Light controlled synthesis of nucleic acids
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![Figure 1.8). [1 ted from [14]. s (rNTP vs. d] However, inwinding ofas template.strands that and, and id17] dNTP), the t involves f the DNA The RNA is used as entical in](https://thumb-eu.123doks.com/thumbv2/123dok_br/15239942.1022849/44.892.274.582.160.539/figure-from-however-inwinding-template-strands-involves-entical.webp)
![Figure 1.20 – Absorption (A) and emission (B) spectra of the coumarin derivatives shown in Figure 1.19. Figure adapted from [145].](https://thumb-eu.123doks.com/thumbv2/123dok_br/15239942.1022849/76.892.129.733.362.608/figure-absorption-emission-spectra-coumarin-derivatives-figure-figure.webp)
![Figure 1.21 – Absorption and emission spectra of ClMMC in cyclohexane (full line) and dioxane:water mixture, 1:4 (dashed lines). Figure taken from [147].](https://thumb-eu.123doks.com/thumbv2/123dok_br/15239942.1022849/78.892.242.609.160.437/figure-absorption-emission-spectra-cyclohexane-dioxane-mixture-figure.webp)
![Figure 1.23 – Effect of the solvent polarity on the non‐radiative rate constant (k nr ) of DEACM. A significant increase in k nr is observed for high polarity solvents. Figure adapted from [157].](https://thumb-eu.123doks.com/thumbv2/123dok_br/15239942.1022849/82.892.257.604.152.412/polarity-radiative-constant-significant-increase-observed-polarity-solvents.webp)
![Table 1.4 – Photophysical and photochemical properties of cyclic adenosine monophosphates esters of differently substituted (coumarin‐4‐yl)methyl alcohols. In CH 3 OH/H 2 O‐HEPES buffer (pH = 7.2). Data taken from [172]. Caged Comp](https://thumb-eu.123doks.com/thumbv2/123dok_br/15239942.1022849/88.892.111.746.223.513/photophysical-photochemical-properties-adenosine-monophosphates-differently-substituted-coumarin.webp)
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