Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand
A mononuclear square planar Ni(II) complex [NiᴵᴵL] (1) with sterically encumbered phenol based tetra dentate N₂O2₂ ligand has been synthesized. Several spectroscopic tools have been employed to characterize this complex. The crystal structure of this Ni(II) complex obtained from single crystal X-ray...
Saved in:
Main Authors: | , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2021
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/153643 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-153643 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1536432021-12-07T08:47:16Z Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand Mandal, Bikramaditya Majee, Mithun Chandra Mandal, Debdas Ganguly, Rakesh School of Physical and Mathematical Sciences Division of Chemistry and Biological Chemistry Science::Chemistry Syntheses Characterization A mononuclear square planar Ni(II) complex [NiᴵᴵL] (1) with sterically encumbered phenol based tetra dentate N₂O2₂ ligand has been synthesized. Several spectroscopic tools have been employed to characterize this complex. The crystal structure of this Ni(II) complex obtained from single crystal X-ray diffraction study reveals that the central metal ion adopts a square planar environment and crystalized in monoclinic space group C 2/c with a = 24.1784 (10), b = 9.3537 (4) and c = 8.3326 (4) with β = 97.0690 (11). The Hirshfeld surface analysis shows halogen-halogen interaction. The Ni(II) complex has been found to be an effective catalyst for the aerial oxidation of 3,5-DTBC to 3,5- DTBQ in methanol. For kinetic study, Michaelis-Menten model has been approached to determine the Kcₐₜ, Kₘ and Vₘₐₓ. The kinetic studies confirm that the turnover number (TON) of complex 1 is 1.762 × 10³ h⁻¹. 2021-12-07T08:47:16Z 2021-12-07T08:47:16Z 2020 Journal Article Mandal, B., Majee, M. C., Mandal, D. & Ganguly, R. (2020). Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand. Journal of Molecular Structure, 1202, 127340-. https://dx.doi.org/10.1016/j.molstruc.2019.127340 0022-2860 https://hdl.handle.net/10356/153643 10.1016/j.molstruc.2019.127340 2-s2.0-85075434362 1202 127340 en Journal of Molecular Structure © 2019 Elsevier B.V. All rights reserved. |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Science::Chemistry Syntheses Characterization |
spellingShingle |
Science::Chemistry Syntheses Characterization Mandal, Bikramaditya Majee, Mithun Chandra Mandal, Debdas Ganguly, Rakesh Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand |
description |
A mononuclear square planar Ni(II) complex [NiᴵᴵL] (1) with sterically encumbered phenol based tetra dentate N₂O2₂ ligand has been synthesized. Several spectroscopic tools have been employed to characterize this complex. The crystal structure of this Ni(II) complex obtained from single crystal X-ray diffraction study reveals that the central metal ion adopts a square planar environment and crystalized in monoclinic space group C 2/c with a = 24.1784 (10), b = 9.3537 (4) and c = 8.3326 (4) with β = 97.0690 (11). The Hirshfeld surface analysis shows halogen-halogen interaction. The Ni(II) complex has been found to be an effective catalyst for the aerial oxidation of 3,5-DTBC to 3,5- DTBQ in methanol. For kinetic study, Michaelis-Menten model has been approached to determine the Kcₐₜ, Kₘ and Vₘₐₓ. The kinetic studies confirm that the turnover number (TON) of complex 1 is 1.762 × 10³ h⁻¹. |
author2 |
School of Physical and Mathematical Sciences |
author_facet |
School of Physical and Mathematical Sciences Mandal, Bikramaditya Majee, Mithun Chandra Mandal, Debdas Ganguly, Rakesh |
format |
Article |
author |
Mandal, Bikramaditya Majee, Mithun Chandra Mandal, Debdas Ganguly, Rakesh |
author_sort |
Mandal, Bikramaditya |
title |
Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand |
title_short |
Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand |
title_full |
Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand |
title_fullStr |
Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand |
title_full_unstemmed |
Synthesis, structure, Hirshfeld surface analysis and catecholase activity of Ni(II) complex with sterically constrained phenol based ligand |
title_sort |
synthesis, structure, hirshfeld surface analysis and catecholase activity of ni(ii) complex with sterically constrained phenol based ligand |
publishDate |
2021 |
url |
https://hdl.handle.net/10356/153643 |
_version_ |
1718928698241974272 |