Shuvankar Dey
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Shuvankar Dey has a total of 47 co-authors. Here are the top co-authors by number of shared publications:
- Vinod Kumar Jain
Department of Chemistry, School of Sciences, Gujarat University, Ahmedabad-380009, India
9 shared publications - Krunal Modi
Department of Humanity and Science, School of Engineering, Indrashil University, Mehsana, India
6 shared publications - Chirag N. Patel
Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, USA
4 shared publications - Anita Kongor
Department of Chemistry Gujarat University 380009 Ahmedabad Gujarat India
3 shared publications Manthan Panchal
3 shared publicationsUrvi Panchal
3 shared publications
Latest Publications
- Open Access
- 17 October 2026
- Published by Springer Nature in Nature Communications
ADAM17 is a broad HIV-1 restriction factor targeted by Nef to restore Env maturation
- 17 October 2026
- Published by Springer Nature in Nature Communications
Open AccessADAM17 is a broad HIV-1 restriction factor targeted by Nef to restore Env maturation
- 1 September 2021
- Published by Elsevier in Journal of Molecular Liquids
- Vol. 337
Detection of small molecular toxins using azacalix[4]arene architecture and its theoretical investigations
- 1 September 2021
- Published by Elsevier in Journal of Molecular Liquids
- Vol. 337
Detection of small molecular toxins using azacalix[4]arene architecture and its theoretical investigations
- 20 August 2021
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 45 (38) , 17902-17908
An oxacalix[4]arene-derived dual-sensing fluorescent probe for the relay recognition of Hg2+ and S2− ions
A rhodamine B-functionalized oxacalix[4]arene architecture has been designed as a dual-responsive probe for the sequential recognition of Hg2+ and S2− ions.
- 20 August 2021
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 45 (38) , 17902-17908
An oxacalix[4]arene-derived dual-sensing fluorescent probe for the relay recognition of Hg2+ and S2− ions
A rhodamine B-functionalized oxacalix[4]arene architecture has been designed as a dual-responsive probe for the sequential recognition of Hg2+ and S2− ions.
- 6 May 2020
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 49 (22) , 7459-7466
An oxacalix[4]arene derived dual sensing fluorescent probe for the detection of As( v ) and Cr( vi ) oxyanions in aqueous media
An oxacalix[4]arene-Ce(III) complex viz. L–Ce(III) has been introduced for the selective detection of As(V) and Cr(VI) oxyanions in aqueous medium. The binding mode of L–Ce(III) + AsO4 3−/CrO4 2− was completely investigated with fluorometric titration, time resolve fluorescent decay and FTIR analyses. Photoinduced electron transfer (PET) and chelation-enhanced fluorescence (CHEF) play an important role in the sensing of these oxyanions. The characteristic fluorescence of the L–Ce(III) complex has been quenched by AsO4 3− and CrO4 2− through cascading the ligating sites. Cyclic voltammetry (CV) experiments with various scan rates suggest that the electrochemical processes on the electrodes were controlled by diffusion. Both the analytes exhibit a lower limit of detection (LOD) below their standard EPA permissible limits. Moreover, the probe successfully detects the oxyanions in environmental real samples with excellent recovery ranging from 97 to 101%.
- 6 May 2020
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 49 (22) , 7459-7466
An oxacalix[4]arene derived dual sensing fluorescent probe for the detection of As( v ) and Cr( vi ) oxyanions in aqueous media
An oxacalix[4]arene-Ce(III) complex viz. L–Ce(III) has been introduced for the selective detection of As(V) and Cr(VI) oxyanions in aqueous medium. The binding mode of L–Ce(III) + AsO4 3−/CrO4 2− was completely investigated with fluorometric titration, time resolve fluorescent decay and FTIR analyses. Photoinduced electron transfer (PET) and chelation-enhanced fluorescence (CHEF) play an important role in the sensing of these oxyanions. The characteristic fluorescence of the L–Ce(III) complex has been quenched by AsO4 3− and CrO4 2− through cascading the ligating sites. Cyclic voltammetry (CV) experiments with various scan rates suggest that the electrochemical processes on the electrodes were controlled by diffusion. Both the analytes exhibit a lower limit of detection (LOD) below their standard EPA permissible limits. Moreover, the probe successfully detects the oxyanions in environmental real samples with excellent recovery ranging from 97 to 101%.
- 1 September 2019
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 896, 194-206
Copper(II)-faciliated synthesis of substituted thioethers and 5-substituted 1H-tetrazoles: Experimental and theoretical studies
- 1 September 2019
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 896, 194-206
Copper(II)-faciliated synthesis of substituted thioethers and 5-substituted 1H-tetrazoles: Experimental and theoretical studies
- 5 December 2018
- Published by Wiley in ChemistrySelect
- Vol. 3 (45) , 12951-12959
Facile Construction and In Silico Study of Quinoline‐Attached Resorcinarene Fluorescent Sensor for the Recognition of Insensitive Munition Compounds
N‐methyl‐4‐nitroaniline (MNA), an insensitive munition is selectively and sensitively recognized by a new resorcinarene bearing quinoline moiety, i.e, Tetra‐Methoxy Resorcinarene Tetra‐Quinoline Acetamide (TMRTQA). A simple and efficient spectrofluorimetric technique demonstrates the quenching of the fluorescence intensity of TMRTQA upon addition of MNA within concentration limits of 2 nM to 1 μM. Binding constant and quantum yield have been determined in this study. Molecular docking studies have been performed to predict the best binding affinity and the possible interactions for the formation of complex between TMRTQA and MNA supporting the 1:1 stoichiometry. Density functional theory calculation also support the excitation wavelength and geometry optimization. MNA being a hazardous environmental pollutant has been successfully detected from the water sample by standard addition method.
- 5 December 2018
- Published by Wiley in ChemistrySelect
- Vol. 3 (45) , 12951-12959
Facile Construction and In Silico Study of Quinoline‐Attached Resorcinarene Fluorescent Sensor for the Recognition of Insensitive Munition Compounds
N‐methyl‐4‐nitroaniline (MNA), an insensitive munition is selectively and sensitively recognized by a new resorcinarene bearing quinoline moiety, i.e, Tetra‐Methoxy Resorcinarene Tetra‐Quinoline Acetamide (TMRTQA). A simple and efficient spectrofluorimetric technique demonstrates the quenching of the fluorescence intensity of TMRTQA upon addition of MNA within concentration limits of 2 nM to 1 μM. Binding constant and quantum yield have been determined in this study. Molecular docking studies have been performed to predict the best binding affinity and the possible interactions for the formation of complex between TMRTQA and MNA supporting the 1:1 stoichiometry. Density functional theory calculation also support the excitation wavelength and geometry optimization. MNA being a hazardous environmental pollutant has been successfully detected from the water sample by standard addition method.
- 10 January 2018
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 42 (4) , 2682-2691
Dual in vitro and in silico analysis of thiacalix[4]arene dinaphthalene sulfonate for the sensing of 4-nitrotoluene and 2,3-dinitrotoluene
A newly synthesized thiacalix[4]arene dinaphthalene sulfonate, i.e. , TCDNS, has been used as a fluorescence quencher for 2,3-DNT as well as 4-NT. The complex was analyzed by ESI-MS and 1 H-NMR titration, which has been further confirmed by the in silico study.
- 10 January 2018
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 42 (4) , 2682-2691
Dual in vitro and in silico analysis of thiacalix[4]arene dinaphthalene sulfonate for the sensing of 4-nitrotoluene and 2,3-dinitrotoluene
A newly synthesized thiacalix[4]arene dinaphthalene sulfonate, i.e. , TCDNS, has been used as a fluorescence quencher for 2,3-DNT as well as 4-NT. The complex was analyzed by ESI-MS and 1 H-NMR titration, which has been further confirmed by the in silico study.