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Composition-dependent nanoelectronics of amido-phenazines: non-volatile RRAM and WORM memory devices.

Scientific reports

Maiti DK, Debnath S, Nawaz SM, Dey B, Dinda E, Roy D, Ray S, Mallik A, Hussain SA.
PMID: 29042660
Sci Rep. 2017 Oct 17;7(1):13308. doi: 10.1038/s41598-017-13754-w.

A metal-free three component cyclization reaction with amidation is devised for direct synthesis of DFT-designed amido-phenazine derivative bearing noncovalent gluing interactions to fabricate organic nanomaterials. Composition-dependent organic nanoelectronics for nonvolatile memory devices are discovered using mixed phenazine-stearic acid (SA)...

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Maiti DK, Debnath S, Nawaz SM, et al. Composition-dependent nanoelectronics of amido-phenazines: non-volatile RRAM and WORM memory devices. Sci Rep. 2017;7(1):13308doi: 10.1038/s41598-017-13754-w.
Maiti, D. K., Debnath, S., Nawaz, S. M., Dey, B., Dinda, E., Roy, D., Ray, S., Mallik, A., & Hussain, S. A. (2017). Composition-dependent nanoelectronics of amido-phenazines: non-volatile RRAM and WORM memory devices. Scientific reports, 7(1), 13308. https://doi.org/10.1038/s41598-017-13754-w
Maiti, Dilip K, et al. "Composition-dependent nanoelectronics of amido-phenazines: non-volatile RRAM and WORM memory devices." Scientific reports vol. 7,1 (2017): 13308. doi: https://doi.org/10.1038/s41598-017-13754-w
Maiti DK, Debnath S, Nawaz SM, Dey B, Dinda E, Roy D, Ray S, Mallik A, Hussain SA. Composition-dependent nanoelectronics of amido-phenazines: non-volatile RRAM and WORM memory devices. Sci Rep. 2017 Oct 17;7(1):13308. doi: 10.1038/s41598-017-13754-w. PMID: 29042660; PMCID: PMC5645374.
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Phenazine production enhances extracellular DNA release via hydrogen peroxide generation in Pseudomonas aeruginosa.

Communicative & integrative biology

Das T, Manefield M.
PMID: 23710274
Commun Integr Biol. 2013 May 01;6(3):e23570. doi: 10.4161/cib.23570.

In Pseudomonas aeruginosa eDNA is a crucial component essential for biofilm formation and stability. In this study we report that release of eDNA is influenced by the production of phenazine in P. aeruginosa. A ∆phzA-G mutant of P. aeruginosa...

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Das T, Manefield M. Phenazine production enhances extracellular DNA release via hydrogen peroxide generation in Pseudomonas aeruginosa. Commun Integr Biol. 2013;6(3):e23570doi: 10.4161/cib.23570.
Das, T., & Manefield, M. (2013). Phenazine production enhances extracellular DNA release via hydrogen peroxide generation in Pseudomonas aeruginosa. Communicative & integrative biology, 6(3), e23570. https://doi.org/10.4161/cib.23570
Das, Theerthankar, and Manefield, Mike. "Phenazine production enhances extracellular DNA release via hydrogen peroxide generation in Pseudomonas aeruginosa." Communicative & integrative biology vol. 6,3 (2013): e23570. doi: https://doi.org/10.4161/cib.23570
Das T, Manefield M. Phenazine production enhances extracellular DNA release via hydrogen peroxide generation in Pseudomonas aeruginosa. Commun Integr Biol. 2013 May 01;6(3):e23570. doi: 10.4161/cib.23570. PMID: 23710274; PMCID: PMC3656008.
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Excited-State Conformational/Electronic Responses of Saddle-Shaped N,N'-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination.

Journal of the American Chemical Society

Zhang Z, Wu YS, Tang KC, Chen CL, Ho JW, Su J, Tian H, Chou PT.
PMID: 26075574
J Am Chem Soc. 2015 Jul 08;137(26):8509-20. doi: 10.1021/jacs.5b03491. Epub 2015 Jun 29.

A tailored strategy is utilized to modify 5,10-dimethylphenazine (DMP) to donor-acceptor type N,N'-disubstituted-dihydrodibenzo[a,c]phenazines. The representative compounds DMAC (N,N'-dimethyl), DPAC (N,N'-diphenyl), and FlPAC (N-phenyl-N'-fluorenyl) reveal significant nonplanar distortions (i.e., a saddle shape) and remarkably large Stokes-shifted emission independent of the...

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Zhang Z, Wu YS, Tang KC, et al. Excited-State Conformational/Electronic Responses of Saddle-Shaped N,N'-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination. J Am Chem Soc. 2015;137(26):8509-20doi: 10.1021/jacs.5b03491.
Zhang, Z., Wu, Y. S., Tang, K. C., Chen, C. L., Ho, J. W., Su, J., Tian, H., & Chou, P. T. (2015). Excited-State Conformational/Electronic Responses of Saddle-Shaped N,N'-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination. Journal of the American Chemical Society, 137(26), 8509-20. https://doi.org/10.1021/jacs.5b03491
Zhang, Zhiyun, et al. "Excited-State Conformational/Electronic Responses of Saddle-Shaped N,N'-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination." Journal of the American Chemical Society vol. 137,26 (2015): 8509-20. doi: https://doi.org/10.1021/jacs.5b03491
Zhang Z, Wu YS, Tang KC, Chen CL, Ho JW, Su J, Tian H, Chou PT. Excited-State Conformational/Electronic Responses of Saddle-Shaped N,N'-Disubstituted-Dihydrodibenzo[a,c]phenazines: Wide-Tuning Emission from Red to Deep Blue and White Light Combination. J Am Chem Soc. 2015 Jul 08;137(26):8509-20. doi: 10.1021/jacs.5b03491. Epub 2015 Jun 29. PMID: 26075574.
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In situ synthesis of hexakis(alkoxy)diquinoxalino[2,3-a:2',3'-c]phenazines: mesogenic phase transition of the electron-deficient discotic compounds.

The Journal of organic chemistry

Ong CW, Liao SC, Chang TH, Hsu HF.
PMID: 15104460
J Org Chem. 2004 Apr 30;69(9):3181-5. doi: 10.1021/jo035840l.

2,3,8,9,14,15-Hexakis(alkoxy)diquinoxalino[2,3-a:2',3'-c]phenazines with alkyl side chains varying from 6 to 12 carbon atoms were readily synthesized by the condensation of hexaketocyclohexane with the respective 1,2-bisalkoxy-4,5-diaminobenzene. Polarization microscopy and DSC studies showed all these compounds to exhibit a very wide mesophase...

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Ong CW, Liao SC, Chang TH, et al. In situ synthesis of hexakis(alkoxy)diquinoxalino[2,3-a:2',3'-c]phenazines: mesogenic phase transition of the electron-deficient discotic compounds. J Org Chem. 2004;69(9):3181-5doi: 10.1021/jo035840l.
Ong, C. W., Liao, S. C., Chang, T. H., & Hsu, H. F. (2004). In situ synthesis of hexakis(alkoxy)diquinoxalino[2,3-a:2',3'-c]phenazines: mesogenic phase transition of the electron-deficient discotic compounds. The Journal of organic chemistry, 69(9), 3181-5. https://doi.org/10.1021/jo035840l
Ong, Chi Wi, et al. "In situ synthesis of hexakis(alkoxy)diquinoxalino[2,3-a:2',3'-c]phenazines: mesogenic phase transition of the electron-deficient discotic compounds." The Journal of organic chemistry vol. 69,9 (2004): 3181-5. doi: https://doi.org/10.1021/jo035840l
Ong CW, Liao SC, Chang TH, Hsu HF. In situ synthesis of hexakis(alkoxy)diquinoxalino[2,3-a:2',3'-c]phenazines: mesogenic phase transition of the electron-deficient discotic compounds. J Org Chem. 2004 Apr 30;69(9):3181-5. doi: 10.1021/jo035840l. PMID: 15104460.
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The reactivity, as electrogenerated bases, of chiral and achiral phenazine radical-anions, including application in asymmetric deprotonation.

Organic & biomolecular chemistry

Alonso AM, Horcajada R, Motevalli M, Utley JH, Wyatt PB.
PMID: 16032362
Org Biomol Chem. 2005 Aug 07;3(15):2842-7. doi: 10.1039/b506309d. Epub 2005 Jul 01.

Radical-anions, electrochemically generated in aprotic solvent from C(2) symmetric homochiral phenazine derivatives, act as chiral electrogenerated bases (EGBs) in the desymmetrisation by selective deprotonation of a prochiral epoxide (3,4-epoxy-2,3,4,5-tetrahydrothiophene-1,1-dioxide); the anion produced is trapped by mesitoic anhydride. The phenazines...

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Alonso AM, Horcajada R, Motevalli M, et al. The reactivity, as electrogenerated bases, of chiral and achiral phenazine radical-anions, including application in asymmetric deprotonation. Org Biomol Chem. 2005;3(15):2842-7doi: 10.1039/b506309d.
Alonso, A. M., Horcajada, R., Motevalli, M., Utley, J. H., & Wyatt, P. B. (2005). The reactivity, as electrogenerated bases, of chiral and achiral phenazine radical-anions, including application in asymmetric deprotonation. Organic & biomolecular chemistry, 3(15), 2842-7. https://doi.org/10.1039/b506309d
Alonso, A Mateo, et al. "The reactivity, as electrogenerated bases, of chiral and achiral phenazine radical-anions, including application in asymmetric deprotonation." Organic & biomolecular chemistry vol. 3,15 (2005): 2842-7. doi: https://doi.org/10.1039/b506309d
Alonso AM, Horcajada R, Motevalli M, Utley JH, Wyatt PB. The reactivity, as electrogenerated bases, of chiral and achiral phenazine radical-anions, including application in asymmetric deprotonation. Org Biomol Chem. 2005 Aug 07;3(15):2842-7. doi: 10.1039/b506309d. Epub 2005 Jul 01. PMID: 16032362.
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A nitrite sensor based on a highly sensitive nitrite reductase mediator-coupled amperometric detection.

Analytical chemistry

Strehlitz B, Gründig B, Schumacher W, Kroneck PM, Vorlop KD, Kotte H.
PMID: 21619176
Anal Chem. 1996 Mar 01;68(5):807-16. doi: 10.1021/ac950692n.

Highly sensitive nitrite sensors have been developed for the first time based on mediator-modified electrodes. Tetraheme cytochrome c nitrite reductase from Sulfurospirillum deleyianum and cytochrome cd(1) nitrite reductase from Paracoccus denitrificans are able to accept electrons from artificial electron...

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Strehlitz B, Gründig B, Schumacher W, et al. A nitrite sensor based on a highly sensitive nitrite reductase mediator-coupled amperometric detection. Anal Chem. 1996;68(5):807-16doi: 10.1021/ac950692n.
Strehlitz, B., Gründig, B., Schumacher, W., Kroneck, P. M., Vorlop, K. D., & Kotte, H. (1996). A nitrite sensor based on a highly sensitive nitrite reductase mediator-coupled amperometric detection. Analytical chemistry, 68(5), 807-16. https://doi.org/10.1021/ac950692n
Strehlitz, B, et al. "A nitrite sensor based on a highly sensitive nitrite reductase mediator-coupled amperometric detection." Analytical chemistry vol. 68,5 (1996): 807-16. doi: https://doi.org/10.1021/ac950692n
Strehlitz B, Gründig B, Schumacher W, Kroneck PM, Vorlop KD, Kotte H. A nitrite sensor based on a highly sensitive nitrite reductase mediator-coupled amperometric detection. Anal Chem. 1996 Mar 01;68(5):807-16. doi: 10.1021/ac950692n. PMID: 21619176.
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Influence of phenothiazines, phenazines and phenoxazine on cation transport in Candida albicans.

Journal of applied microbiology

Calahorra M, Sánchez NS, Peña A.
PMID: 30153370
J Appl Microbiol. 2018 Aug 28; doi: 10.1111/jam.14092. Epub 2018 Aug 28.

AIMS: (i) To analyse the increase in calcium ion uptake caused by several cationic dyes on Candida albicans, (ii) to postulate a mechanism, (iii) to define the effects of Zn ions on the phenomenon, and (iv) to propose the...

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Calahorra M, Sánchez NS, Peña A. Influence of phenothiazines, phenazines and phenoxazine on cation transport in Candida albicans. J Appl Microbiol. 2018;doi: 10.1111/jam.14092.
Calahorra, M., Sánchez, N. S., & Peña, A. (2018). Influence of phenothiazines, phenazines and phenoxazine on cation transport in Candida albicans. Journal of applied microbiology, . https://doi.org/10.1111/jam.14092
Calahorra, M, et al. "Influence of phenothiazines, phenazines and phenoxazine on cation transport in Candida albicans." Journal of applied microbiology vol. (2018). doi: https://doi.org/10.1111/jam.14092
Calahorra M, Sánchez NS, Peña A. Influence of phenothiazines, phenazines and phenoxazine on cation transport in Candida albicans. J Appl Microbiol. 2018 Aug 28; doi: 10.1111/jam.14092. Epub 2018 Aug 28. PMID: 30153370.
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o-Quinones Derived from Tribenzotriquinacenes: Functionalization of Inner Bay Positions and Use for Single-Wing Extensions.

The Journal of organic chemistry

Zhang YF, Tian WF, Cao XP, Kuck D, Chow HF.
PMID: 26937585
J Org Chem. 2016 Mar 18;81(6):2308-19. doi: 10.1021/acs.joc.5b02806. Epub 2016 Mar 03.

Through a surprisingly nonregioselective oxidation process, the reaction of two analogous 2-hydroxy-substituted tribenzotriquinacenes (TBTQs) 8a/8b by o-iodoxybenzoic acid was found to afford the corresponding Cs- and C1-symmetrical TBTQ-o-quinones 6a/6b and 7a/7b, respectively, in 1:1 ratio and excellent combined yields....

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Zhang YF, Tian WF, Cao XP, et al. o-Quinones Derived from Tribenzotriquinacenes: Functionalization of Inner Bay Positions and Use for Single-Wing Extensions. J Org Chem. 2016;81(6):2308-19doi: 10.1021/acs.joc.5b02806.
Zhang, Y. F., Tian, W. F., Cao, X. P., Kuck, D., & Chow, H. F. (2016). o-Quinones Derived from Tribenzotriquinacenes: Functionalization of Inner Bay Positions and Use for Single-Wing Extensions. The Journal of organic chemistry, 81(6), 2308-19. https://doi.org/10.1021/acs.joc.5b02806
Zhang, Yu-Fei, et al. "o-Quinones Derived from Tribenzotriquinacenes: Functionalization of Inner Bay Positions and Use for Single-Wing Extensions." The Journal of organic chemistry vol. 81,6 (2016): 2308-19. doi: https://doi.org/10.1021/acs.joc.5b02806
Zhang YF, Tian WF, Cao XP, Kuck D, Chow HF. o-Quinones Derived from Tribenzotriquinacenes: Functionalization of Inner Bay Positions and Use for Single-Wing Extensions. J Org Chem. 2016 Mar 18;81(6):2308-19. doi: 10.1021/acs.joc.5b02806. Epub 2016 Mar 03. PMID: 26937585.
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A Rapid Synthesis of Some 1,4-aryldiazines by the Use of Lithium Chloride as an Effective Catalyst.

Acta chimica Slovenica

Karami B, Rooydel R, Saeed K.
PMID: 24061189
Acta Chim Slov. 2012 Mar;59(1):183-8.

The synthesis of some 1,4-aryldiazines (novel and known dibenzo[a,c]phenazines and quinoxalines) based on the condensation of 1,2-aryldiamines with aromatic 1,2-dicarbonyl compounds in the presence of lithium chloride as a heterogeneous catalyst is presented as convenient and efficient strategy. This...

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Karami B, Rooydel R, Saeed K. A Rapid Synthesis of Some 1,4-aryldiazines by the Use of Lithium Chloride as an Effective Catalyst. Acta Chim Slov. 2012;59(1):183-8
Karami, B., Rooydel, R., & Saeed, K. (2012). A Rapid Synthesis of Some 1,4-aryldiazines by the Use of Lithium Chloride as an Effective Catalyst. Acta chimica Slovenica, 59(1), 183-8.
Karami, Bahador, et al. "A Rapid Synthesis of Some 1,4-aryldiazines by the Use of Lithium Chloride as an Effective Catalyst." Acta chimica Slovenica vol. 59,1 (2012): 183-8.
Karami B, Rooydel R, Saeed K. A Rapid Synthesis of Some 1,4-aryldiazines by the Use of Lithium Chloride as an Effective Catalyst. Acta Chim Slov. 2012 Mar;59(1):183-8. PMID: 24061189.
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Rhodium-Catalyzed Reaction of Azobenzenes and Nitrosoarenes toward Phenazines.

Organic letters

Xiao Y, Wu X, Wang H, Sun S, Yu JT, Cheng J.
PMID: 30958684
Org Lett. 2019 Apr 19;21(8):2565-2568. doi: 10.1021/acs.orglett.9b00502. Epub 2019 Apr 08.

A rhodium-catalyzed annulative reaction between azobenzenes and nitrosoarenes has been developed, leading to a series of phenazines in moderate to good yields. This procedure proceeds with sequential chelation-assisted addition of aryl C-H to nitrosoarenes and ring closure by electrophilic...

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Xiao Y, Wu X, Wang H, et al. Rhodium-Catalyzed Reaction of Azobenzenes and Nitrosoarenes toward Phenazines. Org Lett. 2019;21(8):2565-2568doi: 10.1021/acs.orglett.9b00502.
Xiao, Y., Wu, X., Wang, H., Sun, S., Yu, J. T., & Cheng, J. (2019). Rhodium-Catalyzed Reaction of Azobenzenes and Nitrosoarenes toward Phenazines. Organic letters, 21(8), 2565-2568. https://doi.org/10.1021/acs.orglett.9b00502
Xiao, Yan, et al. "Rhodium-Catalyzed Reaction of Azobenzenes and Nitrosoarenes toward Phenazines." Organic letters vol. 21,8 (2019): 2565-2568. doi: https://doi.org/10.1021/acs.orglett.9b00502
Xiao Y, Wu X, Wang H, Sun S, Yu JT, Cheng J. Rhodium-Catalyzed Reaction of Azobenzenes and Nitrosoarenes toward Phenazines. Org Lett. 2019 Apr 19;21(8):2565-2568. doi: 10.1021/acs.orglett.9b00502. Epub 2019 Apr 08. PMID: 30958684.
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Synthesis of novel ligands targeting phenazine biosynthesis proteins as a strategy for antibiotic intervention.

Monatshefte fur chemie

Guttenberger N, Schlatzer T, Leypold M, Tassoti S, Breinbauer R.
PMID: 29681660
Monatsh Chem. 2018;149(4):847-856. doi: 10.1007/s00706-017-2100-z. Epub 2017 Nov 30.

No abstract available.

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Guttenberger N, Schlatzer T, Leypold M, et al. Synthesis of novel ligands targeting phenazine biosynthesis proteins as a strategy for antibiotic intervention. Monatsh Chem. 2017;149(4):847-856doi: 10.1007/s00706-017-2100-z.
Guttenberger, N., Schlatzer, T., Leypold, M., Tassoti, S., & Breinbauer, R. (2018). Synthesis of novel ligands targeting phenazine biosynthesis proteins as a strategy for antibiotic intervention. Monatshefte fur chemie, 149(4), 847-856. https://doi.org/10.1007/s00706-017-2100-z
Guttenberger, Nikolaus, et al. "Synthesis of novel ligands targeting phenazine biosynthesis proteins as a strategy for antibiotic intervention." Monatshefte fur chemie vol. 149,4 (2018): 847-856. doi: https://doi.org/10.1007/s00706-017-2100-z
Guttenberger N, Schlatzer T, Leypold M, Tassoti S, Breinbauer R. Synthesis of novel ligands targeting phenazine biosynthesis proteins as a strategy for antibiotic intervention. Monatsh Chem. 2018;149(4):847-856. doi: 10.1007/s00706-017-2100-z. Epub 2017 Nov 30. PMID: 29681660; PMCID: PMC5906492.
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An umpolung strategy for rapid access to thermally activated delayed fluorescence (TADF) materials based on phenazine.

Chemical communications (Cambridge, England)

Zhang H, Guo Q, Cheng H, Ran C, Wu D, Lan J.
PMID: 35018392
Chem Commun (Camb). 2022 Jan 12; doi: 10.1039/d1cc06705b. Epub 2022 Jan 12.

Herein, Ag(I)-promoted regioselective intramolecular radical nucleophilic addition/rearrangement of 2-aryl diazaboroles has been accomplished for the first time to construct phenazine structures. This protocol is an umpolung strategy based on the classical electrophilic mechanism, and therefore, a reversed regioselectivity was...

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Zhang H, Guo Q, Cheng H, et al. An umpolung strategy for rapid access to thermally activated delayed fluorescence (TADF) materials based on phenazine. Chem Commun (Camb). 2022;doi: 10.1039/d1cc06705b.
Zhang, H., Guo, Q., Cheng, H., Ran, C., Wu, D., & Lan, J. (2022). An umpolung strategy for rapid access to thermally activated delayed fluorescence (TADF) materials based on phenazine. Chemical communications (Cambridge, England), . https://doi.org/10.1039/d1cc06705b
Zhang, Huaxing, et al. "An umpolung strategy for rapid access to thermally activated delayed fluorescence (TADF) materials based on phenazine." Chemical communications (Cambridge, England) vol. (2022). doi: https://doi.org/10.1039/d1cc06705b
Zhang H, Guo Q, Cheng H, Ran C, Wu D, Lan J. An umpolung strategy for rapid access to thermally activated delayed fluorescence (TADF) materials based on phenazine. Chem Commun (Camb). 2022 Jan 12; doi: 10.1039/d1cc06705b. Epub 2022 Jan 12. PMID: 35018392.
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Showing 1 to 12 of 112 entries