Arindam Modak

ORCID: 0000-0001-6044-6942
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About
Contact & Profiles
Research Areas
  • Covalent Organic Framework Applications
  • Metal-Organic Frameworks: Synthesis and Applications
  • Catalysis for Biomass Conversion
  • Mesoporous Materials and Catalysis
  • Carbon dioxide utilization in catalysis
  • Electrocatalysts for Energy Conversion
  • Chemical Synthesis and Reactions
  • Advanced battery technologies research
  • Catalysis and Hydrodesulfurization Studies
  • Nanomaterials for catalytic reactions
  • Carbon Dioxide Capture Technologies
  • Catalytic Cross-Coupling Reactions
  • Zeolite Catalysis and Synthesis
  • Catalytic Processes in Materials Science
  • Supercapacitor Materials and Fabrication
  • Polyoxometalates: Synthesis and Applications
  • Advanced Photocatalysis Techniques
  • Fuel Cells and Related Materials
  • Catalysis and Oxidation Reactions
  • CO2 Reduction Techniques and Catalysts
  • Membrane Separation and Gas Transport
  • Asymmetric Hydrogenation and Catalysis
  • Biofuel production and bioconversion
  • Sulfur-Based Synthesis Techniques
  • Recycling and Waste Management Techniques

Amity University
2023-2025

Indian Institute of Technology Delhi
2021-2024

Indian Association for the Cultivation of Science
2014-2023

Ariel University
2019-2023

S.N. Bose National Centre for Basic Sciences
2017-2021

Tianjin University
2016-2017

Dalian Institute of Chemical Physics
2016-2017

Chinese Academy of Sciences
2016-2017

Toyota Central Research and Development Laboratories (Japan)
2015-2016

Japan Science and Technology Agency
2014

Iron containing porous organic polymers (Fe-POPs) have been synthesized by a facile one-pot bottom-up approach to porphyrin chemistry an extended aromatic substitution reaction between pyrrole and dialdehydes in the presence of small amount Fe(III). The Fe-POPs possess very high BET surface area, large micropores showed excellent CO(2) capture (~19 wt%) at 273 K/1 bar.

10.1039/c1cc14275e article EN Chemical Communications 2011-11-17

Catalytic reduction of CO<sub>2</sub>is very challenging from both economics and green chemistry perspectives. This critical review highlights major advancements made in the CO<sub>2</sub>reduction processes their future challenges.

10.1039/d0gc01092h article EN Green Chemistry 2020-01-01

Abstract To overcome the challenges of global warming and environmental pollution it is mandatory to reduce concentration atmospheric carbon dioxide (CO 2 ), which largely accumulated in air through combustion fossil fuels. Thus, sequestration CO physisorption on solid adsorbents their successful conversion into value added fine chemicals are major priority areas research today. Innovation efficient ‐philic together with high mechanical/chemical stability regeneration efficiency most...

10.1002/cctc.201801046 article EN ChemCatChem 2018-08-11

10.1016/j.micromeso.2018.09.018 article EN Microporous and Mesoporous Materials 2018-09-20

Exploring a covalent organic framework (COF) material as an efficient metal-free photocatalyst and adsorbent for the removal of pollutants from contaminated water is very challenging in context sustainable chemistry. Herein, we report new porous crystalline COF, C6-TRZ-TPA via segregation donor-acceptor moieties through extended Schiff base condensation between tris(4-formylphenyl)amine 4,4',4″-(1,3,5-triazine-2,4,6-triyl)trianiline. This COF displayed Brunauer-Emmett-Teller (BET) surface...

10.1021/acs.langmuir.2c03379 article EN Langmuir 2023-03-11

A new functionalized mesoporous polymer (MPTAT-1) has been synthesized via organic–organic radical polymerization of 2,4,6-triallyloxy-1,3,5-triazine (TAT) in aqueous medium the presence an anionic surfactant (sodium dodecyl sulfate) as template. Powder XRD and TEM image analysis suggests ordered 2D-hexagonal arrangement pores material. N2 sorption reveals a moderately good surface area 135 m2 g−1 for this polymer. The template free MPTAT-1 acts excellent support immobilizing Pd(II) at its...

10.1039/c1gc15045f article EN Green Chemistry 2011-01-01

One-pot bottom-up synthesis involving extended aromatic electrophilic substitution on to a pyrrole has been employed for the design of novel triazine-functionalized porphyrin-based porous organic polymer, TPOP-1. Hydrothermal treatment 4,4′,4′′-(1,3,5-triazine-2,4,6-triyl)tris(oxy)tribenzaldehyde and in glacial acetic acid presence FeCl3 leads formation TPOP-1, which is highly robust material, exhibits high surface area bimodal pore sizes ranging from large micropores mesopores. The...

10.1039/c4ta02150a article EN Journal of Materials Chemistry A 2014-05-12

The high surface area of 2D-hexagonal periodic mesoporous organosilica (PMO) containing a phloroglucinol-diimine moiety inside the pore wall has been utilized for grafting Pd(II) at mesopores. This Pd-containing PMO material (Pd-LHMS-3) shows excellent catalytic activity in fluoride-free Hiyama cross-coupling reactions water alkaline pH conditions. Sonogashira cross-couplings between terminal alkynes and aryl halides take place presence hexamine as base absence any Cu co-catalyst. Cyanation...

10.1039/c2gc35820d article EN Green Chemistry 2012-01-01

Surface functionalization of SBA-15 followed by its reaction with Cu(OAc)2 has been carried out to develop a new Cu-grafted functionalized mesoporous material, which catalyzes one-pot three component coupling different aryl halides thiourea and benzyl bromide in aqueous medium produce thioethers very good yields (80–88%).

10.1039/c2cc32676k article EN Chemical Communications 2012-01-01

Bifunctional porous nanomaterials are very demanding in the context of heterogeneous catalysis. A highly ordered 2D-hexagonal bifunctionalized mesoporous SBA-15 type material MPBOS (mesoporous organosilica) has been synthesized via a post synthetic route. The surface functionalized with (3-chloropropyl)triethoxysilane to obtain MPCOS chloro-substituted material, which undergoes an SN2 substitution reaction grafted chloro group amine organic ligand 5-aminoisophthalic acid, presence potassium...

10.1021/acssuschemeng.6b03100 article EN ACS Sustainable Chemistry & Engineering 2017-01-22

The electrochemical urea oxidation reaction (UOR) is considered as a promising renewable source for harvesting energy from waste. We report new synthetic design approach to produce an iron–nickel alloy nanocatalyst metal–organic polymer (MOP) by single-step carbonization process at 500 °C, thus forming core–shell of iron–nickel-coated carbon (C@FeNi) nanostructures wired embedded nanotubes (CNTs) (CNT/C@FeNi). Powder X-ray diffraction confirmed the formation metallic FeNi3 nanoparticles (∼20...

10.1021/acsami.0c22148 article EN ACS Applied Materials & Interfaces 2021-02-10

Abstract Novel organic‐inorganic hybrid mesoporous materials containing diimine moieties inside the pore wall were used for grafting of an oxo‐vanadium Schiff base complex at mesopore surface. The prepared catalyst was found to be highly active and selective oxidation a variety primary, secondary α‐hydroxy carbonyl compounds corresponding aldehydes, ketones 1,2‐dicarbonyl using tert‐ butyl hydroperoxide as oxidant under mild reaction conditions. After completion reaction, could easily...

10.1002/adsc.201100018 article EN Advanced Synthesis & Catalysis 2011-08-01

Metal-free catalysis is particularly challenging in the context of green and sustainable chemistry. High toxicity associated with leaching metals from catalysts has notorious environmental impact. To surmount such an effect, homogeneous organocatalysis can provide a alternative protocol. However, it suffers drawbacks low activity selectivity, because neighboring effect solvent, devoid recyclability for operations. address issues, solid-supported heterogeneous organocatalysts are developed,...

10.1021/acssuschemeng.1c01537 article EN ACS Sustainable Chemistry & Engineering 2021-08-31

A comprehensive and critical in-depth discussion on the development prospect of several advanced materials for conversion CO<sub>2</sub>to value added chemicals is provided, together with their current status, technical feasibility future opportunities.

10.1039/d1ma00107h article EN cc-by-nc Materials Advances 2021-01-01
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