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Gd3TCAS2: An Aquated Gd3+-Thiacalix[4]arene Sandwich Cluster with Extremely Slow Ligand Substitution Kinetics
Author(s) -
Nobuhiko Iki,
Eszter Boros,
Mami Nakamura,
Ryo Baba,
Peter Caravan
Publication year - 2016
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.6b00241
Subject(s) - chemistry , kinetics , dissociation (chemistry) , transmetalation , aqueous solution , ligand (biochemistry) , ion exchange , gadolinium , ion , crystallography , inorganic chemistry , catalysis , organic chemistry , biochemistry , physics , receptor , quantum mechanics
In aqueous solution, Gd(3+) and thiacalix[4]arene-p-tetrasulfonate (TCAS) form the complex [Gd3TCAS2](7-), in which a trinuclear Gd(3+) core is sandwiched by two TCAS ligands. Acid-catalyzed dissociation reactions, as well as transmetalation and ligand exchange with physiological concentrations of Zn(2+) and phosphate, showed [Gd3TCAS2](7-) to be extremely inert compared to other Gd complexes. Luminescence lifetime measurements of the Tb analogue Tb3TCAS2 allowed estimation of the mean hydration number q to be 2.4 per Tb ion. The longitudinal relaxivity of [Gd3TCAS2](7-) (per Gd(3+)) was r1 = 5.83 mM(-1) s(-1) at 20 Hz (37 °C, pH 7.4); however, this relaxivity was limited by an extremely slow water exchange rate that was 5 orders of magnitude slower than the Gd(3+) aqua ion. Binding to serum albumin resulted in no relaxivity increase owing to the extremely slow water exchange kinetics. The slow dissociation and water exchange kinetics of [Gd3TCAS2](7-) can be attributed to the very rigid coordination geometry.

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