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1

Hisham, El-Masri, United States. Agency for Toxic Substances and Disease Registry., United States. Environmental Protection Agency., and Syracuse Research Corporation, eds. Toxicological profile for naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances and Disease Registry, 2005.

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2

United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances Disease Registry, Division of Toxicology, Dept. of Health and Human Services, Public Health Service, 2005.

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3

United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Naftalina, 1-metilnaftalina y 2-metilnaftalina. 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, 2005.

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4

Antsyforov, Gleb I., and Alyona F. Ivanski. Napthalene: Structure, properties, and applications. Nova Science Publishers, 2011.

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5

D, Nitterauer James, and United States. Environmental Protection Agency, eds. Biotransformation of benzothiophene by isopropylbenzene-degrading bacteria. Environmental Protection Agency], 1994.

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6

Nii͡azov, A. N. Naftenaty. Ylym, 1992.

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7

United States. Environmental Protection Agency. Emissions Standards and Engineering Division. and United States. Environmental Protection Agency. Office of Air Quality Planning and Standards., eds. Summary of emissions associated with sources of naphthalene. U.S. Environmental Protection Agency, 1986.

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8

Kreutz, Martin. Halogen-Metall-Austausch bei Bromnaphthalinen: Synthese, Struktur, und Reaktionsweisen mono- und polylithiierter Naphthaline. A.S. Intemann, 1991.

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9

Humans, IARC Working Group on the Evaluation of Carcinogenic Risks to. Some traditional herbal medicines, some mycotoxins, naphthalene and styrene. IARC Press, 2002.

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10

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

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11

National Toxicology Program (U.S.). NTP technical report on the toxicology and carcinogenesis studies of methyl bromide (CAS no. 74-83-9) in B6C3F1 mice (inhalation studies). U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1992.

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12

Joshi, Harshad. Investigation of the catabolic plasmid involvement in naphthalene-degrading strains of Pseudomonas spp.. University of Wolverhampton, 1995.

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13

Haveman, S. A. Biodegradation of a sodium sulphonated naphthalene formaldehyde condensate by bacteria naturally present in granitic groundwater. AECL, Whiteshell Laboratories, 1996.

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14

C, D'Adamo Peter, Bouwer Edward J, and National Risk Management Research Laboratory (U.S.), eds. Bioremediation of BTEX, naphthalene, and phenanthrene in aquifer material using mixed oxygen/nitrate electron acceptor conditions: Project summary. U.S. Environmental Protection Agency, National Risk Management Research Laboratory, 1997.

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15

BV, Hoogovens Groep, and Commission of the European Communities. Directorate-General Energy., eds. The development and implementation of continuous and automated measurement of total sulphur, NH3 and naphthalene of purified coke oven gas: Final report. Commission of the European Communities, 1990.

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16

Crookes, M. J. Enviromental hazard assessment: Halogenated naphthalenes. BuildingResearch Establishment, 1993.

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17

Dordanas, Stratos N. Hē germanikē stolē stē naphthalinē: Epiviōseis tou dosilogismou stē Makedonia, 1945-1974. Vivliōpoleion tēs Hestias, 2011.

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18

Reindl, Michael. Untersuchungen zur metabolischen Bildung und enzymatischen Kontrolle von Chinonen polyzyklischer armonatischer Kohlenwasserstoffe am Beispiel von Naphthalin, Chrysen und Benzo[[alpha]]pyren. [s.n.], 1996.

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19

qızı, Sadıqova Sayalı Allahverdi, and Azärbaycan Milli Elmlär Akademiyası. Terminologiya Komissiyası., eds. Terminologiya mäsäläläri. Elm, 2005.

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20

Naphthalene. VCH, 1992.

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21

Chlorinated naphthalenes. World Health Organization, 2001.

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22

Chlorinated Naphthalenes (Concise International Chemical Assessment Document). World Health Organization, 2003.

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23

Biotransformation of benzothiophene by isopropylbenzene-degrading bacteria. Environmental Protection Agency], 1994.

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24

Toxicological profile for naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene: Draft. The Agency, 1993.

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25

Summary review of health effects associated with naphthalene. Environmental Criteria and Assessment Office, Office of Health and Environmental Assessment, Office of Research and Development, U.S. Environmental Protection Agency, 1988.

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26

Etheridge, Herbert Thomas. Time-resolved measurements of vibrational predissociation in naphthalene-X molecules. 1993.

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27

Harris, Daniel C. Determining Molar Mass by Freezing-Point Depression in Naphthalene. Chemical Education Resources, 1998.

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28

Jones, Timothy J. The solubility of naphthalene in supercritical carbon dioxide: A comparison of the compressed-gas and expanded-liquid treatments. 1986.

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29

Draft toxicological profile for naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances and Disease Registry, 2003.

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30

Berry, Thomas Morris. Alkylation of Benzene, Toluene and Naphthalene and the Chorlination of Acetylene. Creative Media Partners, LLC, 2022.

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31

Berry, Thomas Morris. Alkylation of Benzene, Toluene and Naphthalene and the Chorlination of Acetylene. Creative Media Partners, LLC, 2022.

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32

Chen, Arthur Ming-Jing. The effect of growth conditions on the faceting behaviour of naphthalene and azobenzene. 1985.

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33

Arpe, Hans-Jürgen. Naphthalene and Hydronaphthalenes to Nuclear Technology, Volume A17, Ullmann's Encyclopedia of Industrial Chemistry. 5th ed. Wiley-VCH, 1991.

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34

Personette, William K. A spectroscopic investigation of matrix isolated radical cations of para-dichlorobenzene, para-dimethoxybenzene, and naphthalene. 1993.

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35

(Contributor), WHO, ed. Some Traditional Herbal Medicines, Some Mycotoxins, Naphthalene, and Styrene (Iarc Monographs on the Evaluation of Carcinogenic Risks to Humans). World Health Organisation, 2002.

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36

Elvers, Barbara, and Stephen Hawkins. Ullmann's Encyclopedia of Industrial Chemistry: Naphthalene to Nuclear Technology/Volume A (Ullmann's Encyclopedia of Industrial Chemistry 5th ed Vol a). 5th ed. John Wiley & Sons Ltd (Import), 1991.

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37

The Development and Implementation of Continuous and Automated Measurement of Total Sulphur, [-]NH3[-] and Naphthalene of Purified Coke Oven Gas. European Communities / Union (EUR-OP/OOPEC/OPOCE), 1990.

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38

Eland, John H. D., and Raimund Feifel. Conjugated and aromatic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0006.

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In the vast majority of conjugated and aromatic molecules, the outermost occupied orbitals are either of π‎ character or non-bonding lone pairs belonging to heteroatoms. These are the orbitals from which double ionisation gives rise to most of the distinct bands that can be discerned in their spectra. Double photoionisation spectra of ethylene, butadiene, pyrrole, furan, thiophene, benzene, hexafluorobenzene, toluene, pyridine, pyrazine, pyrimidine, pyridazine, naphthalene, azulene, quinoline, biphenyl, TDME, iron pentacarbonyl, ferrocene, and TMPPD are presented with analysis where possible.
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39

Halogenated Biphenyls, Terphenyls, Naphthalenes, Dibenzodioxins and Related Products. Elsevier, 1989. http://dx.doi.org/10.1016/c2009-0-12642-9.

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40

Halogenated biphenyls, terphenyls, naphthalenes, dibenzodioxins, and related products. 2nd ed. Elsevier, 1989.

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41

Kimbrough, R. D., and A. A. Jensen. Halogenated Biphenyls, Terphenyls, Naphthalenes, Dibenzodioxins and Related Products. Elsevier Science & Technology Books, 2012.

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42

The actions and uses of naphthalin. s.n., 1986.

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43

Harden, Arthur, Carl Schorlemmer, and Harold Govett Colman. A Treatise on Chemistry. Arkose Press, 2015.

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44

Roscoe, Henry E., and Carl Schorlemmer. A Treatise On Chemistry: Metals. Arkose Press, 2015.

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45

Rieble, Anke. Beiträge zur Synthese des Dicyclopenta[b,g]naphthalins und des 2,2'-Bipentalens. 1999.

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46

Hē germanikē stolē stē naphthalinē: Epiviōseis tou dosilogismou stē Makedonia, 1945-1974. Vivliōpoleion tēs Hestias, 2011.

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47

Kind, Lothar Franz. Intramolekulare C-H-Aktivierung von 1-substituierten Naphthalenen: Cyclopalladierung von 1-Naphthylamin-Derivaten und anschliessende Alkylierung. 1997.

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48

Kämmerling, Heinz-Theo. Dien-Addukte an die Naphthalin-[b]-Bindung: Neue o-Chinodimethane mit interessanten Eigenschaften. 1989.

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49

Breisgau, Universität Freiburg im, ed. Untersuchungen über den Resonanz-Ramaneffekt an Anthracen, Naphthalin und p-nitro,-p-dimethylamino-azobenzol. 1986.

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50

Steinfeldt, Wieland. Kationische Cyclopentadienyleisen(II)-, Cyclopentadienyl-ruthenium(II)- und Pentamethylcyclopentadienylruthenium(II)-Naphthalinkomplexe mit alkyl- und alkoxysubstituierten Naphthalinen. 1992.

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