Anil Reddy Marri

Kirk, M. L., Shultz, D. A., Marri, A. R., & Est, A. (2024, March 22). Photoinduced Magnetic Exchange-Jump Promotes Ground State Biradical Electron Spin Polarization. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, Vol. 3. https://doi.org/10.1021/jacs.4c00930

Kirk, M. L., Shultz, D. A., Hewitt, P., Marri, A. R., & Est, A. (2023, August 8). Competitive reversed quartet mechanisms for photogenerated ground state electron spin polarization. CHEMICAL SCIENCE, Vol. 8. https://doi.org/10.1039/d3sc03049

Kirk, M. L., Shultz, D. A., Hewitt, P., Marri, A. R., & Est, A. (2023). Competitive reversed quartet mechanisms for photogenerated ground state electron spin polarization. CHEMICAL SCIENCE, 14(36), 9689–9695. https://doi.org/10.1039/d3sc03049k

Reddy-Marri, A., Marchini, E., Cabanes, V. D., Argazzi, R., Pastore, M., Caramori, S., & Gros, P. C. (2023). Panchromatic light harvesting and record power conversion efficiency for carboxylic/cyanoacrylic Fe(<scp>ii</scp>) NHC co-sensitized FeSSCs. Chemical Science, 14(16), 4288–4301. https://doi.org/10.1039/D2SC05971A

Marri, A. R., Marekha, B., Penfold, T., Haacke, S., & Gros, P. C. (2023). Towards panchromatic Fe(<scp>ii</scp>) NHC sensitizers <i>via</i> HOMO inversion. Inorganic Chemistry Frontiers, 10(1), 118–126. https://doi.org/10.1039/D2QI01903E

Delcroix, M., Reddy Marri, A., Parant, S., Gros, P. C., & Bouché, M. (2023). Water‐Soluble Fe(II) Complexes for Theranostic Application: Synthesis, Photoacoustic Imaging, and Photothermal Conversion. European Journal of Inorganic Chemistry, 5. https://doi.org/10.1002/ejic.202300138

Marri, A. R., Flint, H., Gibson, E. A., & Fielden, J. (2022). Pyridyl anchored indolium dyes for the p-type dye sensitized solar cell. Dyes and Pigments, 202, 110244. https://doi.org/10.1016/j.dyepig.2022.110244

Kirk, M. L., Shultz, D. A., Marri, A. R., Hewitt, P., & van der Est, A. (2022). Single-Photon-Induced Electron Spin Polarization of Two Exchange-Coupled Stable Radicals. Journal of the American Chemical Society, 144(46), 21005–21009. https://doi.org/10.1021/jacs.2c09680

Carrillo, U., Francés-Monerris, A., Marri, A. R., Cebrián, C., & Gros, P. C. (2022). Substituent-Induced Control of <i>fac</i>/<i>mer</i> Isomerism in Azine-NHC Fe(II) Complexes. ACS Organic & Inorganic Au, 2(6), 525–536. https://doi.org/10.1021/acsorginorgau.2c00038

Marri, A. R., Marchini, E., Cabanes, V. D., Argazzi, R., Pastore, M., Caramori, S., … Gros, P. C. (2021). A Series of Iron(II)‐NHC Sensitizers with Remarkable Power Conversion Efficiency in Photoelectrochemical Cells**. Chemistry – A European Journal, 27(65), 16260–16269. https://doi.org/10.1002/chem.202103178

Marri, A. R., Marchini, E., Cabanes, V. D., Argazzi, R., Pastore, M., Caramori, S., & Gros, P. C. (2021). Record power conversion efficiencies for iron(ii)-NHC-sensitized DSSCs from rational molecular engineering and electrolyte optimization. Journal of Materials Chemistry A, 9(6), 3540–3554. https://doi.org/10.1039/d0ta10841c

Hainer, F., Alagna, N., Reddy Marri, A., Penfold, T. J., Gros, P. C., Haacke, S., & Buckup, T. (2021). Vibrational Coherence Spectroscopy Identifies Ultrafast Branching in an Iron(II) Sensitizer. The Journal of Physical Chemistry Letters, 12(35), 8560–8565. https://doi.org/10.1021/acs.jpclett.1c01580

Marri, A. R., Black, F. A., Mallows, J., Gibson, E. A., & Fielden, J. (2019). Pyridinium p-DSSC dyes: An old acceptor learns new tricks. Dyes and Pigments, 165, 508–517. https://doi.org/10.1016/j.dyepig.2019.02.044

El Moll, H., Black, F. A., Wood, C. J., Al-Yasari, A., Reddy Marri, A., Sazanovich, I. V., … Fielden, J. (2017). Increasing p-type dye sensitised solar cell photovoltages using polyoxometalates. Physical Chemistry Chemical Physics, 19(29), 18831–18835. https://doi.org/10.1039/c7cp01558e

Marri, A. R., Cho, K. Y., Lee, A. S., Kim, H.-J., Huy, D. X., Hwang, S. S., & Baek, K.-Y. (2017). Synthesis, characterization and photophysical behavior of heteroleptic ruthenium-complexed ladder-like structured polysilsesquioxanes. Macromolecular Research, 25(6), 591–598. https://doi.org/10.1007/s13233-017-5110-0

Reddy, M. A., Kumar, C. P., Ashok, A., Sharma, A., Sharma, G. D., & Chandrasekharam, M. (2016). Hetero aromatic donors as effective terminal groups for DPP based organic solar cells. RSC Advances, 6(11), 9023–9036. https://doi.org/10.1039/c5ra24610e

Vinayak, B., Reddy, M. A., Chiranjeevi, B., Chandrashekharam, M., Poornachandra, Y., & Ganesh Kumar, C. (2016). Iron-catalyzed cyclization of aminothiols: An easy access to benzothiazoles and evaluation of their antimicrobial and anti-biofilm activities. Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 55B(4), 461–470. Retrieved from http://www.scopus.com/inward/record.url?eid=2-s2.0-85009289882&partnerID=MN8TOARS

Gupta, K. S. V., Zhang, J., Marotta, G., Reddy, M. A., Singh, S. P., Islam, A., … Pastore, M. (2015). Effect of the anchoring group in the performance of carbazole-phenothiazine dyads for dye-sensitized solar cells. Dyes and Pigments, 113, 536–545. https://doi.org/10.1016/j.dyepig.2014.09.032

Sharma, G. D., Anil Reddy, M., Ramana, D. V., & Chandrasekharam, M. (2014). A novel carbazole-phenothiazine dyad small molecule as a non-fullerene electron acceptor for polymer bulk heterojunction solar cells. RSC Advances, 4(63), 33279–33285. https://doi.org/10.1039/c4ra05584e

Lobello, M. G., Wu, K.-L., Reddy, M. A., Marotta, G., Grätzel, M., Nazeeruddin, M. K., … De Angelis, F. (2014). Engineering of Ru(ii) dyes for interfacial and light-harvesting optimization. Dalton Transactions, 43(7), 2726–2732. https://doi.org/10.1039/c3dt53272k

Anil Reddy, M., Vinayak, B., Suresh, T., Niveditha, S., Bhanuprakash, K., Prakash Singh, S., … Chandrasekharam, M. (2014). Highly conjugated electron rich thiophene antennas on phenothiazine and phenoxazine-based sensitizers for dye sensitized solar cells. Synthetic Metals, 195, 208–216. https://doi.org/10.1016/j.synthmet.2014.06.009

Sharma, G. D., Reddy, M. A., Ganesh, K., Singh, S. P., & Chandrasekharam, M. (2014). Indole and triisopropyl phenyl as capping units for a diketopyrrolopyrrole (DPP) acceptor central unit: An efficient D-A-D type small molecule for organic solar cells. RSC Advances, 4(2), 732–742. https://doi.org/10.1039/c3ra44926b

Chandrasekharam, M., Reddy, M. A., Ganesh, K., Sharma, G. D., Singh, S. P., & Rao, J. L. (2014). Synthesis and photovoltaic properties of D-A-D type small molecules containing diketopyrrolopyrrole (DPP) acceptor central unit with different donor terminal units. Organic Electronics, 15(9), 2116–2125. https://doi.org/10.1016/j.orgel.2014.05.033

Marotta, G., Reddy, M. A., Singh, S. P., Islam, A., Han, L., De Angelis, F., … Chandrasekharam, M. (2013). Novel carbazole-phenothiazine dyads for dye-sensitized solar cells: A combined experimental and theoretical study. ACS Applied Materials and Interfaces, 5(19), 9635–9647. https://doi.org/10.1021/am402675q

Agrawal, S., Pastore, M., Marotta, G., Reddy, M. A., Chandrasekharam, M., & De Angelis, F. (2013). Optical properties and aggregation of phenothiazine-based dye-sensitizers for solar cells applications: A combined experimental and computational investigation. Journal of Physical Chemistry C, 117(19), 9613–9622. https://doi.org/10.1021/jp4026305

Chandrasekharam, M., Reddy, M. A., Singh, S. P., Priyanka, B., Bhanuprakash, K., Kantam, M. L., … Han, L. (2012). One bipyridine and triple advantages: tailoring ancillary ligands in ruthenium complexes for efficient sensitization in dye solar cells. Journal of Materials Chemistry, 22(36), 18757. https://doi.org/10.1039/c2jm34558g

Chandrasekharam, M., Srinivasarao, C., Suresh, T., Reddy, M. A., Raghavender, M., Rajkumar, G., … Reddy, P. Y. (2011). High spectral response heteroleptic ruthenium (II) complexes as sensitizers for dye sensitized solar cells. Journal of Chemical Sciences, 123(1), 37–46. https://doi.org/10.1007/s12039-011-0066-7

Chandrasekharam, M., Rajkumar, G., Srinivasa Rao, C., Suresh, T., Anil Reddy, M., Yella Reddy, P., … Graetzel, M. (2011). Polypyridyl Ru(II)-sensitizers with extended π-system enhances the performance of dye sensitized solar cells. Synthetic Metals, 161(11-12), 1098–1104. https://doi.org/10.1016/j.synthmet.2011.03.022