Nasima Yasmin

Nasima Yasmin

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Nasima Yasmin

Aliah Univ, Dept Chem, Kolkata 700160, West Bengal, India

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 June 2020 in Chemnanomat
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Journal Article
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SBSurajit Biswas
Surajit Biswas
RMRostam Ali Molla
Rostam Ali Molla
NYNasima Yasmin
Nasima Yasmin
SISk Manirul Islam
Sk Manirul Islam

18 December 2019 in New Journal of Chemistry
Verified
Journal Article
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SISk Safikul Islam
Sk Safikul Islam
SRSk Riyajuddin
Sk Riyajuddin
RMRostam Ali Molla
Rostam Ali Molla
NYNasima Yasmin
Nasima Yasmin
KGKaushik Ghosh
Kaushik Ghosh
SISk Manirul Islam
Sk Manirul Islam
A novel complex catalyst, POP-palladium(II), has been synthesized. The developed catalyst has been characterized by XRD, EDX, scanning electron microscopy (FE-SEM), HR-TEM, FTIR spectroscopy, UV-vis spectroscopy, TGA and BET isotherm analysis. The reactivity of the incorporated palladium(II) catalyst was tested in the in situ carbonylation of aryl iodides and secondary cyclic amines to the respective α-ketoamides at 80 °C. A large number of aryl iodides combined with CO followed by 2° amines can generate the corresponding α-ketoamides with high selectivity. This Pd(II) complex catalyst exhibits superb catalytic activities and can also be easily recovered after the reaction by an easy filtration method. The catalyst could be reused for up to six consecutive cycles without much loss in its activity.

13 November 2017 in ChemistrySelect
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Journal Article
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SISk. Safikul Islam
Sk. Safikul Islam
PBPiyali Bhanja
Piyali Bhanja
KGKajari Ghosh
Kajari Ghosh
RMRostam Ali Molla
Rostam Ali Molla
NYNasima Yasmin
Nasima Yasmin
SISk Manirul Islam
Sk Manirul Islam

4 October 2024 in Ecotoxicology and Environmental Safety
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Journal Article
Open access
KMKalimuddin Mandal
Kalimuddin Mandal
MMMukti Mohammad
Mukti Mohammad
NYNasima Yasmin
Nasima Yasmin
HGHarun Al Rasid Gazi
Harun Al Rasid Gazi
MIMd. Maidul Islam
Md. Maidul Islam
Environmental pollution poses a major problem now a day. Several dyes, in the form of industrial waste, pollute water body and may cause adverse effects to human health. In this paper ADME and toxicity of fives Phenothiazinium group of dyes Methylene blue (MB), Azure A (AA), Azure B (AB), Azure C (AC) and Toluidine Blue O (TBO) were predicted using Swiss ADME and Protox II tools. Results showed these dyes may herm for living organism due to their carcinogenic, mutagenic and hepatotoxic properties. Removal efficiency of these dyes using okra plant product were determined using spectroscopic, thermodynamic and molecular modeling study. It was revealed that these dyes adsorb on the surface of okra leaf mostly at pH 7.0 and the adsorption isotherms were found to fit in Langmuir and Freundlich isotherm model, while Temkin model fails to do this. Mucilage present in different parts of okra plant plays a significant role on removal of these dyes and is able to remove near about 71-92 % of dyes from water body by itself. As this process did not fit in any of above said adsorption isotherm model, it may be suggested that some other mechanism may happen. Further studies explore that these dyes bound to the hydrophobic pocket of mucilage with binding affinity in the order of 105 M- 1 and the bindings were exothermic in nature with enthalpy change in the range of - 2.94 to - 4.28 kcal/mole. Molecular docking study validate all the experimental results obtained from spectroscopic and thermodynamic study and enlighten the role of structure of dyes on their binding affinity to mucilage. This paper will help to systematically understand the role of okra plant products on removal efficiency of Phenothiazinium group of dyes with their structural variations.

9 August 2024 in Journal of Materials Chemistry B
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RKRousunara Khatun
Rousunara Khatun
MDMalay Dolai
Malay Dolai
MSMihir Sasmal
Mihir Sasmal
AKAtul Katarkar
Atul Katarkar
AIAbu Saleh Musha Islam
Abu Saleh Musha Islam
MAMahammad Ali
Mahammad Ali
A well characterized hexanuclear complex, [Mn6(μ3-O)2(3-MeO-salox)6(OAc)2(H2O)4] (1), selectively interacts with HSA by preferential trapping in the subdomain IIA of site I. It, further, exhibits anticancer activity in lung cancer A549 cells.