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The H<jats:sub>4<\/jats:sub>DOTP<jats:sup>H<\/jats:sup>, H<jats:sub>4<\/jats:sub>DOTP<jats:sup>hm<\/jats:sup> and H<jats:sub>4<\/jats:sub>DOTP<jats:sup>OEt<\/jats:sup> ligands and their Ln<jats:sup>III<\/jats:sup> complexes were characterized by potentiometry and time\u2010resolved luminescence; the Gd<jats:sup>III<\/jats:sup> complexes are thermodynamically much less stable than that of H<jats:sub>4<\/jats:sub>DOTA, and no water is coordinated in the inner sphere. The crystal structures of the free ligand H<jats:sub>4<\/jats:sub>DOTP<jats:sup>OEt<\/jats:sup> and of the Gd<jats:sup>III<\/jats:sup> complexes of H<jats:sub>4<\/jats:sub>DOTP<jats:sup>H<\/jats:sup> and H<jats:sub>4<\/jats:sub>DOTP<jats:sup>OEt<\/jats:sup> were determined by X\u2010ray diffraction. The complexes have the expected octadentate coordination mode with an N<jats:sub>4<\/jats:sub>O<jats:sub>4<\/jats:sub> arrangement; no water molecule is bound to the Gd<jats:sup>III<\/jats:sup> ion. Information on the structures of the Ln<jats:sup>III<\/jats:sup> complexes of all five ligands in aqueous solution were obtained from <jats:sup>1<\/jats:sup>H and <jats:sup>31<\/jats:sup>P NMR spectra. The NMR spectra of the [Ln(DOTP<jats:sup>hm<\/jats:sup>)]<jats:sup>\u2013<\/jats:sup> and [Ln(DOTP<jats:sup>Et<\/jats:sup>)]<jats:sup>\u2013<\/jats:sup> complexes show that these compounds have a clear preference for a specific arrangement of phosphorus atoms which gives rise to the symmetrical <jats:italic>RRRR<\/jats:italic> (or <jats:italic>SSSS<\/jats:italic>) isomer. However, many diastereoisomers were observed for all other complexes. Ln<jats:sup>III<\/jats:sup>\u2010induced <jats:sup>17<\/jats:sup>O NMR shift data reveal that the spatial location of the second\u2010sphere water molecules for the two groups of complexes differs. The parameters governing the effect of the second hydration sphere on the relaxivity of the Gd<jats:sup>III<\/jats:sup> complexes of all ligands were evaluated by EPR, variable\u2010temperature <jats:sup>17<\/jats:sup>O NMR spectroscopy and <jats:sup>1<\/jats:sup>H NMRD relaxometry. The presence of second\u2010sphere water molecules is clearly confirmed, depending on the character of the pendant arms. As the relaxivity does not depend significantly on the nature of the phosphorus substituents and\/or on the isomerism present in solution, the second\u2010sphere water molecules should be located close to the phosphorus\u2013oxygen atoms.(\u00a9 Wiley\u2010VCH Verlag GmbH &amp; Co. KGaA, 69451 Weinheim, Germany, 2009)<\/jats:p>","DOI":"10.1002\/ejic.200800859","type":"journal-article","created":{"date-parts":[[2008,11,7]],"date-time":"2008-11-07T05:10:12Z","timestamp":1226034612000},"page":"119-136","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":63,"title":["Lanthanide(III) Complexes of Phosphorus Acid Analogues of H<sub>4<\/sub>DOTA as Model Compounds for the Evaluation of the Second\u2010Sphere Hydration"],"prefix":"10.1002","volume":"2009","author":[{"given":"Zuzana","family":"Kotkov\u00e1","sequence":"first","affiliation":[]},{"given":"Giovannia A.","family":"Pereira","sequence":"additional","affiliation":[]},{"given":"Kristina","family":"Djanashvili","sequence":"additional","affiliation":[]},{"given":"Jan","family":"Kotek","sequence":"additional","affiliation":[]},{"given":"Jakub","family":"Rudovsk\u00fd","sequence":"additional","affiliation":[]},{"given":"Petr","family":"Hermann","sequence":"additional","affiliation":[]},{"given":"Luce","family":"Vander Elst","sequence":"additional","affiliation":[]},{"given":"Robert N.","family":"Muller","sequence":"additional","affiliation":[]},{"given":"Carlos F. 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