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Journal articles on the topic 'Complexation Reactions'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Toda, Fumio. "Crystalline inclusion complexes as media of molecular recognitions and selective reactions." Pure and Applied Chemistry 73, no. 7 (2001): 1137–45. http://dx.doi.org/10.1351/pac200173071137.

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Hexaol host compounds which include guest molecules maximum in 1:6 ratio were prepared. Aromatic hexaol host, hexahydroxytriphenylene, was found to form chiral inclusion crystal by complexation with achiral guest molecules. Some interesting and important optical resolutions of rac-guests by inclusion complexation with a chiral host were described. When chemical reaction and the inclusion complexation procedures in a water suspension medium are combined, new economical and ecological method of the preparation of optically active compound can be established. When photochemical reactions are carr

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2

Chen, Kunfeng, Shuyan Song, and Dongfeng Xue. "Hopper-like framework growth evolution in a cubic system: a case study of Cu2O." Journal of Applied Crystallography 46, no. 6 (2013): 1603–9. http://dx.doi.org/10.1107/s0021889813022322.

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Crystallization of hopper-like Cu2O cubes is demonstrated in alkaline citrate–copper solution upon the equilibrium between complexation, precipitation and redox reactions. The complexation reactions of Na3cit and NaOH with Cu2+manipulate the current chemical reaction routes, phase transformation, and thus crystallization morphologies and compositions. During the crystallization of Cu2O variations of mother solution such as pH and the concentration of Cu2+(Cu+) are monitored byex situpH measurement and UV–Vis absorption spectroscopy. The shape evolution of Cu2O hopper cubes is consistent with t

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3

Chung, Chung-Sun. "Statistical factors in complexation reactions." Journal of Chemical Education 62, no. 2 (1985): 107. http://dx.doi.org/10.1021/ed062p107.

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4

Nash, Kenneth L., and James C. Sullivan. "Kinetics of actinide complexation reactions." Journal of Alloys and Compounds 271-273 (June 1998): 712–18. http://dx.doi.org/10.1016/s0925-8388(98)00193-5.

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5

Benarie, Michel. "Complexation reactions in aquatic systems." Science of The Total Environment 77, no. 2-3 (1988): 298–99. http://dx.doi.org/10.1016/0048-9697(88)90068-x.

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6

Payehghadr, Mahmood, and Seyed Ebrahim Hashemi. "Solvent effect on complexation reactions." Journal of Inclusion Phenomena and Macrocyclic Chemistry 89, no. 3-4 (2017): 253–71. http://dx.doi.org/10.1007/s10847-017-0759-8.

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7

Clifford, Sarah E., Vanny Tiwow, Aleasia Gendron, et al. "Complexation of Constrained Ligands Piperazine, N-substituted Piperazines, and Thiomorpholine." Australian Journal of Chemistry 62, no. 10 (2009): 1196. http://dx.doi.org/10.1071/ch09313.

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Complexation of the symmetric cyclic diamine piperazine (1,4-diazacyclohexane) has been examined in dry dimethyl formamide by spectrophotometric titrations (with Cu2+, Ni2+) to define formation constants, and by stopped-flow kinetics to define the complexation rates and reaction pathway. Initial formation of a rarely observed η1-piperazine intermediate occurs in a rapid second-order reactions. This intermediate then undergoes two competing reactions: formation of (chelated) η2-piperazine (ML) or the formation of (bridging) μ-piperazine (in M2L and M2L3, speciation depending on relative concent

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8

Sieffert, Nicolas, Amol Thakkar, and Michael Bühl. "Modelling uranyl chemistry in liquid ammonia from density functional theory." Chemical Communications 54, no. 74 (2018): 10431–34. http://dx.doi.org/10.1039/c8cc05382k.

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We developed a computationally-efficient protocol based on Density Functional Theory (DFT) and a continuum solvation model (CSM) to predict reaction free energies of complexation reactions of uranyl in liquid ammonia.

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9

Lavallee, David K. "Complexation and Demetalation Reactions of Porphyrins." Comments on Inorganic Chemistry 5, no. 3 (1986): 155–74. http://dx.doi.org/10.1080/02603598608072281.

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10

Chuen-Ying, Liu, Chang Huan-Tsung, and Hu Cho-Chun. "Complexation reactions in a heterogeneous system." Inorganica Chimica Acta 172, no. 2 (1990): 151–58. http://dx.doi.org/10.1016/s0020-1693(00)80850-6.

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11

Silber, Herbert B. "Europium(III) complexation reactions in water." Inorganica Chimica Acta 139, no. 1-2 (1987): 33–38. http://dx.doi.org/10.1016/s0020-1693(00)84030-x.

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12

Singh, Ajai K. "Organotellurium ligands — designing and complexation reactions." Journal of Chemical Sciences 114, no. 4 (2002): 357–66. http://dx.doi.org/10.1007/bf02703826.

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13

Ilgen, Anastasia G. "Surface Complexation Reactions in Oxide Nanopores." Reviews in Mineralogy and Geochemistry 91A, no. 1 (2025): 337–52. https://doi.org/10.2138/rmg.2025.91a.10.

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14

T., SINGH, and P. SINGH J. "Reactions of Carbonylchlorohydridotris(triphenylphosphine )ruthenium(II) with some Aromatic Thioamides." Journal of Indian Chemical Society Vol. 69, Mar 1992 (1992): 158–59. https://doi.org/10.5281/zenodo.6075439.

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Department of Chemistry, S. G. R. Post-Graduate College, Dobhi, Jaunpur-222 149 <em>Manuscript received 3 May 1991, accepted 5 March 1992</em> Reactions of Carbonylchlorohydridotris(triphenylphosphine)ruthenium(II) with some Aromatic Thioamides.  

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15

Peters, Christoph, Frank Tabellion, Anja Nachbauer, Uwe Fischbeck, Fritz Preuss, and Manfred Regitz. "Organophosphorus Compounds, Part 146* Imidovanadium(V) Complexes as Reaction Partners for Kinetically Stabilized Phosphaalkynes. Synthesis and Reactivity of 3-Aza-l,2,4,6-tetraphospha-quadricyclanes." Zeitschrift für Naturforschung B 56, no. 9 (2001): 951–62. http://dx.doi.org/10.1515/znb-2001-0915.

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The Lewis base adducts of imidovanadium(V) compounds 5a,b undergo chemoselective cyclooligomerization reactions with the kinetically stabilized phosphaalkynes 4a-e to furnish the azatetraphosphaquadricyclanes 6a-f with incorporation of the imido fragment. The reactivity of this novel class of heteropolycyclic compounds has been examined exemplarily for compound 6a. Complexation of one and two phosphorus atoms was achieved by reaction with nonacarbonyldiiron or the tungsten pentacarbonyl-THF complex resulting in the formation of the transition metal compounds 17-20. Reactions of 6a with the sul

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16

Usenik, Andrea, Matija Modrušan, Katarina Leko, et al. "A Combined Thermodynamic and Computational Study of Alkaline Earth Metal Cations Complexation by a Fluorescent Calix[4]arene Receptor." International Journal of Molecular Sciences 26, no. 3 (2025): 1264. https://doi.org/10.3390/ijms26031264.

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Complexation of alkaline earth metal cations with fluorescent tertiary-amide lower-rim calix[4]arene derivative bearing two phenanthridine moieties was studied experimentally (UV spectrophotometry, fluorimetry, isothermal microcalorimetry, NMR spectroscopy) and computationally (classical molecular dynamics and DFT calculations) at 25 °C. The complexation reactions were studied in acetonitrile, methanol, and ethanol, whereby the solvent effect on cation-binding processes was particularly addressed. The complex stability constants and standard reaction thermodynamic quantities (Gibbs energies, e

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17

Tlustý, Martin, Václav Eigner, Hana Dvořáková, and Pavel Lhoták. "The Formation of Inherently Chiral Calix[4]quinolines by Doebner–Miller Reaction of Aldehydes and Aminocalixarenes." Molecules 27, no. 23 (2022): 8545. http://dx.doi.org/10.3390/molecules27238545.

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The formation of inherently chiral calix[4]arenes by the intramolecular cyclization approach suffers from a limited number of suitable substrates for these reactions. Here, we report an easy way to prepare one class of such compounds: calixquinolines, which can be obtained by the reaction of aldehydes with easily accessible aminocalix[4]arenes in acidic conditions (Doebner–Miller reaction). The synthetic procedure represents a very straightforward approach to the inherently chiral macrocyclic systems. The complexation studies revealed the ability of these compounds to complex quaternary ammoni

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18

Chipperfield, J. R. "Complexation Reactions in Aquatic Systems: Analytical Approach." Analytica Chimica Acta 225 (1989): 455. http://dx.doi.org/10.1016/s0003-2670(00)84637-1.

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19

Hosten, Eric, and Hans E. Rohwer. "Complexation reactions of uranyl with arsenazo III." Analytica Chimica Acta 355, no. 1 (1997): 95–100. http://dx.doi.org/10.1016/s0003-2670(97)81616-9.

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20

R., S. Pandey, and S. Pandey C. "Ionophoretic study on complexation reactions of manganese-, iron-, cobalt- and nickel(II) with o-methoxybenzoic acid and nitrilotriacetic acid." Journal of Indian Chemical Society Vol. 76, Jan 1999 (1999): 38–40. https://doi.org/10.5281/zenodo.5848900.

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Divyalok Prakashan, Ahari, P.H.E.D. Colony, Aurangabad-824 101, India Department of Chemistry, S. Sinha College, Aurangabad, India <em>Manuscript received 13 December 1997, revised 28 April 1998, accepted </em>8 <em>June 1998</em> Ternary complexes of Mn<sup>II</sup>, Fe<sup>ll</sup>, Co<sup>ll. </sup>and NI<sup>II</sup> with o-methoxybenzoic acid as primary ligand (HL) and nitrilotriacetic acid (NTA)as secondary ligand (HA) at pH 8.5) µ = 0.1 <em>M) </em>and their binary complexes at different pH have been investigated by ionophoretic technique at 35<sup>°</sup>. The stability

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21

Hamad, Ahmed A., Ramadan Ali, Hassan Refat H. Ali, Dalia M. Nagy, and Sayed M. Derayea. "Facile complexation reactions for the selective spectrofluorimetric determination of albendazole in oral dosage forms and spiked human plasma." RSC Advances 8, no. 10 (2018): 5373–81. http://dx.doi.org/10.1039/c7ra12360d.

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22

Sposito, Garrison. "Surface Reactions in Natural Aqueous Colloidal Systems." CHIMIA 43, no. 6 (1989): 169. https://doi.org/10.2533/chimia.1989.169.

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Natural colloids are mixtures of inorganic and organic polymers resulting from weathering processes. These materials include layer-type aluminosilicates, hydrous oxides, and biodegraded organic matter. Regardless of their molecular structure, these polymeric constituents present reactive functional groups of two principal kinds at the colloid/aqueous solution interface: siloxane ditrigonal cavities and inorganic or organic hydroxy groups. The reactive proportion of each kind of functional group at a colloid surface depends on the extent of chemical weathering and the composition of the materia

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23

Gao, Zhu Qing, Xiao Dong Cai, Lei Lei Cheng, and Kai Cheng Ling. "Studies on the Coordination Reactions of Polyphenols and Vanadium (IV) Using pH-Potentiometry." Advanced Materials Research 396-398 (November 2011): 2225–29. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.2225.

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Protonation constants of pyrocatechol, pyrogallol and gallic acid, and stability constants, thermodynamic properties of their complexes with tetravalent vanadium VO2+ have been calculated by using pH-potentiometry at different temperatures and ionic strength of 0.1mol•L-1NaCl. The results indicated protonation constants and stability constants decrease with increasing temperature. Higher temperature is unfavorable to the complexation reactions. This kind of reaction is exothermic reaction that was spontaneous. Compared with all thermodynamic properties, the enthalpy change is the driving force

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24

Taghdiri, Mehdi, Mahmood Payehghadr, Reza Behjatmanesh-Ardakani, and Homa Gha'ari. "Conductometric Studies of Thermodynamics of Complexation of Co2+, Ni2+, Cu2+, and Zn2+ Cations with Aza-18-crown-6 in Binary Acetonitrile-Methanol Mixtures." Journal of Thermodynamics 2012 (November 11, 2012): 1–10. http://dx.doi.org/10.1155/2012/109132.

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The complexation reactions between aza-18-crown-6 (A18C6) and Co2+, Ni2+, Cu2+, and Zn2+ ions were studied conductometrically in different acetonitrile-methanol mixtures at various temperatures. The formation constants of the resulting 1 : 1 complexes were calculated from the computer fitting of the molar conductance-mole ratio data at different temperatures. Selectivity of A18C6 for Co2+, Ni2+, Cu2+, and Zn2+ cations is sensitive to the solvent composition. At 20°C and in acetonitrile solvent, the stability of the resulting complexes varied in the order but the order was reversed byadding 20%

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25

Taghdiri, Mehdi, Mahmood Payehghadr, Reza Behjatmanesh-Ardakani, Sirous Movahhedi, and Farzaneh Nourifard. "Conductometric Studies of Thermodynamics of 1,10-Didecyl-1,10-diaza-18-crown-6 Complexes with , , , , , , and Ions in Acetonitrile, Methanol, and Ethanol Solutions." Journal of Chemistry 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/318015.

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The complexation reactions between 1,10-didecyl-1,10-diaza-18-crown-6 (DD18C6) and , , , , , and ions were studied conductometrically in acetonitrile, methanol, and ethanol at various temperatures. The formation constants of the resulting 1 : 1 complexes were calculated from the computer fitting of the molar conductance-mole ratio data at different temperatures. In the solvents studied, the stability of the resulting complexes varied in the order acetonitrile ≫ methanol > ethanol. The enthalpy and entropy changes of the complexation reactions were evaluated from the temperature dependence o

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26

Neumajer, Gábor, Gergő Tóth, Szabolcs Béni, and Béla Noszál. "Novel ion-binding C3 symmetric tripodal triazoles: synthesis and characterization." Open Chemistry 12, no. 1 (2014): 115–25. http://dx.doi.org/10.2478/s11532-013-0351-z.

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AbstractNovel C3 symmetric tripodal molecules were synthesized from cyclohexane 1,3,5-tricarboxylic acid. Utilizing click and Sonogashira reactions, ion-binding triazole and pyridazin-3(2H)-one units were incorporated to form polydentate ligands for ion complexation. The structures of the novel C3 symmetric derivatives were extensively characterized by 1H, 13C and 2D NMR techniques along with HRMS and IR. The copper(I)-binding potentials of these ligands were investigated by using them as additives in model copper(I)-catalysed azide-alkyne cycloaddition (CuAAC) reactions. The copper(I) complex

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27

Akan, Zafer, Taner Ozel, Gokhan Oto, and Hulya Ozdemir. "Synthesis of Borono Fluoro Deoxy D glucose as Boron carrier for Boron neutron capture therapy (BNCT)." Medical Science and Discovery 4, no. 7 (2017): 58–64. https://doi.org/10.36472/msd.v4i7.191.

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Objective: The 18F-labeled Deoxy-D-Glucose exhibits high affinity to cancer tissue as a PET (Positron Emission Tomography) imaging agent for metastatic cancers. Complexation of 10B to 18F-DG complex may create a useful BNCT (Boron Neutron Capture Therapy) agent for cancer therapy. In previous studies, complexation and characterization of 10B with DG were evaluated and biodistribution analysis was completed successfully. Radioactive tracer labeled 10B-DG will be a useful approach to uses for BNCT applications. Methods: The 18F-DG synthesized by ion exchange and complexed with 10B(OH)3 via pH re

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28

Romanov, S. R., K. O. Shibaeva, R. R. Minnullin та ін. "α-Carboxylate Phosphabetains in Alkylation and Complexation Reactions". Uchenye Zapiski Kazanskogo Universiteta. Seriya Estestvennye Nauki 165, № 1 (2023): 158–69. http://dx.doi.org/10.26907/2542-064x.2023.1.158-169.

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Alkylation reactions of α-carboxylate phosphabetaines were carried out and studied to enhance the biological activity of previously synthesized carboxylate phosphabetaines. As a result of these reactions, the original structure was destroyed with the formation of quaternary salts of phosphonium triiodide. The structure and composition were confirmed by a complex of physical research methods, including NMR, IR spectroscopy, and elemental analysis. The bactericidal and antimycotic activity of the synthesized salts was assessed. The compounds showed activity similar to that of commercial drugs. T

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29

Tsai, Ming-Shan, U. Narasimha Rao, Peng-Yu Hsueh, and Ming Chang P. Yeh. "Completely Diastereoselective Tricarbonyliron Complexation Reactions of Chiral Dienes." Organometallics 20, no. 2 (2001): 289–95. http://dx.doi.org/10.1021/om000719f.

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30

Sontag, S. Kyle, Jenna A. Bilbrey, N. Eric Huddleston, Gareth R. Sheppard, Wesley D. Allen та Jason Locklin. "π-Complexation in Nickel-Catalyzed Cross-Coupling Reactions". Journal of Organic Chemistry 79, № 4 (2014): 1836–41. http://dx.doi.org/10.1021/jo402259z.

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31

Ford, Randal R., Bei Li Li, Robert H. Neilson, and Randall J. Thoma. "Addition and complexation reactions of a silylated aminomethylenephosphine." Inorganic Chemistry 24, no. 13 (1985): 1993–97. http://dx.doi.org/10.1021/ic00207a009.

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32

Hering, Janet G., and Francois M. M. Morel. "Kinetics of trace metal complexation: ligand-exchange reactions." Environmental Science & Technology 24, no. 2 (1990): 242–52. http://dx.doi.org/10.1021/es00072a014.

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33

Iordanskaya, L. I., L. L. Stotskaya, A. M. Gyul'maliev, and S. G. Gagarin. "Reactivity of propargylamines in complexation and polymerization reactions." Theoretical and Experimental Chemistry 25, no. 5 (1990): 548–51. http://dx.doi.org/10.1007/bf00529974.

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34

Dyrssen, David. "Complexation reactions in aquatic systems — An analytical approach." Marine Chemistry 28, no. 4 (1990): 365–66. http://dx.doi.org/10.1016/0304-4203(90)90054-g.

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35

Geyer, Richard A. "Complexation reactions in aquatic systems (an analytical approach)." Chemical Geology 77, no. 2 (1989): 161–63. http://dx.doi.org/10.1016/0009-2541(89)90142-3.

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36

Friedman, Gerald M. "Complexation reactions in aquatic systems—an analytical approach." Geochimica et Cosmochimica Acta 54, no. 4 (1990): 1195. http://dx.doi.org/10.1016/0016-7037(90)90452-q.

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37

Fukuzumi, Shunichi. "Catalytic control of electron-transfer processes." Pure and Applied Chemistry 75, no. 5 (2003): 577–87. http://dx.doi.org/10.1351/pac200375050577.

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Catalytic control of electron-transfer processes is described for a number of photoinduced and thermal electron-transfer reactions, including back electron transfer in the charge-separated state of artificial photosynthetic compounds. The intermolecular and intramolecular electron-transfer processes are accelerated by complexation of radical anions, produced in the electron transfer, with metal ions that act as Lewis acids. Quantitative measures to determine the Lewis acidity of a variety of metal ions are given in relation with the promoting effects of metal ions in the electron-transfer reac

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38

Quelhas, Alexandre, Thierry Roisnel, Jean-Claude Guillemin, and Yann Trolez. "Synthesis, Characterization and Chemistry of Tetrakis(Propargylisocyanide) Copper(I) Complex." Molbank 2023, no. 1 (2023): M1599. http://dx.doi.org/10.3390/m1599.

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The kinetically unstable propargylisocyanide was reacted with the tetrakis(acetonitrile) copper(I) hexafluorophosphate and the formed complex was then involved in a copper-catalyzed alkyne-azide cycloaddition reaction (CuAAC). After the decomplexation of the adduct, the isocyanide was engaged in a Ugi reaction. By such a complexation, reactions can be carried out on the CC triple bond without the constraint of the instability of the free compound or the competitive reactivity of the isocyanide group.

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39

Usacheva, Tatiana R., Kseniya I. Kuz'mina, Mikhail A. Cheshinskiy, Irina A. Kuz'mina, and Valentin A. Sharnin. "DATABASE ON THERMODYNAMIC PARAMETERS OF REACTIONS OF COMPLEXATION AND SOLVATION IN MIXED SOLVENTS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 59, no. 3 (2018): 86. http://dx.doi.org/10.6060/tcct.20165903.5295.

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Study of the effect of solvation on the thermodynamics and kinetics of complexation reactions in mixed solvents are performed in ISUCT and they are one of the main scientific directions of the university. For systematization of thermodynamic parameters of complexation and solvations in the mixed solvents which were obtained by researchers of ISUCT the database «Thermodynamics of a complex formation and solvation in binary solvents» was developed using a MS Access Database Management System which provides fast search of necessary thermodynamic characteristics and also information on the used me

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40

Patil, Mahendra. "Mechanism of the t-BuOM (M = K, Na, Li)/DMEDA-Mediated Direct C–H Arylation of Benzene: A Computational Study." Synthesis 52, no. 19 (2020): 2883–91. http://dx.doi.org/10.1055/s-0040-1707882.

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Over the past ten years, a combination of organic additive and t-BuOK/t-BuONa has been successfully used for the direct C–H arylation of arenes. Conceptually different from transition-metal-catalyzed cross-coupling reactions, these t-BuOK-mediated reactions have raised significant curiosity among organic chemists. Herein, a systematic computational study of each elementary step of the t-BuOM (M = K, Na, Li)/N 1,N 2-dimethylethane-1,2-diamine (DMEDA) mediated direct C–H arylation of benzene is detailed. The presented mechanistic proposal relies on the complexation and reaction of t-BuOM with DM

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41

Peter, S., and M. S. Selvakumar. "Synthesis and Characterization of Phthalic Acid Complexes with Biologically Active Metal Ions." Mapana - Journal of Sciences 1, no. 2 (2003): 7–11. http://dx.doi.org/10.12723/mjs.2.2.

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Animal and plants contain carboxylic acids, which are involved in their metabolic reactions. It is also well known that metal ions are involved in their metabolic reactions. So far the complexation of carboxylate ions with metal ions has been extensively studied. Since neutral or acidic medium is existing in most of the biological reactions in animals and plants it is interesting to study the complexation of organic carboxylic acids in neutral medium with biologically active metal ions such as manganese, cobalt, nickel, copper and zinc. Complexes of phthalic acid were prepared in neutral mediu

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42

Selvakumar, M. S., and S. R. Bheeter. "Synthesis and Characterization of Benzoic Acid Complexes with Biologically Active Metal Ions." Mapana - Journal of Sciences 4, no. 1 (2005): 85–89. http://dx.doi.org/10.12723/mjs.6.15.

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Animal and plants contain carboxylic acids, which are involved in their metabolic reactions. It is also well known that metal ions are involved in their metabolic reactions. So far the complexation of carboxylate ions with metal ions has been extensively studied. Since neutral or acidic medium is existing in most of the biological reactions in animals and plants it is interested to study the complexation of organic carboxylic acids in neutral medium with biologically active metal ions such as manganese, cobalt, nickel, copper and zinc. Complexes of benzoic acid were prepared in neutral medium

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43

De Proft, Frank, Lies Broeckaert, Jan Turek, Aleš Růžička, and Rudolph Willem. "Reactivity of low-oxidation state tin compounds: an overview of the benefits of combining DFT Theory and experimental NMR spectroscopy." Canadian Journal of Chemistry 92, no. 6 (2014): 447–61. http://dx.doi.org/10.1139/cjc-2013-0521.

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The reactivity and complexation properties of dicoordinated Sn(II) and Sn(0) compounds are reviewed. The (dominant) electrophilicity of the stannylenes was confirmed and quantified through density functional theory (DFT) based reactivity indices. For these compounds, combining theoretical DFT calculations and experimental nuclear magnetic resonance (NMR) spectroscopic results has evidenced their potential to undergo π-complexation from aromatic π clouds in addition to significantly stronger σ-complexation. Moreover, their potential as Lewis bases was scrutinized in their interactions and react

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44

Cindro, Nikola, Josip Požar, Dajana Barišić, et al. "Neutral glycoconjugated amide-based calix[4]arenes: complexation of alkali metal cations in water." Organic & Biomolecular Chemistry 16, no. 6 (2018): 904–12. http://dx.doi.org/10.1039/c7ob02955a.

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45

Makio, Naoaki, Yuki Sakata, Tomoko Kuribara, et al. "(Hexafluoroacetylacetonato)copper(i)–cycloalkyne complexes as protected cycloalkynes." Chemical Communications 56, no. 77 (2020): 11449–52. http://dx.doi.org/10.1039/d0cc05182a.

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Protection method of cycloalkynes by forming (hexafluoroacetylacetonato)copper(i)–cycloalkyne complexes is disclosed. Selective click reactions are realized through the complexation of cycloalkynes with copper.

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46

Avdeeva, V. V., E. A. Malinina, and N. T. Kuznetsov. "Boron cluster anions and their derivatives in complexation reactions." Coordination Chemistry Reviews 469 (October 2022): 214636. http://dx.doi.org/10.1016/j.ccr.2022.214636.

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47

Sposito, Garrison, and Peter Blaser. "Revised Quasiparticle Model of Protonation and Metal Complexation Reactions." Soil Science Society of America Journal 56, no. 4 (1992): 1095–99. http://dx.doi.org/10.2136/sssaj1992.03615995005600040014x.

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Baker, S. Richard, Michael L. F. Cadman, Leslie Crombie, David A. V. Edwards, and Jayshree Mistry. "Magnesium methoxide complexation in the control of chemical reactions." Journal of the Chemical Society, Perkin Transactions 1, no. 22 (1996): 2705. http://dx.doi.org/10.1039/p19960002705.

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Singr, Jai Deo, Marilyn Daisy Milton, Bishan Khandelwal, S. Karthikeyan, and T. P. Singh. "New Acyclic Chalcogen Bearing Ligands and Their Complexation Reactions." Phosphorus, Sulfur, and Silicon and the Related Elements 136, no. 1 (1998): 299–304. http://dx.doi.org/10.1080/10426509808042623.

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Singh, Jai Deo, Marilyn Daisy Milton, Bishan L. Khandelwal, S. Karthikeyan, and T. P. Singh. "New Acyclic Chalcogen Bearing Ligands and their Complexation Reactions." Phosphorus, Sulfur, and Silicon and the Related Elements 136, no. 1 (1998): 299–304. http://dx.doi.org/10.1080/10426509808545955.

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