Double-shot inkjet printing of donor–acceptor-type organic charge-transfer complexes: Wet/nonwet definition and its use for contact engineering

2010 ◽  
Vol 518 (14) ◽  
pp. 3988-3991 ◽  
Author(s):  
Tatsuo Hasegawa ◽  
Maki Hiraoka ◽  
Toshikazu Yamada
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.


2019 ◽  
Vol 25 (59) ◽  
pp. 13547-13565 ◽  
Author(s):  
Karlee P. Castro ◽  
Eric V. Bukovsky ◽  
Igor V. Kuvychko ◽  
Nicholas J. DeWeerd ◽  
Yu‐Sheng Chen ◽  
...  

1984 ◽  
Vol 39 (12) ◽  
pp. 1274-1278 ◽  
Author(s):  
M. H. Abdel-Kader ◽  
R. M. Issa ◽  
M. M. Ayad ◽  
M. S. Abdel-Mottaleb

The charge transfer complexes of 2,3- (I) and 2,6-Dimethylnaphthalenes (II) as electron donors with tri- and di-nitrobenzenes as electron acceptors are prepared and investigated by element analysis, IR. 1H nmr and electronic absorption spectroscopy. The results showed that I yields CT complexes of 1:1 type only while II is capable of forming 1 : 1 and 1 : 2 (donor: acceptor) compounds. The spectral characteristics of the CT complexes are pointed out and discussed. The difference in the donor behaviour between I and II is explained in the light of PPP-MO calculations.


2020 ◽  
Vol 8 (43) ◽  
pp. 15199-15207
Author(s):  
Paul Beyer ◽  
Eduard Meister ◽  
Timo Florian ◽  
Alexander Generalov ◽  
Wolfgang Brütting ◽  
...  

Charge transfer complex (CPX) formation at a donor–acceptor interface reduces the amount of Fermi-level pinning induced interfacial charge transfer.


1973 ◽  
Vol 4 (44) ◽  
pp. no-no
Author(s):  
M. RAILEANU ◽  
I. RADULIAN ◽  
M. OLTENEANU ◽  
M. CONSTANTIN

1998 ◽  
Vol 53 (11) ◽  
pp. 1316-1322 ◽  
Author(s):  
Marc Dötze ◽  
Hendrik Czepat ◽  
Jens Kudnig ◽  
Günter Klar

The title compounds are prepared by slow evaporation of dilute solutions of the components. 2,3,7,8-Tetrakis(methylthio)thianthrene and -selenanthrene give isostructural 2:1 complexes with 7,7,8,8-tetracyanoquinodimethane (TCNQ) built up by donor/acceptor/donor units in which the TCNQ molecule is inserted into the cavity formed by two of the folded, oppositely arranged chalcogenanthrene molecules. These units are connected to chains by S -S contacts via the methylthio groups. From 2,3,7,8-tetrakis(methylthio)thianthrene and tetracyanoethene again a 2:1 complex is obtained, however, with a columnar structure in which two donor stacks are slightly interlinked by an acceptor stack thus forming a structure with alternating donor and acceptor molecules. The molecules are arranged in such a way that an optimum overlap of the HOMOs of the donors and the LUMOs of the acceptors, all of which are of π-type character according to MNDO calculations, is secured.


Author(s):  
Olga A Otmakhova ◽  
Alexey Piryazev ◽  
Galina N Bondarenko ◽  
Georgii A. Shandryuk ◽  
Alexey Merekalov ◽  
...  

Electron donor-acceptor liquid crystals have been attracting considerable attention due to possible applications in optoelectronics and photonics. The creation of such charge transfer complexes is a powerful and flexible instrument...


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