Academic literature on the topic 'Aromatic derivatives'

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Journal articles on the topic "Aromatic 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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Berrío Escobar, Jhon Fernando, Victor Hugo Arango Carmona, Elkin Galeano Jaramillo, et al. "Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells." Ars Pharmaceutica (Internet) 57, no. 4 (2016): 183–91. http://dx.doi.org/10.30827/ars.v57i4.5560.

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Aims: Synthesize tri-acyl ester derivatives of uridine, and evaluate its cytotoxicity against breast cancer cells line. Methods: The tri-esterified uridine derivatives were obtained through Steglich esterification reaction by fatty and aromatic acids, and with acetic anhydride. An acetonide derivative from uridine was prepared with acid catalysis. Compounds were characterized by NMR spectroscopy (1H NMR and 13C NMR), and mass spectrometry. Derivatives were assessed in chinese hamster ovary (CHO-K1) and human breast cancer (MCF-7) cell lines. Results: Five tri-acyl ester derivatives of uridine
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Taylor, Roger. "Aromatic fullerene derivatives." Phys. Chem. Chem. Phys. 6, no. 2 (2004): 328–31. http://dx.doi.org/10.1039/b312502p.

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Tori, Motoo, Masakazu Sono, Keiko Takikawa, et al. "Oxidation Reactions of Marchantin A Trimethyl Ether and Some Aromatic Compounds using m-Chloroperbenzoic Acid. Formation of Muconic Acid Ester and m-Chlorobenzoate." Journal of Chemical Research 23, no. 8 (1999): 470–71. http://dx.doi.org/10.1177/174751989902300808.

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On treatment with m-chloroperbenzoic acid, dihydroeugenol methyl ether and marchantin A trimethyl ether afford muconic acid ester derivatives by oxidation of the aromatic ring as well as hydroxylated derivatives; the m-chlorobenzoate of the dihydroeugenol derivative is also observed for the former.
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Cao, Fengyi, Genxing Zhu, Meng Song, Xiaoli Zhao, Gangqing Ma, and Mengqing Zhang. "Study on the self-assembly of aromatic antimicrobial peptides based on different PAF26 peptide sequences." e-Polymers 22, no. 1 (2022): 276–84. http://dx.doi.org/10.1515/epoly-2022-0012.

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Abstract Antimicrobial peptide (AMP) self-assembly is an effective way to synthesis antimicrobial biomaterials. In previous studies, we found PAF26 AMP (Ac-RKKWFW-NH2) and its derivative K2–F2 peptide (Ac-KKRKKWFWFF-NH2) could both self-assemble into hydrogels, but they had distinct microscopic structures. Therefore, in this work five PAF26 peptide derivatives with different numbers of aromatic amino acids are designed to better understand the self-assembly mechanism of aromatic AMP. The transmission electron microscopy, infrared spectroscopy, circular dichroism, and fluorescence spectroscopy
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Simon, Péter, Bálint Lőrinczi, and István Szatmári. "Alkoxyalkylation of Electron-Rich Aromatic Compounds." International Journal of Molecular Sciences 25, no. 13 (2024): 6966. http://dx.doi.org/10.3390/ijms25136966.

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Alkoxyalkylation and hydroxyalkylation methods utilizing oxo-compound derivatives such as aldehydes, acetals or acetylenes and various alcohols or water are widely used tools in preparative organic chemistry to synthesize bioactive compounds, biosensors, supramolecular compounds and petrochemicals. The syntheses of such molecules of broad relevance are facilitated by acid, base or heterogenous catalysis. However, degradation of the N-analogous Mannich bases are reported to yield alkoxyalkyl derivatives via the retro-Mannich reaction. The mutual derivative of all mentioned species are quinone m
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Arsianti, Ade, Chie Aoki Utsubo, Fadilah Fadilah, et al. "SYNTHESIS AND ANTI-HEPATITIS C VIRUS ACTIVITY OF GALLIC ACID DERIVATIVES WITH CHIRAL CENTER." Asian Journal of Pharmaceutical and Clinical Research 10, no. 7 (2017): 164. http://dx.doi.org/10.22159/ajpcr.2017.v10i7.18162.

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Objective: In this work, we aim to synthesize gallic acid derivatives with chiral center and to evaluate its anti-hepatitis C virus (anti-HCV) activity.Methods: Synthesis of the target derivatives was started from esterification of commercially available boc deprotection (Boc)-L-threonine with allyl bromide, followed by Boc with HCl/EtOAc, amidation, and Sharpless asymmetric dihydroxylation with (DHQ)2PHAL or (DHQD)2PHAL as a ligand to give desired gallic acid derivatives. The synthesized gallic acid derivatives were then evaluated for anti-HCV activity and cytotoxicity.Results: The target der
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Cambie, RC, PS Rutledge, RJ Stevenson, and PD Woodgate. "Synthesis of Phthalide Derivatives of Podocarpic Acid Via Directed ortho Metalation: a Route to Highly Substituted Octahydrochrysene Derivatives." Australian Journal of Chemistry 47, no. 5 (1994): 913. http://dx.doi.org/10.1071/ch9940913.

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Two phthalide derivatives (7) and (8) have been prepared from podocarpic acid (1) via directed ortho metallation. The ring-c aromatic 16-oxa-17-oxo androstane analogue (8) was reacted with dimethyl acetylenedicarboxylate to give the 1,4-epoxy decahydrochrysene derivatives (9) and (10). The stereoisomer (10) was aromatized under acidic conditions to give the chrysen-1-ol derivative (11).
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Abdel-Latif, Nehad A. "Synthesis and Antidepressant Activity of Some New Coumarin Derivatives." Scientia Pharmaceutica 73, no. 4 (2005): 193–216. http://dx.doi.org/10.3797/scipharm.aut-05-15.

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The coumarin-3-cinnamoyl derivatives 2a-d were prepared via Claisen-Schmidt condensation of 3-acetylcoumarin 1 with different aromatic aldehydes. Cycloaddition reaction of 2b,e with guanidine and thiourea yielded the corresponding aminopyrmimidine 3a,b and thioxypyrimidine derivatives 4a,b, respectively. Compounds 4a,b were condensed with chloroacetic acid or 3-bromopropionic acid to yield coumarin 3-thiazolo-pyrimidine 5a,b and thiazinopyrimidine 6a,b derivatives, respectively. Compounds 4a,b were condensed with chloroacetic acid and aromatic aldehyde to yield the aryl methylene derivatives 7
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Afef, Meftah, Messaoudi Nassiba, Khelifa Foudil, Bourhane Djebar Abdallah, and Bachari Khaldoun. "The Attitude In Vitro of 10 Ubiquitous Bacteria in Seawater Polluted by Benzene and Toluene." INTERNATIONAL JOURNAL OF AGRICULTURE AND BIOLOGICAL SCIENCES 5, May & June 2021 (2021): 122–41. https://doi.org/10.5281/zenodo.5150052.

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<em>This study focuses on specifying a number of ubiquitous non-fastidious bacteria isolated from urine hospitalized patients for their abilities to degrade benzene and toluene. Using the MALDI-Tof technique (Bruker Daltonics), these opportunist bacteria have been identified. The bacteria were inoculated and incubated in sterile water contaminated with pure benzene and toluene for 63 days, at room temperature with continuous oxygenation. Analysis by Gas Chromatography/ Mass Spectrometry (GC / MS) HP6890 / HP 5973 MS (Agilent Technologies) allowed us to determine the concentration of each hydro
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Dissertations / Theses on the topic "Aromatic derivatives"

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Alaviuhkola, T. (Terhi). "Aromatic borate anions and thiophene derivatives for sensor applications." Doctoral thesis, University of Oulu, 2007. http://urn.fi/urn:isbn:9789514286575.

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Abstract This study was part of a project targeted at developing chemical sensors for organic cations and metal ions by exploiting the interactions between cations and anionic borate derivatives. As well, the chemical synthesis of thiophene monomers with charged or neutral ion-recognition sites was investigated. The primary task in the first part of the work was to prepare anionic receptor molecules based on synthesized borate derivatives and study their complexation with N-heteroaromatic and tropylium cations. The complexation was studied in solution by 1H NMR and ESIMS techniques and in so
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Blencowe, Peter Stewart. "Application of dioxinone derivatives for synthesis of aromatic compounds." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/44181.

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This thesis describes synthetic organic chemistry of 2,2,6-Trimethyl-4H-1,3-dioxin-4-one derivatives for the synthesis of aromatic compounds including salicylates, gamma resorcylates, hydroquinones and anilines. Using a biomimetic approach dioxinone derivatives acted as masked poly-carbonyl derivatives which cyclized giving the aromatic molecules in a de novo manner. The synthesis of the substrates was carried out by a variety of methods to introduce different functional groups prior to cyclization. Cross metathesis of a vinyl dioxinone gave access to a variety of substrates capable of cycliza
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Al-Ktaifani, Mahmoud M. "Novel chemistry of the aromatic P₃Câ‚‚'tBuâ‚‚ anion and its derivatives." Thesis, University of Sussex, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288611.

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Pei, Baojian. "Anthracene capped benzoxadisilole, naphthoxadisilole and isobenzofuran : applications in the preparations of triptycynes and iptycene derivatives." HKBU Institutional Repository, 2011. http://repository.hkbu.edu.hk/etd_ra/1212.

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Hollin, Jonathan. "I. Contorted Polycyclic Aromatic Hydrocarbons: Attempted Synthesis Of [12]circulene Derivatives Ii. Synthesis And Characterization Of Novel [1]benzothieno[3,2-B][1]benzothiophene Derivatives." ScholarWorks @ UVM, 2019. https://scholarworks.uvm.edu/graddis/992.

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There has been increasing interest in the development of organic materials due to their unique structural and electronic properties. Organic compounds have the advantage of being able to be deposited from solution, leading to low-cost, high-area electronics production. Contorted polycyclic aromatic hydrocarbons have been shown to have potential for use in organic field-effect transistors (OFETs) and organic photovoltaic devices (OPVs) due to their supramolecular properties and charge carrier mobilities. Thiophene-based materials have also shown great promise in OFETs due to their high charge c
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Rodríguez, López Marco Tulio. "Synthesis of Peropyrene and Tetracene Derivatives for Photochemical Applications." Thesis, University of North Texas, 2015. https://digital.library.unt.edu/ark:/67531/metadc801958/.

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A novel route for the synthesis of the polycyclic aromatic hydrocarbon peropyrene (Pp) is reported along with the efforts to synthesize derivatives of Pp, 2,2′- and 5,5′-linked tetracene dimers as candidates for study as singlet fission materials in photovoltaic devices. Peropyrene was synthesized by the McMurry coupling conditions from phenalenone and low-valent titanium species. The crystal structure of Pp is formed by π-stacked molecular pairs in a herringbone arrangement. The direct functionalization of Pp was studied, and several indirect methods for the functionalization of Pp via phenal
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Conde, Amanda Solis. "Synthesis of 5-methyl-3-phenyl-1,3,4-oxadiazol-2(3H)-one derivatives by electrophilic aromatic substitution." Wright State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=wright1547584724393162.

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Fetters, Hannah. "Functionalized PEEK Analogues from 2,4- and 3,5- Difluorobenzophenone Derivatives." Wright State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1559497023409191.

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Appleton, Anthony Lucas. "Synthesis and characterization of large linear heteroacenes and their derivatives." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/37225.

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The work presented in this thesis is primarily concerned with the synthesis and characterization of large, linear heteroacenes and their derivatives. We have been able to significantly expand on the types of materials available for application in organic electronic device architectures. In particular, the work focused on solution processible and novel derivatives of thiadiazoles, diazatetracenes, diazapentacenes, tetrazapentacences, and N,N-dihydrotetraazaheptacene. Extensive computational studies have been performed in order to better understand the optoelectronic properties of these mater
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Driega, Alex B. (Alexander Brooke) Carleton University Dissertation Chemistry. "An analysis of factors contributing to isotropic [superscript] 13C shifts in 1,2- Dialkoxybenzene and Cyclohexane derivatives." Ottawa, 1992.

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Books on the topic "Aromatic derivatives"

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Aliyev, Ismayil A., Boris A. Trofimov, and Lyudmila A. Oparina. Aromatic Thiols and Their Derivatives. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69621-4.

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Mulder, Patricius Petrus Johannes. Synthesis and spectroscopy of substituted aceanthrylenes and acephenanthrylenes. P.P.J. Mulder, 1992.

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Thomson, R. H. Naturally occurring quinones IV: Recent advances. 4th ed. Blackie Academic & Professional, 1997.

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Thomson, R. H. Naturally occurring quinones IV: Recent advances. 4th ed. Blackie Academic & Professional, 1997.

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C, Chuang J., and United States. Environmental Protection Agency., eds. Polycyclic aromatic hydrocarbons and their derivatives in indoor and outdoor air in an eight-home study. U.S. Environmental Protection Agency, 1992.

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Dimashki, Marwan. Characterisation, concentrations and phase distribution of polycyclic aromatic hydrocarbons (PAH) and their nitrated derivatives (Nitro-PAH) in the urban atmosphere. University of Birmingham, 1998.

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United States. National Aeronautics and Space Administration., ed. [Theoretical calculations on the electron absorption spectra of selected polycyclic aromatic hydrocarbons (PAH) and derivatives]: A final technical report for NASA-Ames agreement no. NCC 2-733. National Aeronautics and Space Administration, 1993.

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Lednicer, Daniel. The organic chemistry of drug synthesis. Wiley, 1995.

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Lednicer, Daniel. The organic chemistry of drug synthesis. Wiley, 1990.

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Georgiev, V. St. Noncondensed Aromatic Derivatives, Part 5 (Noncondensed Aromatic Derivatives). S. Karger AG (Switzerland), 1985.

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Book chapters on the topic "Aromatic derivatives"

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Aliyev, Ismayil A., Boris A. Trofimov, and Lyudmila A. Oparina. "Aromatic Sulfides." In Aromatic Thiols and Their Derivatives. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69621-4_2.

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Franck, Heinz-Gerhard, and Jürgen Walter Stadelhofer. "Production and uses of benzene derivatives." In Industrial Aromatic Chemistry. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73432-8_5.

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Franck, Heinz-Gerhard, and Jürgen Walter Stadelhofer. "Production and uses of toluene derivatives." In Industrial Aromatic Chemistry. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73432-8_6.

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Franck, Heinz-Gerhard, and Jürgen Walter Stadelhofer. "Production and uses of xylene derivatives." In Industrial Aromatic Chemistry. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73432-8_7.

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Aliyev, Ismayil A., Boris A. Trofimov, and Lyudmila A. Oparina. "Aromatic Disulfides, Sulfoxides, Sulfones, and Other Derivatives of Aromatic Thiols." In Aromatic Thiols and Their Derivatives. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69621-4_3.

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Aliyev, Ismayil A., Boris A. Trofimov, and Lyudmila A. Oparina. "Synthesis of Aromatic Thiols." In Aromatic Thiols and Their Derivatives. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69621-4_1.

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Kameda, Takayuki. "Atmospheric Reactions of PAH Derivatives: Formation and Degradation." In Polycyclic Aromatic Hydrocarbons. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6775-4_7.

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Aliyev, Ismayil A., Boris A. Trofimov, and Lyudmila A. Oparina. "Electronic and Conformational Structure of Aromatic Thiols and Their Derivatives." In Aromatic Thiols and Their Derivatives. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69621-4_6.

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Aliyev, Ismayil A., Boris A. Trofimov, and Lyudmila A. Oparina. "Acylated Aromatic Sulfides in Organic Synthesis." In Aromatic Thiols and Their Derivatives. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69621-4_5.

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Aliyev, Ismayil A., Boris A. Trofimov, and Lyudmila A. Oparina. "Reactivity of Aromatic Thiols and Their Derivatives." In Aromatic Thiols and Their Derivatives. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-69621-4_4.

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Conference papers on the topic "Aromatic derivatives"

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Lukovits, I., T. Kosztolányi, E. Kálmán, and G. Pálinkás. "Corrosion Inhibitors: Correlation between Chemical Structure and Efficiency." In CORROSION 1999. NACE International, 1999. https://doi.org/10.5006/c1999-99242.

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Abstract Corrosion inhibition efficiencies of heterocyclic, aromatic or partially saturated aromatic compounds (pyrimidines, benzothiazole derivatives, amino-acids containing an aromatic part, pyridines and quinolines) were correlated with quantum chemical indices of the respective molecules. Inhibition efficiencies measured in acidic solutions containing 0.001 and 0.01 mol/L of the inhibitor, respectively, were collected. The quantum chemical calculations were done by using the simple Hückel method. Comparison of inhibition efficiencies and the differences between energies of the highest occu
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Soriaga, Manuel P., G. M. Berry, C. Bhardwaj, et al. "Chemisorption of Organic Molecules on Metal Electrode Surfaces." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90300.

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Abstract The chemisorption of various organic functional groups from aqueous solutions onto smooth single-crystal and polycrystalline electrodes, and the resistance of the resulting monolayer intermediates towards electrochemical oxidation have been studied; these investigations were motivated by the need to understand, at the atomic level, metal passivation by monolayer organic coatings. The electrodes employed were Rh, Pd, Ir, Pt, and Au whose anodic dissolution is preceded by surface-oxide formation even in highly acidic media. Resistance towards anodic oxidation can thus be associated with
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Kouznetsov, D. L., O. Yu Podkopaeva, Yu V. Chizhov, G. P. Antroshenko, S. M. Shevchenko, and A. I. Altsybeeva. "Relationship between the Structure and Activity of Volatile Corrosion Inhibitors Derived from Cyclic Amines." In CORROSION 2001. NACE International, 2001. https://doi.org/10.5006/c2001-01192.

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Abstract Products of the condensation reaction between morpholine or cyclohexylamine and benzaldehydes have been used extensively as volatile inhibitors of atmospheric corrosion, as well as components of lubricant compositions, biocides and preservatives in automotive cooling liquids and fuels. In this study, we examined the relationship between the electronic structure and inhibition performance of the compounds in an atmospheric corrosion test. The condensation products have significantly lower vapor pressure than parent amines, resulting in longer residence times of inhibitor species at a m
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Markova, Mariia, Antonina Stepacheva, Vladimir Molchanov, Galina Demidenko, and Mikhail Sulman. "FISCHER-TROPSCH SYNTHESIS OVER POLYMER SUPPORTED PROMOTED IRON CATALYSTS." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s17.12.

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In recent decades, the interest of researchers has focused on the development of methods for obtaining alternative energy sources. Fischer-Tropsch synthesis is one of the methods for obtaining a wide range of hydrocarbons and their derivatives. Ru, Ni, Fe and Co are the widely used catalytically active metals in FTS. To increase the activity of the catalyst, as well as increase the yield of target products, promoters are introduced into catalytic systems. In FTS, oxides of alkaline and rare earth metals, oxides of lanthanides and actinides, and noble metals are used as modifiers. In this work,
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Ward, Eric C., Al L. Foster, Ivonne C. Weidner, and Dane E. Glaser. "Looking for an Alternative Yellow Metal Corrosion Inhibitor." In CORROSION 2004. NACE International, 2004. https://doi.org/10.5006/c2004-04079.

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Abstract For the last thirty years, benzotriazole and its derivatives have dominated industrial yellow metal corrosion inhibitors. By far, the most popular of these has been tolyltriazole. It has become the industry standard and is, today, usually the only copper corrosion inhibitor considered by water treatment experts. However, even though it dominates all other competitors, tolyltriazole does have its weaknesses in certain applications. Tests have shown that chlorine added as a biocide can penetrate the thin tolyltriazole film, causing accelerated corrosion rates. The tenacious, hydrophobic
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Miller, Terry A. "Laser spectroscopy of aromatic and organometallic radicals." In OSA Annual Meeting. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.thi1.

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Laser induced fluorescence techniques can be used to obtain rotationally resolved electronic spectra of moderately large aromatic and organometallic radicals cooled to &lt;2 K in a supersonic free jet expansion. Aromatic organic radicals studied include cyclopentadienyl, benzyl, triphenyl methyl, and substituted derivatives thereof. Organometallic radicals studied include Cd and Zn monomethyl as well as group IIA and IIB derivatives of cyclopentadienyl, methylcyclopentadienyl, and pyrrolyl radicals.
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Nedeljković, Nikola V., Vladimir D. Dobričić, Marina Ž. Mijajlović, et al. "„IN SILICO“ PREDICTION OF PHARMACOKINETIC PROPERTIES AND DRUGLIKENESS OF NOVEL THIOUREA DERIVATIVES OF NAPROXEN." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.371n.

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Masking the carboxyl group of naproxen with other functional groups may be a promising strategy to decrease its gastrointestinal toxicity. Thiourea moiety has been described as an important pharmacophore in a variety of pharmacologically active compounds, including anti-inflammatory, antiviral, anticancer, hypoglycemic and antimicrobial agents. Our research group has previously designed twenty novel thiourea derivatives of naproxen, containing amino acids (glycine, L-alanine, β-alanine, L-valine and L-phenylalanine – compounds 1,2,3,4 and 5, respectively), their methyl (6–10) and ethyl esters
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Stanculescu, Anca I., Laura Tugulea, Florin G. Stanculescu, and Marcela Socol. "Fluorescence of substituted aromatic derivatives crystalline materials for optical nonlinear applications." In SPIE Proceedings, edited by Valentin I. Vlad. SPIE, 2004. http://dx.doi.org/10.1117/12.583028.

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Jatunov, Sorel, Antonio Franconetti, Manuel Gómez-Guillén, and Francisca Cabrera-Escribano. "Design of Aromatic Aldehyde Chitosan Derivatives for Biological and Industrial Applications." In The 16th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01126.

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Franconetti, Antonio, Pedro Dominguez-Rodriguez, Lidia Contreras-Bernal, Sorel Jatunov, and Francisca Cabrera-Escribano. "Unprecedented Ureidyl-Chitosan Derivatives: An Interesting Tool for Anchoring Aromatic Moieties." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-d007.

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Reports on the topic "Aromatic derivatives"

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Brel, Valery K. Development of the New Approaches in Designing of Fluoroorganic Derivatives Sulfur (Unsaturated, Heterocyclic, Aromatic Molecular Systems and Polyfunctional Organic Compounds). Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada447113.

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Su, Lin. Gas phas thermal reactions of aromatic ethers; Generation of p-xylylene and its derivative by zinc induced dehalogenation. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7121515.

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