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个人简介

招收博士后、研究生等,提供良好的学习发展平台,有意者请联系:gqchen@szu.edu.cn或0755-26923007 陈国强, 男,博士,副教授。2011年7月毕业于中国科学院上海有机化学研究所获理学博士学位,2011年9月至2017年6月先后在香港大学和德国明斯特大学从事博士后研究。2017年7月作为海外高层次人才引进深圳大学,任化学与环境工程学院副教授。主要从事主族元素有机(磷/硼、氮/硼受阻Lewis酸碱对化学),金属有机(络合物的合成及其催化应用)等方面的研究,研究兴趣包括:非金属碳氢键活化、二氧化碳的高效利用等。目前主持国家自然科学青年基金1项、广东省教育厅青年创新人才项目1项,深圳市海外高层次人才科研启动项目1项,至今已在J. Am. Chem. Soc.; Angew. Chem. Int. Ed.; Chem. Sci.; Chem. Common.; Chem. Eur. J.等化学核心期刊上发表论文十余篇。 工作及教育经历: 2017/07–至今,深圳大学化学与环境工程学院,副教授 2012/10–2017/06,德国明斯特大学有机化学所,博士后 2011/09–2012/09,香港大学化学系,博士后 2006/09–2011/07,中国科学院上海有机化学研究所,博士 2002/09–2006/06,中山大学化学与化学工程学院,学士

研究领域

主要从事主族元素有机(磷/硼、氮/硼受阻Lewis酸碱对化学),金属有机(络合物的合成及其催化应用)等方面的研究,研究兴趣包括:非金属碳氢键活化、二氧化碳的高效利用等

主持的科研项目: 1、 国家自然科学基金青年基金项目(项目负责人, 2019-2021年) 2、 广东省教育厅青年创新人才项目(项目负责人, 2019-2020年) 3、 深圳市海外高层次人才科研启动项目(项目负责人, 2018-2020年)

近期论文

查看导师最新文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

1. G.-Q. Chen, C. G. Daniliuc, G. Kehr, G. Erker*, “Making Use of the Functional Group Combination of a Phosphane/Borane Lewis Pair Connected by an Unsaturated Four-Carbon Bridge” Eur. J. Inorg. Chem. 2017, 4519-4524. 2. G.-Q. Chen, G. Kehr, C. G. Daniliuc, M. Bursch, S. Grimme, G. Erker*, “Intermolecular Redox-Neutral Amine C-H Functionalization Induced by the Strong Boron Lewis Acid B(C6F5)3 in the Frustrated Lewis Pair Regime" Chem. Eur. J. 2017, 23, 4723-4729. 3. G.-Q. Chen, G. Kehr, C. Mück-Lichtenfeld, C. G. Daniliuc, G. Erker*, “Phospha-Claisen type reactions at frustrated Lewis pair frameworks” J. Am. Chem. Soc. 2016, 138, 8554-8559. 4. G.-Q. Chen, G. Kehr, C. G. Daniliuc, C. Mück-Lichtenfeld, G. Erker*, “Formation of thermally robust frustrated Lewis pairs by electrocyclic ring closure reactions” Angew. Chem. Int. Ed. 2016, 55, 5526-5530. 5. G.-Q. Chen, G. Kehr, C. G. Daniliuc, G. Erker*, “Nitro-redox reactions at a frustrated borane/phosphane Lewis pair” Dalton. Trans. 2016, 45, 6820-6823. 6. G.-Q. Chen, F. Türkyilmaz, C. G. Daniliuc, C. Bannwarth, S. Grimme, G. Kehr, G. Erker*, “Enamine/butadienylborane cycloaddition in the frustrated Lewis pair regime” Org. Biomol. Chem. 2015, 13, 10477-10486. 7. G.-Q. Chen, G. Kehr, C. G. Daniliuc, B. Wibbeling, G. Erker*, “Bifunctional behavior of unsaturated intramolecular phosphane-borane frustrated Lewis pair derived from uncatalyzed 1,4-hydrophosphination of a dienylborane” Chem. Eur. J. 2015, 21, 12449-12455. 8. G.-Q. Chen, G. Kehr, C. G. Daniliuc, G. Erker*, “1,1-alkenylboration of diarylphosphino-enynes: convenient synthetic entry to vicinal P/B Lewis pairs at extended conjugated π-frameworks” Org. Biomol. Chem. 2015, 13, 764-769. 9. P. Moquist#, G.-Q. Chen#, C. Mück-Lichtenfeld, K. Bussmann, C. G. Daniliuc, G. Kehr, G. Erker*, “α-CH acidity of alkyl-B(C6F5)2 compounds – the role of stabilized borata-alkene formation in frustrated Lewis pair chemistry” Chem. Sci. 2015, 6, 816-825. (#co-first author) 10. G.-Q. Chen, Z.-J. Xu, C.-Y. Zhou, C.-M. Che*, “Selective oxidation of terminal aryl and aliphatic alkenes to aldehydes catalyzed by iron(III) porphyrins with triflate as a counter anion” Chem. Commun. 2011, 47, 10963-10965. 11. G.-Q. Chen, Z.-J. Xu, Y. Liu, C.-Y. Zhou, C.-M. Che*, “Iron-catalyzed nitrene insertion reaction for facile construction of amide compounds” Synlett 2011, 1174-1178. 12. G.-Q. Chen, Z.-J. Xu, S. L.-F. Chan, C.-Y. Zhou, C.-M. Che*, “Homogeneous silver(I) salts and heterogeneous Ag3PW12O40-catalyzed intermolecular allylation of arenes with allylic alcohols” Synlett 2011, 2713-2718. 13. T. Özgün, G.-Q. Chen, C. G. Daniliuc, A. C. McQuilken, T. H. Warren, R. Knitsch, H. Eckert, G. Kehr, G. Erker*, “Unsaturated vicinal frustrated Lewis pair formation by electrocyclic ring closure and their reaction with nitric oxide” Organometallics 2016, 35, 3667-3680. 14. Y. Liu, G.-Q. Chen, C.-W. Tse, X. Guan, Z.-J. Xu, J-S. Huang, C.-M. Che*, “[Fe(F20TPP)Cl]-catalyzed amination with arylamines and {[Fe(F20TPP)(NAr)](PhI=NAr)}+. intermediate assessed by high-resolution ESI-MS and DFT calculations” Chem. Asian. J. 2015, 10, 100-105. 15. T. W.-S. Chow, G.-Q. Chen, Y. Liu, C.-Y. Zhou, C.-M. Che*, “Practical iron-catalyzed atom/group transfer and insertion reactions” Pure Appl. Chem. 2012, 84, 1685-1704.

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