107321-41-5Relevant academic research and scientific papers
A rodlike organogelator: Fibrous aggregation of azobenzene derivatives with a syn-chiral carbonate moiety
Mamiya, Jun-Ichi,Kanie, Kiyoshi,Hiyama, Tamejiro,Ikeda, Tomiki,Kato, Takashi
, p. 1870 - 1871 (2002)
A chiral azobenzene derivative containing a cyclic syn-carbonate moiety functions as a gelator for various organic solvents; the dipole-dipole interaction drives the fibrous self-assembly of the rodlike gelator.
A Redox Isomerization Strategy for Accessing Modular Azobenzene Photoswitches with near Quantitative Bidirectional Photoconversion
Zhu, Jie S.,Larach, Julio M.,Tombari, Robert J.,Gingrich, Phillip W.,Bode, Stanley R.,Tuck, Jeremy R.,Warren, Hunter T.,Son, Jung-Ho,Duim, Whitney C.,Fettinger, James C.,Haddadin, Makhluf J.,Tantillo, Dean J.,Kurth, Mark J.,Olson, David E.
supporting information, p. 8765 - 8770 (2019/11/11)
Photoswitches capable of accessing two geometric states are highly desirable, especially if their design is modular and incorporates a pharmacophore tethering site. We describe a redox isomerization strategy for synthesizing p-formylazobenzenes from p-nit
Smaragdyrin-azobenzene conjugates: Syntheses, structure, and spectral and electrochemical properties
Gokulnath, Sabapathi,Prabhuraja, Viswanathan,Sankar, Jeyaraman,Chandrashekar, Tavarekere K.
, p. 191 - 200 (2007/10/03)
The syntheses, characterization, and spectral properties of smaragdyrin-azobenzene conjugates are reported. Our synthetic strategy involves linking the azobenzene group in one of the precursors to a dipyrromethane subunit, which was achieved by reaction o
Azobenzene-porphyrins
Hunter,Hunter, Christopher A.,Sarson,Sarson, Luke D.
, p. 699 - 702 (2007/10/02)
A series of covalently-connected azobenzene-porphyrin derivatives have been synthesised and their photochemical properties investigated. The photochemistry of the porphyrin components is essentially unaltered, but photochemical isomerisation of the azobenzene components can not be detected.
