SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:kth-159355"
 

Search: onr:"swepub:oai:DiVA.org:kth-159355" > Alkali-metal ion co...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Alkali-metal ion coordination in uranyl(VI) poly-peroxide complexes in solution. Part 1 : the Li+, Na+ and K+ - peroxide-hydroxide systems

Zanonato, Pier Luigi (author)
Di Bernardo, Plinio (author)
Vallet, Valerie (author)
show more...
Szabo, Zoltan (author)
KTH,Organisk kemi
Grenthe, Ingmar (author)
KTH,Kemi
show less...
 (creator_code:org_t)
2015
2015
English.
In: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; 44:4, s. 1549-1556
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • The alkali metal ions Li+, Na+ and K+ have a profound influence on the stoichiometry of the complexes formed in uranyl(VI)-peroxide-hydroxide systems, presumably as a result of a templating effect, resulting in the formation of two complexes, M[(UO2)(O-2)(OH)](2)(-) where the uranyl units are linked by one peroxide bridge, mu-eta(2)-eta(2), with the second peroxide coordinated "end-on", eta(2), to one of the uranyl groups, and M[(UO2)(O-2)(OH)](4)(3-), with a four-membered ring of uranyl ions linked by mu-eta(2)-eta(2) peroxide bridges. The stoichiometry and equilibrium constants for the reactions: M+ + 2UO(2)(2+) + 2HO(2)(-) + 2H(2)O -> M[(UO2)(O-2)(OH)] 2 - + 4H(+) (1) and M+ + 4UO(2)(2+) + 4HO(2)(-) + 4H(2)O -> M[(UO2)(O-2)(OH)](4)(3-) + 8H(+) (2) have been measured at 25 degrees C in 0.10 M (tetramethyl ammonium/M+)NO3 ionic media using reaction calorimetry. Both reactions are strongly enthalpy driven with large negative entropies of reaction; the observation that Delta H(2) approximate to 2 Delta H(1) suggests that the enthalpy of reaction is approximately the same when peroxide is added in bridging and "end-on" positions. The thermodynamic driving force in the reactions is the formation of strong peroxide bridges and the role of M+ cations is to provide a pathway with a low activation barrier between the reactants and in this way "guide" them to form peroxide bridged complexes; they play a similar role as in the synthesis of crown-ethers. Quantum chemical (QC) methods were used to determine the structure of the complexes, and to demonstrate how the size of the M+-ions affects their coordination geometry. There are several isomers of Na[(UO2)(O-2)(OH)](2)(-) and QC energy calculations show that the ones with a peroxide bridge are substantially more stable than the ones with hydroxide bridges. There are isomers with different coordination sites for Na+ and the one with coordination to the peroxide bridge and two uranyl oxygen atoms is the most stable one.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Keyword

Water Exchange-Reaction
Basis-Sets
Chemical-Equilibria
Free-Energy
Solvation
Pseudopotentials
Hydrogen
Atoms

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view