Nonradiative Transition of Phosphorescent Charge-Transfer States of Ruthenium(II)-to-2,2‘-Biquinoline and Ruthenium(II)-to-2,2‘:6‘,2‘‘-Terpyridine in the Solid State

1998 ◽  
Vol 37 (12) ◽  
pp. 3093-3098 ◽  
Author(s):  
Ashraful Islam ◽  
Noriaki Ikeda ◽  
Akio Yoshimura ◽  
Takeshi Ohno
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Nonradiative Transition

Solid-state redox couple mediated water splitting

2021 ◽  
Author(s):  
Duanduan Liu ◽  
Wei Wei ◽  
Maidina Mahemu ◽  
Hao Qin ◽  
Kai Zhu ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Water Splitting ◽  
Redox Couple ◽  
Electrochemical Water Splitting

The solid-state redox couple is a vital charge transfer medium for electrochemical water splitting.

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

The lowest energy excited states of the binuclear silver(I) halide complexes, Ag2(dmb)2X2. Metal-centered or charge transfer states?

1994 ◽  
Vol 72 (3) ◽  
pp. 705-713 ◽  
Author(s):  
Daniel Piché ◽  
Pierre D. Harvey
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Excited States ◽  
Silver Halide ◽  
Molecular Orbital Calculations ◽  
Isocyanide Ligands ◽  
Visible Spectra ◽  
Halide Complexes ◽  
The Media ◽  
Uv Visible

The nature of the lowest energy excited states of the Ag2(dmb)2X2 complexes (X = Cl, Br, I; dmb = 1,8-diisocyano-ρ-menthane) have been addressed both experimentally and theoretically. It is shown that the lowest energy excited states of the complexes are charge transfer states from the silver-halide frame to the isocyanide ligands (M/XLCT) based upon UV-visible spectra and emission polarization ratio measurements, and extended Hückel molecular orbital calculations (EHMO). The metal-centered dσ* → pσ bands have been observed in the higher energy region of the spectra (232–242 nm). The complexes are luminescent (440 ≤ λe ≤ 480 nm) both in a glass and in the solid state at 77 K where the emission lifetimes, τe, range from 20 to 90 µs, which depend upon the nature of the halide (for the solid state data) and the media. No emission is observed at room temperature.

Bonding and interlayer charge transfer in the solid state compound Na1.9Cu2Se2Cu2O

1995 ◽  
Vol 216 (2) ◽  
pp. 177-182 ◽  
Author(s):  
Gerardo Chacon ◽  
Xiangyun Long ◽  
Chong Zheng
Keyword(s):  
Charge Transfer ◽  
Solid State

Charge-Transfer Crystal with Segregated Packing Structure Constructed with Hexaarylbenzene and Tetracyanoquinodimethane

CrystEngComm ◽  
2021 ◽  
Author(s):  
Rempei Ando ◽  
Mingoo Jin ◽  
Hajime Ito
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
Electron Donor ◽  
Packing Structure ◽  
Donor And Acceptor ◽  
Solid State Materials ◽  
Electron Donor And Acceptor ◽  
Acceptor Molecules

Charge-transfer (CT) crystals bearing segregated domains between the electron donor and acceptor molecules are a promising platform for developing new organic functional solid-state materials. However, there is limited diversity in...

scholarly journals Emission Quenching and First Evidence of Tb3+-to-As5+ Charge Transfer in Terbium(III) Ion-Doped YVxAs1–xO4 Solid-State Solution

2020 ◽  
Vol 124 (31) ◽  
pp. 17364-17371
Author(s):  
Marta Wujczyk ◽  
Adam Watras ◽  
Philippe Boutinaud ◽  
Marco Bettinelli ◽  
Sara Targonska ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
State Solution ◽  
Emission Quenching
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