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- Synthesis and properties of new 9,10-anthraquinone derived compounds for molecular electronics. Nadine Seidel, Torsten Hahn, Simon Liebing, Wilhelm Seichter, Jens Kortus, Edwin Weber
, New J. Chem.
, 2013
, 37
, 601
- Photophysical properties of 2-amino-9,10-anthraquinone: evidence for structural changes in the molecule with solvent polarity. P. Dahiya, M. Kumbhakar, D. K. Maity, T. Mukherjee, J. P. Mittal, A. B. R. Tripathi, N. Chattopadhyay, H. Pal
, Photochem. Photobiol. Sci.
, 2005
, 4
, 100
- Photoreduction of 2-methyl-1-nitro-9,10-anthraquinone in the presence of 1-phenylethanol. Henry Gruen, Helmut Görner
, Photochem. Photobiol. Sci.
, 2008
, 7
, 1344
- 470. Chemistry of indanthrone. Part I. The mode of formation of indanthrone from 2-aminoanthraquinone and potassium hydroxide. William Bradley, Edward Leete
, J. Chem. Soc.
, 1951
, 2129
- High-performance supercapacitor electrodes based on graphene hydrogels modified with 2-aminoanthraquinone moieties. Qiong Wu, Yiqing Sun, Hua Bai, Gaoquan Shi
, Phys. Chem. Chem. Phys.
, 2011
, 13
, 11193
- 471. Chemistry of indanthrone. Part II. The formation of dianthraquionyl-N-methylamines. William Bradley, Edward Leete
, J. Chem. Soc.
, 1951
, 2147
- Quinone-functionalised carbons as new materials for electrochemical carbon dioxide capture. Niamh A. Hartley, Suzi M. Pugh, Zhen Xu, Daniel C. Y. Leong, Adam Jaffe, Alexander C. Forse
, J. Mater. Chem. A
, 2023
, 11
, 16221
- Covalently functionalized carbon nanotubes as stable cathode materials of lithium/organic batteries. G. Charrier, A. Desrues, C. Barchasz, J. Leroy, R. Cornut, B. Jousselme, S. Campidelli
, J. Mater. Chem. A
, 2016
, 4
, 15036
- Pulse radiolysis of 9,10-anthraquinones. Part 2.—Triplet excited states. B. E. Hulme, E. J. Land, G. O. Phillips
, J. Chem. Soc., Faraday Trans. 1
, 1972
, 68
, 2003
- 474. Chemistry of indanthrone. Part V. Tert.-butyl derivatives of indanthrone and flavanthrone. The mode of formation of flavanthrone in the alkali fusion of 2-aminoanthraquinone. William Bradley, Harry E. Nursten
, J. Chem. Soc.
, 1951
, 2170