Relevant bibliographies by topics / P-nitroaniline

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  2. Dissertations / Theses
  3. Books
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Academic literature on the topic 'P-nitroaniline'

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Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "P-nitroaniline"

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RACHANA, RASTOGI, and K. GUPTA V. "Determination of meta-, para- and ortho-Nitroanilines using Spectrophotometric and Thermal Gradient Chromatographic Methods." Journal of Indian Chemical Society Vol. 75, Apr 1998 (1998): 267–68. https://doi.org/10.5281/zenodo.5924251.

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School of Studies in Chemistry, Pt. Ravi Shankar Shukla University, Raipur-492 010 <em>Manuscript received 1 August 1997, accepted 8 August 1997</em> A new sensitive spectrophotometric method based on diazotization and coupling reaction has been developed to determine the meta-, para- and ortho-nitroanilines. The nitroanilines were diazotized and coupled with phloroglucinol to give yellow azo-dyes, having &lambda;<sub>max</sub> at 405, 435 and 450 nm respectively. The color systems obeyed Beer&#39;s law in the range 0.04-0.4 ppm for m-nitroaniline, 0.08-0.8&nbsp;ppm for p-nitroaniline and 0.12
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Deshmukh, Arundhati, Sujoy Bandyopadhyay, Anto James, and Abhijit Patra. "Trace level detection of nitroanilines using a solution processable fluorescent porous organic polymer." Journal of Materials Chemistry C 4, no. 20 (2016): 4427–33. http://dx.doi.org/10.1039/c6tc00599c.

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Sensitive detection of environmentally hazardous nitroanilines, especially p-nitroaniline in solution as well as in contact mode, was achieved employing a solution processable fluorescent porous organic polymer.
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Lemmerer, Andreas, and David G. Billing. "p-Nitroaniline hydrobromide." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1562—o1564. http://dx.doi.org/10.1107/s1600536806010166.

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The crystal stucture of p-nitroaniline hydrobromide, C6H7N2O2 +·Br− or O2NC6H4NH3 +·Br−, exhibits ionic layers separated by hydrocarbon layers. The hydrocarbon layers stack head-to-tail but no π–π interactions are observed. In the inorganic layer, the ammonium group, Br− anion and nitro group interact to form a three-dimensional hydrogen-bonded network. The structure is compared with that of the related compound O2NC6H4NH3 +·Cl−.
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Szostak, M. Magdalena, Bolesław Kozankiewicz, and Józef Lipiński. "Low-temperature photoluminescence of p-nitroaniline and o-methyl-p-nitroaniline crystals." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 67, no. 5 (2007): 1412–16. http://dx.doi.org/10.1016/j.saa.2006.10.038.

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Kimura, Y., S. Ibaraki, R. Hirano, Y. Sugita, Y. Yasaka, and M. Ueno. "Photoexcitation dynamics of p-nitroaniline and N,N-dimethyl-p-nitroaniline in 1-alkyl-3-methylimidazolium-cation based ionic liquids with different alkyl-chain lengths." Physical Chemistry Chemical Physics 19, no. 33 (2017): 22161–68. http://dx.doi.org/10.1039/c7cp03610h.

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Von Niessen, W. "Valence ionization spectrum of p-nitroaniline." Journal of Physical Chemistry 92, no. 5 (1988): 1035–39. http://dx.doi.org/10.1021/j100316a010.

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Varghese, Anju Linda, P. L. Maria Linsha, and George Mathai. "Exploring the Third-Order Non-linear Optical Responses and Optical Limiting Properties of p-Nitroaniline Picrate: A Theoretical and Experimental Study." Asian Journal of Chemistry 36, no. 9 (2024): 2013–18. http://dx.doi.org/10.14233/ajchem.2024.31999.

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The current study investigates the nonlinear optical behaviour of p-nitroaniline picrate, which has been synthesized and characterized. Its third-order non-linear optical properties were investigated via Z-scan studies. p-Nitroaniline picrate demonstrates a reverse saturable absorption, as indicated by a positive absorption coefficient (b), which is of the order 10–12 m/W. Closed aperture data indicate a positive refractive non-linearity due to self-focusing, with non-linear refractive index (n2), third-order susceptibility (χ(3)) and second-order hyperpolarizability (g) in order of 10–19 m2/W
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Wijaya, Karna, Iqmal Tahir, and Ahmad Baikuni. "THE SYNTHESIS OF Cr2O3-PILLARED MONTMORILLONITE (CrPM) AND ITS USAGE FOR HOST MATERIAL OF p-NITROANILINE." Indonesian Journal of Chemistry 2, no. 1 (2010): 12–21. http://dx.doi.org/10.22146/ijc.21928.

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The synthesis of Cr2O3-pillared montmorillonite (CrPM) and its usage for host material of p-nitroaniline have been conducted. The Cr2O3-pillared montmorillonite clays was prepared by a direct ion exchange method. First, the polyhydroxychromium as a pillaring spesies was intercalated into the interlayer region of the montmorillonite clays (purified clay in the monocation form), result in a montmorillonite-polyoxychromium intercalation compound. The precursors/pillaring spesies was not stable, hence it must be stabilized by calcination in order to transform the polyoxychromium via dehydration an
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Yang, Ming, Qian Sun, and Cai Yun Li. "Preparation and Characterization of Molecularly Imprinted Polymer Microspheres of p-Nitroaniline." Applied Mechanics and Materials 71-78 (July 2011): 3411–14. http://dx.doi.org/10.4028/www.scientific.net/amm.71-78.3411.

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Polystyrene microspheres were prepared by the emulsifier-free polymerization method. Using the polystyrene microspheres as seeds, p-nitroaniline as template molecules, the monodispersed molecularly imprinted polymer microspheres (MIPMs) were prepared by a single-step swelling and polymerization method. The monodispersed molecular imprinted polymers with porous structure were characterized by SEM, and UV-visible spectrophotometry. The adsorption performance of MIPMs for p-nitroaniline was investigated.
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A., P. MISHRA, K. SRIVASTAVA S., and VIBHUTI SRIVASTAVA (MISS). "Complexes of Cobalt-, Nickel- and Copper(II) with 2-Furfurylidene-p-nitroaniline and 2-Furfurylidene-m-nitroaniline Schiff Bases." Journal of Indian Chemical Society Vol. 73, Jun 1996 (1996): 261–63. https://doi.org/10.5281/zenodo.5897556.

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Inorganic Laboratories, Chemistry Department, Dr. H. S. Gour University, Sagar-470 003 <em>Manuscript received 5 September 1994, accepted 4 November 1994</em> Complexes of Cobalt-, Nickel- and Copper(II) with 2-Furfurylidene-<em>p</em>-nitroaniline and 2-Furfurylidene-m-nitroaniline Schiff Bases.
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Dissertations / Theses on the topic "P-nitroaniline"

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Sen, Deser. "Effect Of Compatibilizers On The Gas Separation Performance Of Polycarbonate Membranes." Master's thesis, METU, 2003. http://etd.lib.metu.edu.tr/upload/1262963/index.pdf.

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In this study, the effect of compatibilizers on the gas separation performance of polycarbonate (PC) membranes was investigated. Membranes were prepared by solvent evaporation method. They were characterized by single gas permeability measurements of O2, N2, H2 and CO2 as well as scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and Fourier transform infrared spectrometry (FTIR). Membranes containing 0.5 to 10 w% p-nitroaniline (pNA) were prepared to study the effect of compatibilizer concentration on the membrane performance. Permeabilities of all gases decre
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Sen, Deger. "Polycarbonate Based Zeolite 4a Filled Mixed Matrix Membranes: Preparation, Characterization And Gas Separation Performances." Phd thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/12609348/index.pdf.

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Developing new membrane morphologies and modifying the existing membrane materials are required to obtain membranes with improved gas separation performances. The incorporation of zeolites and low molecular-weight additives (LMWA) into polymers are investigated as alternatives to modify the permselective properties of polymer membranes. In this study, these two alternatives were applied together to improve the separation performance of a polymeric membrane. The polycarbonate (PC) chain characteristics was altered by incorporating p-nitroaniline (pNA) as a LMWA and the PC membrane morphology wa
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Gorai, S. "Preferential Solvation of P-nitroaniline in Alcohol-dioxan Binary Solvent Mixture." Thesis, 2010. http://ethesis.nitrkl.ac.in/1576/2/Sukhamoy.pdf.

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The Preferential solvation of p-nitroaniline (PNA) has been investigated by monitoring the intramolecular charge transfer band in different alcohol-dioxan binary solvent mixtures. The plots of observed spectroscopic transition energy vs. mole fraction confirm the presence of preferential solvation in the mixtures. In the higher mole fraction of alcohol PNA is preferentially solvated by dioxan while in the higher mole fraction of dioxan it is preferentially solvated by alcohol. This type of preferential solvation has been explained by hydrogen bonding between PNA and the solvent molecules. Bes
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Huang, Jyunjie, and 黃俊傑. "Adsorption Studies of p-Nitroaniline onto Surface Activation and Modification of MWCNTs." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/60145046982637543808.

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碩士<br>明志科技大學<br>化學工程研究所<br>101<br>The adsorption for P-Nitroaniline(PNA) by modified multiwalled carbon nanotubes (MWCNTs) were investigated in this study. MWCNTs were modified by H2SO4/HNO3,CO2 and KOH. The influences of the functional groups of MWCNTs were observed by modified MWCNTs. After modification, the MWCNTs broke into smaller sizes with defects on their surface. From Raman spectral analysis , the degree of graphitization is the order of ACID-MWCNT > COM-MWCNT > KOH-MWCNT > CO2-MWCNT. From thermogravimetry analysis, the residual mass of samples is the order of KOH-MWCNT > COM-MWCNT >A
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Wang, Wei-Chieh, and 王威傑. "nfrared Electroabsorption study of N,N-Dimethyl-p-nitroaniline in Mixed Solvents of Acetonitrile and Tetrachloroethylene: Solvation of the Solute and Association Structure of Acetonitrile." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/12642915343488722917.

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碩士<br>國立交通大學<br>應用化學研究所<br>99<br>N,N-Dimethyl-p-nitroaniline (DMPNA) in mixed solvents of acetonitrile (ACN) and tetrachloroethylene (C2Cl4) was studied with FT-IR spectroscopy and IR electroabsorption spectroscopy. Previous studies using Raman and IR electroabsorption spectroscopy show that p-nitroaniline (PNA), an analogue of DMPNA, forms specific solvation structures with ACN in ACN/CCl4. To examine the effect of N,N-dimethyl substitution on the formation of those solvation structures, we measured the ACN mole fraction dependence of FT-IR spectra and the angle χ dependence of IR electroabso
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Books on the topic "P-nitroaniline"

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NTP technical report on the toxicology and carcinogenesis studies of p-nitroaniline (CAS no. 100-01-6) in B6C3F mice (gavage studies). U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Toxicology Program, 1993.

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Book chapters on the topic "P-nitroaniline"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with 2-furfurylidene-p-nitroaniline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_509.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 2-furfurylidene-p-nitroaniline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_211.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 2-furfurylidene-p-nitroaniline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_201.

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Agarwal, Rekha Rani, and Nupur Jain. "Pesticide substance of p-nitroaniline degradation by photo-catalytic reaction using semiconductor ZnO and H2O2 for sustainable development." In Recent Advances in Sciences, Engineering, Information Technology & Management. CRC Press, 2024. https://doi.org/10.1201/9781003598152-82.

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Feddern, Vivian, Vanessa Gressler, Anildo Cunha, and Danniele Miranda Bacila. "Determination of p-Nitroaniline Residues in Chicken Meat by Salting-out Liquid-Liquid Extraction (SALLE) Followed by Derivatization and LC-MS/MS Analysis." In Methods and Protocols in Food Science. Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-3806-4_14.

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Hayashi, S., and Y. Komori. "13-P-06-Dynamics of p-nitroaniline in the micropore of zeolite ZSM-5 studied by solid-state NMR." In Studies in Surface Science and Catalysis. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)81785-7.

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Paschoal Diego, Costa Marcello F., Junqueira Georgia M.A., and Dos Santos Hélio F. "Gaussian basis sets for ab initio calculation of NLO properties of polyatomic molecules." In Atomic and Molecular Nonlinear Optics: Theory, Experiment and Computation. IOS Press, 2011. https://doi.org/10.3233/978-1-60750-742-0-129.

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In this paper, basis sets for H, C, N and O atoms were adjusted to obtain electric properties of diatomic molecules. The dipole moment, polarizability and first-order hyperpolarizability were calculated for H2, CH+, CN-and CO molecules and the basis sets modified to reproduce the reference data available. A sequential methodology was used, where the basis set for H is firstly adjusted and then used to fit the basis set for C in the CH+molecule and so on. The final basis sets were (7s2p1d)&amp;rarr;[3s2p1d] for H and (9s5p2d)&amp;rarr;[5s3p2d] for C and O. In the case of N atom, the best basis
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Conference papers on the topic "P-nitroaniline"

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Block, S., and G. J. Piermarini. "The Pressure Synthesis Of P-Nitroaniline Condensation Products." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by Robert L. Gunshor. SPIE, 1988. http://dx.doi.org/10.1117/12.943951.

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Bouchouit, K., Z. Essaidi, E. Bendeif, N. Benali-cherif, and B. Sahraoui. "Structural Phase Transition and Nonlinear Optical Properties in P-Nitroaniline." In 2nd International Conference on Transparent Optical Networks "Mediterranean Winter" 2008. ICTON-MW'08. IEEE, 2008. http://dx.doi.org/10.1109/ictonmw.2008.4773107.

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Muto, Shinzo, Tohru Okada, and Hiroshi Ito. "Highly efficient second-harmonic generation in mixture films of p-nitroaniline and methacrylate polymers." In SPIE's 1993 International Symposium on Optics, Imaging, and Instrumentation, edited by Gustaaf R. Moehlmann. SPIE, 1993. http://dx.doi.org/10.1117/12.165281.

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de Matos Gomes, Etelvina, E. Nogueira, Michael S. Belsley, and M. Margarida R. Costa. "Modification of the nonlinear optical, dielectric, and structural properties of p-nitroaniline and 2-methyl-4-nitroaniline crystals through recrystallization under a strong dc electric field." In XVII International Conference on Coherent and Nonlinear Optics (ICONO 2001), edited by Konstantin N. Drabovich, Nikolai S. Kazak, Vladimir A. Makarov, and Alexander P. Voitovich. SPIE, 2002. http://dx.doi.org/10.1117/12.475914.

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Watanabe, Toshiyuki, and Seizo Miyata. "Effect Of Crystallization Process On The Second Harmonic Generation Of Poly(Oxyethylene)/P-Nitroaniline Systems." In 33rd Annual Techincal Symposium, edited by Garo Khanarian. SPIE, 1990. http://dx.doi.org/10.1117/12.962112.

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Bardo, Richard D. "Theoretical Study Of The Existence Of Metastable Semiconducting P-Nitroaniline Formed At High Shock Pressure." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by Robert L. Gunshor. SPIE, 1988. http://dx.doi.org/10.1117/12.943952.

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Ura, S., R. Ohyama, T. Suhara, and H. Nishihara. "Electrooptic Waveguide Grating Using New Nonlinear-Optic Polymer p-NAn-PVA." In Nonlinear Guided-Wave Phenomena. Optica Publishing Group, 1991. http://dx.doi.org/10.1364/nlgwp.1991.md3.

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A new polymer p-NAn-PVA illustrated in Fig. 1 was developed by N. Ogata et al.1) for implementing second-order nonlinear-optic (NLO) devices. p-NA (p-Nitroaniline) is introduced as side-chain to PVA (Polyvinyl Alcohol) main-chain via acetal-linkage, and second-order NLO effects emerge by electric-field induced side-chain alignment (poling). This polymer has some attractive features besides fabrication easiness. Large NLO susceptibility is expected since p-NA has large polarizability and is highly doped (x=0.82), and the relaxation is small in comparison with dispersive type NLO polymers becaus
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Moerner, W. E., J. C. Scott, S. Ducharme, et al. "Photorefractivity in doped nonlinear polymers." In OSA Annual Meeting. Optica Publishing Group, 1991. http://dx.doi.org/10.1364/oam.1991.mj3.

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Photorefractive polymer materials offer a number of potential advantages over inorganic materials, particularly low cost of material, low dc dielectric constant, ease of fabrication, and compatibility with integrated optics. Our first reports of photorefractivity in an organic polymer1 established the presence of the effect by a combination of hologram erasability, correlation with photoconductivity and electro-optic response, and enhancement by external fields in numerous samples (≃350 μm thick) of the epoxy polymers bisA-NPDA (bisphenol-A-diglycidylether-nitrophenylenediamine) or NA-APNA (N,
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Walba, David M., Peter L. Cobben, Daniel J. Dyer, Uwe Müller, Renfan Shao, and Noel A. Clark. "Orientation of the Disperse Red 1 Chromophore Along the Polar Axis in Ferroelectric Liquid Crystals." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.tue.3.

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Organic thin films with large second order nonlinear susceptibility χ(2) are of potential utility in fast integrated electro-optic modulators. Ferroelectric liquid crystals (FLCs), possessing a thermodynamically stable polar structure, and therefore non-zero χ(2) with infinite "thermal stability," combined with good processibility on semiconductor substrates, seem to provide an excellent approach to creation of χ(2) thin films. Indeed, we have outlined in detail an approach for achieving useful χ(2) values in FLCs by orientation of the p-nitroaniline unit along the FLC polar axis. [1] This app
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Suzuki, A., Y. Matsuoka, Y. Kitahara, and A. J. Ikushima. "Evaluation of Nonlinear Optical Host-Guest Systems with Long Lifetime." In Nonlinear Optics. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/nlo.1992.md25.

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Host-guest systems which consist of transparent polymer matrices and optical nonlinear active molecules, are one of the key materials for optical nonlinear devices. For practical use, the materials should have both large nonlinearity and long lifetime. Such host-guest systems, made of poly-acrylamide derivatives and p-nitroaniline, have been developed in the group of present authors1). The lifetimes at room temperature are expected to be more than several 10 years, as were estimated from the changes in nonlinear susceptibility over 180 days. Such a conventional evaluation might not be sufficie
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