13673-30-8Relevant academic research and scientific papers
Syntheses of shuttlecock- and bowl-equipped phenylazopyridines and photomodulation of their coordination ability to Zn-porphyrin
Suwa, Kazuya,Otsuki, Joe,Goto, Kei
supporting information; experimental part, p. 2106 - 2108 (2009/07/19)
Shuttlecock- and bowl-equipped 4-(phenylazo)pyridine derivatives, which bear substituents that allow the pyridine moiety to protrude in the trans form but hinder it in the cis form, have been designed and synthesized. These molecules show cis/trans photoisomerization despite the presence of bulky substituents. 1H NMR titration with Zn-porphyrin showed that the trans isomers coordinate to Zn-porphyrin much stronger than the cis isomers.
REDUCTION OF AROMATIC NITRO GROUPS WITH HEXAMETHYLDISILANE1): REACTIONS WITH HEXAMETHYLDISILANE AND FLUORIDE ION-II2).
Vorbrueggen, Helmut,Krolikiewicz, Konrad
, p. 1259 - 1262 (2007/10/02)
Reduction of aromatic nitro compounds with hexamethyldisilane and fluoride ion in THF at 24 deg C gives the corresponding azo- and azoxy-compounds in high yields.Hexamethyldisilane converts commercial tetrabutylammoniumfluoride-dihydrate into a highly reactive catalyst.
