Browsing Faculty of Science by Author "Luhanga, P.V.C."
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Nijegorodov, N.; Luhanga, P.V.C.; King, J.G. (Regional Energy Resources Information Center (RERIC) Asian Institute of Technology. http://www.rericjournal.ait.ac.th/index.php/reric/index, December NaN, 2005)[more][less]
Abstract: Please refer to the attached article for the ABSTRACT. Due to technical problems with some scientific formulae it was not possible to upload the abstract HERE. URI: http://hdl.handle.net/10311/408 Files in this item: 1
Nijegorodov_IEJ_2005.pdf (2.539Mb) -
Nijegorodov, N.; Zvolinski, V.; Luhanga, P.V.C.; Mabbs, R.; Ahmad, J. (Elsevier Ltd. www.elsevier.com/locate/saa, NaN, 2006)[more][less]
Abstract: The multi-banded fluorescence and laser properties of 11 new amino- and tosylamino derivatives of 2,5-di(phenyl)-1,3,4-oxadiazole and oxadiazole in various solvents at 293 K are reported. All the compounds investigated possess intra-molecular hydrogen quasi-bond (IHB) of 4.6-5.2 kcal mol-1 in the ground state. In the excited state they can undergo protolytic dissociation or intra-molecular photon-initiated transfer of proton and reveal anomalous fluorescence which cannot be explained within the framework of the Kasha and Kasha-Vavilov rules. Depending upon the excitation wavelength, solvent, concentration and pH of the medium, the compounds studied show a single, double, triple or even a four-banded fluorescence, which has not been reported earlier. The nature of multi-banded fluorescence is explained in terms of the possible photochromic processes in excited states. Quantum yields and decay times of the different fluorescence bands are reported. Anomalous dependence of quantum yield upon concentration of the solution is observed. Laser properties of the compounds studied are carefully tested. Laser action based on the fluorescence of the so-called bi-radical molecules is reported. Various possible arrangements of singlet and triplet levels of compounds investigated are discussed. URI: http://hdl.handle.net/10311/176 Files in this item: 2
license.txt (1.998Kb) -
Nijegorodov, N.; Zvolinsky, V.; Luhanga, P.V.C. (Elsevier Science Ltd. www.elsevier.com/locate/jphotochem, NaN, 2008)[more][less]
Abstract: Intramolecular processes and fluorescence properties of 32 specially chosen aromatic molecules, different in degrees of planarity and rigidity, but family related in -structure are experimentally and theoretically (using the PPP-method) studied at room temperature (293 K). The quantum yields of fluorescence , and decay times τf, of deaerated and non-deaerated cyclohexane solutions are measured. The oscillator strength fe, the fluorescence rate constants kf, the natural lifetimes τT o , and the intersystem crossing rate constants kST, are calculated. The investigations showed the following differences in the behaviour of the fluorescence parameters in transition from the non-planar molecule to the planar and more rigid-type: the value of the symmetry line wave-number υ00 (the frequency of the S0→S1 * transition) and the Stokes shift υST, decrease. The oscillator strength and fluorescence constant, normally decrease. The change in the quantum yield of the fluorescence depends upon the changes in the kf and kST values. Furthermore, the intersystem crossing rate constant generally decreases, sometimes very significantly. However, there are some interesting exceptions. For example, the kST value of the non-planar molecule of 9,10-diphenylanthracene is less than the kST value of the planar and very rigid molecule of anthracene. This important phenomenon is explained. The differences of the intramolecular processes of planar and non-planar molecules are discussed. The photochemical stability of planar and non-planar molecules is studied. The effect of planarity, rigidity and molecular symmetry upon laser properties is also traced. URI: http://hdl.handle.net/10311/367 Files in this item: 1
Nijegorodov_JPPaC196_2008.pdf (1.901Mb)
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