Relevant bibliographies by topics / Anthracene

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Anthracene'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Anthracene"

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Boyd, Simon, Nuno M. Cabral, Kenneth P. Ghiggino, Martin J. Grannas, W. David McFadyen, and Peter A. Tregloan. "Nickel complexation and photophysics of alkylanthracenyl dioxocyclam macrocycle derivatives." Australian Journal of Chemistry 53, no. 8 (2000): 651. http://dx.doi.org/10.1071/ch00106.

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Ligands H2L in which (10-R-anthracen-9-yl)methyl moieties (R = H, Me, Et) are covalently joined (6-position) to the 5,7-dioxocyclam macrocycle framework have been prepared and their nickel(II) complexes isolated and characterized. X-Ray crystal structures of NiIIL (R = H, Me) complexes show that in both structures the anthracene moieties are folded around towards the mean plane of the macrocycles; dihedral angles between the mean anthracene and macrocyclic planes of c. 22˚ are subtended. 1H n.m.r. spectrometry indicates that the folded conformations are retained in solution. Absorption and flu
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Boyd, Simon, Kenneth P. Ghiggino, and W. David McFadyen. "Photochemistry of Anthracene-Appended Cobalt(III) Cyclam Complexes." Australian Journal of Chemistry 61, no. 8 (2008): 585. http://dx.doi.org/10.1071/ch08189.

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The photochemistry of two anthracene-appended cobalt(iii) cyclam complexes is explored with a view to demonstrate a photoactivated ligand release process. The ligand exchange processes that occur in the complexes cis-[CoL(NO2)(ONO)]+ and trans-[CoL(NO2)(ONO)]+ in which L = 6-(anthracen-9-ylmethyl)-1,4,8,11-tetraazacyclotetradecane were monitored upon illumination of the anthracenyl chromophore at 360 nm in the presence of a large excess of thiocyanate. The trans-[CoL(NO2)(ONO)]+ complex underwent a ligand exchange reaction in the absence of light and displayed an enhancement of the reaction up
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Byrne, Andrew J., Sandra A. Bright, James P. McKeown, et al. "Synthesis and Pro-Apoptotic Effects of Nitrovinylanthracenes and Related Compounds in Chronic Lymphocytic Leukaemia (CLL) and Burkitt’s Lymphoma (BL)." Molecules 28, no. 24 (2023): 8095. http://dx.doi.org/10.3390/molecules28248095.

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Chronic lymphocytic leukaemia (CLL) is a malignancy of the immune B lymphocyte cells and is the most common leukaemia diagnosed in developed countries. In this paper, we report the synthesis and antiproliferative effects of a series of (E)-9-(2-nitrovinyl)anthracenes and related nitrostyrene compounds in CLL cell lines and also in Burkitt’s lymphoma (BL) cell lines, a rare form of non-Hodgkin’s immune B-cell lymphoma. The nitrostyrene scaffold was identified as a lead structure for the development of effective compounds targeting BL and CLL. The series of structurally diverse nitrostyrenes was
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Marzoq Hadi Al Fahd, Thawab M. R. Albugami, Mohamed T. Selim, and Mohamed H. EL-Saeid. "Impact of Photo-remediation on Anthracene PAHs in treated wastewater using ZnO/TiO2/H2O2 Catalysis." Open Access Research Journal of Science and Technology 11, no. 1 (2024): 059–70. http://dx.doi.org/10.53022/oarjst.2024.11.1.0068.

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The remediation of carcinogenic Polycyclic Aromatic Hydrocarbons )PAHs( such as Anthracene (3 Rings) in different sources of wastewater was examined using a mix of Zink Oxide, Titanium Oxide, and Hydrogen peroxide (ZnO/ TiO2/H2O2). Eleven wastewater sources were collected from different industrial wastewater and treated wastewater (5 Farms, Main treatment plant, Tanning factory treated wastewater, Tanning factory non-treated wastewater, Carton factories, Factories Lake, and Grease refining plants. Anthracene was extracted by QuEChERS methodology and Analyzed by GCMSMS/TQD. Remediation techniqu
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Choi, Michael T. M., Qingchuan Yang, Thomas C. W. Mak, and Dennis K. P. Ng. "Synthesis and Molecular Structure of a Head-to-Tail [4+4] Dimer of a Hexa-Substituted Anthracene." Journal of Chemical Research 2002, no. 12 (2002): 644–46. http://dx.doi.org/10.3184/030823402103171122.

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Tang, Jian-Hong, and Yu-Wu Zhong. "Anthracene-Containing Metallacycles and Metallacages: Structures, Properties, and Applications." Inorganics 10, no. 7 (2022): 88. http://dx.doi.org/10.3390/inorganics10070088.

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Due to its highly conjugated panel-like structure and unique photophysical and chemical features, anthracene has been widely used for fabricating attractive and functional supramolecular assemblies, including two-dimensional metallacycles and three-dimensional metallacages. The embedded anthracenes in these assemblies often show synergistic effects on enhancing the desired supramolecular and luminescent properties. This review focuses on the metallasupramolecular architectures with anthracene-containing building blocks, as well as their applications in host-guest chemistry, stimulus response,
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Khanra, Somnath, Sabyasachi Ta, Milan Ghosh, Sudeshna Chatterjee, Pallabi Mukherjee, and Debasis Das. "Al3+ triggered aggregation induced emission of an anthracence based azine derivative in SDS medium." New Journal of Chemistry 44, no. 20 (2020): 8477–85. http://dx.doi.org/10.1039/d0nj00968g.

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Single crystal X-ray structurally characterized anthracene appended unsymmetrical azine derivative, viz. 4-(anthracen-9-ylmethylene-hydrazonomethyl)-2-methoxy-phenol (L5) shows Al<sup>3+</sup> assisted aggregation induced emission in SDS medium.
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Roitershtein, D. M., K. A. Lyssenko, I. E. Nifant’ev, and M. E. Minyaev. "Lutetium Cyclopentadienyl Complex with the 2,6-Di-tert-Butylanthracene Dianion." Russian Journal of Coordination Chemistry 49, no. 6 (2023): 369–76. http://dx.doi.org/10.1134/s1070328423700586.

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Abstract The reaction of 2,6-di(tert-butyl)anthracene with potassium graphite and monocyclopentadienyllutetium dichloride tetrahydrofuranate in THF gave the anthracenide complex [(η5-C5H5)Lu(η2-2,6-tBu2C14H8)(THF)2] (I), which was studied by X-ray diffraction (CCDC no. 2215512). Complex I crystallizes in the orthorhombic space group P212121. The structural rigidity of the Lu(O)2Cp(anthracene) crystallographic node was demonstrated. The retention of the structure of complex I in solution was confirmed by NMR techniques.
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Roitershtein, D. M., K. A. Lyssenko, I. E. Nifant’ev, and M. E. Minyaev. "Lutetium Cyclopentadienyl Complex with the 2,6-Di-tert-Butylanthracene Dianion." Координационная химия 49, no. 6 (2023): 367–74. http://dx.doi.org/10.31857/s0132344x22600497.

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The reaction of 2,6-di(tert-butyl)anthracene with potassium graphite and monocyclopentadienyllutetium dichloride tetrahydrofuranate in THF gave the anthracenide complex [(η5-C5H5)Lu(η2-2,6-tBu2C14H8)(THF)2] (I), which was studied by X-ray diffraction (CCDC no. 2215512). Complex I crystallizes in the orthorhombic space group P212121. The structural rigidity of the Lu(O)2Cp(anthracene) crystallographic node was demonstrated. The retention of the structure of complex I in solution was confirmed by NMR techniques.
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Lamm, Jan-Hendrik, Johanna Glatthor, Jan-Henrik Weddeling, et al. "Polyalkynylanthracenes – syntheses, structures and their behaviour towards UV irradiation." Org. Biomol. Chem. 12, no. 37 (2014): 7355–65. http://dx.doi.org/10.1039/c4ob00735b.

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A series of 1,5-, 1,8-, 9,10- and 1,8,10-alkynyl-substituted anthracenes have been synthesised. Amongst others, 9,10-bis[(trimethylsilyl)ethynyl]anthracene was photo-dimerised. The photodimer is thermally unstable as was investigated by VT NMR spectroscopy.
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Dissertations / Theses on the topic "Anthracene"

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Davis, Nicola Kathleen Sybille. "Anthracene-fused porphyrins." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:86b0efea-d33a-42e2-9304-82d94e8f895a.

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This thesis describes the synthesis of a novel family of porphyrins fused to anthracenes, together with investigations into their optical and electrochemical properties, as well as exploring their potential for application in dye-sensitised solar cells. Chapter 1 gives an overview of the structure-property relationships of large planar pi- systems for organic electronic applications. Porphyrins are introduced as suitable building blocks for such systems, and approaches for extending the pi-conjugation of these macrocycles are presented. A literature review of porphyrins fused to aromatic units
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Destecroix, Harry. "Anthracene based synthetic lectins." Thesis, University of Bristol, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.682557.

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Over the past 40 years there has been substantial interest in continuous glucose monitors (CGMs) for diabetes management. Much of the work has focused on the use of enzymes, lectins (carbohydrate binding proteins) or boronic acids as the sensing element, but instability and biocompatibility has hindered development. This has presented an 0pp0l1unity for supramolecular chemists to make synthetic lectins for glucose that respond in real time to glucose in the blood. However, carbohydrate recognition in water presents a challenge due to the hydromimetic nature of the substrate. Moreover, subtle s
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Najah, Zaid. "Asymmetric synthesis using anthracene auxiliaries." Thesis, University of Sheffield, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555128.

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Diels-Alder reaction conditions of the chiral anthracene auxiliary, 9-(l-methoxyethyl) anthracene and 2-cyclopenten-I-one were optimised using the microwave irradiation to give three regioisomers in 80: 12:8 ratio. Flash chromatography purification afforded the desired adduct in 45% yield. Subsequent asymmetric transformations on the major cycloadduct were performed in good yield with excellent levels of diastereoselectivity. Alkylation-reduction reactions sequence on the ketone cycloadduct furnished the desired ketones in 65-75% yield and up to 92:8 diastereoselectivity. Corresponding alcohol
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Moran, Nina. "Novel anthracene-tagged DNA sensors." Thesis, University of Exeter, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.425489.

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Duprey, Jean-Louis Henry Alan. "Studies on Anthracene Tagged Oligonucleotides." Thesis, University of Birmingham, 2011. http://etheses.bham.ac.uk//id/eprint/1286/.

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This thesis describes the synthesis, characterization and study of a range of oligonucleotides that were modified by the inclusion of a non-nucleosidic anthracene unit. This involved the synthesis of different stereoisomers of a non-nucleosidic backbone attached to DNA via a carbon chain linker. These monomers were then coupled to short (15-mer) oligonucleotide chains using solid state DNA synthesis and purified using RP-HPLC. Two systems were studied: a duplex with anthracene functioning as a non-bonding base opposite of a natural nucleobase and a wedge type system. The probes were then exami
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Dujols, Virginie Elisabeth. "Rhodamine & anthracene-based chemosensors /." The Ohio State University, 1996. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487941504294111.

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Wandtke, Sebastian. "Anthracene Based Colorimetric Molecular Sensors." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2014. http://hdl.handle.net/11858/00-1735-0000-0022-5DBE-D.

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Jiménez, Isaac Ojea. "Asymmetric transformations of chiral anthracene derivatives." Thesis, University of Sheffield, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.420699.

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Bullen, Gemma Anne. "Anthracene tagged biomolecules for DNA binding." Thesis, University of Birmingham, 2015. http://etheses.bham.ac.uk//id/eprint/6369/.

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Within this thesis, the use of anthracene to perform various applications within biomolecules is assessed. Anthracene displays two interesting photo properties which make it an appealing molecule for incorporation; fluorescence and photodimerisation. The former is utilised to develop a single nucleotide polymorphism detection assay which is shown to allow for determination of the base present in a complementary strand of DNA. In addition to this, the photodimerisation properties of anthracene are used within a protein for the first time. This is utilised to develop a photoswitched binding prot
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Mashau, Sharon Ntevheleni. "The preparation of pitches from anthracene oil." Pretoria : [S.n.], 2007. http://upetd.up.ac.za/thesis/available/etd-06242008-075035/.

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Books on the topic "Anthracene"

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United States. Environmental Protection Agency and Clement Associates, eds. Toxicological profile for benz[a]anthracene. Oak Ridge National Laboratory, 1990.

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United States. Environmental Protection Agency and Clement Associates, eds. Toxicological profile for dibenz[a,h]anthracene. [Public Health Service, Agency for Toxic Substances and Disease Registry], 1990.

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Nguyen, An Hoang. Theoretical study of intra-molecular dynamics in anthracene. National Library of Canada = Bibliothèque nationale du Canada, 1992.

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Derner, Harald. Untersuchungen über den Resonanz-Ramaneffekt an Anthracen, Naphthalin und p-nitro-p-dimethylamino-azobenzol. Hochschulverlag, 1986.

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Rabjohns, Michael Alan. Synthesis of aromatic polymers containing Anthracene units by a precursor route. University of Manchester, 1993.

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Heldt, Janina. Spektroskopowe i laserowe właściwości pochodnych 9-acetoksy-10-(4ʼ-acetoksyfenylo) antracenu. Uniwersytet Gdański, 1991.

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Traczewska, Teodora Małgorzata. Biotoksyczność produktów mikrobiologicznych przemian antracenu i fenantrenu w wodzie oraz możliwość ich usuwania. Oficyna Wydawnicza Politechniki Wrocławskiej, 2003.

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McElroy, Anne Elizabeth. Benz(a)anthracene in benthic marine environments: Bioavailability, metabolism, and physiological effects on the polychaete Nereis virens. Woods Hole Oceanographic Institution, 1985.

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Fulmer, David. Anthracite. Bang Bang Lulu, 2015.

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Cattafi, Bartolo. Anthracite =: Antracite. Arc, 2000.

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Book chapters on the topic "Anthracene"

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Gooch, Jan W. "Anthracene." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_680.

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Gooch, Jan W. "Anthracene Oil." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_681.

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Nayak, Susri, Sthitaprajna Nath Sharma, Smruti Prajna Pradhan, Subhashree Nayak, and Lipika Patnaik. "Anthracene in Aquatic Ecosystems." In Toxicity of Aquatic System and Remediation. CRC Press, 2024. http://dx.doi.org/10.1201/9781003297901-7.

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Franck, Heinz-Gerhard, and Jürgen Walter Stadelhofer. "Anthracene — production and uses." In Industrial Aromatic Chemistry. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73432-8_11.

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Winkelmann, J. "Diffusion of anthracene (1); air (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_928.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "224 C14H13N Anthracene – ammonia (1/1)." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_355.

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Winkelmann, Jochen. "Diffusion coefficient of anthracene in hexane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_813.

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Winkelmann, Jochen. "Diffusion coefficient of anthracene in heptane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_814.

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Winkelmann, Jochen. "Diffusion coefficient of anthracene in octane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_815.

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Winkelmann, Jochen. "Diffusion coefficient of anthracene in hexadecane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_816.

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Conference papers on the topic "Anthracene"

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Bykov, Alexey, Galina Demidenko, Linda Nikoshvili, and Elena Bakhvalova. "INFLUENCE OF THE NATURE OF AROMATIC POLYMER AS A PT PARTICLE STABILIZER ON ITS ACTIVITY AND SELECTIVITY IN THE LIQUID-PHASE HYDROGENATION OF AROMATIC AND POLYAROMATIC SUBSTRATES." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s17.16.

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A series of platinum catalytic systems stabilized in aromatic polymers were obtained in this work. Commercially available styrene-divinylbenzene (MN100) and polymers synthesized by one-stage crosslinking by the Friedel-Crafts reaction from benzene, naphthalene, and an equimolar benzene-naphthalene mixture were used as polymers. The obtained systems were tested in liquid-phase hydrogenation reactions of benzene, toluene, and benzene-toluene mixture, as well as anthracene in a dodecane medium. The reaction products were studied using GC-MS. Polymers and catalytic systems were studied using diffu
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Shahani, M. N. F., R. B. N. Dharmasiri, H. O. T. O. Perera, et al. "Microbial Degradation of Anthracene and Pyrene in Urban Roadside Soils for a Sustainable Environment: An Evaluation of Bioremediation Potential." In 2024 International Conference on Advances in Technology and Computing (ICATC). IEEE, 2024. https://doi.org/10.1109/icatc64549.2024.11025288.

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Prakash, Kunal, and Nainy Khera. "Anthracene-Oxazine based reversible ink." In The 23rd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecsoc-23-06457.

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Vyas, Arpita, Nitin A. Mirgane, S. V. Moharil, and Aarti Iyer Muley. "Photoluminescence in anthracene and it’s derivatives." In INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2015): Proceeding of International Conference on Condensed Matter and Applied Physics. Author(s), 2016. http://dx.doi.org/10.1063/1.4946110.

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Mal'tsev, Eugene I., Mariy A. Brusentseva, Vladimir I. Berendyaev, Vladislav A. Kolesnikov, Boris V. Kotov, and Anatoly V. Vannikov. "Electroluminescent properties of anthracene-containing polyimides." In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, edited by Zakya H. Kafafi. SPIE, 1999. http://dx.doi.org/10.1117/12.372729.

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Sukhinina, N. S., A. A. Zhokhov, V. M. Masalov, I. I. Khodos, and G. A. Emelchenko. "C8 microcrystals synthesized by anthracene carbonization." In THE 9TH INTERNATIONAL CONFERENCE ON STRUCTURAL ANALYSIS OF ADVANCED MATERIALS - ICSAAM 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5140296.

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Sadiq Mahdi AL-Khateeb, Dalia. "Synthesis of Anthracene and Benzene Derivatives from Glycerol and Study of the Effectiveness of Biological." In XI. International Scientific Congress of Pure, Applied and Technological Sciences (MINAR Congress). Rimar Academy, 2024. https://doi.org/10.47832/minarcongress11-11.

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This research includes the synthesis of benzene and poly hydroxyl anthracene derivatives from the reaction of glycerol with ethanoic acid using the catalyst poly allyl sulfonic acid benzene and produces glycerol tri acetate and this latter compound is reacted with Benzene, anthracene and their derivatives in the presence of copper silicate (catalyst )and then analyze these compounds using the catalyst agent hydrochloric acid and these compounds were diagnosed using infrared, element analysis and thin-layer chromatography technology of these compounds and measure the degree of Boiling point and
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Singh, L. K., and Anju Jaiswal. "Direct Current Conductivity Measurement on Anthracene Single Crystal." In 2015 Fifth International Conference on Communication Systems and Network Technologies (CSNT). IEEE, 2015. http://dx.doi.org/10.1109/csnt.2015.258.

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Koyasu, Kiichirou, Toshio Nishi, Tatsuhiko Nishi, et al. "Determination of Energy Gap of Anthracene Thin Film." In 2008 MRS Fall Meetin. Materials Research Society, 2008. http://dx.doi.org/10.1557/proc-1115-h08-27.

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Yang Shengke, Zhu Tao, and Kang Hua. "Research on anthracene absorption in Weihe River sediments." In 2011 International Symposium on Water Resource and Environmental Protection (ISWREP). IEEE, 2011. http://dx.doi.org/10.1109/iswrep.2011.5893311.

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Reports on the topic "Anthracene"

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Pavlopoulos, T. G. Triplet-Triplet Absorption and Polarization Spectra of Anthracene. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada235895.

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Fung, D. P. C., C. Fairbridge, and R. Anderson. Gasification reactivity of Canadian anthracite and semi -anthracite chars. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/302659.

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Dougherty, Dennis A. New Synthetic Receptor Derived from Bridged Anthracenes. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada237461.

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Merritt, R. D. Alaska bituminous coal and anthracite. Alaska Division of Geological & Geophysical Surveys, 1988. http://dx.doi.org/10.14509/1364.

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Killmeyer, R. P., P. H. Zandhuis, M. V. Ciocco, W. Weldon, T. West, and D. Petrunak. Fine Anthracite Coal Washing Using Spirals. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/781457.

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Simmon, F. J., D. V. Keller, Marino Jr., Keller J., Ask D. S., and T. E. Developing Anthracite Coal Water Slurry Fuel. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada274852.

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Bartis, J. T., and A. K. Inberman. Anthracite R&D needs - CRADA 89-001. Final report. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/582173.

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Leeladee, Pannee. Cooperative small-molecule activation toward sustainable catalysis. Faculty of Science, Chulalongkorn University, 2018. https://doi.org/10.58837/chula.res.2018.47.

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In this research, a series of copper complexes containing polypyridyl ligands were designed to study the influence from ligands, nuclearity, solvents and secondary coordination on reactivity toward small-molecule activation. This structure-reactivity relationship was used in investigation for oxygen reduction reactions (ORR), and applied in detection of ascorbic acid (AsH₂). Firstly, copper (II) complexes containing polypyridyl derivatives ligands (i.e., Cu(dpa), Cu(adpa) and Cu₂ (addpa)) were synthesized and fully characterized by elemental analysis, mass spectrometry and X-ray crystallograph
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9

Water quality of large discharges from mines in the anthracite region of eastern Pennsylvania. US Geological Survey, 1996. http://dx.doi.org/10.3133/wri954243.

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10

Quality of water in mines in the Western Middle Coal Field, Anthracite Region, east-central Pennsylvania. US Geological Survey, 1987. http://dx.doi.org/10.3133/wri854038.

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