakuchi, Synthesis of syndiotactic-rich star-shaped poly(methyl methacrylate) by core-first group transfer polymerization using N-(trimethylsilyl)bis(trifluoromethanesulfonyl)imide. J. Polym. Sci., Part A: Polym. Chem., 2012, 50, 3277-3285.

40. N. Xiao, Y.-G. Chen, X.-D. Shen, C.-H. Zhang, S. Yano, M. Gottschaldt, U. Schubert, T. Kakuchi, T. Satoh, Synthesis of miktoarm star copolymer Ru(II) complexes by click-to-chelate approach. Polym. J., 2012, 45, 216-225.

41. Y.-C. Chiu, Y.-G. Chen, C.-C. Kuo, S.-H. Tung, T. Kakuchi, W.-C. Chen, Synthesis, morphology, and sensory applications of multifunctional rod–coil–coil triblock copolymers and their electrospun nanofibers. ACS Appl. Mater. & Interfaces, 2012, 4, 3387-3395.

42. K. Fuchise, Y.-G. Chen, K. Takada, T. Satoh, T. Kakuchi, Effect of counter anions on kinetics and stereoregularity for the strong brønsted acid-promoted group transfer polymerization of N,N-dimethylacrylamide. Macromol. Chem. Phys., 2012, 213, 1604-1611.

43. K. Takada, K. Fuchise, Y.-G. Chen, T. Satoh, T. Kakuchi, Controlled polymerization of methyl acrylate for high-molecular-weight polymers by pentafluorophenylbis(triflyl)methane-promoted group transfer polymerization using triisopropylsilyl ketene acetal. J. Polym. Sci., Part A: Polym. Chem., 2012, 50, 3560-3566.

44.Y.-G. Chen, K. Fuchise, A. Narumi, S. Kawaguchi, T. Satoh, T. Kakuchi, Core-first synthesis of three-, four-, and six-armed star-shaped poly(methyl methacrylate)s by group transfer polymerization using phosphazenebase. Macromolecules 2011, 44, 9091-9098.

45. T. Kakuchi, Y.-G. Chen, J. Kitakado, K. Mori, K. Fuchise, T. Satoh, Organic superbase as an efficient catalyst for group transfer polymerization of methyl methacrylate. Macromolecules 2011, 44, 4641-4647.

46. J.-C. Hsu#, Y.-G. Chen#, T. Kakuchi, W.-C. Chen, Synthesis of linear and star-shaped poly[4-(diphenylamino)benzyl methacrylate]s by group transfer polymerization and their electrical memory device applications. Macromolecules, 2011, 44, 5168-5177.

47. I. Otsuka, K. Fuchise, S. Halila, S. Fort, K. Aissou, I. Paintrand, Y.-G. Chen, A. Narumi, T. Kakuchi, R. Borsali, Thermoresponsive vesicular morphologies obtained by self-assemblies of hybrid oligosaccharide-block-poly(N-isopropylacrylamide) copolymer systems. Langmuir 2010, 26, 2325-2332.

48. S.-T. Lin, K. Fuchise, Y.-G. Chen, R. Sakai, T. Satoh, T. Kakuchi. W.-C. Chen, Synthesis, thermomorphic characteristics, and fluorescent properties of poly[2,7-(9,9-dihexylfluorene)]-block-poly(N-isopropylacrylamide)-block-poly(N-hydroxyethylacrylamide) rod-coil-coil triblock copolymers. Soft Matter 2009, 5, 3761-3770.

49.Y.-G. Chen, M. Sone, K. Fuchise, R. Sakai, R. Kakuchi, Q. Duan, J.-L. Sun, A. Narumi, T. Satoh, T. Kakuchi, Structural effect of a series of block copolymers consisting of poly(N-isopropylacrylamide) and poly(N-hydroxyethylacrylamide) on thermoresponsive behavior. React. Funct. Polym., 2009, 69, 463-469.

50. A. Narumi, Y.-G. Chen, M. Sone, K. Fuchise, R. Sakai, T. Satoh, T. Kakuchi, Poly(N-hydroxyethylacrylamide) prepared by atom transfer radical polymerization as a nonionic, water-soluble, and hydrolysis-resistant polymer and/or segment of block copolymer with a well-defined molecular weight. Macromol. Chem. Phys., 2009, 210, 349-358.