scholarly journals PAH/PAH(CF 3 ) n Donor/Acceptor Charge‐Transfer Complexes in Solution and in Solid‐State Co‐Crystals

2019 ◽  
Vol 25 (59) ◽  
pp. 13547-13565 ◽  
Author(s):  
Karlee P. Castro ◽  
Eric V. Bukovsky ◽  
Igor V. Kuvychko ◽  
Nicholas J. DeWeerd ◽  
Yu‐Sheng Chen ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Charge Transfer Complexes ◽  
Donor Acceptor

Solid State Structural Properties of Multibridged [3n]Cyclophanes and Their Charge Transfer Complexes

ChemInform ◽  
2004 ◽  
Vol 35 (13) ◽  
Author(s):  
Mikio Yasutake ◽  
Toru Koga ◽  
Chultack Lim ◽  
Ming Zhou ◽  
Wakana Matsuda-Sentou ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Structural Properties ◽  
Charge Transfer Complexes

Crystal growth and characterization of solvated organic charge-transfer complexes built on TTF and 9-dicyanomethylenefluorene derivatives

CrystEngComm ◽  
2015 ◽  
Vol 17 (32) ◽  
pp. 6227-6235 ◽  
Author(s):  
Amparo Salmerón-Valverde ◽  
Sylvain Bernès
Keyword(s):  
Charge Transfer ◽  
Crystal Growth ◽  
Charge Transfer Complexes ◽  
Organic Complexes ◽  
Donor Acceptor ◽  
Degree Of Charge Transfer

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.

Charge Transfer Complexes of Aromatic Nitrocompounds with Disubstituted Naphthalenes. I.Spectroscopic Investigation of the Donor Behaviour of the 2,6- and 23-Dimethylnaphthalene

1984 ◽  
Vol 39 (12) ◽  
pp. 1274-1278 ◽  
Author(s):  
M. H. Abdel-Kader ◽  
R. M. Issa ◽  
M. M. Ayad ◽  
M. S. Abdel-Mottaleb
Keyword(s):  
Charge Transfer ◽  
Spectral Characteristics ◽  
Charge Transfer Complexes ◽  
Element Analysis ◽  
H Nmr ◽  
Aromatic Nitrocompounds ◽  
Donor Acceptor ◽  
The Difference ◽  
Donor Behaviour ◽  
Ct Complexes

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.

Investigation of Charge-Transfer Interaction in Mixed Stack Donor–Acceptor Cocrystals Toward Tunable Solid-State Emission Characteristics

2018 ◽  
Vol 18 (10) ◽  
pp. 6001-6008 ◽  
Author(s):  
Rabia Usman ◽  
Arshad Khan ◽  
Mingliang Wang ◽  
Yi Luo ◽  
Weiwei Sun ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Emission Characteristics ◽  
Charge Transfer Interaction ◽  
Donor Acceptor

Behavior of charge transfer complexes for solid state cells

1981 ◽  
Vol 5 ◽  
pp. 693-695
Author(s):  
A.V. Distefano ◽  
J.I. Franco ◽  
L. Perissinotti ◽  
N.E. Walsöe de Reca
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Charge Transfer Complexes

scholarly journals Fermi level pinned molecular donor/acceptor junctions: reduction of induced carrier density by interfacial charge transfer complexes

2020 ◽  
Vol 8 (43) ◽  
pp. 15199-15207
Author(s):  
Paul Beyer ◽  
Eduard Meister ◽  
Timo Florian ◽  
Alexander Generalov ◽  
Wolfgang Brütting ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Fermi Level ◽  
Carrier Density ◽  
Charge Transfer Complex ◽  
Charge Transfer Complexes ◽  
Interfacial Charge Transfer ◽  
Fermi Level Pinning ◽  
Donor Acceptor ◽  
Interfacial Charge

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

Sign in / Sign up

Export Citation Format

Share Document