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The substituent group effect on the morphology and memory performance of phenazine derivatives . Pei-Yang Gu, Yong Ma, Jing-Hui He, Guankui Long, Chengyuan Wang, Wangqiao Chen, Yi Liu, Qing-Feng Xu, Jian-Mei Lu, Qichun Zhang
, J. Mater. Chem. C
, 2015
, 3
, 3167
705. Polynuclear heterocyclic systems. Part II. Hydroxyderivatives . G. M. Badger, R. S. Pearce, R. Pettit
, J. Chem. Soc.
, 1951
, 3204
Organic small molecule-based RRAM for data storage and neuromorphic computing . Boyuan Mu, Hsiao-Hsuan Hsu, Chi-Ching Kuo, Su-Ting Han, Ye Zhou
, J. Mater. Chem. C
, 2020
, 8
, 12714
Novel phenazine crystals enable direct electron transfer to methanogens in anaerobic digestion by redox potential modulation . Sabrina Beckmann, Cornelia Welte, Xiaomin Li, Yee M. Oo, Lena Kroeninger, Yooun Heo, Miaomiao Zhang, Daniela Ribeiro, Matthew Lee, Mohan Bhadbhade, Christopher E. Marjo, Jan Seidel, Uwe Deppenmeier, Mike Manefield
, Energy Environ. Sci.
, 2016
, 9
, 644
Pigments of Pseudomonas species. Part V. Biosynthesis of pyocyanin and the pigments of Ps. aureofaciens . M. E. Flood, R. B. Herbert, F. G. Holliman
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 622
Pigments of Pseudomonas species. Part II. Structure of aeruginosin B . R. B. Herbert, F. G. Holliman
, J. Chem. Soc. C
, 1969
, 2517
359. The phenazine series. Part VI. Reactions of alkyl phenazonium salts; the phenazyls . Henry McIlwain
, J. Chem. Soc.
, 1937
, 1704
Notes . J. P. Varma, Bhola Nath, J. S. Aggarwal, Justus K. Landquist, R. E. Bowman, D. D. Evans, K. R. Bharucha, M. J. S. Dewar, T. Mole, E. F. M. Stephenson, M. G. Brown, W. Rigby, S. C. Abrahams, J. C. Speakman, T. Davies, L. A. K. Staveley, T. G. Halsall, D. B. Thomas, J. L. Drummond, G. A. Welch, A. L. Green
, J. Chem. Soc.
, 1956
, 2550