Relevant bibliographies by topics / Bivalent Metal Ion Complexes

Contents

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

Academic literature on the topic 'Bivalent Metal Ion Complexes'

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

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Journal articles on the topic "Bivalent Metal Ion Complexes"

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M., SATYANARAYAN REDDY, and VENKATESHWAR REDDY K. "Equilibrium Studies on the System 4,6-Dimethyl-2-mercaptopyrimidine- Bivalent Metal Ion Complexes." Journal of Indian Chemical Society Vol. 73, Jul 1996 (1996): 345–46. https://doi.org/10.5281/zenodo.5897747.

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Department of Chemistry,&nbsp;Osmania University ,&nbsp;Hyderabad -500 007 <em>Manuscript received 6 September 1994,&nbsp;revised 28 October&nbsp;1994, accepted 25 November 1994</em> Equilibrium Studies on the System 4,6-Dimethyl-2-mercaptopyrimidine- Bivalent Metal Ion Complexes.
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MAHMOUD, A. S. MONSHI. "Transition Metal Complexes of 5-[ 4' -(Nitrophenyl)azo]salicylaldehyde-3-thiosemicarbazone." Journal of Indian Chemical Society Vol. 75, Mar 1998 (1998): 158–59. https://doi.org/10.5281/zenodo.5915665.

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Department of Chemistry, King Saud University, P.O. Box 2455, Riyadh-11451, Saudi Arabia <em>Manuscript received 25 September 1996, revised 2 June 1997, accepted 12 June 1997</em> Metal complexes formed by the interaction of 5-[4&#39;-(nitrophenyl)azo]salicylaldehyde-3-thiosemicarbazone [HAT] with some bivalent metal ion have been prepared. The ligand behaves as neutral bidentate, as mononegative bidentate or tridentate ligand.
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Chandra, Sulekh, Smriti Raizada, Monika Tyagi, and Archana Gautam. "Synthesis, Spectroscopic, and Antimicrobial Studies on Bivalent Nickel and Copper Complexes of Bis(thiosemicrbazone)." Bioinorganic Chemistry and Applications 2007 (2007): 1–7. http://dx.doi.org/10.1155/2007/51483.

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A series of metal complexes of Cu(II) and Ni(II) having the general composition[M(L)X2]with benzil bis(thiosemicarbazone) has been prepared and characterized by element chemical analysis, molar conductance, magnetic susceptibility measurements, and spectral (electronic, IR, EPR, mass) studies. The IR spectral data suggest the involvement of sulphur and azomethane nitrogen in coordination to the central metal ion. On the basis of spectral studies, an octahedral geometry has been assigned for Ni(II) complexes but a tetragonal geometry for Cu(II) complexes. The free ligand and its metal complexes
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Chandra, Sulekh, Shikha Parmar, and Yatendra Kumar. "Synthesis, Spectroscopic, and Antimicrobial Studies on Bivalent Zinc and Mercury Complexes of 2-Formylpyridine Thiosemicarbazone." Bioinorganic Chemistry and Applications 2009 (2009): 1–6. http://dx.doi.org/10.1155/2009/851316.

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A series of metal complexes of Zn(II) and Hg(II) having the general composition [where L = 2-formylpyridine thiosemicarbazone; M = Zn(II) and Hg(II); X = , and ] have been prepared and characterized by elemental chemical analysis, molar conductance, and spectral (IR and mass) studies. The IR spectral data suggests the involvement of sulphur and azomethane nitrogen in coordination to the central metal ion. On the basis of spectral studies, a tetrahedral geometry has been assigned for Zn(II) and Hg(II) complexes. The free ligand and its metal complexes have been tested in vitro against a number
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Sunita, Sharma, and Varshney Gaurav. "Use of metal co-ordination compounds as antimicrobial agents." Journal of Indian Chemical Society Vol. 92, Mar 2015 (2015): 313–18. https://doi.org/10.5281/zenodo.5674938.

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Department of Chemistry, Govt. Raza P.G. College, Rampur-244 901, Uttar Pradesh, India Department of Chemistry, IFTM University, Moradabad-244 102, Uttar Pradesh, India <em>E-mail </em>: varshneygaurav.varshney@gmail.com <em>Manuscript received online 01 March 2014, revised 18 September 2014, accepted 06 October 2014</em> Mixed ligand transition metal complexes of Mn<sup>II</sup>, Co<sup>I</sup><sup>I</sup>, Ni<sup>II</sup>, Cu<sup>II</sup> and Zn<sup>II</sup> ions with dibasic oxalic acid as primary ligand and benzoyl hydrazine as secondary ligand have been synthesized. Their conventional phy
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A., Reiss, D. Rudorf W., Blejoiu S., and Deva R. "Transition metal complexes of heterocyclic ligands. Part- IV. Complexes of 6-aryl-3-cyano-4-trifluoromethylpyridine-2(1H)-thione with palladium- and platinum(II)." Journal of Indian Chemical Society Vol. 77, Sep 2000 (2000): 438–39. https://doi.org/10.5281/zenodo.5870062.

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University of Craiova, Faculty of Chemistry, 13, A. I. Cuza 1100-Craiova, Romania Martin-Luther-University, Halle Wittenberg, Institut of Organic Chemistry, 06099 Halle (Saale), Germany Microbiological Laboratory, C. F. R. Polyclinic, 60, Stirbei Voda, 1100-Craiova, Romania <em>Manuscript received 13 March 2000. accepted 20 May 2000</em> The complexes of bivalent Pd and Pt with 6-aryl-3-cyano-4-tritluoromethylpyridine-2(1<em>H</em>)-thione have been synthesized. IR and NM R investigations show that the thioncs are bonded to the metal ion through the sulfur atom. The thioncs and their complexes
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M., M. MOSTAFA, K. T. MAKY A., and M. IBRAHIM K. "Metal Complexes Derived from Isobutyric Acid Hydrazide with Some Bivalent Metal Ions." Journal of Indian Chemical Society Vol. 62, Jan 1985 (1985): 27–30. https://doi.org/10.5281/zenodo.6302306.

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Department of Chemistry, Faculty of Science, Mansoura University, Egypt <em>Manuscript received 16 November 1983, accepted 10 August 1984</em> The preparation and characterisation of some new metal complexes derived from, isobutyric acid hydrazide (IBH), of the types [M(IBH)X<sub>2</sub>]. [M(IBH)<sub>2</sub>X<sub>2</sub>(M = Co<sup>II</sup>, Ni<sup>II</sup>, Cu<sup>ll</sup>, Zn<sup>II</sup>, Cd<sup>II</sup> and Hg<sup>II</sup>&nbsp;; X = CI, Br) and [M(IBH)<sub>3</sub>X<sub>2</sub>.H<sub>2</sub>O] (M=Co<sup>II</sup>, Ni<sup>II</sup>, Cu<sup>II</sup>, Zn<sup>II</sup> and Cd<sup>II</sup>) are r
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Singh, D. P., V. Malik, R. Kumar, K. Kumar, and J. Singh. "Synthesis and spectral and antibacterial studies of bivalent transition metal ion macrocyclic complexes." Russian Journal of Coordination Chemistry 35, no. 10 (2009): 740–45. http://dx.doi.org/10.1134/s1070328409100054.

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Sharma, Sangita, Dipika Dalwadi, and Madhurjya Neog. "A study of the formation constants of ternary and quaternary complexes of some bivalent transition metals." Journal of the Serbian Chemical Society 75, no. 1 (2010): 75–82. http://dx.doi.org/10.2298/jsc1001075s.

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The formation of hetero-ligand 1:1:1, M(II)-Opda-Sal/Gly ternary and 1:1:1:1, M(II)-Opda-Sal-Gly quaternary complexes, where M(II) = Ni, Cu, Zn and Cd; Opda = o-phenylenediamine, Sal = salicylic acid, Gly = glycine, was studied pH-metrically in aqueous medium. The formation constants for the resulting ternary and quaternary complexes were evaluated at a constant ionic strength, ? = 0.20 mol dm-3 and temperature, 30?0.1 ?C. The order of the formation constants in terms of the metal ion for both type of complexes was found to be Cu(II) &gt; Ni(II) &gt; Zn(II) &gt; Cd(II). This order was explaine
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R., N. PATHAK, та K. MISHRA L. "Complexes of β-Isatin-4,4-dimethyl-3-thiosemicarbazone with some Bivalent Metal Ions". Journal of Indian Chemical Society Vol. 65, Feb 1988 (1988): 119–20. https://doi.org/10.5281/zenodo.6035487.

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Chemistry Department, Tata College, Chaibasa-833 202 Chemistry Department, Patna University, Patna-800 005 <em>Manuscript received 27 November 1986, revised 9 December 1987,</em><em>accepted 24 December 1987</em> Complexes of <em>&beta;</em>-Isatin-4,4-dimethyl-3-thiosemicarbazone with some Bivalent Metal Ions.
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Dissertations / Theses on the topic "Bivalent Metal Ion Complexes"

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Congreve, Aileen. "Responsive lanthanide complexes for metal ion sensing." Thesis, Durham University, 2004. http://etheses.dur.ac.uk/3668/.

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The speciation and distribution of zinc (II) within cells is not well established and the range of zinc (II) probes available are of limited use. The quest was to develop responsive lanthanide complexes to bind selectively and respond (by change in hydration state) to biologically relevant concentrations of zinc at physiological pH for possible application in MRI and luminescence. A pyridyl sulfonamide ligand with an a-CH(_2)NHSO(_2)CF(_3) substituent was found to have the desired properties for strong zinc (II) coordination. The presence of a methyl group at 6', inhibited the formation of rel
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Iskra, Andreas. "Photofragmentation studies of metal ion-molecule complexes and metal oxides." Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:d3663b37-7954-47a3-83e3-4a9ad7b9e3e7.

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Gas phase metal-containing complexes provide suitable systems in which to study fundamental binding motifs between a metal ion and molecules in the absence of any solvent, support or competing charge effects. In this thesis, metal-containing species are explored experimentally using infrared resonance enhanced photodissociation (IR-REPD) spectroscopy and velocity map imaging (VMI). The experimental results are further interpreted with the aid of spectral simulations based on density functional theory (DFT). These are the first studies reported using a newly built IR-REPD spectrometer equipped
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Kumari, Sudesh. "ELECTRON AND ION SPECTROSCOPY OF METAL HYDROCARBON COMPLEXES." UKnowledge, 2014. http://uknowledge.uky.edu/chemistry_etds/30.

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Metal-hydrocarbon complexes were prepared in a laser-vaporization molecular beam source and studied by single-photon zero electron kinetic energy (ZEKE) and mass-analyzed threshold ionization (MATI) spectroscopy. The ionization energies and vibrational frequencies of the metal complexes were measured from the ZEKE and MATI spectra. Metal-ligand bonding and low-lying electronic states of the neutral and ionized complexes were analyzed by combining the spectroscopic measurements with quantum chemical calculations and spectral simulations. In this dissertation, the metal complexes of mesitylene,
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Asgariyeh, Mohammed Mehdi. "Aspects of chemistry of metal ion complexes of butylphosphoric acids." Thesis, Imperial College London, 1989. http://hdl.handle.net/10044/1/47339.

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Walker, Nicholas R. "Gas-phase studies of multiply-charged transition metal complexes." Thesis, University of Sussex, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299030.

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Wei, Shiqiang. "Metal ion interactions in the environment /." Uppsala : Swedish Univ. of Agricultural Sciences (Sveriges lantbruksuniv.), 1999. http://epsilon.slu.se/avh/1999/91-576-5495-6.pdf.

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Hunter, Mary Josephine. "Encapsulated metal ions : mononuclear complexes of Schiff-base macrocycles and cryptands." Thesis, Open University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.277902.

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Sarowar, Chowdhury Hasan Chemistry Faculty of Science UNSW. "Electrospray ionisation fourier transform ion cyclotron resonance and quadrupole ion trap mass spectrometry of metal-flavonoid complexes." Publisher:University of New South Wales. Chemistry, 2009. http://handle.unsw.edu.au/1959.4/43658.

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Positive-ion electrospray ionisation Fourier transform ion cyclotron resonance and ion trap mass spectrometry have been used to investigate the reactions of the flavonoids 3-hydroxyflavone, 5-hydroxyflavone, 5-methoxyflavoe, quercetin, quercitrin and rutin with monovalent Li+, Na+, K+ and Cs+, divalent Cu2+, Zn2+ and Pb2+ and trivalent La3+ and Eu3+ metal cations. The effect of capillary-skimmer potential difference and the ion residence time in the hexapole ion trap of the Fourier transform ion cyclotron resonance mass spectrometer are systematically investigated for the flavonoid-alkali and
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Bloom, Alex. "Identification and structural insights into immobilised metal ion affinity purified nuclear protein complexes." Thesis, University of Sheffield, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522493.

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Melton, Darren Landon. "Metal ion complexing properties of the two-dimensional, highly preorganized ligand 1, 10-Phenanthroline-2, 9-Dicarboxylic acid /." Electronic version (PDF), 2005. http://dl.uncw.edu/etd/2005/meltond/darrenmelton.pdf.

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Books on the topic "Bivalent Metal Ion Complexes"

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Beynek, N. Metal-ion control in the template synthesis of helical complexes. UMIST, 1997.

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Astrid, Sigel, and Sigel Helmut, eds. Probing of nucleic acids by metal ion complexes of small molecules. Marcel Dekker, 1996.

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Geraldes, Carlos F. G. C. Lanthanide and Other Transition Metal Ion Complexes and Nanoparticles in Magnetic Resonance Imaging. CRC Press, 2024. http://dx.doi.org/10.1201/9781003374688.

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(Editor), Yitzhak Marcus, and Arup K. SenGupta (Editor), eds. Ion Exchange & Solvent Extraction (Ion Exchange and Solvent Extraction). CRC, 2001.

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Marcus, Yitzhak, and Arup K. SenGupta. Ion Exchange and Solvent Extraction. Taylor & Francis Group, 2004.

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Treatment of plating wastewaters containing metal cyanide complexes by a gas membrane-ion exchange process. University of Minnesota, Water Resources Research Center, 1989.

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Ion Exchange and Solvent Extraction: A Series of Advances, Volume 14. Taylor & Francis Group, 2001.

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Marcus, Yitzhak, and Arup K. SenGupta. Ion Exchange and Solvent Extraction: A Series of Advances, Volume 17. Taylor & Francis Group, 2004.

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Marcus, Yitzhak, and Arup K. SenGupta. Ion Exchange and Solvent Extraction: A Series of Advances, Volume 16. Taylor & Francis Group, 2004.

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SenGupta, Arup K. Ion Exchange and Solvent Extraction: A Series of Advances, Volume 20. Taylor & Francis Group, 2016.

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Book chapters on the topic "Bivalent Metal Ion Complexes"

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Morrow, Janet R., Kimberly A. Kolasa, Shahid Amin, and K. O. Aileen Chin. "Metal Ion Macrocyclic Complexes as Artificial Ribonucleases." In Advances in Chemistry. American Chemical Society, 1996. http://dx.doi.org/10.1021/ba-1995-0246.ch016.

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Afanas'ev, Igor B. "The Formation of Superoxide Adducts by Metal Complexes." In Superoxide Ion Chemistry and Biological Implications. CRC Press, 2024. https://doi.org/10.1201/9781003574538-8.

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Armentrout, P. B. "Guided-Ion Beam Studies of Ionic Transition Metal Clusters and Complexes." In Metal-Ligand Interactions. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0155-1_2.

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Busch, Daryle H. "Synthesis of Macrocyclic Complexes Using Metal Ion Templates." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch19.

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Scrimin, Paolo, Paolo Tecilla, and Umberto Tonellato. "Supramolecular Functions of Designed Transition Metal Ion Complexes." In Chemistry at the Beginning of the Third Millennium. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-04154-3_4.

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Dunbar, Robert C. "Spectroscopy of Metal-Ion Complexes with Peptide-Related Ligands." In Topics in Current Chemistry. Springer International Publishing, 2014. http://dx.doi.org/10.1007/128_2014_578.

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Inokuchi, Yoshiya. "Gas-Phase Spectroscopy of Metal Ion–Benzo-Crown Ether Complexes." In Physical Chemistry of Cold Gas-Phase Functional Molecules and Clusters. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9371-6_5.

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Echegoyen, Luis, and Eduardo Perez-Cordero. "Redox Chemistry of Metal Ion Complexes: Preparation of New Materials." In Transition Metals in Supramolecular Chemistry. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-015-8380-0_6.

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Hettich, Robert L., and Ben S. Freiser. "Gas-Phase Photodissociation of Transition Metal Ion Complexes and Clusters." In ACS Symposium Series. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0359.ch010.

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Marusak, Rosemary A., Thomas P. Shields, and A. Graham Lappin. "Chiral Recognition by Metal-Ion Complexes in Electron-Transfer Reactions." In Electron Transfer in Biology and the Solid State. American Chemical Society, 1989. http://dx.doi.org/10.1021/ba-1990-0226.ch013.

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Conference papers on the topic "Bivalent Metal Ion Complexes"

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Johnson, Richard E., and Vinod S. Agarwala. "Fluorescence Based Chemical Sensors for Corrosion Detection." In CORROSION 1997. NACE International, 1997. https://doi.org/10.5006/c1997-97304.

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Abstract Several fluorescent materials have been identified as possible corrosion sensing coatings. These are either redox or metal ion complex materials. The redox materials are nonfluorescent in the reduced state and become fluorescent upon oxidation. Incorporated into paint coatings, they provide an early warning of corrosive conditions at the metal or alloy surface. The metal ion complex materials only fluoresce when the organic compound complexes with metal ions such as those generated in corrosion reactions. Fluorescent materials have been incorporated into paint coatings and on metal su
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Shaw, S. S., and K. S. Sorbie. "Structure and Stoichiometry of Mixed Divalent Metal (Ca2+/Mg2+/Sr2+/Ba2+) Phosphonate Scale Inhibitor Complexes for Application in Precipitation Squeeze Processes." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05646.

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Abstract In oilfield applications, various divalent cations are present in field produced waters, e.g. Ca2+, Mg2+, Sr2+ and Ba2+. The interaction of these cations with phosphonate scale inhibitors (SI) is important both for scale inhibition and inhibitor retention mechanisms. In this paper, the properties of precipitated “mixed” Ca2+/M2+ phosphonate SI complexes formed by 9 common phosphonate species are investigated, where M2+ may be Mg2+, Sr2+, or Ba2+. These 2 and 3 metal ion complexes with SI are of the form SI_CaN1_SrN2 and SI_CaN1_MgN2_BaN3, where the stoichiometry N1, N2 and N3, are the
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Jaeger, Paul. "Adsorbed Inhibitor Fragments Observed on Alloyed Thin Films Identified by TOF-SIMS." In CORROSION 2001. NACE International, 2001. https://doi.org/10.5006/c2001-01199.

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Abstract Time-of-Flight Secondary Ion Mass Spectroscopy TOFSIMS was used to identify the different fragmented species associated with the adsorption of a triazole based inhibitor on alloyed thin films. Copper, cobalt-iron, nickel-manganese, and nickel-iron alloyed films were immersed in an inhibited aqueous solution. Inspection of the positive and negative spectra indicated different fragmented complexes of the inhibitor. In some cases the primary metal of the alloy was where the inhibitor fragments adsorbed thus excluding or lightly covering the secondary alloy. In many cases there are differ
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Mangalagiu, Violeta, Dorina Amariucai-Mantu, Dumitrela Diaconu, and Vasilichia Antoci. "BENZIMIDAZOLE � PYRIDINE: A NEW TYPE OF HGHLY SENSITIVE CHEMOSENSOR FOR ZN2+." In SGEM International Multidisciplinary Scientific GeoConference. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024v/6.2/s23.01.

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Discovery of new chemosensors for M2+ cations represent a continuously and challenging issue for researcher because of their potential applications in nano and micro technologies. Among the other metals, zinc is the second most abundant transition metal ion in human body and plays a crucial role in many biological and environmental processes. In this work we present the design, synthesis and characterization of a Zn2+ chemosensors and its coordination complexes based on podants with benzimidazole - pyridine skeleton. The new chemosensor have in the same molecule a ?�reach heterocycles (benzimi
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Haskaj, Adelina, Musaj Pacarizi, Sonja Lepitkova, Berat Sinan, Bahri Sinani, and Elida Dreshaj. "THE POTENTIAL COMPLEXING IMPACT OF SOME ORGANIC COMPOUNDS AMINE AND CARBOXYL GROUPS ON TRANSITION METALS." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s18.42.

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Environmental water chemistry is substantially aided by modern electrochemical research. Sensitive voltammetric techniques are much more useful for metal species in natural waters, where complexation with organic molecules predominates. Many environmental electrochemists are still interested in determining the stability constants of metal ion complexes with various ionic species found in natural waterways. The aim of this work is to investigate the possible influence of complexation of amine and carboxyl groups of some organic molecules (with EDTA, NTA and aniline, using differential pulse pol
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Iwawaki, Hirohito, and Kazuhiro Toba. "Corrosion Behavior of Steels in Concentrated NH4HS Environments." In CORROSION 2007. NACE International, 2007. https://doi.org/10.5006/c2007-07576.

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Abstract Abrupt rise in a corrosion rate has been observed when the concentration of NH4HS reached a certain value suggesting that a change in the corrosion mechanism is taking place. In order to elucidate the reason for accelerated metal loss under highly concentrated solutions, corrosion tests were executed in medium and high concentrated solutions at a static condition. Though significant corrosion observed in rich solutions is often ascribed to formation of the iron complex, its presence has not been proved. In the current work, the aggressive environment was successfully generated in a la
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Wei, Zhenqiang, Paul Duby, and Ponisseril Somasundaran. "Surfactants as Green Inhibitors for Pitting Corrosion of Stainless Steels." In CORROSION 2004. NACE International, 2004. https://doi.org/10.5006/c2004-04539.

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Abstract Recently sodium dodecylsulfate (SDS) and some other surfactants have been shown to be promising inhibitors for the pitting corrosion of stainless steels and aluminum alloys in chloride media. In the present research, the effect of other compounds such as multivalent metal cations and other surfactants on the pitting inhibition of 304 stainless steel by SDS was investigated to determine its inhibition behavior in relevant mixed systems. It was shown that calcium ion increased the pitting inhibition efficiency of SDS. The efficiency increase was attributed to the increased SDS adsorptio
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Shoesmith, D. W. "Used Fuel and Uranium Dioxide Dissolution Studies – A Review Report No.: NWMO-TR-2007-03." In CORROSION 2008. NACE International, 2008. https://doi.org/10.5006/c2008-08rts04.

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Abstract The extensive studies of used fuel dissolution inside a failed nuclear waste container have been reviewed. The primary controlling factor is the redox condition set at the fuel surface by water radiolysis, its evolution with time as radiation fields decay, and how it is influenced by the presence of oxidant scavengers, especially H2, produced by corrosion of the steel liner in the container. If the container fails early, and oxidizing conditions are established, dissolution will be a corrosion reaction driven by radiolytically-produced H2O2. As radiation fields decay and conditions be
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Malenov, Dušan P., Katarina A. Ćeranić, Dubravka Z. Vojislavljević-Vasilev та Snežana D. Zarić. "Modeling ion-π interactions of transition metal complexes". У 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.621m.

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Interactions of π-systems with ions are very important for many chemical and biological systems. In this work we show how transition metal coordination strengthens cation-π interactions, and how it makes anion-π interactions of some systems possible. The calculations showed that cation-π interactions between ferrocene and alkali metal ions are stronger than cation-π interactions of benzene. The strongest cation-π interaction is between ferrocene and Li+, with interaction energy of -44.0 kcal/mol, while benzene-Li+ interaction has the energy of -36.1 kcal/mol. Cation-π interactions can also inv
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Petrović, Biljana. "TRANSITION METAL ION COMPLEXES AS POTENTIAL ANTITUMOR AGENTS." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac,, 2021. http://dx.doi.org/10.46793/iccbi21.009p.

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Discovery of the antitumor activity of platinum complex, cisplatin, cis-Pt(NH3)2Cl2, and later carboplatin and oxaliplatin, led to the intensive investigation of the potential antitumor activity of the huge number of platinum complexes. Furthermore, it is well-known that platinum complexes express toxicity, numerous side effects and resistance, so the scientists make a lot of efforts to synthetize, beside Pt(II) and Pt(IV), other non-platinum compounds with potential antitumor activity, such as Pd(II), Ru(II/III) and Au(III) complexes. The goal of this study is to summarize the results of the
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Reports on the topic "Bivalent Metal Ion Complexes"

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Thompson, Richard C. The Redox Chemistry of Some Peroxo and Superoxo Metal Ion Complexes. Defense Technical Information Center, 1987. http://dx.doi.org/10.21236/ada189159.

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Crowley, David, Yitzhak Hadar, and Yona Chen. Rhizosphere Ecology of Plant-Beneficial Microorganisms. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7695843.bard.

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Abstract:
Rhizoferrin, a siderophore produced by Rhizopus arrhizus, has been shown in previous studies to be an outstanding Fe carrier to plants. However, calculations based on stability constants and thermodynamic equilibrium lead to contradicting conclusions. In this study a kinetic approach was employed to elucidate this apparent contradiction and to determine the behavior of rhizoferrin under conditions representing soil and nutrient solutions. Stability of Fe3+ complexes in nutrient solution, rate of metal exchange with Ca, and rate of Fe extraction by the free ligand were monitored for rhizoferrin
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