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Journal articles on the topic '2-Nitrobiphenyl'

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Published: 4 June 2021

Last updated: 11 February 2022

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1

Novina, J. Josephine, G. Vasuki, Sushil Kumar, and K. R. Justin Thomas. "4,4′-Dibromo-2-nitrobiphenyl." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (2012): o319. http://dx.doi.org/10.1107/s1600536812000347.

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2

Vieira, Vanessa C. M., James A. Golen, Arnold L. Rheingold, and David R. Manke. "Dimethyl 2-nitrobiphenyl-4,4′-dicarboxylate." Acta Crystallographica Section E Structure Reports Online 70, no. 3 (2014): o371. http://dx.doi.org/10.1107/s1600536814004218.

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The title compound, C16H13NO6, exhibits a biphenyl unit with a dihedral angle between the two aryl rings of 56.01 (5)°. The two ester groups vary slightly from planarity, with aryl–ester dihedral angles of 4.57 (5) and 16.73 (5)°. The nitro group is turned from the aromatic unit with an aryl–nitro dihedral angle of 48.66 (4)°. In the crystal, molecules are connected by weak C—H...O interactions, forming a three-dimensional network.

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3

Sekine, A., Y. Ohashi, K. Yoshimura, M. Yagi, and J. Higuchi. "2-Nitrobiphenyl and 2,2'-dinitrobiphenyl." Acta Crystallographica Section C Crystal Structure Communications 50, no. 7 (1994): 1101–4. http://dx.doi.org/10.1107/s0108270194001009.

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4

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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5

Wang, Qing Xiu, Li Jie Duan, Bo Yang Qu, Juan Wang, and Fu De Liu. "Synthesis and Optical/Electrochemical Properties of Conjugated Polymers with Diphenyl and Thiophene in Main Chain." Advanced Materials Research 1035 (October 2014): 497–501. http://dx.doi.org/10.4028/www.scientific.net/amr.1035.497.

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Two thiophene derivatives 4,4'-di (thiophen-2-yl) biphenyl and 4,4'-di (thiophen-2-yl) -2-nitrobiphenyl ,which were used as monomers for preparing poly (4,4'-di (thiophen-2-yl) biphenyl) (DPBT) and poly (4,4'-di (thiophen-2-yl)-2-nitrobiphenyl) (DPNT) by ferric chloride oxidation polymerization, were synthesized via Suzuki reaction with 4,4'-dibromobiphenyl as the raw material. UV-vis absorption spectra, fluorescence spectra, photoluminescence spectra and electrochemical properties of the polymers were recorded and used for calculating the band-gap (Eg), HOMO orbital energy (EHOMO) and LUMO or

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6

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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7

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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8

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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9

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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10

CAI, Bang-cheng, Shi-xiang GAO та Gen-fa LU. "β-Cyclodextrin and its derivatives-enhanced solubility and biodegradation of 2-nitrobiphenyl". Journal of Environmental Sciences 18, № 6 (2006): 1157–60. http://dx.doi.org/10.1016/s1001-0742(06)60055-7.

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11

Bell, AJ, and RW Read. "Synthesis of Polynitro-Substituted 2'-Nitrobiphenyl-2-Amines, Analogs of Polynitro Benzo[c]cinnoline Oxide Derivatives." Australian Journal of Chemistry 40, no. 11 (1987): 1813. http://dx.doi.org/10.1071/ch9871813.

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2',3,4',5- and 2',3,5,6'-Tetranitrobiphenyl-2-amines, and 2',3,4',5,6'- and 2',4,4',6,6'-pentanitrobiphenyl-2-amines, have been synthesized for the first time, along with the known 2,4,8- and 2,4,10-trinitrobenzo[c]cinnoline 6-oxides and 1,3,7,9-tetranitrobenzo [c]cinnoline 5- oxide. The benzocinnoline oxide derivatives were found to have higher densities and thermal stability than those of the corresponding biphenylamines. These observations are discussed in terms of structure.

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12

Liu, Fu De, Yong Zhou, and Hai Yan Wu. "Synthesis and Characterization of Copolymers Consisting of 3-Hexylthiophene and Biphenyl Derivatives." Applied Mechanics and Materials 331 (July 2013): 478–82. http://dx.doi.org/10.4028/www.scientific.net/amm.331.478.

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Two novel copolymers consisting of 3-hexylthiophene and 4,4-di (thiophen-2-yl) biphenyl (DTBHT) or 4,4-di (thiophen-2-yl)-2-nitrobiphenyl (DTNHT) were synthesized. Both of the copolymers show lower HOMO energy level (-5.62, -5.51 eV) than that of the P3HT (-5.1 eV). Compared to DTBHT, adding nitro group in DTNHT improves effective conjugation of the main chain and successfully lowers the electrochemical bandgap of the copolymers from 2.39 to 2.28 eV and optical band-gap from 2.17 to 2.07 eV with significant increase in fluorescence quantum yield from 0.140 to 0.252. Keywords: biphenyl, 3-Hexyl

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13

Tanigaki, Katsumi, Mikio Yagi, and Jiro Higuchi. "A new ground-state triplet species formed from 2-nitrobiphenyl by ultraviolet light irradiation." Chemical Physics Letters 153, no. 1 (1988): 57–60. http://dx.doi.org/10.1016/0009-2614(88)80132-5.

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14

Higuchi, Jiro, Michinori Fujisawa, Yasushi Yokoyama, and Mikio Yagi. "Electron paramagnetic resonance study on the triplet species produced from 2-nitrobiphenyl derivatives by UV irradiation." Journal of Photochemistry and Photobiology A: Chemistry 124, no. 1-2 (1999): 53–65. http://dx.doi.org/10.1016/s1010-6030(99)00075-1.

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15

Yoshida, Ai, Kazunobu Sato, Takeji Takui, et al. "Electronic and Molecular Structures of a Stable Triplet Species Generated from 2-Nitrobiphenyl after UV Irradiation." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 306, no. 1 (1997): 373–78. http://dx.doi.org/10.1080/10587259708044589.

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16

Higuchi, Jiro, Kimihiro Yoshimura, and Mikio Yagi. "Electron Paramagnetic Resonance of a Triplet Species Observed in 2-Nitrobiphenyl Single Crystal after Ultraviolet Light Irradiation." Journal of Physical Chemistry 99, no. 13 (1995): 4441–46. http://dx.doi.org/10.1021/j100013a012.

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17

Peng, Haixia, Xuxing Chen, Yanhong Chen, Qian He, Yuyuan Xie та Chunhao Yang. "Solvent-free synthesis of δ-carbolines/carbazoles from 3-nitro-2-phenylpyridines/2-nitrobiphenyl derivatives using DPPE as a reducing agent". Tetrahedron 67, № 32 (2011): 5725–31. http://dx.doi.org/10.1016/j.tet.2011.06.027.

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18

Guo, Li-Rong, Xiao-Liang Tang, Zheng-Hua Ju, Kai-Ming Zhang, Hui-E. Jiang, and Wei-Sheng Liu. "Lanthanide metal–organic frameworks constructed by asymmetric 2-nitrobiphenyl-4,4′-dicarboxylate ligand: syntheses, structures, luminescence and magnetic investigations." CrystEngComm 15, no. 44 (2013): 9020. http://dx.doi.org/10.1039/c3ce41370e.

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19

Peng, Haixia, Xuxing Chen, Yanhong Chen, Qian He, Yuyuan Xie та Chunhao Yang. "ChemInform Abstract: Solvent-Free Synthesis of δ-Carbolines/Carbazoles from 3-Nitro-2-phenylpyridines/2-Nitrobiphenyl Derivatives Using DPPE as a Reducing Agent." ChemInform 42, № 49 (2011): no. http://dx.doi.org/10.1002/chin.201149035.

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20

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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21

Jing, Xue-Hui, Xiu-Chun Yi, En-Qing Gao, and Vladislav A. Blatov. "Synthesis, structure, topology and magnetic properties of cobalt(ii) coordination polymers with 2-nitrobiphenyl-4,4′-dicarboxylic acid and bis(pyridyl) ligands." Dalton Transactions 41, no. 47 (2012): 14316. http://dx.doi.org/10.1039/c2dt31917a.

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22

Kadiyala, Venkateswarlu, Lloyd J. Nadeau, and Jim C. Spain. "Construction of Escherichia coli Strains for Conversion of Nitroacetophenones to ortho-Aminophenols." Applied and Environmental Microbiology 69, no. 11 (2003): 6520–26. http://dx.doi.org/10.1128/aem.69.11.6520-6526.2003.

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ABSTRACT The predominant bacterial pathway for nitrobenzene (NB) degradation uses an NB nitroreductase and hydroxylaminobenzene (HAB) mutase to form the ring-fission substrate ortho-aminophenol. We tested the hypothesis that constructed strains might accumulate the aminophenols from nitroacetophenones and other nitroaromatic compounds. We constructed a recombinant plasmid carrying NB nitroreductase (nbzA) and HAB mutase A (habA) genes, both from Pseudomonas pseudoalcaligenes JS45, and expressed the enzymes in Escherichia coli JS995. IPTG (isopropyl-β-d-thiogalactopyranoside)-induced cells of s

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23

Wang, Wei, Xinhua Peng, and Nan Chen. "Regioselective Nitration of Inactive 4,4-Dibromobiphenyl with Nitrogen Dioxide and Molecular Oxygen over Zeolites: An Efficient Preparation of 4,4'-Dibromo-2-nitrobiphenyl." Journal of the Korean Chemical Society 58, no. 1 (2014): 72–75. http://dx.doi.org/10.5012/jkcs.2014.58.1.72.

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24

Crotti, Corrado, Sergio Cenini, Angela Bassoli, Bruno Rindone та Francesco Demartin. "Synthesis of carbazole by Ru3(CO)12-catalyzed reductive carbonylation of 2-nitrobiphenyl: the crystal and molecular structure of Ru3(μ3-NC6H4-o-C6H5)2(CO)9". Journal of Molecular Catalysis 70, № 2 (1991): 175–87. http://dx.doi.org/10.1016/0304-5102(91)80159-z.

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25

Kapoor, Ramesh, Anand Gupta, Pratibha Kapoor, and Paloth Venugopalan. "Synthesis and characterization of di-n-butyltin(IV) complexes with 4?/2?-nitrobiphenyl-2-carboxylic acids: X-ray crystal structures of [{(n-C4H9)2Sn(OCOC12H8NO2?4?)}2O]2 and (n-C4H9)2Sn{OCOC12H8NO2?4?}2." Applied Organometallic Chemistry 17, no. 8 (2003): 600–606. http://dx.doi.org/10.1002/aoc.480.

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26

Kuethe, Jeffrey T, and Karla G Childers. "Suzuki–Miyaura Cross‐Coupling of 2‐Nitroarenediazonium Tetrafluoroborates: Synthesis of Unsymmetrical 2‐Nitrobiphenyls and Highly Functionalized Carbazoles." Advanced Synthesis & Catalysis 350, no. 10 (2008): 1577–86. http://dx.doi.org/10.1002/adsc.200800162.

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27

Freeman, Adam W., Marie Urvoy, and Megan E. Criswell. "Triphenylphosphine-Mediated Reductive Cyclization of 2-Nitrobiphenyls: A Practical and Convenient Synthesis of Carbazoles." Journal of Organic Chemistry 70, no. 13 (2005): 5014–19. http://dx.doi.org/10.1021/jo0503299.

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28

Milano, Jean Claude, Jean Michel Robert, Jean-Louis Vernet, and Bernard Gallot. "The thioether spacer in liquid crystalline polysiloxanes with cyano- and nitrobiphenyl mesogens." Macromolecular Chemistry and Physics 200, no. 7 (1999): 1580–86. http://dx.doi.org/10.1002/(sici)1521-3935(19990701)200:7<1580::aid-macp1580>3.0.co;2-a.

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29

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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30

"SYNTHESIS OF BIARYLS VIA PALLADIUM-CATALYZED CROSS-COUPLING: 2-METHYL-4'-NITROBIPHENYL." Organic Syntheses 66 (1988): 67. http://dx.doi.org/10.15227/orgsyn.066.0067.

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31

BELL, A. J., and R. W. READ. "ChemInform Abstract: Synthesis of Polynitro-Substituted 2′-Nitrobiphenyl-2-amines, Analogues of Polynitro Benzo(c)cinnoline Oxide Derivatives." ChemInform 19, no. 11 (1988). http://dx.doi.org/10.1002/chin.198811184.

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32

"SYNTHESIS OF 2-SUBSTITUTED BIARYLS VIA Cu/Pd-CATALYZED DECARBOXYLATIVE CROSS-COUPLING OF 2-SUBSTITUTED POTASSIUM BENZOATES: 4-METHYL-2'-NITROBIPHENYL AND 2-ACETYL-4'-METHYLBIPHENYL." Organic Syntheses 85 (2008): 196. http://dx.doi.org/10.15227/orgsyn.085.0196.

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33

Freeman, Adam W., Marie Urvoy, and Megan E. Criswell. "Triphenylphosphine-Mediated Reductive Cyclization of 2-Nitrobiphenyls: A Practical and Convenient Synthesis of Carbazoles (IV)." ChemInform 36, no. 45 (2005). http://dx.doi.org/10.1002/chin.200545142.

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34

Kuethe, Jeffrey T., and Karla G. Childers. "ChemInform Abstract: Suzuki-Miyaura Cross-Coupling of 2-Nitroarenediazonium Tetrafluoroborates: Synthesis of Unsymmetrical 2-Nitrobiphenyls and Highly Functionalized Carbazoles." ChemInform 39, no. 43 (2008). http://dx.doi.org/10.1002/chin.200843127.

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35

Elumalai, Vijayaragavan, Alexander H. Sandtorv, and Hans-Rene Bjoersvik. "ChemInform Abstract: A Highly Efficient Pd(PPh3)4-Catalyzed Suzuki Cross-Coupling Method for the Preparation of 2-Nitrobiphenyls from 1-Chloro-2-nitrobenzenes and Phenylboronic Acids." ChemInform 47, no. 29 (2016). http://dx.doi.org/10.1002/chin.201629098.

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