scholarly journals Ultrafast kinetics of linkage isomerism in Na2[Fe(CN)5NO] aqueous solution revealed by time-resolved photoelectron spectroscopy

2017 ◽  
Vol 4 (4) ◽  
pp. 044031 ◽  
Author(s):  
Azhr A. Raheem ◽  
Martin Wilke ◽  
Mario Borgwardt ◽  
Nicholas Engel ◽  
Sergey I. Bokarev ◽  
...  
2015 ◽  
Vol 17 (47) ◽  
pp. 31978-31987 ◽  
Author(s):  
Franziska Buchner ◽  
Berit Heggen ◽  
Hans-Hermann Ritze ◽  
Walter Thiel ◽  
Andrea Lübcke

Time-resolved photoelectron spectroscopy is performed on aqueous guanosine solution to study its excited-state relaxation dynamics.


1988 ◽  
Vol 44 (12) ◽  
pp. 1309-1314 ◽  
Author(s):  
Andrew J. Dixon ◽  
Paul Glyn ◽  
Michael A. Healy ◽  
P.Michael Hodges ◽  
Timothy Jenkins ◽  
...  

2013 ◽  
Vol 15 (27) ◽  
pp. 11402 ◽  
Author(s):  
Franziska Buchner ◽  
Hans-Hermann Ritze ◽  
Jan Lahl ◽  
Andrea Lübcke

2017 ◽  
Vol 19 (4) ◽  
pp. 507-516 ◽  
Author(s):  
Elena Appiani ◽  
Rachele Ossola ◽  
Douglas E. Latch ◽  
Paul R. Erickson ◽  
Kristopher McNeill

The rate constant for the reaction between furfuryl alcohol (FFA) and singlet oxygen (1O2) in aqueous solution was measured as a function of temperature, pH and salt content employing both steady-state photolysis (β value determination) and time-resolved singlet oxygen phosphorescence methods.


2019 ◽  
Author(s):  
Hao Wu ◽  
Jeffrey Ting ◽  
Siqi Meng ◽  
Matthew Tirrell

We have directly observed the <i>in situ</i> self-assembly kinetics of polyelectrolyte complex (PEC) micelles by synchrotron time-resolved small-angle X-ray scattering, equipped with a stopped-flow device that provides millisecond temporal resolution. This work has elucidated one general kinetic pathway for the process of PEC micelle formation, which provides useful physical insights for increasing our fundamental understanding of complexation and self-assembly dynamics driven by electrostatic interactions that occur on ultrafast timescales.


1990 ◽  
Vol 55 (8) ◽  
pp. 1984-1990 ◽  
Author(s):  
José M. Hernando ◽  
Olimpio Montero ◽  
Carlos Blanco

The kinetics of the reactions of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione to form the corresponding monocomplexes have been studied spectrophotometrically in the range 5 °C to 16 °C at I 25 mol l-1 in aqueous solution. In the proposed mechanism for the two complexes, the enol form reacts with the metal ion by parallel acid-independent and inverse-acid paths. The kinetic constants for both pathways have been calculated at five temperatures. Activation parameters have also been calculated. The results are consistent with an associative activation for Fe(H2O)63+ and dissociative activation for Fe(H2O)5(OH)2+. The differences in the results for the complexes of heptanediones studied are interpreted in terms of steric factors.


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