ABSTRACT
In the title compound, C19H15NO, the dihedral angle between the benzene rings of the carbazole moiety is 1.73â (12)° and the meth-oxy-substituted phenyl ring deviates from the mean plane of the carbazole grouping (r.m.s. deviation = 0.020â Å) by 56.78â (8)°. In the crystal, weak C-Hâ¯π inter-actions link the mol-ecules. The two-dimensional fingerprint plots derived from the Hirshfeld surface indicate that Hâ¯H (51.2%) and Câ¯H/Hâ¯C (39.9%) contacts dominate the packing.
ABSTRACT
Imidazole-based donor-acceptor materials are well known for their polarity-controlled trade-off phenomenon between the localized excitation-based short-wavelength (SW) emission in nonpolar solvents and charge transfer dominated long-wavelength (LW) emission in polar solvents. To attain concurrent SW- and LW-based dual-emission characteristics, a series of imidazole-based donor-acceptor fluorophores (CBImDCN, TPImDCN, PZImDCN) possessing different electron-donating groups such as carbazole, triphenylamine, and phenothiazine linked via the N-position of the imidazole core unit were synthesized and verified by NMR and mass spectroscopic techniques. As a result, the strong donating TPImDCN and PZImDCN exhibited dual emission in different solvents of varying polarity, covering the blue (SW) and green/orange (LW) regions. On the other hand, in contrast, only an SW emission band is observed with the weak donating CBImDCN. Moreover, PZImDCN shows panchromatic emission under 365 nm illumination, while only orange color emission is observed under visible light excitation, revealing two different origins of SW and LW emissions, as also evidenced from DFT calculations. Overall, this work reveals a new approach for attaining concurrent SW and LW emission characteristics from imidazole-based D-A materials and sheds light on the design and development of novel panchromatic emitters with intriguing properties for lighting and display applications.
ABSTRACT
A significant decrease in performance was observed for commercial Pt/C due to electrochemical oxidation of the carbon support and subsequent detachment and agglomeration of Pt particles. The Pt/TiO(2) cathode catalyst exhibited excellent fuel cell performance and ultrahigh stability under accelerated stress test conditions and can be considered as a promising alternative for improving the reliability and durability of PEMFCs.
