87337-01-7Relevant academic research and scientific papers
Cooperative assembly of binary molecular components into tubular structures for multiple photonic applications
Liao, Qing,Fu, Hongbing,Wang, Chen,Yao, Jiannian
, p. 4942 - 4946 (2011)
Take the tube: Tubular structures can be fabricated by the cooperative self-assembly of the binary molecular components TPI and APO (see picture). This method can also be used to make a single binary tube capable of performing multiple photonic functions,
Structures and Photochemical Reactions of 1-(9-Anthryl)-2-aroylethylenes: Competing cis-trans Isomerization and Skeletal Rearrangement
Mori, Yukie,Maeda, Koko
, p. 106 - 112 (1994)
(Z)-3-(9-Anthryl)-1-phenylpropenone, cis-(I), C23H16O, Mr=308.38, orthorhombic, P212121, a=14.992 (3), b=19.124 (4), c=5.614 (1) Angstroem, V=1609.4 (6) Angstroem3, Z=4, Dx=1.273 g cm-
PHOTOCHEMISTRY OF THE ANTHRACENE CHROMOPHORE: NOVEL ISOMERIZATION OF 1-(9-ANTHRYL)-2-BENZOYLETHYLENES
Becker, Hans-Dieter,Becker, Hans-Christian,Sandros, Kjell,Andersson, Kjell
, p. 1589 - 1592 (2007/10/02)
Photoexcited cis-1-(9-anthryl)-2-benzoylethylenes undergo a novel type of isomerization by skeletal rearrangement to give furano-annelated 5H-dibenzocycloheptenes.
On the Relationship between Molecular Geometry and Excited-State Properties of 9-Anthrylalkenes
Becker, Hans-Dieter,Andersson, Kjell
, p. 4542 - 4549 (2007/10/02)
The excited-state properties of a series of 1-substituted and 1,1-disubstituted 2-(9-anthryl)alkenes have been investigated in terms of their fluorescence spectra and photochemical isomerizations.Large Stokes shifts of up to 10000 cm-1 between absorption and emission maxima are attributed to geometrical differences between the ground state and the emitting excited state.The : ratio of the photostationary state was found to depend markedly on the nature of the 1-substituent.Photochemical isomerization of 1,3- and 1,5-bis(9-anthryl)-substituted trans olefins results in the formation of intramolecular or cycloaddition products.The cycloaddition reactions of carbonyl-substituted anthracenes are suggested to involve the triplet excited state.
