个人简历

教育背景\r
1978.9-1979.6 苍南县灵溪中学\r
1979.9-1983.7 杭州大学化学系 学士\r
1983.9-1986.6 上海有机所 硕士\r
1986.7-1990.6 上海有机所 西柏林工业大学 合培博士\r
1990.7-1991.11 上海有机所 助研\r
1991.12-1995.7 南加州大学 博士后\r
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担任职位\r
1990-1991 上海有机化学研究所助理研究员\r
1991-1995 南加州大学博士后研究员\r
1995-1998 香港中文大学助理教授\r
1998-2002 香港中文大学副教授\r
2002-2006 香港中文大学教授\r
2006-2013 香港中文大学化学讲座教授\r
2013年至今 香港中文大学卓敏化学讲座教授

研究领域

""有机金属化学领域，重点是碳硼烷，超级碳硼烷和碳硼烷金属络合物，并应用于有机，无机和材料化学的研究领域""""

近期论文

Catalytic Cascade Dehydrogenative Cross-Coupling of BH/CH and BH/NH: One-Pot Process to Carborano-Isoquinolinone Au, Y. K.; Lyu, H.; Quan, Y.; Xie, Z. J. Am. Chem. Soc. 2019, 141, 12855-12862. \r
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How long a C–C bond can be? An example of extraordinary long C–C single bond in 1,2-diarylamino-o-carborane Wu, Y.; Zhang, J.; Xie, Z. Chin. Chem. Lett. 2019, ASAP. \r
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Rhodium catalyzed cascade cyclization featuring B–H and C–H activation: one-step construction of carborane-fused N-polyheterocycles Lyu, H.; Zhang, J.; Yang, J.; Quan, Y.; Xie, Z. J. Am. Chem. Soc. 2019, 141, 4219-4224. \r
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Controlled functionalization of o-carborane viatransition metal catalyzed B–H activation Quan, Y.; Xie, Z. Chem. Soc. Rev. 2019, ASAP. \r
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Nucleophilic substitution: a facile strategy for selective B–H functionalization of carboranes Quan, Y.; Tang, C.; Zhang, J.;Xie, Z. Dalton Trans. 2019, ASAP.\r
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Copper catalyzed/mediated direct B–H alkenylation/alkynylation in carboranes Chen, Y.; Au, Y. K.; Quan, Y.; Xie, Z.Sci China Chem, 2019, 62, 74-79.\r
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Regioselective Nucleophilic Alkylation/Arylation of B–H Bonds in o-Carboranes: An Alternative Method for Selective Cage Boron Functionalization Tang, C.; Zhang, J.; Zhang, J.; Xie, Z.J. Am. Chem. Soc., 2018, 140, 16423-16427.\r
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Broad Scope Extra‐Annular [4 + 2] Cycloaddition of o‐Carboryne with Styrenes: Efficient Route to Carborane‐Fused Polycyclics Zhang, J.; Xie, Z. Chin. J. Chem. 2018, 36, 1041-1046.\r
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Rhodium catalyzed cascade cyclization featuring B–H and C–H activation: one-step construction of carborane-fused N-polyheterocycles Lyu, H.; Quan, Y.; Xie, Z. Chem. Sci., 2018, 9, 6390-6394\r
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Reaction of o‐Carboryne with Furans: Facile Synthesis of Carborane-Fused Oxanorbornenes and Their Derivatives Zhang, R.; Yuan, Y.; Qiu, Z.; Xie, Z. Chin. J. Chem. 2018, 36, 273-279.\r
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16th International Meeting on Boron Chemistry (IMEBORON XVI) Xie, Z. Pure Appl. Chem. 2018, 90, 605. \r
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Enantioselective Synthesis of Chiral-at-Cage o-Carboranes via Pd-Catalyzed Asymmetric B–H Substitution Cheng, R.; Li, B.; Wu, J.; Zhang, J.; Qiu, Z.; Tang, W.; You, S. L.; Tang, Y.; Xie, Z. J. Am. Chem. Soc. 2018, 140, 4508-4511. \r
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Transition‐Metal‐Like Behavior of Monovalent Boron Compounds: Reduction, Migration, and Complete Cleavage of CO at a Boron Center Wang, H.; Wu, L.; Lin, Z.; Xie, Z.Angew. Chem. Int. Ed. 2018, 57, 8708-8713.\r
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Borylene Insertion into Cage B–H Bond: A Route to Electron-Precise B–B Single Bond Wang, H.; Zhang, J.; Lee, H. K.; Xie, Z. J. Am. Chem. Soc. 2018, 140, 3888-3891. \r
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Synthesis, structure and reactivity of a carborane-fused silylene 1-{[PhC(NtBu)2]Si}-1,2-C2B10H11 Wang, H.; Zhang, J.; Xie, Z. J. Organomet. Chem. 2018, 865, 173-177. \r
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Transition‐Metal‐Catalyzed Selective Cage B−H Functionalization of o‐Carboranes Quan, Y.; Qiu, Z.; Xie, Z. Chem. Eur. J. 2018, 24, 2795-2805. \r
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Cage carbon-substitute does matter for aggregation-induced emission features of o-carborane-functionalized anthracene triads Wu, X.; Guo, J.; Quan, Y.; Jia, W.; Jia, D.; Chen, Y.; Xie, Z. J. Mater. Chem. C 2018, 15, 4140-4149. \r
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Synthesis of carborane-fused carbo- and heterocycles via zirconacyclopentane intermediates Cui, C. X.; Ren, S.; Qiu, Z.; Xie, Z. Dalton Trans. 2018, 47, 2453-2459. \r
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Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles Chan, T. L.; Xie, Z. Chem. Sci. 2018, 9, 2284-2289. \r
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Cyclic amino(carboranyl) silylene: synthesis, structure and reactivity Wang, H.; Chan, T. L.; Xie, Z. Chem. Commun. 2018, 54, 385-388. \r
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Broad Scope [4 + 2] Cycloaddition of o-Carboryne with Pentafulvenes Using 1-Li-2-OTf-o-C2B10H10 as Precursor Zhang, J.; Qiu Z.; Xie, Z. Organometallics 2017, 36, 3806-3811.