@article {4983,
	title = {Seven-coordinate [(ReON4X2)-O-V](+) complexes (X = O and Cl)},
	journal = {Inorganic Chemistry},
	volume = {39},
	number = {26},
	year = {2000},
	note = {ISI Document Delivery No.: 385TFTimes Cited: 10Cited Reference Count: 29},
	month = {Dec},
	pages = {5958-5963},
	type = {Article},
	abstract = {The oxorhenium(V) complexes with ligands containing N-4 (H(2)pmen) and N4O2 (H(2)bbpen, H(2)Clbbpen, and H(2)bped) donor atom sets have been synthesized. X-ray crystallographic analyses of the [ReO(H(2)pmen)Cl-2](+), [ReO(bbpen)](+), and [ReO(bped)](+) complexes showed that all three cations share a rate seven-coordinate structure with a distorted pentagonal bipyramidal geometry, which represents a novel and potentially general structural motif in Re-V=O complexes. H-1 NMR spectroscopy shows that the structures of the complexes are retained in the solution.},
	keywords = {CHELATION, CHEMISTRY, LIGANDS, N3O2, pyridyl, RADIOPHARMACEUTICALS, rhenium, technetium, TRIS(2-PYRIDYLMETHYL)AMINE},
	isbn = {0020-1669},
	url = {<Go to ISI>://000166019200010},
	author = {Xu, L. and Setyawati, I. A. and Pierreroy, J. and Pink, M. and Young, V. G. and Patrick, B. O. and Rettig, S. J. and Orvig, Chris}
}
@article {4410,
	title = {Complexation of gallium(III) by 2-hydroxynicotinic acid and 3-hydroxypicolinic acid in aqueous solution},
	journal = {Inorganica Chimica Acta},
	volume = {273},
	number = {1-2},
	year = {1998},
	note = {ISI Document Delivery No.: ZP204Times Cited: 17Cited Reference Count: 27XXXIII International Conference on Coordination ChemistryAUG 30-SEP 04, 1998FLORENCE, ITALY},
	month = {May},
	pages = {47-53},
	type = {Proceedings Paper},
	abstract = {The deprotonations of 2-hydroxynicotinic acid (H(2)nic) and 3-hydroxypicolinic acid (H(2)pic) and the complexation of these molecules with Ga3+ were studied by H-1 NMR, UV-Vis spectrophotometry and potentiometric titration. Both ligands bind Ga3+ at very low pH; the ligand binds in the monodeprotonated form. The stability constants of the [Ga(HL)(n)]((3-n)+) (L = nic or pic; n = 1, 2, or 3) complexes were measured at 25 degrees C, 1.0 M NaCl (for beta(1)) and 0.16 M NaCl (for beta(2) and beta(3)); for H(2)nic (H(2)pic), log beta(1) = 6.78 (7.04), log beta(2) = 12.43 (13.09) and log beta(3) = 16.20 (17.74). At higher pH, polynuclear mixed ligand-hydroxo species form, although their composition and stability could not be determined. These complexes undergo hydrolysis to form [Ga(OH)(4)](-) above pH 7. (C) 1998 Elsevier Science S.A. All rights reserved.},
	keywords = {3-HYDROXY-4-PYRIDINONES, aluminum, CHELATION, CHEMISTRY, COMPLEXES, EQUILIBRIUM, GA-68, gallium complexes, hydroxynicotinic acid, hydroxypicolinic acid complexes, INDIUM COMPLEXES, INVIVO, LIGANDS, RADIOPHARMACEUTICALS},
	isbn = {0020-1693},
	url = {<Go to ISI>://000073728200008},
	author = {Stephens, A. K. W. and Orvig, Chris}
}
@article {3855,
	title = {Selectivity of potentially hexadentate amine phenols for Ga3+ and In3+ in aqueous solution},
	journal = {Inorganic Chemistry},
	volume = {35},
	number = {3},
	year = {1996},
	note = {ISI Document Delivery No.: TT717Times Cited: 29Cited Reference Count: 48},
	month = {Jan},
	pages = {715-724},
	type = {Article},
	abstract = {{A new series of linear N4O2 amine phenols (H(2)badd, H(2)Brbadd, and H(2)Clbadd) based on N,N{\textquoteright}-bis(3-aminopropyl)-ethylenediamine (tnentn) were prepared and characterized by spectroscopic techniques. Monocationic hexadentate metal complexes with the tnentn-based amine phenols were obtained from the reactions of Ga3+ and In3+ with the Linear amine phenol in the presence of a weak base (acetate). The molecular structure of [Ga(Brbadd)]ClO4 has been determined by X-ray crystallography; crystals of [Ga(Brbadd)][ClO4] (C22H30Br2ClGaN4O6) are orthorhombic: a = 12.462(1) Angstrom},
	keywords = {ACID, aluminum, CHELATION, CRYSTAL, GA-68, gallium, IONS, LIGANDS, STABILITIES, TRIVALENT METAL-COMPLEXES},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1996TT71700029},
	author = {Wong, E. and Caravan, P. and Liu, S. and Rettig, S. J. and Orvig, Chris}
}
@article {2952,
	title = {PHARMACOKINETICS OF ALUMINUM 3-HYDROXYPYRIDIN-4-ONE COMPLEXES - IMPLICATIONS FOR ALUMINUM REDISTRIBUTION SUBSEQUENT TO CHELATION-THERAPY},
	journal = {Toxicology},
	volume = {92},
	number = {1-3},
	year = {1994},
	note = {ISI Document Delivery No.: PK035Times Cited: 14Cited Reference Count: 34},
	month = {Sep},
	pages = {193-202},
	type = {Article},
	abstract = {The pharmacokinetics of selected aluminum-hydroxypyridinone (Al-HP) complexes were determined in rats to better understand the relationship between their disposition and elimination parameters and the safety of HPs in the chelation therapy of Al intoxication. Five complexes were administered as i.v. bolus doses of Al-HP (0.25 mmol/kg Al-0.75 mmol/kg HP). The Al-HP steady state volumes of distribution ranged from 220 to 871 ml/kg, suggesting that each complex distributed out of the vascular compartment (which should have been approximate to 65 ml/kg). Systemic clearances ranged from 189 to 906 ml/h per kg. Elimination half-lives (t(1/2)) and mean residence times ranged from 0.36 to 0.84 and 0.52 to 1.20 h, respectively. The Al-CP20 complex had a short t(1/2) and a midrange volume of distribution. It demonstrated no apparent toxicity, whereas myoclonic seizures were observed after Al-CP22, Al-CP24 and Al-CP94 administration. The most appropriate choice for Al chelation among the HPs tested may be CP20. Characterization of the distribution and elimination of Al-HP complexes improves the understanding of potential toxicity that may be associated with HP therapy of Al intoxication.},
	keywords = {3-HYDROXY-4-PYRIDINONES, 3-HYDROXYPYRIDIN-4-ONES, aluminum, ALUMINUM CHELATION, ALUMINUM TOXICITY, CHELATION, DESFERRIOXAMINE, ENCEPHALOPATHY, gallium, INTOXICATION, INVITRO, IRON CHELATORS, OCULAR TOXICITY, pharmacokinetics, RENAL-FAILURE, SUBCUTANEOUS DEFEROXAMINE},
	isbn = {0300-483X},
	url = {<Go to ISI>://A1994PK03500015},
	author = {Allen, D. D. and Orvig, Chris and Yokel, R. A.}
}
@article {2837,
	title = {ROUTES TO RUTHENIUM(II) BROMO(SULFOXIDE) COMPLEXES, INCLUDING THE SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF A NEUTRAL DILITHIUM DIRUTHENIUM(II) COMPLEX CONTAINING TERMINAL AND BRIDGING TETRAMETHYLENE SULFOXIDE LIGANDS},
	journal = {Inorganica Chimica Acta},
	volume = {207},
	number = {1},
	year = {1993},
	note = {ISI Document Delivery No.: LB776Times Cited: 7Cited Reference Count: 36},
	month = {May},
	pages = {97-103},
	type = {Article},
	abstract = {{The dimeric Ru(II) complex [Br6(TMSO)2Ru2(mu2-TMSO)2(mu3-TMSO)2Li2(TMSO)2] (1) has been isolated from solutions containing RuCl3.3H3O, LiBr and TMSO (TMSO = tetramethylene sulfoxide, O and S indicating oxygen- and sulfur-bonding, respectively). Crystals of 1 are monoclinic},
	keywords = {CHELATION, CRYSTAL-STRUCTURE, DIMETHYLSULFOXIDE, OXIDATION, SOLUTION CHEMISTRY, SULFOXIDE)RUTHENIUM(II), SULFOXIDE)TETRACHLORORUTHENATE(III), VERSATILE STARTING MATERIALS},
	isbn = {0020-1693},
	url = {<Go to ISI>://A1993LB77600014},
	author = {Jaswal, J. S. and Yapp, D. T. T. and Rettig, S. J. and James, Brian R. and Skov, K. A.}
}
