Relevant bibliographies by topics / Naphthalene derivatives

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

Academic literature on the topic 'Naphthalene derivatives'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 July 2025

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Journal articles on the topic "Naphthalene derivatives"

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Jurczak, Janusz, Agnieszka Cholewiak, and Pawel Stepniak. "Linear Neutral Receptors for Anions: Synthesis, Structure and Applications." Synthesis 50, no. 23 (2018): 4555–68. http://dx.doi.org/10.1055/s-0037-1609943.

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A selective digest of linear anion receptors based on different aromatic skeletons is presented. Since the structures of anions vary from one to another, different strategies have been developed over recent years in order to bind anions efficiently and selectively. Rigidity, number of hydrogen bond donors, steric hindrance, and special preorganization of linear receptors are analyzed to shed light on the rational design of anion receptors.1 Introduction2 1,3- and 1,2-Benzene Derivatives3 1,3- and 5,7-Azulene Derivatives4 1,8-Naphthalene Derivatives5 1,8-Anthracene Derivatives6 2,6-Pyridine Der
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El-Dossoki, Farid I. "Protonation and Solvation Thermodynamics of Some Naphthol Derivatives in KCl Aqueous Solution of Different Ionic Strengths." Journal of Chemistry 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/7234320.

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The acid-base properties of naphthalen-1-ol (L1), naphthalene-1,5-diol (L2), and 4-amino-3-hydroxynaphthalene-1-sulphonic acid (L3) were characterized from pH-metric measurements in pure water and in different concentrations (0–4 mol kg−1) of aqueous KCl solutions at the temperature range ofT= (293.15 to 213.15) K at 5 K intervals. The results reveal that naphthalen-1-ol and naphthalene-1,5-diol molecules have two ionisable protons (of the hydroxyl groups) while 4-amino-3-hydroxynaphthalene-1-sulphonic acid has three ionisable protons (hydrogen ion of the hydroxyl group, SO3H, andNH3+). Modeli
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Ibrahim, Mohamed N., Salaheddin A. I. Sharif, Ahmad N. EL-Tajory, and Asma A. Elamari. "Synthesis and Antibacterial Activities of Some Schiff Bases." E-Journal of Chemistry 8, no. 1 (2011): 212–16. http://dx.doi.org/10.1155/2011/258340.

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Schiff basesp-hydroxybenzylidene-2-carboxyaniline,p-nitrobenz-ylidene-2-carboxyaniline,p-(N, N-dimethyl)aminobenzylidene-2-carboxyaniline,N-(4-hydroxybezylidene)-benzene-1,2-diamine,N--(4-nitrobezylidene)benzene-1,2-diamine,N-(4-(N, N-dimethylaminobezylidene)benzene-1,2-diamine,N-(4-(N,N-dimethylamino)benzylidene)naphthalen-1-amine,N-(4-nitrobenzylidene)naphthalen-1-amine,N--(4-chlorobenzylidene)naphthalen-1-amine,sodium-4-(4-(N,N-dimethyl amino)benzylideneamino)naphthalene-1-sulfonate,sodium -4-(4-nitrobenzylidene-amino)naphthalene-1-sulfonate and sodium-4-(4-chlorobenzylideneamino) naphthale
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Lauro, Figueroa-Valverde, Diaz-Cedillo Francisco, Rosas-Nexticapa Marcela, et al. "Synthesis and Biological Activity of a Bis-steroid-methanocyclobutanaphthalene- dione Derivative against Ischemia/Reperfusion Injury via Calcium Channel Activation." Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry 19, no. 4 (2020): 393–412. http://dx.doi.org/10.2174/1871523018666191003152854.

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Background: There is some experimental data on the effect exerted by some steroid derivatives against ischemia/reperfusion injury; however, the molecular mechanism is very confusing, perhaps this phenomenon could be due to the protocols used and/or differences in the chemical structure of each one of the steroid derivatives. Objective: The aim of this study was to synthesize a new bis-steroid-methanocyclobutanaphthalene- dione derivative using some tools chemical. Methodology: The biological activity exerted by the bis-steroid-methanocyclobutanaphthalene- dione derivative against ischemia/repe
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Haget, Y., N. B. Chanh, A. Meresse, et al. "Isomorphism and mixed crystals in 2-R-naphthalenes: evidence of structural subfamilies and prediction of metastable forms." Journal of Applied Crystallography 32, no. 3 (1999): 481–88. http://dx.doi.org/10.1107/s0021889899002423.

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Solid–liquid binary phase diagrams and isothermal unit-cell parameters as a function of composition are given for the high-temperature form (P21/a,Z= 2) mixed crystals generated by 2-fluoronaphthalene, naphthalene and 2-naphthol with four other β derivatives of naphthalene. The study leads to the distinction between two high-temperature forms (or types of packing). The first one (type 1) is taken by five 2-R-naphthalenes (R= F, Cl, Br, SH, CH3; the first subfamily), the second one (type 2) by naphthalene itself and 2-naphthol (R= H, OH; the second subfamily). The crystallographic data also all
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Mukherjee, Anurag, and Suhrit Ghosh. "Core-Substituted Naphthalene-Diimides (cNDI) and Related Derivatives: Versatile Scaffold for Supramolecular Assembly and Functional Materials." Organic Materials 03, no. 03 (2021): 281–92. http://dx.doi.org/10.1055/a-1530-0476.

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Naphthalene-diimide (NDI)-derived building blocks have been explored extensively for supramolecular assembly as they exhibit attractive photophysical properties, suitable for applications in organic optoelectronics. Core-substituted derivatives of the NDI chromophore (cNDI) differ significantly from the parent NDI dye in terms of optical and redox properties. Adequate molecular engineering opportunities and substitution-dependent tunable optoelectronic properties make cNDI derivatives highly promising candidates for supramolecular assembly and functional materials. This short review discusses
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V, BALIAH, and BALASUBRAMANIYAN V. "Dipole Moments of some Naphthalene Derivatives. A Study of the Conformational Preferences of Substituent Groups." Journal of Indian Chemical Society Vol.70, Sep 1993 (1993): 755–61. https://doi.org/10.5281/zenodo.5939741.

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Department of Chemistry, Annamalai&nbsp;University, Annamalainagar-608 002 Department of Chemistry, H P T College, Nasik-422 005 <em>Manuscript received 31 October 1991, revised 11 March 1993, accepted 30 March 1993</em> The electric dipole moments of more than fifty naphthalene derivatives have been determined. Steric, polar and field effects existing in disubstituted naphthalenes are studied by comparing the observed dipole moments with those calculated by vector addition of group moments. The conformational preferences of the substituent groups in a number of disubstituted naphthalenes are
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Xu, Zhiyong, Ting Feng, Zhenchang Wen, et al. "New Naphthalene Derivatives from the Mangrove Endophytic Fungus Daldinia eschscholzii MCZ-18." Marine Drugs 22, no. 6 (2024): 242. http://dx.doi.org/10.3390/md22060242.

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Five new naphthalene derivatives dalesconosides A–D, F (1–4, 6), a known synthetic analogue named dalesconoside E (5), and eighteen known compounds (7–24) were isolated from Daldinia eschscholzii MCZ-18, which is an endophytic fungus obtained from the Chinese mangrove plant Ceriops tagal. Differing from previously reported naphthalenes, compounds 1 and 2 were bearing a rare ribofuranoside substituted at C-1 and the 5-methyltetrahydrofuran-2,3-diol moiety, respectively. Their structures were determined by detailed nuclear magnetic resonance (NMR) and mass spectroscopic (MS) analyses, while the
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Akshara, Vinayakrishnan* Malavika K. Aneesha Thomas Aswagosh K. "The Study of Insilco Design and Biological Evaluation of Naphthalene Derivatives." International Journal of Pharmaceutical Sciences 3, no. 1 (2025): 1964–69. https://doi.org/10.5281/zenodo.14724043.

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Naphthalene is an aromatic compound that contain two fused benzene rings. Naphthalene derivatives has diverse biological activities and gained attention as potential therapeutic agents. In this study we applied Insilco drug design techniques to evaluate pharmacokinetic properties, biological activities and binding affinity of 2-(bromomethyl) naphthalene, 8-amino-2-naphthol and acenaphthalene. The molecular structures were created by using King Draw, followed by the prediction of key pharmacokinetic parameters (solubility, permeability, toxicity, etc.) using Swiss ADME. Biological activity pred
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Fryzuk, Michael D., Peihua Yu, and Brian O. Patrick. "Synthesis, structure, and reactivity of diamidophosphine complexes of yttrium and the lanthanides." Canadian Journal of Chemistry 79, no. 7 (2001): 1194–200. http://dx.doi.org/10.1139/v01-087.

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The reaction of the dilithiodiamidophosphine ligand precursor PhP(CH2SiMe2NPh)2Li2(THF)2([NPN]Li2(THF)2) with LnCl3(THF)3 (Ln = Y, Sm, Ho, Yb, Lu; THF = tetrahydrofuran) in refluxing toluene generates the mononuclear complexes [NPN]LnCl(THF) in good yield. The molecular structures have been shown to be five-coordinate in the solid state and in solution. Attempts to prepare alkyl derivatives have only met with partial success; the reaction of MeMgCl with [NPN]YCl(THF) generates the partially characterized mixed-metal derivative [NPN]YMe2MgCl. The reaction with LiAlH4 results in complete ligand
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Dissertations / Theses on the topic "Naphthalene derivatives"

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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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Knight, Lorraine Shirley. "The synthesis of derivatives of naturally occurring naphthalenes." Doctoral thesis, University of Cape Town, 1988. http://hdl.handle.net/11427/17082.

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Includes bibliographical references.<br>The ansamycins are a large group of natural products which have attracted considerable attention, largely as a result of their range of biological activity. The laboratory synthesis of an ansamycin has been simplified into the independent construction of the aromatic nucleus and the ansa chain, followed by their combination to form the macrocyle. The project described in Chapter 1 was designed to devise a novel, convenient, and efficient synthesis of a substituted 1,4-naphthoquinone which would function as a model for the naphthoquinonoid nucleus of the
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Clark, G. R. "Studies on syntheses of cyclic derivatives of biphenylene and naphthalene." Thesis, University of Bristol, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.371991.

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Fuller, Amy L. "Applications of X-ray crystallography : studies into the structural perturbations of peri-substituted naphthalene derivatives /." St Andrews, 2009. http://hdl.handle.net/10023/826.

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Fuller, Amy L. "Applications of X-ray crystallography : studies into the structural perturbations of peri-substituted naphthalene derivatives." Thesis, University of St Andrews, 2010. http://hdl.handle.net/10023/826.

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The majority of research in this thesis uses X-ray crystallography to investigate the structural features of peri-substituted naphthalene compounds. X-ray crystallography is introduced in chapter one, followed by a discussion on modes of distortion peri-substituted naphthalene derivatives can undergo, in chapter two. In chapter three, compounds having non-bonded -SPh and -EPh (E = S, Se, or Te) peri-substituents are compared. These similar compounds react differently when oxidized with bromine. The oxidation products are used to discuss a recently proposed mechanism and a more specific mechani
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Etheridge, Forrest Samuel. "Tuning the Opto-Electronic Properties of Organic Semiconductors: Derivatives ofAzadipyrromethene, Naphthalene Diimide and Poly(3-hexylthiophene)." Case Western Reserve University School of Graduate Studies / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=case1459352863.

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Jia, Shuanglong. "Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives." Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLY012/document.

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Les réactions multicomposantes jouent un rôle important en chimie organique. Ce sont des réactions qui mettent en jeu au moins trois réactifs de départ et qui permettent d’obtenir des produits considérés comme des éléments intéressants pour la synthèse de molécules complexes ou de composés bioactifs. Grâce à leur versatilité, ces réactions sont considérées comme des outils précieux pour la préparation de bibliothèques de composés organiques dans le domaine de la recherche pharmaceutique et de la synthèse de produits naturels.La réaction de Passerini, combinée à une addition de Michael et à une
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Kasturi, Chandrika. "Photochemical inactivation of viruses using psoralen, naphthalene and porphyrin derivatives : development of a protocol for the selective inactivation of viruses in blood products /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487846354482773.

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Jia, Shuanglong. "Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives." Electronic Thesis or Diss., Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLY012.

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Les réactions multicomposantes jouent un rôle important en chimie organique. Ce sont des réactions qui mettent en jeu au moins trois réactifs de départ et qui permettent d’obtenir des produits considérés comme des éléments intéressants pour la synthèse de molécules complexes ou de composés bioactifs. Grâce à leur versatilité, ces réactions sont considérées comme des outils précieux pour la préparation de bibliothèques de composés organiques dans le domaine de la recherche pharmaceutique et de la synthèse de produits naturels.La réaction de Passerini, combinée à une addition de Michael et à une
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Ndube, Ncediwe. "Determination of fumonisins in maize by High Performance Liquid Chromatography with fluorescence and ultraviolet detection of o-phthaldialdehyde, naphthalene-2,3-dicarboxaldehyde and dansyl chloride derivatives." Thesis, University of the Western Cape, 2011. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_2588_1320667169.

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Fumonisins, carcinogenic mycotoxins produced by various Fusarium species, occur naturally in maize and maize-based food products. They are hazards for animal and human health as they cause cancer in rodents and have been associated with oesophageal cancer and neural tube defects in humans. The most abundant naturally occurring fumonisins analogues in maize are fumonisin B1, B2 and B3 (FB1, FB2 and FB3). For analytical determination, they mostly require suitable extraction, clean-up and pre or post-column derivatization together with reversed-phase HPLC separation. o- Phthaldialdehyde (OPA) had
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Books on the topic "Naphthalene derivatives"

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

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

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Book chapters on the topic "Naphthalene derivatives"

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Dinsdale, D., and R. D. Verschoyle. "Pulmonary Toxicity of Naphthalene Derivatives in the Rat." In Mechanisms and Models in Toxicology. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72558-6_54.

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Takenaka, Shigeori. "Cyclic Naphthalene Diimide Derivatives as Novel DNA Ligands." In Handbook of Chemical Biology of Nucleic Acids. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-1313-5_31-1.

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Takenaka, Shigeori. "Cyclic Naphthalene Diimide Derivatives as Novel DNA Ligands." In Handbook of Chemical Biology of Nucleic Acids. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-19-9776-1_31.

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Gurung, Sumiran Kumar, Sangeeta Kumari, and Neelima Mondal. "Oxidative Stress Modulation by G-quadruplex Binder-Naphthalene Diimide Derivatives and Its Therapeutic Potential." In Handbook of Oxidative Stress in Cancer: Therapeutic Aspects. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-5422-0_259.

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Prasad De, Sankar, and Ajay Misra. "Excited-State Intramolecular Proton Transfer Processes on Some Isomeric Naphthalene Derivatives: A Density Functional Theory Based Computational Study." In Hydrogen Bonding and Transfer in the Excited State. John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470669143.ch26.

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Netter, K. J., B. Hahnemann, S. A. Mangoura, et al. "Selective Inducers of the Coh-Locus Enhance the Metabolisms of Coumarin- and of Quinoline-Derivatives but Not That of Naphthalenes." In Advances in Experimental Medicine and Biology. Springer New York, 1991. http://dx.doi.org/10.1007/978-1-4684-5877-0_46.

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Venkatasubramanian, N., Thuy D. Dang, Soo-Young Park, Vladyslav Kholodovych, and William J. Welsh. "Poly(benzobisoxazole), Naphthalene Derivatives." In Polymer Data Handbook. Oxford University PressNew York, NY, 2009. http://dx.doi.org/10.1093/oso/9780195181012.003.0063.

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Abstract Major Applications of Interest High performance fibers, films, and coatings. Synthesis Polycondensation of 2,6-naphthalenedicarboxylic acid or 1,5-naphthalenedicarboxylic acid with 4,6-diaminoresorcinol dihydrochloride in 83% polyphosphoric acid (PPA)(1−4) using the ‘P2O5 adjustment method’.(5) Although Naph-2,6-PBO composition is mentioned in the Japanese patent (reference 3), the properties of this rigid-rod polymer have not been described in the literature. Processing Isotropic films are mainly cast from dilute methanesulfonic acid solutions. Fabrication of the polymeric fibers is
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Venkatasubramanian, N., Thuy D. Dang, Soo-Young Park, Vladyslav Kholodovych, and William J. Welsh. "Poly(benzobisthiazole), Naphthalene Derivatives." In Polymer Data Handbook. Oxford University PressNew York, NY, 2009. http://dx.doi.org/10.1093/oso/9780195181012.003.0065.

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Abstract Major Applications of Interest High performance fibers, films, and coatings Synthesis Polycondensation of 2,6-naphthalenedicarboxylic acid or 1,5-naphthalenedicarboxylic acid with 2,5-diamino-1,4-benzenedithiol dihydrochloride in 83 % polyphosphoric acid (PPA) using the ‘P2O5 adjustment method’. Processing Isotropic films are mainly cast from dilute methanesulfonic acid solutions. Fabrication of the polymeric fibers is from the lyotropic liquid crystalline phase of the polymer in PPA; polymer fibers are spun from the dope by a dry-jet wet spinning technique, a variation of wet extrusi
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Alberti, M. N., M. D. Tzirakis, and M. Orfanopoulos. "Photooxidation of Naphthalene Derivatives." In Peroxides, Inorganic Esters (RO-X, X=Hal, S, Se, Te, N). Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-038-00465.

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"5 Naphthalene and Anthracene Derivatives." In Natural Poisons and Venoms. De Gruyter, 2024. http://dx.doi.org/10.1515/9783110728538-005.

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Conference papers on the topic "Naphthalene derivatives"

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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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Dyadyuchenko, L. V., and I. G. Dmitrieva. "Study of the growth-regulating activity of pyrazolopyridine derivatives on soybean plants." In CURRENT STATE, PROBLEMS AND PROSPECTS OF THE DEVELOPMENT OF AGRARIAN SCIENCE. Federal State Budget Scientific Institution “Research Institute of Agriculture of Crimea”, 2020. http://dx.doi.org/10.33952/2542-0720-2020-5-9-10-19.

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The aim of this work was to find new active substances to create domestic soybean growth regulators. The screening was carried out in a series of naphthalene-2-sulfonyl amide derivatives. Substances with high growth-stimulating activity were identified.
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Hewett, Daniel, Timothy Zwier, and Victoria Boulos. "ISOMER-SPECIFIC SPECTROSCOPY OF ETHYL NAPHTHALENE DERIVATIVES: SPECTROSCOPIC FOUNDATION FOR UNDERSTANDING ETHYL-BRIDGED DINAPHTHYLS." In 73rd International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.wj07.

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Kux, U., and M. Iyod. "Syntheses and properties of new donors: 1,6-methano[10]annulene- and naphthalene-derivatives with tetrathiafulvalene substituents." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835495.

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Kobayashi, Naofumi, Hiroyuki Kuwae, Juro Oshima, et al. "Deep-blue light emission with a wide-bandgap naphthalene-derivative liquid organic semiconductor host." In SPIE OPTO, edited by Christopher E. Tabor, François Kajzar, Toshikuni Kaino, and Yasuhiro Koike. SPIE, 2017. http://dx.doi.org/10.1117/12.2251640.

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Pramod, A. G., and C. G. Renuka. "Theoretical analysis of 3,3’-(naphthalen-2-ylmethylene) bis (4-hydroxy-2H-chromen-2-one) coumarin derivative." In 3RD INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC-2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0001780.

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Mella-Raipán, J., C. F. Lagos, J. Romero-Parra, et al. "Docking and Synthesis of a series of 1-(naphthalen-1- ylmethyl)-2-(pyridin-2-yl)-1H-benzo[d]imidazole derivatives designed as novel CB1 cannabinoid ligands." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0233-1.

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