135761-45-4Relevant articles and documents
Extremely efficient and reversible visible-light photochromism and accompanying switch of electronic communication in N-phenylcarbazole-appended diethynylethene
Hayashi, Mikihiro,Sakamoto, Ryota,Nishihara, Hiroshi
supporting information; experimental part, p. 8610 - 8613 (2012/08/27)
Photoisomerization: N-phenylcarbazole-conjugated dimethyl 2,3-diethynylfumarate/maleate, E/Z-4, shows highly efficient and reversible visible-light E/Z photoisomerization (φtotal=0.40) upon excitation with an intramolecular charge-transfer band. This photochromism induces switching of electronic communication between the two N-phenylcarbazole moieties in the one-electron oxidized mixed-valent state (see scheme). Copyright
Javelin-, hockey stick-, and boomerang-shaped liquid crystals. Structural variations on p-quinquephenyl
Dingemans, Theo J.,Murthy, N. Sanjeeva,Samulski, Edward T.
, p. 8845 - 8860 (2007/10/03)
The ramifications of changing molecular geometry in a series of all-aromatic liquid crystals derived from p-quinquephenyl are reported. Substituting heterocyclic rings such as thiophene, oxadiazole, oxazole, or 1,3-phenylene into the p-quinquephenylene core affects molecular shape changes via the substituent's exocyclic bond angle. In general, we found that introducing nonlinearity into molecules depresses the melting transition temperature. The symmetric (boomerang-shaped) molecules, 2,5-bisbiphenyl-4-yl-1,3,4-oxadiazole, 2,5-bisbiphenyl-4-yl-oxazole, and 1,3-bisbiphenyl-4-yl-benzene, melt into isotropic phases showing small monotropic mesophases. By contrast, the asymmetric (hockey stick-shaped) mesogens, 2-terphenyl-4-yl-5-phenyl thiophene and 2-terphenyl-4-yl-5-phenyl-1,3,4-oxadiazole, exhibit more stable enantiotropic liquid crystalline phases. The hockey stick-shaped mesogens exhibit a smectic phase as well as a nematic phase. High-temperature X-ray determination of the smectic layer spacing gives an unambiguous picture of interdigitated, bilayerlike supramolecular architecture in the smectic phase. There are associated changes in the mesogen's electrostatic profile when a heterocycle is introduced into the quinquiphenylene framework (e.g., conjugation is perturbed). Our findings suggest that steric packing considerations dominate the phase preferences (nematic versus smectic phases). However, electronic considerations (conjugation) appear to control the range of mesomorphism in this new family of nonlinear liquid crystals.
