Direct structural characterization of charge localization in metal to ligand charge transfer complexes

1988 ◽  
Author(s):  
L. K. Orman ◽  
D. R. Anderson ◽  
J. B. Hopkins
1999 ◽  
Vol 53 ◽  
pp. 721-730 ◽  
Author(s):  
David M. Schubert ◽  
David E. Harwell ◽  
Carolyn B. Knobler ◽  
M. Frederick Hawthorne ◽  
Stefan Sjöberg ◽  
...  

2001 ◽  
Vol 56 (3) ◽  
pp. 297-300 ◽  
Author(s):  
G. C. Papavassiliou ◽  
Yohji Misaki ◽  
Kazuko Takahashi ◽  
Jun-ichi Yamada ◽  
G. A. Mousdis ◽  
...  

Abstract The preparation and characterization of some π-donors with a pyrazine-edge-group as well as with tetrathiapentalene-, thiophene-, and dihydrobenzoselenophene-spacer-groups are de­ scribed. Some of these donors give conducting charge transfer complexes with TCNQ and/or cation radical salts with I3-, BF4-and PF6-as counter anions.


1989 ◽  
Vol 28 (15) ◽  
pp. 2930-2939 ◽  
Author(s):  
Joel S. Miller ◽  
Daniel T. Glatzhofer ◽  
Dermot M. O'Hare ◽  
William M. Reiff ◽  
Animesh Chakraborty ◽  
...  

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.


2020 ◽  
Vol 31 (10) ◽  
pp. 2143-2153
Author(s):  
Lauren E. Pepi ◽  
Zachary J. Sasiene ◽  
Praneeth M. Mendis ◽  
Glen P. Jackson ◽  
I. Jonathan Amster

2007 ◽  
Vol 469 (1) ◽  
pp. 99-110 ◽  
Author(s):  
Neelu Chouhan ◽  
M. L. Kalra ◽  
Sudhish Kumar ◽  
Y. N. Singh ◽  
Suresh C. Ameta

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