Evaluation of Standard Changes in Free Energy During Complexation of p-chlorobenzoylthioacetophenone with Some Bivalent Transition Metals

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Published

12-12-2022

DOI:

https://doi.org/10.58414/SCIENTIFICTEMPER.2022.13.2.23

Keywords:

Free energy, p-chlorobenzoylthioacetophenone, Potentiometric Titration, Stability Constant, Solution equilibria

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Issue

Vol. 13 No. 02 (2022): The Scientific Temper

Section

Articles

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Copyright (c) 2022 The Scientific Temper

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This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

Authors

  • Hashmat Ali University Department of Chemistry, Sido Kanhu Murmu University, Dumka-814110, Jharkhand, India
  • Nishant Soren University Department of Chemistry, Sido Kanhu Murmu University, Dumka-814110, Jharkhand, India
  • Rohit Kumar Ravi University Department of Chemistry, Sido Kanhu Murmu University, Dumka-814110, Jharkhand, India
  • Kunal Kumar University Department of Chemistry, Sido Kanhu Murmu University, Dumka-814110, Jharkhand, India
  • Anjali University Department of Chemistry, Sido Kanhu Murmu University, Dumka-814110, Jharkhand, India

Abstract

Para-chlorobenzoylthioacetophenone is an organic ligand of monothio-β-diketone class. Stability constants of bivalent complexes of manganese, nickel, palladium and platinum at three different temperatures were determined using Calvin-Bjerrum’s pH-metric technique as adopted by Irving and Rossotti. From the data of stability constant of the complexes obtained, standard changes in free energy at the said temperatures namely 283K, 293K and 303K were determined with the help of thermodynamic relation, ΔG° = −2.303 RT Log β. Standard changes in free energy contributing towards complex formation have been discussed.

How to Cite

Ali, H., Soren, N., Ravi, R. K., Kumar, K., & Anjali. (2022). Evaluation of Standard Changes in Free Energy During Complexation of p-chlorobenzoylthioacetophenone with Some Bivalent Transition Metals. The Scientific Temper, 13(02), 156–159. https://doi.org/10.58414/SCIENTIFICTEMPER.2022.13.2.23

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