Search Options

Sort by:

Sort search results by

Publication Type:

Publication Type filter

Open access:

Publication Date:

Periodicals:

Periodicals filter

Search results

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).
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.
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
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.
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.
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).
Online since: January 2005
Authors: X.F. Rui, Y.Y. Fu, Han Zhang, Y.W. Liu
The structure of the nanowires was investigated by XRD analysis.
Kung, Transition Metal Oxides: Surface Chemistry and Catalysis (Elsevier, New York, 1989)
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).
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).
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).