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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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Optimum removal conditions of aniline compounds in simulated wastewater by laccase from white-rot fungi.

Journal of environmental health science & engineering

Yang B, Wang Y, Liu Z, Liu J, Cai J.
PMID: 31321041
J Environ Health Sci Eng. 2019 Jan 15;17(1):135-140. doi: 10.1007/s40201-018-00334-x. eCollection 2019 Jun.

BACKGROUND: Aniline compounds are widely applied as important chemical raw materials. However, they are so toxic and harmful to humans and environment that they need to be removed by an effective and economic approach, such as enzymatic reaction, which...

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Yang B, Wang Y, Liu Z, et al. Optimum removal conditions of aniline compounds in simulated wastewater by laccase from white-rot fungi. J Environ Health Sci Eng. 2019;17(1):135-140doi: 10.1007/s40201-018-00334-x.
Yang, B., Wang, Y., Liu, Z., Liu, J., & Cai, J. (2019). Optimum removal conditions of aniline compounds in simulated wastewater by laccase from white-rot fungi. Journal of environmental health science & engineering, 17(1), 135-140. https://doi.org/10.1007/s40201-018-00334-x
Yang, Bo, et al. "Optimum removal conditions of aniline compounds in simulated wastewater by laccase from white-rot fungi." Journal of environmental health science & engineering vol. 17,1 (2019): 135-140. doi: https://doi.org/10.1007/s40201-018-00334-x
Yang B, Wang Y, Liu Z, Liu J, Cai J. Optimum removal conditions of aniline compounds in simulated wastewater by laccase from white-rot fungi. J Environ Health Sci Eng. 2019 Jan 15;17(1):135-140. doi: 10.1007/s40201-018-00334-x. eCollection 2019 Jun. PMID: 31321041; PMCID: PMC6581990.
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The Effect of Hydrogen Bonding and Azomethine Group Orientation on Liquid Crystal Properties in Benzylidene Aniline Compounds.

Acta chimica Slovenica

Kshash AH.
PMID: 33533423
Acta Chim Slov. 2020 Sep;67(3):739-747.

This study examines the effects of substituents and hydrogen bonding, orientations of imine linkage on the behavior of benzylidene aniline compounds as liquid crystals (LC). Compounds 4-carboxy benzylidene-4-X-aniline (X = H, F, Cl, Br, CH3, OCH3) 1a-6a were synthesized...

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Kshash AH. The Effect of Hydrogen Bonding and Azomethine Group Orientation on Liquid Crystal Properties in Benzylidene Aniline Compounds. Acta Chim Slov. 2020;67(3):739-747
Kshash, A. H. (2020). The Effect of Hydrogen Bonding and Azomethine Group Orientation on Liquid Crystal Properties in Benzylidene Aniline Compounds. Acta chimica Slovenica, 67(3), 739-747.
Kshash, Abdullah Hussein. "The Effect of Hydrogen Bonding and Azomethine Group Orientation on Liquid Crystal Properties in Benzylidene Aniline Compounds." Acta chimica Slovenica vol. 67,3 (2020): 739-747.
Kshash AH. The Effect of Hydrogen Bonding and Azomethine Group Orientation on Liquid Crystal Properties in Benzylidene Aniline Compounds. Acta Chim Slov. 2020 Sep;67(3):739-747. PMID: 33533423.
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Preparation of Ce-PbO(2) modified electrode and its application in detection of anilines.

Talanta

Ai S, Gao M, Zhang W, Wang Q, Xie Y, Jin L.
PMID: 18969316
Talanta. 2004 Feb 27;62(3):445-50. doi: 10.1016/j.talanta.2003.08.019.

The effect of Ce(III) on the morphology and structure of lead dioxide (PbO(2)) modified electrode was studied in this paper. The results obtained by cyclic voltammetry (CV), X-ray diffractometion (XRD) and scanning tunneling micrograph (STM) indicated that the Ce-doped...

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Ai S, Gao M, Zhang W, et al. Preparation of Ce-PbO(2) modified electrode and its application in detection of anilines. Talanta. 2004;62(3):445-50doi: 10.1016/j.talanta.2003.08.019.
Ai, S., Gao, M., Zhang, W., Wang, Q., Xie, Y., & Jin, L. (2004). Preparation of Ce-PbO(2) modified electrode and its application in detection of anilines. Talanta, 62(3), 445-50. https://doi.org/10.1016/j.talanta.2003.08.019
Ai, Shiyun, et al. "Preparation of Ce-PbO(2) modified electrode and its application in detection of anilines." Talanta vol. 62,3 (2004): 445-50. doi: https://doi.org/10.1016/j.talanta.2003.08.019
Ai S, Gao M, Zhang W, Wang Q, Xie Y, Jin L. Preparation of Ce-PbO(2) modified electrode and its application in detection of anilines. Talanta. 2004 Feb 27;62(3):445-50. doi: 10.1016/j.talanta.2003.08.019. PMID: 18969316.
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Mechanistic studies of the rhodium-catalyzed direct C-H amination reaction using azides as the nitrogen source.

Journal of the American Chemical Society

Park SH, Kwak J, Shin K, Ryu J, Park Y, Chang S.
PMID: 24450395
J Am Chem Soc. 2014 Feb 12;136(6):2492-502. doi: 10.1021/ja411072a. Epub 2014 Jan 30.

Direct C-H amination of arenes offers a straightforward route to aniline compounds without necessitating aryl (pseudo)halides as the starting materials. The recent development in this area, in particular in the metal-mediated transformations, is significant with regard to substrate scope...

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Park SH, Kwak J, Shin K, et al. Mechanistic studies of the rhodium-catalyzed direct C-H amination reaction using azides as the nitrogen source. J Am Chem Soc. 2014;136(6):2492-502doi: 10.1021/ja411072a.
Park, S. H., Kwak, J., Shin, K., Ryu, J., Park, Y., & Chang, S. (2014). Mechanistic studies of the rhodium-catalyzed direct C-H amination reaction using azides as the nitrogen source. Journal of the American Chemical Society, 136(6), 2492-502. https://doi.org/10.1021/ja411072a
Park, Sae Hume, et al. "Mechanistic studies of the rhodium-catalyzed direct C-H amination reaction using azides as the nitrogen source." Journal of the American Chemical Society vol. 136,6 (2014): 2492-502. doi: https://doi.org/10.1021/ja411072a
Park SH, Kwak J, Shin K, Ryu J, Park Y, Chang S. Mechanistic studies of the rhodium-catalyzed direct C-H amination reaction using azides as the nitrogen source. J Am Chem Soc. 2014 Feb 12;136(6):2492-502. doi: 10.1021/ja411072a. Epub 2014 Jan 30. PMID: 24450395.
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Selective utilization of methoxy groups in lignin for .

Chemical science

Mei Q, Shen X, Liu H, Liu H, Xiang J, Han B.
PMID: 30774905
Chem Sci. 2018 Nov 01;10(4):1082-1088. doi: 10.1039/c8sc03006e. eCollection 2019 Jan 28.

The utilization of lignin as a feedstock to produce valuable chemicals is of great importance. However, it is a great challenge to produce pure chemicals because of the complex structure of lignin. The selective utilization of specific groups on...

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Mei Q, Shen X, Liu H, et al. Selective utilization of methoxy groups in lignin for . Chem Sci. 2018;10(4):1082-1088doi: 10.1039/c8sc03006e.
Mei, Q., Shen, X., Liu, H., Liu, H., Xiang, J., & Han, B. (2019). Selective utilization of methoxy groups in lignin for . Chemical science, 10(4), 1082-1088. https://doi.org/10.1039/c8sc03006e
Mei, Qingqing, et al. "Selective utilization of methoxy groups in lignin for ." Chemical science vol. 10,4 (2019): 1082-1088. doi: https://doi.org/10.1039/c8sc03006e
Mei Q, Shen X, Liu H, Liu H, Xiang J, Han B. Selective utilization of methoxy groups in lignin for . Chem Sci. 2018 Nov 01;10(4):1082-1088. doi: 10.1039/c8sc03006e. eCollection 2019 Jan 28. PMID: 30774905; PMCID: PMC6346405.
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Mechanisms and Models of Adsorption: TiO.

ACS omega

Abodif AM, Meng L, Ma S, Ahmed ASA, Belvett N, Wei ZZ, Ning D.
PMID: 32566828
ACS Omega. 2020 Jun 01;5(23):13630-13640. doi: 10.1021/acsomega.0c00619. eCollection 2020 Jun 16.

Here, 3,4-dimethylaniline (3,4-DMA) was selected as a representative organic substance of aniline compounds. A biochar-titanium dioxide (BC-TiO

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Abodif AM, Meng L, Ma S, et al. Mechanisms and Models of Adsorption: TiO. ACS Omega. 2020;5(23):13630-13640doi: 10.1021/acsomega.0c00619.
Abodif, A. M., Meng, L., Ma, S., Ahmed, A. S. A., Belvett, N., Wei, Z. Z., & Ning, D. (2020). Mechanisms and Models of Adsorption: TiO. ACS omega, 5(23), 13630-13640. https://doi.org/10.1021/acsomega.0c00619
Abodif, Ahmed M, et al. "Mechanisms and Models of Adsorption: TiO." ACS omega vol. 5,23 (2020): 13630-13640. doi: https://doi.org/10.1021/acsomega.0c00619
Abodif AM, Meng L, Ma S, Ahmed ASA, Belvett N, Wei ZZ, Ning D. Mechanisms and Models of Adsorption: TiO. ACS Omega. 2020 Jun 01;5(23):13630-13640. doi: 10.1021/acsomega.0c00619. eCollection 2020 Jun 16. PMID: 32566828; PMCID: PMC7301375.
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A STUDY OF THE ANTISEPTIC PROPERTIES OF CERTAIN ORGANIC COMPOUNDS.

The Journal of experimental medicine

Kligler IJ.
PMID: 19868219
J Exp Med. 1918 Apr 01;27(4):463-76. doi: 10.1084/jem.27.4.463.

THIS STUDY OF THE INHIBITIVE EFFECT OF ANILINE AND SOME OF ITS DERIVATIVES AND OF THE TRIPHENYLMETHANE DYES ON CERTAIN BACTERIA WARRANTS THE FOLLOWING TENTATIVE CONCLUSIONS: 1. The composition and reaction of the medium exert a marked influence on...

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Kligler IJ. A STUDY OF THE ANTISEPTIC PROPERTIES OF CERTAIN ORGANIC COMPOUNDS. J Exp Med. 1918;27(4):463-76doi: 10.1084/jem.27.4.463.
Kligler, I. J. (1918). A STUDY OF THE ANTISEPTIC PROPERTIES OF CERTAIN ORGANIC COMPOUNDS. The Journal of experimental medicine, 27(4), 463-76. https://doi.org/10.1084/jem.27.4.463
Kligler, I J. "A STUDY OF THE ANTISEPTIC PROPERTIES OF CERTAIN ORGANIC COMPOUNDS." The Journal of experimental medicine vol. 27,4 (1918): 463-76. doi: https://doi.org/10.1084/jem.27.4.463
Kligler IJ. A STUDY OF THE ANTISEPTIC PROPERTIES OF CERTAIN ORGANIC COMPOUNDS. J Exp Med. 1918 Apr 01;27(4):463-76. doi: 10.1084/jem.27.4.463. PMID: 19868219; PMCID: PMC2125947.
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Implementation and study of dopant-assisted photoionization with a miniature capillary inlet ion trap mass spectrometer.

Rapid communications in mass spectrometry : RCM

Zhang Q, Tian Y, Aliang M, Yu Q, Wang X.
PMID: 31658505
Rapid Commun Mass Spectrom. 2020 Mar 30;34(6):e8621. doi: 10.1002/rcm.8621.

RATIONALE: Dopant-assisted photoionization (PI) has been widely used in the mass spectrometric analysis of volatile compounds. Exploring simple doping methods will benefit parameter optimization and promote the application of this technique.METHODS: A previously built miniature ion trap mass spectrometer...

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Zhang Q, Tian Y, Aliang M, et al. Implementation and study of dopant-assisted photoionization with a miniature capillary inlet ion trap mass spectrometer. Rapid Commun Mass Spectrom. 2020;34(6):e8621doi: 10.1002/rcm.8621.
Zhang, Q., Tian, Y., Aliang, M., Yu, Q., & Wang, X. (2020). Implementation and study of dopant-assisted photoionization with a miniature capillary inlet ion trap mass spectrometer. Rapid communications in mass spectrometry : RCM, 34(6), e8621. https://doi.org/10.1002/rcm.8621
Zhang, Qian, et al. "Implementation and study of dopant-assisted photoionization with a miniature capillary inlet ion trap mass spectrometer." Rapid communications in mass spectrometry : RCM vol. 34,6 (2020): e8621. doi: https://doi.org/10.1002/rcm.8621
Zhang Q, Tian Y, Aliang M, Yu Q, Wang X. Implementation and study of dopant-assisted photoionization with a miniature capillary inlet ion trap mass spectrometer. Rapid Commun Mass Spectrom. 2020 Mar 30;34(6):e8621. doi: 10.1002/rcm.8621. PMID: 31658505.
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[Aqueous Fingerprint of Printing and Dyeing Wastewater].

Guang pu xue yu guang pu fen xi = Guang pu

Wang SF, Wu J, Cheng C, Yang L, Zhao YF, Lü Q, Fu XM.
PMID: 26964226
Guang Pu Xue Yu Guang Pu Fen Xi. 2015 Dec;35(12):3440-3.

Aqueous fingerprint has an advantage to represent the organic components of water samples as compared to traditional parameters such as chemical oxygen demand (COD) and total organic carbon (TOC). Printing and dyeing wastewater is one of the major types...

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Wang SF, Wu J, Cheng C, et al. [Aqueous Fingerprint of Printing and Dyeing Wastewater]. Guang Pu Xue Yu Guang Pu Fen Xi. 2015;35(12):3440-3
Wang, S. F., Wu, J., Cheng, C., Yang, L., Zhao, Y. F., Lü, Q., & Fu, X. M. (2015). [Aqueous Fingerprint of Printing and Dyeing Wastewater]. Guang pu xue yu guang pu fen xi = Guang pu, 35(12), 3440-3.
Wang, Shi-feng, et al. "[Aqueous Fingerprint of Printing and Dyeing Wastewater]." Guang pu xue yu guang pu fen xi = Guang pu vol. 35,12 (2015): 3440-3.
Wang SF, Wu J, Cheng C, Yang L, Zhao YF, Lü Q, Fu XM. [Aqueous Fingerprint of Printing and Dyeing Wastewater]. Guang Pu Xue Yu Guang Pu Fen Xi. 2015 Dec;35(12):3440-3. Chinese. PMID: 26964226.
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Reactions for making widely used aniline compounds break norms of synthesis.

Nature

Schmidt VA.
PMID: 32760040
Nature. 2020 Aug;584(7819):46-47. doi: 10.1038/d41586-020-02283-8.

No abstract available.

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Schmidt VA. Reactions for making widely used aniline compounds break norms of synthesis. Nature. 2020;584(7819):46-47doi: 10.1038/d41586-020-02283-8.
Schmidt, V. A. (2020). Reactions for making widely used aniline compounds break norms of synthesis. Nature, 584(7819), 46-47. https://doi.org/10.1038/d41586-020-02283-8
Schmidt, Valerie A. "Reactions for making widely used aniline compounds break norms of synthesis." Nature vol. 584,7819 (2020): 46-47. doi: https://doi.org/10.1038/d41586-020-02283-8
Schmidt VA. Reactions for making widely used aniline compounds break norms of synthesis. Nature. 2020 Aug;584(7819):46-47. doi: 10.1038/d41586-020-02283-8. PMID: 32760040.
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One-pot preparation of an organic polymer monolith by thiol-ene click chemistry for capillary electrochromatography.

Journal of separation science

Wang J, Shen S, Lu X, Ye F.
PMID: 28586155
J Sep Sci. 2017 Aug;40(15):3144-3152. doi: 10.1002/jssc.201700110. Epub 2017 Jun 29.

A novel organic monolith was successfully fabricated by a one-pot thiol-ene click reaction of triallyl isocyanurate with pentaerythritol tetrakis-(2-mercaptoacetate) and mercaptopropionic acid in the presence of porogens. We investigated the effects of the ratio of monomer and cross-linking agent,...

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Wang J, Shen S, Lu X, et al. One-pot preparation of an organic polymer monolith by thiol-ene click chemistry for capillary electrochromatography. J Sep Sci. 2017;40(15):3144-3152doi: 10.1002/jssc.201700110.
Wang, J., Shen, S., Lu, X., & Ye, F. (2017). One-pot preparation of an organic polymer monolith by thiol-ene click chemistry for capillary electrochromatography. Journal of separation science, 40(15), 3144-3152. https://doi.org/10.1002/jssc.201700110
Wang, Jiannan, et al. "One-pot preparation of an organic polymer monolith by thiol-ene click chemistry for capillary electrochromatography." Journal of separation science vol. 40,15 (2017): 3144-3152. doi: https://doi.org/10.1002/jssc.201700110
Wang J, Shen S, Lu X, Ye F. One-pot preparation of an organic polymer monolith by thiol-ene click chemistry for capillary electrochromatography. J Sep Sci. 2017 Aug;40(15):3144-3152. doi: 10.1002/jssc.201700110. Epub 2017 Jun 29. PMID: 28586155.
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