| Year |
Citation |
Score |
| 2023 |
Mishra A, Sharma GD. Harnessing the Structure-Performance Relationships in Designing Non-Fused Ring Acceptors for Organic Solar Cells. Angewandte Chemie (International Ed. in English). e202219245. PMID 36798969 DOI: 10.1002/anie.202219245 |
0.341 |
|
| 2020 |
Pradhan R, Malhotra P, Gupta G, Singhal R, Sharma GD, Mishra A. Efficient Fullerene-Free Organic Solar Cells Using a Coumarin-Based Wide Bandgap Donor Material. Acs Applied Materials & Interfaces. PMID 32799443 DOI: 10.1021/acsami.0c12147 |
0.35 |
|
| 2017 |
Arora N, Wetzel C, Dar MI, Mishra A, Yadav P, Steck C, Zakeeruddin SM, Bäuerle P, Grätzel M. Donor-Acceptor-Type S,N-Heteroacene-Based Hole-Transporting Materials for Efficient Perovskite Solar Cells. Acs Applied Materials & Interfaces. PMID 29185697 DOI: 10.1021/Acsami.7B10039 |
0.559 |
|
| 2016 |
Bi D, Mishra A, Gao P, Franckevičius M, Steck C, Zakeeruddin SM, Nazeeruddin MK, Bäuerle P, Grätzel M, Hagfeldt A. High-Efficiency Perovskite Solar Cells Employing a S,N-Heteropentacene-based D-A Hole-Transport Material. Chemsuschem. PMID 26813331 DOI: 10.1002/Cssc.201501510 |
0.586 |
|
| 2015 |
Wetzel C, Brier E, Vogt A, Mishra A, Mena-Osteritz E, Bäuerle P. Fused Thiophene-Pyrrole-Containing Ring Systems up to a Heterodecacene. Angewandte Chemie (International Ed. in English). PMID 26136252 DOI: 10.1002/Anie.201502840 |
0.484 |
|
| 2015 |
Götz G, Zhu X, Mishra A, Segura JL, Mena-Osteritz E, Bäuerle P. π-Conjugated [2]Catenanes Based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7193-210. PMID 25820180 DOI: 10.1002/Chem.201406039 |
0.504 |
|
| 2015 |
Perera IR, Daeneke T, Makuta S, Yu Z, Tachibana Y, Mishra A, Bäuerle P, Ohlin CA, Bach U, Spiccia L. Application of the tris(acetylacetonato)iron(III)/(II) redox couple in p-type dye-sensitized solar cells. Angewandte Chemie (International Ed. in English). 54: 3758-62. PMID 25631105 DOI: 10.1002/Anie.201409877 |
0.515 |
|
| 2014 |
Mishra A, Popovic D, Vogt A, Kast H, Leitner T, Walzer K, Pfeiffer M, Mena-Osteritz E, Bäuerle P. A-D-A-type S,N-heteropentacenes: next-generation molecular donor materials for efficient vacuum-processed organic solar cells. Advanced Materials (Deerfield Beach, Fla.). 26: 7217-23. PMID 25244527 DOI: 10.1002/Adma.201402448 |
0.563 |
|
| 2014 |
Weidelener M, Powar S, Kast H, Yu Z, Boix PP, Li C, Müllen K, Geiger T, Kuster S, Nüesch F, Bach U, Mishra A, Bäuerle P. Synthesis and characterization of organic dyes with various electron-accepting substituents for p-type dye-sensitized solar cells. Chemistry, An Asian Journal. 9: 3251-63. PMID 25234556 DOI: 10.1002/Asia.201402654 |
0.577 |
|
| 2014 |
Mercier LG, Mishra A, Ishigaki Y, Henne F, Schulz G, Bäuerle P. Acceptor-donor-acceptor oligomers containing dithieno[3,2-b:2',3'-d]pyrrole and thieno[2,3-c]pyrrole-4,6-dione units for solution-processed organic solar cells. Organic Letters. 16: 2642-5. PMID 24796375 DOI: 10.1021/Ol500809E |
0.543 |
|
| 2014 |
Wetzel C, Mishra A, Mena-Osteritz E, Liess A, Stolte M, Würthner F, Bäuerle P. Synthesis and structural analysis of thiophene-pyrrole-based S,N-heteroacenes. Organic Letters. 16: 362-5. PMID 24359234 DOI: 10.1021/Ol403153Z |
0.57 |
|
| 2013 |
Weidelener M, Wessendorf CD, Hanisch J, Ahlswede E, Götz G, Lindén M, Schulz G, Mena-Osteritz E, Mishra A, Bäuerle P. Dithienopyrrole-based oligothiophenes for solution-processed organic solar cells. Chemical Communications (Cambridge, England). 49: 10865-7. PMID 24126293 DOI: 10.1039/C3Cc46066E |
0.526 |
|
| 2013 |
Schmid S, Mishra A, Wunderlin M, Bäuerle P. Mannose-functionalized dendritic oligothiophenes: synthesis, characterizations and studies on their interaction with Concanavalin A. Organic & Biomolecular Chemistry. 11: 5656-65. PMID 23877421 DOI: 10.1039/C3Ob41113C |
0.449 |
|
| 2013 |
Mishra A, Mena-Osteritz E, Bäuerle P. Synthesis, photophysical and electrochemical characterization of terpyridine-functionalized dendritic oligothiophenes and their Ru(II) complexes. Beilstein Journal of Organic Chemistry. 9: 866-76. PMID 23766802 DOI: 10.3762/Bjoc.9.100 |
0.467 |
|
| 2013 |
Powar S, Daeneke T, Ma MT, Fu D, Duffy NW, Götz G, Weidelener M, Mishra A, Bäuerle P, Spiccia L, Bach U. Highly efficient p-type dye-sensitized solar cells based on tris(1,2-diaminoethane)cobalt(II)/(III) electrolytes. Angewandte Chemie (International Ed. in English). 52: 602-5. PMID 23169678 DOI: 10.1002/Anie.201206219 |
0.544 |
|
| 2012 |
Potratz S, Mishra A, Bäuerle P. Thiophene-based donor-acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition. Beilstein Journal of Organic Chemistry. 8: 683-92. PMID 23015814 DOI: 10.3762/Bjoc.8.76 |
0.502 |
|
| 2012 |
Fitzner R, Mena-Osteritz E, Mishra A, Schulz G, Reinold E, Weil M, Körner C, Ziehlke H, Elschner C, Leo K, Riede M, Pfeiffer M, Uhrich C, Bäuerle P. Correlation of π-conjugated oligomer structure with film morphology and organic solar cell performance. Journal of the American Chemical Society. 134: 11064-7. PMID 22694124 DOI: 10.1021/Ja302320C |
0.539 |
|
| 2012 |
Mishra A, Bäuerle P. Small molecule organic semiconductors on the move: promises for future solar energy technology. Angewandte Chemie (International Ed. in English). 51: 2020-67. PMID 22344682 DOI: 10.1002/Anie.201102326 |
0.561 |
|
| 2011 |
Zhang XL, Huang F, Nattestad A, Wang K, Fu D, Mishra A, Bäuerle P, Bach U, Cheng YB. Enhanced open-circuit voltage of p-type DSC with highly crystalline NiO nanoparticles. Chemical Communications (Cambridge, England). 47: 4808-10. PMID 21416106 DOI: 10.1039/C0Cc05445C |
0.479 |
|
| 2011 |
Steinberger S, Mishra A, Reinold E, Levichkov J, Uhrich C, Pfeiffer M, Bäuerle P. Vacuum-processed small molecule solar cells based on terminal acceptor-substituted low-band gap oligothiophenes. Chemical Communications (Cambridge, England). 47: 1982-4. PMID 21221436 DOI: 10.1039/C0Cc04541A |
0.564 |
|
| 2011 |
Steinberger S, Mishra A, Reinold E, Müller CM, Uhrich C, Pfeiffer M, Bäuerle P. A-D-A-D-A-type oligothiophenes for vacuum-deposited organic solar cells. Organic Letters. 13: 90-3. PMID 21133358 DOI: 10.1021/Ol102603N |
0.526 |
|
| 2011 |
Schmid S, Mishra A, Bäuerle P. Carbohydrate-functionalized oligothiophenes for concanavalin A recognition. Chemical Communications (Cambridge, England). 47: 1324-6. PMID 21103559 DOI: 10.1039/C0Cc03908J |
0.437 |
|
| 2009 |
Mishra A, Pootrakulchote N, Fischer MK, Klein C, Nazeeruddin MK, Zakeeruddin SM, Bäuerle P, Grätzel M. Design and synthesis of a novel anchoring ligand for highly efficient thin film dye-sensitized solar cells. Chemical Communications (Cambridge, England). 7146-8. PMID 19921011 DOI: 10.1039/B912506J |
0.543 |
|
| 2009 |
Mishra A, Ma CQ, Janssen RA, Bäuerle P. Shape-persistent oligothienylene-ethynylene-based dendrimers: synthesis, spectroscopy and electrochemical characterization. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 13521-34. PMID 19876965 DOI: 10.1002/Chem.200901242 |
0.537 |
|
| 2009 |
Sauvage F, Fischer MK, Mishra A, Zakeeruddin SM, Nazeeruddin MK, Bäuerle P, Grätzel M. A dendritic oligothiophene ruthenium sensitizer for stable dye-sensitized solar cells. Chemsuschem. 2: 761-8. PMID 19569164 DOI: 10.1002/Cssc.200900058 |
0.553 |
|
| 2009 |
Mishra A, Fischer MK, Bäuerle P. Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationships to design rules. Angewandte Chemie (International Ed. in English). 48: 2474-99. PMID 19294671 DOI: 10.1002/Anie.200804709 |
0.545 |
|
| 2009 |
Mishra A, Ma CQ, Bäuerle P. Functional oligothiophenes: molecular design for multidimensional nanoarchitectures and their applications. Chemical Reviews. 109: 1141-276. PMID 19209939 DOI: 10.1021/Cr8004229 |
0.386 |
|
| 2002 |
Newkome GR, Mishra A, Moorefield CN. Improved synthesis of an ethereal tetraamine core for dendrimer construction. The Journal of Organic Chemistry. 67: 3957-60. PMID 12027725 DOI: 10.1021/Jo025625P |
0.423 |
|
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