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Journal articles on the topic '4-Nitrobiphenyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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1

Chao, Xuqiang, Xiuqin Zhang, Kai Wang, Jun Ji, and Qiang Chen. "4-Methoxy-3-nitrobiphenyl." Acta Crystallographica Section E Structure Reports Online 68, no. 1 (2011): o114. http://dx.doi.org/10.1107/s1600536811052846.

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2

Kolehmainen, Erkki, Vladimir Nikiforov, Konstantin Troshin, and Arto Valkonen. "2,5-Dimethyl-4′-nitrobiphenyl." Acta Crystallographica Section E Structure Reports Online 62, no. 11 (2006): o4989—o4990. http://dx.doi.org/10.1107/s1600536806040955.

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3

Barek, Jiří, Gulamustafa Malik, and Jiří Zima. "The voltammetric determination of 4-nitrobiphenyl." Collection of Czechoslovak Chemical Communications 56, no. 3 (1991): 595–601. http://dx.doi.org/10.1135/cccc19910595.

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Optimum conditions were found for the determination of 4-nitrobiphenyl by fast scan differential pulse voltammetry at a hanging mercury drop electrode in the concentration range 1 . 10-5 to 2 . 10-7 mol l-1. A further increase in sensitivity was attained by adsorptive accumulation of this substance on the surface of the working electrode, permitting determination in the concentration range (2 – 10) . 10-8 mol l-1 with one minute accumulation of the substance in unstirred solution or (2 – 10) . 10-9 mol l-1 with three-minute accumulation in stirred solution. Linear scan voltammetry can be used

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4

Xia, Lingling, Jiawen Ni, Pengyan Wu, et al. "Photoactive metal–organic framework as a bifunctional material for 4-hydroxy-4′-nitrobiphenyl detection and photodegradation of methylene blue." Dalton Transactions 47, no. 46 (2018): 16551–57. http://dx.doi.org/10.1039/c8dt03278e.

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A photoactive MOF showed ultra-selectivity and sensitivity towards 4-hydroxy-4′-nitrobiphenyl (HNBP) with a LOD of around 50 nM and highly efficient photocatalytic activity for the photodegradation of methylene blue.

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5

Barlin, GB, and C. Jiravinyu. "Potential Antimalarials. XI. 4'-Chloro-3-(substituted amino)-methyl-5-(7-trifluoromethylquinolin-4-ylamino)biphenyl-2-ols." Australian Journal of Chemistry 43, no. 7 (1990): 1301. http://dx.doi.org/10.1071/ch9901301.

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Syntheses are reported for 3-(t-butylamino)methyl-4′-chloro-5-(7′-trifluoromethylquinolin-4′-(ylamino)biphenyl-2-ol (5b) and analogous Mannich bases from diethylamine, pyrrolidine, piperidine, 3- and 4-methylpiperidine, 4-benzylpiperidine and 4-benzylpiperazine via N- substituted 3-aminomethyl-4′-chloro-5-nitrobiphenyl-2-ols (9). These compounds have been prepared for evaluation as antimalarials.

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6

Masciocchi, Norberto, Angelo Sironi, Norberto Masciocchi, and Mirka Bergamo. "Comments on the elusive crystal structure of 4-iodo-4′-nitrobiphenyl." Chemical Communications, no. 13 (1998): 1347–48. http://dx.doi.org/10.1039/a803486i.

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7

Ning, S. "Reductive metabolism of 4-nitrobiphenyl by rat liver fraction." Carcinogenesis 18, no. 6 (1997): 1233–40. http://dx.doi.org/10.1093/carcin/18.6.1233.

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8

Kutsumizu, Shoichi, Takanari Yamaguchi, Ryuji Kato, Tatsuya Ichikawa, and Shinichi Yano. "Cubic D Phase of 4′-n-Pentadecyloxy-3′-Nitrobiphenyl-4-Carboxylic Acid." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 330, no. 1 (1999): 359–65. http://dx.doi.org/10.1080/10587259908025610.

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9

Barek, Jiří, Antonín Berka, Marion Müller, Miroslav Procházka, and Jiří Zima. "Chemical destruction of 4-nitrobiphenyl in laboratory waste and its monitoring by differential pulse polarography and voltammetry and by high-performance liquid chromatography." Collection of Czechoslovak Chemical Communications 51, no. 8 (1986): 1604–8. http://dx.doi.org/10.1135/cccc19861604.

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A method for destruction of the carcinogenic 4-nitrobiphenyl in laboratory waste was elaborated based on its reduction with powdered zinc and oxidation of the produced 4-aminobiphenyl with potassium permanganate. The efficiency of the method can be checked by high-performance liquid chromatography, differential pulse polarography, and differential pulse voltammetry.

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10

Ojha, Durga Prasad. "Molecular Ordering of 4-Acetyl-2'-Nitrobiphenyl - A Computational Analysis." Zeitschrift für Naturforschung A 55, no. 11-12 (2000): 918–22. http://dx.doi.org/10.1515/zna-2000-11-1216.

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Abstract The molecular ordering of some biphenyl derivatives like 4-acetyl-2'-nitrobiphenyl (ANBP), 4-nitro-2-biphenylamine (NBPA) and 4-acetyl-3'-chlorobiphenyl (ACBP) has been examined using basic con-cepts of quantum mechanics and intermolecular forces. The CNDO/2 method has been employed to compute the net atomic charge and atomic dipole components at each atomic centre. The modified Ray-leigh-Schrödinger perturbation theory along with the multicentred-multipole expansion method has been employed to evaluate long-range interactions while a '6-exp' potential function has been assumed for sh

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11

Swaminathan, Santhanam, and James F. Hatcher. "Xanthine oxidase-mediated mutagenicity of the bladder carcinogen 4-nitrobiphenyl." Mutation Research/Genetic Toxicology 172, no. 1 (1986): 37–45. http://dx.doi.org/10.1016/0165-1218(86)90103-5.

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12

Hernández, P., F. Galan-Estella, and L. Hernández. "Determination of 4-nitrobiphenyl by adsorptive stripping square-wave polarography." Analytica Chimica Acta 271, no. 2 (1993): 217–21. http://dx.doi.org/10.1016/0003-2670(93)80048-p.

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13

Lee, Gisang, Taehyung Jang, Sebok Lee, Hyeongyeol Oh, Hohjai Lee, and Yoonsoo Pang. "Excited-state dynamics of 4-dimethylamino-4′-nitrobiphenyl confined in AOT reverse micelles." Journal of Molecular Liquids 305 (May 2020): 112873. http://dx.doi.org/10.1016/j.molliq.2020.112873.

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14

Kutsumizu, Shoichi, Makoto Yamada, Shinichi Yano, Kenji Tadano, Shuichi Nojima, and Takanari Yamaguchi. "Cubic Phases of 4'-n-docosyloxy-3'-nitrobiphenyl-4-carboxylic Acid (ANBC-22)." Molecular Crystals and Liquid Crystals 412, no. 1 (2004): 49–58. http://dx.doi.org/10.1080/15421400490431183.

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15

Labat, Gaël, Norwid-Rasmus Behrnd, Gaëtan Couderc, et al. "Polymorphism, polar morphology and absolute structure determination of 4-iodo-4′-nitrobiphenyl (INBP)." CrystEngComm 12, no. 4 (2010): 1252–62. http://dx.doi.org/10.1039/b915469h.

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16

Kutsumizu, Shoichi, Koushi Morita, Tatsuya Ichikawa, Shinichi Yano, Shuichi Nojima, and Takanari Yamaguchi. "Cubic phases of 4′-n-alkoxy-3′-nitrobiphenyl-4-carboxylic acids (ANBC-n)." Liquid Crystals 29, no. 11 (2002): 1447–58. http://dx.doi.org/10.1080/02678290260372646.

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17

Mandle, Richard J., Stephen J. Cowling, and John W. Goodby. "Evaluation of 4-alkoxy-4′-nitrobiphenyl liquid crystals for use in next generation scattering LCDs." RSC Advances 7, no. 64 (2017): 40480–85. http://dx.doi.org/10.1039/c7ra06886g.

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A combination of microscopy, X-ray scattering, calorimetry and applied electric field studies demonstrates the 4-alkoxy-4′-nitrobiphenyls are potentially of use for next generation, backlight free scattering mode LCD devices.

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18

Zhang, Wanqiang. "Crystal Structure of 3-Amino-5,6-Dimethyl-2-Nitrobiphenyl-4-Carbonitrile." Crystal Structure Theory and Applications 02, no. 03 (2013): 120–23. http://dx.doi.org/10.4236/csta.2013.23016.

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19

Kutsumizu, Shoichi, Makoto Yamada, Takanari Yamaguchi, Katsufumi Tanaka, and Ryuichi Akiyama. "Electric Field-Induced Cubic Phase in 4‘-n-Docosyloxy-3‘-nitrobiphenyl-4-carboxylic Acid." Journal of the American Chemical Society 125, no. 10 (2003): 2858–59. http://dx.doi.org/10.1021/ja029014q.

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20

Kutsumizu, Shoichi, Ryuji Kato, Minoru Yamada, and Shinichi Yano. "Structural Studies of 4‘-n-Alkoxy-3‘-nitrobiphenyl-4-carboxylic Acids by Infrared Spectroscopic Analysis." Journal of Physical Chemistry B 101, no. 50 (1997): 10666–73. http://dx.doi.org/10.1021/jp9717913.

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21

Sarma, Jagarlapudi A. R. P., Frank H. Allen, Vanessa J. Hoy, et al. "Design of an SHG-active crystal, 4-iodo-4′-nitrobiphenyl: the role of supramolecular synthons." Chemical Communications, no. 1 (1997): 101–2. http://dx.doi.org/10.1039/a605044a.

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22

Burgener, Matthias, Hanane Aboulfadl, Gaël Charles Labat, et al. "Peculiar orientational disorder in 4-bromo-4′-nitrobiphenyl (BNBP) and 4-bromo-4′-cyanobiphenyl (BCNBP) leading to bipolar crystals." IUCrJ 3, no. 3 (2016): 219–25. http://dx.doi.org/10.1107/s2052252516006709.

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180° orientational disorder of molecular building blocks can lead to a peculiar spatial distribution of polar properties in molecular crystals. Here we present two examples [4-bromo-4′-nitrobiphenyl (BNBP) and 4-bromo-4′-cyanobiphenyl (BCNBP)] which develop into a bipolar final growth state. This means orientational disorder taking place at the crystal/nutrient interface produces domains of opposite average polarity for as-grown crystals. The spatial inhomogeneous distribution of polarity was investigated by scanning pyroelectric microscopy (SPEM), phase-sensitive second harmonic microscopy (P

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23

Maeda, Yoji, S. Krishna Prasad, Shoichi Kutsumizu, and Shinichi Yano. "In situobservation of the pressure-induced mesophase for 4′-n-hexadecyloxy-3′-nitrobiphenyl-4-carboxylic acid." Liquid Crystals 30, no. 1 (2003): 7–16. http://dx.doi.org/10.1080/0267829021000046418.

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24

Kutsumizu, Shoichi, Tatsuya Ichikawa, Shinichi Yano, and Shuichi Nojima. "A cubic–cubic phase transition of 4′-n-hexacosyloxy-3′-nitrobiphenyl-4-carboxylic acid (ANBC-26)." Chemical Communications, no. 13 (1999): 1181–82. http://dx.doi.org/10.1039/a902975c.

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25

SATO, AYAKO. "Calorimetric study on the thermotropic cubic mesogen, 4'-n-hexadecyloxy-3'-nitrobiphenyl-4-carboxylic acid, ANBC(16)." Liquid Crystals 26, no. 3 (1999): 341–49. http://dx.doi.org/10.1080/026782999205119.

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26

Hulliger, J., and P. J. Langley. "On intrinsic and extrinsic defect-forming mechanisms determining the disordered structure of 4-iodo-4′-nitrobiphenyl crystals." Chemical Communications, no. 23 (1998): 2557–58. http://dx.doi.org/10.1039/a806895j.

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27

Bokare, Alok D., and Archita Patnaik. "Structure of Mesogenic 4′-Hexadecyloxy-3′-Nitrobiphenyl-4-Carboxylic Acid (ANBC-16) at the Air--Water Interface." Molecular Crystals and Liquid Crystals 383, no. 1 (2002): 49–55. http://dx.doi.org/10.1080/713738766.

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28

Burgener, Matthias, Gaël Labat, Michel Bonin, Alessio Morelli, and Jürg Hulliger. "Pyroelectric and piezoelectric scanning microscopy applied to reveal the bipolar state of 4-iodo-4′-nitrobiphenyl (INBP)." CrystEngComm 15, no. 38 (2013): 7652. http://dx.doi.org/10.1039/c3ce40902c.

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29

Ghosh, Rajib, Amitabha Nandi, and Dipak K. Palit. "Solvent sensitive intramolecular charge transfer dynamics in the excited states of 4-N,N-dimethylamino-4′-nitrobiphenyl." Physical Chemistry Chemical Physics 18, no. 11 (2016): 7661–71. http://dx.doi.org/10.1039/c5cp07778h.

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Solvent sensitive excited state dynamics of DNBP is explored. In polar solvents, the ultrafast barrierless TICT process is the major relaxation pathway, whereas, in nonpolar solvents the excited state undergoes the PICT process, followed by efficient intersystem crossing to the triplet state.

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30

Maeda, Yoji, Koushi Morita, and Shoichi Kutsumizu. "Thermal behaviour under pressure of the thermotropic cubic mesogen 4′- n -alkoxy-3′-nitrobiphenyl-4-carboxylic acids." Liquid Crystals 30, no. 2 (2003): 157–64. http://dx.doi.org/10.1080/0267829031000065164.

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31

Barek, Jiří, Antonín Berka, Marion Müller, and Jiří Zima. "Determination of 4-nitrobiphenyl and 4-aminobiphenyl by controlled-potential coulometry, differential pulse polarography and differential pulse voltammetry." Collection of Czechoslovak Chemical Communications 50, no. 12 (1985): 2853–62. http://dx.doi.org/10.1135/cccc19852853.

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Conditions were sought for the determination of 4-nitrobiphenyl by controlled-potential coulometry based on its reduction on a mercury pool electrode and for its polarographic determination on a dropping mercury electrode, with detection limits of 0.7 μmol l-1 for TAST polarography and 0.06 μmol l-1 for DP polarography. The reduction of this compound on a glassy carbon electrode was employed for its determination with detection limits of 10 μmol l-1 for DC voltammetry on a rotating electrode and 1 μmol l-1 for DP voltammetry on a stationary electrode. For 4-aminobiphenyl, its oxidation on a gl

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32

Li, Jie, Dong Xue, and Zun-Ting Zhang. "Crystal structure of 3-amino-5-(furan-2-yl)-2-nitrobiphenyl-4-carbonitrile, C17H11N3O3." Zeitschrift für Kristallographie - New Crystal Structures 222, no. 3 (2007): 297–98. http://dx.doi.org/10.1524/ncrs.2007.0126.

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33

Kutsumizu, Shoichi, Koushi Morita, Shinichi Yano, and Shuichi Nojima. "Cubic phases of binary systems of 4′-n-tetradecyloxy-3′-nitrobiphenyl-4-carboxylic acid (ANBC-14)-n-alkane." Liquid Crystals 29, no. 11 (2002): 1459–68. http://dx.doi.org/10.1080/02678290260372655.

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34

Yoshioka, Tadao, Yasuko Takou, and Takayoshi Uematsu. "Mutagenicity of N-arylacetohydroxamic acids and their O-glucosides derived from chlorinated 4-nitrobiphenyl ethers." Mutation Research/Genetic Toxicology 170, no. 3 (1986): 93–102. http://dx.doi.org/10.1016/0165-1218(86)90021-2.

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35

Hiremath, Rupa, Stephen W. Varney, and Jennifer A. Swift. "Oriented Crystal Growth of 4-Iodo-4‘-nitrobiphenyl on Polar Self-Assembled Monolayer Templates: A Case for “Chemical Epitaxy”." Chemistry of Materials 16, no. 24 (2004): 4948–54. http://dx.doi.org/10.1021/cm048560a.

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36

Kutsumizu, Shoichi, Tatsuya Ichikawa, Minoru Yamada, Shuichi Nojima, and Shinichi Yano. "Phase Transitions of 4‘-n-Hexacosyloxy-3‘-nitrobiphenyl-4-carboxylic Acid (ANBC-26): Two Types of Thermotropic Cubic Phases." Journal of Physical Chemistry B 104, no. 44 (2000): 10196–205. http://dx.doi.org/10.1021/jp0018652.

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37

Zugenmaier, Peter, and Wojciech Kuczynski. "Comparison of the Crystal and Molecular Structures of Three Similar 4-Heptyl-biphenyl Compounds: 4-Heptyl-4′-cyanobiphenyl, 4-Heptyl-3′-cyanobiphenyl, and 4-Heptyl-4′-nitrobiphenyl." Molecular Crystals and Liquid Crystals 457, no. 1 (2006): 93–103. http://dx.doi.org/10.1080/15421400600598297.

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38

Govindarasu, K., and E. Kavitha. "Vibrational spectra, molecular structure, NBO, UV, NMR, first order hyperpolarizability, analysis of 4-Methoxy-4′-Nitrobiphenyl by density functional theory." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 122 (March 2014): 130–41. http://dx.doi.org/10.1016/j.saa.2013.10.122.

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39

Maeda, Yoji, Gui-Ping Cheng, Shoichi Kutsumizu, and Shinichi Yano. "Thermal behaviour of the thermotropic cubic mesogen 4'-n-hexadecyloxy-3'-nitrobiphenyl-4-carboxylic acid (ANBC-16) under hydrostatic pressure." Liquid Crystals 28, no. 12 (2001): 1785–91. http://dx.doi.org/10.1080/02678290110078801.

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40

Urban, Ján, Petr Kuzmič, David Šaman, and Milan Souček. "Regioselectivity of nucleophilic aromatic photosubstitution in the biphenyl series. Photohydrolysis of some dimethoxynitrobiphenyls." Collection of Czechoslovak Chemical Communications 52, no. 10 (1987): 2482–91. http://dx.doi.org/10.1135/cccc19872482.

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Anaerobic photolysis of dimethoxynitrobiphenyls IIIa-VIa in aqueous alkaline tert-butanol gave products of nucleophilic photosubstitution of methoxyl by hydroxide anion, while the dimethoxybiphenyls Ia and IIa were found unreactive. Regioselectivity of the reaction was examined in view of a possible “extended meta activation” by the nitro group. The most reactive substrate IIIa gives both C-3 and C-4 substitution products with an unsubstantial preference for the latter, which opposes the “extended meta selectivity” rule. All of the other compounds obey the rule, and 3,4-dimethoxy-3'-nitrobiphe

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41

TANSHO, MASATAKA, YOSHITO ONODA, SHOICHI KUTSUMIZU, SHINICHI YANO, and RYUJI KATO. "14N NMR studies on an optically isotropic liquid crystalline D phase of 4'-n-alkoxy-3'-nitrobiphenyl-4-carboxylic acids (ANBC)." Liquid Crystals 24, no. 4 (1998): 525–29. http://dx.doi.org/10.1080/026782998206975.

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42

Massé, Robert, Mohamed Badr, Christiane Ayotte, and Michel Sylvestre. "Gas chromatographie‐mass spectrometric characterization of bacterial metabolites of 4‐nitrobiphenyl formed in gram negative strain B‐206†." Toxicological & Environmental Chemistry 10, no. 3 (1985): 225–46. http://dx.doi.org/10.1080/02772248509357104.

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43

Jin, Peipei, Jing Long, Yong Du, Xuming Zheng, and Jiadan Xue. "Hydrogen bond configuration and protonation of ground and lowest excited triplet states of 4‑amino‑4′‑nitrobiphenyl based on nanosecond transient absorption spectroscopy." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 217 (June 2019): 44–50. http://dx.doi.org/10.1016/j.saa.2019.03.054.

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44

Kutsumizu, Shoichi, Kouhei Hosoyama, Makoto Yamada, et al. "Smectic C to Cubic Phase Transition of 4′-n-Docosyloxy-3′-nitrobiphenyl-4-carboxylic Acid (ANBC-22) and Alternating-Current Electric Field Effect." Journal of Physical Chemistry B 113, no. 3 (2009): 640–46. http://dx.doi.org/10.1021/jp806972x.

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45

Kutsumizu, Shoichi, Hisato Kobayashi, Naotake Nakamura, Tatsuya Ichikawa, Shinichi Yano, and Shuichi Nojima. "X-ray Characterization of Two Cubic Phases and a Structured Liquid Phase of 4′-n-Alkoxy-3′-nitrobiphenyl-4-carboxylic Acids (ANBC-n)." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 347, no. 1 (2000): 239–48. http://dx.doi.org/10.1080/10587250008024845.

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46

Hori, Ryo, Yohei Miwa, Katsuhiro Yamamoto, and Shoichi Kutsumizu. "Phase Structure and Phase Transition Mechanism for Light-Induced Ia3d Cubic Phase in 4′-n-Docosyloxy-3′-nitrobiphenyl-4-carboxlic acid/Ethyl 4-(4′-n-docosyloxyphenylazo)benzoate Binary Mixture." Journal of Physical Chemistry B 118, no. 13 (2014): 3743–49. http://dx.doi.org/10.1021/jp4127978.

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47

Hirayama, Teruhisa, Kazuhiko Iguchi, Sachiyo Yoshida, Yukinori Yamanaka, and Tetsushi Watanabe. "Structural determination of a directly mutagenic amino-nitrobiphenyl as the S9 metabolite of 2,4,2′,4′-tetranitrobiphenyl in Salmonella typhimuriumTA98." Mutation Research Letters 262, no. 3 (1991): 203–7. http://dx.doi.org/10.1016/0165-7992(91)90023-w.

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48

Hori, Ryo, Yohei Miwa, Katsuhiro Yamamoto, and Shoichi Kutsumizu. "Correction to “Phase Structure and Phase Transition Mechanism for Light-Induced Ia3d Cubic Phase in 4′-n-Docosyloxy-3′-nitrobiphenyl-4-carboxlic acid/Ethyl 4-(4′-n-Docosyloxyphenylazo)benzoate Binary Mixture”." Journal of Physical Chemistry B 118, no. 40 (2014): 11862. http://dx.doi.org/10.1021/jp509310h.

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49

Nadeau, L. J., Z. He, and J. C. Spain. "Production of 2-amino-5-phenoxyphenol from 4-nitrobiphenyl ether using nitrobenzene nitroreductase and hydroxylaminobenzene mutase from Pseudomonas pseudoalcaligenes JS45." Journal of Industrial Microbiology and Biotechnology 24, no. 4 (2000): 301–5. http://dx.doi.org/10.1038/sj.jim.2900821.

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50

Hori, Ryo, Daisuke Furukawa, Katsuhiro Yamamoto, and Shoichi Kutsumizu. "Light-Driven Phase Transition in a Cubic-Phase-Forming Binary System Composed of 4′-n-Docosyloxy-3′-nitrobiphenyl-4-carboxylic Acid and an Azobenzene Derivative." Chemistry - A European Journal 18, no. 24 (2012): 7346–50. http://dx.doi.org/10.1002/chem.201200810.

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