Chandan Kumar Tiwari

ORCID: 0000-0001-5470-4191
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About
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Research Areas
  • Metal-Organic Frameworks: Synthesis and Applications
  • Metal-Catalyzed Oxygenation Mechanisms
  • Crystallization and Solubility Studies
  • Nanocluster Synthesis and Applications
  • Electrocatalysts for Energy Conversion
  • X-ray Diffraction in Crystallography
  • Quantum Dots Synthesis And Properties
  • Chromium effects and bioremediation
  • Supramolecular Chemistry and Complexes
  • Copper-based nanomaterials and applications
  • Advanced Photocatalysis Techniques
  • Fuel Cells and Related Materials
  • Covalent Organic Framework Applications
  • Supramolecular Self-Assembly in Materials
  • Heavy Metal Exposure and Toxicity
  • Environmental remediation with nanomaterials
  • Advanced oxidation water treatment
  • Metal complexes synthesis and properties
  • Polyoxometalates: Synthesis and Applications
  • Nitric Oxide and Endothelin Effects
  • Vanadium and Halogenation Chemistry
  • Electrochemical Analysis and Applications
  • Advanced Nanomaterials in Catalysis
  • Organometallic Complex Synthesis and Catalysis
  • CO2 Reduction Techniques and Catalysts

University of Rochester
2023-2024

Carestream (United States)
2023-2024

Robert Bosch (Germany)
2023

Ben-Gurion University of the Negev
2019-2022

Indian Association for the Cultivation of Science
2019

Recent investigations reveal that by providing active sites for O–O bond formation, Fe(III) oxyhydroxides (FeOOH) dramatically enhance the oxygen evolution activities of iron-containing abundant-earth CoOxHy and NiOxHy electrocatalysts. In contrast to α-Fe2O3 (hematite), however, little detailed information is available concerning fundamental reactivities themselves. We here report a macroanion-like polyoxometalate cluster-anion complex 2.6 nm γ-FeOOH nanocrystals, 1, not only catalyzes...

10.1021/acscatal.1c02824 article EN ACS Catalysis 2021-08-30

Dissolution of the polyoxometalate (POM) cluster anion H5[PV2Mo10O40] (1; a mixture positional isomers) in 50% aq H2SO4 dramatically enhances its ability to oxidize methylarenes, while fully retaining high selectivities typical this versatile oxidant. To better understand impressive reactivity, we now provide new information regarding nature 1 (115 mM) (9.4 M) H2SO4. Data from 51V NMR spectroscopy and cyclic voltammetry reveal that as volume water is incrementally increased 50%, V(V) ions...

10.1021/acs.inorgchem.9b03747 article EN cc-by Inorganic Chemistry 2020-03-05

Both natural enzymatic systems and synthetic porous material catalysts utilize well-defined uniform channels to dictate reaction selectivities on the basis of size or shape. Mimicry this design element in homogeneous is generally difficult owing flexibility inherent most small molecular species. Herein, we report synthesis a tripodal ligand scaffold that orients narrow rigid cavity atop accessible metal coordination space. The permanent void formed through macrocyclization whereby...

10.1021/acs.inorgchem.3c01335 article EN cc-by Inorganic Chemistry 2023-07-18

The formation of small 1 to 3 nm organic-ligand free metal-oxide nanocrystals (NCs) is essential utilization their attractive size-dependent properties in electronic devices and catalysis. We now report that hexaniobate cluster-anions, [Nb6 O19 ]8- , can arrest the growth NCs stabilize them as water-soluble complexes. This exemplified by hexaniobate-complexed 2.4-nm monoclinic-phase CuO (1), whose ca. 350 Cu-atom cores feature quantum-confinement effects impart an unprecedented ability...

10.1002/anie.202213762 article EN cc-by Angewandte Chemie International Edition 2022-12-29

The selective uptake of guests by capsules, cages, and containers, porous solid-state materials such as zeolites metal–organic frameworks (MOFs), is generally controlled pore size the dimensions chemical properties interior host domains. For soluble structures, however, few options are available for modifying their outer pores to impart chemoselectivity similarly sized guests. We now show that using alkane-coated gold cores structural building units (SBUs) hydrophobic self-assembly...

10.1021/jacs.9b07284 article EN Journal of the American Chemical Society 2019-08-14

Porous organic cages (POCs) and metal-organic polyhedra (MOPs) function as zero-dimensional porous materials, able to mimic many functions of insoluble framework materials while offering processability advantages. A popular approach access tailored metal-based motifs in extended network is postsynthetic metalation, which allows metal installation be decoupled from assembly. Surprisingly, this has only sparingly been reported for molecular materials. In report, we demonstrate metalation...

10.1021/acs.organomet.4c00247 article EN cc-by Organometallics 2024-09-12

Abstract The formation of small 1 to 3 nm organic‐ligand free metal‐oxide nanocrystals (NCs) is essential utilization their attractive size‐dependent properties in electronic devices and catalysis. We now report that hexaniobate cluster‐anions, [Nb 6 O 19 ] 8− , can arrest the growth NCs stabilize them as water‐soluble complexes. This exemplified by hexaniobate‐complexed 2.4‐nm monoclinic‐phase CuO ( ), whose ca. 350 Cu‐atom cores feature quantum‐confinement effects impart an unprecedented...

10.1002/ange.202213762 article EN cc-by Angewandte Chemie 2022-12-29

…(PCH1) containing four contiguous heptagons was synthesized by Juan Casado, Junzhi Liu et al. in their Communication (e202217124).Thefour form aZshape the central p-electron skeleton, giving PCH1 a butterfly-shaped conformation.Nonlinear Optics In Research Article (e202216523), Qingyun Wan, Chi-Ming Che report controlled self-assembly of gold(I) complexes with nonlinear optical and waveguide properties through multiple kinetic aggregation states.Metal-Organic Frameworks Ac hiral...

10.1002/ange.202381011 article EN Angewandte Chemie 2023-02-20

Water oxidation is a multielectron complex reaction that produces molecular oxygen as the final product. The article addresses lack of confirmation product formation in electrochemical evolution (OER) studies, despite extensive research conducted on catalysts for water splitting. It critically evaluates trend observed many studies solely rely methods OER quantification without confirming via complementary analytical techniques. omission measuring evolved gas leaves crucial gap process and...

10.3390/catal14010013 article EN Catalysts 2023-12-22
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