Relevant bibliographies by topics / Anthracen

Contents

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

Academic literature on the topic 'Anthracen'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Anthracen"

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Berg, David J., and Brendan Twamley. "Crystal structure of a binuclear mixed-valence ytterbium complex containing a 2-anthracene-substituted phenoxide ligand." Acta Crystallographica Section E Crystallographic Communications 75, no. 9 (2019): 1367–71. http://dx.doi.org/10.1107/s205698901901154x.

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Reaction of 2-(anthracen-9-yl)phenol (HOPhAn, 1) with divalent Yb[N(SiMe3)2]2·2THF in THF–toluene mixtures affords the mixed-valence YbII–YbIII dimer {[2-(anthracen-9-yl)phenolato-κO]bis(tetrahydrofuran)ytterbium(III)}-tris[μ-2-(anthracen-9-yl)phenolato]-κ4 O:O;κO:1,2-η,κO-{[2-(anthracen-9-yl)phenolato-κO]ytterbium(II)} toluene trisolvate, [Yb2(C20H13O)5(C4H8O)2]·3C7H7 or [YbIII(THF)2(OPhAn)](μ-OPhAn)3[YbII(OPhAn)]·3C7H7 (2), as the major product. It crystallized as a toluene trisolvate. The Yb—O bond lengths in the crystal structure of this dimer clearly identify the YbII and YbIII centres. I
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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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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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Liu, Dan, Chenguang Li, Shujie Niu, et al. "A case study of tuning the crystal polymorphs of organic semiconductors towards simultaneously improved light emission and field-effect properties." Journal of Materials Chemistry C 7, no. 20 (2019): 5925–30. http://dx.doi.org/10.1039/c9tc01321k.

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Simultaneously improved light emission and field-effect performance were achieved for an anthracene derivative, 1,4-di(anthracen-9-yl)buta-1,3-diyne (DABD) in its β-phase crystals, suggesting their potential applications in integrated optoelectronic devices.
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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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Kabay, Nilgün, Burak Doğan Bozer, Aslı Öztürk Kiraz, Yasemin Baygu, İzzet Kara, and Yaşar Gök. "Synthesis, characterization and structural computational investigation of novel Zn(II) phthalocyanines containing peripheral anthracene moieties." Journal of Porphyrins and Phthalocyanines 23, no. 07n08 (2019): 943–59. http://dx.doi.org/10.1142/s1088424619500913.

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New zinc(II) phthalocyanines (ZnPc-I and ZnPc-II) containing four peripheral anthracene pendant groups were synthesized by cyclotetramerization of (E)-4-(3-(4-((anthracen-9-yl-methylene)amino)phenoxy)propoxy)phthalonitrile and 4-(3-(4-((anthracen-9-ylmethyl)amino)phenoxy)propoxy)phthalonitrile. All compounds were characterized using a combination of analytical and spectroscopic techniques such 1H, [Formula: see text]C NMR, FT-IR, UV-vis and MS spectral data. The molecular geometry and gauge including atomic orbital (GIAO) 1H and [Formula: see text]C chemical shift values of the compounds in th
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Dong, Zhenming, Bo Liu, Xinxin Cui, and Yufang Liu. "2-(Anthracen-9-yl)-10-methoxybenzo[h]quinoline acetone hemisolvate." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2535. http://dx.doi.org/10.1107/s1600536812031807.

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The asymmetric unit of the title structure, C28H19NO·0.5C3H6O, comprises one 2-(anthracen-9-yl)-10-methoxybenzo[h]quinoline molecule and an acteone molecule with an occupany of 0.5. The solvent molecule is disordered around a centre of symmetry. Its occupancy was determined from NMR data and kept fixed during the refinement. The two conjugated ring systems of the molecule are almost perpendicular to each other; the interplanar angle between the anthracene and quinoline ring systems is 84.9 (2)°.
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Zainuri, Dian Alwani, Ibrahim Abdul Razak, and Suhana Arshad. "Crystal structures, DFT studies and UV–visible absorption spectra of two anthracenyl chalcone derivatives." Acta Crystallographica Section E Crystallographic Communications 74, no. 10 (2018): 1491–96. http://dx.doi.org/10.1107/s2056989018013087.

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The crystal structures of (E)-1-(anthracen-9-yl)-3-(3H-indol-2-yl)prop-2-en-1-one, C25H17NO, and (E)-1-(anthracen-9-yl)-3-[4-(dimethylamino)naphthalen-1-yl]prop-2-en-1-one, C29H23NO, are reported. In each case the anthracene ring system and pendant ring system are almost perpendicular to each other [dihedral angles = 75.57 (7)° and 70.26 (10)°, respectively]. In the extended structures, weak N—H...O, C—H...O and C—H...π interactions influence the centrosymmetric crystal packing. Density functional theory calculations were carried out using a 6–311 G++(d,p) basis set and the calculated structur
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Liao, Chung-Ping, Otto Phanstiel, Mark E. Lasbury, et al. "Polyamine Transport as a Target for Treatment of Pneumocystis Pneumonia." Antimicrobial Agents and Chemotherapy 53, no. 12 (2009): 5259–64. http://dx.doi.org/10.1128/aac.00662-09.

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ABSTRACT Polyamine levels are greatly increased in alveolar macrophages (AMs) during Pneumocystis pneumonia (PCP), leading to increased production of H2O2, which causes AMs to undergo apoptosis. One of the mechanisms by which polyamine levels in AMs are elevated is enhanced uptake of exogenous polyamines. In this study, the possibility of targeting polyamine uptake as a treatment for PCP was examined. Four anthracene- and one benzene-polyamine conjugates that are potential polyamine transport inhibitors, including N1-anthracen-9-ylmethyl-butane-1,4-diamine; N-(4-aminobutyl)-N-anthracen-9-ylmet
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Lee, Jaehyun, Seungho Kim, Jee-Hwan Kim, and Jongwook Park. "A New Anthracene Derivative Containing t-Butyl Group for Solution Process Organic Light-Emitting Diodes." Journal of Nanoscience and Nanotechnology 15, no. 10 (2015): 8285–88. http://dx.doi.org/10.1166/jnn.2015.11258.

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4-(10-(3′,5′-diphenylbiphenyl-4-yl)anthracen-9-yl)-N,N-diphenylaniline [TATa] and a new anthracene derivative of 4-(2 or 3-tert-butyl-10-(3′,5′-diphenylbiphenyl-4-yl)anthracen-9-yl)-N,N-diphenylaniline [T-TATa] isomer by introduced t-butyl group were synthesized. OLED devices of TATa and T-TATa were fabricated by solution process. Its physical properties such as optical, electrochemical, and electroluminescent properties were also investigated. Two compounds were used as emitting layer (EML) in OLED device: ITO/PEDOT (40 nm)/synthesized materials (60 nm)/TPBi (20 nm)/LiF (1 nm)/Al (200 nm). Th
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Dissertations / Theses on the topic "Anthracen"

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Kunze, Markus. "Neue Fluoreszenzfarbstoffe mit Anthracen- und Fluoranthengrundgerüst." Diss., lmu, 2004. http://nbn-resolving.de/urn:nbn:de:bvb:19-24692.

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Kahlert, Björn. "Synthese supramolekulare Eigenschaften von Klammermolekülen mit Anthracen-Seitenwänden." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=978757556.

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Mack, Min Jung [Verfasser]. "Synthese von Anthracen-funktionalisierten Polymeren und Photodimerisierungseffekte / Min Jung Mack." Aachen : Shaker, 2005. http://d-nb.info/1186587563/34.

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Lamm, Jan-Hendrik [Verfasser]. "Anthracen-basierte Poly-Lewis-Säuren - Synthese, Charakterisierung und Wirt-Gast-Chemie / Jan-Hendrik Lamm." Bielefeld : Universitätsbibliothek Bielefeld, 2014. http://d-nb.info/1196644152/34.

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Gloza, Steffi [Verfasser], and Matthias [Gutachter] Lehmann. "Synthese und Charakterisierung von Anthracen- und Anthrachinon-substituierten sternförmigen Mesogenen / Steffi Gloza. Gutachter: Matthias Lehmann." Würzburg : Universität Würzburg, 2015. http://d-nb.info/110325961X/34.

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Schneider, Marc Andre. "Iridium- und Rhodiumhydrido-Komplexe mit 1,8-Bis(diorganylphosphino)anthracen-Liganden als thermostabile homogene Katalysatoren für die Dehydrierung von Alkanen." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968540732.

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Polomska, Marta Ewa. "Towards a total synthesis of mensacarcin." Doctoral thesis, [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=976248018.

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Bladholm, Viktor. "Organic Fillers for Solid Rocket Fuel." Thesis, KTH, Skolan för kemi, bioteknologi och hälsa (CBH), 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-259589.

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Idag är de vanligaste använda raketerna flytande-bränsle- och fast-bränsle- raketer. Flytande-bränsle-raketer har fördelen att det kan manövreras men de har en komplex design och problem med förvaring. Fast-bränsle-raketer har en enkel design och kan förvaras men de har en miljöpåverkan och bränslet kan vara svårhanterligt. En tredje typ av raketer, hybridraketer, kan kombinera enkelheten från fasta-bränsle-raketer med manövreringsbarheten från vätske-bränsle-raketer. Trots fördelarna med hybridraketer används de inte på grund av att bränslet har låg regressionshastighet och låg densitet. Orga
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Pijeat, Joffrey. "Anthracenylporphyrin based building blocks for the bottom-up fabrication of nitrogen-doped graphene nanostructures." Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS346/document.

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La synthèse de graphène par approche « bottom-up » fait l’objet de nombreux travaux de recherche ayant pour but de contrôler les propriétés électroniques et optiques de ce matériau par la fabrication de nanostructures avec une précision atomique. D’autre part, le contrôle de dopant dans le graphène permettant d’en moduler les propriétés suscite un grand intérêt et dans ce contexte l’utilisation de porphyrines avec un taux d’azote contrôlé est attrayante. Par leurs ressemblances structurelles, les porphyrines π-étendues peuvent être considérées comme des nanoparticules de graphène dopées à l’az
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Yospanya, Wijak. "Studies on supramolecular photochirogenesis mediated by synthetic antibody and chiral silica-organic hybrid nanoribbons." Thesis, Bordeaux, 2020. http://www.theses.fr/2020BORD0088.

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Dû à l’augmentation de la demande de nouveaux matériaux chiraux, la préparation de molécules chirales est actuellement l'un des domaines les plus essentiels de la chimie synthèse chimique. La photoréaction supramoléculaire est une stratégie efficace de photoréaction régio- et énantio-sélective qui permet d’éviter le problème de la courte durée de vie de l’état excité de la molécule clé-intermédiaire, ainsi que des faibles interactions dues aux états excités. Cette thèse décrit, la photocyclodimérisation supramoléculaire du 2-anthracènecarboxylate à l’aide de deux procédés différents dans l'eau
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Books on the topic "Anthracen"

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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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Bergman, Nicholas H. Bacillus anthracis and anthrax. John Wiley & Sons, 2011.

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Bergman, Nicholas H., ed. Bacillus anthracis and Anthrax. John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470891193.

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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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Newman, Melvin S. The chemistry and biology of benz(a)anthracenes. Cambridge University Press, 1988.

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B, Tierney, and Veerarghavan S, eds. The chemistry and biology of benz(a)anthracenes. Cambridge University Press, 1988.

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Newman, Melvin S. The chemistry and biology of benz(a)anthracenes. Cambridge University Press, 2009.

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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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Anthrax decontamination: Hearing before a subcommittee of the Committee on Appropriations, United States Senate, One Hundred Seventh Congress, first session : special hearing, November 28, 2001, Washington, DC. U.S. G.P.O., 2002.

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Böhm, R. Schnelle und automatisierbare diagnosemethoden für Bacillus anthracis als Testkeim bei Untersuchungen zur Umwelthygiene. Paul Parey Scientific Publishers, 1988.

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Book chapters on the topic "Anthracen"

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Franck, Heinz-Gerhard, and Jürgen Walter Stadelhofer. "Anthracen — Herstellung und Verwendung." In Industrielle Aromatenchemie. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-662-07875-4_11.

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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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Shroot, B., and H. Schaefer. "Anthralin." In Pharmacology of the Skin II. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74054-1_34.

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Antwerpen, Markus, Paola Pilo, Pierre Wattiau, Patrick Butaye, Joachim Frey, and Dimitrios Frangoulidis. "Bacillus anthracis." In BSL3 and BSL4 Agents. Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527645114.ch15.

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Thorne, Curtis B. "Bacillus anthracis." In Bacillus subtilis and Other Gram-Positive Bacteria. ASM Press, 2014. http://dx.doi.org/10.1128/9781555818388.ch8.

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Koehler, Theresa M. "Bacillus anthracis." In Gram-Positive Pathogens. ASM Press, 2014. http://dx.doi.org/10.1128/9781555816513.ch54.

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Challacombe, Jean F., Richard T. Okinaka, A. Christine Munk, Thomas S. Brettin, and Paul Keim. "Bacillus anthracis." In Genomes of Foodborne and Waterborne Pathogens. ASM Press, 2014. http://dx.doi.org/10.1128/9781555816902.ch12.

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Chaubey, Vikas P., Kevin B. Laupland, Christopher B. Colwell, et al. "Bacillus anthracis." In Encyclopedia of Intensive Care Medicine. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-00418-6_1188.

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Mogridge, J., S. Shadomy, and P. Turnbull. "Bacillus Anthracis." In Pathogenesis of Bacterial Infections in Animals. Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9780470958209.ch6.

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Conference papers on the topic "Anthracen"

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Valverde-Aguilar, Guadalupe, Jorge Garcia-Macedo, Xianghuai Wang, Jeffrey I. Zink, and Stephen F. Nelsen. "Photoinduced electron transfer in 2- tert -butyl-3-(anthracen-9-yl)-2,3-diazabicyclo[2.2.2]octane." In SPIE Optics + Photonics, edited by Zeno Gaburro and Stefano Cabrini. SPIE, 2006. http://dx.doi.org/10.1117/12.680904.

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Haidar, Samer, Annika Meyers, Andre Bollacke, and Joachim Jose. "Synthesis and Biological Determination of a New Anthracen-9,10-dione Derivative as a Human CK2 Inhibitor." In 1st International Electronic Conference on Medicinal Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a042.

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Weaver, John, Tae Jin Kang, Kimberly Raines, et al. "The Protective Role of Bacillus Anthracis Exosporium in Macrophage-Mediated Killing by Nitric Oxide." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176138.

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The ability of the endospore-forming, gram-positive bacterium Bacillus anthracis to survive exposure to antibacterial killing mechanisms by activated macrophages is key to its germination and survival. These antibacterial killing mechanisms include, but are not limited to the generation of free radicals such as nitric oxide (•NO) and superoxide (O2•−) from the upregulation of inducible nitric oxide synthase (NOS 2) along with products derived from them, e.g., peroxynitrite (ONOO−), as part of microbicidal activity. However questions still remain as to how these species are involved in microbia
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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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Siegrist, Jonathan, Mary Amasia, Horacio Kido, Jim Zoval, and Marc Madou. "Microfluidic CD-Based Systems Toward Rapid Anthrax Detection in Whole Blood." In ASME 2008 3rd Frontiers in Biomedical Devices Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/biomed2008-38094.

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Anthrax is an acute and deadly disease caused by the bacterium Bacillus anthracis. Upon exposure, usually through inhalation, ingestion, or cutaneous contact, B. anthracis spores begin multiplying, creating a life-threatening situation. If not quickly detected and treated, humans can die within several days. With renewed bio-terrorism concerns, there is a need for a rapid and automated system capable of sample (respiratory or blood) to answer (positive infection) so that quarantine procedures and treatment can be administered immediately. Microfluidic platforms hold great promise of fulfilling
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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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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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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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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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Reports on the topic "Anthracen"

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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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Peterson, Scott N. Macrophage Responses to B. Anthracis. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada428855.

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Hanna, Philip C. Macrophage Responses to B. Anthracis. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada456287.

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Leighton, Terrance. Recombinant Antibodies Specific to Bacillus Anthracis Spores. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada406971.

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Smith, Lisa S., Vipin K. Rastogi, and Michelle R. Ziemski. Disinfection of Vegetative Cells of Bacillus anthracis. Defense Technical Information Center, 2016. http://dx.doi.org/10.21236/ad1006130.

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Sutton, M., S. Kane, and J. Wollard. Methyl Iodide Fumigation of Bacillus Anthracis Spores. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1070161.

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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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Little, Stephen F., and Gregory B. Knudson. Identification of Vaccine Resistant Isolates of Bacillus anthracis. Defense Technical Information Center, 1985. http://dx.doi.org/10.21236/ada162002.

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DelVecchio, Vito G., and Alexander Walz. Computer Simulation of the Virulome of Bacillus anthracis Using Proteomics. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada455249.

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Brittingham, Katherine C., Gordon Ruthel, Rekha G. Panchal, Claudette L. Fuller, and Wilson J. Ribot. Dendritic Cells Endocytose Bacillus Anthracis Spores: Implications for Anthrax Pathogenesis. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada434591.

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