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Publications (2019)

1. R Sharma, M Thomas, R Misra*, F D'Souza, Strong Ground and Excited State Charge Transfer in C3-Symmetric Truxene Derived, Low Band Gap, Phenothiazine-Tetracyanobutadine (TCBD) and Expanded TCBD Conjugates, Angew. Chem. Int. Ed., 2019, 58, 4350-4355. DOI: https://doi.org/10.1002/anie.201814388

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2. F Khan, A Ekbote and R Misra*, Reversible mechanochromism and aggregation induced enhanced emission in phenothiazine substituted tetraphenylethylene, New J. Chem., 2019, 43, 16156-16163. DOI: https://doi.org/10.1039/C9NJ03290H

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3. Y Rout, SM Mobin and R Misra*, Tetracyanobutadiene (TCBD) functionalized benzothiadiazole derivatives: effect of donor strength on the [2+2] cycloaddition–retroelectrocyclization reaction., New J. Chem., 2019, 43, 12299-12307. DOI: https://doi.org/10.1039/C9NJ01887E

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4. Y Rout, Y Jang, HB Gobeze, R Misra*, F D’Souza*, Conversion of Large-Bandgap Triphenylamine–Benzothiadiazole to Low-Bandgap, Wide-Band Capturing Donor–Acceptor Systems by Tetracyanobutadiene and/or Dicyanoquinodimethane Insertion for Ultrafast Charge Separation, J. Phys. Chem. C., 2019, 123, 23382-23389. DOI: https://doi.org/10.1021/acs.jpcc.9b06632

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5. B Carlotti*, M Poddar, F Elisei, A Spalletti and R Misra*, Energy-Transfer and Charge-Transfer Dynamics in Highly Fluorescent Naphthalimide–BODIPY Dyads: Effect of BODIPY Orientation, J. Phys. Chem. C., 2019, 123, 24362-24374. DOI: https://doi.org/10.1021/acs.jpcc.9b06632

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6. Y Patil, R Misra*, Rational molecular design towards NIR absorption: efficient diketopyrrolopyrrole derivatives for organic solar cells and photothermal therapy, J. Mater. Chem. C, 2019, 7, 13020-13031. DOI: https://doi.org/10.1039/C9TC03640G

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7. Y Patil, R Misra*, Metal Functionalized Diketopyrrolopyrroles: A Promising Class of Materials for Optoelectronic Applications, Chem. Rec., 2019, 19, 1-9. DOI: https://doi.org/10.1002/tcr.201900061

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8. B Sekaran, Y Jang, R Misra*, F D’Souza, Push–Pull Porphyrins via β‐Pyrrole Functionalization: Evidence of Excited State Events Leading to High‐Potential Charge‐Separated States, Chem. Eur. J., 2019, 25, 12991-13001. * DOI: https://doi.org/10.1002/chem.201902286

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9. M Poddar, G Sivakumar, R Misra*, Donor–acceptor substituted 1,8-naphthalimides: design, synthesis, and structure–property relationship. J. Mater. Chem. C, 2019, 7, 14798-14815. DOI: https://doi.org/10.1039/C9TC02634G

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