Relevant bibliographies by topics / Acenaphthylene

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

Academic literature on the topic 'Acenaphthylene'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Acenaphthylene"

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Sugimoto, Toshiya, Masatomo Nojima, and Shigekazu Kusabayashi. "Ozonolysis of acenaphthylene and 1-substituted acenaphthylenes." Journal of Organic Chemistry 55, no. 12 (1990): 3816–20. http://dx.doi.org/10.1021/jo00299a024.

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2

Yavari, Issa, and Aliyeh Khajeh-Khezri. "Recent Advances in the Synthesis of Hetero- and Carbocyclic Compounds­ and Complexes Based on Acenaphthylene-1,2-dione." Synthesis 50, no. 20 (2018): 3947–73. http://dx.doi.org/10.1055/s-0037-1610209.

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Acenaphthylene-1,2-dione has been utilized in a wide range of reactions as a starting material for the synthesis of hetero- and carbocyclic compounds and complexes. This review provides a short summary of the recent advances in the application of acenaphthylene-1,2-dione in the synthesis of hetero- and carbocyclic systems and bioactive compounds. In addition, the applications of acenaphthylene-1,2-dione in the synthesis of spiro compounds, propellanes, and ligands in catalyst reactions, from 2002 to early 2018, are included.1 Introduction2 Synthesis of Spiro Compounds Employing Acenaphthylene-
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3

Brown, RFC, KJ Coulston, FW Eastwood, and S. Saminathan. "Detection of the 1,2-Didehydronaphthalene to 1H-Indenylidenecarbene Rearrangement by Intramolecular Trapping in a Flash Vacuum Pyrolytic Reaction." Australian Journal of Chemistry 40, no. 1 (1987): 107. http://dx.doi.org/10.1071/ch9870107.

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Flash vacuum pyrolysis of 9-methyl-1,3-dihydronaphtho[1,2-c]furan-1,3-dione (8) at 750-880� gave exclusively 1H-cyclopent[ cd ]indene (9) and of 8-methyl-1,2-dihydrocyclobuta[a]naphthalene-1.2-dione (10) at 600-840� gave a mixture of (9) and acenaphthylene. Acenaphthylen-4-ol (12) was synthesized and found to be stable to flash vacuum pyrolysis over thetemperature range 600-900�. These findings are discussed in relation to the rearrangement described in the title.
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Poonthrigpun, Siriwat, Kobchai Pattaragulwanit, Sarunya Paengthai, et al. "Novel Intermediates of Acenaphthylene Degradation by Rhizobium sp. Strain CU-A1: Evidence for Naphthalene-1,8-Dicarboxylic Acid Metabolism." Applied and Environmental Microbiology 72, no. 9 (2006): 6034–39. http://dx.doi.org/10.1128/aem.00897-06.

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ABSTRACT The acenaphthylene-degrading bacterium Rhizobium sp. strain CU-A1 was isolated from petroleum-contaminated soil in Thailand. This strain was able to degrade 600 mg/liter acenaphthylene completely within three days. To elucidate the pathway for degradation of acenaphthylene, strain CU-A1 was mutagenized by transposon Tn5 in order to obtain mutant strains deficient in acenaphthylene degradation. Metabolites produced from Tn5-induced mutant strains B1, B5, and A53 were purified by thin-layer chromatography and silica gel column chromatography and characterized by mass spectrometry. The r
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Chandralekha, Kuppan, Deivasigamani Gavaskar, Adukamparai Rajukrishnan Sureshbabu, and Srinivasakannan Lakshmi. "Crystal structure of 5′′-(4-chlorobenzylidene)-4′-(4-chlorophenyl)-1′-methyltrispiro[acenapthylene-1,2′-pyrrolidine-3′,1′′-cyclohexane-3′′,2′′′-[1,3]dioxane]-2(1H),6′′-dione." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (2015): o814—o815. http://dx.doi.org/10.1107/s2056989015018034.

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In the title compound, C36H29Cl2NO4, two spiro links connect the methyl-substituted pyrrolidine ring to the acenaphthylene and cyclohexanone rings. The cyclohexanone ring is further connected to the dioxalane ring by a third spiro junction. The five-membered ring of the acenaphthylen-1-one ring system adopts a flattened envelope conformation, with the ketonic C atom as the flap, whereas the dioxalane and pyrrolidine rings each have a twist conformation. The cyclohexenone ring assumes a boat conformation. An intramolecular C—H...O hydrogen-bond interaction is present. In the crystal, molecules
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Thimmarayaperumal, Solaimalai, and Sivakumar Shanmugam. "Ultrasound-assisted one-pot multicomponent 1,3-dipolar cycloaddition strategy: combinatorial synthesis of spiro-acenaphthylene-S,S-acetal and 2H-pyranone derivatives." New Journal of Chemistry 42, no. 6 (2018): 4061–66. http://dx.doi.org/10.1039/c7nj04627h.

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The stereo/regio/chemoselective syntheses of a library of novel spiro[acenaphthylene-1,3′-pyrrolizin]-2-one and spiro[acenaphthylene-1,5′-pyrrolo[1,2-c]thiazol]-2-one have been achieved through 1,3-dipolar cycloaddition.
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Chandralekha, Kuppan, Deivasigamani Gavaskar, Adukamparai Rajukrishnan Sureshbabu, and Srinivasakannan Lakshmi. "Crystal structure of 5′′-benzylidene-1′-methyl-4′-phenyltrispiro[acenaphthylene-1,2′-pyrrolidine-3′,1′′-cyclohexane-3′′,2′′′-[1,3]dioxane]-2,6′′-dione." Acta Crystallographica Section E Crystallographic Communications 72, no. 3 (2016): 387–90. http://dx.doi.org/10.1107/s2056989016002875.

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In the title compound, C36H31NO4, two spiro links connect the methyl-substituted pyrrolidine ring to the acenaphthylene and cyclohexanone rings. The cyclohexanone ring is further connected to the dioxalane ring by a third spiro junction. The five-membered ring of the acenaphthylen-1-one ring system adopts a flattened envelope conformation with the ketonic C atom as flap, whereas the dioxalane and pyrrolidine rings each have a twist conformation. The cyclohexanone ring assumes a boat conformation. Three intramolecular C—H...O hydrogen bonds involving both ketonic O atoms as acceptors are presen
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İşci, Ümit, Sevinc Zehra Topal, Emel Önal, et al. "Synthesis and characterization of a new meso-tetra-dihydro benzocyclobutacenaphthylene free-base porphyrin." Journal of Porphyrins and Phthalocyanines 22, no. 01n03 (2018): 173–80. http://dx.doi.org/10.1142/s1088424618500062.

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A meso-tetra-6b,10b-dihydrobenzo[j]cyclobut[a]acenaphthylene free-base porphyrin was synthesised and its photophysical, photochemical and electrochemical properties were compared with those of free-base meso-tetraphenylporphyrin. The frontier orbitals and the HOMO–LUMO energy gaps of both compounds were also determined. It was demonstrated that the meso6b,10b-Dihydrobenzo[j]cyclobut[a]acenaphthylene porphyrin retained the same properties as the tetraphenylporphyrin.
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Lefkaditis, Demetrics A., Nicolaos G. Argyropoulos, and Demetrios N. Nicolaides. "Preparation and Catalytic Hydrogenation of Spiro[acenaphthylene-dioxazoles] and spiro[acenaphthylene-isoxazoles]." Liebigs Annalen der Chemie 1986, no. 11 (1986): 1863–71. http://dx.doi.org/10.1002/jlac.198619861106.

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Neumann, Gerd, and Klaus Müllen. "Reduktive Alkylierungen von Acenaphthylen und Synthese von Acephenanthrylen." CHIMIA 39, no. 9 (1985): 275. https://doi.org/10.2533/chimia.1985.275.

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The as yet unknown reductive alkylation of acenaphthylene with 1,n-dihalogenoalkanes is investigated. The techniques applied are the direct spectroscopic characterization of the ionic intermediates and the systematic variation of those reaction conditions which are relevant for the ion pair structures. By controlling the regioselectivity as well as the formation of cyclized/non-cyclized and monomeric/polymeric products one can substantially improve on the synthesis of several acenaphthylene derivatives.
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Dissertations / Theses on the topic "Acenaphthylene"

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Yuan, Bingxin. "Acenaphthylene Based CP-PAH Materials for Organic Semiconductors." OpenSIUC, 2016. https://opensiuc.lib.siu.edu/dissertations/1233.

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Organic-based electronic devices have received considerable attention because of their presumable advantages over traditional inorganic-based electronics, such as low cost, flexibility, and applicability for large area production. Because of the possible commercialization of electronic products based on organic conducting materials, it is important to develop a variety of organic semiconductors (OSCs) that are categorized as hole transporting (p-type), electron-transporting (n-type) or ambipolar transporting (both hole and electron). P-type OSCs have been the most thoroughly studied. N-type s
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Diamond, Louise M. "Synthetic, structural and spectroscopic studies of peri-substituted systems and their complexes." Thesis, University of St Andrews, 2014. http://hdl.handle.net/10023/6135.

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The family of polycyclic aromatic hydrocarbons naphthalene, acenaphthene and acenaphthylene, containing rigid organic backbones, allow the study of non-bonded intramolecular interactions. Due to the rigid framework, heteroatoms that are substituted at the peri-positions (positions 1- and 8- of the naphthalene ring and positions 5- and 6- of the acenaphthene and acenaphthylene rings) are forced to occupy space that is closer than the sum of their van der Waals radii, resulting in severe steric strain and unique interactions. In spite of this, a vast amount of peri-substituted naphthalenes have
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Yongfeng, Lin, and 林永峯. "Simplified Numerical Simulation of Acenaphthylene Decomposition in a Plasma Reactor by Computational Fluid Dynamics Method." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/98433467015897767887.

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碩士<br>國立屏東科技大學<br>環境工程與科學系所<br>100<br>The United States Environmental Protection Agency （US EPA） ranked acenaphthylene （Acpy） as 16 among polycyclic aromatic hydrocarbons （PAHs） in terms of priority air pollutants. Despite the use of plasma technology in recent years to treat and decompose toxic compounds, power consumption costs during plasma operations are prohibitively high. Reducing plasma operational costs and validating the destructive efficiency of toxic compounds by using plasma are thus of priority concern. This study simulated an atmospheric plasma reactor by using a method based on
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Po-WeiLin and 林柏緯. "Palladium-Catalyzed Annulation: Attempts to Synthesize Acenaphthylene Derivatives and Fragment of Defect Structure in Carbon Nanotubes." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/84xuz9.

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Books on the topic "Acenaphthylene"

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Banisaukas, John James. Photodissociation of the acenaphthene, acenaphthylene, and benzofluorene cations. 2003.

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Book chapters on the topic "Acenaphthylene"

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Winkelmann, J. "Diffusion of acenaphthylene (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_924.

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Cabaness, W. R., S. A. Zamzam, and C. T. Chen. "Exciton Migration in Copolymers of Acenaphthylene." In ACS Symposium Series. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0358.ch027.

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Wohlfarth, Ch. "Partial specific volume of poly(acenaphthylene)." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_164.

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Wohlfarth, Ch. "Second virial coefficient of poly(acenaphthylene)." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_346.

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Vogt, J. "743 C12H8 Acenaphthylen." In Asymmetric Top Molecules. Part 3. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_165.

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"ACENAPHTHYLENE." In Groundwater Chemicals Desk Reference. CRC Press, 2007. http://dx.doi.org/10.1201/9781420009132-8.

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Lin, W. C., and Y. T. Wu. "From Acenaphthylene." In Monocyclic Arenes, Quasiarenes, and Annulenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-01101.

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"acenaphthylene, n." In Oxford English Dictionary, 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/7521764898.

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"Photochemical Dimerization of Acenaphthylene and Related Compounds." In CRC Handbook of Organic Photochemistry and Photobiology, Volumes 1 & 2. CRC Press, 2003. http://dx.doi.org/10.1201/9780203495902-27.

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Tominaga, Y. "From 3,4,7,8-Tetrahydro-8b,8c-diazacyclopenta[]acenaphthylene." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01747.

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Conference papers on the topic "Acenaphthylene"

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Semenikhin, A. S., A. S. Savchenkova, I. V. Chechet, S. G. Matveev, M. Frenklach, and A. M. Mebel. "BRIDGING NUCLEATION REACTIONS BETWEEN ACENAPHTHYLENE AND NAPHTHALENE: A THEORETICAL STUDY." In 9TH INTERNATIONAL SYMPOSIUM ON NONEQUILIBRIUM PROCESSES, PLASMA, COMBUSTION, AND ATMOSPHERIC PHENOMENA. TORUS PRESS, 2020. http://dx.doi.org/10.30826/nepcap9a-09.

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The formation of soot during combustion of hydrocarbon fuels is a rather complex process and one of its stages is nucleation. In recent years, the physical mechanism that takes into account the appearance of the initial soot nuclei has been increasingly studied. The main ideas and disadvantages of this mechanism were recently considered by M. Frenklach and A. Mebel, who also proposed a new chemical nucleation mechanism for pyrene dimerization.
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