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| 1 | 显示文摘 | Yanlong Qian Keleypette Dono Jiling Huang | 2001 | Journal of Applied Polymer Science2001，81，： | 1 |
| 2 | 显示文摘 | Keleypette Dono Jiling Huang Haiyan Ma | 2000 | Journal of Applied Polymer Science2000，77，： | 1 |
| 3 | Chlorination of differentially ringsubstituted titanocene complex by SO2Cl2/SOCl2 and X-my structure of chlorinated product TiCl2显示文摘 | Jiling Huang Quiqian Huang YangLong Qian | 1998 | Polyhedron1998，17，15： | 1 |
| 4 | Elevated p53 expression levels correlate with tumor progression and poor prognosis in patients exhibiting esophageal squamous cell carcinoma显示文摘 | Kate Huang Lin Chen Jiling Zhang | 2014 | Oncol Let2014，8，： | 1 |
| 5 | The ring - opening of dicyclopentadiene with titanocene complexes显示文摘 | Liu Jianfei Zhang Danfeng Huang Jiling | 1999 | Joumal of Molec- ular Catalysis A1999，142，3： | 1 |
| 6 | Ethylene trimeri- zation with a half-sandwich titanium complex bearing a pen- dant thienyl group显示文摘 | Huang Jiling Wu Tianzhi Qian Yanlong | 2003 | Chem Commun2003，39，22： | 1 |
| 7 | Catalytic trimeriza- tion of ethylene by half-sandwich titanium complexes bear- ing a pendant ethereal group显示文摘 | Wu Tianzhi Qian Yanlong Huang Jiling | 2004 | Journal of Molecular Catal- ysis A: Chemical2004，214，2： | 1 |
| 8 | Ring opening metath- esis polymerization of Norbornene Catalyzed by MC14 2L/CH3Li 显示文摘 | Huang Jiling Keleypette Dono Ma Haiyan | 1999 | Chinese Journal of Catalysis1999，20，5： | 1 |
| 9 | Catalytic Synthesis of Polymethyl Methacrylate by Mixed Ligand Schiff Base Lanthanocene Complexes显示文摘 | Yousaf MUHAMMAD 1, HUANG Jiling 1, FENG Zuofeng 1, QIAN Yanlong 1, SUN Junquan 2, PAN Zhida 2(1 Laboratory of Organometallic Chemistry, East China University of Science and Technology, Shanghai 200237, China 2 Material and Chemical Engineering Co | 2000 | 催化学报2000，21，4： | 0 |
| 10 | Synthesis and Characterization of Cyclopentadienylchromium Complexes Bearing a Pendant o-Me_2N-C_6H_4-C(CH_3)(CH_3)-Group as Catalysts for Ethylene Polymerization显示文摘 | QIAN Yanlong, ZHANG Hao, HUANG Jiling (Laboratory of Organometallic Chemistry, East China University of Science and Technology, Shanghai 200237, China) | 2003 | 催化学报2003，24，7： | 0 |
| 11 | Access to High-Molecular-Weight Polyethylenes through High Temperature Ethylene Polymerization Catalysed by Ethylene-Bridged ansa-(3-R-Cyclopentadienyl)(Fluorenyl) Zirconocene Complexes显示文摘A series of C1-symmetric ethylene-bridged ansa-(3-R-cyclopentadienyl)(fluorenyl) metallocene complexes(Zr: 1-5;Hf: 6) have been synthesized, characterized and investigated as catalyst precursors for the high temperature ethylene polymerization. Using methylaluminoxane(MAO) as the cocatalyst, zirconium complexes 1-5 bearing a bulky substituent on the 3-position of the cyclopendienyl ring showed high catalytic activities up to 1.48×10^(7) g PE·mol_(Zr)^(-1)·h^(-1) toward the polymerization of ethylene and afforded polyethylenes with high molecular weights(1.49×10^(5)-6.31×10^(5) g/mol), meanwhile exhibting great thermal stability at high temperatures up to 120 ℃ together with a long catalytic life time up to 2 h. By adopting low Al/Zr ratios, such as 125, polyethylenes with ultra high molecular weights up to 2.86×106 g/mol were obtained. It is worthy of noting that zirconium complexes 1-4 bearing a substituent with an aryl pendant showed temperature-dependent activities, which increased rapidly with the increase of polymerization temperature, thus weak interaction of the pendent aryl group with the cationic active center is proposed to account for the very low activities displayed at low temperatures. In contrast to zirconocene complexes 1-5, hafnocene complex 6 only displayed very low catalytic activities toward the polymerization of ethylene and afforded polyethylenes with molecular weights ten times smaller than those obtained by zirconocene complexes 1-5. Zirconocene complexes 1-5 were also able to catalyse the polymerization of propylene at high temperatures, but only afforded waxes with low molecular weights. | Bo Li Haiyan Ma Jiling Huang | 2024 | Chinese Journal of Polymer Science2024，42，1： | 0 |
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