Barada Prasanna Dash

ORCID: 0000-0001-8855-0813
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Research Areas
  • Boron Compounds in Chemistry
  • Radiopharmaceutical Chemistry and Applications
  • Luminescence and Fluorescent Materials
  • Organoboron and organosilicon chemistry
  • Supramolecular Chemistry and Complexes
  • Boron and Carbon Nanomaterials Research
  • Dendrimers and Hyperbranched Polymers
  • Synthesis of heterocyclic compounds
  • Synthesis and Reactions of Organic Compounds
  • Synthesis and Characterization of Heterocyclic Compounds
  • Metal complexes synthesis and properties
  • Quinazolinone synthesis and applications
  • Synthesis and Biological Evaluation
  • Chemical Synthesis and Analysis
  • X-ray Diffraction in Crystallography
  • Synthesis and biological activity
  • Supercapacitor Materials and Fabrication
  • Porphyrin and Phthalocyanine Chemistry
  • Crystallization and Solubility Studies
  • Extraction and Separation Processes
  • RNA Interference and Gene Delivery
  • Synthesis of Tetrazole Derivatives
  • Metal Extraction and Bioleaching
  • Crystallography and molecular interactions
  • Electrocatalysts for Energy Conversion

National Institute of Technology Rourkela
2025

Siksha O Anusandhan University
2014-2024

National Bureau of Soil Survey and Land Use Planning
2021

University of Manchester
2018

Northern Illinois University
2008-2018

Utkal University
1975-2016

Ravenshaw University
2016

Southern Methodist University
2008-2010

Indian Institute of Technology Bombay
2005

A series of C(3)-symmetric pi-conjugated compounds containing three to six o-carborane clusters have been synthesized by employing palladium-catalyzed Suzuki coupling reactions and acetylation reactions, followed silicon tetrachloride mediated trimerization reactions. Carborane-containing extended trimers were found emit blue light. Incorporation into systems led 22-70% enhancement their relative fluorescence quantum yields. Decapitation made these water soluble, aqueous solutions also be...

10.1021/ja101845m article EN Journal of the American Chemical Society 2010-04-16

Robust three-dimensional structure, aromaticity, high chemical and thermal stability of polyhedral boron clusters make them promising candidates for use in materials science. Boron have been used the synthesis luminescent materials, polymers, coordination polymers or metal–organic frameworks, dendrimers, liquid crystals, nonlinear optical materials. Some these as molecular building blocks nanoscience. This review summarizes applications

10.1039/c1nj20228f article EN New Journal of Chemistry 2011-01-01

The ability of ortho-, meta- and para-carboranes to enhance the emission intensity has been compared. For this purpose a series carborane-appended 1,3,5-triphenylbenzene (TB) 1,3,5- tris(biphenyl-4-yl)benzene (TBB) containing three para-carborane clusters directly attached conjugated cores have synthesized employing Suzuki, Heck, trimerization reactions. incorporation icosahedral carboranes was associated with red shift in UV absorption spectrum up 13 nm as well enhancements intensities...

10.1021/ic200010q article EN Inorganic Chemistry 2011-05-25

Symmetrical star-shaped molecules with carborane clusters on the periphery have been synthesized in good yields via silicon tetrachloride mediated cyclotrimerization reactions of 9-benzyl derivatives carboranes acetyl group substitution benzene ring. Facile functionalization these symmetrical core structures 1-iodoheptane and trivinylchlorosilane produce compounds which could be used as liquid crystalline substances precursors for synthesis higher order carbosilane dendrons.

10.1021/ol8005248 article EN Organic Letters 2008-05-09

Phenylene-cored small dendrimers containing three to nine peripheral o-carborane clusters were synthesized via Cu(I)-catalyzed Huisgen-type azide alkyne cycloaddition reactions. The resulting have been characterized by IR and NMR spectroscopy MALDI-TOF mass spectral analysis. biological evaluation of branched dendrimer 16 carborane cages has carried out using human liver cancer cells (SK-Hep1). Dendrimer was accumulated in the SK-Hep1 a concentration-dependent manner. highest boron...

10.1021/om201255b article EN Organometallics 2012-01-20

The synthesis and thermal properties of phenylene triazine core based symmetrical macromolecules containing three to six cobaltabis(dicarbollide) clusters are reported. zwitterionic oxonium derivative cobaltabis(dicarbollide), [3,3′-Co(8-C4H8O2-1,2-C2B9H10)(1′,2′-C2B9H11)], has been used for the synthetic transformations, silicon tetrachloride triflic acid were as cyclotrimerization reagents. Compounds multiple found be extremely thermally stable, only a 10−30% mass loss occurred up 700 °C.

10.1021/om100365t article EN Organometallics 2010-07-12

The advancements in the synthetic chemistry of carboranes and metallacarboranes have given rise to diversified uses medicinal chemistry, resulting many new medical applications. An overview is presented emphasizing use nanoparticles, dendrimers, porphyrins carbohydrates as boron carriers. A review with 80 references.

10.1135/cccc2010050 article EN Collection of Czechoslovak Chemical Communications 2010-01-01

Large dendrimers, noted G(n)-3(n+2)cage, containing 3(n+2) o-carborane cluster cages MeC(2)B(10)H(10) at their peripheries (n = number of generation G(n)) have been synthesized by Huisgen-type azide alkyne Cu(I)-catalyzed dipolar "click" cycloaddition reactions (CuAAC) between an monomeric ethynyl group and arene-centered azido-terminated dendrimers G(n)-3(n+2)N(3) generations 0, 1, 2. Attempts to synthesize higher-generation this family yielded insoluble materials. The carborane G(0)-9cage,...

10.1021/ic101729s article EN Inorganic Chemistry 2010-10-15

A series of carborane-appended 5-thio-D-glucopyranose (5-TDGP) derivatives containing one to two 5-TDGP moieties were synthesized via click cycloaddition reaction as well following the traditional methods. Among carboranyl-5-TDGP derivatives, decapitated nido-carboranyl derivative 18 was found be highly water-soluble and therefore its preliminary biodistribution study conducted. comparative biological evaluation 18versus carboranyl-D-glucopyranose analog 19 with human hepatocellular...

10.1039/c2dt30874f article EN Dalton Transactions 2012-01-01

The facile synthesis of a thermally stable carborane appended symmetrical star-shaped molecule having six bulky o-carborane clusters on the periphery, thereby containing sixty boron atoms was accomplished via cobalt-catalyzed [2 + 2 2] cycloaddition reaction.

10.1039/b905076k article EN Chemical Communications 2009-01-01

Borylative fusion of BSe and BTz containing donor–acceptor oligomers gives fused boracycles with a reduction in the energy LUMO by up to 0.65 eV. This leads red shift emission <italic>ca.</italic> 200 nm use these materials for fabrication NIR OLEDs.

10.1039/c8tc05131c article EN Journal of Materials Chemistry C 2018-12-19

Diels–Alder reactions have been accomplished with ethylene as the dienophile through use of inverse-electron demand chemistry. As a key aspect chemistry, dienes are part tri- or dicationic superelectrophilic systems. Theoretical calculations reveal that highly charged superelectrophiles possess exceptionally low lying LUMOs, and this facilitates cycloaddition chemistry ethylene. The has used to prepare series tetrahydroquinoline products. This represents first application activation in...

10.1021/acs.orglett.8b00367 article EN Organic Letters 2018-03-26

Coke oven wastewater containing high concentrations of phenol and chemical oxygen demand (COD) was collected from a local steel plant Odisha. The treatment coke carried out by using Mobil Composition Matter No. 41 (MCM-41) nanoadsorbent. effect various adsorption parameters, such as temperature (°C), initial pH, agitation speed (rpm), MCM-41 dosage (g/L) on investigated two-level factorial experimental design. Enhancing had positive the performance, whereas with increasing negative removal...

10.1061/(asce)hz.2153-5515.0000384 article EN Journal of Hazardous Toxic and Radioactive Waste 2018-01-06

Boron-rich dendritic glycoconjugates of ortho -carborane clusters containing three to six peripheral hydrophilic glucose moieties have been found be promising anticancer agents.

10.1039/d3nj00182b article EN cc-by-nc New Journal of Chemistry 2023-01-01

Abstract o ‐Carborane was covalently linked to the side chain of a polystyrene polymer by “click” reaction provide acarborane‐appended polymer. The initial step involved radical polymerization p ‐chloromethylstyrene with AIBN followed replacement chloro units azido groups; final employed Cu I ‐catalyzedHuisgen‐type between azidomethyl‐appended and ethynyl‐terminated carborane unit yielding desired carborane‐appended polystyrene. Size exclusion chromatography (SEC) this showed polydispersity...

10.1002/ejic.201100360 article EN European Journal of Inorganic Chemistry 2011-06-09

This manuscript describes the development of a remarkably general palladium-catalyzed monoacylation carbazoles using toluene derivatives playing dual role acyl source and organic solvent. The method uses NHPI as cocatalyst oxygen sole oxidant. Interestingly, acylation monosubstituted N-pyridylcarbazoles takes place regioselectively at C-8 position. scope is explored aldehyde source. highly site-selective proceeds through radical process.

10.1021/acs.joc.0c01746 article EN The Journal of Organic Chemistry 2020-12-31

The role of carborane clusters in organometallic chemistry is diverse. A number cage systems such as C(2)B(4), C(2)B(9) and C(2)B(10) have been extensively used for the synthesis numerous metallacarboranes s, p, d f-block elements. An introduction to provided with an emphasis on recent advances

10.1039/c001994a article EN Dalton Transactions 2010-01-01

In the reactions of 2,3-pyrazinedicarboxylic anhydride with amines and anilines, pyrazine carboxamides are formed in good to excellent yields. A mechanism is proposed involving ring opening decarboxylation heterocyclic ring. Based on other similar decarboxylations, this suggests involvement an N-heterocyclic carbene intermediate leading product.

10.1021/ol402200x article EN Organic Letters 2013-09-09

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTCarboranylpyrroles: A Synthetic InvestigationRashmirekha Satapathy†, Barada Prasanna Dash†, Chong Zheng†, John A. Maguire‡, and Narayan S. Hosmane*†View Author Information† Department of Chemistry Biochemistry, Northern Illinois University, DeKalb, 60115-2862, United States‡ Chemistry, Southern Methodist Dallas, Texas 75275-0314, States *Email: [email protected]Cite this: J. Org. Chem. 2011, 76, 9, 3562–3565Publication Date (Web):March 16,...

10.1021/jo2000463 article EN The Journal of Organic Chemistry 2011-03-16
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