Relaxivity Studies on Dinitroxide and Polynitroxyl Functionalized Dendrimers:  Effect of Electron Exchange and Structure on Paramagnetic Relaxation Enhancement

The 1H NMR relaxivity of o- and p-dinitroxide-substituted phthalate esters and a series of nitroxyl-functionalized poly(propylene imine) dendrimers has been measured in acetonitrile and methanol. Studies of dinitroxide relaxivity indicate that the electron exchange rate has only a small effect on re...

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Veröffentlicht in:The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2003-10, Vol.107 (41), p.8467-8475
Hauptverfasser: Maliakal, Ashok J, Turro, Nicholas J, Bosman, Anton W, Cornel, Jeroen, Meijer, E. W
Format: Artikel
Sprache:eng
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Zusammenfassung:The 1H NMR relaxivity of o- and p-dinitroxide-substituted phthalate esters and a series of nitroxyl-functionalized poly(propylene imine) dendrimers has been measured in acetonitrile and methanol. Studies of dinitroxide relaxivity indicate that the electron exchange rate has only a small effect on relaxivity. Outer-sphere relaxivity has been measured using benzene as a probe molecule. In studies on dendritic polynitroxides, the per-nitroxide-based outer-sphere relaxivity nearly doubles for the generation 5 nitroxyl-functionalized dendrimer as compared to a mononitroxide model. This relaxivity enhancement may be due to crowding of dendrimer surface groups in higher generation dendrimers. Water relaxivity has been measured for these polynitroxides as well, and a significant inner-sphere contribution to relaxivity is found. Dendritic polynitroxides exhibit higher per-nitroxide-based water relaxivity as compared to a mononitroxide model. This relaxivity enhancement is attributed to an increase in rotational correlation time (τc) for the dendritic polynitroxides.
ISSN:1089-5639
1520-5215
DOI:10.1021/jp0350666