Relevant bibliographies by topics / Aromatic nuclei

Contents

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

Academic literature on the topic 'Aromatic nuclei'

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

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Journal articles on the topic "Aromatic nuclei"

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Vácha, R., J. Čechmánková, and J. Skála. "Polycyclic aromatic hydrocarbons in soil and selected plants." Plant, Soil and Environment 56, No. 9 (2010): 434–43. http://dx.doi.org/10.17221/7/2010-pse.

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The influence of soil load with polycyclic aromatic hydrocarbons (PAHs) on their contents in selected plants was investigated. A set of experiments was realized in three years. The influence of extreme soil load with PAHs (soil contaminated by floods and sludge application) on their content in plants was observed in a pot trial. A laboratory column extract trial investigated PAHs transfer from the soil into soil solution in different conditions. The results showed that the transfer of PAHs into plants is influenced mainly by chemical characteristics of the substances (the number and position o
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Korvezee, A. E., and F. E. C. Scheffer. "On substitutions in aromatic nuclei." Recueil des Travaux Chimiques des Pays-Bas 69, no. 4 (2010): 496–502. http://dx.doi.org/10.1002/recl.19500690415.

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Postigo, Al. "Aromatic radical perfluoroalkylation reactions." Canadian Journal of Chemistry 90, no. 6 (2012): 493–97. http://dx.doi.org/10.1139/v2012-026.

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This account intends to cover recent literature on radical perfluoroalkylation reactions of aromatic nuclei in organic and aqueous media. Emphasis will be placed on radical aromatic perfluoroalkylation reactions in water or aqueous media, with the aim of exploring aromatic radical reactivity in a benign environment.
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Kantlehner, Willi, Erwin Haug, Oliver Scherr, Edmont V. Stoyanov, Jochen Mezger, and Georg Ziegler. "Orthoamide, LX [1]. N,N,N’,N’-Tetraformylhydrazin – ein breit anwendbares Formylierungsmittel für aromatische Verbindungen / Orthoamide, LX [1]. N,N,N’,N’-Tetraformylhydrazine – a Formylation Agent for Aromatic Compounds of Wide Scope." Zeitschrift für Naturforschung B 59, no. 4 (2004): 357–65. http://dx.doi.org/10.1515/znb-2004-0402.

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KeywordsThe reagent system formed from N,N,N’,N’-tetraformylhydrazine (3) and aluminum chloride allows the formylation of aromatic compounds. The scope of the method is comparable with the Olah formylation and the Groß-Rieche procedure, since benzene and fluorobenzene can be formylated. Two formyl groups are transferred from 3 to the aromatic nuclei when a molar ratio 4:1:4 (aluminum chloride/3/aromatic compound) is chosen.
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Rozental, Ester, Moshe Goldberg, Harold Basch, and Shmaryahu Hoz. "Charge transfer complexes between azidopentazole and aromatic nuclei." Journal of Molecular Structure: THEOCHEM 674, no. 1-3 (2004): 153–57. http://dx.doi.org/10.1016/j.theochem.2004.02.001.

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KUMYKOV, R. M., A. B. ITTIEV, and K. V. BAMBETOV. "New polynaphthylimides based on 3,3'-diamino-4,4'-dichloroarylenes and aroylene-bis(naphthalic anhydrides) with improved solubility, thermal and fire resistance." Plasticheskie massy, no. 7-8 (October 25, 2022): 10–12. http://dx.doi.org/10.35164/0554-2901-2022-7-8-10-12.

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Soluble polynaphthylimides not previously described were obtained by reacting 3,3'-diamino-4,4'-dichloroarylenes with aroylene-bis(naphthalic anhydrides) containing dichloroethylene, ether, and carbonyl groups. The infl uence of introduced chlorine atoms into aromatic nuclei, dichloroethylene, carbonyl and methylene groups between the phenyl nuclei of the central fragments of macromolecules on the solubility, thermal and strength properties of the synthesized polymers has been studied.
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Ota, E., Yu Hongan, and S. Otani. "Growth of Condensed Aromatic Nuclei in Some Condensed Polynuclear Aromatic (COPNA) Resins by Heating." TANSO 1987, no. 128 (1987): 12–17. http://dx.doi.org/10.7209/tanso.1987.12.

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Suzuki, Satoshi, Thi Bach Tuyet Lam†, and Kenji Iiyama. "5-Hydroxyguaiacyl nuclei as aromatic constituents of native lignin." Phytochemistry 46, no. 4 (1997): 695–700. http://dx.doi.org/10.1016/s0031-9422(97)00348-8.

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Wang, Kailiang, Maoyun Lü, Ao Yu, Xiaoqing Zhu, and Qingmin Wang. "Iron(III) Chloride Catalyzed Oxidative Coupling of Aromatic Nuclei." Journal of Organic Chemistry 74, no. 2 (2009): 935–38. http://dx.doi.org/10.1021/jo8021633.

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Liu, Shiqi, Shuxun Sang, Tian Wang, Yi Du, Jinlong Jia, and Huihuang Fang. "The effects of CO2 on organic groups in bituminous coal and high-rank coal via Fourier transform infrared spectroscopy." Energy Exploration & Exploitation 36, no. 6 (2018): 1566–92. http://dx.doi.org/10.1177/0144598718764752.

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The interactions between supercritical CO2 and coal and their effects on changes in the coal pore structure and organic groups play a critical role in the CO2 geological storage-enhanced coalbed methane recovery. To investigate the effects of supercritical CO2 on organic groups in coals of different ranks and its mechanisms under different temperature and pressure conditions, CO2 sequestration processes in bituminous coals and high-rank coals were replicated using a high-pressure reactor. Four coal samples of different ranks were exposed to supercritical CO2 and water under three temperatures
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Dissertations / Theses on the topic "Aromatic nuclei"

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Silver, David J. "Occupational exposure to ultrafine particles and polycyclic aromatic hydrocarbons from candle emissions." [Tampa, Fla] : University of South Florida, 2005. http://purl.fcla.edu/usf/dc/et/SFE0001426.

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Myers, Eddie Leonard. "Heterocyclic aromatic nucleic acids." Thesis, McGill University, 2002. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=79056.

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In order to investigate the role played by the aromatic moiety of Aromatic Peptide Nucleic Acids (APNAs) in their ability to hybridize with RNA and DNA, as well as improve the solubility of APNA oligomers in aqueous solutions, a new generation of heterocyclic monomers were designed. APNA monomers, where the nucleobase can be thymine, cytosine adenine or guanine, with backbones contain thiophene and pyridine moieties were synthesized. Suitably protected APNA-APNA and PNA-APNA dimers were also synthesized as building blocks for the solid phase synthesis of APNA-PNA chimeras and APNA homop
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Boyd, Michael J. "Synthesis of aromatic peptide nucleic acids." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0007/MQ43635.pdf.

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Živković, Aleksandra. "RNA recognition by fluoro aromatic substituted nucleic acid analogues." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=976480190.

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Fader, Lee David 1974. "Design, synthesis and physicochemical properties of aromatic peptide nucleic acids." Thesis, McGill University, 2002. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=82867.

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Synthetic methods were developed for the preparation of several structurally diverse aromatic peptide nucleic acid (APNA) monomers containing all four natural DNA bases. This set of building blocks was useful for the preparation of oligomers designed to evaluate the hybridization properties of novel peptide nucleic acid (PNA) analogues, which incorporate aromatic rings into their backbone. Protocols for the solid-phase synthesis of APNA-PNA chimeras and APNA homopolymers were also developed.<br>Thermal denaturation experiments involving APNA-PNA chimeras demonstrated that APNA backbones
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Tikilili, Phumza Vuyokazi. "Biodegradation of complex aromatic compounds in nuclear process water." Diss., University of Pretoria, 2010. http://hdl.handle.net/2263/25979.

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Nuclear energy generation results in the production of effluents and radioactive waste that are very difficult to treat and dispose. A considerable fraction of nuclear waste is discharged in the form of complex mixtures of hazardous organic compounds and metallic radionuclides. The most serious pollution is caused by polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls that are very difficult to remove from the environment. The nuclear industry faces certain challenges related to treatment and safe disposal of these mixed radioactive organic wastes due to the toxicity and reca
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Lunetta, Jacqueline F. "The stereoselective synthesis of a novel aromatic peptide nucleic acid, APNA, oligomer." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq25983.pdf.

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McClellan, Lindsay Rene. "Characterization of ARNT (Aryl Hydrocarbon Receptor Nuclear Translocator) Expression in the Soft-shell Clam (Mya arenaria)." Fogler Library, University of Maine, 2007. http://www.library.umaine.edu/theses/pdf/McClellanLR2007.pdf.

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Hardy, Stella Jane. "Photochemistry and photopolymerisation activity of novel aromatic carbonyl photoinitiators." Thesis, Manchester Metropolitan University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359296.

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The photochemistry and photopolymerisation activity of eight novel aromatic carbonyl photoinitiators have been examined. Five of these were t-butyl perester derivatives, three of 9-fluorenone and these were compared with fluorenone itself and the other two of benzophenone and this was used for comparison also. The remaining three compounds incorporated acetophenone type chromophores bound onto a polysiloxane backbone and these were compared to diethoxyacetophenone. The photochemistry was examined using UV/Vis absorption spectroscopy, luminescence, and flash photolysis, both conventional micros
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Song, Li. "Liquid Phase Carbon-Thirteen Dynamic Nuclear Polarization Study of Monosubstituted Aromatic Compounds." Thesis, Virginia Tech, 1997. http://hdl.handle.net/10919/36999.

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In this work, liquid phase Carbon-thirteen DNP experimental data were collected in a flow transfer system for different mono-substituted aromatic compounds, such as, anisole, nitrobenzene and halobenzenes. These substitute groups covered a wide range of electronic effects from strong electron donating groups to strong electron withdrawing groups. Hammett linear free energy relationship was used to quantitatively study the electronic effect of substituent on the carbon-thirteen DNP enhancement. It was found that the carbon-thirteen DNP enhancements at meta and para positions exhibits a reasonab
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Books on the topic "Aromatic nuclei"

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Center, Langley Research, ed. Finite-perturbation intermediate-neglect-of-differential-overlap molecular orbital calculations of nuclear magnetic resonance spin-spin coupling constants for polycyclic aromatic hydrocarbons and aromatic nitrogen heterocyclics. North Carolina State University, 1985.

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L, Anisimova I., Denisov A. I͡U︡, Kopti͡u︡g V. A, Mamati͡u︡k V. I, and Podgornai͡a︡ M. I, eds. Spektry vysokogo razreshenii͡a︡ I͡A︡MR ¹N i ¹³S monozameshchennykh piridinov. Novosibirskiĭ in-t organicheskoĭ khimii SO AN SSSR, 1985.

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Pohjanvirta, Raimo. The AH receptor in biology and toxicology. Wiley, 2011.

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Induction of nuclear anomalies in the gastrointestinal tract by polyclic aromatic hydrocarbons. U.S. Environmental Protection Agency, 1992.

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Kuznetsov, Yuriy, Inna Levina, and Igor Zavarzin. Estrogens and antiestrogens. Modern synthetic approaches to directed modification of estra-1,3,5(10)-triene steroids: goals, reactions, and methods. LCC MAKS Press, 2021. http://dx.doi.org/10.29003/m2020.978-5-317-06626-0.

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The monograph summarizes the information over the past 20 years on the currently widely used and promising methods for the synthesis of estra-1,3,5(10)-triene derivatives by modifying natural estrogens - estrone and estradiol. The main practical goals of modifying this class of steroids and achievements in the chemistry of steroidal antiestrogens, which are promising drugs for hormonal therapy, are considered. Special attention is paid to the stereochemical features of the reactions and the specific problems of modification of the steroid nucleus of estratrienes associated with the presence of
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Finite-perturbation intermediate-neglect-of-differential-overlap molecular orbital calculations of nuclear magnetic resonance spin-spin coupling constants for polycyclic aromatic hydrocarbons and aromatic nitrogen heterocyclics. North Carolina State University, 1985.

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Pohjanvirta, Raimo. AH Receptor in Biology and Toxicology. Wiley & Sons, Incorporated, John, 2011.

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Pohjanvirta, Raimo. AH Receptor in Biology and Toxicology. Wiley & Sons, Incorporated, John, 2011.

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Pohjanvirta, Raimo. AH Receptor in Biology and Toxicology. Wiley & Sons, Incorporated, John, 2011.

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Pohjanvirta, Raimo. Ah Receptor in Biology and Toxicology. Wiley & Sons, Incorporated, John, 2012.

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Book chapters on the topic "Aromatic nuclei"

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Snape, Timothy J. "Aromatic Rearrangements in Which the Migrating Group Migrates to the Aromatic Nucleus." In Arene Chemistry. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch18.

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Kanno, Manabu, Hirohiko Kono, Sheng H. Lin, and Yuichi Fujimura. "Laser-Induced Electronic and Nuclear Coherent Motions in Chiral Aromatic Molecules." In Quantum Systems in Chemistry and Physics. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5297-9_6.

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Wu, Xuan, Wenyu Li, Li Lin, et al. "Thermodynamic Equilibrium Analysis of Steam Reforming Reaction of Radioactive Waste Oil." In Springer Proceedings in Physics. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-1023-6_97.

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AbstractAt present, there are much radioactive waste oil temporarily stored in nuclear fuel processing plants, nuclear industry research institutes and operating nuclear power plants in China, which brings great storage pressure and safety risks to the operating nuclear facilities. In this paper, the components analysis of 40# waste oil used in nuclear facilities was carried out, and the elemental composition and chemical composition of the waste oil were obtained. The analysis showed that the main elements in the waste oil were C and H, and the main chemical components were alkanes, alkenes,
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Majumder, Moumita, and N. Sathyamurthy. "A theoretical investigation on the effect of π–π stacking interaction on 1H isotropic chemical shielding in certain homo- and hetero-nuclear aromatic systems." In Highlights in Theoretical Chemistry. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-31750-7_5.

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Wilson, N. H. "Aromatic compounds with condensed nuclei." In Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds. Elsevier, 1991. http://dx.doi.org/10.1016/b978-044453347-0.50131-2.

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Sainsbury, Malcolm. "Polycyclic arenes." In Aromatic Chemistry. Oxford University Press, 1992. http://dx.doi.org/10.1093/hesc/9780198556749.003.0007.

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This chapter discusses polycyclic arenes. The fusion of benzene rings leads to an array of polycyclic arenes, of which naphthalene, anthracene, and phenanthrene are the best known. Other compounds in the series include chrysene, pyrene, tetracene, and coronene. Many polycyclic aromatic hydrocarbons are found in coal tar, and are formed when plant materials are partially combusted. Some are procarcinogens, that are oxidized within the body to the true cancer-promoting compounds. Very large polycyclic systems are known, and graphite consists of planes derived from an infinite linear fusion of be
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Harwood, Laurence M. "Acid catalysed aromatic rearrangements." In Polar Rearrangements. Oxford University Press, 1992. http://dx.doi.org/10.1093/hesc/9780198556701.003.0006.

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This chapter reviews arbitrary distinction to create the classification of aromatic rearrangements. It considers reactions that are initiated by the generation of an arenium ion and involve migration around the aromatic ring or from a side chain onto the aromatic nucleus. It also points out that the migration terminus positioned on an aromantic ring is initiated by protonation or by a Lewis acid, which is commonly a consequence of equilibration to form thermodynamically stable products. The chapter highlights intramolecular migration, which occurs via a π-complex that leads to equilibration be
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Crowe, Jonathan, and Tony Bradshaw. "Compounds and chemical bonding: bringing atoms together." In Chemistry for the Biosciences. Oxford University Press, 2021. http://dx.doi.org/10.1093/hesc/9780198791041.003.0003.

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This chapter examines compounds and chemical bonding. A compound is a substance that comprises atoms of more than one element. Chemical bonds hold the components of a compound together and are formed by the redistribution of valence electrons between atoms. According to the octet rule, valence electrons are redistributed so that atoms achieve full valence shells that typically contain eight electrons. The chapter then differentiates between the two types of chemical bond: ionic and covalent. An ionic bond forms when one or more electrons are totally transferred from one atom to another to gene
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Davies, David T. "Introduction." In Aromatic Heterocyclic Chemistry. Oxford University Press, 1992. http://dx.doi.org/10.1093/hesc/9780198556602.003.0001.

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This introductory chapter provides an overview of heterocyclic chemistry, which is a large and important branch of organic chemistry. Heterocycles occur in nature, for instance in nucleic acids and indole alkaloids. Synthetic heterocycles have widespread uses as herbicides, fungicides, insecticides, dyes, organic conductors, and, of course, pharmaceutical products such as the anti-ulcer drug. Any ring system containing at least one heteroatom can be described as heterocyclic. This broad definition encompasses both aromatic heterocycles and their non-aromatic counterparts. Aromatic heterocycles
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Calderón-Garcidueñas, Lilian, José Avila-Ramírez, Ana Calderón-Garcidueñas, et al. "Cerebrospinal Fluid Biomarkers in Highly Exposed PM2.5 Urbanites: The Risk of Alzheimer’s and Parkinson’s Diseases in Young Mexico City Residents." In Advances in Alzheimer’s Disease. IOS Press, 2021. http://dx.doi.org/10.3233/aiad210039.

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Exposure to fine particulate matter (PM2.5) and ozone (O3) above US EPA standards is associated with Alzheimer’s disease (AD) risk, while Mn toxicity induces parkinsonism. Mexico City Metropolitan Area (MCMA) children have pre- and postnatal sustained and high exposures to PM2.5, O3, polycyclic aromatic hydrocarbons, and metals. Young MCMA residents exhibit frontal tau hyperphosphorylation and amyloid-β (Aβ)1–42 diffuse plaques, and aggregated and hyperphosphorylated α-synuclein in olfactory nerves and key brainstem nuclei. We measured total prion protein (TPrP), total tau (T-tau), tau phospho
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Conference papers on the topic "Aromatic nuclei"

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D. Lakićević, M., J. Kovačević-Dojčinović, and L. Č. Popović. "X-RAY HARDNESS RATIO AND MID-INFRARED PARAMETERS FOR AGNS." In XIV SERBIAN-BULGARIAN ASTRONOMICAL CONFERENCE. Astronomical Observatory, Volgina 7, 11060 Belgrade 38, Serbia, 2025. https://doi.org/10.69646/14sbac18p.

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We use the resulting parameters of the two different model decompositions of mid-infrared (MIR) spectra of 1) active and star-forming galaxies and 2) active galactic nuclei (AGN). These resulting parameters are the AGN, polycyclic aromatic hydrocarbons – PAH, H II and stellar contribution components, silicate contribution, etc. It is found that some of these parameters correlate with X-ray hardness ratios (especially HR1). This reveals the insight in the X-ray energy bands that influence the MIR parameters and it can point to the AGN sources that are more obscured. These correlations indicate
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Yi, Junghwa, Julien Manin, Kevin Wan, Dario Lopez Pintor, Tuan Nguyen, and Adam Dempsey. "Effect of Fuel Chemical Structure on Soot Formation in Sustainable Aviation Fuels." In Energy & Propulsion Conference & Exhibition. SAE International, 2024. http://dx.doi.org/10.4271/2024-01-4310.

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&lt;div class="section abstract"&gt;&lt;div class="htmlview paragraph"&gt;Sustainable Aviation Fuels (SAFs) offer great promises towards decarbonizing the aviation sector. Due to the high safety standards and global scale of the aviation industry, SAFs pose challenges to aircraft engines and combustion processes, which must be thoroughly understood. Soot emissions from aircrafts play a crucial role, acting as ice nuclei and contributing to the formation of contrail cirrus clouds, which, in turn, may account for a substantial portion of the net radiative climate forcing. This study focuses on u
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Teulade-Fichou, Marie-Paule, Markus Kaiser, Matthieu Sainlos, et al. "Customized fused aromatics for structural recognition of nucleic acids." In XIIIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507245.

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Böge, Nicolas, Sarah Krüger, and Chris Meier. "Synthesis of N2- and C8-N-Ac-DNA-adducts of aromatic amines." In XIVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2008. http://dx.doi.org/10.1135/css200810137.

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Xia, Yi, Jinqiao Wan, Fanqi Qu, and Ling Peng. "Synthesis of nucleoside analogues with aromatic systems appended on the triazole nucleobase." In XIVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2008. http://dx.doi.org/10.1135/css200810224.

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Tikilili, P. V., E. M. N. Chirwa, Carlos Granja, and Claude Leroy. "Microbial Degradation of Polycyclic Aromatic Hydrocarbons and Characterization of Bacteria." In NUCLEAR PHYSICS METHODS AND ACCELERATORS IN BIOLOGY AND MEDICINE: Fifth International Summer School on Nuclear Physics Methods and Accelerators in Biology and Medicine. AIP, 2010. http://dx.doi.org/10.1063/1.3295668.

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Asher, Sanford A. "Ultraviolet resonance Raman studies of monocyclic and polycyclic aromatic hydrocarbons." In International Laser Science Conference. Optica Publishing Group, 1986. http://dx.doi.org/10.1364/ils.1986.tue1.

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UV resonance Raman studies of benzene have demonstrated that the Raman intensities are dominated by vacuum UV transitions. Because of the weak oscillator strengths and the significant homogeneous linewidths in the condensed phase, little Raman enhancement iscontributed by the ~240-260-nm B2 u transition. In the gas phase, however, the smaller homogeneous linewidth results in resonance enhancement. We show experimentally the distinction between resonance Raman scattering and single vibrational level fluorescence. Raman studies of substituted benzene derivatives illustrate that the resonance enh
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Nakajima, S., Y. Iijima, T. Inoue, M. Taniuchi, and K. Ujiie. "Anomalous magnetic properties of polycondensate of fused poly nuclear aromatics(COPNA) resin." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834740.

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Wierzbicki, Teresa A., Ivan C. Lee, and Ashwani K. Gupta. "Catalytic Oxidation of Jet Fuel Surrogates in a Meso-Scale Combustor." In ASME 2015 Power Conference collocated with the ASME 2015 9th International Conference on Energy Sustainability, the ASME 2015 13th International Conference on Fuel Cell Science, Engineering and Technology, and the ASME 2015 Nuclear Forum. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/power2015-49208.

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Oxidation behavior of dodecane and two mixtures of dodecane and m-xylene (90/10 wt. % and 80/20 wt. %) over an Rh catalyst in a meso-scale heat recirculating combustor was examined to isolate the effect of aromatic content on performance. The fuel conversion, product speciation and reaction kinetics were calculated, and the global combustion behavior observed. The results showed that increasing the amount of m-xylene in the fuel increased the fuel conversion from 85% (pure dodecane) to 92% (90/10) and further to 98% (80/20). The presence of xylene also significantly increased CO2/H2O selectivi
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Andrejević, Tina P., Darko P. Ašanin, Nada D. Savić, Nevena Lj Stevanović, Miloš I. Djuran, and Biljana Đ. Glišić. "DNA/BSA BINDING STUDY OF DINUCLEAR GOLD(III) COMPLEXES WITH AROMATIC NITROGEN-CONTAINING HETEROCYCLES AS BRIDGING LIGANDS." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.312a.

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In recent decades, a special attention has been devoted to gold(III) complexes as potential antitumor agents due to their structural similarity to platinum(II) complexes. One of the possible mechanisms of the mode of antitumor activity of gold(III) complexes could include their interaction with DNA. However, the effectiveness of the therapeutic agents also depends on the degree of its binding to proteins present in the blood plasma, because, in this way, it is transported to the cell. Considering this, we investigated the interactions of three dinuclear gold(III) complexes of the general formu
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