Browsing by Subject "Chemical binding"
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Item Open Access Design strategies for ratiometric chemosensors: modulation of excitation energy transfer at the energy donor site(2009) Guliyev, R.; Coskun, A.; Akkaya, E. U.Excitation energy transfer, when coupled to an ion-modulated ICT chromophore, creates novel opportunities in sensing. The direction of energy transfer and the point of ICT modulation can be varied as desired. In our previous work, we have shown that energy transfer efficiency between two energetically coupled fluorophores will be altered by the metal ion binding to the ICT chromophore carrying a ligand. There are two beneficial results: increased pseudo-Stokes shift and expanded dynamic range. Here, we explored the consequences of the modulation of energy transfer efficiency at the energy donor site, in a molecular design which has an ICT type metal ion-sensitive chromophore placed as the energy donor in the dyad. Clear advantages emerge compared to the acceptor site modulation: unaltered emission wavelength in the red end of the visible spectrum, while keeping a large Stokes shift and the ratiometric character. © 2009 American Chemical Society.Item Open Access Pyramidalized double bonds containing endoperoxide linkages: photooxygenation of dimethyl cis-3,8-dihydroheptalene-3,8, dicarboxylate(American Chemical Society, 1999) Saraçoǧlu, N.; Menzek, A.; Sayan, Ş.; Salzner, U.; Balci, M.Diels-Alder cycloaddition utilizing singlet oxygen as the dienophile with dimethyl cis-3,8-dihydroheptalene-3,8-dicarboxylate (5) has been investigated, and monoaddition product 7 has been isolated. The addition of a second singlet oxygen to the cycloheptatriene unit in 7 gave syn- bis(norcaradiene) bis(endoperoxide) 4. 1H NMR spectral studies and theoretical calculations indicate the increased pyramidalization in syn-4 compared with carbon analogue. The increased pyramidalization results from hyperconjugation between the central π-bond and the four adjacent C-O bonds and by rehybridization at C3, C4, C5, and C6. Furthermore, the increased reactivity for syn-4, which is probably arising from further folding of the central double bond, is also in agreement with theoretical calculations.