Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Reversible O-H bond activation by an intramolecular frustrated Lewis pair
Ist Teil von
Dalton transactions : an international journal of inorganic chemistry, 2019-02, Vol.48 (9), p.2896-2899
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
The interactions of the O-H bonds in alcohols, water and phenol with dimethylxanthene-derived frustrated Lewis pairs (FLPs) have been probed. Within the constraints of this backbone framework, the preference for adduct formation or O-H bond cleavage to give the corresponding zwitterion is largely determined by p
K
a
considerations. In the case of the PPh
2
/B(C
6
F
5
)
2
system and
p
-
t
BuC
6
H
4
OH, an equilibrium is established between the two isomeric forms which allows the thermodynamic parameters associated with zwitterion formation
via
O-H bond cleavage to be probed.
The interactions of the O-H bonds in alcohols, water and phenol with dimethylxanthene-derived frustrated Lewis pairs (FLPs) have been probed.