Jun Ren

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Organization: Hubei University
Department: Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials – College of Chemistry and Chemical Engineering
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Co-reporter:Zhu Yu, Zaiwen Tian, Zhengqian Li, Zaoli Luo, Yan Li, Yi Li, Jun Ren
Sensors and Actuators B: Chemical 2016 Volume 223() pp:172-177
Publication Date(Web):February 2016
DOI:10.1016/j.snb.2015.09.082
In this paper, a thioacetal chemosensor 1 incorporating simultaneously a carbazole moiety and an azobenzene moiety was synthesized. Among other metal ions, Hg2+ proved to be able to selectively induce both color and fluorescence changes of 1. The mechanism of Hg2+-promoted cleavage of thioacetal was confirmed by 1H NMR experiments. Upon the addition of Hg2+ into the yellow CH3CN/H2O solution of 1, the resultant azobenzene-containing thioglycolamide was precipitated from the solution as a mercuric salt, leading to a colorless solution. Therefore, a novel color change pattern was developed.
Co-reporter:Zaoli Luo, Kai Yin, Zhu Yu, Mengxue Chen, Yan Li, Jun Ren
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2016 Volume 169() pp:38-44
Publication Date(Web):5 December 2016
DOI:10.1016/j.saa.2016.06.022
•A novel turn-on fluorescent sensor based on quinoline and naphthalimide was designed and synthesized.•The sensor is highly sensitive and selective to hydrogen sulfate with 8-fold fluorescence enhancement.•The sensing mechanism has been suggested to proceed via a hydrolysis process.A new fluorescence turn-on chemosensor 1 based on quinoline and naphthalimide was prepared and its anion sensing toward various anions behavior was explored in this paper. Sensor 1 exhibited a highly selective fluorescent response toward HSO4− with an 8-fold fluorescence intensity enhancement in the presence of 10 equiv. of HSO4− in DMSO-H2O (1/1, v/v) solution. The sensor also displayed high sensitivity to hydrogen sulfate and the detection limit was calculated to be 7.79 × 10− 7 M. The sensing mechanism has been suggested to proceed via a hydrolysis process of the Schiff base group. The hydrolysis product has been isolated and further identified by 1H NMR and MS.
Co-reporter:Zhengqian Li, Ying Zhou, Kai Yin, Zhu Yu, Yan Li, Jun Ren
Dyes and Pigments 2014 Volume 105() pp:7-11
Publication Date(Web):June 2014
DOI:10.1016/j.dyepig.2013.12.032
•A new fluorescence chemosensor based on coumarin and naphthalimide was synthesized.•The chemosensor exhibits high selectivity for Fe3+ with fluorescence-enhancement.•The detection limit could reach 0.388 μM.A new Fe3+-selective “turn-on” chemosensor 1 based on coumarin and naphthalimide was designed and synthesized. The chemosensor exhibits high selectivity for Fe3+ over other ions (Mn2+, Co2+, Ni2+, Cu2+, Ag+, Cd2+, Pb2+, Ca2+, Al3+, Ba2+, Hg2+, Li+, Mg2+, Sr2+, Zn2+ and K+) with fluorescence-enhancement in THF-H2O solution. The binding ratio of 1-Fe3+ complex was determined to be 1:1 according to the Job plot. The association constant Ka of Fe3+ binding with sensor 1 was (2.589 ± 0.206) × 103 M−1. The detection limit was calculated to be 0.388 μM.
Co-reporter:Jun Ren, Zhen Wu, Ying Zhou, Yan Li, Zuxun Xu
Dyes and Pigments 2011 Volume 91(Issue 3) pp:442-445
Publication Date(Web):December 2011
DOI:10.1016/j.dyepig.2011.04.012
A colorimetric chemosensor TBS-NA, 4-(tert-butyldimethylsilyloxy)-N-butyl-naphthalimide was designed and synthesized. Addition of fluoride ion to a CH3CN solution of TBS-NA can result in an obvious color change (from colorless to yellow) and UV–Vis absorption spectral change in a short time. This indicated that TBS-NA had highly selectivity for fluoride detection over other anions, such as Cl−, Br−, I−, HSO4−, ClO4− and AcO− in CH3CN solutions, and the selectively detection was due to the selective cleavage of Si–O bond in TBS-NA by fluoride. The detection limit was calculated to be 0.59 μM.Highlights► The sensor TBS-NA can detect fluoride ion with high selectivity in CH3CN solution over other anions. ► Addition of fluoride ion to a CH3CN solution of TSB-NA can result in an obvious color change (from colorless to yellow) and UV–Vis absorption spectral change in a short time. ► The absorbance of TBS-NA at 474 nm increased linearly with the concentration of fluoride from 10 to 100 μM. ► The detection limit was calculated to be 0.59 μM.
Co-reporter:Yuan Zhou, Guichun Yang, Cuifen Lu, Junqi Nie, Zuxing Chen, Jun Ren
Catalysis Communications (5 February 2016) Volume 75() pp:23-27
Publication Date(Web):5 February 2016
DOI:10.1016/j.catcom.2015.11.017
•The new POSS that supported the prolinamide-type catalysts was synthesized and used to catalyze asymmetric Aldol reactions.•The higher ee value has been obtained after the C2-symmetric bisprolinamide chrial catalyst was immobilized onto the POSS.•The POSS supported catalyst could be recycled simply and reused in five consecutive cycles maintaining its effectiveness.POSS supported prolinamide-type catalysts were synthesized and used to catalyze asymmetric Aldol reactions between unmodified ketones and aldehydes. Immobilization of the prolinamide-type catalysts onto POSS resulted in good yields and improved diastereoselectivity as well as enantioselectivity. The POSS-supported catalysts were recycled simply by precipitation and filtration, and could be reused in five consecutive cycles without losing its effectiveness.
2-Butanone, 4-hydroxy-4-(3-nitrophenyl)-, (4R)-
Benzonitrile, 4-[(1R)-1-hydroxy-3-oxobutyl]-
Cyclohexanone, 2-[(R)-hydroxy(4-nitrophenyl)methyl]-, (2S)-
Cyclopentanone, 2-[(R)-hydroxy(4-nitrophenyl)methyl]-, (2S)-
3-Pentanone, 1-hydroxy-1-(4-nitrophenyl)-, (1R)-
2-Butanone, 4-hydroxy-4-(4-nitrophenyl)-, (4R)-
2-Butanone, 4-hydroxy-4-phenyl-, (4R)-