60273-43-0Relevant articles and documents
Substituent site effect induced assemblies of porphyrin derivatives on graphite surface characterized using a scanning probe microscope
Li, Min,Xu, Haijun,Yang, Yanlian,Zhao, Lina,Shen, Zhen,Zeng, Qingdao,Wang, Chen
, p. 1764 - 1766 (2014)
The assembly behavior of both symmetrically substituted tetraphenylporphyrin (TPP) (sym-16OTPP, meso-tetra(3,5-dihexadecyloxyphenyl)) and asymmetrically substituted tetraphenylporphyrin (TPP) (asym-16OTPP, meso-tetra(3,4-dihexadecyloxyphenyl)) on a highly
Rationally designed anion-responsive-organogels: Sensing F-via reversible color changes in gel-gel states with specific selectivity
Lin, Qi,Zhu, Xin,Fu, Yong-Peng,Zhang, You-Ming,Fang, Ran,Yang, Li-Zi,Wei, Tai-Bao
, p. 5715 - 5723 (2014)
Through the rational introduction of the multi self-assembly driving forces and F- sensing sites into a gelator molecule, low-molecular-weight organogelators L1 and L2 were designed and synthesized. L1 and L2 showed excellent gelation ability i
Discotic liquid crystals of transition metal complexes 56 ?: Synthesis of mesogenic phthalocyanine-fullerene dyads and influence of the substitution position of alkoxy chains and the kind of terminal groups on appearance of the helical supramolecular stru
Ishikawa, Kohei,Watarai, Ayumi,Yasutake, Mikio,Ohta, Kazuchika
, p. 693 - 715 (2018/07/30)
We have synthesized twelve novel discotic columnar liquid crystals based on a phenoxy-group-substituted phthalocyaninato copper(II) complex having the same alkoxy chain of C16H33O at different positions in the phenoxy group: The parent compounds {0a~0c-16
Photoluminescent discotic liquid crystals derived from tris(N-salicylideneaniline) and stilbene conjugates: Structure-property correlations
Achalkumar, Ammathnadu S.,Veerabhadraswamy,Hiremath, Uma S.,Rao, Doddamane S. Shankar,Prasad, Subbarao Krishna,Yelamaggad, Channabasaveshwar V.
, p. 291 - 305 (2016/05/24)
Luminescent discotic liquid crystals based on tris(N-salicylideneaniline)s [TSANs] bearing trans-stilbene fluorophores have been synthesized. Their mesomorphic and photophysical properties were studied. These TSANs existing in the form of C3h and Cs geometrical isomers of the keto-enamine tautomer self-assemble to form the columnar phase and exhibit fluorescence both in solution and mesophase states. These columnar mesophases also exhibit frozen (glassy) columnar phase, which ensures preserved fluorescence intensity, defect free alignment and simultaneous restriction on the motion of ionic impurities. These features make them promising candidates for the use in organic light emitting diodes, particularly as emissive layers. This study also led to an understanding about the dependence of their mesomorphism (mesophase type, stability and thermal range) and photophysical features on the number and pattern of their peripheral substitution, in comparison to the analogous columnar liquid crystalline TSANs reported earlier.