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Journal articles on the topic 'Bivalent Metal'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Sharfalddin, Abeer A., Abdul-Hamid Emwas, Mariusz Jaremko, and Mostafa A. Hussien. "Synthesis and theoretical calculations of metal-antibiotic chelation with thiamphenicol: in vitro DNA and HSA binding, molecular docking, and cytotoxicity studies." New Journal of Chemistry 45, no. 21 (2021): 9598–613. http://dx.doi.org/10.1039/d1nj00293g.

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2

AFKAR, K. ABD EL-HADI, H. H. EL-GHANDOUR AHMED, K. A. IBRAHIM MOHAMED, and M. DAR WISH FAIZA. "Complexes of 3-(p-Tolyl)-1-phenylpyrazol-5-ylthiourea with some Bivalent Metal Ions." Journal of Indian Chemical Society Vol. 72, Jul 1995 (1995): 469–70. https://doi.org/10.5281/zenodo.5905426.

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Chemistry Department, Faculty of Science, Cairo University. Giza, Egypt <em>Manuscript received 20 December 1988. revised 28 December 1993, accepted 20 January 1994</em> Complexes of 3-(p-Tolyl)-1-phenylpyrazol-5-ylthiourea with some Bivalent Metal Ions

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3

HARI, PRASAD SRIVASTAVA, and TIWARI DIWAKAR. "Biamperometric Determination of some Bivalent Metal Ions." Journal of Indian Chemical Society Vol. 70, Oct 1993 (1993): 847–49. https://doi.org/10.5281/zenodo.5939687.

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Department of Chemistry, Banaras Hindu University, Varanasi-221 005 <em>Manuscript received 1 September 1991, revised 2 April 1993, accepted 8 April 1993</em> Biamperometric Determination of some Bivalent Metal Ions

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4

Varadwaj, Pradeep R., Arpita Varadwaj, and Bih-Yaw Jin. "Ligand(s)-to-metal charge transfer as a factor controlling the equilibrium constants of late first-row transition metal complexes: revealing the Irving–Williams thermodynamical series." Physical Chemistry Chemical Physics 17, no. 2 (2015): 805–11. http://dx.doi.org/10.1039/c4cp03953j.

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5

S., N. LIMAYE, and C. SAXENA M. "Some Ligational Aspects of Tartrazine. Stabilities and c.f.s.e. of Its Binary Complexes with Some Bivalent Metal lons." Journal of Indian Chemical Society Vol. 62, Mar 1985 (1985): 192–93. https://doi.org/10.5281/zenodo.6303192.

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Department of Chemistry, Dr. H. S. Gour Vishwavidyalaya, Sagar-470 003 <em>Manuscript received 13 March 1984, received 16 July 1984, accepted 19 January 1985</em> Practical<em> </em>proton-ligand stability constant of tartrazine (trzne) and metal-ligand stability constants of its 1 : 1 binary complexes with some bivalent metal ions, <em>\(viz\)., </em>UO\(_2^2\)+, VO<sup>2+</sup>, Be<sup>2+</sup>, Mn<sup>2+</sup>,+ Co<sup>2+</sup>,+ Ni<sup>2+</sup>, Cu<sup>2+</sup>+, Zn<sup>2+</sup>, Cd<sup>2+</sup> have been determined pH-metrically using Irving-Rossolti titration technique at 25° an

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6

R., C. SHARMA, K. VAR.SHNBY V., and AMBWANI J. "Synthetic and Antimicrobial Studies of some Bivalent Metal Chelates of Heterocyclic Anils." Journal of Indian Chemical Society Vol. 69, Nov 1992 (1992): 772–74. https://doi.org/10.5281/zenodo.6044034.

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Department of Chemistry, Institute of Basic Sciences, Khandari Road, Agra-282 002 <em>Manuscript received 3 May 1990, revised 20 July 1992, accepted 31 July 1992</em> Synthetic and Antimicrobial Studies of some Bivalent Metal Chelates of Heterocyclic Anils.  

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7

Verma, V. P., and A. Khushu. "Thermal and other studies on bivalent metal selenltes." Journal of Thermal Analysis 35, no. 4 (1989): 1157–63. http://dx.doi.org/10.1007/bf01913033.

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8

Kar, L., P. Matsumura, and M. E. Johnson. "Bivalent-metal binding to CheY protein. Effect on protein conformation." Biochemical Journal 287, no. 2 (1992): 521–31. http://dx.doi.org/10.1042/bj2870521.

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CheY is a 14 kDa cytoplasmic protein that is activated by the transfer of a phosphoryl moiety to Asp-57 from phosphoCheA during signal transduction in bacterial chemotaxis. It has been established that metal ions are necessary for the autophosphorylation of CheA, the transfer of phosphate from phosphoCheA to CheY and the autodephosphorylation of phosphoCheY. In this work, paramagnetic relaxation enhancement has been used in conjunction with one- and two-dimensional n.m.r. to study the interaction of CheY with bivalent metal ions. These studies have led to the discovery of two conformations of

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9

S., N. DUBEY, and K. VAID BEENA. "Triazoles as Complexing Agents :Synthesis and Characterisation of some Bivalent Metal with Bi- and Tridentate Schiff Bases." Journal of Indian Chemical Society Vol. 69, Nov 1992 (1992): 774–77. https://doi.org/10.5281/zenodo.6044073.

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Department of Chemistry, Kurukshetra University, Kurukshetra-132 119 <em>Manuscript received 31 October 1990, revised 20 July 1992, accepted 31 July 1992</em> Triazoles as Complexing Agents :Synthesis and Characterisation of some Bivalent Metal with Bi- and Tridentate Schiff Bases. 

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10

A., K. DWIVEDI, S. OJHA V., N. TIWARI H., and K. MISHRA L. "Donor Behaviour of some MorpholineN- thiohydrazones with some Bivalent Metal Ions." Journal of Indian Chemical Society Vol. 72, Jun 1995 (1995): 403–5. https://doi.org/10.5281/zenodo.5904989.

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Department of Chemistry, Patna Universtty, Patna-800 005 <em>Manuscript received 12 October 1993, accepted 31 December 1993</em> Donor Behaviour of some MorpholineN-thiohydrazones with some Bivalent Metal Ions

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11

Yeung, I. Y. L., E. Phillips, D. A. Mann, and C. H. Barton. "Oxidant regulation of the bivalent cation transporter Nramp1." Biochemical Society Transactions 32, no. 6 (2004): 1008–10. http://dx.doi.org/10.1042/bst0321008.

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Nramp1 (murine natural resistance-associated macrophage protein 1 gene)/Slc11a1 (solute carrier family 11 member a1 gene) encodes a bivalent-metal/iron transporter that is expressed within late endosomes/lysosomes of macrophages. A functionally null Nramp1 allele that exhibits impaired bivalent cation transport enables excessive growth of intracellular pathogens. Iron is important for many cellular activities, including defence against pathogens; however, redox-active/free iron can participate in Fenton chemistry that generates reactive oxygen species. Using Raw264.7 cells, non-functional for

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12

A., P. GUPTA, QURESHI M., SHARMA V., C. KAUSHIK R., and O. GUPTA H. "Ion-exchange Behaviour of Stannic Tungstophosphate towards Bivalent Metal Ions." Journal of Indian Chemical Society Vol. 63, Feb 1986 (1986): 206–9. https://doi.org/10.5281/zenodo.6254062.

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Chemistry Department, Delhi College of Engineering, Kaskinere Gate, Delhi-110 006 Chemical Laboratorys, Z. H. College of Engineering and Technology, Aligarh Muslim University, Aligarh-202 001 <em>Manuscript received 19 September 1984, revised 16 August 1985, accepted 29 October 1985</em> Sn<em><sup>Iv </sup></em>tungstophosphate (Sn-W-P) was prepared by adding 01 <em>M</em> Sn<em><sup>Iv </sup></em>chloride solution to 0.1 <em>M </em>tungstophosphoric acid solution in different volume ratios. The dried gel of Sn-W-P was reused in 6 <em>M </em>phosphoric acid for 100 h before bre

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13

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> ; 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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14

Xiao, Jun, Miyamoto Chikanori, Ke-Feng Yu, Seki Hideshi, Maruyama Hideo, and Pei-Min He. "Biosorption of heavy metals onto nonliving Laminaria japonica." Water Science and Technology 65, no. 8 (2012): 1514–20. http://dx.doi.org/10.2166/wst.2012.042.

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In this paper, study of the biosorption of Cd2+ and Pb2+ by nonliving Laminaria japonica in a batch adsorption system is described. The content of acidic sites and the dissociation constant of carboxylic acid functional groups (metal-binding site) of L. japonica were experimentally determined by conductometric and potentiometric titrations and theoretically predicated by using monodentate and bidentate binding models. The models are based on the monodentate or bidentate binding reactions of bivalent metal ions to acidic sites. The acidic site content and carboxylic acid dissociation constants

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15

G, P. SENGUPTA, R. BERA C., and N. GHOSH N. "Stability Constants of some Bivalent transition Metal Chelates of Salicylidene Sulpbanilamide." Journal of Indian Chemical Society Vol. 64, Feb 1987 (1987): 117–18. https://doi.org/10.5281/zenodo.6201154.

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Department of Chemistry Visha-Varathi University, Shantiniketan -731 235 <em>Manuscript received 20 march 1986, revised 18 November 1986, accepted 3 January 1987</em> Stability Constants of some Bivalent transition Metal Chelates of Salicylidene Sulpbanilamide  

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16

Jahan, Israt, Md Amirul Islam, Tahmid Hasan Rupam, Mujib L. Palash, and Bidyut Baran Saha. "Water adsorption characterization of bivalent metal doped HKUST-1." Thermal Science and Engineering Progress 35 (October 2022): 101453. http://dx.doi.org/10.1016/j.tsep.2022.101453.

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17

Cheng, Ji Jian. "Crystallization Behavior of some Bivalent Metal Containing Fluorozirconate Glasses." Materials Science Forum 67-68 (January 1991): 219–24. http://dx.doi.org/10.4028/www.scientific.net/msf.67-68.219.

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18

Singh, B., and A. K. Srivastav. "Studies on Some Bivalent Metal Complexes of Schiff Bases." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 24, no. 9 (1994): 1523–36. http://dx.doi.org/10.1080/00945719408002578.

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19

Narvekar, Kedar U., and Bikshandarkoil R. Srinivasan. "Crystal structures of two isostructural bivalent metal N-benzoylglycinates." Acta Crystallographica Section E Crystallographic Communications 76, no. 8 (2020): 1260–65. http://dx.doi.org/10.1107/s2056989020009287.

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The crystal structures of two coordination compounds of N-benzoylglycine, viz. catena-poly[[[diaquabis(N-benzoylglycinato)cobalt(II)]-μ-aqua] dihydrate], {[Co(C9H8NO3)2(H2O)3]·2H2O} n , 1, and catena-poly[[[diaquabis(N-benzoylglycinato)nickel(II)]-μ-aqua] dihydrate], {[Ni(C9H8NO3)2(H2O)3]·2H2O} n , 2, are described. The structures of 1 and 2 were reported previously [Morelock et al. (1979). J. Am. Chem. Soc. 101, 4858–4866] and redetermined in this work to determine the H-atom coordinates. In the isostructural compounds, the central metal is located on an inversion centre and exhibits a distor

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20

S., N. DUBEY, and P. YADAV (Mrs.). "Synthesis and Characterisation of some Bivalent Metal lon Complexes of Thiocyanate or Iodide and Thiocarbohydrazide." Journal of Indian Chemical Society Vol. 68, Jun 1991 (1991): 350–52. https://doi.org/10.5281/zenodo.6156461.

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Department of Chemistry, Kurukshetra University, Kurukshetra-132 119 <em>Manuscript received 26 December 1990, revised 6 May 1991. </em><em>accepted 27 May 1991</em> Synthesis and Characterisation of some Bivalent Metal lon Complexes of Thiocyanate or Iodide and Thiocarbohydrazide.  

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21

CLUGSTON, Susan L., Rieko YAJIMA, and John F. HONEK. "Investigation of metal binding and activation of Escherichia coli glyoxalase I: kinetic, thermodynamic and mutagenesis studies." Biochemical Journal 377, no. 2 (2004): 309–16. http://dx.doi.org/10.1042/bj20030271.

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GlxI (glyoxalase I) isomerizes the hemithioacetal formed between glutathione and methylglyoxal. Unlike other GlxI enzymes, Escherichia coli GlxI exhibits no activity with Zn2+ but maximal activation with Ni2+. To elucidate further the metal site in E. coli GlxI, several approaches were undertaken. Kinetic studies indicate that the catalytic metal ion affects the kcat without significantly affecting the Km for the substrate. Inductively coupled plasma analysis and isothermal titration calorimetry confirmed one metal ion bound to the enzyme, including Zn2+, which produces an inactive enzyme. Iso

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22

A., K. SINHA, D. SINGH P., N. KFSHARI B., and K. MISHRA L. "Complexes of some Bivalent Metal Ions with 4-Salicylaldimino-3-mercapto-5-phenyl 1 ,2,4-triazole." Journal of Indian Chemical Society Vol. 66, Jun 1989 (1989): 408–9. https://doi.org/10.5281/zenodo.6140175.

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Department of Chemistry, Patna University, Patna-800 005  Manuscript <em>received 10 February 1988, revised 27 January 1989, accepted 18 April 1989</em> <em>Complexes of some Bivalent Metal Ions with 4-Salicylaldimino-3-mercapto-5-phenyl 1 ,2,4-triazole </em>

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23

Теруков, Е. И., А. В. Марченко, А. А. Лужков, П. П. Серегин та К. Б. Шахович. "Сверхтонкие взаимодействия в узлах меди диэлектрических и сверхпроводящих металлооксидов меди". Письма в журнал технической физики 46, № 21 (2020): 52. http://dx.doi.org/10.21883/pjtf.2020.21.50199.18037.

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The method of Mössbauer spectroscopy on isotopes 61Cu (61Ni) shows that for bivalent copper dielectric metal oxides, a combined quadrupole and Zeeman interaction of 61Ni nuclei with local fields in copper sites is observed, whereas for superconducting metal oxides, only quadrupole interaction of the nuclei 61Ni is detected. For all the metal oxides under consideration, the equal in value valence contribution to the electric field gradient tensor was found.

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24

FAZLUR, RAHMAN, N. RASTOGI S., and K. JETLEY U. "Stability Constants of some Bivalent Metal Complexes with 2-Hydroxy-3,5-dimethylacetophenone Oxime." Journal of Indian Chemical Society Vol. 67, April 1990 (1990): 342. https://doi.org/10.5281/zenodo.6163860.

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Chemical Laboratories, D. N. College, Meerut-250 002 <em>Manuscript received 23 March 1989, revised 15 September 1989, accepted 10 November 1989</em> Stability Constants of some Bivalent Metal Complexes with 2-Hydroxy-3,5-dimethylacetophenone Oxime.

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25

Papavassilioua, G. C., G. A. Mousdis, A. Terzis, and C. P. Raptopoulou. "Excitonic Bands in the Optical Absorption Spectra of (Bu4N)CuBr2, (Et4N)2Cu2Br4, (Pr4N)2Cu4Br6, (Bu4N)2Cu2I4, (Me4N)Cu2I3, (Pr4N)4Ag4I8, (Me4N)Ag2I3, (Et4N)Ag2Br3, and Similar Compounds." Zeitschrift für Naturforschung B 54, no. 1 (1999): 109–12. http://dx.doi.org/10.1515/znb-1999-0120.

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The title compounds (natural low-dimensional semiconductor systems) exhibit strong excitonic optical absorption bands in the UV spectral region, because of the quantum confinement of excitons, as in the cases of bivalent-metal and trivalent-metal halide complexes. The excitonic bands are shifted to longer wavelengths, approaching those of the corresponding bulk materials, as the anion-size or the anion-dimensionality increases.

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26

(MISS), S. PATNAIK, and PANDA C. "pH-metric Study of Bivalent Metal Chelates using D(+)-Saccharic Acid as Secondary Ligand." Journal of Indian Chemical Society Vol. 74, Apr 1997 (1997): 330–31. https://doi.org/10.5281/zenodo.5881005.

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Department of Chemistry, Regional Engineering College, Rourkela-769 008 <em>Manuscript received 16 March 1995, revised 23 August 1995, accepted 14 December 1995</em> pH-metric Study of Bivalent Metal Chelates using D(+)-Saccharic Acid as Secondary Ligand

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27

Gao, Xiaokang, Yunzhe Li, Yu Qin, et al. "Reversible and oriented immobilization of histidine-tagged protein on silica gel characterized by frontal analysis." RSC Advances 5, no. 31 (2015): 24449–54. http://dx.doi.org/10.1039/c5ra01012h.

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Utilizing N,N′-bis(carboxymethyl)-L-lysine (ANTA) combined with bivalent metal cation Ni<sup>2+</sup>, which leaving free sites for the reversible binding of gene recombinant histidine-tagged β<sub>2</sub>-adrenoceptor onto silica gel.

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28

D., C. DASH, K. PANDA A., MOHANTY H., and RENJITHA KUMARI (MISS). "Synthesis of Complexes of 2-(Benzothiazolyl-2' -aminoimino )-1,2-diphenylethanone with some Bivalent Transition Metal Ions." Journal of Indian Chemical Society Vol. 74, Oct 1997 (1997): 791–92. https://doi.org/10.5281/zenodo.5897067.

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P. G. Department of Chemistry, Sambalpur University, Jyotivihar-768 019 <em>Manuscript received 23 May /996, accepted 18 November 1996</em> Synthesis of Complexes of 2-(Benzothiazolyl-2' -aminoimino )-1,2-diphenylethanone with some Bivalent Transition Metal Ions.

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29

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, Osmania University , Hyderabad -500 007 <em>Manuscript received 6 September 1994, revised 28 October 1994, accepted 25 November 1994</em> Equilibrium Studies on the System 4,6-Dimethyl-2-mercaptopyrimidine- Bivalent Metal Ion Complexes.

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30

R., C. SHARMA, AMBWANI J., and K. VARSHNEY V. "Synthetic and Antimicrobial Studies of some Heterocyclic Hydrazones and their Bivalent Metal Complexes." Journal of Indian Chemical Society Vol. 69, Nov 1992 (1992): 770–72. https://doi.org/10.5281/zenodo.6043985.

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Department of Chemistry. Institute of Basic Sciences, Khandari Road. Agra-282 002 <em>Manuscript received 27 November 1991, revised 20 July 1992, accepted 31 July 1992</em> Synthetic and Antimicrobial Studies of some Heterocyclic Hydrazones and their Bivalent Metal Complexes.    

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31

Ding, Yingchun, Qijiu Deng, Caiyin You, Yunhua Xu, Jilin Li, and Bing Xiao. "Assessing electrochemical properties and diffusion dynamics of metal ions (Na, K, Ca, Mg, Al and Zn) on a C2N monolayer as an anode material for non-lithium ion batteries." Physical Chemistry Chemical Physics 22, no. 37 (2020): 21208–21. http://dx.doi.org/10.1039/d0cp02524k.

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We perform first-principles molecular dynamics (FPMD) simulations together with a CI-NEB method to explore the structure, electrochemical properties and diffusion dynamics of a C<sub>2</sub>N monolayer saturated with various univalent, bivalent and trivalent metal ions.

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32

M., S. MAYADEO, H. SINHA C., and S. KALE S. "Stability Constants of some Bivalent Metal Ion Chelates of Schiff Bases derived from : 2,4-Dihydroxybenzaldehyde." Journal of Indian Chemical Society Vol. 63, Jul 1986 (1986): 694–96. https://doi.org/10.5281/zenodo.6275233.

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Department of Chemistry, Ramnarain Ruia College, Matunga, Bombay-400 019 <em>Manuscript received 19 February 1986, revised .17 June 1986, accepted 25 June 1986</em> Stability Constants of some Bivalent Metal Ion Chelates of Schiff Bases derived from : 2,4-Dihydroxybenzaldehyde

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33

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>β</em>-Isatin-4,4-dimethyl-3-thiosemicarbazone with some Bivalent Metal Ions.

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34

Xue, Jingjing, Xinpeng Li, Rongri Tan, and Wenjun Zong. "Molecular dynamics simulations of A-DNA in bivalent metal ions salt solution." Chinese Physics B 31, no. 4 (2022): 048702. http://dx.doi.org/10.1088/1674-1056/ac3caa.

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A-form DNA is one of the biologically active double helical structure. The study of A-DNA structure has an extensive application for developing the field of DNA packaging in biotechnology. In aqueous solution, the A-DNA structure will have a free transformation, the A-DNA structure will be translated into B-form structure with the evolution of time, and eventually stabilized in the B-DNA structure. To explore the stability function of the bivalent metal ions on the A-DNA structure, a series of molecular dynamics simulations have been performed on the A-DNA of sequence (CCCGGCCGGG). The results

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35

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'-(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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36

Prasad, Bipin Bihari, and Ramjee Sah. "A biomimicing approach to the mixed ligand complexes of bivalent transition metal." International Journal of Applied Sciences and Biotechnology 1, no. 1 (2013): 16–20. http://dx.doi.org/10.3126/ijasbt.v1i1.7922.

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Metal complexes of the type ML1L2[M=Cu(II), Ni(II), and Co(II), L1=?,?'-dipyridyl(dipy.), L2=2-hydroxybenzalidine anthranilic acid (HBAA)] have been synthesized by using ?,?'-dipyridyl(dipy.), 2-hdroxybenzalidine anthranilic acid (HBAA) and metal(II) acetate. The resulting mixed ligand metal complexes have been characterized on the basis of elemental analysis, IR-spectra, electronic spectra, magnetic susceptibilities and molar conductance measurements. The antifungal and antibacterial activities of ligands and there metal complexes have been screened against Aspergillus flavus, Aspergillus fum

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37

J, K. NEPAL, and N. DUBEY S. "Equilibrium Study of the Complex Formation of some Bivalent Transition Metal Ions with Sulphur Oxygen Donor Ligands." Journal of Indian Chemical Society Vol. 65, Nov 1988 (1988): 795. https://doi.org/10.5281/zenodo.7077704.

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Department of Chemistrv, Kurukshetra University, Kurukshetra.-132 119 <em>Manuscript received 18 July 1986, revised 19 July 1988, accepted 29 July 1988</em> Equilibrium Study of the Complex Formation of some Bivalent Transition Metal Ions with Sulphur Oxygen Donor Ligands.

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38

A., H. M. SIDDALINGAIAH, and Y. KARIDURAGANAVAR M. "Synthesis and Evaluation of Thermodynamic Functions for Complexation Reactions involving Bivalent Metal Ions and Di(2-ethylphenyl)carbazone." Journal of Indian Chemical Society Vol. 73, Dec 1996 (1996): 671–73. https://doi.org/10.5281/zenodo.5928689.

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Department of Chemistry, Karnatak University, Dharwad-580 003 <em>Manuscript received  26 September 1994, revised 31 March 1995, accepted 22 May 1995</em> Synthesis and Evaluation of Thermodynamic Functions for Complexation Reactions involving Bivalent Metal Ions and Di(2-ethylphenyl)carbazone.

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39

Schutzbach, Maximilian, Steffen Kiemel, Robert Miehe, Ekrem Köse, Alexander Mages, and Alexander Sauer. "Comparative Life Cycle Sustainability Assessment of Mono- vs. Bivalent Operation of a Crucible Melting Furnace." Sustainability 14, no. 14 (2022): 8826. http://dx.doi.org/10.3390/su14148826.

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The benefits of energy flexibility measures have not yet been conclusively assessed from an ecological, economic, and social perspective. Until now, analysis has focused on the influence of changes in the energy system and the ecological and economic benefits of these. Therefore, the objective of this study was to perform a life cycle sustainability assessment of energy flexibility measures on the use case of a bivalent crucible melting furnace in comparison with a monovalent one for aluminum light metal die casting. The system boundary was based on a cradle-to-gate approach in Germany and inc

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Bennett, A. J., and C. R. Bagshaw. "The kinetics of bivalent metal ion dissociation from myosin subfragments." Biochemical Journal 233, no. 1 (1986): 173–77. http://dx.doi.org/10.1042/bj2330173.

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Bivalent metal ions have multiple roles in subunit association and ATPase regulation in scallop adductor-muscle myosin. To help elucidate these functions, the rates of Ca2+ and Mg2+ dissociation from the non-specific high-affinity sites on the regulatory light chains were measured and compared with those of rabbit skeletal-muscle myosin subfragments. Ca2+ dissociation had a rate constant of about 0.7 s-1 in both species, as measured by the time course of the pH change on EDTA addition. Mg2+ dissociation had a rate constant of 0.05 s-1, as monitored by its displacement with the paramagnetic Mn2

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Singh, B. "Studies on Thioamidopyridine Complexes of some 3d Bivalent Metal Ions." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 17, no. 5 (1987): 457–68. http://dx.doi.org/10.1080/00945718708070210.

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Dunstan, P. Oliver. "Thermochemistry of Morpholine Adducts of Some Bivalent Transition Metal Bromides." Journal of Chemical & Engineering Data 54, no. 3 (2009): 842–46. http://dx.doi.org/10.1021/je8006315.

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Liu, Yongxin, Dan Liu, and Cheng Wang. "Bivalent metal-based MIL-53 analogues: Synthesis, properties and application." Journal of Solid State Chemistry 223 (March 2015): 84–94. http://dx.doi.org/10.1016/j.jssc.2014.06.029.

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Urusov, V. S., and V. B. Dudnikova. "Semiempirical approximation for atomization energy of bivalent metal halide crystals." Theoretical and Experimental Chemistry 21, no. 6 (1986): 674–78. http://dx.doi.org/10.1007/bf00945145.

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Singh, Bachcha, and Ashutosh K. Srivastav. "2-Aminoacetophenone-2-thenoylhydrazone complexes of bivalent 3d metal ions." Transition Metal Chemistry 14, no. 6 (1989): 415–19. http://dx.doi.org/10.1007/bf01092581.

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Yaocheng, Shi, Song QingBao, Wu Xiaoli, and Ma Yongxiang. "Formylferrocene 2-thenoyl hydrazone and its bivalent transition metal complexes." Polyhedron 13, no. 14 (1994): 2101–5. http://dx.doi.org/10.1016/s0277-5387(00)81489-8.

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SATO, Hisakuni. "Ion exchange chromatography of bivalent metal ions by conductivity detection." Bunseki kagaku 34, no. 10 (1985): 606–11. http://dx.doi.org/10.2116/bunsekikagaku.34.10_606.

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Ayene, Iraimoudi S., Cameron J. Koch, and Robert E. Krisch. "DNA strand breakage by bivalent metal ions and ionizing radiation." International Journal of Radiation Biology 83, no. 3 (2007): 195–210. http://dx.doi.org/10.1080/09553000601146956.

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Preigh, Michael J., Fu-Tyan Lin, Kamal Z. Ismail, and Stephen G. Weber. "Bivalent metal ion-dependent photochromism and photofluorochromism from a spiroquinoxazine." Journal of the Chemical Society, Chemical Communications, no. 20 (1995): 2091. http://dx.doi.org/10.1039/c39950002091.

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Rakha, Tawfik H., Ahmed A. El-Asmy, Mohsen M. Mostafa, and Abd El-Ghany El-Kourshy. "Synthesis and structural studies on bivalent metal complexes of benzenesulphonylhydrazine." Transition Metal Chemistry 12, no. 2 (1987): 125–27. http://dx.doi.org/10.1007/bf01022337.

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