27. Tetracyanobutadiene Bridged Push-Pull Chromophores: Development of New Generation Optoelectronic Materials

Y. Patil, H. Butenschön, R. Misra, Chem. Rec. 2022, e202200208.

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26. Organic Molecular and Polymeric Electrets Toward Soft Electronics (HOT Article)

Guo, Z.†, Patil Y.†, Shinohara, A., Nagura, K., Yoshida, M., Nakanishi T. Mol. Syst. Des. Eng. 2022, 7, 537-552. IF = 4.935 Link ( † indicates equal contribution).

 

 

 

 

 

 

 

 

 

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25.Photoinduced Charge Separation Prompted Intervalence Charge Transfer in a Bis(thienyl) diketopyrrolopyrrole Bridged Donor-TCBD Push-Pull System.
F. Khan, Y. Jang, Y. Patil, R. Misra, F. D'Souza, Angew. Chem. Int. Ed., 2021, 60, 20518-20527.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

24. Interfacing High‐Energy Charge Transfer States to a Near‐IR Sensitizer for Efficient Electron Transfer upon Near‐IR Irradiation. 

D. Pinjari, A. Alsaleh, Y. Patil, R. Misra, F. D'Souza, Angew. Chem. Int. Ed., 2020, 59, 23697-23705.

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23. Formation of Highly Efficient, Long‐Lived Charge Separated States in Star‐Shaped Ferrocene‐ Diketopyrrolopyrrole‐Triphenylamine Donor‐Acceptor‐Donor Conjugates.

C. Popli, Y. Jang, Y. Patil, R. Misra, F. D'Souza, Chem. Eur. J., 2020, DOI:10.1002/chem.202002851. 

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22. Rational molecular design towards NIR absorption: efficient diketopyrrolopyrrole derivatives for organic solar cells and photothermal therapy- Review Article

Patil, Y., Misra, R., J. Mater. Chem. C, 2019, 7, 13020-13031.(Review) (Impact Factor = 6.641).

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21. Metal Functionalized Diketopyrrolopyrroles: A Promising Class of Materials for Optoelectronic Applications-Review Article

Patil, Y., Misra, R., Chem. Rec. 2019, DOI:org/10.1002/tcr.201900061. (Review) 

 

 

 

 

 

 

 

 

 

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20. Small molecule based non-fullerene acceptors: A comparative study – Review Article

Patil, Y., Misra, R., Chem. Rec. 2018, 18, 1350. (Review).

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19. Diketopyrrolopyrrole-based and tetracyano-bridged small molecules for bulk heterojunction organic solar cells–Focus Review.

Patil, Y., Misra, R., Chem. Asian J. 2018, 13, 220 – 229 (Review) 

 

 

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18. Near-infrared absorbing tetracyanobutadiene bridged diketopyrrolopyrroles.

Patil, Y., Popli, C., Misra, R. New J. Chem. 2018, 42, 3892-3899.

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17. Design and synthesis of N-phenyl carbazole substituted diketopyrrolopyrrole based monomers and dimers: A comparative study.

Popli, C., Patil, Y., Misra, R. Eur. J. Org. Chem., 2018, 2018, 6474-6481

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16. Ferrocene-diketopyrrolopyrrole based non-fullerene acceptors for bulk heterojunction polymer solar cells.

Patil, Y., Misra, R., Singhal R., Sharma, G. D. J. Mater. Chem. A, 2017, 5, 13625–13633.

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15. Design and synthesis of near-infrared absorbing diketopyrrolopyrroles

Patil, Y., Misra, R. PhD Thesis

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14. Small molecule carbazole based diketopyrrolopyrroles with tetracyanobutadiene acceptor unit as Non-Fullerene Acceptor for Bulk Heterojunction Organic Solar Cells.

Patil, Y., Misra, R., Keshtov, M. L., Sharma, G. D. J. Mater. Chem. A 2017, 5, 3311-   3319.

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13. Ferrocene-diketopyrrolopyrrole based small molecule donor for bulk heterojunction solar cells.

Patil, Y., Misra, R., Singh, M. K., Sharma, G. D. Phys. Chem. Chem. Phys. 2017, 19, 7262-7269. 

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12. Near-infrared absorbing metal functionalized diketopyrrolopyrroles.

Patil, Y., Shinde, J., Misra, R. J. Organomet. Chem. 2017, 852, 48 – 53.

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11. Tetracyanobutadiene bridged Ferrocene and Triphenylamine functionalized Pyrazabole dimers.

Patil, Y., Misra, R. J. Organomet. Chem. 2017, 840, 23-29. 

 

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10. Donor Substituted Pyrazabole Monomers and Dimers: Design, Synthesis and Properties.

Patil, Y., Jadhav, T., Dhokale, B., Butenschön, H., Misra, R. ChemistrySelect 2017, 2, 415–420. 

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9. 1,1,4,4-Tetracyanobuta-1,3-diene Substituted Diketopyrrolopyrroles: An Acceptor for Solution Processable Organic Bulk Heterojunction Solar Cells.

Patil, Y., Misra, R., Keshtov, M. L., Sharma, G. D. J. Phys. Chem. C 2016, 120, 6324−6335. 

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8. D-A-D-p-D-A-D Type Diketopyrrolopyrrole Based Small Molecule Electron Donor for Bulk Heterojunction Organic Solar Cells.

Patil, Y., Misra, R., Sharma, A., Sharma G. D. Phys. Chem. Chem. Phys. 2016, 18, 16950-16957. 

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7. Small molecules based N-phenyl carbazole Substituted Diketopyrrolopyrroles as donor for solution processed bulk heterojunction organic solar cells.

Patil, Y., Misra, R., Chen, F. C., Sharma, G. D. Phys. Chem. Chem. Phys. 2016, 18, 22999-23005. 

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6. Symmetrical and Unsymmetrical Triphenylamine based Diketopyrrolopyrroles and their use as Donor for Solution Processed Bulk Heterojunction Organic Solar Cells.

Patil, Y., Misra, R., Chen, F. C., Keshtov, M. L., Sharma, G. D. RSC Adv. 2016,  6, 99685-99694.

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5. Tuning of the HOMO-LUMO gap of symmetrical and unsymmetrical ferrocenyl diketopyrrolopyrroles.

Patil, Y., Jadhav, T., Dhokale, B., Misra, R. Eur. J. Org. Chem. 2016, 4, 733–738. 

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4. Design and Synthesis of Low HOMO–LUMO Gap N-phenyl Carbazole Substituted Diketopyrrolopyrroles.

Patil, Y., Jadhav, T., Dhokale, B., Misra, R. Asian J. Org. Chem. 2016, 5, 1008–1014. 

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3. Multi-Stimuli Responsive Donor–Acceptor Tetraphenylethylene Substituted Benzothiadiazoles

Jadhav, T., Dhokale, B., Patil, Y., Shaikh, M. M., Misra, R., J. Phys. Chem. C, 2016, 120, 24030–24040. 

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2. Symmetrical and unsymmetrical ferrocenyl perylenediimides: Design, synthesis and properties.

Dhokale, B., Jadhav, T., Patil, Y.,  Misra, R., Dyes and Pigments, 2016, 134, 164–170. 

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1. Aggregation induced emission and mechanochromism in tetraphenylethene substituted pyrazabole.

Jadhav, T., Dhokale, B., Patil, Y., Misra, R., RSC Adv., 2015, 5, 68187-68191.