Relevant bibliographies by topics / Naphthalenol

Contents

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

Academic literature on the topic 'Naphthalenol'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Naphthalenol"

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Zhang, Wang, Xinye Zhao, Weijing Gu, et al. "A novel naphthalene-based fluorescent probe for highly selective detection of cysteine with a large Stokes shift and its application in bioimaging." New Journal of Chemistry 42, no. 22 (2018): 18109–16. http://dx.doi.org/10.1039/c8nj04425b.

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An efficient naphthalene-based fluorescent probe (BTNA) for cysteine (Cys) has been rationally designed and synthesized in this work, which consists of a 6-(2-benzothiazolyl)-2-naphthalenol (BNO) fluorophore connected with an acrylate group (the fluorescence quenching and response group).
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Rojas, Janne, Alexis Buitrago, Luis B. Rojas, Antonio Morales, and Shirley Baldovino. "Chemical Composition of the Essential Oil of Leaves and Roots of Ottoa oenanthoides (Apiaceae) from Mérida, Venezuela." Natural Product Communications 5, no. 7 (2010): 1934578X1000500. http://dx.doi.org/10.1177/1934578x1000500728.

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Essential oils extracted by hydrodistillation from leaves and roots of Ottoa oenanthoides Kunth (Apiaceae) were analyzed by GC/MS. The oils, obtained in yields of 0.10% and 0.66%, respectively, each contained four compounds, which were identified from their mass spectra and retention indices (RI). The major compound identified was 2-methoxy-8-methyl-1,4-naphthalindione (59.9% leaves, and 62.8%, roots), followed by 7-methoxy-1-naphthol (18.3% leaves and 17.3% roots), 2-naphthalenol (18.6% leaves and 15.0% roots), and 3-methoxy-2-naphthalenol (3.1% leaves and 2.1% roots). To the best of our know
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Marciniak, Bernard, Ewa Rozycka-Sokolowska, and Volodymyr Pavlyuk. "2-Naphthalenol." Acta Crystallographica Section E Structure Reports Online 59, no. 1 (2002): o52—o53. http://dx.doi.org/10.1107/s1600536802022808.

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Rozycka-Sokolowska, Ewa, Bernard Marciniak, and Volodymyr Pavlyuk. "Redetermination of 1-naphthalenol." Acta Crystallographica Section E Structure Reports Online 60, no. 5 (2004): o884—o885. http://dx.doi.org/10.1107/s1600536804009225.

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Pickering, R. E., D. L. Bymaster, and E. J. Eisenbraun. "Synthesis of 1,2,3,4-tetrahydronaphthalene-1-13C, naphthalene-1-13C, and 1-naphthalenol-1-13C." Journal of Labelled Compounds and Radiopharmaceuticals 22, no. 11 (1985): 1149–54. http://dx.doi.org/10.1002/jlcr.2580221107.

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Lauro, Figueroa‐Valverde, Díaz‐Cedillo Francisco, Gobato Ricardo, et al. "Design and synthesis of two Strychnidin‐oxiran‐naphthalenol derivatives and their theoretical evaluation as noradrenaline and serotonin reuptake inhibitors." Vietnam Journal of Chemistry 60, no. 2 (2022): 245–56. http://dx.doi.org/10.1002/vjch.202100128.

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AbstractSeveral agents have been used as biogenic amine reuptake inhibitors for depression such as imipramine, fluoxetine, reboxetine, and others; however, some of these drugs can produce some secondary effects such as tiredness and psychomotor retardation. Analyzing these data, the aim of this study was to synthesize two Strychnidin‐oxiran‐naphthalenol derivatives using some chemical tools. Besides, the theoretical interaction of Strychnin‐oxiran‐naphthalenol derivatives (compounds 7 and 8) as noradrenaline and serotonin reuptake inhibitors was evaluated using two proteins (1ieo and 5i6z) as
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Halton, Brian, Carissa S. Jones, Peter T. Northcote, and Roland Boese. "Studies in the Cycloproparene Series: Formation of a New Dimer of 1H-Cyclopropa[b]naphthalene." Australian Journal of Chemistry 52, no. 4 (1999): 285. http://dx.doi.org/10.1071/c98179.

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1-(Trimethylsilyl)-1H-cyclopropa[b]naphthalene (10) and its 1-methyl derivative (11) have been isolated as pure compounds from use of a lipophilic size exclusion gel. Acylation of the 1H-cyclopropa[b]naphthalenyl anion (2) is effected with N,N -dimethyl-benzamide and -acetamide to give (5) and (6), respectively. Analogous reactions with the 1-(trimethylsilyl)-1H-cyclopropa[b]naphthalenyl anion (9) do not yield the 1-acyl-1-(trimethylsilyl)-1H-cyclopropa[b]naphthalenes (12) and (13); instead the novel 6-methyl- 7H-dibenzo[b,g]fluorene (15) results from attempted acetylation. Compound (15), a fo
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SELVARAJU, K., K. KIRUBAVATHI, and S. KUMARARAMAN. "INVESTIGATION ON THE PHYSICOCHEMICAL PROPERTIES OF NONLINEAR OPTICAL SINGLE CRYSTAL: 2-NAPHTHALENOL." Modern Physics Letters B 23, no. 09 (2009): 1221–27. http://dx.doi.org/10.1142/s0217984909019363.

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Single crystals of 2-Naphthalenol (2N), new organic nonlinear optical (NLO) material, have been grown by slow evaporation solution growth technique at room temperature. The crystal system has been confirmed from the single crystal X-ray diffraction analysis. The functional groups were identified using FTIR spectroscopy. UV-vis-NIR spectrum showed absence of absorption in the wavelength region 400–1400 nm. The second harmonic generation efficiency is two times higher than that of standard potassium dihydrogen phosphate (KDP).
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Jeevalatha, A., R. V. Kalaimathi, Afroze Naveed Basha, et al. "Profile of bioactive compounds in Rosmarinus officinalis." Journal of Drug Delivery and Therapeutics 12, no. 1 (2022): 114–22. http://dx.doi.org/10.22270/jddt.v12i1.5189.

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Plant Based Natural Products (PBNPs) have contributed to the development of drugs for diverse indications. Worldwide interest in use of PBNPs has been growing, and its beneficial effects being rediscovered for the development of drug leads. Literature survey on indigenous traditional knowledge bestows ethnopharmacological potentials of PBNPs, has inspired research in drug design and discovery; PBNPs provide a baseline for the development of novel drug leads against various pharmacological targets. Reports indicate that rosemary essential oil (ROEO) extracts show biological bioactivities such a
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Chen, Xia, Xiao-Yu Zhou, and Ming Bao. "Base-Catalyzed Nucleophilic Addition Reaction of Indoles with Vinylene Carbonate: An Approach to Synthesize 4-Indolyl-1,3-dioxolanones." Molecules 28, no. 21 (2023): 7450. http://dx.doi.org/10.3390/molecules28217450.

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The N-functionalized indole is a privileged structural framework in a wide range of bioactive molecules. The nucleophilic addition between indoles with vinylene carbonate proceeded smoothly in the presence of K2CO3 as the catalyst to produce novel indolyl-containing skeletons and 4-indolyl-1,3-dioxolanones in satisfactory to excellent yields (up to >97% yield). Various synthetically useful functional groups, such as halogen atoms, cyano, nitro, and methoxycarbonyl groups, remained intact during the regioselective N-H addition reactions. The developed catalytic system also could accommodate
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Dissertations / Theses on the topic "Naphthalenol"

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Hibbeln, Kim Sabine. "Effect of kaolinite and cadmium on the biodegradation of naphthalene and substituted naphthalenes." Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=24011.

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The objectives of this study were to look at the effect of kaolinite and cadmium on the biodegradation of naphthalene and substituted naphthalenes. The kaolinite mineral is present in many Quebec soils and is a primary constituent of tropical soils. Since kaolinite is also a well defined mineral, experiments were performed to examine the effect kaolinite might play on the degradation of naphthalene, 2-methyl naphthalene, and 2-naphthol in the presence and absence of cadmium. Furthermore, the results from these analyses were used to interpret the behaviour in the mineralization experiments of e
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Glass, Adam Cameron 1983. "The Synthesis of Novel and Sterically Demanding Tetra-ortho-substituted Aryl Naphthalenes." Thesis, University of Oregon, 2011. http://hdl.handle.net/1794/11978.

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xiv, 326 p. : ill. (some col.)<br>Tetra-ortho -substituted aryl naphthalenes (TOANs) are a motif of great importance, being present in biologically active natural products, chiral ligands, and building blocks relevant to materials science. The synthesis of sterically demanding and enantioenriched TOANs continues to be a challenge for current synthetic methods. Herein, we describe the highly effective synthesis of a variety of sterically demanding and enantioenriched TOANs through a rearrangement-based method. Our method utilizes a cyclopropyl carbinol moiety as the key rearrangement precurs
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Quinn, Samuel. "Colouring naphthalene diimides." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/50038/.

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Naphthalene diimides have been explored in a wide variety of ways; They are a promising candidate for organic electronics, boasting the ability to form n-type semiconductor materials, the stability of their anions further aiding in this regard. Their electron poor aromatic core can be used in host guest chemistry to generate interlocked species. The ability to tune their electronic properties and how this could be manipulated to create photovoltaic devices is primarily focus of this thesis. A series of naphthalene diimides substituted at the core with morpholine moieties have been synthesized
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Swigelaar, Wendell Peter. "The synthesis of 3-allyl-4-ethyl-2- (1'-hydroxyethyl)-1-methoxynaphthalene and its behaviour towards base- and palladium-promoted cyclisation under aerobic and anaerobic conditions." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&amp.

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Over the years, Giles and co-workers have established that, upon treatment with potassium tert-butoxide, tetra-substituted naphthalenes undergo cyclisations to afford naphthopyrans. It was suggested that these base-induced cyclisations was as a result of the reacting centers being forced into close proximity as a consequence of steric crowding.<br /> <br /> This thesis describes the synthesis of 3-allyl-4-ethyl-2-(1&prime<br>-hydroxyethyl)-1-methoxy-naphthalene 177 and its behaviour towards Pd(0) and potassium tert-butoxide under aerobic and anaerobic conditions, to verify whether the base-pro
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Nehls, Benjamin S. "Naphthalene based conjugated materials." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=976731363.

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Kim, Michelle B. "The Hydrolysis of Naphthalene Diimides." Digital Archive @ GSU, 2007. http://digitalarchive.gsu.edu/chemistry_theses/7.

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The hydrolyses of naphthalene diimides (NDIs) bearing aliphatic side chains with N-methylpyrrolidinium groups placed two (1) and three (5) atoms from the central core were studied. The Ka values for the first and second hydrolyses for 1 were 2.5 ± 0.2 x 105 M-1 and 2.0 ± 0.1 x 102 M-1, respectively; for 5 they were 1.4 ± 0.1 x 105 M-1 and 44 ± 2 M-1, respectively. NDI 1 hydrolyzed 6.8 times faster than did 5. The rates for the first and second hydrolyses of 1 at 100 mM hydroxide measured by stopped-flow were 17.0 ± 0.2 s-1 and 53.0 ± 0.1 x 10-2 s-1, respectively. NMR showed both the syn and an
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黃文菁 and Man-ching Wong. "Synthesis of the naturally occurring 1, 2-naphthalenedione, azanzoneA." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1993. http://hub.hku.hk/bib/B31211033.

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Wong, Man-ching. "Synthesis of the naturally occurring 1, 2-naphthalenedione, azanzone A /." [Hong Kong : University of Hong Kong], 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13457093.

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Gubellini, Federico. "Designing heterogeneous catalysts for naphthalene isopropylation." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2020. http://amslaurea.unibo.it/20659/.

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2,6 di-isopropylnaphthalene is a plant growth regulator and it is used for the manufacturing of products intended to prevent sprouting of stored potatoes; despite that in the last decades it has been mainly produced as a precursor of the corresponding dicarboxylic acid (2,6-naphthalene dicarboxylic acid) which is, with ethylene glycol, the monomer for polyethylene naphthalate (PEN) polymerization. PEN results appealing for many uses for which PET is more commonly utilized; the most relevant, higher glass transition temperature (PEN 122°C, PET 80°C), higher Young’s modulus (PEN 5200 MPa, PET 3
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Bakker, M. G. "ESR studies on some naphthalene derivatives." Thesis, University of Canterbury. Chemistry, 1985. http://hdl.handle.net/10092/8639.

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ESR Spectroscopy has been used to study conformational interconversion and addivity relationships in a number of series of naphthalene derivatives. Oscillation of the alkyl rings in 1,2,3,6,7,8-hexahydropyrene ions, and the ions of the related 5, 6 and 7 membered ring compounds has been studied. The temperature dependance of the ESR spectra have been used to assign the coupling constants. The aromatic ring coupling constants in the asymmetric compounds have been assigned on the basis of an additivity relationship. The ESR spectra of a number of methylnaphthalene anions have been recorded and
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Books on the topic "Naphthalenol"

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

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

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

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

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Book chapters on the topic "Naphthalenol"

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Vogt, J. "731 C10H8O 1-Naphthalenol." In Asymmetric Top Molecules. Part 3. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_153.

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Winkelmann, Jochen. "Diffusion coefficient of 1-(2-phenyldiazenyl)-2-naphthalenol in ethanol." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_869.

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Winkelmann, Jochen. "Diffusion coefficient of 1-(2-phenyldiazenyl)-2-naphthalenol in benzene." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_872.

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Winkelmann, Jochen. "Diffusion coefficient of 1-(2-phenyldiazenyl)-2-naphthalenol in cyclohexanol." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_873.

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Winkelmann, Jochen. "Diffusion coefficient of 4-(2-phenyldiazenyl)-1-naphthalenol in hexadecane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_877.

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Winkelmann, Jochen. "Diffusion coefficient of 4-(2-phenyldiazenyl)-1-naphthalenol in ethanol." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_880.

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Winkelmann, Jochen. "Diffusion coefficient of 1-(2-phenyldiazenyl)-2-naphthalenol in tetrachloro-methane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_868.

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Winkelmann, Jochen. "Diffusion coefficient of 1-(2-phenyldiazenyl)-2-naphthalenol in propan-2-one." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_870.

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Winkelmann, Jochen. "Diffusion coefficient of 1-(2-phenyldiazenyl)-2-naphthalenol in octan-1-ol." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_874.

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Winkelmann, Jochen. "Diffusion coefficient of 1-(2-phenyldiazenyl)-2-naphthalenol in 1,2,3-triacetoxy-propane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_875.

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Conference papers on the topic "Naphthalenol"

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Hill, Jeffrey R., and Dana D. Dlott. "Vibrational Relaxation and Energy Transfer in Ordered and Disordered Molecular Crystals." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1986. http://dx.doi.org/10.1364/up.1986.tuf2.

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Vibrational energy transfer in condensed phases is a process which occurs on the picosecond time scale. In our lab, we are studying this process in complex molecules in the well-defined environment of a single molecular crystal. We have measured the lifetime of several vibrons in the model system naphthalene, and then extended these studies to several partially deuterated naphthalenes [1,2]. Vibrations in pure crystals form delocalized vibron bands which relax by emission of optical phonons. In disordered or mixed crystals, excited vibrations scatter off impurities and transfer energy to adjac
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Jia, Dan, Huimin Liu, and Dongyan Gu. "Preparation of Naphthalene Molecularly Imprinted Absorbent and its adsorption for Naphthalene." In 2017 3rd International Forum on Energy, Environment Science and Materials (IFEESM 2017). Atlantis Press, 2018. http://dx.doi.org/10.2991/ifeesm-17.2018.288.

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Melker, Alexander I., Dimitri A. Kornilov, Tatiana V. Vorobyeva, and Denis Kalinin. "Conformational transitions in naphthalene." In SPIE Proceedings, edited by Alexander I. Melker. SPIE, 2004. http://dx.doi.org/10.1117/12.555442.

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Junbiao Peng, Runguang Son, Yuguang Ma, Haifeng Zhang, and Shiyong Liu. "Electroluminescent of plasma polymerized naphthalene." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835421.

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Ciocci, Richard C. "Characterizing Naphthalene via Material Flow Analysis." In ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-82808.

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An Environmental Protection Agency-funded project centers on the material flow analysis of naphthalene-containing products in an effort to eliminate, reduce, or replace the sources of naphthalene. The analysis commences with manufacturers who use naphthalene-containing products in their processes. Also, the analysis works in reverse by starting with the naphthalene user, as the material will be traced to the source in an effort to identify elimination/reduction opportunities throughout the material’s life cycle. A particular focus is the potential for removal of naphthalene from the primary pr
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Ciocci, Richard, Daniel Massey, and Steve Funck. "Developing a Process to Identify Material Flow of a Priority Chemical." In ASME 2006 International Mechanical Engineering Congress and Exposition. ASMEDC, 2006. http://dx.doi.org/10.1115/imece2006-13727.

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An Environmental Protection Agency-funded project was the material flow analysis of naphthalene-containing products in an effort to eliminate, reduce, or replace the sources of naphthalene. The project analysis began with manufacturers who use naphthalene-containing products in their processes. It identifies the basic characteristics of naphthalene as a common polynuclear aromatic hydrocarbon, which is released to the environment. Included are likely sources of naphthalene emissions and releases as they were identified for further investigation. This paper, which is the sequel to IMECE 2005-82
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Nikulina, N., Sergey Nikulin, and A. Dmitrenkov. "PRODUCTION OF MODIFIED WOOD USING VINYL NAPHTHALENE DERIVATIVE." In ENERGY-SAVING AND ENVIRONMENTALLY SAFE TECHNOLOGIES OF THE TIMBER INDUSTRY – 2025. FSBE Institution of Higher Education Voronezh State University of Forestry and Technologies named after G.F. Morozov, 2025. https://doi.org/10.58168/e-sestti2025_284-288.

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The compositions for processing natural birch wood, obtained on the basis of ethenyl derivatives of naphthalene, are investigated in the work. A solution of naphthalene derivatives in toluene with additives of pinane hydroperoxide was used for wood processing. The removal of toluene from modified timber samples was combined with radical polymerization of ethenyl naphthalene derivatives in an autoclave at 160-165 0C for 5 hours. The polymer content in the timber varied from 10 to 26%. Manufactured timber products containing ethenyl naphthalene derivatives will provide products based on them not
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Hourani, Michel J. "Alkylated Naphthalenes as High Performance Synthetic Lubricating Fluids." In STLE/ASME 2006 International Joint Tribology Conference. ASME, 2006. http://dx.doi.org/10.1115/ijtc2006-12113.

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Song, Fu, Yifei Shi, Shiru Jia, Zhilei Tan, and Huabing Zhao. "Advances of naphthalene degradation in Pseudomonas putida ND6." In ADVANCES IN ENERGY SCIENCE AND ENVIRONMENT ENGINEERING II: Proceedings of 2nd International Workshop on Advances in Energy Science and Environment Engineering (AESEE 2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5029792.

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Dixon, D., W. Wilson, V. Steullet, and S. Takenaka. "Studies of Naphthalene Diimides as DNA-binding Agents." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02060.

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Reports on the topic "Naphthalenol"

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Buchholz, Bruce A. Mechanism for Clastogenic Activity of Naphthalene. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1226965.

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Buchholz, Bruce A. Mechanism for Clastogenic Activity of Naphthalene. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1281678.

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Buchholz, Bruce A. Metabolic Mechanisms of Naphthalene Toxicity in Lung. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1529177.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7149929.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6884708.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6929711.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6986489.

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Ghoshal, S., A. Ramaswami, and R. G. Luthy. Biodegradation of naphthalene from coal tar. Research progress report. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10178125.

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Lotufo, Guilherme, Mandy Michalsen, Danny Reible, et al. Interlaboratory study of polyethylene and polydimethylsiloxane polymeric samplers for ex situ measurement of freely dissolved hydrophobic organic compounds in sediment porewater. Engineer Research and Development Center (U.S.), 2024. http://dx.doi.org/10.21079/11681/48512.

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Abstract:
We evaluated the precision and accuracy of multilaboratory measurements for determining freely dissolved concentrations (Cfree) of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in sediment porewater using polydimethylsiloxane and low-density polyethylene polymeric samplers. Four laboratories exposed performance reference compound (PRC) preloaded polymers to actively mixed and static ex situ sediment for approximately one month or more. For Cfree results, intralaboratory precision was high for single compounds; most PAHs and PCBs variability was low. Variability w
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Buchholz, B. A. Mechanism for Clastogenic Activity of Naphthalene. Quarterly Technical Progress Report. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1239176.

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