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The influence of the trans -ligand to NO on the thermal stability of the photoinduced side-bond coordinated linkage isomer
Ist Teil von
New journal of chemistry, 2022-07, Vol.46 (26), p.12641-12650
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2022
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
The influence of the
trans
-to-NO ligand (X) on the thermal stability of the transient side-on coordinated nitrosyl linkage isomer (MS2) is investigated in a series of
trans
-[RuNOPy
4
X](PF
6
)
2
(X = F
−
(RuF), Cl
−
(RuCl), Br
−
(RuBr) and OH
−
(RuOH)) compounds. Based on differential scanning calorimetry (DSC) and IR-spectroscopy investigations, activation energies (
E
a
) and frequency factors (
k
0
) are determined for MS1 → GS and MS2 → GS reactions. Calculated decay temperatures (
T
d
) of both processes correlate with Mulliken electronegativities of X and Hirshfeld charges of the (RuNO) unit, and the increase in the electronegativity of X or in the positive charge on the (RuNO) group leads to an increase in the thermal stability of the MS2 isomer with almost linear dependence. Since the MS2 isomer is a transient state in MS1 isomer formation or the NO release reaction, the obtained correlation can be used for the design of compounds with higher quantum yields of these processes.