Relevant bibliographies by topics / Ligands. Coordination compounds. Gold compounds

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Academic literature on the topic 'Ligands. Coordination compounds. Gold compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Ligands. Coordination compounds. Gold compounds"

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Oroz, Miguel Monge, Annette Schier, and Hubert Schmidbaur. "(Tnmethylphosphine)(triphenylsilyl)gold(I) and Related Compounds." Zeitschrift für Naturforschung B 54, no. 1 (1999): 26–29. http://dx.doi.org/10.1515/znb-1999-0108.

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Mononuclear coordination compounds of the type (R3P)AuSiR′3 with R = R’ = Ph and R = Me, R′ = Ph have been obtained from reactions of the corresponding halide complexes (R3P)AuCl with the silyllithium reagent LiSiPh3. The fully phenylated species undergoes ligand redistribution in solution to give homoleptic ionic species. (Me3P)AuSiPh3 is less susceptible to this process and crystallizes from solutions as the heteroleptic complex. The crystal structure of this compound has been determined by X-ray diffraction. In the crystal lattice the molecules are not associated.
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Goitia, Helen, M. Villacampa, Antonio Laguna, and M. Gimeno. "Cytotoxic Gold(I) Complexes with Amidophosphine Ligands Containing Thiophene Moieties." Inorganics 7, no. 2 (2019): 13. http://dx.doi.org/10.3390/inorganics7020013.

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A new phosphine ligand bearing a thiophene moiety, C4H3SNHCOCH2CH2PPh2 (L), has been prepared by reaction of the aminophosphine Ph2PCH2CH2NH2 with thiophenecarbonylchloride in the presence of triethylamine. The coordination behavior towards gold(I), gold(III) and silver(I) species has been studied and several metal compounds of different stoichiometry have been achieved, such as [AuL2]OTf, [AuXL] (X = Cl, C6F5), [Au(C6F5)3L], [AgL2]OTf or [Ag(OTf)L]. Additionally, the reactivity of the chloride gold(I) species with biologically relevant thiolates was explored, thus obtaining the neutral thiola
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Diamant, Viktor. "NOVEL NON-AQUEOUS ELECTROLYTES BASED ON COORDINATION BORON COMPOUNDS." Ukrainian Chemistry Journal 87, no. 3 (2021): 41–60. http://dx.doi.org/10.33609/2708-129x.87.03.2021.41-60.

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The review provides a classification of electrolytes for modern chemical power sources, supercapacitors, sodium and lithium-ion batteries depending on changes in the physicochemical properties of salts and the products of their interaction with the solvent. A comparative analysis of physicochemical properties of salts depending on the structure of the cation and anion, and the influence of these properties on the properties of final solutions of electrolytes on the example of different classes of ionic liquids and chelatoborates of alkali metals and ammonium was conducted. The dependence of th
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Schmidbaur, Hubert, Gabriele Weidenhiller, Aref A. M. Aly, Oliver Steigelmann, and Gerhard Müller. "Gold(I)-Komplexe sekundärer Phosphine / Gold(I) Complexes of Secondary Phosphines." Zeitschrift für Naturforschung B 44, no. 12 (1989): 1503–8. http://dx.doi.org/10.1515/znb-1989-1206.

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Gold(I) complexes with secondary phosphines R2PH (la—d) of the type R2PH · AuCl (2a—d) have been obtained in good yield from reactions of (carbonyl)chlorogold(I) and the corresponding ligand in diethylether. Both compounds 2a, b bearing aromatic substituents with R = 2,4,6-trimethylphenyl (mesityl) and 2-methylphenyl (o-tolyl), and compounds 2c, d with the bulky alkyl substituents R = t-butyl and R = cyclohexyl, resp., are air-stable crystalline solids. — The coordination compounds have been characterized by NMR and IR data, and — in the cases of 2b and 2c — by single crystal X-ray diffraction
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Cinellu, Maria Agostina, Laura Maiore, Annette Schier, Hubert Schmidbaur, and Davide Rossi. "Synthesis, Solution Behavior, Molecular and Supramolecular Structures of the Water-soluble Gold(I) Saccharinate Complexes M[Au(Sac)2] (M = Na, K, NH4)." Zeitschrift für Naturforschung B 63, no. 9 (2008): 1027–34. http://dx.doi.org/10.1515/znb-2008-0902.

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Three gold(I) saccharinate complexes of the type M[Au(Sac)2] (M = Na, K and NH4) have been prepared by treatment of Au(tht)Cl (tht = tetrahydrothiophene) with saccharine and MOH in MeOHacetone. The compounds are very stable in the solid state but moderately soluble and of limited stability in water. Single crystal X-ray diffraction analysis of the three compounds revealed a linear coordination of the gold atom by the two N-bonded saccharinato ligands. For M = Na, the two heterobicyclic ligands are roughly coplanar with a cis orientation of the two carbonyl groups which allows for a chelation o
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Habermehl, Nicolle C., Fabian Mohr, Dana J. Eisler, Michael C. Jennings, and Richard J. Puddephatt. "Organogold(I) macrocycles and [2]catenanes containing pyridyl and bipyridyl substituents — Organometallic catenanes as ligands." Canadian Journal of Chemistry 84, no. 2 (2006): 111–23. http://dx.doi.org/10.1139/v05-229.

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The synthesis of achiral gold(I) macrocycles [RCH(4-C6H4OCH2C≡CAu)2(µ-Ph2PZPPh2)] and the corresponding chiral gold(I) [2]catenanes, bearing substituents R = 2-pyridyl, 4-pyridyl, and 4-(2,2′-bipyridyl), is reported. The gold(I) compounds form by self-assembly on reaction of oligomeric digold(I) diacetylides [{RCH(4-C6H4OCH2C≡CAu)2}n] or the isocyanide complexes [RCH(4-C6H4OCH2C≡CAuC≡N-t-Bu)2] with diphosphine ligands Ph2PZPPh2, Z = CC or (CH2)n with n = 2–5, or on reaction of [Au2(O2CCF3)2(µ-Ph2PZPPh2)] with diacetylenes RCH(4-C6H4OCH2C≡CH)2 in the presence of a base. The equilibrium between
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Jurgens, Sophie, Fritz E. Kuhn, and Angela Casini. "Cyclometalated Complexes of Platinum and Gold with Biological Properties: State-of-the-Art and Future Perspectives." Current Medicinal Chemistry 25, no. 4 (2018): 437–61. http://dx.doi.org/10.2174/0929867324666170529125229.

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Background: The inherent problems accompanying chemotherapy necessitate the development of new anticancer approaches. The development of compounds that can disrupt cancerous cellular machinery by novel mechanisms, via interactions with proteins and non-canonical DNA structures (e.g. G-quadruplexes), as well as by alteration of the intracellular redox balance, is nowadays focus of intense research. In this context, organometallic compounds of the noble metals Pt and Au have become prominent experimental therapeutic agents. This review provides an overview of the Pt(II) and Au(III) cyclometalate
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Fernández-Vega, Lauren, Valeria A. Ruiz Silva, Tania M. Domínguez-González, et al. "Evaluating Ligand Modifications of the Titanocene and Auranofin Moieties for the Development of More Potent Anticancer Drugs." Inorganics 8, no. 2 (2020): 10. http://dx.doi.org/10.3390/inorganics8020010.

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Over time platinum-based anticancer drugs have dominated the market, but their side effects significantly impact the quality of life of patients. Alternative treatments are being developed all over the world. The titanocene and auranofin families of compounds, discovered through an empirical search for other metal-based therapeutics, hold tremendous promise to improve the outcomes of cancer treatment. Herein we present a historical perspective of these compounds and review current efforts focused on the evolution of their ligands to improve their physiological solution stability, cancer select
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Börner, Martin, Laura Blömer, Marcus Kischel, et al. "Deposition of exchange-coupled dinickel complexes on gold substrates utilizing ambidentate mercapto-carboxylato ligands." Beilstein Journal of Nanotechnology 8 (July 5, 2017): 1375–87. http://dx.doi.org/10.3762/bjnano.8.139.

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The chemisorption of magnetically bistable transition metal complexes on planar surfaces has recently attracted increased scientific interest due to its potential application in various fields, including molecular spintronics. In this work, the synthesis of mixed-ligand complexes of the type [NiII 2L(L’)](ClO4), where L represents a 24-membered macrocyclic hexaazadithiophenolate ligand and L’ is a ω-mercapto-carboxylato ligand (L’ = HS(CH2)5CO2 − (6), HS(CH2)10CO2 − (7), or HS(C6H4)2CO2 − (8)), and their ability to adsorb on gold surfaces is reported. Besides elemental analysis, IR spectroscop
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Deaton, Joseph C., and Henry R. Luss. "Gold(I) coordination compounds with mesoionic thiolate ligands and the crystal and molecular structure of bis(1,4,5-trimethyl-1,2,4-triazolium-3-thiolate)gold(I) tetrafluoroborate." Journal of the Chemical Society, Dalton Transactions, no. 18 (1999): 3163–67. http://dx.doi.org/10.1039/a903597d.

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Dissertations / Theses on the topic "Ligands. Coordination compounds. Gold compounds"

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Coetzee, Jacorien. "New developments in the coordination chemistry of gold(1), gold(II) and gold(III) with C-, N-, P-and S-Donor ligands /." Link to the online version, 2007. http://hdl.handle.net/10019/412.

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Coetzee, Jacorien. "New developments in the coordination chemistry of Gold(I), Gold(II) and Gold(III) with C-, N- , P-and S-donor ligands." Thesis, Stellenbosch : University of Stellenbosch, 2007. http://hdl.handle.net/10019.1/1702.

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Thesis (MSc (Chemistry and Polymer Science))--University of Stellenbosch, 2007.<br>A comprehensive, comparative structural study of gold(I), gold(II) and gold(III) compounds with the general formula [Aux(C6F5)y(tht)z] (tht = tetrahydrothiophene) was performed. The series of compounds included the unprecedented dinucleur gold(II) compound, tetrakis(pentafluorophenyl)bis(tetrahydrothiophene)digold(II), which could be prepared in a rational manner. This very unique compound represents the first example of an unbridged dinucleur gold(II) compound in which the gold(II) centres are not stabilis
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Gabrielli, William Fullard. "Utilisation of various bonding modes of nitrogen-rich heterocycles in gold(I) chemistry." Thesis, Stellenbosch : University of Stellenbosch, 2006. http://hdl.handle.net/10019.1/1258.

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Thesis (PhD (Chemistry and Polymer Science))—University of Stellenbosch, 2006.<br>This study describes the exploitation of numerous donor ligand possibilities presented by selected nitrogen-rich heterocyclic ligands towards gold(I). The preparation and structural characterisation of novel gold(I) complexes, apart from conventional gold(I) bonding possibilities, also encompassed a study of bi- and polytopic bonding modes within a range of multifunctional ligands.
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De, Jongh Leigh-Anne. "Imine-donor complexes with group 6 and group 11 transition metals : coordination and dynamics." Thesis, Stellenbosch : Stellenbosch University, 2008. http://hdl.handle.net/10019.1/2001.

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Thesis (MSc (Chemistry and Polymer Science))--Stellenbosch University, 2008.<br>In this study the coordination of ligands with several coordination sites, 2-aminoazoles (2- amino-4-methylthiazole), 2-aminobenzothiazole, 2-aminobenzoimidazole and 2- aminothiazoline and a biguanidine (N-(2-methylphenyl)imidodicarbonimidic diamide) to soft metal centres [gold(I) (group 11), chromium(0) (group 6) and tungsten (0) (group 6)] was investigated. The aminoazoles have three coordination sites, an exocyclic amine nitrogen, an endocyclic imine nitrogen and an endocyclic thioether sulphur. The biguan
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DuPont, Julie A. "The coordination chemistry of thioether-supported, low-valent cobalt complexes." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file 3.92 Mb., 165 p, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3200521.

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Garnier, Delphine. "Open-shell Coordination Compounds based on Cyanide and Scorpionate Ligands." Thesis, Paris 6, 2015. http://www.theses.fr/2015PA066296/document.

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Cette thèse porte sur la synthèse et la caractérisation de complexes octaédrique de fer(II) et fer(III) coordinés par un ligand tridente de type scorpionate (symétrie fac) et par trois ligands cyanures. Leur utilisation en tant que metalloligand face à des ions métalliques partiellement bloqués est étudiée. Les ligands cyanures, de par leur caractère ambidente, permettent un accès facile aux espèces hétérobimétalliques. De plus, ces ligands sont connus pour transmettre efficacement l'interaction d'échange magnétique et donc pour favoriser la communication électronique intramoléculaire entre le
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Ng, Fei-yeung, and 吳飛洋. "Structure and properties of self-assembled coordination compounds: homoleptic d10-metal aryl/alkylacetylides, ruthenium n-heterocyclesand picolinates." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B37878566.

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Taylor, Steven John. "Exploratory studies of novel ligand systems." Thesis, Rhodes University, 1992. http://hdl.handle.net/10962/d1004973.

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A range of novel ligand systems have been developed in three distinct phases and preliminary studies have been initiated to evaluate their complexation potential. Phase I incorporated the synthesis of single strand ligand systems, which were mainly based on amino acid residues. Techniques have been developed for the attachment of these ligand systems onto, firstly, a styrene monomer, and then later onto a pseudo-styrene linking group, viz. the p-toluoyl group. The linking reactions were based on the formation of amides or esters by the reaction of an acid chloride system with an amine or alcoh
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Kui, Chi-fai. "Non-covalent weak interactions in group IV, PT(II) and AU(I) organometallic complexes synthesis, structures and properties /." Click to view the E-thesis via HKUTO, 2005. http://sunzi.lib.hku.hk/hkuto/record/B32021331.

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Ng, Fei-yeung. "Structure and properties of self-assembled coordination compounds : homoleptic d10-metal aryl/alkylacetylides, ruthenium n-heterocycles and picolinates." View the Table of Contents & Abstract, 2006. http://sunzi.lib.hku.hk/hkuto/record/B36587126.

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Books on the topic "Ligands. Coordination compounds. Gold compounds"

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Transition metal complexes of neutral [Eta]1-carbon ligands. Springer Verlag, 2010.

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P-stereogenic ligands in enantioselective catalysis. Royal Society of Chemistry, 2011.

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Constable, Edwin C. Metals and ligand reactivity. E. Horwood, 1990.

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Constable, Edwin C. Metals and ligand reactivity. Ellis Horwood, 1990.

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Organotransition metal chemistry: From bonding to catalysis. University Science Books, 2010.

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Cornejo, Adolfo F. A. Solution and solid state studies of metal complexes of some EDTA and calixarene derivatives. University College Dublin, 1998.

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Yamaguchi, Ryohei. Ligand platforms in homogenous catalytic reactions with metals: Practice and applications for green organic transformations. Wiley, 2015.

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Wilkinson, G., and R. Gillard. Comprehensive Coordination Chemistry Synthesis Reactions: Properties & Applications Coordination Compounds Ligands (Comprehensive Coordination Chemistry Synthesis Reactions). Reader's Digest Young Families, 1987.

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A, Buslaev I͡U︡, ed. Complex formation and stereochemistry of coordination compounds. Nova Science Publishers, 1996.

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Ligands: Synthesis, Characterization and Role in Biotechnology. Nova Science Pub Inc, 2014.

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Book chapters on the topic "Ligands. Coordination compounds. Gold compounds"

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Boucher, L. J., Karl Koeber, Mirjana Kotowski, and Dieter Tille. "Complexes with Ligands Containing Sulfur." In Coordination Compounds 7. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-662-07506-7_4.

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Boucher, L. J., Karl Koeber, Mirjana Kotowski, and Dieter Tille. "Complexes with Ligands Containing Selenium or Tellurium." In Coordination Compounds 7. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-662-07506-7_5.

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Crassous, J., C. Lescop, and R. Réau. "Coordination-Driven Supramolecular Assembly of Phosphole-Based π-Conjugated Ligands." In Phosphorus Compounds. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3817-3_11.

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Sabbatini, N., S. Perathoner, and L. De Cola. "Effects of Macrocyclic and Cryptand Ligands on Photophysics of Eu3+ Ions." In Photochemistry and Photophysics of Coordination Compounds. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72666-8_5.

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Lees, A. J., M. J. Schadt, and L. Chan. "Photoexcitation of W(CO)6 Solutions Containing α-Diimine Ligands. Kinetics and Mechanism of Chelation for a Series of Photoproduced W(CO)5(α-Diimine) Intermediates." In Photochemistry and Photophysics of Coordination Compounds. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72666-8_42.

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Knorr, Michael, and Fabrice Guyon. "Luminescent Oligomeric and Polymeric Copper Coordination Compounds Assembled by Thioether Ligands." In Macromolecules Containing Metal and Metal-Like Elements. John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470604090.ch3.

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Wickham, Geoffrey, Laurence Wakelin, Brian Palmer, et al. "Cis-Diammineplatinum(II) Complexes Tethered to DNA-Affinic Ligands: Antitumour Activity and DNA-Binding Properties." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-0738-7_5.

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Haeberlin, S. Trebert, F. Lux, T. Spruss, R. Gust, and H. Schönenberger. "Determination of Platinum and Biologically Essential Trace Elements by Neutron Activation Analysis in Pharmacokinetic Studies on Cisplatin Derivatives with Estrophilic Ligands." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1717-3_39.

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Coluccia, Mauro, Maria A. Mariggiò, Angela Boccarelli, et al. "Iminoethers as Carrier Ligands: A Novel trans-Platinum Complex Possessing in Vitro and in Vivo Antitumour Activity." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy 2. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-0218-4_3.

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Gonzalez-Gallardo, Sandra, Ganesan Prabusankar, Thomas Cadenbach, et al. "Structure and Bonding of Metal-Rich Coordination Compounds Containing Low Valent Ga(I) and Zn(I) Ligands." In Structure and Bonding. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-05243-9_5.

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Conference papers on the topic "Ligands. Coordination compounds. Gold compounds"

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"The process of catalytic hydration of acetylene compounds using a homogeneous catalyst based on gold (I) complex with water-soluble organophosphorus ligands." In Chemical technology and engineering. Lviv Polytechnic National University, 2021. http://dx.doi.org/10.23939/cte2021.01.150.

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