Academic literature on the topic 'Dibenzo'

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Journal articles on the topic "Dibenzo"

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Zhu, Xiu Hua, Cheng Zhi Zhou, Ran Ran, Zhen Wang, Xin Dong Ma, and Xiao Xiao Li. "Levels and Distributions of Six Toxic PAHs in the Urban Air of Dalian, China During Heating Periods." Advanced Materials Research 518-523 (May 2012): 2572–75. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.2572.

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Superscript text Superscript textThe concentration of six potential carcinogenic compounds (3-Methylcholanthrene, Dibenz(a,h)acridine, Dibenz(a,i)acridine, Dibenzo(a,e)pyrene, Dibenzo(a,h)pyrene, Dibenzo(a,i)pyrene ) in the urban air of Dalian, China were monitored from November 2009 to March 2010 with active high-volume sampler. They were detected in gaseous phase and particulate phase, respectively. The total concentration of them was 563.2 pg m-3, and they were mainly found in particulate phase with the concentration of 540.5 pg m-3 while the concentration in the gas phase only was 22.7 pg
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Tucker, Sheryl A., William E. Acree, and Christopher Upton. "Polycyclic Aromatic Nitrogen Heterocycles. Part V: Fluorescence Emission Behavior of Select Tetraaza- and Diazaarenes in Nonelectrolyte Solvents." Applied Spectroscopy 47, no. 2 (1993): 201–6. http://dx.doi.org/10.1366/0003702934048235.

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Fluorescence emission spectra are reported for tricycloquinazoline, dibenzo[c,f][2,7]naphthyridine, dibenzo[a,c]phenazine, dibenz[b,h]-indeno[1,2,3de][1,6]naphthyridine, and dibenz[c,f]indeno[l,2,3ij]-[2,7]naphthyridine dissolved in organic nonelectrolyte solvents of varying polarity and acidity. Results of these experiments were used to screen PANHs for potential probe character. The effect of nitromethane as a selective quenching agent on both the unprotonated and protonated PANHs was also examined. Nitromethane was found to quench fluorescence emission of dibenzo[c,f][2,7]naphthyridine. Emi
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Amszi, Vicki L., Yvonne Cordero, Bradley Smith, et al. "Spectroscopic Investigation of Fluorescence Quenching Agents: Effect of Nitromethane on the Fluorescence Emission Behavior of Select Cyclopenta-PAH, Aceanthrylene, and Fluorene Derivatives." Applied Spectroscopy 46, no. 7 (1992): 1156–61. http://dx.doi.org/10.1366/0003702924124213.

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Nitromethane is examined as a selective fluorescence quenching agent for “alternant” alkyl-substituted polycyclic aromatic hydrocarbons (PAHs). Fluorescence emission behavior is reported for 11 H-benz[bc]aceanthrylene, 4 H-cyclopenta[def]phenanthrene, 4 H-cyclopenta[def]chrysene, 13 H-dibenzo[a,g]fluorene, 13 H-dibenzo[a,i]fluorene, 4 H-benzo[b]cyclopenta[mno]chrysene, 4 H-cyclopenta[pqr]picene, 7 H-dibenzo[c,g]fluorene, 9 H-benz(6,7)indeno[1,21]phenanthrene, 4 H-benzo[b]cyclopenta[jkl]triphenylene, 13 H-dibenz[bc,k]aceanthrylene, 13 H-dibenz[bc,l]aceanthrylene, and 4 H-benzo[def]cyclopenta[mn
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Payili, Nagaraju, Santhosh Reddy Rekula, Anjaiah Aitha, V. V. S. R. N. Anji Karun Mutha, Challa Gangu Naidu, and Satyanarayana Yennam. "Synthesis of dibenzo[a,d]cycloheptanoids via aryne insertion into 2-arylidene-1,3-indandiones." Organic & Biomolecular Chemistry 17, no. 43 (2019): 9442–46. http://dx.doi.org/10.1039/c9ob01900f.

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Krawczyk, Hanna. "Dibenzo[b,f]oxepine Molecules Used in Biological Systems and Medicine." International Journal of Molecular Sciences 24, no. 15 (2023): 12066. http://dx.doi.org/10.3390/ijms241512066.

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In this short review, including 113 references, issues related to dibenzo[b,f]oxepine derivatives are presented. Dibenzo[b,f]oxepine scaffold is an important framework in medicinal chemistry, and its derivatives occur in several medicinally relevant plants. At the same time, the structure, production, and therapeutic effects of dibenzo[b,f]oxepines have not been extensively discussed thus far and are presented in this review. This manuscript addresses the following issues: extracting dibenzo[b,f]oxepines from plants and its significance in medicine, the biosynthesis of dibenzo[b,f]oxepines, th
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Dastan, Arif, Nurullah Saracoglu, and Haydar Kilic. "The Dibenzosuberenone Scaffold as a Privileged Substructure: From Synthesis to Application." Synthesis 50, no. 03 (2017): 391–439. http://dx.doi.org/10.1055/s-0036-1589518.

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Numerous studies on dibenzosuberenones, especially on 5-dibenzosuberenones, have emerged in recent years. This review focuses on the chemistry of dibenzosuberenones, including their synthesis and applications, which are currently used as tools by the synthetic and biological communities.1 Introduction2 5-Dibenzosuberenone (5H-Dibenzo[a,d]cyclohepten-5-one)2.1 Synthesis of 5-Dibenzosuberenone2.2 Reactions of 5-Dibenzosuberenone3 5H-Dibenzo[a,c]cyclohepten-5-one3.1 Synthesis of 5H-Dibenzo[a,c]cyclohepten-5-one3.2 Reactions of 5H-Dibenzo[a,c]cyclohepten-5-one4 6H-Dibenzo[a,c]cyclohepten-6-one and
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Maier, David Irving Hermann, Barend Christiaan Buurman Bezuidenhoudt, and Charlene Marais. "Strategies in the synthesis of dibenzo[b,f]heteropines." Beilstein Journal of Organic Chemistry 19 (May 22, 2023): 700–718. http://dx.doi.org/10.3762/bjoc.19.51.

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The dibenzo[b,f]azepine skeleton is important in the pharmaceutical industry, not only in terms of existing commercial antidepressants, anxiolytics and anticonvulsants, but also in reengineering for other applications. More recently, the potential of the dibenzo[b,f]azepine moiety in organic light emitting diodes and dye-sensitized solar cell dyes has been recognised, while catalysts and molecular organic frameworks with dibenzo[b,f]azepine derived ligands have also been reported. This review provides a brief overview of the different synthetic strategies to dibenzo[b,f]azepines and other dibe
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Bremner, JB, та W. Jaturonrusmee. "Manganese(III) Acetate-Induced Formation of a Fused, Chloro-Substituted β-Lactam Derivative From a Chloroacetamide". Australian Journal of Chemistry 43, № 8 (1990): 1461. http://dx.doi.org/10.1071/ch9901461.

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Reaction of 1-chloroacetyl-5-methoxy-2,3-dihydro-1H-dibenzo[de,h]quinoline (1) with manganese(III) acetate in acetic acid at 50° gave the novel fused spiro derivative 11-chloro-4-methoxy-1,2-dihydro-6H-azeto[2,1-f]dibenzo[de,h]quinoline-6,12(11H)-dione (6) in 21% yield, together with 5-methoxy-7H-dibenzo[de,h]quinolin-7-one (3), 5-methoxy-2,3-dihydro-7H-dibenzo[de,h]quinolin-7-one (4), and 1- chloroacetyl-5-methoxy-2,3-dihydro-1H-dibenzo[de,h]-quinolin-7-yl ethanoate (5) in 1, 3 and 44% yields respectively. Compound (5) was shown to be a precursor of (3), (4) and (6).
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Gao, Xingbao, Bingjing Ji, Dahai Yan, Qifei Huang, and Xuemei Zhu. "A full-scale study on thermal degradation of polychlorinated dibenzo-p-dioxins and dibenzofurans in municipal solid waste incinerator fly ash and its secondary air pollution control in China." Waste Management & Research: The Journal for a Sustainable Circular Economy 35, no. 4 (2016): 437–43. http://dx.doi.org/10.1177/0734242x16677078.

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Degradation of polychlorinated dibenzo- p-dioxins and dibenzofurans in municipal solid waste incinerator fly ash is beneficial to its risk control. Fly ash was treated in a full-scale thermal degradation system (capacity 1 t d−1) to remove polychlorinated dibenzo- p-dioxins and dibenzofurans. Apart from the confirmation of the polychlorinated dibenzo- p-dioxin and dibenzofuran decomposition efficiency, we focused on two major issues that are the major obstacles for commercialising this decomposition technology in China, desorption and regeneration of dioxins and control of secondary air pollut
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Matsubara, Hiroshi, Mitsunobu Osatani, Koji Yano, Tomohiro Adachi, and Koji Yamamoto. "Synthesis and Characterisation of [2.2](5,13)Dibenzo[c;1]chrysenophane." Journal of Chemical Research 23, no. 1 (1999): 12–13. http://dx.doi.org/10.1177/174751989902300112.

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High-dilution coupling of 5,13-bis(bromomethyl)dibenzo[ c;1]chrysene (7) and 5,13-bis(sulfanylmethyl)dibenzo[ c;1]-chrysene 8 afforded the dithia derivative 9 which was converted, via the disulfone 10, into an unusually strained compound, [2.2](5,13)dibenzo[ c;1]chrysenophane 5.
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Dissertations / Theses on the topic "Dibenzo"

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Joseph-Charles, Julienne. "Etudes chromatographiques et spectrophotométriques de molécules tricycliques dibenzo- et pyridobenzo- cycloheptaatomiques." Bordeaux 2, 1992. http://www.theses.fr/1992BOR2E004.

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Ebert, Jörg. "Untersuchungen zur Optimierung der Analytik der polybromierten Dibenzo-p-dioxine und Dibenzofurane." [S.l. : s.n.], 1998. http://deposit.ddb.de/cgi-bin/dokserv?idn=955472636.

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Chatkittikunwong, Watcharee. "Analytical synthesis and stability studies of halogenated dibenzo-p-dioxins and dibenzofurans." Thesis, University of East Anglia, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335138.

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Wessels, Hanlie R. "Dibenzo-30-crown-10: Synthetic optimization and studies of the binding conformation." Diss., Virginia Tech, 2018. http://hdl.handle.net/10919/95205.

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Dibenzo-30-crown-10 (DB30C10) is one of the first-generation macrocyclic hosts discovered by Pedersen. Crown ethers originally attracted attention due to their ability to encapsulate metal cations and render them soluble in organic solvents. These studies helped to launch host-guest chemistry as a discipline within supramolecular chemistry. Crown ethers form complex molecules containing organic cations and neutral organic molecules. Additionally, they form components in supramolecular architectures such as catenanes, rotaxanes, and supramolecular polymers. They have been used as selective host
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Memetzidis, Georgios. "Pharmacochimie de la tetrahydro-5,6,13,13a 8h-dibenzo (a, g) quinolizine ou berbine." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13159.

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Palamede, Audrey. "Stabilization of chlorinated dibenzo-p-dioxins, dibenzofurans and chlordecone in soils from three former industrial areas. : Leaching behavior of chlorinated dibenzo-p-dioxins, dibenzofurans and chlordecone from three soils." Thesis, Umeå universitet, Kemiska institutionen, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-163550.

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Poblete, González Cristián Ignacio. "Estudio de las especies transientes generadas durante la fotorreducción por aminas de oxoisoaporfinas : 5-metoxi-7H-dibenzo[de,h]quinolin-7-ona y 7H-dibenzo[de,h]quinolin-7-ona." Tesis, Universidad de Chile, 2007. http://repositorio.uchile.cl/handle/2250/105633.

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Memoria para optar al título de Químico Farmacéutico<br>Los sistemas fotosintéticos naturales y artificiales en los cuales la energía de la luz es colectada y almacenada como energía química, es un proceso de conversión que es iniciado con la transferencia fotoinducida de un electrón, que es seguida por otras etapas químicas que permiten la separación y estabilización cinética de los llamados “sistemas de carga separada”. Este es el caso de las 7H-dibenzo[de,h]quinolin-7-onas, conocidas como oxoisoaporfinas, que al ser fotorreducidas en presencia de aminas generan fotoproductos iónicos
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Schmidt, Eva. "Duplikatstudie zur alimentären Aufnahme von polychlorierten Dibenzo-p-dioxinen und Dibenzofuranen bei Kindern." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=963979094.

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Disse, Gerhard. "Bilanzierung von polychlorierten Dibenzo-p-dioxinen und Dibenzofuranen bei der Fermentierung von Klärschlamm /." Inhaltsverzeichnis, 1997. http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&doc_number=007734926&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA.

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Akki, Umesh. "Gas phase formation pathways and mechanisms of polychlorinated dibenzo-p-dioxins and dibenzofurans." Diss., Georgia Institute of Technology, 1998. http://hdl.handle.net/1853/23157.

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Books on the topic "Dibenzo"

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Dibenzo-p-dioxinas policloradas. Agencia para Sustancias Tóxicas y el Registro de Enfermedades, División de la Toxicología, Departamento de Salud y Servicios Humanos de los EE.UU., Servicio de Salud Pública, 1998.

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Chlorinated dibenzo-p-dioxins (CDDs). U.S. Dept. of Health and Human Services, Agency for Toxic Substances and Disease Registry, 1998.

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C, Melber, Kielhorn J, WHO Task Group on Environmental Health Criteria for Polybrominated Dibenzo-p-Dioxins and Dibenzofurans., et al., eds. Polybromated dibenzo-p-dioxins and dibenzofurans. World Health Organization, 1998.

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Humans, IARC Working Group on the Evaluation of Carcinogenic Risks to. Polychlorinated dibenzo-para-dioxins and polychlorinated dibenzofurans. IARC Press, 1997.

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United States. Environmental Protection Agency. Environmental Criteria and Assessment Office (Cincinnatti, Ohio), ed. Health assessment document for polychlorinated dibenzo-p-dioxins. U.S. Environmental Protection Agency, Office of Research and Development, Office of Health and Environmental Assessment, Environmental Criteria and Assessment Office, 1985.

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United States. Environmental Protection Agency. Office of Health and Environmental Assessment, ed. Health assessment document for polychlorinated dibenzo-p-dioxins. U.S. Environmental Protection Agency, Office of Health and Environmental Assessment, 1988.

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Ontario. Ministry of the Environment., ed. Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs). Ontario Ministy of the Environment, 1985.

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Ontario. Ministry of the Environment., ed. Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs). Ontario Ministy of the Environment, 1985.

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Canada. Commercial Chemicals Evaluation Branch. Polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans: Scientific justification. Environment Canada, 1997.

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Sheffield, Arthur. Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs): Sources and releases. Environmental Protection Service, 1985.

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Book chapters on the topic "Dibenzo"

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Kannan, Kurunthachalam, Chunyang Liao, and Hyo-Bang Moon. "Polybrominated Dibenzo-P-Dioxins and Dibenzofurans." In Dioxins and Health. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118184141.ch9.

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Demaison, J. "116 C20H10 Dibenzo[ghi,mno]fluoranthene." In Symmetric Top Molecules. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-47532-3_118.

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Hemming, Jarl, Bjarne Holmbom, and Bengt Larsson. "Formation of Chlorinated dibenzo-p-dioxins and Dibenzo Furans during Chlorination of Aquatic Humic Substances." In Organic Micropollutants in the Aquatic Environment. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3356-2_64.

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Stringer, Ruth, and Paul Johnston. "Polychlorinated dibenzo-p-dioxins, dibenzofurans and related compounds." In Chlorine and the Environment. Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-015-9813-2_12.

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Adriaens, P., A. L. Barkovskii, M. Lynam, J. Damborský, and M. Kutý. "Polychlorinated Dibenzo-p-Dioxins in Anaerobic Soils and Sediments." In Biodegradability Prediction. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-5686-8_6.

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Fiedler, Heidelore. "Release Inventories of Polychlorinated Dibenzo-p-Dioxins and Polychlorinated Dibenzofurans." In The Handbook of Environmental Chemistry. Springer International Publishing, 2015. http://dx.doi.org/10.1007/698_2015_432.

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Damborsky, Jirí, Mary Lynam, and Michal Kuty. "Structure-Biodegradability Relationships for Chlorinated Dibenzo-p-Dioxins and Dibenzofurans." In Biodegradation of Dioxins and Furans. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-662-06068-1_7.

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Hanf, V., W. Körner, A. Faust, et al. "Konzentrationen polychlorierter Dibenzo-p-dioxine und Dibenzofurane in menschlichem Nabelschnurgewebe." In Gynäkologie und Geburtshilfe 1992. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77857-5_652.

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Parsons, John R., and Merel Toussaint. "Microbial Degradation of Polychlorinated Dibenzo-p-dioxins and Polychlorinated Dibenzofurans." In ACS Symposium Series. American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2001-0772.ch013.

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Echner, H., and W. Voelter. "Application of the 10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5-yl (5H-dibenzo-suberyl, Sub) and 5H-dibenzo[a,d]-cyclohepten-5-yl (5H-dibenzosuberenyl, Dbs) groups for thiol protection in Fmoc solid phase peptide chemistry." In Peptides 1994. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_61.

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Conference papers on the topic "Dibenzo"

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Brebels, Sonny, Tom Cardeynaels, Louis Jackers, et al. "Isomeric modulation of thermally activated delayed fluorescence properties in dibenzo[a,c]phenazine-based (deep) red emitters." In Organic and Hybrid Light Emitting Materials and Devices XXVIII, edited by Tae-Woo Lee, Franky So, and Ji-Seon Kim. SPIE, 2024. http://dx.doi.org/10.1117/12.3027330.

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S.L., Summoogum, Dlugogorski B.Z., Altarawneh M., Mackie J.C., and Kennedy E.M. "Decomposition of Dibenzo–p–Dioxin in Fires." In Sixth International Seminar on Fire and Explosion Hazards. Research Publishing Services, 2011. http://dx.doi.org/10.3850/978-981-08-7724-8_11-03.

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Gunasekaran, Suman, Xiushang Xu, Scott Renken, et al. "Electronic excitation dynamics of dibenzo [a,i] pyrene oligomers." In Physical Chemistry of Semiconductor Materials and Interfaces XXI, edited by Andrew J. Musser and Derya Baran. SPIE, 2022. http://dx.doi.org/10.1117/12.2636030.

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Marra, Giacomo, Marco Bortoluzzi, and Lodovico Agostinis. "One-Pot Synthesis of Phosphoramidates from dibenzo[1,3,2]dioxaphosphepine-6-oxide." In ECSOC 2023. MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16174.

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Zimmermann, Ralf. "Dibenzo-p-dioxin and its chlorinated congeners: Molecular geometry and electronic structure." In The ninth international symposium on resonance ionization spectroscopy:New directions and applications. AIP, 1998. http://dx.doi.org/10.1063/1.57186.

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Jeyabalan, Jeyaprakash, Farrukh Aqil, Srivani Ravoori, Manicka V. Vadhanam, and Ramesh C. Gupta. "Abstract 5557: Steady DNA adduct accumulation by dibenzo[a,l]pyrene implants." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-5557.

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Bonati, L., E. Fraschini, M. Lasagni, U. Cosentino, G. Moro, and D. Pitea. "Electrostatic descriptors in relation to biological activity of some chlorinated dibenzo-p-dioxins." In Advances in biomolecular simulations. AIP, 1991. http://dx.doi.org/10.1063/1.41317.

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Bonati, Laura, Emanuela Palma Modoni, Elena Fraschini, and Demetrio Pitea. "The local softness in the study of polychlorinated dibenzo-p-dioxin biological activity." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47832.

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Lu, Gui-Ning, Xue-Qin Tao, and Zhi Dang. "Theoretical Indicators for Proposing Reductive Dechlorination Pathways of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans." In 2011 International Conference on Computer Distributed Control and Intelligent Environmental Monitoring (CDCIEM). IEEE, 2011. http://dx.doi.org/10.1109/cdciem.2011.415.

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Wurrey, Charles J., Billy J. Fairless, and Harry E. Kimball. "Analysis Of Halogenated Dibenzo-P-Dioxins And Dibenzofurans Using Matrix Isolation GC/FT-IR." In Intl Conf on Fourier and Computerized Infrared Spectroscopy, edited by David G. Cameron. SPIE, 1989. http://dx.doi.org/10.1117/12.969443.

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Reports on the topic "Dibenzo"

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Leckey, J. H. Polychlorinated dibenzo-p-dioxin and polychlorinated dibenzofuran formation and emission in the thermal desorption waste treatment process. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/290997.

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Huszthy, P., J. S. Bradshaw, C. Y. Zhu, T. Wang, and R. M. Izatt. Recognition of the Enantiomers of Chiral Organic Ammonium Salts by Chiral Dibenzyl- and Diphenyl-Substituted Diamido-or Dithionoamidopyridino-18- crown-6 Ligands. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada248026.

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Synthesis of 6-Methyl-9-n-propyldibenzo thiophene-4-ol ammended to 6-Methyl-9-(1-methylethyl)-dibenzo thiophene-4-ol. Quarterly technical progress report No. 6, October 28, 1991--January 26, 1992. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10158452.

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