A Srinivasan
Affiliations: | Chemistry | National Institute of Science Education and Research |
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Sign in to add traineeSuritra Bandyopadhyay | grad student | 2020-2022 | National Institute of Science Education and Research, Bhubaneswar |
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Dash S, Ghosh A, Srinivasan A, et al. (2019) Protonation-Triggered Hückel and Möbius Aromatic Transformations in Nonaromatic Core-Modified [30]Hexaphyrin(2.1.1.2.1.1) and Annulated [28]Hexaphyrin(2.1.1.0.1.1). Organic Letters |
Ghosh A, Dash S, Srinivasan A, et al. (2019) Two non-identical twins in one unit cell: characterization of 34π aromatic core-modified octaphyrins, their structural isomers and anion bound complexes. Chemical Science. 10: 5911-5919 |
Chandrashekar TK, Ghosh A, Dash S, et al. (2018) [24]π Core-modified Non-fused Pentaphyrin with Möbius aromaticity. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Chatterjee T, Srinivasan A, Ravikanth M, et al. (2016) Smaragdyrins and Sapphyrins Analogues. Chemical Reviews |
Chandrashekar TK, Ghosh A, Srinivasan A, et al. (2016) [40]π Fused and Nonfused Core-Modified Nonaphyrins: Syntheses and Structural Diversity. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Chandrashekar TK, Karthik G, Cha WY, et al. (2016) Phenylene Bridged Core-Modified Planar Aromatic Octaphyrin: Aromaticity, Photophysical and Anion Receptor Properties. Chemistry, An Asian Journal |
Chandrashekar TK, Ghosh A, Chaudhary A, et al. (2016) [32]π Fused Core-Modified Heptaphyrin with Möbius Aromaticity. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Karthik G, Srinivasan A, Suresh CH, et al. (2014) Fused core-modified planar antiaromatic 32π heptaphyrins: unusual synthesis and structural diversity. Chemical Communications (Cambridge, England). 50: 12127-30 |
Karthik G, Srinivasan A, Chandrashekar TK. (2014) meso-Aryl core-modified fused sapphyrins: syntheses and structural diversity. Organic Letters. 16: 3472-5 |
Lim JM, Ganesan K, Sung YM, et al. (2014) Photophysical properties of bridged core-modified hexaphyrins: conjugational perturbation of thiophene bridges. Chemical Communications (Cambridge, England). 50: 4358-60 |