American Chemical Society, The Journal of Physical Chemistry A, 41(107), p. 8467-8475, 2003
DOI: 10.1021/jp0350666
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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.