Özdemir, Tuğba2016-01-082016-01-082010http://hdl.handle.net/11693/15096Ankara : The Graduate Program of Materials Science and Nanotechnology and the Institute of Engineering and Sciences of Bilkent University, 2010.Thesis (Master's) -- Bilkent University, 2010.Includes bibliographical references leaves 74-77.Dyes having solid state fluorescence are playing an important role for organic light emitting devices (OLED), optoelectronic devices and photoelectric conversion. However, emissive solids are not common because of the quenching resulting from the packing. With these considerations, we have synthesized and characterized novel boradiazaindacene BODIPY-based dye with bulky substituents (3,5-di-tert-butylphenyl) to prevent π-π stacking of the chromophore. We have succesfully demonstrated that by simple modulation of BODIPY core with very bulky groups lead us to have a bright emissive compounds in solid state. In the second part of this research, we developed BODIPY based near-IR dye as a selective, ratiometric and water-soluble fluorophore for Zn (II) cation. We functionalized the versatile BODIPY from its 3 and 5 positions for long wavelength emission the zinc selective chemosensor.xv, 116 leaves, illustrationsEnglishinfo:eu-repo/semantics/openAccessSolid state fluorescenceChemosensorBoradiazaindaceneNear-IR dyesπ-π stackingStokes’ shiftQP519.9.F56 O93 2010Fluorescent probes.Fluorescence spectroscopy.Fluorescent Dyes.Nanostructured materials.Light emitting diodes.Solid state emissive bodipy dyes with bulky substituents as spacers and a sensitive and selective ratiometric near IR fluorescent probe for zinc ions based on the distyryl-bodipy fluorophoreThesisB122588