A photoswitchable methylene-spaced fluorinated aryl azobenzene monolayer grafted on silicon
Aryldiazonium-terminated methylene-spaced trifluoromethylazobenzene derivatives have been synthesized. Their self-assembled monolayers (SAMs) on a silicon surface allow for a stable and reversible molecular photoswitch.
The invention disclosed in this document is related to the field of pesticides and their use in controlling pests. A compound having the following structure is disclosed.
-
Page/Page column 11
(2010/08/18)
Syntheses of new functionalized azobenzenes for potential molecular electronic devices
New non-symmetrical azobenzene derivatives have been synthesized as potential molecular electronic switching device candidates. The Oxone mediated oxidation of anilines provided nitroso-functionalized arenes, which were then condensed with substituted anilines to provide a series of azobenzene derivatives that could be further converted into oligo(phenylene ethynylene)s or diazonium salts. The resulting thiolacetates, thiols, or diazonium salts are capable of forming molecular layers on the surface of gold or silicon, thereby paving the way for molecular electronics testing.
Yu, Byung-Chan,Shirai, Yasuhiro,Tour, James M.
p. 10303 - 10310
(2007/10/03)
More Articles about upstream products of 1961-53-1