Experimental and theoretical investigation of the catalytic performance of reduced Schiff base and Schiff base iron complexes: Transformation to magnetically retrievable catalyst

Author(s):  
Rimpa Mondal ◽  
Aratrika Chakraborty ◽  
Rinku Ghanta ◽  
María Isabel Menéndez ◽  
Tanmay Chattopadhyay
2020 ◽  
Vol 49 (43) ◽  
pp. 15461-15472
Author(s):  
Arnab Mandal ◽  
Abani Sarkar ◽  
Amit Adhikary ◽  
Debabrata Samanta ◽  
Debasis Das

A DFT-based mechanistic study of phosphatase and phenoxazine synthase activities of Schiff base and reduced Schiff base complexes.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Mainak Karmakar ◽  
Antonio Frontera ◽  
Shouvik Chattopadhyay

The formation of an infinite 1D assembly is governed by the H-bonding interactions in the solid state structure of the two zinc complexes. It has been analyzed energetically using DFT calculations and several computational tools.


2011 ◽  
Vol 37 (1) ◽  
pp. 31-35 ◽  
Author(s):  
Jian-zhang Li ◽  
Xi-yang He ◽  
Jun Zeng ◽  
Zheng-hua Xiao ◽  
Sheng-ying Qin

2014 ◽  
Vol 692 ◽  
pp. 240-244
Author(s):  
Gong De Wu ◽  
Xiao Li Wang ◽  
Zhi Li Zhai

A series of transition metal alanine-salicylaldehyde Schiff base chromium (III) complexes immobilized on MCM-41 were prepared and characterized by various physico-chemical measurements such as FIIR, XRD, HRTEM, N2 sorption and elemental analysis. The immobilized complexes were effective and stable catalysts for the epoxidation of styrene and cyclohexene with 30% hydrogen peroxide. Moreover, the metal centers were found to play important roles in the catalytic performance of immobilized complex catalysts.


2018 ◽  
Vol 4 (4) ◽  
pp. 51 ◽  
Author(s):  
Monotosh Mondal ◽  
Maharudra Chakraborty ◽  
Michael G. B. Drew ◽  
Ashutosh Ghosh

Three trinuclear Ni(II)-Na(I) complexes,[Ni2(L1)2NaCl3(H2O)]·H2O (1), [Ni2(L2)2NaCl3(H2O)] (2), and [Ni2(L3)2NaCl3(OC4H10)] (3) have been synthesized using three different NNO donor tridentate reduced Schiff base ligands, HL1= 2-[(3-methylamino-propylamino)-methyl]-phenol, HL2= 2-[(3-methylamino-propylamino)-methyl]-4-chloro-phenol, and HL3= 2-[(3-methylamino-propylamino)-methyl]-6-methoxy-phenol that had been structurally characterized. Among these complexes, 1 and 2 are isostructural in which dinuclearNi(II) units act as metalloligands to bind Na(I) ions via phenoxido and chlorido bridges. The Na(I) atom is five-coordinated, and the Ni(II) atom possesses hexacordinated distorted octahedral geometry. In contrast, in complex 3, two -OMe groups from the dinuclear Ni(II) unit also coordinate to Na(I) to make its geometry heptacordinated pentagonal bipyramidal. The magnetic measurements of complexes 1–3 indicate ferromagnetic interactions between dimeric Ni(II) units with J = 3.97 cm−1, 4.66 cm−1, and 5.50 cm−1for 1–3, respectively, as is expected from their low phenoxido bridging angles (89.32°, 89.39°, and 87.32° for 1–3, respectively). The J values have been calculated by broken symmetry DFT method and found to be in good agreement with the experimental values.


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