| Year |
Citation |
Score |
| 2021 |
Oh S, Nikolaev A, Tagami K, Tran T, Lee D, Mukherjee S, Segalman RA, Han S, Read de Alaniz J, Chabinyc ML. Redox-Active Polymeric Ionic Liquids with Pendant N-Substituted Phenothiazine. Acs Applied Materials & Interfaces. PMID 33480673 DOI: 10.1021/acsami.0c20462 |
0.6 |
|
| 2020 |
Xie R, Mukherjee S, Levi AE, Reynolds VG, Wang H, Chabinyc ML, Bates CM. Room temperature 3D printing of super-soft and solvent-free elastomers. Science Advances. 6. PMID 33188029 DOI: 10.1126/sciadv.abc6900 |
0.6 |
|
| 2020 |
Levi AE, Fu L, Lequieu J, Horne JD, Blankenship J, Mukherjee S, Zhang T, Fredrickson GH, Gutekunst WR, Bates CM. Efficient Synthesis of Asymmetric Miktoarm Star Polymers. Macromolecules. 53: 702-710. PMID 32489220 DOI: 10.1021/acs.macromol.9b02380 |
0.6 |
|
| 2018 |
Thilagar P, Mukherjee S. Renaissance of Organic Triboluminescent Materials. Angewandte Chemie (International Ed. in English). PMID 30565815 DOI: 10.1002/anie.201811542 |
1 |
|
| 2016 |
Sarkar T, Banerjee S, Mukherjee S, Hussain A. Mitochondrial selectivity and remarkable photocytotoxicity of a ferrocenyl neodymium(iii) complex of terpyridine and curcumin in cancer cells. Dalton Transactions (Cambridge, England : 2003). PMID 26947919 DOI: 10.1039/c5dt04775g |
1 |
|
| 2016 |
Banerjee S, Dixit A, Maheswaramma KS, Maity B, Mukherjee S, Kumar A, Karande AA, Chakravarty AR. Photocytotoxic ternary copper(II) complexes of histamine Schiff base and pyridyl ligands Journal of Chemical Sciences. 128: 165-175. DOI: 10.1007/s12039-015-1017-5 |
1 |
|
| 2015 |
Mukherjee S, Thilagar P. Boron clusters in luminescent materials. Chemical Communications (Cambridge, England). PMID 26574714 DOI: 10.1039/c5cc08213g |
1 |
|
| 2015 |
Mukherjee S, Thilagar P. Recent advances in purely organic phosphorescent materials. Chemical Communications (Cambridge, England). 51: 10988-1003. PMID 26036713 DOI: 10.1039/c5cc03114a |
1 |
|
| 2014 |
Mukherjee S, Thilagar P. Fine-tuning solid-state luminescence in NPIs (1,8-naphthalimides): impact of the molecular environment and cumulative interactions. Physical Chemistry Chemical Physics : Pccp. 16: 20866-77. PMID 25168634 DOI: 10.1039/c4cp02071e |
1 |
|
| 2014 |
Mukherjee S, Thilagar P. Fine-tuning dual emission and aggregation-induced emission switching in NPI-BODIPY dyads. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9052-62. PMID 24895089 DOI: 10.1002/chem.201305049 |
1 |
|
| 2014 |
Mukherjee S, Thilagar P. Insights into the AIEE of 1,8-naphthalimides (NPIs): inverse effects of intermolecular interactions in solution and aggregates. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8012-23. PMID 24848578 DOI: 10.1002/chem.201304694 |
1 |
|
| 2014 |
Swamy P CA, Mukherjee S, Thilagar P. Multichannel-emissive V-shaped boryl-BODIPY dyads: synthesis, structure, and remarkably diverse response toward fluoride. Inorganic Chemistry. 53: 4813-23. PMID 24801770 DOI: 10.1021/ic402470a |
1 |
|
| 2014 |
Swamy PC, Mukherjee S, Thilagar P. Dual binding site assisted chromogenic and fluorogenic recognition and discrimination of fluoride and cyanide by a peripherally borylated metalloporphyrin: overcoming anion interference in organoboron based sensors. Analytical Chemistry. 86: 3616-24. PMID 24571811 DOI: 10.1021/ac500230p |
1 |
|
| 2014 |
Sarkar SK, Mukherjee S, Thilagar P. Going beyond red with a tri- and tetracoordinate boron conjugate: intriguing near-IR optical properties and applications in anion sensing. Inorganic Chemistry. 53: 2343-5. PMID 24520954 DOI: 10.1021/ic402441w |
1 |
|
| 2013 |
Mukherjee S, Thilagar P. Molecular flexibility tuned emission in "V" shaped naphthalimides: Hg(II) detection and aggregation-induced emission enhancement (AIEE). Chemical Communications (Cambridge, England). 49: 7292-4. PMID 23846300 DOI: 10.1039/c3cc43351j |
1 |
|
| 2013 |
Swamy CA, Mukherjee S, Thilagar P. Dual emissive borane-BODIPY dyads: molecular conformation control over electronic properties and fluorescence response towards fluoride ions. Chemical Communications (Cambridge, England). 49: 993-5. PMID 23254480 DOI: 10.1039/c2cc38352g |
1 |
|
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