Thermal and light-induced reduction of the ruthenium complex cation Ru(bpy)33+ in aqueous solution

1984 ◽  
Vol 106 (17) ◽  
pp. 4772-4783 ◽  
Author(s):  
Pushpito K. Ghosh ◽  
Bruce S. Brunschwig ◽  
Mei Chou ◽  
Carol Creutz ◽  
Norman Sutin
1984 ◽  
Vol 15 (49) ◽  
Author(s):  
P. K. GHOSH ◽  
B. S. BRUNSCHWIG ◽  
M. CHOU ◽  
C. CREUTZ ◽  
N. SUTIN

Author(s):  
Isabelle M. Dixon ◽  
Sylvestre Bonnet ◽  
Fabienne Alary ◽  
Jérôme Cuny

1980 ◽  
Vol 35 (9) ◽  
pp. 1096-1103 ◽  
Author(s):  
Matthias Kretschmer ◽  
Lutwin Labouvie ◽  
Karl-W. Quirin ◽  
Helmut Wiehn ◽  
Ludwig Heck

Acidity constants of ammine complexes of tetravalent platinum in aqueous solutions have been determined by a spectrophotometric method at very low ionic strengths and extrapolated to zero ionic strength. Temperature variations of pK-values (25 °C and 50 °C) yield thermodynamic parameters for two successive deprotonation steps of hexaammineplatinum(IV), pentaamminechloroplatinum(IV), and tris(ethylenediamine)pla- tinum(IV) complexes and for the deprotonation of pentaammineaquacobalt(III) ion.The enthalpy changes for the first and second steps are similar and range from 50 to 75 kJ/mole while for the aqua ligand of Co(III) 33 kJ/mole are found. The very large dif­ference in the entropy changes (about 70 to 80 J/K mole for the first step and -10 to + 20 J/K mole for the second step) is interpreted by a model of solvation change. The primary hydration sphere of strongly oriented and immobilized water dipoles around the highly charged complex cation is transformed to a hydrogen-bonded solvation sheath when the electric field of the complex is weakened upon release of the first proton.


1922 ◽  
Vol 4 (6) ◽  
pp. 741-757 ◽  
Author(s):  
Jacques Loeb

1. Experiments on anomalous osmosis suggested that salts with trivalent cations, e.g. LaCl3, caused isoelectric gelatin to be positively charged, and salts with tetravalent anions, e.g. Na4Fe(CN)6, caused isoelectric gelatin to be negatively charged. In this paper direct measurements of the P.D. between gels of isoelectric gelatin and an aqueous solution as well as between solutions of isoelectric gelatin in a collodion bag and an aqueous solution are published which show that this suggestion was correct. 2. Experiments on anomalous osmosis suggested that salts like MgCl2, CaCl2, NaCl, LiCl, or Na2SO4 produce no charge on isoelectric gelatin and it is shown in this paper that direct measurements of the P.D. support this suggestion. 3. The question arose as to the nature of the mechanism by which trivalent and tetravalent ions cause the charge of isoelectric proteins. It is shown that salts with such ions act on isoelectric gelatin in a way similar to that in which acids or alkalies act, inasmuch as in low concentrations the positive charge of isoelectric gelatin increases with the concentration of the LaCl3 solution until a maximum is reached at a concentration of LaCl3 of about M/8,000; from then on a further increase in the concentration of LaCl3 diminishes the charge again. It is shown that the same is true for the action of Na4Fe(CN)6. From this it is inferred that the charge of the isoelectric gelatin under the influence of LaCl3 and Na4Fe(CN)6 at the isoelectric point is due to an ionization of the isoelectric protein by the trivalent or tetravalent ions. 4. This ionization might be due to a change of the pH of the solution, but experiments are reported which show that in addition to this influence on pH, LaCl3 causes an ionization of the protein in some other way, possibly by the formation of a complex cation, gelatin-La. Na4Fe(CN)6 might probably cause the formation of a complex anion of the type gelatin-Fe(CN)6. Isoelectric gelatin seems not to form such compounds with Ca, Na, Cl, or SO4. 5. Solutions of LaCl3 and Na4Fe(CN)6 influence the osmotic pressure of solutions of isoelectric gelatin in a similar way as they influence the P.D., inasmuch as in lower concentrations they raise the osmotic pressure of the gelatin solution until a maximum is reached at a concentration of about M/2,048 LaCl3 and M/4,096 Na4Fe(CN)6. A further increase of the concentration of the salt depresses the osmotic pressure again. NaCl, LiCl, MgCl2, CaCl2, and Na2SO4 do not act in this way. 6. Solutions of LaCl3 have only a depressing effect on the P.D. and osmotic pressure of gelatin chloride solutions of pH 3.0 and this depressing effect is quantitatively identical with that of solutions of CaCl2 and NaCl of the same concentration of Cl.


2009 ◽  
Vol 64 (3) ◽  
pp. 269-273 ◽  
Author(s):  
Xiuhong Xu ◽  
Fang Luo ◽  
Weihong Luo ◽  
Ji Chen

A new polyoxotungstate complex [Na2(H2O)8][Na8(H2O)20][Cu(en)2][W12O42] ・3H2O (1) (en = ethylenediamine) has been synthesized in aqueous solution and characterized by elemental analysis, IR spectroscopy and TG analysis, together with a single crystal X-ray diffraction study. In compound 1, the Cu(en)22+ complex cation links the [W12O42]12− anions to form a 1D chain, and the 1D chains are further interconnected with Na8(H2O)208+ and Na2(H2O)82+ cations to construct a new 3D framework.


1988 ◽  
Vol 41 (5) ◽  
pp. 635 ◽  
Author(s):  
LR Gahan ◽  
TW Hambley ◽  
PC Healy

Sodium diethyldithiocarbamate, Na[Et2dtc], reacts with (8-methyl-3,6,10,13,16,19-hexaazabicyclo[6.6.6]icosan-1-aminium)cobalt(III) chloride, [Co( AMMEsarH )]Cl4, in aqueous solution to form the compound [Co( AMMEsar )][Et2dtc]3 which is readily soluble in organic solvents. Crystals are trigonal, space group R3c (3m, No. 167) with a 13.864(4), c 36.42(2)Ǻ, Z 6. A full-matrix least-squares refinement on 952 reflections, with I > 2.5σ(I), converged with final R of 0.037. The structure consists of the [Co( AMMEsar )]3+ cation and three [Et2dtc]- anions. The primary aminium group on one trigonal cap of the cage is deprotonated to an amine. Strong hydrogen bonds exist between the sulfur atoms of the diethyldithiocarbamate anions and the protons of the secondary amines of the complex cation, which is stabilized in the lel conformation.


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