Relevant bibliographies by topics / Anthracene-9-carboxylic acid

Academic literature on the topic 'Anthracene-9-carboxylic acid'

Author: Grafiati
Published: 14 March 2023

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Journal articles on the topic "Anthracene-9-carboxylic acid"

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Fitzgerald, L. J., and R. E. Gerkin. "Anthracene-9-carboxylic Acid." Acta Crystallographica Section C Crystal Structure Communications 53, no. 1 (January 15, 1997): 71–73. http://dx.doi.org/10.1107/s0108270196011213.

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Khanra, Partha, Md Elias Uddin, Nam Hoon Kim, Tapas Kuila, Seung Hee Lee, and Joong Hee Lee. "Electrochemical performance of reduced graphene oxide surface-modified with 9-anthracene carboxylic acid." RSC Advances 5, no. 9 (2015): 6443–51. http://dx.doi.org/10.1039/c4ra12356e.

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3

Li, Qi, Qian Zhang, Wu-Ji Wei, A.-Ni Wang, Ji-Xiang Hu, and Guo-Ming Wang. "Light actuated stable radicals of the 9-anthracene carboxylic acid for designing new photochromic complexes." Chemical Communications 57, no. 35 (2021): 4295–98. http://dx.doi.org/10.1039/d1cc00920f.

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The crystalline 9-anthracene carboxylic acid and the constructed mononuclear complex were for the first time discovered to show radical-induced photochromism and photomagnetism after Xe lamp light irradiation.
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Ghoneim, N., D. Scherrer, and P. Suppan. "Dual luminescence, structure and excimers of 9-anthracene carboxylic acid." Journal of Luminescence 55, no. 5-6 (August 1993): 271–75. http://dx.doi.org/10.1016/0022-2313(93)90022-f.

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Ahmed, Adeeba, Md Serajul Haque Faizi, Aiman Ahmad, Musheer Ahmad, and Igor O. Fritsky. "Crystal structure and Hirshfeld surface analysis of 4-{[(anthracen-9-yl)methyl]amino}benzoic acid." Acta Crystallographica Section E Crystallographic Communications 76, no. 1 (January 1, 2020): 62–65. http://dx.doi.org/10.1107/s2056989019016207.

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In the molecule of the title anthracene derivative, C22H17NO2, the benzene ring is inclined to the mean plane of the anthracene ring system (r.m.s. deviation = 0.024 Å) by 75.21 (9)°. In the crystal, molecules are linked by pairs of O—H...O hydrogen bonds, forming classical carboxylic acid inversion dimers with an R 2 2(8) ring motif. The dimers are linked by C—H...π interactions, forming a supramolecular framework.
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Bose, Saswata, Tapas Kuila, Ananta Kumar Mishra, Nam Hoon Kim, and Joong Hee Lee. "Preparation of non-covalently functionalized graphene using 9-anthracene carboxylic acid." Nanotechnology 22, no. 40 (September 12, 2011): 405603. http://dx.doi.org/10.1088/0957-4484/22/40/405603.

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Khanra, Partha, Tapas Kuila, Seon Hyeong Bae, Nam Hoon Kim, and Joong Hee Lee. "Electrochemically exfoliated graphene using 9-anthracene carboxylic acid for supercapacitor application." Journal of Materials Chemistry 22, no. 46 (2012): 24403. http://dx.doi.org/10.1039/c2jm34838a.

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8

Abdel-Mottaleb, M. S. A., H. R. Galal, A. F. M. Dessouky, M. El-Naggar, D. Mekkawi, S. S. Ali, and G. M. Attya. "Fluorescence and photostability studies of anthracene-9-carboxylic acid in different media." International Journal of Photoenergy 2, no. 1 (2000): 47–53. http://dx.doi.org/10.1155/s1110662x00000076.

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Electronic absorption and fluorescence spectra of anthracene-9-carboxylic acid (ANCA) were studied in different homogeneous solvents, binary protic/aprotic solvent mixtures and in heterogeneous solutions of the cationic cetyltrimethyl ammonium bromide (CTAB) micelle. Different chemical species of ANCA were identified spectroscopically in different media. The results are discussed on the basis of a mechanism that involves two equilibria: acid-base equilibrium and monomer-dimer equilibrium. These equilibria were found to be very sensitive to the nature of the medium and the concentration of ANCA.Moreover, while it is photostable in most solvents studied, the ANCA was found to be photolabile in aqueous media of different pHs. The acid-base catalyzed photodegradation rate was studied by following up absorption and/or fluorescence intensities as a function of illumination dose. The determined rate of the photochemical degradation of ANCA depends on the nature of the medium. The first order degradation rate constant is remarkably enhanced in heterogeneous medium of CTAB. As expected, the determined activation energy is low (∼3.2 kJ.mol-1). This result favors photooxidation process. Anthraquinone was the main photodegradation product obtainedvia9,9′-dicarboxylic head-to-head dimer of anthracene that was identified by GC-Mass technique.
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9

Skupińska, Katarzyna, Monika Zylm, Irena Misiewicz, and Teresa Kasprzycka-Guttman. "Interaction of anthracene and its oxidative derivatives with human serum albumin." Acta Biochimica Polonica 53, no. 1 (January 9, 2006): 101–12. http://dx.doi.org/10.18388/abp.2006_3368.

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Binding affinities of ten polycyclic aromatic hydrocarbons to albumin were determined: anthracene, its eight oxy-derivatives: anthraquinone, 9-anthracenemethanol, 9-anthraldehyde, 9-anthracenecarboxylic acid, 1,4-dihydroxyanthraquinone, 1,5-dihydroxyanthraquinone, 1,8-dihydroxyanthraquinone, 2,6-dihydroxyanthraquinone and benzo[a]pyrene. The quenching of albumin fluorescence was used to measure the PAH - protein interaction. The theoretical curve of calculated fluorescence was fitted to experimental data after necessary corrections regarding PAHs fluorescence and inner filter effect. From the numerical fitting the final association constants were calculated. Anthracene and anthraquinone failed to quench the albumin fluorescence. 9-anthracenecarboxylic acid showed the highest, while 9-anthracenemethanol the weakest albumin binding affinity. The affinity constants determined for 9-anthraldehyde and benzo[a]pyrene were of the same magnitude and indicated low-affinity binding to albumin. The constants obtained for the four dihydroxyanthraquinones were higher, but dissimilar, which suggests that the position of the functional group in anthracene molecule influences the binding constant. Moreover, this study suggests that the type of substituent plays a significant role in PAH-albumin complex formation. The carboxylic group increases the binding affinity of the anthracene molecule the most rather than the presence of both carbonyl and hydroxyl groups. The lowest affinity constants were obtained for aldehyde, methyl and carbonyl substituents.
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Hardy, Jake, Matthew W. Brett, Aurélien Rossi, Isabella Wagner, Kai Chen, Mattie S. M. Timmer, Bridget L. Stocker, Michael B. Price, and Nathaniel J. L. K. Davis. "Energy Transfer between Anthracene-9-carboxylic Acid Ligands and CsPbBr3 and CsPbI3 Nanocrystals." Journal of Physical Chemistry C 125, no. 2 (January 7, 2021): 1447–53. http://dx.doi.org/10.1021/acs.jpcc.0c09161.

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Book chapters on the topic "Anthracene-9-carboxylic acid"

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Jaramillo-González, Caterine, Rodrigo Morales Cueto, and William Rodríguez-Córdoba. "Absorption and Emission Spectra of Anthracene-9-Carboxylic Acid in Solution Within the Polarizable Continuum Model." In Concepts of Mathematical Physics in Chemistry: A Tribute to Frank E. Harris - Part B, 61–94. Elsevier, 2016. http://dx.doi.org/10.1016/bs.aiq.2015.05.004.

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