Anil Reddy Marri

Photoinduced Magnetic Exchange-Jump Promotes Ground State Biradical Electron Spin Polarization

Kirk, M. L., Shultz, D. A., Marri, A. R., & Est, A. (2024, March 22). JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, Vol. 3.

Competitive reversed quartet mechanisms for photogenerated ground state electron spin polarization

Kirk, M. L., Shultz, D. A., Hewitt, P., Marri, A. R., & Est, A. (2023, August 8). CHEMICAL SCIENCE, Vol. 8.

Competitive reversed quartet mechanisms for photogenerated ground state electron spin polarization

CHEMICAL SCIENCE, 14(36), 9689–9695.

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.

Towards panchromatic Fe(<scp>ii</scp>) NHC sensitizers <i>via</i> HOMO inversion

Inorganic Chemistry Frontiers, 10(1), 118–126.

Water‐Soluble Fe(II) Complexes for Theranostic Application: Synthesis, Photoacoustic Imaging, and Photothermal Conversion

European Journal of Inorganic Chemistry, 5.

Pyridyl anchored indolium dyes for the p-type dye sensitized solar cell

Dyes and Pigments, 202, 110244.

Single-Photon-Induced Electron Spin Polarization of Two Exchange-Coupled Stable Radicals

Journal of the American Chemical Society, 144(46), 21005–21009.

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.

A Series of Iron(II)‐NHC Sensitizers with Remarkable Power Conversion Efficiency in Photoelectrochemical Cells**

Chemistry – A European Journal, 27(65), 16260–16269.

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.

Vibrational Coherence Spectroscopy Identifies Ultrafast Branching in an Iron(II) Sensitizer

The Journal of Physical Chemistry Letters, 12(35), 8560–8565.

Pyridinium p-DSSC dyes: An old acceptor learns new tricks

Dyes and Pigments, 165, 508–517.

Increasing p-type dye sensitised solar cell photovoltages using polyoxometalates

Physical Chemistry Chemical Physics, 19(29), 18831–18835.

Synthesis, characterization and photophysical behavior of heteroleptic ruthenium-complexed ladder-like structured polysilsesquioxanes

Macromolecular Research, 25(6), 591–598.

Hetero aromatic donors as effective terminal groups for DPP based organic solar cells

RSC Advances, 6(11), 9023–9036.

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. http://www.scopus.com/inward/record.url?eid=2-s2.0-85009289882&partnerID=MN8TOARS

Effect of the anchoring group in the performance of carbazole-phenothiazine dyads for dye-sensitized solar cells

Dyes and Pigments, 113, 536–545.

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.

Engineering of Ru(ii) dyes for interfacial and light-harvesting optimization

Dalton Transactions, 43(7), 2726–2732.

Highly conjugated electron rich thiophene antennas on phenothiazine and phenoxazine-based sensitizers for dye sensitized solar cells

Synthetic Metals, 195, 208–216.

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.

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.

Novel carbazole-phenothiazine dyads for dye-sensitized solar cells: A combined experimental and theoretical study

ACS Applied Materials and Interfaces, 5(19), 9635–9647.

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.

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.

High spectral response heteroleptic ruthenium (II) complexes as sensitizers for dye sensitized solar cells

Journal of Chemical Sciences, 123(1), 37–46.

Polypyridyl Ru(II)-sensitizers with extended π-system enhances the performance of dye sensitized solar cells

Synthetic Metals, 161(11-12), 1098–1104.