Structure and Reversible Anion Exchange in Copper Hydroxy Double Salts

Author(s):  
Catherine S. Bruschini ◽  
Michael J. Hudson
ChemInform ◽  
2010 ◽  
Vol 24 (28) ◽  
pp. no-no
Author(s):  
M. MEYN ◽  
K. BENEKE ◽  
G. LAGALY

1993 ◽  
Vol 32 (7) ◽  
pp. 1209-1215 ◽  
Author(s):  
Martina Meyn ◽  
Klaus Beneke ◽  
Gerhard Lagaly

1997 ◽  
pp. 403-411
Author(s):  
Catherine S. Bruschini ◽  
Michael J. Hudson

2015 ◽  
Vol 44 (47) ◽  
pp. 20728-20734 ◽  
Author(s):  
Miao Jin ◽  
Dominic E. M. Spillane ◽  
Carlos F. G. C. Geraldes ◽  
Gareth R. Williams ◽  
S. W. Annie Bligh

Chelated Gd3+complexes were loaded into hydroxy double salts and found to retain their proton relaxivity properties after intercalation.


1998 ◽  
Vol 13 (4) ◽  
pp. 848-851 ◽  
Author(s):  
Hiroyuki Morioka ◽  
Hideyuki Tagaya ◽  
Masa Karasu ◽  
Jun-ichi Kadokawa ◽  
Koji Chiba

Hydroxy double salts (HDS's) comprise a class of layered materials that are similar to layered double hydroxides (LDH's) and show a comparable intracrystalline reactivity. Their anion exchange reactions occur with preincorporated anions in the hydroxide layer and with anions bound as gegenions of the positively charged layers, respectively. In this study, nitrate and acetate anions of HDS's were exchanged with anionic monoand di-carboxylic acids, and we confirmed that interlayer spacing of HDS's increased depending on the size of mono- and di-carboxylic acids. Moreover, we have prepared photofunctional materials by exchange reaction with azobenzene-p-carboxylic acid and 4–4′-azobenzenedicarboxylic acid.


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