Department of Physics
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Item Solvent effects on the absorption and fluorescence spectra of quinine sulphate: Estimation of ground and excited-state dipole moments(AIP, 2012-06) Pant, Debi D.Ground and excited state dipole moments of probe quinine sulphate (QS) was obtained using Solvatochromic shift method. Higher dipole moment is observed for excited state as compared to the ground state which is attributed to the higher polarity of excited state.Item Interaction of quinine sulfate with anionic micelles of sodium dodecylsulfate: A time-resolved fluorescence spectroscopy at different pH(Elsevier, 2015-09) Pant, Debi D.Photophysical behavior and rotational relaxation dynamics of quinine sulfate (QS) in anionic surfactant, sodium dodecylsulfate (SDS) at different pH have been studied using steady state and time resolved fluorescence spectroscopy. It has been observed that the cationic form of quinine sulfate (at pH 2) forms a fluorescent ion pair complex with the surfactant molecules at lower concentrations of surfactant. However, for higher concentrations of SDS, the probe molecules bind strongly with the micelles and reside at the water–micelle interface. At pH 7, QS is singly protonated in bulk aqueous solution. At lower concentrations of SDS aggregation between probe and surfactant molecules has been observed. However, for higher concentrations of SDS, an additional fluorescence peak corresponding to dicationic form of QS appears and this has been attributed to double protonation of the QS molecule in micellar solution. At pH 7, in the presence of SDS micelles, the photophysical properties of QS showed substantial changes compared to that in the bulk water solution. At pH 12, an increase in fluorescence intensity and lifetime has been observed and this has been attributed to the increase in radiative rate due to the incorporation of QS at the micelle–water interface. The local pH at micellar surface has been found different from the pH of bulk solution.Item Solvent effect on absorption and fluorescence spectra of cinchonine and cinchonidine dications: Estimation of ground and excited state dipole moments by experimental and numerical studies(Elsevier, 2015-06) Pant, Debi D.Absorption and fluorescence spectra of dications of cinchonine (C2 +) and cinchonidine (Cd2 +) have been measured at room temperature in solvents of different polarities. Ground and excited state electric dipole moments are determined experimentally using solvatochromic shift method based on bulk solvent properties. Theoretical calculations are done using B3LYP/6-31G(D) and CIS/6-31G(D) levels of theory for ground and excited states, respectively. Both experimental and theoretical studies reveal that excited state dipole moment (μe) values are higher than corresponding ground state dipole moment (μg) value of C2 + and Cd2 +, which is attributed to the higher polarity of excited states compared to the ground state polarity of these molecules.Item Estimation of ground and excited state dipole moments of quinidine and quinidine dication: Experimental and numerical methods(Elsevier, 2013-03) Pant, Debi D.Absorption and fluorescence spectra of quinidine (QD) and quinidine dication (QD2 +) have been measured at room temperature in solvents of different polarities. Ground and excited state electric dipole moments are determined experimentally using solvatochromic shift method based on bulk solvent properties. Numerical calculations are also performed using B3LYP/6-31G(D) level of theory for ground state and CIS/6-31G(D) level of theory for first excited singlet state. From both experimental and numerical studies it has been observed that dipole moment values of excited states (μe) are higher than corresponding ground state value (μg), of QD and QD2 +, which is attributed to the higher polarity of excited states of QD and QD2 + molecules.Item Photophysics of protonated 6-methoxyquinoline: steady state and time-dependent fluorescence(Elsevier, 1990-11) Pant, Debi D.Nanosecond time-resolved emission spectroscopy was used to investigate the excited state solute—solvent interaction in 6-methoxyquinoline. A red shift in the emission maximum is observed on excitation at the red edge of the absorpton band which depends on the temperature and viscosity of the medium. The fluorescence lifetime is dependent on the emission and excitation wavelengths. A significant change in the energy of emission is observed on the nanosecond time scale. The room temperature data can be explained using the Bakhshiev formulation of solvent relaxation. However, transient and steady state fluorescence studies from 80 to 290 K reveal that, at 160 K, a rapid relaxation process occurs (not solvent relaxation). The photophysics of 6-methoxyquinoline are similar to those of the quinine dication which exhibits two relaxation processes (from 80 to 290 K) — a charge-transfer process around 160 K and a solvent relaxation process at ambient temperature.Item Photophysics of doubly-charged quinine: Steady state and time-dependent fluorescence(Elsevier, 1990-04) Pant, Debi D.The quinine dication in aqueous solution (1 N H2SO4) gives two fluorescence lifetimes (τ1 = 2.80 ns and τ2 = 19.36 ns) at ambient temperature. τ2 shows a small increase with an increase in acid concentration between 0.1 N and 15 N. Quenching by Cl− shows that τ1 and τ2 are differentially quenched. The Stern—Volmer quenching constant KSV for τ1 is 10 M−1 and for τ2 is 75 M−1. In addition, KSV is dependent on emission wavelength. In acidified solution, τ2 increases with an increase in emission wavelength, whereas τ1 exhibits a behaviour which resembles a two-state mechanism with a negative amplitude in the region of longer emission wavelength. However, the two-state theory does not give an entirely satisfactory mechanism for the time-dependent emission. Time-resolved emission spectroscopy (TRES) shows a spectral relaxation which partially explains the dependence of τ2 on emission wavelength in accordance with Bakhshiev formulation. Transient and steady state fluorescence studies from 80 to 290 K show that at 160 K there is a rapid relaxation process resulting in an increase in τ2 and a sudden spectral shift. We propose that the complex behaviour of quinine decay consists of two major relaxation processes: a charge-transfer process which occurs around 160 K and a solvent reorientation process which occurs in the fluid medium.Item Structure and Intermolecular Dynamics of Liquids: Femtosecond Optical Kerr Effect Measurements in Nonpolar Fluorinated Benzenes(Elsevier, 1998-07) Pant, Debi D.Polar solvation dynamics of a 95:5% (v/v) water/acetone mixture have been measured at the ZrO2 nanoparticle surface by time-resolved fluorescence of a probe molecule adsorbed to the particle surface. The interfacial solvent response displays two sub-picosecond diffusive components with the same time constants as bulk solution. However, the relative amplitudes for the individual relaxation components are significantly different, leading to a faster average solvation response for molecules at the ZrO2 surface. Furthermore, the overall fluorescence Stokes shift is approximately three times smaller for dye molecules adsorbed to the nanoparticle surface. Implications for electron injection into semiconductor nanoparticles are discussed.Item Estimation of ground and excited state dipole moments of synthesized coumarin derivative [N-(2-oxo-2H-chromen-4-yl)imino]triphenyl-phosphorane(Elsevier, 2014-12) Pant, Debi D.Electronic absorption and fluorescence spectra of coumarin derivative [N-(2-oxo-2H-chromen-4-yl)imino] triphenyl phosphorane have been recorded at room temperature in wide range of solvents of different polarities. The absorption maximum remains almost unchanged with the increase in solvent polarity, whereas, a red shift in fluorescence emission maximum was observed. Synthesized compound [N-(2-oxo-2H-chromen-4-yl)imino] triphenyl phosphorane was characterized by 1H and 13C NMR, and FT-IR spectral studies. The ground and excited state dipole moments of molecule were obtained from Bakhshiev's and Bilot–Kawski's equations by means of the solvatochromic shift method. Very high value of dipole moment is observed for excited state as compared to ground state value and this is attributed to more polar excited state of the molecule. Numerical calculations are performed using B3LYP/6-31G+(d) and B3LYP/6-31G(d) level of theory for ground state in Gaussian 03. Studies in different solvents are also done using the CPCM method and UA0 radii with the same level of theory. A critical analysis between the values of dipole moment in gas phase and various solvents is also carried out for ground state.Item Solvatochromic shift and estimation of dipole moment of quinine sulfate(Elsevier, 2012-02) Pant, Debi D.The absorption and fluorescence spectra of quinine sulfate (QS) have been recorded at room temperature in wide range of solvents of different polarities. The ground-state dipole moment of QS was obtained from quantum mechanical calculations and the excited state dipole moment of QS was estimated from Bakhshiev's and Bilot–Kawski's equations by means of solvatochromic shift method. Higher value of dipole moment has been observed for excited state as compared to the corresponding ground state value and this is attributed to the more polar excited state of QS.Item Fluorescence Quenching of a Benzimidazolium–based Probe for Selective Detection of Picric Acid in Aqueous Medium(Wiley, 2016-06) Pant, Debi D.; Sakhuja, RajeevA novel fluorescent coumaryl linked benzimidazolium salt has found to be highly selective for nanomolar detection of explosive picric acid, over other aromatic explosives in aqueous medium. The quenching constant and detection limit of the sensor was found to be KSV=1.58 × 104 M−1 and 208 nM respectively for picric acid. UV-Visible studies, time resolved fluorescence results and Density Functional Theory (DFT) calculations inferred the ground-state charge-transfer complex formation as the predominant quenching mechanism for picric acid detection.