scholarly journals A method to calculate the NMR spectra of paramagnetic species using thermalized electronic relaxation

2021 ◽  
pp. 106939
Author(s):  
Andrew J. Pell
1986 ◽  
Vol 64 (1) ◽  
pp. 71-75 ◽  
Author(s):  
Daniel Cozak ◽  
François Gauvin ◽  
Jacques Demers

The paramagnetic 1H nmr spectra for manganocene (1) and 1.1′-dimethylmanganocene (2), and the 13C nmr spectra for 1,1′-diethylmanganocene (3) have been recorded in toluene solvent over a −90 to 90 °C temperature range. 1 shows a low field and a high field ring proton resonance in its spectrum near −59 °C. At higher temperatures the low field resonance is prevalent and becomes gradually averaged due to a fast spin exchange process that dominates the spectrum at 90 °C. For the ring substituted derivatives 2 and 3, resonances due to only one paramagnetic species were detected in the low temperature range. Above ambient temperature a new spectrum due to rapid spin exchange averaging is observed for these complexes. Results are readily interpreted in terms of ground state molecular cross-over exchanges between the 2E2g, 6A1g, and 2A1g spin states of the complexes.


2004 ◽  
Vol 852 ◽  
Author(s):  
Eleonora Del Federico ◽  
Wolfgang Schoefberger ◽  
Rajeev Kumar ◽  
Wen Ling ◽  
Sofia M. Kapetanaki ◽  
...  

ABSTRACTWe report on a study of ultramarine pigments via Colorimetry, resonance Raman, and 27Al, 29Si solid-state NMR spectroscopy. NMR parameters are shown to correlate well with the intensities of Raman signals corresponding to the chromophores S3−. and S2−.. Further, a correlation is established between the colorimetric parameters L* (lightness) and C* (chromaticity) and the paramagnetic shift in NMR spectra for both 27Al and 29Si. The parameter h (hue) appeared not to vary over the range of paramagnetic host concentrations studied. Preliminary results on faded pigments in both acidic and basic media show that the concentration of diamagnetic guest molecules in the sodalite lattice rises, and some of the paramagnetic species are replaced.


1985 ◽  
Vol 46 (7) ◽  
pp. 1205-1209 ◽  
Author(s):  
R. Blinc ◽  
S. Žumer ◽  
D.C. Ailion ◽  
J. Nicponski

1980 ◽  
Vol 41 (C1) ◽  
pp. C1-25-C1-31 ◽  
Author(s):  
N. S. Dixon ◽  
L. S. Fritz ◽  
Y. Mahmud ◽  
B. B. Triplett ◽  
S. S. Hanna ◽  
...  

2020 ◽  
Author(s):  
Pankaj Attri ◽  
Anan Teruki ◽  
Ryo Arita ◽  
Takamasa Okumura ◽  
Hayate Tanaka ◽  
...  

2019 ◽  
Author(s):  
Matthew M. Brister ◽  
Carlos Crespo-Hernández

<p></p><p> Damage to RNA from ultraviolet radiation induce chemical modifications to the nucleobases. Unraveling the excited states involved in these reactions is essential, but investigations aimed at understanding the electronic-energy relaxation pathways of the RNA nucleotide uridine 5’-monophosphate (UMP) have not received enough attention. In this Letter, the excited-state dynamics of UMP is investigated in aqueous solution. Excitation at 267 nm results in a trifurcation event that leads to the simultaneous population of the vibrationally-excited ground state, a longlived <sup>1</sup>n<sub>O</sub>π* state, and a receiver triplet state within 200 fs. The receiver state internally convert to the long-lived <sup>3</sup>ππ* state in an ultrafast time scale. The results elucidate the electronic relaxation pathways and clarify earlier transient absorption experiments performed for uracil derivatives in solution. This mechanistic information is important because long-lived nπ* and ππ* excited states of both singlet and triplet multiplicities are thought to lead to the formation of harmful photoproducts.</p><p></p>


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