issue contents
August 2017 issue
![Highlighted illustration](/x/issues/2017/08/00/graphics/coverill.gif)
Cover illustration: The organic fluorophores commonly known as BODIPY dyes are a class of compounds that are characterized by intense fluorescence, high stability and relatively small Stokes shifts. In 2-[4-(dimethylamino)phenyl]-3,3-difluoro-3H-naphtho[1,2-e][1,3,2]oxazaborinin-2-ium-3-uide, a twist about the N-C single bond is observed, making the cross conjugation not as efficient as in the case of a planar structure. The borone complex displays a tetrahedral geometry. In the crystal, molecules are conected by weak C-HF hydrogen bonds. See: Dziuk, Osmialowski, Skotnicka, Ejsmont & Zarychta [IUCrData (2017). 2, x171141].
metal-organic compounds
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
organic compounds
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![R_{2}^{2}](/x/issues/2017/08/00/su4159/teximages/su4159fi1.gif)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)