Highly twisted biphenyl-linked carbazole–benzimidazole hybrid bipolar host materials for efficient PhOLEDs

2014 ◽  
Vol 2 (40) ◽  
pp. 8554-8563 ◽  
Author(s):  
Shuo-Hsien Cheng ◽  
Wen-Yi Hung ◽  
Ming-Hung Cheng ◽  
Hsiao-Fan Chen ◽  
Atul Chaskar ◽  
...  

Three highly twisted bipolar molecules with different degree of charge transfer characters are developed to serve as PhOLEDs host materials.

CrystEngComm ◽  
2015 ◽  
Vol 17 (32) ◽  
pp. 6227-6235 ◽  
Author(s):  
Amparo Salmerón-Valverde ◽  
Sylvain Bernès

A series of solvated donor–acceptor organic complexes were shown to slowly release the lattice solvent while the degree of charge transfer decreases steadily. This behavior is not observed in the case of a hydrate.


2015 ◽  
Vol 51 (81) ◽  
pp. 15071-15074 ◽  
Author(s):  
Bora Joo ◽  
Eung-Gun Kim

Choosing a small active space of electrons for charge analysis allows the model-free determination of the degree of charge transfer.


Nanoscale ◽  
2017 ◽  
Vol 9 (40) ◽  
pp. 15303-15313 ◽  
Author(s):  
Xiaolei Wang ◽  
Peng Li ◽  
Xiao Xia Han ◽  
Yasutaka Kitahama ◽  
Bing Zhao ◽  
...  

The synergistic effect in ZnO-TiO2/N3/Ag can generate extra enhancements in the SERS intensity and degree of CT.


2017 ◽  
Vol 53 (70) ◽  
pp. 9701-9704 ◽  
Author(s):  
Jian-Zhen Liao ◽  
Jian-Fei Chang ◽  
Lingyi Meng ◽  
Hai-Long Zhang ◽  
Sa-Sa Wang ◽  
...  

Lone pair-π interaction-induced variation of the degree of charge-transfer was successfully used for switching the conductance of a photochromic coordination network.


1968 ◽  
Vol 0 (0) ◽  
pp. 1297-1302 ◽  
Author(s):  
R. J. W. Le Fèvre ◽  
D. V. Radford ◽  
P. J. Stiles

2003 ◽  
Vol 59 (4) ◽  
pp. 505-511 ◽  
Author(s):  
Amparo Salmerón-Valverde ◽  
Sylvain Bernès ◽  
Juan Gerardo Robles-Martínez

A new organic charge-transfer complex, C18H7N5O8·C6H4S4, has been prepared using TTF (tetrathiafulvalene) as a donor (D) and MeDC2TNF (9-dicyanomethylene-4,5,7-trinitro-fluorene-2-carboxylic acid methyl ester) as an acceptor (A). Two monoclinic polymorphs of the 1:1 salt were crystallized and characterized by X-ray diffraction. Form α crystallizes in space group P21/n with Z′ = 1, while form β crystallizes in space group C2/c with Z′ = 1\over 2 and the MeDC2TNF moiety disordered across a twofold axis. Both phases have mixed-stack crystal packings, which are characteristic of semiconducting one-dimensional organic complexes. However, the observed crystal packings are significantly different, with a single D...A interlayer separation of 3.452 Å for the disordered β polymorph and interlayer separations of 3.378 and 3.483 Å in the case of the ordered α form. These variations are reflected in the degree of charge transfer, δ, which was estimated on the basis of the b 2u stretching-mode frequency shift observed in the IR spectra for the cyano groups of the MeDC2TNF radical anion. The fact that the charge transfer is more efficient for α-(TTF-MeDC2TNF) than for β-(TTF-MeDC2TNF) (δ = 0.35 and 0.31, respectively) is consistent with the structural features observed for each crystalline form.


RSC Advances ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 6658-6680
Author(s):  
Jayaraman Jayabharathi ◽  
Venugopal Thanikachalam ◽  
Ganapathy Abirama Sundari

CDDPI:Ir(ppy)3 exhibits higher efficiencies: L = 8812 cd m−2; ηex = 19.0%; ηc = 27.5 cd A−1; ηp = 33.0 lm W−1 at 2.7 V.


2006 ◽  
Vol 84 (2) ◽  
pp. 154-163 ◽  
Author(s):  
Mark E Smith ◽  
Richard L Cordiner ◽  
David Albesa-Jové ◽  
Dmitri S Yufit ◽  
František Hartl ◽  
...  

The cyanoacetylide complex Fe(C≡CC≡N)(dppe)Cp (3) is readily obtained from sequential reaction of Fe(C≡CSiMe3)(dppe)Cp with methyllithium and phenyl cyanate. Complex 3 is a good metalloligand, and coordination to the metal fragments [RhCl(CO)2], [Ru(PPh3)2Cp]+, and [Ru(dppe)Cp*]+ affords the corresponding cyanoaceylide-bridged heterobimetallic complexes. In the case of the 36-electron complexes [Cp(dppe)Fe-C≡CC≡N-MLn]n+, spectroscopic and structural data are consistent with a degree of charge transfer from the iron centre to the rhodium or ruthenium centre via the C3N bridge, giving rise to a polarized ground state. Electrochemical and spectroelectrochemical methods reveal significant interactions between the metal centres in the oxidized (35 electron) derivatives, [Cp(dppe)Fe-C≡CC≡N-MLn](n+1)+. Key words: cyanide, cyanoacetylide, crystal structure.


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