T
Tridib K. Sarma
Researcher at Indian Institute of Technology Indore
Publications - 79
Citations - 2495
Tridib K. Sarma is an academic researcher from Indian Institute of Technology Indore. The author has contributed to research in topics: Nanoparticle & Catalysis. The author has an hindex of 25, co-authored 74 publications receiving 2014 citations. Previous affiliations of Tridib K. Sarma include University of Tokyo & Shanghai University.
Papers
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Synthesis of Au nanoparticle–conductive polyaniline composite using H2O2 as oxidising as well as reducing agent
TL;DR: A new method of synthesis of an Au nanoparticle-conductive polyaniline composite is reported by using H2O2 both for reduction of HAuCl4 and polymerization of aniline in the same aqueous medium, with electrical conductivity measured to be two orders of magnitude higher than the polymer itself.
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Retention of Enzymatic Activity of α-Amylase in the Reductive Synthesis of Gold Nanoparticles
Abhijit Rangnekar,Tridib K. Sarma,Atul K. Singh,Jashmini Deka,Aiyagari Ramesh,Arun Chattopadhyay +5 more
TL;DR: The generation of Au nanoparticles (NPs) is reported, using a pure enzyme for the reduction of AuCl4-, with the retention of enzymatic activity in the complex.
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Carbon dot reduced palladium nanoparticles as active catalysts for carbon–carbon bond formation
TL;DR: Carbon dots were used as a reducing agent for the synthesis of Pd nanoparticles coated with ultrathin carbon dot shells of ca.
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Protonation-coupled redox reactions in planar antiaromatic meso-pentafluorophenyl-substituted o-phenylene-bridged annulated rosarins
Masatoshi Ishida,Soo Jin Kim,Christian Preihs,Kei Ohkubo,Jong Min Lim,Byung Sun Lee,Jung Su Park,Vincent M. Lynch,Vladimir V. Roznyatovskiy,Tridib K. Sarma,Pradeepta K. Panda,Chang-Hee Lee,Shunichi Fukuzumi,Dongho Kim,Jonathan L. Sessler,Jonathan L. Sessler +15 more
TL;DR: The stepwise nature of the proton-coupled reduction observed in the planar rosarin stands in marked contrast to that seen for non-annulated rosarins and other ostensibly antiaromatic expanded porphyrinoids.
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Dinaphthoporphycenes: synthesis and nonlinear optical studies.
TL;DR: Naphthobipyrrole-derived porphycenes are synthesized for the first time via McMurry coupling of the β-alkylated 2,9-diformylnaphthopyrrole derivatives, which were prepared easily from 2,3-naphthalene bishydrazine in four steps.