Year |
Citation |
Score |
2022 |
Patil Y, Butenschön H, Misra R. Tetracyanobutadiene Bridged Push-Pull Chromophores: Development of New Generation Optoelectronic Materials. Chemical Record (New York, N.Y.). e202200208. PMID 36202630 DOI: 10.1002/tcr.202200208 |
0.596 |
|
2021 |
D'Souza F, Khan F, Jang Y, Patil Y, Misra R. Photoinduced Charge Separation Prompted Intervalence Charge Transfer in a Bis(thienyl)diketopyrrolopyrrole Bridged Donor-TCBD Push-Pull System. Angewandte Chemie (International Ed. in English). PMID 34258866 DOI: 10.1002/anie.202108293 |
0.778 |
|
2020 |
D'Souza F, Pinjari D, Alsaleh A, Patil Y, Misra R. Interfacing High-Energy Charge Transfer States to a Near-IR Sensitizer for Efficient Electron Transfer upon Near-IR Irradiation. Angewandte Chemie (International Ed. in English). PMID 33027554 DOI: 10.1002/anie.202013036 |
0.767 |
|
2020 |
D'Souza F, Popli C, Jang Y, Patil Y, Misra R. Formation of Highly Efficient, Long-Lived Charge Separated States in Star-Shaped Ferrocene-Diketopyrrolopyrrole-Triphenylamine Donor-Acceptor-Donor Conjugates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32589288 DOI: 10.1002/Chem.202002851 |
0.768 |
|
2020 |
Pinjari D, Alsaleh AZ, Patil Y, Misra R, D'Souza F. Cover Picture: Interfacing High‐Energy Charge‐Transfer States to a Near‐IR Sensitizer for Efficient Electron Transfer upon Near‐IR Irradiation (Angew. Chem. Int. Ed. 52/2020) Angewandte Chemie International Edition. 59: 23345-23345. DOI: 10.1002/anie.202014552 |
0.777 |
|
2020 |
Pinjari D, Alsaleh AZ, Patil Y, Misra R, D'Souza F. Titelbild: Interfacing High‐Energy Charge‐Transfer States to a Near‐IR Sensitizer for Efficient Electron Transfer upon Near‐IR Irradiation (Angew. Chem. 52/2020) Angewandte Chemie. 132: 23549-23549. DOI: 10.1002/ange.202014552 |
0.778 |
|
2019 |
Patil Y, Misra R. Metal Functionalized Diketopyrrolopyrroles: A Promising Class of Materials for Optoelectronic Applications. Chemical Record (New York, N.Y.). PMID 31833617 DOI: 10.1002/Tcr.201900061 |
0.563 |
|
2019 |
Patil Y, Misra R. Rational molecular design towards NIR absorption: efficient diketopyrrolopyrrole derivatives for organic solar cells and photothermal therapy Journal of Materials Chemistry C. 7: 13020-13031. DOI: 10.1039/C9Tc03640G |
0.582 |
|
2018 |
Patil Y, Misra R. Small Molecule Based Non-fullerene Acceptors: A Comparative Study. Chemical Record (New York, N.Y.). PMID 29888443 DOI: 10.1002/Tcr.201800037 |
0.604 |
|
2018 |
Patil Y, Popli C, Misra R. Near-infrared absorbing tetracyanobutadiene-bridged diketopyrrolopyrroles New Journal of Chemistry. 42: 3892-3899. DOI: 10.1039/C7Nj05162J |
0.751 |
|
2018 |
Popli C, Patil Y, Misra R. Design and Synthesis of N
-Phenylcarbazole-Substituted Diketopyrrolopyrrole-Based Monomers and Dimers: A Comparative Study European Journal of Organic Chemistry. 2018: 6474-6481. DOI: 10.1002/Ejoc.201801072 |
0.73 |
|
2017 |
Patil Y, Misra R, Singh MK, Sharma GD. Ferrocene-diketopyrrolopyrrole based small molecule donors for bulk heterojunction solar cells. Physical Chemistry Chemical Physics : Pccp. PMID 28239736 DOI: 10.1039/C7Cp00231A |
0.642 |
|
2017 |
Patil Y, Misra R, Singhal R, Sharma GD. Ferrocene-diketopyrrolopyrrole based non-fullerene acceptors for bulk heterojunction polymer solar cells Journal of Materials Chemistry A. 5: 13625-13633. DOI: 10.1039/C7Ta03322B |
0.578 |
|
2017 |
Patil Y, Misra R, Keshtov ML, Sharma GD. Small molecule carbazole-based diketopyrrolopyrroles with tetracyanobutadiene acceptor unit as a non-fullerene acceptor for bulk heterojunction organic solar cells Journal of Materials Chemistry A. 5: 3311-3319. DOI: 10.1039/C6Ta09607G |
0.607 |
|
2017 |
Patil Y, Shinde J, Misra R. Near-infrared absorbing metal functionalized diketopyrrolopyrroles Journal of Organometallic Chemistry. 852: 48-53. DOI: 10.1016/J.Jorganchem.2017.10.014 |
0.61 |
|
2017 |
Patil Y, Misra R. Tetracyanobutadiene bridged ferrocene and triphenylamine functionalized pyrazabole dimers Journal of Organometallic Chemistry. 840: 23-29. DOI: 10.1016/J.Jorganchem.2017.03.048 |
0.691 |
|
2016 |
Patil Y, Misra R, Chen FC, Sharma GD. Small molecule based N-phenyl carbazole substituted diketopyrrolopyrroles as donors for solution-processed bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics : Pccp. PMID 27489031 DOI: 10.1039/C6Cp03767D |
0.607 |
|
2016 |
Patil Y, Misra R, Sharma A, Sharma GD. D-A-D-π-D-A-D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics : Pccp. PMID 27292157 DOI: 10.1039/C6Cp02700H |
0.604 |
|
2016 |
Patil Y, Misra R, Chen FC, Keshtov ML, Sharma GD. Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells Rsc Advances. 6: 99685-99694. DOI: 10.1039/C6Ra10442H |
0.638 |
|
2016 |
Jadhav T, Dhokale B, Patil Y, Mobin SM, Misra R. Multi-Stimuli Responsive Donor–Acceptor Tetraphenylethylene Substituted Benzothiadiazoles The Journal of Physical Chemistry C. 120: 24030-24040. DOI: 10.1021/Acs.Jpcc.6B09015 |
0.751 |
|
2016 |
Patil Y, Misra R, Keshtov ML, Sharma GD. 1,1,4,4-Tetracyanobuta-1,3-diene Substituted Diketopyrrolopyrroles: An Acceptor for Solution Processable Organic Bulk Heterojunction Solar Cells Journal of Physical Chemistry C. 120: 6324-6335. DOI: 10.1021/Acs.Jpcc.5B12307 |
0.643 |
|
2016 |
Dhokale B, Jadhav T, Patil Y, Misra R. Symmetrical and unsymmetrical ferrocenyl perylenediimides: Design, synthesis and properties Dyes and Pigments. 134: 164-170. DOI: 10.1016/J.Dyepig.2016.07.006 |
0.799 |
|
2016 |
Patil Y, Jadhav T, Dhokale B, Misra R. Design and Synthesis of Low HOMO-LUMO GapN-Phenylcarbazole-Substituted Diketopyrrolopyrroles Asian Journal of Organic Chemistry. 5: 1008-1014. DOI: 10.1002/Ajoc.201600194 |
0.747 |
|
2015 |
Jadhav T, Dhokale B, Patil Y, Misra R. Aggregation induced emission and mechanochromism in tetraphenylethene substituted pyrazabole Rsc Advances. 5: 68187-68191. DOI: 10.1039/C5Ra12697E |
0.759 |
|
2015 |
Patil Y, Jadhav T, Dhokale B, Misra R. Tuning of the HOMO-LUMO Gap of Symmetrical and Unsymmetrical Ferrocenyl-Substituted Diketopyrrolopyrroles European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201501123 |
0.781 |
|
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