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Online since: June 2006
Authors: Vyacheslav F. Kalinin, Sergey V. Mischenko, Aleksey G. Tkachev, Vladimir L. Negrov
These materials
are filament carbon structures with a diameter from 1 to hundreds of nanometers and with lengths to
several micrometers.
Digurov: Continuous process of carbon nanofibres obtaining (J. of Applied Chemistry, Vol. 77, R 2, 2004), p. 193196 (in Russian) [7] N.
Digurov: Continuous process of carbon nanofibres obtaining (J. of Applied Chemistry, Vol. 77, R 2, 2004), p. 193196 (in Russian) [7] N.
Online since: January 2017
Authors: Rui Min Lu, Shu Ying Li, Shi Qiang Cui
Study on the Synthesis and Application of a Material 1-[2-Methyl-5-Phenyl-3-Thienyl]-2-[2-Methyl-5- (3-Aldehyde-4-Methoxy)-3-Thienyl] Perfluorocyclopentene
Rui-Min LU1, Shu-Ying LI1, Shi-Qiang CUI1,a,*
1Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang, Jiangxi, China
acuisq2006@163.com
*Corresponding author
Keywords: Diarylethene, Photochromism, Fluorescence.
Synthesis of crystal structure and photochromism of new diarylethenes with a benzene moiety.
Synthesis of crystal structure and photochromism of new diarylethenes with a benzene moiety.
Online since: October 2008
Authors: Marcelo Henrique Prado da Silva, Luis Henrique Leme Louro, C. Marques
Surface chemistry accounts for
bioactivity, the ability of chemically bonding to bone.
(a) (b) Figure 3 - Porous Nb2O5 sample showing macroporous structure (a) and nanometric features on the interconnections walls.
(a) (b) Figure 3 - Porous Nb2O5 sample showing macroporous structure (a) and nanometric features on the interconnections walls.
Online since: October 2011
Authors: Xiao Guang Ren, Jie Yang
The organic compounds containing N, S or O atom lone pair are easy with the metal electronic structure of covalent bonds to form a solid, so that it is potential as a metal corrosion inhibitor.
Desalination [ J ] , 2007, 206(1~3) : 169 [7] Qiangqiang Liao, Wei Li, Yijiu Li, Qi Zhou, sodium diethyldithiocarbamate inhibition of brass performance, Applied Chemistry, 26 (10) :1127-1130 In Chinese
Desalination [ J ] , 2007, 206(1~3) : 169 [7] Qiangqiang Liao, Wei Li, Yijiu Li, Qi Zhou, sodium diethyldithiocarbamate inhibition of brass performance, Applied Chemistry, 26 (10) :1127-1130 In Chinese
Online since: May 2014
Authors: Zhi Mao, Ting Ting Wang
Introduction
Fractional models have been increasingly shown by many scientists to describe adequately the problems with memory and nonlocal properties in fluid mechanics, viscoelasticity, physics, biology, chemistry, finance and other areas of applications [1].
In particular, the fractional diffusion equation has been used to model many important physical phenomena ranging from amorphous, colloid, glassy, and porous materials through fractals, percolation clusters, random and disordered media to comb structures, dielectrics and semiconductors, polymers and biological systems [2,3].
In particular, the fractional diffusion equation has been used to model many important physical phenomena ranging from amorphous, colloid, glassy, and porous materials through fractals, percolation clusters, random and disordered media to comb structures, dielectrics and semiconductors, polymers and biological systems [2,3].
Online since: December 2012
Authors: Feng Jiang, Jun Yu, Jian Jun Chen
DDS technology is based on Shannon Theorem, and it uses the full digital structure and through the control phase accumulators, wave data storage, D/A converter and low pass filter composition.
References [1] Ogle B.M, Cascalho M, Platt J.L: Nature Reviews Molecular Cell Biology Vol. 6 (2005), p.567 [2] Robinson J.M, Roos D.S, Davidson R.L, et al: Journal of Cell Science Vol. 40 (1979), p.63 [3] Wiegand R, Weber G, Zimmermann K, et al: Journal of Cell Science Vol. 88 (1987), p. 145 [4] Zimmermann U: Biochim Biophys Acta Vol. 694 (1982), p. 227 [5] CaoY,Yang J,Yin Z.Q, et al: Microfludics& Nanofluidics Vol. 5 (2008), p. 669 [6] Stromberg A, Karlsson A, Ryttsen F, et al: Analytical Chemistry Vol. 73 (2001), p.126 [7] J Tierney, C.M.
References [1] Ogle B.M, Cascalho M, Platt J.L: Nature Reviews Molecular Cell Biology Vol. 6 (2005), p.567 [2] Robinson J.M, Roos D.S, Davidson R.L, et al: Journal of Cell Science Vol. 40 (1979), p.63 [3] Wiegand R, Weber G, Zimmermann K, et al: Journal of Cell Science Vol. 88 (1987), p. 145 [4] Zimmermann U: Biochim Biophys Acta Vol. 694 (1982), p. 227 [5] CaoY,Yang J,Yin Z.Q, et al: Microfludics& Nanofluidics Vol. 5 (2008), p. 669 [6] Stromberg A, Karlsson A, Ryttsen F, et al: Analytical Chemistry Vol. 73 (2001), p.126 [7] J Tierney, C.M.
Online since: December 2014
Authors: Shou Zhi Pu, Jing Jing Liu, Hong Jing Jia
Synthesis and Properties of 1-(2-methyl-3-benzothienyl)-2-[2-methyl-5-(3-trifluoromethyl)-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 were confirmed by 1H NMR (400 MHz, CDCl3, TMS): δ 1.56 (s, 3H, -CH3), 2.31 (s, 3H, -CH3), 7.25 (s, 1H, thiophene-H),7.33-7.40 (m, 2H, benzo[b]thiophene-H), 7.65 (d, 2H, J = 8.0 Hz, benzene-H), 7.71 (d, 2H, J = 8.0 Hz, benzene-H), 7.85 (d, 1H, J = 8.0 Hz, benzo[b]thiophene-H), 7.90 (d, 1H, J = 8.0 Hz, benzo[b]thiophene-H).
The structure of diarylethene 1o were confirmed by 1H NMR (400 MHz, CDCl3, TMS): δ 1.56 (s, 3H, -CH3), 2.31 (s, 3H, -CH3), 7.25 (s, 1H, thiophene-H),7.33-7.40 (m, 2H, benzo[b]thiophene-H), 7.65 (d, 2H, J = 8.0 Hz, benzene-H), 7.71 (d, 2H, J = 8.0 Hz, benzene-H), 7.85 (d, 1H, J = 8.0 Hz, benzo[b]thiophene-H), 7.90 (d, 1H, J = 8.0 Hz, benzo[b]thiophene-H).