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Preparation and Instability of Nanocrystalline Cuprous Nitride.

Inorganic chemistry

Reichert MD, White MA, Thompson MJ, Miller GJ, Vela J.
PMID: 26091284
Inorg Chem. 2015 Jul 06;54(13):6356-62. doi: 10.1021/acs.inorgchem.5b00679. Epub 2015 Jun 19.

Low-dimensional cuprous nitride (Cu3N) was synthesized by nitridation (ammonolysis) of cuprous oxide (Cu2O) nanocrystals using either ammonia (NH3) or urea (H2NCONH2) as the nitrogen source. The resulting nanocrystalline Cu3N spontaneously decomposes to nanocrystalline CuO in the presence of both...

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Reichert MD, White MA, Thompson MJ, et al. Preparation and Instability of Nanocrystalline Cuprous Nitride. Inorg Chem. 2015;54(13):6356-62doi: 10.1021/acs.inorgchem.5b00679.
Reichert, M. D., White, M. A., Thompson, M. J., Miller, G. J., & Vela, J. (2015). Preparation and Instability of Nanocrystalline Cuprous Nitride. Inorganic chemistry, 54(13), 6356-62. https://doi.org/10.1021/acs.inorgchem.5b00679
Reichert, Malinda D, et al. "Preparation and Instability of Nanocrystalline Cuprous Nitride." Inorganic chemistry vol. 54,13 (2015): 6356-62. doi: https://doi.org/10.1021/acs.inorgchem.5b00679
Reichert MD, White MA, Thompson MJ, Miller GJ, Vela J. Preparation and Instability of Nanocrystalline Cuprous Nitride. Inorg Chem. 2015 Jul 06;54(13):6356-62. doi: 10.1021/acs.inorgchem.5b00679. Epub 2015 Jun 19. PMID: 26091284.
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Mechanism of the Gibbs Reaction. Part 4.(1) Indophenol Formation via N-Chlorobenzoquinone Imine Radical Anions. The Aza-S(RN)2 Chain Reaction Mechanism. Chain Initiation with 1,4-Benzoquinones and Cyanide Ion.

The Journal of organic chemistry

Pallagi I, Toró A, Horváth G.
PMID: 11674654
J Org Chem. 1999 Sep 03;64(18):6530-6540. doi: 10.1021/jo982113v.

The mechanism of the Gibbs reaction, a colorimetric phenol assay that applies N-chlorobenzoquinone imines 1 in an aqueous basic medium, was investigated. It is concluded that N-chloroimine radical anion 7 generated in a single electron transfer (SET) from the...

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Pallagi I, Toró A, Horváth G. Mechanism of the Gibbs Reaction. Part 4.(1) Indophenol Formation via N-Chlorobenzoquinone Imine Radical Anions. The Aza-S(RN)2 Chain Reaction Mechanism. Chain Initiation with 1,4-Benzoquinones and Cyanide Ion. J Org Chem. 1999;64(18):6530-6540doi: 10.1021/jo982113v.
Pallagi, I., Toró, A., & Horváth, G. (1999). Mechanism of the Gibbs Reaction. Part 4.(1) Indophenol Formation via N-Chlorobenzoquinone Imine Radical Anions. The Aza-S(RN)2 Chain Reaction Mechanism. Chain Initiation with 1,4-Benzoquinones and Cyanide Ion. The Journal of organic chemistry, 64(18), 6530-6540. https://doi.org/10.1021/jo982113v
Pallagi, István, et al. "Mechanism of the Gibbs Reaction. Part 4.(1) Indophenol Formation via N-Chlorobenzoquinone Imine Radical Anions. The Aza-S(RN)2 Chain Reaction Mechanism. Chain Initiation with 1,4-Benzoquinones and Cyanide Ion." The Journal of organic chemistry vol. 64,18 (1999): 6530-6540. doi: https://doi.org/10.1021/jo982113v
Pallagi I, Toró A, Horváth G. Mechanism of the Gibbs Reaction. Part 4.(1) Indophenol Formation via N-Chlorobenzoquinone Imine Radical Anions. The Aza-S(RN)2 Chain Reaction Mechanism. Chain Initiation with 1,4-Benzoquinones and Cyanide Ion. J Org Chem. 1999 Sep 03;64(18):6530-6540. doi: 10.1021/jo982113v. PMID: 11674654.
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Inhibition of Water Splitting Increases the Susceptibility of Photosystem II to Photoinhibition.

Plant physiology

Wang WQ, Chapman DJ, Barber J.
PMID: 16668844
Plant Physiol. 1992 May;99(1):16-20. doi: 10.1104/pp.99.1.16.

Photosystem II (PSII)-enriched membrane particles were isolated from peas (Pisum sativum L.) and treated in several different ways to inhibit the water oxidation reactions, but not reaction center function itself, as judged by the light-induced rate of reduction of...

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Wang WQ, Chapman DJ, Barber J. Inhibition of Water Splitting Increases the Susceptibility of Photosystem II to Photoinhibition. Plant Physiol. 1992;99(1):16-20doi: 10.1104/pp.99.1.16.
Wang, W. Q., Chapman, D. J., & Barber, J. (1992). Inhibition of Water Splitting Increases the Susceptibility of Photosystem II to Photoinhibition. Plant physiology, 99(1), 16-20. https://doi.org/10.1104/pp.99.1.16
Wang, W Q, et al. "Inhibition of Water Splitting Increases the Susceptibility of Photosystem II to Photoinhibition." Plant physiology vol. 99,1 (1992): 16-20. doi: https://doi.org/10.1104/pp.99.1.16
Wang WQ, Chapman DJ, Barber J. Inhibition of Water Splitting Increases the Susceptibility of Photosystem II to Photoinhibition. Plant Physiol. 1992 May;99(1):16-20. doi: 10.1104/pp.99.1.16. PMID: 16668844; PMCID: PMC1080399.
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Regulation of the Photosynthesis Rhythm in Euglena gracilis: II. Involvement of Electron Flow through Both Photosystems.

Plant physiology

Lonergan TA, Sargent ML.
PMID: 16660924
Plant Physiol. 1979 Jul;64(1):99-103. doi: 10.1104/pp.64.1.99.

Rhythmic changes in the light reactions of Euglena gracilis have been found which help to explain the basic reactions effected in the circadian rhythm of O(2) evolution. Diurnal changes in the slope of light intensity plots indicated that the...

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Lonergan TA, Sargent ML. Regulation of the Photosynthesis Rhythm in Euglena gracilis: II. Involvement of Electron Flow through Both Photosystems. Plant Physiol. 1979;64(1):99-103doi: 10.1104/pp.64.1.99.
Lonergan, T. A., & Sargent, M. L. (1979). Regulation of the Photosynthesis Rhythm in Euglena gracilis: II. Involvement of Electron Flow through Both Photosystems. Plant physiology, 64(1), 99-103. https://doi.org/10.1104/pp.64.1.99
Lonergan, T A, and Sargent, M L. "Regulation of the Photosynthesis Rhythm in Euglena gracilis: II. Involvement of Electron Flow through Both Photosystems." Plant physiology vol. 64,1 (1979): 99-103. doi: https://doi.org/10.1104/pp.64.1.99
Lonergan TA, Sargent ML. Regulation of the Photosynthesis Rhythm in Euglena gracilis: II. Involvement of Electron Flow through Both Photosystems. Plant Physiol. 1979 Jul;64(1):99-103. doi: 10.1104/pp.64.1.99. PMID: 16660924; PMCID: PMC543032.
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Stimulation of Photosystem I Electron Transport by High Concentration of 3-(3,4-Dichlorophenyl)-1,1-dimethyl Urea in Uncoupled Chloroplasts.

Plant physiology

Ramanujam P, Gnanam A, Bose S.
PMID: 16662131
Plant Physiol. 1981 Dec;68(6):1485-7. doi: 10.1104/pp.68.6.1485.

The light saturated rate of photosystem I-dependent electron transport (ascorbate/dichlorophenol-indophenol --> methyl vilogen in presence of 1 micromolar 3-[3,4-dichlorophenyl]-1,1-dimethyl urea [DCMU]) was increased by a high concentration of DCMU added to broken and uncoupled chloroplasts isolated from pea (Pisum...

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Ramanujam P, Gnanam A, Bose S. Stimulation of Photosystem I Electron Transport by High Concentration of 3-(3,4-Dichlorophenyl)-1,1-dimethyl Urea in Uncoupled Chloroplasts. Plant Physiol. 1981;68(6):1485-7doi: 10.1104/pp.68.6.1485.
Ramanujam, P., Gnanam, A., & Bose, S. (1981). Stimulation of Photosystem I Electron Transport by High Concentration of 3-(3,4-Dichlorophenyl)-1,1-dimethyl Urea in Uncoupled Chloroplasts. Plant physiology, 68(6), 1485-7. https://doi.org/10.1104/pp.68.6.1485
Ramanujam, P, et al. "Stimulation of Photosystem I Electron Transport by High Concentration of 3-(3,4-Dichlorophenyl)-1,1-dimethyl Urea in Uncoupled Chloroplasts." Plant physiology vol. 68,6 (1981): 1485-7. doi: https://doi.org/10.1104/pp.68.6.1485
Ramanujam P, Gnanam A, Bose S. Stimulation of Photosystem I Electron Transport by High Concentration of 3-(3,4-Dichlorophenyl)-1,1-dimethyl Urea in Uncoupled Chloroplasts. Plant Physiol. 1981 Dec;68(6):1485-7. doi: 10.1104/pp.68.6.1485. PMID: 16662131; PMCID: PMC426126.
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Light Activation of Purified Aconitase by Washed Thylakoid Membranes of Pea (Pisum sativum L.).

Plant physiology

Mohamed AH, Anderson LE.
PMID: 16662812
Plant Physiol. 1983 Feb;71(2):248-50. doi: 10.1104/pp.71.2.248.

Purified aconitase, an iron-sulfur protein, from either beef heart mitochondria or pig heart can be activated fully by light when combined with washed thylakoid membranes from pea (Pisum sativum L.) chloroplasts. The light activation of the enzyme does not...

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Mohamed AH, Anderson LE. Light Activation of Purified Aconitase by Washed Thylakoid Membranes of Pea (Pisum sativum L.). Plant Physiol. 1983;71(2):248-50doi: 10.1104/pp.71.2.248.
Mohamed, A. H., & Anderson, L. E. (1983). Light Activation of Purified Aconitase by Washed Thylakoid Membranes of Pea (Pisum sativum L.). Plant physiology, 71(2), 248-50. https://doi.org/10.1104/pp.71.2.248
Mohamed, A H, and Anderson, L E. "Light Activation of Purified Aconitase by Washed Thylakoid Membranes of Pea (Pisum sativum L.)." Plant physiology vol. 71,2 (1983): 248-50. doi: https://doi.org/10.1104/pp.71.2.248
Mohamed AH, Anderson LE. Light Activation of Purified Aconitase by Washed Thylakoid Membranes of Pea (Pisum sativum L.). Plant Physiol. 1983 Feb;71(2):248-50. doi: 10.1104/pp.71.2.248. PMID: 16662812; PMCID: PMC1066019.
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Control of the Photosynthetic Apparatus of Acetabularia mediterranea by Blue Light : Analysis by Light-Saturation Curves.

Plant physiology

Wennicke H, Schmid R.
PMID: 16665593
Plant Physiol. 1987 Aug;84(4):1252-6. doi: 10.1104/pp.84.4.1252.

During growth, Acetabularia mediterranea requires the action of blue light to maintain high rates of photosynthesis. In the present study, blue light-dependent alterations of the photosynthetic apparatus, which can be detected by analysis of light-saturation curves and by measurements...

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Wennicke H, Schmid R. Control of the Photosynthetic Apparatus of Acetabularia mediterranea by Blue Light : Analysis by Light-Saturation Curves. Plant Physiol. 1987;84(4):1252-6doi: 10.1104/pp.84.4.1252.
Wennicke, H., & Schmid, R. (1987). Control of the Photosynthetic Apparatus of Acetabularia mediterranea by Blue Light : Analysis by Light-Saturation Curves. Plant physiology, 84(4), 1252-6. https://doi.org/10.1104/pp.84.4.1252
Wennicke, H, and Schmid, R. "Control of the Photosynthetic Apparatus of Acetabularia mediterranea by Blue Light : Analysis by Light-Saturation Curves." Plant physiology vol. 84,4 (1987): 1252-6. doi: https://doi.org/10.1104/pp.84.4.1252
Wennicke H, Schmid R. Control of the Photosynthetic Apparatus of Acetabularia mediterranea by Blue Light : Analysis by Light-Saturation Curves. Plant Physiol. 1987 Aug;84(4):1252-6. doi: 10.1104/pp.84.4.1252. PMID: 16665593; PMCID: PMC1056760.
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The identity of the indophenol-reducing substance in the Jensen rat sarcoma.

The Biochemical journal

Kellie AE, Zilva SS.
PMID: 16746144
Biochem J. 1936 Jul;30(7):1216-20. doi: 10.1042/bj0301216.

No abstract available.

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Kellie AE, Zilva SS. The identity of the indophenol-reducing substance in the Jensen rat sarcoma. Biochem J. 1936;30(7):1216-20doi: 10.1042/bj0301216.
Kellie, A. E., & Zilva, S. S. (1936). The identity of the indophenol-reducing substance in the Jensen rat sarcoma. The Biochemical journal, 30(7), 1216-20. https://doi.org/10.1042/bj0301216
Kellie, A E, and Zilva, S S. "The identity of the indophenol-reducing substance in the Jensen rat sarcoma." The Biochemical journal vol. 30,7 (1936): 1216-20. doi: https://doi.org/10.1042/bj0301216
Kellie AE, Zilva SS. The identity of the indophenol-reducing substance in the Jensen rat sarcoma. Biochem J. 1936 Jul;30(7):1216-20. doi: 10.1042/bj0301216. PMID: 16746144; PMCID: PMC1263167.
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Spectrophotometric determination of cyclotrimethylenetrinitramine (RDX) in explosive mixtures and residues with the Berthelot reaction.

Analytica chimica acta

Uzer A, Erçağ E, Apak R.
PMID: 18331858
Anal Chim Acta. 2008 Mar 31;612(1):53-64. doi: 10.1016/j.aca.2008.02.015. Epub 2008 Feb 15.

On-site colorimetric methods are a valuable, cost-effective tool to assess the nature and extent of contamination in remediated sites and to enable on-site screening for police criminology laboratories. The existing colorimetric method for cyclotrimethylenetrinitramine (RDX) based on a Griess...

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Uzer A, Erçağ E, Apak R. Spectrophotometric determination of cyclotrimethylenetrinitramine (RDX) in explosive mixtures and residues with the Berthelot reaction. Anal Chim Acta. 2008;612(1):53-64doi: 10.1016/j.aca.2008.02.015.
Uzer, A., Erçağ, E., & Apak, R. (2008). Spectrophotometric determination of cyclotrimethylenetrinitramine (RDX) in explosive mixtures and residues with the Berthelot reaction. Analytica chimica acta, 612(1), 53-64. https://doi.org/10.1016/j.aca.2008.02.015
Uzer, A, et al. "Spectrophotometric determination of cyclotrimethylenetrinitramine (RDX) in explosive mixtures and residues with the Berthelot reaction." Analytica chimica acta vol. 612,1 (2008): 53-64. doi: https://doi.org/10.1016/j.aca.2008.02.015
Uzer A, Erçağ E, Apak R. Spectrophotometric determination of cyclotrimethylenetrinitramine (RDX) in explosive mixtures and residues with the Berthelot reaction. Anal Chim Acta. 2008 Mar 31;612(1):53-64. doi: 10.1016/j.aca.2008.02.015. Epub 2008 Feb 15. PMID: 18331858.
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The indophenol oxidase of mammalian and avian tissues.

The Journal of physiology

Vernon HM.
PMID: 16993086
J Physiol. 1911 Sep 11;43(1):96-108. doi: 10.1113/jphysiol.1911.sp001461.

No abstract available.

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Vernon HM. The indophenol oxidase of mammalian and avian tissues. J Physiol. 1911;43(1):96-108doi: 10.1113/jphysiol.1911.sp001461.
Vernon, H. M. (1911). The indophenol oxidase of mammalian and avian tissues. The Journal of physiology, 43(1), 96-108. https://doi.org/10.1113/jphysiol.1911.sp001461
Vernon, H M. "The indophenol oxidase of mammalian and avian tissues." The Journal of physiology vol. 43,1 (1911): 96-108. doi: https://doi.org/10.1113/jphysiol.1911.sp001461
Vernon HM. The indophenol oxidase of mammalian and avian tissues. J Physiol. 1911 Sep 11;43(1):96-108. doi: 10.1113/jphysiol.1911.sp001461. PMID: 16993086; PMCID: PMC1512748.
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Visible spectrophotometric determination of cephalosporins and penicillins by indophenol derivatization with and without alkaline degradation to ammonia.

Journal of pharmaceutical and biomedical analysis

Fogg AG, Abdalla MA.
PMID: 16867666
J Pharm Biomed Anal. 1985;3(4):315-21. doi: 10.1016/0731-7085(85)80038-8.

Cephalosporins and penicillins give reproducible yields of ammonia on degradation in 0.5 M sodium hydroxide solution at 100 degrees C: the ammonia formed was determined in the degraded solutions using the indophenol reaction. In another approach the ammonia driven...

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Fogg AG, Abdalla MA. Visible spectrophotometric determination of cephalosporins and penicillins by indophenol derivatization with and without alkaline degradation to ammonia. J Pharm Biomed Anal. 1985;3(4):315-21doi: 10.1016/0731-7085(85)80038-8.
Fogg, A. G., & Abdalla, M. A. (1985). Visible spectrophotometric determination of cephalosporins and penicillins by indophenol derivatization with and without alkaline degradation to ammonia. Journal of pharmaceutical and biomedical analysis, 3(4), 315-21. https://doi.org/10.1016/0731-7085(85)80038-8
Fogg, A G, and Abdalla, M A. "Visible spectrophotometric determination of cephalosporins and penicillins by indophenol derivatization with and without alkaline degradation to ammonia." Journal of pharmaceutical and biomedical analysis vol. 3,4 (1985): 315-21. doi: https://doi.org/10.1016/0731-7085(85)80038-8
Fogg AG, Abdalla MA. Visible spectrophotometric determination of cephalosporins and penicillins by indophenol derivatization with and without alkaline degradation to ammonia. J Pharm Biomed Anal. 1985;3(4):315-21. doi: 10.1016/0731-7085(85)80038-8. PMID: 16867666.
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Photosynthetic properties of permaplasts of anacystis.

Plant physiology

Ward B, Myers J.
PMID: 16658214
Plant Physiol. 1972 Nov;50(5):547-50. doi: 10.1104/pp.50.5.547.

A treatment procedure using lysozyme and ethylenediaminetetracetic acid gave intact but permeable cells (permeaplasts) of Anacystis nidulans. Rates of electron transport from water to carbon dioxide, ferricyanide, 2,6-dichlorophenol indophenol, benzoquinone, and methyl viologen, and from reduced indophenol to methyl...

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Ward B, Myers J. Photosynthetic properties of permaplasts of anacystis. Plant Physiol. 1972;50(5):547-50doi: 10.1104/pp.50.5.547.
Ward, B., & Myers, J. (1972). Photosynthetic properties of permaplasts of anacystis. Plant physiology, 50(5), 547-50. https://doi.org/10.1104/pp.50.5.547
Ward, B, and Myers, J. "Photosynthetic properties of permaplasts of anacystis." Plant physiology vol. 50,5 (1972): 547-50. doi: https://doi.org/10.1104/pp.50.5.547
Ward B, Myers J. Photosynthetic properties of permaplasts of anacystis. Plant Physiol. 1972 Nov;50(5):547-50. doi: 10.1104/pp.50.5.547. PMID: 16658214; PMCID: PMC366187.
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