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Online since: October 2012
Authors: Shi Qiang Cui, Shou Zhi Pu, Shu Hong Jing
Photochromic Composite Properties and Application in Optical Memory of a Diarylethene with Benzofuran unit
Shuhong Jing, Shiqiang Cui and Shouzhi Pu*
Jiangxi Key Laboratory of Organic Chemistry,
Jiangxi Science and Technology Normal University, Nanchang 330013, P.
The structure of 1a was characterized by 1H NMR. 1H NMR (400 MHz, CDCl3, ppm): δ 2.08(s, 3H, -CH3), 2.27 (s, 3H, -CH3), 4.05 (t, 2H, dioxolane-H), 4.14 (t, 2H, dioxolane-H), 5.82 (s, 1H, dioxolane-H), 6.83 (s, 1H, thiophene-H), 6.87 (d, 1H, benzofuran -H), 6.89 (t, 1H, benzofuran -H), 7.01 (t, 1H, benzofuran -H), 7.18 (d, 1H, benzofuran -H), 7.34 (d, 2H, benzene-H), 7.38 (d, 2H, benzene-H).
The structure of 1a was characterized by 1H NMR. 1H NMR (400 MHz, CDCl3, ppm): δ 2.08(s, 3H, -CH3), 2.27 (s, 3H, -CH3), 4.05 (t, 2H, dioxolane-H), 4.14 (t, 2H, dioxolane-H), 5.82 (s, 1H, dioxolane-H), 6.83 (s, 1H, thiophene-H), 6.87 (d, 1H, benzofuran -H), 6.89 (t, 1H, benzofuran -H), 7.01 (t, 1H, benzofuran -H), 7.18 (d, 1H, benzofuran -H), 7.34 (d, 2H, benzene-H), 7.38 (d, 2H, benzene-H).
Online since: February 2014
Authors: Shu Heng Liu
Study of phenyl phenol formaldehyde resin and its curing performance of aniline
LIU Shu Heng 1, a
1 Department of Chemistry and Environmental Science, Cangzhou Normal University,
Cangzhou,061000, Hebei, China
aliushuheng65@sina.com
Keywords: modified,phenol formaldehyde resin,welding.
For the first aniline modified phenol formaldehyde resin was prepared in this paper, first,presents the structure of the resin.
For the first aniline modified phenol formaldehyde resin was prepared in this paper, first,presents the structure of the resin.
Online since: July 2014
Authors: Hai Jiao Yu, Chen Ci Ma, Yang Yu
INTRODUCTION
Aerobic granular sludge process has been proposed as a promising approach to control water contamination in recent years [1, 2].Due to the its own characteristic of structure,simultaneous removal of nitrogen and phosphorous was achieved successfully in a one-reactor system,the system had the distinctive advantages of high activity of microorganisms,good performance of solid-liquid separation,high resistance to organic impact load and long biological chain.Because of all the advantages of AGS system,it had broad development prospect [3].In this study,we compared the influence of dissolved oxygen and organic compound on the municipal wastewater removal performance of aerobic granular sludge process by dynamic tests.The aim of the study was to provide technical support and theoretical basis for the stable operation of aerobic granular sludge process and practical engineering application.
Chemistry & Bioengineering, Vol. 26 (2009) No.1, p.15
Chemistry & Bioengineering, Vol. 26 (2009) No.1, p.15
Online since: January 2012
Authors: Si Ying Zhao, Kai Cheng Zhang
Synthesis and Characterizations of Monodispersed Nanotriangle of Gold
Kaicheng Zhang and Siying Zhao
School of Chemistry and Environmental Engineering
Wuhan Polytechnic University, Wuhan, Hubei Province, China
zhangkaichengwhpu@126.com
Keywords: gold; nanotriangle; Growth from solutions.
Fig. 3a was shown the triangular structure of gold with average side of 50-150 nm.
Fig. 3a was shown the triangular structure of gold with average side of 50-150 nm.
Online since: October 2011
Authors: Abdol Ghaffar Ebadi, Somayeh Alami
Acknowledgement
All authors strongly will present special thanks for Department of Chemistry in IAU, Jouybar branch and also IAU, Tabriz branch for their scientific and finance supports.
Therefore this molecule can be used on structure of rotaxanes and catenanes in nano machines.
Therefore this molecule can be used on structure of rotaxanes and catenanes in nano machines.
Online since: January 2014
Authors: Guan Ming Liao, Zhi Yuan Sun, Shou Zhi Pu
Synthesis and Properties of 1-[2,5-dimethyl-3-thienyl]-2-[2-methyl-5- (p-N,N-dimethylaminophenyl)-3-thienyl]perfluorocyclopentene
Guanming Liao, Zhiyuan Sun and Shouzhi Pu*
Jiangxi Key Lab of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013, China
pushouzhi@tsinghua.org.cn
Keywords: Diarylethene; Photochromism; Kinetic; Fluorescence.
The structure of compound 1o was confirmed by 1H NMR. 1H NMR (400 MHz, CDCl3): δ 2.18 (s, 3H, –CH3), 2.26 (s, 3H, –CH3), 2.31 (s, 3H, –CH3), 2.96 (s, 6H, –NCH3), 6.68 (d, 2H), 6.95 (s, 2H), 7.32–7.43 (m, 2H).
The structure of compound 1o was confirmed by 1H NMR. 1H NMR (400 MHz, CDCl3): δ 2.18 (s, 3H, –CH3), 2.26 (s, 3H, –CH3), 2.31 (s, 3H, –CH3), 2.96 (s, 6H, –NCH3), 6.68 (d, 2H), 6.95 (s, 2H), 7.32–7.43 (m, 2H).
Online since: November 2011
Authors: Shi Qiang Cui, Shou Zhi Pu, Zhi Peng Tong
Synthesis and Properties of a New Photochromic Compound Bearing Isoxazol Moiety
Zhipeng Tong, Shouzhi Pu* and Shiqiang Cui
Jiangxi Key Laboratory of Organic Chemistry
Jiangxi Science and Technology Normal University, Nanchang 330013, P.R.China
pushouzhi@tsinghua.org.cn
Keywords: Diarylethene; Photochromism; Fluorescence switching.
The structure of compound 1a was confirmed by 1H NMR(400 MHz, CDCl3): δ 2.03 (s, 3H, -CH3), 2.06 (s, 3H, -CH3), 2.24 (s, 3H, -CH3), 3.97 (s, 3H, -OCH3), 7.03 (d, 1H, phenyl-H), 7.19 (s, 1H, thiophene-H), 7.69 (d, 1H, phenyl-H), 7.97 (s, 1H, phenyl-H), 10.49 (s, 1H, -CHO).
The structure of compound 1a was confirmed by 1H NMR(400 MHz, CDCl3): δ 2.03 (s, 3H, -CH3), 2.06 (s, 3H, -CH3), 2.24 (s, 3H, -CH3), 3.97 (s, 3H, -OCH3), 7.03 (d, 1H, phenyl-H), 7.19 (s, 1H, thiophene-H), 7.69 (d, 1H, phenyl-H), 7.97 (s, 1H, phenyl-H), 10.49 (s, 1H, -CHO).
Online since: April 2011
Authors: Shou Zhi Pu, Shi Qiang Cui, Gang Liu, Wei Jun Liu
Synthesis a New Photochromic Diarylethene Based on Five-membered Heterocycle and Hexatomic Ring Aryl for Optical Storage
Shiqiang Cui, Shouzhi Pu*, Gang Liu, Weijun Liu
Jiangxi Key Laboratory of Organic Chemistry,
Jiangxi Science and Technology Normal University,
Nanchang 330013, P.
The structure of 1a was characterized by 1H NMR. 1H NMR (400 MHz, CDCl3, ppm): δ 2.02 (s, 3H, -CH3), 3.82 (s, 3H, -OCH3), 6.87 (d, 2H, J = 8.4Hz, benzene-H), 7.07 (s, 1H, thiophene-H), 7.37 (d, 2H, J = 8.4Hz, benzene-H), 7.53-7.60(t, 1H, benzene-H), 7.62 (d, 1H, J = 8.0Hz, benzene-H), 7.68(d, 1H, J = 7.6Hz, benzene-H), 7.70-7.74(t, 1H, benzene-H).
The structure of 1a was characterized by 1H NMR. 1H NMR (400 MHz, CDCl3, ppm): δ 2.02 (s, 3H, -CH3), 3.82 (s, 3H, -OCH3), 6.87 (d, 2H, J = 8.4Hz, benzene-H), 7.07 (s, 1H, thiophene-H), 7.37 (d, 2H, J = 8.4Hz, benzene-H), 7.53-7.60(t, 1H, benzene-H), 7.62 (d, 1H, J = 8.0Hz, benzene-H), 7.68(d, 1H, J = 7.6Hz, benzene-H), 7.70-7.74(t, 1H, benzene-H).
Online since: October 2014
Authors: Shou Zhi Pu, Jing Jing Liu, Hong Jing Jia
Synthesis and Properties Study of 1-[2-methyl-5-(3-trifluoromethyl)-3-thienyl]-2-[2-methyl-5- (9-phenanthren-e)-3-thienyl]perfluorocyclopentene
Jingjing Liu, Hongjing Jia and Shouzhi Pu*
Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University
Nanchang 330013, P.R.China
pushouzhi@tsinghua.org.cn
Keywords: Diarylethene, Photochromism, Kinetic, Fluorescence.
The structure of diarylethene 1o was confirmed by 1H NMR (400 MHz, CDCl3, TMS): δ 2.13 (s, 3H, -CH3), 2.15 (s, 3H, -CH3), 7.21 (s, 1H, thiophene-H), 7.26 (s, 1H, thiophene-H), 7.31 (d, 1H, J = 8.0 Hz, benzene-H), 7.40-7.65 (m, 4H, phenanthren-H), 7.67 (d, 1H, J = 8.0 Hz, benzene-H),7.69 (d, 1H, J = 8.0 Hz, benzene-H),7.71 (d, 1H, J = 8.0 Hz, benzene-H), 7.79 (s, 1H, phenanthren-H), 7.88 (d, 1H, J = 8.0 Hz, phenanthren-H), 8.11 (d, 1H, J = 8.0 Hz, phenanthren-H), 8.70 (d, 1H, J = 8.0 Hz, phenanthren-H), 8.76 (d, 1H, J = 8.0 Hz, phenanthren-H).
The structure of diarylethene 1o was confirmed by 1H NMR (400 MHz, CDCl3, TMS): δ 2.13 (s, 3H, -CH3), 2.15 (s, 3H, -CH3), 7.21 (s, 1H, thiophene-H), 7.26 (s, 1H, thiophene-H), 7.31 (d, 1H, J = 8.0 Hz, benzene-H), 7.40-7.65 (m, 4H, phenanthren-H), 7.67 (d, 1H, J = 8.0 Hz, benzene-H),7.69 (d, 1H, J = 8.0 Hz, benzene-H),7.71 (d, 1H, J = 8.0 Hz, benzene-H), 7.79 (s, 1H, phenanthren-H), 7.88 (d, 1H, J = 8.0 Hz, phenanthren-H), 8.11 (d, 1H, J = 8.0 Hz, phenanthren-H), 8.70 (d, 1H, J = 8.0 Hz, phenanthren-H), 8.76 (d, 1H, J = 8.0 Hz, phenanthren-H).