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1. The chemistry and technology of naphthalene compounds
by Donaldson, Norman
1958, xv, 512 p. illus.
Naphthalene
Book
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2. The oxidation of naphthalene to phthalonic acid by alkaline solutions of permanganate
by Daly, Richard Arthur
1907, University of Toronto studies. Papers from the chemical laboratories, Volume no. 64, [93]-106
Book
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3. Chlorinated naphthalenes
by Howe, Paul D and World Health Organization (WHO) and International Labour Organisation and World Health Organization and United Nations . Environment Programme (UNEP) and United Nations Environment Programme and Inter-Organization Programme for the Sound Management of Chemicals and International Program on Chemical Safety and International Labour Organisation (ILO)
2001, Concise international chemical assessment document, ISBN 9789241530347, Volume 34.
Toxicology | Naphthalene | Naphtalene -- Environmental aspects | Naphtalene -- Toxicology | Environmental aspects | Health risk assessment | Physiological effect | Chlorohydrocarbons
Book
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4. Full Text The Toxicological Effects of Halogenated Naphthalenes: A Review of Aryl Hydrocarbon Receptor-Mediated (Dioxin-like) Relative Potency Factors
by Falandysz, Jerzy and Fernandes, Alwyn and Gregoraszczuk, Ewa and Rose, Martin
Journal of Environmental Science and Health, Part C, ISSN 1059-0501, 07/2014, Volume 32, Issue 3, pp. 239 - 272
There is no doubt that chloronaphthalenes (PCNs) and their brominated counterparts (PBNs) are dioxin-like compounds, but there is less evidence for mixed... 
persistent organic pollutants (POPs) | dioxin-like compounds | mixed brominated/chlorinated naphthalenes | polybrominated naphthalenes | dioxin-like toxicity | polychlorinated naphthalenes | INDIVIDUAL POLYCHLORINATED NAPHTHALENES | HALOWAX SERIES | DRUG-METABOLIZING-ENZYMES | IMMATURE MALE-RAT | DIBENZO-P-DIOXINS | MASS-SPECTROMETRY | CHLORONAPHTHALENE MIXTURES | CHLORINATED NAPHTHALENES | ENVIRONMENTAL SCIENCES | BY-SIDE IMPURITIES | ONCOLOGY | BALTIC SEA | TOXICOLOGY | Naphthalenes - chemistry | Animals | Gas Chromatography-Mass Spectrometry | Rats, Wistar | Rats | Body Burden | Male | Halogens - chemistry | Naphthalenes - pharmacokinetics | Naphthalenes - toxicity | Receptors, Aryl Hydrocarbon - drug effects
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5. Full Text Depurinating naphthalene–DNA adducts in mouse skin related to cancer initiation
by Saeed, Muhammad and Higginbotham, Sheila and Gaikwad, Nilesh and Chakravarti, Dhrubajyoti and Rogan, Eleanor and Cavalieri, Ercole
Free Radical Biology and Medicine, ISSN 0891-5849, 2009, Volume 47, Issue 7, pp. 1075 - 1081
Naphthalene has been shown to be a weak carcinogen in rats. To investigate its mechanism of metabolic activation and cancer initiation, mice were topically... 
Depurinating naphthalene–DNA adducts | Naphthalene | 1,2-Naphthalene quinone ultimate carcinogenic metabolite | Stable naphthalene–DNA adducts | Metabolic activation of naphthalene | Depurinating naphthalene-DNA adducts | Stable naphthalene-DNA adducts | ORTHO-QUINONES | MECHANISM | N7GUANINE ADDUCTS | ESTRADIOL-3,4-QUINONE | BIOCHEMISTRY & MOLECULAR BIOLOGY | 1,2-Naphthalene quinone ultimate | METABOLIC-ACTIVATION | IDENTIFICATION | REPAIR | ENDOCRINOLOGY & METABOLISM | MUTATIONS | carcinogenic metabolite | TUMOR INITIATION | MAMMARY-GLAND | Naphthalenes - chemistry | Skin Neoplasms - pathology | Animals | Mice, Inbred SENCAR | DNA Adducts - chemistry | Mice | Naphthalenes - toxicity | Skin Neoplasms - chemically induced | Naphthalenes - metabolism | DNA Adducts - metabolism | Purines | Metabolites | Surface active agents | Analysis | DNA | Quinone | Hydrocarbons | Hormones, Sex | Sulfates | Mass spectrometry | Ethylenediamines | Benzene | Index Medicus
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6. The course of the oxidation of [b]- naphthoquinone to phthalic acid, and the detection and estimation of [a]-naphthoquinone
: [b]-B-naphthoquinone, phthalonic acid and phthalic acid
by Boswell, Maitland Crease and Toronto, Ont. University.Theses (Ph.D.)
1907, 20
Naphthalene | Phthalic acid
Book
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7. Impact of Thermal Remediation on the Degradation of Naphthalene by Indigenous Anaerobic Bacteria in Hydrocarbon Contaminated Soil
by Newfield, Kirstin
03/2014
Thermal remediation is an efficient and cost effective method for the removal of organic compounds from the subsurface. However, complete removal of these... 
Naphthalene Degradation | 0775 | Bioremediation
Dissertation
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8. Anion induced supramolecular polymerization: a novel approach for the ultrasensitive detection and separation of F− (Electronic supplementary information (ESI) available: Experimental details and characterization data; fluorescence spectra; fluorescence titrations for target ions and so on. See DOI: 10.1039/c8cc09876j)
by Qi Lin and Guan-Fei Gong and Yan-Qing Fan and Yan-Yan Chen and Jiao Wang and Xiao-Wen Guan and Juan Liu and You-Ming Zhang and Hong Yao and Tai-Bao Wei
Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2019, Volume 55, Issue 22, pp. 3247 - 3250
A novel approach for the ultrasensitive detection and separation of F− has been successfully developed. F− could induce a tripodal naphthalene imide sensor... 
Naphthalene | Separation | Fluorescence | Polymerization
Journal Article
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9. Full Text Facile Deposition of Multicolored Electrochromic Metal–Organic Framework Thin Films
by Wade, Casey R and Li, Minyuan and Dincă, Mircea
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2013, Volume 52, Issue 50, pp. 13377 - 13381
Metal–organic frameworks: The solvothermal reaction of Zn2+ ions and bis‐ (pyrazolyl)naphthalene diimide readily affords strongly adhering, electroactive... 
naphthalene diimide | electrochemistry | metal–organic frameworks | electrochromic materials | thin films | metal-organic frameworks | SUBSTITUTED NAPHTHALENE DIIMIDE | TUNGSTEN-OXIDE | COORDINATION | BISIMIDES | REDOX PROPERTIES | ADSORPTION | CHEMISTRY, MULTIDISCIPLINARY | COLORATION EFFICIENCY MEASUREMENTS | CHARGE MOBILITY | CHEMISTRY | DEVICES | Thin films | Electrochemistry | Electrochemical reactions | Dielectric films | Pictures | Cycles | Spectroscopy | Glass | Electrochromism | Metal-organic frameworks | Deposition | Diimide
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10. Synthesis of Macrocyclic Hexamine from Naphthalene-based C2-Symmetric Chiral Diamine and Dialdehyde
by Suguru Ito and Shiori Okada and Rika Sue and Masatoshi Asami
Chemistry Letters, ISSN 0366-7022, 01/2018, Volume 47, Issue 3, p. 340
A naphthalene-based C2-symmetric chiral diamine was obtained with high enantioselectivity by the double asymmetric addition of diethylzinc to... 
Hexamine | Naphthalene | Enantiomers
Journal Article
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11. Full Text Rationally Designed Surfactants for Few-Layered Graphene Exfoliation: Ionic Groups Attached to Electron-Deficient π‑Conjugated Unit through Alkyl Spacers
by Zhang, Lu and Zhang, Zijian and He, Chaozheng and Dai, Liming and Liu, Jun and Wang, Lixiang
ACS Nano, ISSN 1936-0851, 07/2014, Volume 8, Issue 7, pp. 6663 - 6670
Mass production of graphene with low cost and high throughput is very important for practical applications of graphene materials. The most promising approach... 
naphthalene diimide | ultrasonic exfoliation | dispersion | graphene | surfactant
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12. The role of fluoride in anion–π interaction with naphthalene diimide (Electronic supplementary information (ESI) available. See DOI: 10.1039/c9cc01795j)
by Teck Lip Dexter Tam and Jian Wei Xu
Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2019, Volume 55, Issue 44, pp. 6225 - 6228
The role of fluoride in anion–π interaction with naphthalene diimide (NDI) is dependent on the solvent used. Here we show that in polar aprotic solvents like... 
Solvents | Anions | Naphthalene | Fluorides | Diimide
Journal Article
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13. Full Text Structural Basis for Telomeric G-Quadruplex Targeting by Naphthalene Diimide Ligands
by Collie, Gavin W and Promontorio, Rossella and Hampel, Sonja M and Micco, Marialuisa and Neidle, Stephen and Parkinson, Gary N
Journal of the American Chemical Society, ISSN 0002-7863, 02/2012, Volume 134, Issue 5, pp. 2723 - 2731
The folding of the single-stranded 3′ end of the human telomere into G-quadruplex arrangements inhibits the overhang from hybridizing with the RNA template of... 
IN-VITRO | INHIBITION | RECOGNITION | SMALL-MOLECULE | DNA | SEQUENCE | ANTITUMOR-ACTIVITY | BINDING | CANCER | CHEMISTRY, MULTIDISCIPLINARY | K+ SOLUTION | Imides - pharmacology | Naphthalenes - chemical synthesis | Naphthalenes - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Imides - chemical synthesis | Models, Molecular | Crystallography, X-Ray | Structure-Activity Relationship | Antineoplastic Agents - chemistry | Naphthalenes - pharmacology | Telomere - chemistry | DNA - chemistry | Imides - chemistry | Hydrogen Bonding | Cell Line, Tumor | G-Quadruplexes | Ligands | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Molecular Structure | Drug Screening Assays, Antitumor | Telomeres | Ligand binding (Biochemistry) | Naphthalene | Analysis | Cancer cells | Physiological aspects | Research | Chemical properties | Structure | Hydrogen bonding
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14. Full Text Does a concomitant exposure to lead influence unfavorably the naphthalene subchronic toxicity and toxicokinetics?
by Katsnelson, Boris A and Minigaliyeva, Ilzira A and Degtyareva, Tamara D and Privalova, Larisa I and Beresneva, Tatyana A
Environmental Toxicology and Chemistry, ISSN 0730-7268, 01/2014, Volume 33, Issue 1, pp. 152 - 157
Rats were given 20 times during 40 d either naphthalene per gavage or the same and lead acetate intraperitoneally in single doses corresponding to 5% of the... 
Naphthalene urine excretion | Naphthalene and lead toxic effect | ENVIRONMENTAL SCIENCES | MECHANISMS | TOXICOLOGY | HEAVY-METALS | Naphthalenes - urine | Animals | Drug Interactions | Rats | Female | Lead - pharmacokinetics | Naphthalenes - pharmacokinetics | Naphthalenes - toxicity | Lead - toxicity | Index Medicus
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15. Full Text Aromatic‐Diimide‐Based n‐Type Conjugated Polymers for All‐Polymer Solar Cell Applications
by Yang, Jing and Xiao, Bo and Tang, Ailing and Li, Jianfeng and Wang, Xiaochen and Zhou, Erjun
Advanced Materials, ISSN 0935-9648, 11/2019, Volume 31, Issue 45, pp. e1804699 - n/a
All‐polymer solar cells (all‐PSCs) have attracted immense attention in recent years due to their advantages of tunable absorption spectra and electronic energy... 
naphthalene diimide (NDI) | perylene diimide (PDI) | aromatic diimide | all‐polymer solar cells (all‐PSCs) | electron acceptors | all-polymer solar cells (all-PSCs) | HIGH-PERFORMANCE | POWER CONVERSION EFFICIENCY | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | DONOR | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | COPOLYMERS | ADDITIVE-FREE | CHEMISTRY, MULTIDISCIPLINARY | FIELD-EFFECT TRANSISTORS | SOLVENT | ABSORPTION | NAPHTHALENE DIIMIDE | ELECTRON-ACCEPTORS | Solar cells | Naphthalene | Energy levels | Photovoltaic cells | Absorption spectra | Polymers | Diimide | Energy conversion efficiency
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16. Phototriggered Supramolecular Polymerization of Barbituric Acid Rosette
by Mitsuaki Yamauchi and Norimichi Kanao and Bimalendu Adhikari and Takashi Karatsu and Shiki Yagai
Chemistry Letters, ISSN 0366-7022, 01/2017, Volume 46, Issue 1, p. 111
Supramolecular polymerization of a naphthalene-azobenzene dyad bearing a barbituric acid hydrogen-bonding unit was studied in nonpolar media. The length of... 
Naphthalene | Polymerization | Supramolecular polymers
Journal Article
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17. Full Text Fluoro‐Substituted n‐Type Conjugated Polymers for Additive‐Free All‐Polymer Bulk Heterojunction Solar Cells with High Power Conversion Efficiency of 6.71
by Jung, Jae Woong and Jo, Jea Woong and Chueh, Chu‐Chen and Liu, Feng and Jo, Won Ho and Russell, Thomas P and Jen, Alex K.‐Y
Advanced Materials, ISSN 0935-9648, 06/2015, Volume 27, Issue 21, pp. 3310 - 3317
Fluorinated n‐type conjugated polymers are used as efficient electron acceptor to demonstrate high‐performance all‐polymer solar cells. The exciton generation,... 
all‐polymer solar cells | fluorination | naphthalene di‐imide | conjugated polymers | Conjugated polymers | All-polymer solar cells | Fluorination | Naphthalene di-imide | naphthalene di-imide | all-polymer solar cells | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | DIIMIDE | OPEN-CIRCUIT VOLTAGE | MOBILITY | PERFORMANCE | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | CHEMISTRY, MULTIDISCIPLINARY | FIELD-EFFECT TRANSISTORS | SOLUBILITY | DIKETOPYRROLOPYRROLE | ACCEPTORS | FULLERENE | AGGREGATION | Solar cells | Energy use | Polymer industry | Solar batteries | Polymers | Blends | Photocurrent | Photovoltaic cells | Heterojunctions | Charge | Energy conversion efficiency
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18. Full Text Synthesis of Arylnaphthalene Lignan Scaffold by Gold-Catalyzed Intramolecular Sequential Electrophilic Addition and Benzannulation
by Gudla, Vanajakshi and Balamurugan, Rengarajan
The Journal of Organic Chemistry, ISSN 0022-3263, 12/2011, Volume 76, Issue 24, pp. 9919 - 9933
An intramolecular approach to generate compounds containing an arylnaphthalene lignan scaffold in high yields is presented. It involves a sequential... 
POLYSUBSTITUTED NAPHTHALENE DERIVATIVES | LACTONES | ONE-POT SYNTHESIS | NATURAL-PRODUCTS | REGIOSELECTIVE SYNTHESIS | BIOLOGICAL EVALUATION | CHEMISTRY, ORGANIC | NONREDOX 5-LIPOXYGENASE INHIBITORS | ANTIVIRAL ACTIVITY | SUBSTITUTED NAPHTHALENES | PHYLLANTHUS-MYRTIFOLIUS | Naphthalenes - chemical synthesis | Naphthalenes - chemistry | Magnetic Resonance Spectroscopy | Gold Compounds - chemistry | Lignans - chemistry | Stereoisomerism | Dioxolanes - chemistry | Biological Factors - chemical synthesis | Lactones - chemical synthesis | Cyclization | Lignans - chemical synthesis | Molecular Structure | Catalysis | Lactones - chemistry | Gold | Carbonyl compounds | Usage | Naphthalene | Aromatic amines | Analysis | Chemical bonds | Ring formation (Chemistry) | Chemical properties
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19. Full Text Frontispiece: Recent Advances in the Core‐Annulation of Naphthalene Diimides
by Insuasty, Alberto and Maniam, Subashani and Langford, Steven J
Chemistry – A European Journal, ISSN 0947-6539, 05/2019, Volume 25, Issue 29, p. n/a
Naphthalene diimides (NDIs) are robust, planar molecules with tuneable electronic properties. Their electron deficient polycyclic aromatic structure yields... 
carbocycles | annulenes | annulation | heterocycles | naphthalene diimides | Organic chemistry | Chemical reactions | Properties (attributes) | Naphthalene | Electron affinity
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20. Full Text Frontispiece: Harnessing Brightness in Naphthalene Diimides
by Maniam, Subashani and Higginbotham, Heather F and Bell, Toby D. M and Langford, Steven J
Chemistry – A European Journal, ISSN 0947-6539, 05/2019, Volume 25, Issue 29, p. n/a
The development of brightly emissive compounds is of great research and commercial interest. Naphthalene diimides have been widely used for both fundamental... 
absorption coefficient | molecular brightness | fluorescence | quantum yield | naphthalene diimides | Fluorescence | Diimide | Naphthalene
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