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Preparation and analytical application of the novel Hg(II)-selective membrane electrodes based on oxime compounds.

Journal of colloid and interface science

Sardohan-Koseoglu T, Kir E, Dede B.
PMID: 25585282
J Colloid Interface Sci. 2015 Apr 15;444:17-23. doi: 10.1016/j.jcis.2014.12.025. Epub 2014 Dec 26.

Novel Hg(II)-selective poly(vinyl) chloride (PVC) membrane electrodes based on oxime compounds of (4-(4-methylphenylaminoisonitrosoacetyl)biphenyl, I1; 4-(4-clorophenylaminoisonitrosoacetyl)biphenyl, I2; N,N-bis[1-(4-phenylphenyl)-2-hydroxyimino-2-(4-chloroaniline)-1-ethylidene]-diethylenetriamine, I3 and N,N-bis[1-(4-phenylphenyl)-2-hydroxyimino-2-(4-chloroaniline)-1-ethylidene]- 1,3-propanediamine), I4 were developed. Effects of the species and ratios of ionophore, plasticizer, PVC and lipophilic additive on the...

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Sardohan-Koseoglu T, Kir E, Dede B. Preparation and analytical application of the novel Hg(II)-selective membrane electrodes based on oxime compounds. J Colloid Interface Sci. 2014;444:17-23doi: 10.1016/j.jcis.2014.12.025.
Sardohan-Koseoglu, T., Kir, E., & Dede, B. (2015). Preparation and analytical application of the novel Hg(II)-selective membrane electrodes based on oxime compounds. Journal of colloid and interface science, 44417-23. https://doi.org/10.1016/j.jcis.2014.12.025
Sardohan-Koseoglu, Tugba, et al. "Preparation and analytical application of the novel Hg(II)-selective membrane electrodes based on oxime compounds." Journal of colloid and interface science vol. 444 (2015): 17-23. doi: https://doi.org/10.1016/j.jcis.2014.12.025
Sardohan-Koseoglu T, Kir E, Dede B. Preparation and analytical application of the novel Hg(II)-selective membrane electrodes based on oxime compounds. J Colloid Interface Sci. 2015 Apr 15;444:17-23. doi: 10.1016/j.jcis.2014.12.025. Epub 2014 Dec 26. PMID: 25585282.
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Aerobic versus anaerobic metabolism of halogenated anilines by aParacoccus sp.

Microbial ecology

Bollag JM, Russel S.
PMID: 24233397
Microb Ecol. 1976 Mar;3(1):65-73. doi: 10.1007/BF02011454.

AParacoccus sp. which transforms aniline and different halogen-substituted derivatives under aerobic and anaerobic conditions was isolated from the soil. In experiments with(14)C-ring-labeled 4-chloroaniline, approximately 60% of the radioactive material disappeared from the growth medium after incubation under anaerobiosis within...

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Bollag JM, Russel S. Aerobic versus anaerobic metabolism of halogenated anilines by aParacoccus sp. Microb Ecol. 1976;3(1):65-73doi: 10.1007/BF02011454.
Bollag, J. M., & Russel, S. (1976). Aerobic versus anaerobic metabolism of halogenated anilines by aParacoccus sp. Microbial ecology, 3(1), 65-73. https://doi.org/10.1007/BF02011454
Bollag, J M, and Russel, S. "Aerobic versus anaerobic metabolism of halogenated anilines by aParacoccus sp." Microbial ecology vol. 3,1 (1976): 65-73. doi: https://doi.org/10.1007/BF02011454
Bollag JM, Russel S. Aerobic versus anaerobic metabolism of halogenated anilines by aParacoccus sp. Microb Ecol. 1976 Mar;3(1):65-73. doi: 10.1007/BF02011454. PMID: 24233397.
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Isostructuralism among bridge-flipped' isomeric benzylideneanilines and phenylhydrazones.

Acta crystallographica. Section B, Structural science

Ojala WH, Smieja JM, Spude JM, Arola TM, Kuspa MK, Herrera N, Ojala CR.
PMID: 17507762
Acta Crystallogr B. 2007 Jun;63:485-96. doi: 10.1107/S0108768107018034. Epub 2007 May 16.

Bridge-flipped' isomers may be defined as pairs of molecules related by a reversal of a bridge of atoms connecting two major parts of the individual molecules. This kind of isomerism is commonly found among benzylideneanilines and phenylhydrazones. Isostructural pairs...

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Ojala WH, Smieja JM, Spude JM, et al. Isostructuralism among bridge-flipped' isomeric benzylideneanilines and phenylhydrazones. Acta Crystallogr B. 2007;63:485-96doi: 10.1107/S0108768107018034.
Ojala, W. H., Smieja, J. M., Spude, J. M., Arola, T. M., Kuspa, M. K., Herrera, N., & Ojala, C. R. (2007). Isostructuralism among bridge-flipped' isomeric benzylideneanilines and phenylhydrazones. Acta crystallographica. Section B, Structural science, 63485-96. https://doi.org/10.1107/S0108768107018034
Ojala, William H, et al. "Isostructuralism among bridge-flipped' isomeric benzylideneanilines and phenylhydrazones." Acta crystallographica. Section B, Structural science vol. 63 (2007): 485-96. doi: https://doi.org/10.1107/S0108768107018034
Ojala WH, Smieja JM, Spude JM, Arola TM, Kuspa MK, Herrera N, Ojala CR. Isostructuralism among bridge-flipped' isomeric benzylideneanilines and phenylhydrazones. Acta Crystallogr B. 2007 Jun;63:485-96. doi: 10.1107/S0108768107018034. Epub 2007 May 16. PMID: 17507762.
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In Vitro toxicity of 2- and 4-chloroaniline: comparisons with 4-amino-3-chlorophenol, 2-amino-5-chlorophenol and aminophenols.

Toxicology in vitro : an international journal published in association with BIBRA

Valentovic MA, Ball JG, Hong SK, Rogers BA, Meadows MK, Harmon RC, Rankin GO.
PMID: 20650255
Toxicol In Vitro. 1996 Dec;10(6):713-20. doi: 10.1016/s0887-2333(96)00060-4.

Chloroanilines have been associated with renal and hepatic toxicity. This study (a) examined the in vitro hepatic and renal toxicity of 2-chloroaniline and 4-chloroaniline, (b) further examined whether aromatic ring hydroxylation would increase toxicity of the parent compound and...

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Valentovic MA, Ball JG, Hong SK, et al. In Vitro toxicity of 2- and 4-chloroaniline: comparisons with 4-amino-3-chlorophenol, 2-amino-5-chlorophenol and aminophenols. Toxicol In Vitro. 1996;10(6):713-20doi: 10.1016/s0887-2333(96)00060-4.
Valentovic, M. A., Ball, J. G., Hong, S. K., Rogers, B. A., Meadows, M. K., Harmon, R. C., & Rankin, G. O. (1996). In Vitro toxicity of 2- and 4-chloroaniline: comparisons with 4-amino-3-chlorophenol, 2-amino-5-chlorophenol and aminophenols. Toxicology in vitro : an international journal published in association with BIBRA, 10(6), 713-20. https://doi.org/10.1016/s0887-2333(96)00060-4
Valentovic, M A, et al. "In Vitro toxicity of 2- and 4-chloroaniline: comparisons with 4-amino-3-chlorophenol, 2-amino-5-chlorophenol and aminophenols." Toxicology in vitro : an international journal published in association with BIBRA vol. 10,6 (1996): 713-20. doi: https://doi.org/10.1016/s0887-2333(96)00060-4
Valentovic MA, Ball JG, Hong SK, Rogers BA, Meadows MK, Harmon RC, Rankin GO. In Vitro toxicity of 2- and 4-chloroaniline: comparisons with 4-amino-3-chlorophenol, 2-amino-5-chlorophenol and aminophenols. Toxicol In Vitro. 1996 Dec;10(6):713-20. doi: 10.1016/s0887-2333(96)00060-4. PMID: 20650255.
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Metabolism of 4-Chloronitrobenzene by the Yeast Rhodosporidium sp.

Applied and environmental microbiology

Corbett MD, Corbett BR.
PMID: 16345757
Appl Environ Microbiol. 1981 Apr;41(4):942-9. doi: 10.1128/aem.41.4.942-949.1981.

The yeast Rhodosporidium sp. metabolized 4-chloronitrobenzene by a reductive pathway to give 4-chloroacetanilide and 4-chloro-2-hydroxyacetanilide as the major final metabolites. The intermediate production of 4-chloronitrosobenzene, 4-chlorophenylhydroxylamine, and 4-chloroaniline was demonstrated by high-pressure liquid chromatography. Additional studies with selected metabolites...

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Corbett MD, Corbett BR. Metabolism of 4-Chloronitrobenzene by the Yeast Rhodosporidium sp. Appl Environ Microbiol. 1981;41(4):942-9doi: 10.1128/aem.41.4.942-949.1981.
Corbett, M. D., & Corbett, B. R. (1981). Metabolism of 4-Chloronitrobenzene by the Yeast Rhodosporidium sp. Applied and environmental microbiology, 41(4), 942-9. https://doi.org/10.1128/aem.41.4.942-949.1981
Corbett, M D, and Corbett, B R. "Metabolism of 4-Chloronitrobenzene by the Yeast Rhodosporidium sp." Applied and environmental microbiology vol. 41,4 (1981): 942-9. doi: https://doi.org/10.1128/aem.41.4.942-949.1981
Corbett MD, Corbett BR. Metabolism of 4-Chloronitrobenzene by the Yeast Rhodosporidium sp. Appl Environ Microbiol. 1981 Apr;41(4):942-9. doi: 10.1128/aem.41.4.942-949.1981. PMID: 16345757; PMCID: PMC243838.
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A concise and efficient concurrent synthesis of 6,11-dihydrodibenzo[b,e]azepines and 5,6,11,12-tetrahydrodibenzo[b,f]azocines and their conversion to 4-oxo-8,13-dihydro-4H-benzo[5,6]azepino[3,2,1-ij]quinoline-5-carboxylates and N-acetyl-5,6,11,12-tetrahydrodibenzo[b,f]azocines: synthetic sequence, spectroscopic characterization and the structures of two products.

Acta crystallographica. Section C, Structural chemistry

Acosta Quintero LM, Palma A, Cobo J, Glidewell C.
PMID: 31166916
Acta Crystallogr C Struct Chem. 2019 Jun 01;75:650-656. doi: 10.1107/S2053229619005746. Epub 2019 May 15.

Reaction of 2-allyl-N-benzyl-4-fluoroaniline or 2-allyl-N-benzyl-4-chloroaniline with 98% sulfuric acid leads to the concurrent formation of halogeno-substituted 11-ethyl-6,11-dihydrodibenzo[b,e]azepines, (II), and halogeno-substituted 11-methyl-5,6,11,12-tetrahydrodibenzo[b,f]azocines, (III), in each case in (II):(III) molar ratios of ca 2:1. Further reaction of (II) leads to ethyl...

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Acosta Quintero LM, Palma A, Cobo J, et al. A concise and efficient concurrent synthesis of 6,11-dihydrodibenzo[b,e]azepines and 5,6,11,12-tetrahydrodibenzo[b,f]azocines and their conversion to 4-oxo-8,13-dihydro-4H-benzo[5,6]azepino[3,2,1-ij]quinoline-5-carboxylates and N-acetyl-5,6,11,12-tetrahydrodibenzo[b,f]azocines: synthetic sequence, spectroscopic characterization and the structures of two products. Acta Crystallogr C Struct Chem. 2019;75:650-656doi: 10.1107/S2053229619005746.
Acosta Quintero, L. M., Palma, A., Cobo, J., & Glidewell, C. (2019). A concise and efficient concurrent synthesis of 6,11-dihydrodibenzo[b,e]azepines and 5,6,11,12-tetrahydrodibenzo[b,f]azocines and their conversion to 4-oxo-8,13-dihydro-4H-benzo[5,6]azepino[3,2,1-ij]quinoline-5-carboxylates and N-acetyl-5,6,11,12-tetrahydrodibenzo[b,f]azocines: synthetic sequence, spectroscopic characterization and the structures of two products. Acta crystallographica. Section C, Structural chemistry, 75650-656. https://doi.org/10.1107/S2053229619005746
Acosta Quintero, Lina M, et al. "A concise and efficient concurrent synthesis of 6,11-dihydrodibenzo[b,e]azepines and 5,6,11,12-tetrahydrodibenzo[b,f]azocines and their conversion to 4-oxo-8,13-dihydro-4H-benzo[5,6]azepino[3,2,1-ij]quinoline-5-carboxylates and N-acetyl-5,6,11,12-tetrahydrodibenzo[b,f]azocines: synthetic sequence, spectroscopic characterization and the structures of two products." Acta crystallographica. Section C, Structural chemistry vol. 75 (2019): 650-656. doi: https://doi.org/10.1107/S2053229619005746
Acosta Quintero LM, Palma A, Cobo J, Glidewell C. A concise and efficient concurrent synthesis of 6,11-dihydrodibenzo[b,e]azepines and 5,6,11,12-tetrahydrodibenzo[b,f]azocines and their conversion to 4-oxo-8,13-dihydro-4H-benzo[5,6]azepino[3,2,1-ij]quinoline-5-carboxylates and N-acetyl-5,6,11,12-tetrahydrodibenzo[b,f]azocines: synthetic sequence, spectroscopic characterization and the structures of two products. Acta Crystallogr C Struct Chem. 2019 Jun 01;75:650-656. doi: 10.1107/S2053229619005746. Epub 2019 May 15. PMID: 31166916.
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Crystal structure of N-8-azanaphtylmethylene-4-chloroaniline.

Analytical sciences : the international journal of the Japan Society for Analytical Chemistry

Oztürk S, Aygün M, Ocal N, Yolaçan C, Fun HK.
PMID: 11707956
Anal Sci. 2001 Jun;17(6):797-8. doi: 10.2116/analsci.17.797.

No abstract available.

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Oztürk S, Aygün M, Ocal N, et al. Crystal structure of N-8-azanaphtylmethylene-4-chloroaniline. Anal Sci. 2001;17(6):797-8doi: 10.2116/analsci.17.797.
Oztürk, S., Aygün, M., Ocal, N., Yolaçan, C., & Fun, H. K. (2001). Crystal structure of N-8-azanaphtylmethylene-4-chloroaniline. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 17(6), 797-8. https://doi.org/10.2116/analsci.17.797
Oztürk, S, et al. "Crystal structure of N-8-azanaphtylmethylene-4-chloroaniline." Analytical sciences : the international journal of the Japan Society for Analytical Chemistry vol. 17,6 (2001): 797-8. doi: https://doi.org/10.2116/analsci.17.797
Oztürk S, Aygün M, Ocal N, Yolaçan C, Fun HK. Crystal structure of N-8-azanaphtylmethylene-4-chloroaniline. Anal Sci. 2001 Jun;17(6):797-8. doi: 10.2116/analsci.17.797. PMID: 11707956.
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Generation and reactivity of the 4-aminophenyl cation by photolysis of 4-chloroaniline.

The Journal of organic chemistry

Guizzardi B, Mella M, Fagnoni M, Freccero M, Albini A.
PMID: 11559186
J Org Chem. 2001 Sep 21;66(19):6353-63. doi: 10.1021/jo0104680.

4-Chloroaniline and its N,N-dimethyl derivative are photostable in cyclohexane but undergo efficient photoheterolysis in polar media via the triplet state and give the corresponding triplet phenyl cations. CASSCF and UB3LYP calculations show that the 4-aminophenyl triplet cation has a...

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Guizzardi B, Mella M, Fagnoni M, et al. Generation and reactivity of the 4-aminophenyl cation by photolysis of 4-chloroaniline. J Org Chem. 2001;66(19):6353-63doi: 10.1021/jo0104680.
Guizzardi, B., Mella, M., Fagnoni, M., Freccero, M., & Albini, A. (2001). Generation and reactivity of the 4-aminophenyl cation by photolysis of 4-chloroaniline. The Journal of organic chemistry, 66(19), 6353-63. https://doi.org/10.1021/jo0104680
Guizzardi, B, et al. "Generation and reactivity of the 4-aminophenyl cation by photolysis of 4-chloroaniline." The Journal of organic chemistry vol. 66,19 (2001): 6353-63. doi: https://doi.org/10.1021/jo0104680
Guizzardi B, Mella M, Fagnoni M, Freccero M, Albini A. Generation and reactivity of the 4-aminophenyl cation by photolysis of 4-chloroaniline. J Org Chem. 2001 Sep 21;66(19):6353-63. doi: 10.1021/jo0104680. PMID: 11559186.
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Pathways of Nitrosobenzene Reduction by Thiols in Alcoholic Media.

The Journal of organic chemistry

Montanari S, Paradisi C, Scorrano G.
PMID: 11674462
J Org Chem. 1999 May 14;64(10):3422-3428. doi: 10.1021/jo981889t.

The biologically important reaction of nitrosobenzenes with thiols has been investigated in 2-propanol solution at room temperature, experimental conditions which allow for the detection and characterization of key intermediates. Final stable products of such complex reactions include azoxybenzenes and...

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Montanari S, Paradisi C, Scorrano G. Pathways of Nitrosobenzene Reduction by Thiols in Alcoholic Media. J Org Chem. 1999;64(10):3422-3428doi: 10.1021/jo981889t.
Montanari, S., Paradisi, C., & Scorrano, G. (1999). Pathways of Nitrosobenzene Reduction by Thiols in Alcoholic Media. The Journal of organic chemistry, 64(10), 3422-3428. https://doi.org/10.1021/jo981889t
Montanari, Stefano, et al. "Pathways of Nitrosobenzene Reduction by Thiols in Alcoholic Media." The Journal of organic chemistry vol. 64,10 (1999): 3422-3428. doi: https://doi.org/10.1021/jo981889t
Montanari S, Paradisi C, Scorrano G. Pathways of Nitrosobenzene Reduction by Thiols in Alcoholic Media. J Org Chem. 1999 May 14;64(10):3422-3428. doi: 10.1021/jo981889t. PMID: 11674462.
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Photochemical reaction of N,N-dimethyl-4-chloroaniline with dienes: new synthetic paths via a phenyl cation.

Chemistry (Weinheim an der Bergstrasse, Germany)

Guizzardi B, Mella M, Fagnoni M, Albini A.
PMID: 12658653
Chemistry. 2003 Apr 04;9(7):1549-55. doi: 10.1002/chem.200390178.

The irradiation of N,N-dimethyl-4-chloroaniline in the presence of open-chain dienes in acetonitrile leads to addition of the aminophenyl and chloro groups across one of the double bonds; transannular cyclization takes place with cyclic dienes, leading to an arylnortricyclene from...

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Guizzardi B, Mella M, Fagnoni M, et al. Photochemical reaction of N,N-dimethyl-4-chloroaniline with dienes: new synthetic paths via a phenyl cation. Chemistry. 2003;9(7):1549-55doi: 10.1002/chem.200390178.
Guizzardi, B., Mella, M., Fagnoni, M., & Albini, A. (2003). Photochemical reaction of N,N-dimethyl-4-chloroaniline with dienes: new synthetic paths via a phenyl cation. Chemistry (Weinheim an der Bergstrasse, Germany), 9(7), 1549-55. https://doi.org/10.1002/chem.200390178
Guizzardi, Benedetta, et al. "Photochemical reaction of N,N-dimethyl-4-chloroaniline with dienes: new synthetic paths via a phenyl cation." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 9,7 (2003): 1549-55. doi: https://doi.org/10.1002/chem.200390178
Guizzardi B, Mella M, Fagnoni M, Albini A. Photochemical reaction of N,N-dimethyl-4-chloroaniline with dienes: new synthetic paths via a phenyl cation. Chemistry. 2003 Apr 04;9(7):1549-55. doi: 10.1002/chem.200390178. PMID: 12658653.
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Bioassay of p-Chloroaniline for Possible Carcinogenicity (CAS No. 106-47-8).

National Toxicology Program technical report series

[No authors listed]
PMID: 12778190
Natl Toxicol Program Tech Rep Ser. 1979;189:1-105.

p-Chloroaniline, a dye and chemical intermediate, was selected for bioassay by the National Cancer Institute because of the high incidence of bladder cancer observed among dye manufacturing industry workers. A bioassay for the possible carcinogenicity of p-chloroaniline was conducted...

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Bioassay of p-Chloroaniline for Possible Carcinogenicity (CAS No. 106-47-8). Natl Toxicol Program Tech Rep Ser. 1979;189:1-105
(1979). Bioassay of p-Chloroaniline for Possible Carcinogenicity (CAS No. 106-47-8). National Toxicology Program technical report series, 1891-105.
"Bioassay of p-Chloroaniline for Possible Carcinogenicity (CAS No. 106-47-8)." National Toxicology Program technical report series vol. 189 (1979): 1-105.
Bioassay of p-Chloroaniline for Possible Carcinogenicity (CAS No. 106-47-8). Natl Toxicol Program Tech Rep Ser. 1979;189:1-105. PMID: 12778190.
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Solarylations via 4-aminophenyl cations.

The Journal of organic chemistry

Dichiarante V, Fagnoni M, Albini A.
PMID: 20104916
J Org Chem. 2010 Feb 19;75(4):1271-6. doi: 10.1021/jo902669j.

The application of the photo-S(N)1 reaction on some 4-chloroanilines was explored under solar irradiation in view of obtaining a convenient metal-free arylation method. Several reactions previously carried out by UV irradiation, as well as some new ones, where either...

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Dichiarante V, Fagnoni M, Albini A. Solarylations via 4-aminophenyl cations. J Org Chem. 2010;75(4):1271-6doi: 10.1021/jo902669j.
Dichiarante, V., Fagnoni, M., & Albini, A. (2010). Solarylations via 4-aminophenyl cations. The Journal of organic chemistry, 75(4), 1271-6. https://doi.org/10.1021/jo902669j
Dichiarante, Valentina, et al. "Solarylations via 4-aminophenyl cations." The Journal of organic chemistry vol. 75,4 (2010): 1271-6. doi: https://doi.org/10.1021/jo902669j
Dichiarante V, Fagnoni M, Albini A. Solarylations via 4-aminophenyl cations. J Org Chem. 2010 Feb 19;75(4):1271-6. doi: 10.1021/jo902669j. PMID: 20104916.
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Showing 1 to 12 of 38 entries