Xian-man Zhang

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Organization: Shaoxing University
Department: Institute of Applied Chemistry
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Co-reporter:Linjun Shao, Chenze Qi and Xian-Man Zhang  
RSC Advances 2014 vol. 4(Issue 95) pp:53105-53108
Publication Date(Web):08 Oct 2014
DOI:10.1039/C4RA08469A
Chlorinated polyvinylchloride (CPVC) nanofiber mats were prepared by an electrospinning technique, and then treated with amines of different chemical structures, followed by immobilization of palladium catalysts (CPVC–NH2–Pd), which have been demonstrated as efficient, stable and easily recyclable heterogeneous catalysts. Their catalytic activities could be correlated with the binding energies of the palladium species with the amine chelating ligands.
Co-reporter:Chenze Qi;Linjun Shao;Yueqing Lu;Chen Wang
Journal of Physical Organic Chemistry 2012 Volume 25( Issue 6) pp:523-528
Publication Date(Web):
DOI:10.1002/poc.1950

An experimental approach was developed to determine the intrinsic thermolysis rate constants of the central carbon–carbon bond during the dl/meso isomerization of diethyl 2,3-dicyano-2,3-di(p-substituted phenyl)succinates (G=H, Me, OMe, Cl, and NO2) at temperatures ranging from 80 to 120 °C. The obtained rate constants are significantly affected by the polarity of the para substituents, in sharp contrast to their negligible effects on the dl/meso isomerization equilibrium constants. Moreover, the substituent effects on the activation enthalpies can be linearly correlated with the Hammett substituent resonance constants and the homolytic dissociation enthalpies (bond dissociation energies) of the benzylic C–H bonds of ethyl 2-cyano-2-(p-substituted phenyl)acetates. Copyright © 2011 John Wiley & Sons, Ltd.

Co-reporter:Minfeng Zeng, Xin Zhang, Linjun Shao, Chenze Qi, Xian-Man Zhang
Journal of Organometallic Chemistry 2012 704() pp: 29-37
Publication Date(Web):
DOI:10.1016/j.jorganchem.2012.01.003
Co-reporter:Minfeng Zeng, Yijun Du, Chenze Qi, Shufeng Zuo, Xiudong Li, Linjun Shao and Xian-Man Zhang  
Green Chemistry 2011 vol. 13(Issue 2) pp:350-356
Publication Date(Web):24 Dec 2010
DOI:10.1039/C0GC00780C
An efficient and recyclable ligand-free heterogeneous catalyst has been prepared by the immobilization of palladium onto ground pearl shell powders (Pd/shell powders, Pd/SP). The catalytic activity and recyclability of the prepared Pd/SP along with the charcoal and calcium carbonate supported palladium (Pd/C and Pd/CaCO3) catalysts have been evaluated using the reductive homocoupling of aromatic halides. Pd/SP not only has higher catalytic activity, but also exhibits much stronger stability than Pd/C and Pd/CaCO3. The remarkable Pd/SP stability has been attributed to the chelation of palladium species with the surface chitin and protein molecules of the supported pearl shell powders. The X-ray photoelectron spectroscopy (XPS) studies show that the reductive Pd0 species can be regenerated in situ from the oxidative Pd2+ species for the Pd/SP catalyzed reductive homocoupling of aromatic halides in ethanol/DMSO solution, suggesting that the heterogeneous and homogeneous palladium catalysis proceeds through a similar Pd0/Pd2+ cycle catalytic mechanism.
(E)-Butyl 3-(4-acetylphenyl)acrylate
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2-Propenoic acid, 3-(4-nitrophenyl)-, butyl ester, (2E)-
2-Propenoic acid, 3-(4-bromophenyl)-, butyl ester, (2E)-
(E)-Butyl 3-(4-fluorophenyl)acrylate