Puhui Xie
Henan Agricultural University
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Featured researches published by Puhui Xie.
Chemical Papers | 2010
Puhui Xie; Fengqi Guo; Weifeng Wang; Xiyang Liu
Effect of the addition of six different anions on the absorption and fluorescence spectra of acridine yellow G (AYG) was examined. Only the F− anion could induce a visible color change observable with naked eye and a strong fluorescence quenching with KSV of 8.3 × 104 mol−1 L in CH3CN solutions. Calculated results of the interaction between the F− anion and acridine yellow G using the B3LYP/6-31G(d) program showed that the intermolecular charge transfer through the formation of an H-bond between AYG and F− is an essential sensor mechanism.
International Journal of Biological Macromolecules | 2018
Guo-Yu Yang; Qiu Jin; Cui-Lian Xu; Sufang Fan; Caixia Wang; Puhui Xie
Four novel coumarin-functionalized chitosan derivatives 4a-4d were synthesized via condensation reactions of thiosemicarbazide chitosan with coumarin derivatives. Their structures were confirmed by FT-IR, 13C NMR, XRD and elemental analysis. Their antifungal activities against three kinds of phytopathogens, Alternaria solani sorauer (A. solani), Fusarium oxysporum f.sp. vasinfectum (F. oxysporum) and Fusarium moniliforme (F. moniliforme), were tested using the mycelial growth rate in vitro at 0.1, 0.5, and 1.0mg/mL. The degree of substitution for 4a-4d ranged from 40 to 60%. At 1mg/mL, 4a inhibited F. moniliforme growth by 58.1%, and had an inhibitory index against F. Moniliforme of 77.2%. Derivative 4a was more effective than unmodified chitosan whose antifungal index was 9.7%. The fungicidal tests showed that the synthesized chitosan derivatives have higher activity against the tested fungi compared to unmodified chitosan. Moreover, the introduction of halogen atoms into the chitosan derivatives causes an increase in antifungal activity.
Journal of Chemical Sciences | 2015
Puhui Xie; Guangqin Gao; Wenjie Zhang; Guoyu Yang; Qiu Jin
AbstractA novel fluorescent turn-on probe (compound 1) for bisulfite based on 7-nitrobenz-2-oxa-1,3-diazole (NBD) chromophore has been developed. Its sensing behavior toward various anions was investigated by absorption and fluorescence techniques. This probe shows a selective, turn-on fluorescent response and ratiometric colorimetric response toward bisulfite in aqueous acetonitrile solutions. The possible recognition mechanism of probe 1toward bisulfite was illustrated by MS spectra analysis and DFT calculations Probe 1 was used to determine bisulfite in real-life samples with good recoveries. Graphical AbstractA novel fluorescent turn-on probe (compound 1) for bisulfite based on 7-nitrobenz-2-oxa-1,3-diazole (NBD) chromophore has been developed. Probe 1 shows a selective, turn-on fluorescent response and ratiometric colorimetric response toward bisulfite in aqueous acetonitrile solutions.
Journal of Luminescence | 2014
Puhui Xie; Fengqi Guo; Ruirui Xia; Yao Wang; Denghui Yao; Guoyu Yang; Lixia Xie
Journal of Luminescence | 2011
Puhui Xie; Fengqi Guo; Dan Li; Xiyang Liu; Lu Liu
Journal of Fluorescence | 2014
Puhui Xie; Fengqi Guo; Sen Yang; Denghui Yao; Guoyu Yang; Lixia Xie
Journal of Luminescence | 2013
Puhui Xie; Fengqi Guo; Yue Xiao; Qiu Jin; Denghui Yao; Zhaohui Huang
Journal of Fluorescence | 2015
Puhui Xie; Fengqi Guo; Lingyu Wang; Sen Yang; Denghui Yao; Guoyu Yang
Journal of Fluorescence | 2013
Puhui Xie; Yue Xiao; Denghui Yao; Qiu Jin; Fengqi Guo
Research on Chemical Intermediates | 2015
Meiling Gao; Puhui Xie; Lingyu Wang; Xiaohui Miao; Fengqi Guo