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128G. A. Planes, J. L. Rodríguez, M. C. Miras, G. García, E. Pastor and C. A. Barbero.
Spectroscopic evidence for intermediate species formed during aniline polymerization and polyaniline degradation, Phys. Chem. Chem. Phys., 2010, 12, 10584. Lukasz Dobrzycki and Krzysztof Woźniak.
Structures of hybrid inorganic–organic salts with benzidine dication derivatives, CrystEngComm, 2008, 10, 525. Christina E. Costin-Hogan, Chun-Long Chen, Emma Hughes, Austin Pickett, Richard Valencia, Nigam P. Rath and Alicia M. Beatty.
“Reverse” engineering: Toward 0-D cadmium halideclusters, CrystEngComm, 2008, 10, 1910. Ying Yan, Sai-Feng Xue, Hang Cong, Jian-Xing Zhang, Yun-Qian Zhang, Qian-Jiang Zhu and Zhu Tao.
Exclusion complexes of the HCl salts of benzidine and bis(4-aminophenyl) methane with two methyl-substituted cucurbiturils, New J. Chem., 2009, 33, 2136. Sandeep-Kumar Mourya, Devasish Bose, Abhilasha Durgbanshi, Josep Esteve-Romero and Samuel Carda-Broch.
Determination of some banned aromatic amines in waste water using micellar liquid chromatography, Anal. Methods, 2011, 3, 2032. Zhanguang Chen, Guomin Zhang, Xi Chen, Yurui Peng, Yuejuan Lin and Simin Lu.
A resonance light scattering amplification system for determination of trace amounts of benzidine in surface water, Anal. Methods, 2011, 3, 1845. Chuan-Feng Chen.
Novel triptycene-derived hosts: synthesis and their applications in supramolecular chemistry, Chem. Commun., 2011, 47, 1674. Karolína Šišková, Martin Kubala, Panagiotis Dallas, Dalibor Jančík, Alain Thorel, Petr Ilík and Radek Zbořil.
The effect of surface modification on the fluorescence and morphology of CdSe nanoparticles embedded in a 3D phosphazene-based matrix: nanowire-like quantum dots, J. Mater. Chem., 2011, 21, 1086. Henry D. Tran, Julio M. D'Arcy, Yue Wang, Peter J. Beltramo, Veronica A. Strong and Richard B. Kaner.
The oxidation of aniline to produce “polyaniline”: a process yielding many different nanoscale structures, J. Mater. Chem., 2011, 21, 3534. Peter Kovacic and Ratnasamy Somanathan.
Novel, unifying mechanism for aromatic primary-amines (therapeutics, carcinogens and toxins): electron transfer, reactive oxygen species, oxidative stress and metabolites, Med. Chem. Commun., 2011, 2, 106.