Solid-state study of charge-transfer interactions in copolymers

1990 ◽  
Vol 23 (24) ◽  
pp. 5127-5132 ◽  
Author(s):  
Alexandra Simmons ◽  
Almeria Natansohn
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
State Study

Liquid− and solid−state study of charge-transfer (CT) interaction between drug triamterene as a donor and tetracyanoethylene (TCNE) as an acceptor

2021 ◽  
pp. 116261
Author(s):  
Abdel Majid A. Adam ◽  
Moamen S. Refat ◽  
Tariq A. Altalhi ◽  
Fahad S. Aldawsari ◽  
Ghaferah H. Al-Hazmi
Keyword(s):  
Charge Transfer ◽  
Solid State ◽  
State Study

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

scholarly journals Four Thermochromic o-Hydroxy Schiff Bases of α-Aminodiphenylmethane: Solution and Solid State Study

Crystals ◽  
2017 ◽  
Vol 7 (1) ◽  
pp. 25 ◽  
Author(s):  
Marija Zbačnik ◽  
Katarina Pičuljan ◽  
Jelena Parlov-Vuković ◽  
Predrag Novak ◽  
Andreas Roodt
Keyword(s):  
Solid State ◽  
Schiff Bases ◽  
State Study

scholarly journals From μ3- to μ- Agostic Methyl Coordination: NMR and Solid State Study of Donor Ligands Uptake by the Triangular Cluster Anion [Re3(μ-H)3(μ3-CH3)(CO)9]-

2021 ◽  
pp. 120641
Author(s):  
Daniela Maggioni ◽  
Donato Tunzi ◽  
Pasquale Illiano ◽  
Pierluigi Mercandelli ◽  
Angelo Sironi ◽  
...  
Keyword(s):  
Solid State ◽  
Cluster Anion ◽  
Donor Ligands ◽  
State Study

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.

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