issue contents
September 2017 issue
![Highlighted illustration](/x/issues/2017/09/00/graphics/coverill.gif)
Cover illustration: 4-Cyano-3,5-bis(phenyl)pyrazole, a symmetrically phenyl substituted 4-cyano pyrazole, was prepared as a precursor for the preparation of scorpionate ligands. The C-CN fragments in the two independent molecules in the asymmetric unit deviate only slightly from linearity, with bonding angles of 179.4 (2) and 178.9 (2)°. In the crystal, molecules are linked by pairs of N-H
N hydrogen bonds, forming inversion dimers with an R22(6) ring motif. See: Zhao, Adeyemi & Pompilius [IUCrData (2017). 2, x171257].
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)
![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)
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)
![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)
addenda and errata
![cross.png](/logos/buttonlogos/cross.png)
![cross.png](/logos/buttonlogos/cross.png)
![Open Access](/logos/open.png)