Yuting Leng

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Organization: Zhengzhou University
Department: The College of Chemistry and Molecular Engineering, Key Laboratory of Chemical Biology and Organic Chemistry of Henan Province
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Co-reporter:Shuaijiang Ma, Shiwei Wang, Qian Li, Yuting Leng, Lianhui Wang, and Guo-Hua Hu
Industrial & Engineering Chemistry Research July 19, 2017 Volume 56(Issue 28) pp:7971-7971
Publication Date(Web):June 21, 2017
DOI:10.1021/acs.iecr.7b01812
This work provides a new method to prepare poly(vinyl alcohol) (PVA) hydrogel. Compared with the traditional repeated freeze–thaw method, the physical cross-linking method was adopted to prepare a high-strength hydrogel in one step. The morphology, melting, and crystallization behavior and mechanical properties of the hydrogel were investigated. The hydrogel has a high water content and reswelling rate, as well as a high melting temperature and mechanical strength. It also has a stable cross-linked structure in the temperature range of 25–65 °C. The hydrogel fracture surface shows ductile and brittle fracture morphology. The protrusions in the hydrogel three-dimensional topography are more numerous and homogeneous when the solvent preparation ratio is 4–6. On the basis of the good plasticity of the hydrogels, tubular hydrogels with inner diameters of 1–6 mm are also prepared to widen their applications.
Co-reporter:Hui-Jie Qiao, Fan Yang, Shi-Wei Wang, Yu-Ting Leng, Yang-Jie Wu
Tetrahedron 2015 Volume 71(Issue 49) pp:9258-9263
Publication Date(Web):9 December 2015
DOI:10.1016/j.tet.2015.10.035
An efficient and general protocol for palladium-catalyzed chelation-assisted ortho-nitration of 2-arylbenzoxazoles has been developed. This nitration exhibits high regioselectivity for the substrates, and the reaction could tolerate many functional groups such as F, Cl, Br, CH3, CH3O, affording ortho-nitration products in moderate to good yields. Moreover, some 2-arylbenzoxazole heterocyclic analogues proceed well under this catalytic system. Further studies have been performed to obtain insight into the mechanism.This palladium-catalyzed ortho-nitration could tolerate many functional groups in the 2-arylbenzoxazole (e.g. F, Cl, Br, CH3 and CH3O), affording ortho-nitration products in moderate to good yields. Moreover, some 2-arylbenzoxazole heterocyclic analogues proceed well under this catalytic system.
Co-reporter:Gaizhi Ma;Huijie Qiao;Fan Yang;Shiwei Wang;Yangjie Wu
Applied Organometallic Chemistry 2014 Volume 28( Issue 1) pp:44-47
Publication Date(Web):
DOI:10.1002/aoc.3069

The palladacycle-catalyzed esterification of a variety of aldehydes with alcohols was developed. This reaction allows formation of esters in moderate to excellent yields not only for various aldehydes but also alcohols. In addition, the esterification could proceed well under mild conditions with a low catalyst loading of 0.0625 mol%. Copyright © 2013 John Wiley & Sons, Ltd.

Co-reporter:Guangwei Chen;Fan Yang;Shiwei Wang;Yangjie Wu
Chinese Journal of Chemistry 2013 Volume 31( Issue 12) pp:1488-1494
Publication Date(Web):
DOI:10.1002/cjoc.201300675

Abstract

An efficient palladacycle-catalyzed aromatic carbonylation reaction of aryl formates with aryl iodides or bromides has been developed. Commercially available and easily prepared aryl formates were employed as carbonyl sources without the use of external carbon monoxide. The present catalytic system shows broad functional group tolerance and affords aryl benzoate derivatives in good to excellent yields.

Co-reporter:Gaizhi Ma, Yuting Leng, Yusheng Wu, Yangjie Wu
Tetrahedron 2013 69(2) pp: 902-909
Publication Date(Web):
DOI:10.1016/j.tet.2012.10.080
2-Octanol, 4-nitrobenzoate
Cyclohexanecarboxylic acid, (4-methoxyphenyl)methyl ester
Palladium, di-m-chlorobis[2-[1-[(4-methylphenyl)imino-kN]ethyl]ferrocenyl-kC]di-
Chloro [2-[1-[(4-methylphenyl)imino]ethyl]ferro Cenyl-c,n]triphenylphosphine)-palladium
Benzoic acid, 3-nitro-, hexyl ester
p-Methoxybenzoic acid, hexyl ester
BUTYL 3-METHOXYBENZOATE