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Goutam Kumar Lahiri

Researcher at Indian Institute of Technology Bombay

Publications -  323
Citations -  9268

Goutam Kumar Lahiri is an academic researcher from Indian Institute of Technology Bombay. The author has contributed to research in topics: Ruthenium & Catalysis. The author has an hindex of 47, co-authored 301 publications receiving 8362 citations. Previous affiliations of Goutam Kumar Lahiri include University of Stuttgart & Indian Institutes of Technology.

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Unconventional mixed-valent complexes of ruthenium and osmium

TL;DR: The strategies employed include the use of multidentate ligands (which give rise to multinuclear and chelate complexes) and the use several redox active components (non-innocent ligands and oxidation-state ambivalence).
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Biomimetic sensor for certain catecholamines employing copper(II) complex and silver nanoparticle modified glassy carbon paste electrode

TL;DR: The prepared modified electrode shows several advantages such as simple preparation method, high sensitivity, high stability, ease of preparation and regeneration of the electrode surface by simple polishing along with excellent reproducibility.
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Separating innocence and non-innocence of ligands and metals in complexes [(L)Ru(acac)2](n) (n = -1, 0, +1; L = o-iminoquinone or o-iminothioquinone).

TL;DR: X-ray structure analysis of (L)Ru(acac)(2) (L(1) = o-iminoquinone) revealed C-C intra-ring, C-O, and C-N distances which suggest a Ru(III)-iminosemiquinone oxidation state distribution with antiparallel spin-spin coupling.
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Ruthenium and osmium complexes of N,O chelators: syntheses, oxidation levels, and distortion parameters

TL;DR: In this paper, les coordinats N, O concernes sont: R-quinoleinol-8, N-arylsalicylaldimine, and N-yrlsalicyclicylldimine.
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Intramolecular Valence and Spin Interaction in meso and rac Diastereomers of a p-Quinonoid-Bridged Diruthenium Complex

TL;DR: The neutral compounds contain a severely twisted L(2-) bridging ligand with 43-48 degree dihedral angles between the planes of the hydroquinone dianion and those of the ortho positioned pyrazolyl substituents and are characterized structurally, magnetically, electrochemically, and spectroscopically as well as spectroelectrochemically in the accessible redox states.