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Structural, Photophysical, and Electrochemical Properties of Doubly Fused Porphyrins and Related Fused Chlorins Chaudhri N, Cong L, Bulbul AS, Grover N, Osterloh WR, Fang YY, Sankar M, Kadish KM Inorganic Chemistry, 59(2), 1481, 2020 |
2 |
beta-Functionalized Dibenzoporphyrins with Mixed Substituents Pattern: Facile Synthesis, Structural, Spectral, and Electrochemical Redox Properties Grover N, Chaudhri N, Sankar M Inorganic Chemistry, 58(4), 2514, 2019 |
3 |
Selective Conversion of Planar trans-Chlorins into Highly Twisted Doubly Fused Porphyrins or Chlorins via Oxidative Fusion Chaudhri N, Grover N, Sankar M Inorganic Chemistry, 57(11), 6658, 2018 |
4 |
Synthesis and Electrochemical Characterization of Acetylacetone (acac) and Ethyl Acetate (EA) Appended beta-Trisubstituted Push-Pull Porphyrins: Formation of Electronically Communicating Porphyrin Dimers Chaudhri N, Cong L, Grover N, Shan WQ, Anshul K, Sankar M, Kadish KM Inorganic Chemistry, 57(21), 13213, 2018 |
5 |
Nickel-Induced Skeletal Rearrangement of Free Base trans-Chlorins into Monofused Ni-II-Porphyrins: Synthesis, Structural, Spectral, and Electrochemical Redox Properties Chaudhri N, Grover N, Sankar M Inorganic Chemistry, 57(18), 11349, 2018 |
6 |
Facile Conversion of Ni(II) Cyclopropylchlorins into Novel ss-Substituted Porphyrins through Acid-Catalyzed Ring-Opening Reaction Grover N, Chaudhri N, Sankar M Inorganic Chemistry, 56(1), 424, 2017 |
7 |
Versatile Synthetic Route for beta-Functionalized Chlorins and Porphyrins by Varying the Size of Michael Donors: Syntheses, Photophysical, and Electrochemical Redox Properties Chaudhri N, Grover N, Sankar M Inorganic Chemistry, 56(19), 11532, 2017 |
8 |
Activation of Molecular Oxygen by a Molybdenum(IV) Imido Compound Zwettler N, Grover N, Belaj F, Kirchner K, Mosch-Zanetti NC Inorganic Chemistry, 56(17), 10147, 2017 |
9 |
Acylase-containing polyurethane coatings with anti-biofilm activity Grover N, Plaks JG, Summers SR, Chado GR, Schurr MJ, Kaar JL Biotechnology and Bioengineering, 113(12), 2535, 2016 |
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Newly identified bacteriolytic enzymes that target a wide range of clinical isolates of Clostridium difficile Mehta KK, Paskaleva EE, Wu X, Grover N, Mundra RV, Chen KV, Zhang YR, Yang ZY, Feng HP, Dordick JS, Kane RS Biotechnology and Bioengineering, 113(12), 2568, 2016 |