K
Kushal Ghale
Researcher at Louisiana State University
Publications - 6
Citations - 580
Kushal Ghale is an academic researcher from Louisiana State University. The author has contributed to research in topics: Polymerization & Chain transfer. The author has an hindex of 5, co-authored 6 publications receiving 457 citations.
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Journal ArticleDOI
Pd-Ir Core-Shell Nanocubes: A Type of Highly Efficient and Versatile Peroxidase Mimic
Xiaohu Xia,Jingtuo Zhang,Ning Lu,Moon J. Kim,Kushal Ghale,Ye Xu,Erin McKenzie,Jiabin Liu,Haihang Ye +8 more
TL;DR: A type of highly efficient peroxidase mimic that was engineered by depositing Ir atoms as ultrathin skins on Pd nanocubes (i.e., Pd-Ir cubes) exhibited significantly enhanced efficiency, with catalytic constants more than 20- and 400-fold higher than those of the initial Pd cubes and horseradish per oxidase (HRP), respectively.
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N-Heterocyclic Carbene-Mediated Zwitterionic Polymerization of N-Substituted N-Carboxyanhydrides toward Poly(α-peptoid)s: Kinetic, Mechanism, and Architectural Control
TL;DR: Kinetic studies reveal that the propagating intermediates for the polymerization in low dielectric solvents maintain cyclic architectures with two chain ends in close contact through Coulombic interaction, which facilitates quasi-living polymerization behavior in cyclic zwitterionic species.
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DFT-Based Method for More Accurate Adsorption Energies: An Adaptive Sum of Energies from RPBE and vdW Density Functionals
Alyssa J. R. Hensley,Kushal Ghale,Carolin Rieg,Thanh Dang,Emily S. Anderst,Felix Studt,Charles T. Campbell,Jean-Sabin McEwen,Ye Xu +8 more
TL;DR: In this paper, the authors present a method for accurately predicting adsorption energies on transition-metal surfaces based on DFT calculations, using an adaptively weighted sum of energies from RPBE and optB86b-vdW (or optB88-vdw) density functionals.
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Crystallization and Melting Behaviors of Cyclic and Linear Polypeptoids with Alkyl Side Chains
TL;DR: In this article, a series of cyclic and linear poly(N-alkyl glycine)s (a.k.a. polypeptoids) with various linear and branched alkyl side chains (n = 2, 4, 6, 8, 10, 12, and 14) were synthesized by N-heterocyclic carbene or benzylamine-initiated polymerizations of the corresponding N-alky N-carboxyanhydride (R-NCAs), respectively.
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Synthesis and characterization of cyclic and linear helical poly(α-peptoid)s by N-heterocyclic carbene-mediated ring-opening polymerizations of N-substituted N-carboxyanhydrides†
TL;DR: Intrinsic viscosity measurements confirm the architectural difference between the polymers prepared by the two methods and reveals that both cyclic and linear poly[(S)-N-CHMePh-glycine]s behave as random-coil polymers in 0.1M LiBr/Dimethylformamide (DMF) solution.