Partha Hazra

ORCID: 0000-0003-0422-1399
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Research Areas
  • Photochemistry and Electron Transfer Studies
  • Spectroscopy and Quantum Chemical Studies
  • Surfactants and Colloidal Systems
  • DNA and Nucleic Acid Chemistry
  • Advanced biosensing and bioanalysis techniques
  • Luminescence and Fluorescent Materials
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Porphyrin and Phthalocyanine Chemistry
  • Supramolecular Chemistry and Complexes
  • Protein Interaction Studies and Fluorescence Analysis
  • Photoreceptor and optogenetics research
  • Molecular Sensors and Ion Detection
  • Free Radicals and Antioxidants
  • Cancer therapeutics and mechanisms
  • Organic Light-Emitting Diodes Research
  • Analytical Chemistry and Chromatography
  • Ionic liquids properties and applications
  • RNA Interference and Gene Delivery
  • Lipid Membrane Structure and Behavior
  • Supramolecular Self-Assembly in Materials
  • Molecular spectroscopy and chirality
  • biodegradable polymer synthesis and properties
  • Advanced Nanomaterials in Catalysis
  • Nanoplatforms for cancer theranostics

Indian Institute of Science Education and Research Berhampur
2013-2025

Indian Institute of Science Education and Research Mohali
2013-2025

Indian Institute of Science Education and Research Kolkata
2013-2025

Indian Institute of Science Education and Research, Bhopal
2013-2025

Indian Institute of Science Education and Research, Tirupati
2013-2025

Indian Institute of Science Education and Research Pune
2014-2024

Indian Institute of Space Science and Technology
2021

Savitribai Phule Pune University
2015-2018

Jadavpur University
2016

Indian Institute of Science Bangalore
2012-2015

The ordered modular structure of a covalent organic framework (COF) facilitates the selective incorporation electronically active segments that can be tuned to function cooperatively. This designability inspires developing COF-based single-source white light emitters, required in next-generation solid-state lighting. Here, we present new anthracene-resorcinol-based COF exhibiting emission. keto-enol tautomers give rise dual emission, which by O-donor and N-donor solvents. Importantly, when...

10.1021/jacs.8b08312 article EN Journal of the American Chemical Society 2018-09-26

Establishing the structure–property relationship for multi-stimuli responsive mechanochromic materials based on charge transfer luminogens.

10.1039/c8sc00143j article EN cc-by Chemical Science 2018-01-01

The relative retardation of intramolecular charge transfer (ICT) and the solvation dynamics coumarin 152 in pure AOT, water, methanol, acetonitrile, formamide reverse micelles have been investigated using picosecond time-resolved emission spectroscopy. rate ICT has retarded almost 7 times at w0 = 4 32 compared to that water. is also observed methanol acetonitrile comparison acetonitrile. In time 12.22 ns, but water 7.27 ns. slow observed. much smaller several thousand fold decrease pool...

10.1021/la025881x article EN Langmuir 2002-09-06

Abstract This article reports the p K a shift of an anti‐cancer drug, 20( S )‐camptothecin (CPT), upon encapsulation into nanocavity cucurbit[7]uril (CB7) macrocycle. Steady‐state, time‐resolved fluorescence and electrospray ionisation mass spectrometry (ESI‐MS) studies provide evidence for formation both 1:1 2:1 (CB7 ⋅ CPT) stoichiometries. Astonishingly, we have found that protonation CPT takes place at higher concentration macrocycle (≥50 μ M ) when stoichiometric complex develops....

10.1002/cphc.201200879 article EN ChemPhysChem 2013-02-07

Abstract Mechanistic details of DNA compaction is essential blue print for gene regulation in living organisms. Many vitro studies have been implemented using several agents. However, these compacting agents may some kinds cytotoxic effects to the cells. To minimize this aspect, research works had performed, but people never focused green solvent, i.e. room temperature ionic liquid as agent. best our knowledge, first ever report where we shown that guanidinium...

10.1038/srep09137 article EN cc-by Scientific Reports 2015-03-16

This research article explores the distinct TADF efficiency of three donor-acceptor based regio-isomers: DPAOCN (ortho-isomer), DPAMCN (meta-isomer), and DPAPCN (para-isomer). exhibits maximum in both solution solid-state with an impressive reverse inter-system crossing (RISC) rate ∼106 s-1; underlying cause being minimum singlet-triplet splitting energy or ΔEST SOC (spin-orbit coupling) between S1 & T1 states. Apart from TADF, differences crystal packing regio-isomers result intriguing bulk...

10.1039/d3sc04280d article EN cc-by-nc Chemical Science 2023-01-01

This work reports that ligand engineering can modulate the triplet harvesting mechanism in iodide-bridged rhombic Cu2I2 complexes. Complex-1, with a smaller Cu-Cu distance, exhibits phosphorescence from 3(M+X)LCT and 3CC states 66% quantum yield, whereas an increased distance complex-2 results switch of emission to TADF, which occurs via 1/3(M+X)LCT 83% yield. The TADF property has been utilized for fabrication pc-LED emitting efficient warm white light. Moreover, high charge-transfer nature...

10.1021/acs.jpclett.4c01122 article EN The Journal of Physical Chemistry Letters 2024-05-31

Organic-inorganic hybrid metal halides have become enormously important in optoelectronics, sensing, photosensitization, etc. In this study, we report a structural transition from staircase configuration to cubane Cu(I) iodide-based polymers influenced by the coordination behavior of two different π*-acceptor ligands. The polymer structure, coordinated with 3-cyanopyridine, demonstrates efficient thermally activated delayed fluorescence (metal+halide)-to-ligand charge transfer [1/3(M+X)LCT]...

10.1021/acs.jpclett.4c03267 article EN The Journal of Physical Chemistry Letters 2025-02-04

In this work, "isobutrin", an ecofriendly sensitizer that is extracted from Butea monosperma (commonly known as "Flame of the Forest") flowers, introduced. It a bright yellow pigment belonging to chalcone class and examined for optoelectronic applications. observed chelation dye with Ti ions results into strong dye-TiO2 charge transfer (DTCT) band in visible region. This Ti-Isobutrin chelate stable, irreversible its formation studied using Benesi–Hildebrand plot. The locations HOMO–LUMO...

10.1021/am200341y article EN ACS Applied Materials & Interfaces 2011-05-24

Abstract Flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) are derivatives of riboflavin (RF), a water‐soluble vitamin, more commonly known as vitamin B 2 . Flavins have attracted special attention in the last few years because recent discovery large number flavoproteins. In this work, these flavins used extrinsic fluorescence markers for probing microheterogeneous environment well‐known transport protein, human serum albumin (HSA). Steady‐state time‐resolved experiments...

10.1002/cphc.201200044 article EN ChemPhysChem 2012-04-24

In this study, the urea dynamics inside AOT reverse micelle (RM) has been monitored without intervention of water using time-resolved fluorescence techniques from picosecond to nanosecond time regime. It observed that is severely retarded compared RM due formation highly networked cluster RM. Time-resolved anisotropy study also confirms existence a confined environment around dye at higher concentrations micelle. The urea-water mixtures with increasing concentration get insight about effect...

10.1021/jp206069z article EN The Journal of Physical Chemistry A 2011-08-30

Host–guest interactions between cucurbit[7]uril (CB7) and a cardiotonic drug, milrinone, have been explored using steady state pico-second time-resolved techniques. A novel fluorescence switch from ultraviolet (UV) to visible (cyan) is observed as consequence of upward pKa shift the drug inside nano-cavity cucurbit[7]uril.

10.1039/c3cp54895c article EN Physical Chemistry Chemical Physics 2014-01-01

Graphene oxide based molecular switching of ellipticine (E) has been utilized to probe its efficient loading onto graphene (GO) and subsequent release intra-cellular biomolecules like DNA/RNA. The green fluorescence E switches blue in GO back with polynucleotides. intensified emission the ellipticine-GO (E-GO) complex human serum albumin (HSA), a bluish upon addition dsDNA. Electron microscopy reveals formation distinctive 3D assemblies involving biomolecule(s) probably through non-covalent...

10.1039/c3nr06081k article EN Nanoscale 2013-12-12

Herein, we have reported a new strategy for the synthesis of highly stable fluorescent copper nanoclusters (CuNCs) with l-cysteine (Cys) as protecting ligand within water nanopool reverse micelles (RMs). In present work, efforts are also given to address origin excitation-dependent fluorescence spectral shift CuNCs. From our experiments, elucidated that broad from CuNCs in RMs consists two spectrally overlapped bands corresponding metal-core and surface states The intrinsic emission...

10.1021/acs.jpcc.7b11457 article EN The Journal of Physical Chemistry C 2018-02-21

The G-quadruplex (GQ-DNA), an alternative structure motif of DNA, has emerged as a novel and exciting target for anticancer drug discovery. GQ-DNA formed in the presence monovalent cations (Na(+)/K(+)) by human telomeric DNA is point interest due to their direct relevance cellular aging abnormal cell growths. Small molecules that selectively stabilize structures are considered be potential therapeutic agents. Herein, we probe proflavine (a well-known intercalator, hence acting...

10.1021/jp506267b article EN The Journal of Physical Chemistry B 2014-09-02

The solvation dynamics of methanol and acetonitrile in n-heptane /AOT/ n-heptane/ AOT/acetonitrile reverse micelles have been investigated by picosecond time resolved emission spectroscopy using Coumarin 490 (C-490) as a probe. We observed substantially slower (order few ns) compared to pure solvents. is dependent on the w value (w = [polar solvent]/[AOT]) case but there little dependence micelles. different explained basis presence absence hydrogen bonding network.

10.1039/b109447e article EN Physical Chemistry Chemical Physics 2002-03-04
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