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Institution

Henan Normal University

EducationXinxiang, China
About: Henan Normal University is a education organization based out in Xinxiang, China. It is known for research contribution in the topics: Catalysis & Ionic liquid. The organization has 10863 authors who have published 11077 publications receiving 166773 citations.


Papers
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Journal ArticleDOI
TL;DR: This paper further improves the determination of DPH compared to the previous methods, and proposes a new method based on the formation of a pink compound from the reaction of D PH, sodium 1,2-naphthoquinone-4-sulfonate and Zeph.

78 citations

Journal ArticleDOI
TL;DR: It is shown that saturation recovery from infective individuals leads to vital dynamics, such as bistability and periodicity, when the basic reproduction number R(0) is less than unity.

77 citations

Journal ArticleDOI
TL;DR: It is showed that low level of Hg(II) can be effectively preconcentrated by this new selective solid phase extractor.

77 citations

Journal ArticleDOI
TL;DR: Rh(III)-catalyzed C–H activation of nitrones and azomethine imines in the context of dipolar addition with alkylidenecyclopropanes (ACPs) have been realized and bridged cycles are delivered.
Abstract: Bridged cycles are an important class of structural motif in various biologically active molecules. Rh(III)-catalyzed C–H activation of nitrones and azomethine imines in the context of dipolar addition with alkylidenecyclopropanes (ACPs) have been realized. By taking advantage of the ring strain in ACPs, the reaction with aryl nitrones delivered bridged [3.2.1] bicyclic isoxazolidines, and reaction with azomethine imines afforded bridged tricyclic pyrazolones under the same conditions, where both the nitrone and azomethine imine act as a dipolar directing group. All the reactions occurred under mild conditions with broad substrates scope, high efficiency, and >20:1 diastereoselectivity. The synthetic applications of this protocol have also been demonstrated.

77 citations

Journal ArticleDOI
Yuanchao Pei1, Zhiyong Li1, Li Liu1, Jianji Wang1, Huiyong Wang1 
TL;DR: In this article, it was found that aqueous solution of a hydrophilic ionic liquid (IL), 1-butyl-3-methylimidazolium dicyanamide ([C4mim][N(CN)2]), could be separated into two phases by inorganic salts such as K2HPO4 and K3PO4.
Abstract: In the present work, it was found that aqueous solution of a hydrophilic ionic liquid (IL), 1-butyl-3-methylimidazolium dicyanamide ([C4mim][N(CN)2]), could be separated into an aqueous two-phase system (ATPS) by inorganic salts such as K2HPO4 and K3PO4. The top phase is IL-rich, while the bottom phase is phosphate-rich. It was shown that 82.7%–100% bovine serum albumin (BSA) could be enriched into the top phase and almost quantitative saccharides (arabinose, glucose, sucrose, raffinose or dextran) were preferentially extracted into the bottom phase in a single-step extraction by [C4mim][N(CN)2] + K2HPO4 ATPS. The extraction efficiency of BSA from the aqueous saccharide solutions was influenced by the molecular structure of saccharides. The conductivity, dynamic light scattering (DLS) and transmission electron microscopy (TEM) were combined to investigate the microstructure of the IL-rich top phase and the possible mechanism for the selective separation. It is suggested that the formation of the IL aggregate and the IL aggregate-BSA complex plays a significant role in the separation of BSA from aqueous saccharide solutions. This is the first example for the selective separation by ILs-based ATPSs. It is expected that these findings would have potential applications in bio-analysis, separation, and IL recycle.

77 citations


Authors

Showing all 10953 results

NameH-indexPapersCitations
Hua Zhang1631503116769
Jie Wu112153756708
Peng Wang108167254529
Lei Liu98204151163
Lixia Zhang9335147817
Zhongwei Chen9251133700
Wei Chen9093835799
Zhiguo Ding8881735162
Xiaolong Wang8196631455
Junhua Li7748021626
Jiujun Zhang7627639624
Lei Liao7527618815
Peng Xu75115125005
Wei Wang75116723558
Tony D. James7343521605
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202349
2022173
20211,281
20201,042
2019987
2018818