@article {1267,
	title = {Carbohydrate-appended 2,2 {\textquoteright}-dipicolylamine metal complexes as potential imaging agents},
	journal = {Inorganic Chemistry},
	volume = {44},
	number = {8},
	year = {2005},
	note = {ISI Document Delivery No.: 916GWTimes Cited: 44Cited Reference Count: 58},
	month = {Apr},
	pages = {2698-2705},
	type = {Article},
	abstract = {Three discrete carbohydrate-appended 2,2{\textquoteright}-dipicolylamine ligands were complexed to the {M(CO)3}(+) (M = Tc-99m/ Re) core: 2-(bis(2-pyridinylmethyl)amino)ethyl-beta-D-glucopyranoside (L-1), 2-(bis(2-pyridinylmethyl)amino)ethyl-beta-Dxylopyranoside (L-2), and 2-(bis(2-pyridinylmethyl)amino)ethyl-alpha-D-mannopyranoside (L-3). An ethylene spacer is used to separate the carbohydrate moiety and the dipicolylamine (DPA) function in all three ligands. The Re complexes [Re(L1-3)(CO)(3)]Br were characterized by H-1 and C-13 1D/2D NMR spectroscopies, which confirmed the pendant nature of the carbohydrate moieties in solution. NMR measurements also established the long-range asymmetric effect of the carbohydrate functions on the chelating portion of the ligand. One analogue, [Re(L-1)(CO)(3)]Cl, was characterized in the solid state by X-ray crystallography. Further characterization was provided by IR spectroscopy, elemental analysis, conductivity, and mass spectrometry. Radiolabeling of L-1-L-3 with [Tc-99m(H2O)(3)(CO)(3)](+) afforded high yield compounds of identical character to the Re analogues. The radiolabeled compounds were found to be stable toward ligand exchange in the presence of a large excess of either cysteine or histidine over a 24-h period.},
	keywords = {AMINO-SUGARS, ANTITUMOR-ACTIVITY, BOMBESIN ANALOG, D-GLUCOSE, HIGH-AFFINITY, IN-VITRO, LIGANDS, PALLADIUM(II) COMPLEXES, RHENIUM CARBONYL-COMPLEXES, STRUCTURAL-CHARACTERIZATION, TRIDENTATE},
	isbn = {0020-1669},
	url = {<Go to ISI>://000228374400020},
	author = {Storr, T. and Sugai, Y. and Barta, C. A. and Mikata, Y. and Adam,Michael J. and Yano, S. and Orvig, Chris}
}
@article {1267,
	title = {Carbohydrate-appended 2,2 {\textquoteright}-dipicolylamine metal complexes as potential imaging agents},
	journal = {Inorganic Chemistry},
	volume = {44},
	number = {8},
	year = {2005},
	note = {ISI Document Delivery No.: 916GWTimes Cited: 44Cited Reference Count: 58},
	month = {Apr},
	pages = {2698-2705},
	type = {Article},
	abstract = {Three discrete carbohydrate-appended 2,2{\textquoteright}-dipicolylamine ligands were complexed to the {M(CO)3}(+) (M = Tc-99m/ Re) core: 2-(bis(2-pyridinylmethyl)amino)ethyl-beta-D-glucopyranoside (L-1), 2-(bis(2-pyridinylmethyl)amino)ethyl-beta-Dxylopyranoside (L-2), and 2-(bis(2-pyridinylmethyl)amino)ethyl-alpha-D-mannopyranoside (L-3). An ethylene spacer is used to separate the carbohydrate moiety and the dipicolylamine (DPA) function in all three ligands. The Re complexes [Re(L1-3)(CO)(3)]Br were characterized by H-1 and C-13 1D/2D NMR spectroscopies, which confirmed the pendant nature of the carbohydrate moieties in solution. NMR measurements also established the long-range asymmetric effect of the carbohydrate functions on the chelating portion of the ligand. One analogue, [Re(L-1)(CO)(3)]Cl, was characterized in the solid state by X-ray crystallography. Further characterization was provided by IR spectroscopy, elemental analysis, conductivity, and mass spectrometry. Radiolabeling of L-1-L-3 with [Tc-99m(H2O)(3)(CO)(3)](+) afforded high yield compounds of identical character to the Re analogues. The radiolabeled compounds were found to be stable toward ligand exchange in the presence of a large excess of either cysteine or histidine over a 24-h period.},
	keywords = {AMINO-SUGARS, ANTITUMOR-ACTIVITY, BOMBESIN ANALOG, D-GLUCOSE, HIGH-AFFINITY, IN-VITRO, LIGANDS, PALLADIUM(II) COMPLEXES, RHENIUM CARBONYL-COMPLEXES, STRUCTURAL-CHARACTERIZATION, TRIDENTATE},
	isbn = {0020-1669},
	url = {<Go to ISI>://000228374400020},
	author = {Storr, T. and Sugai, Y. and Barta, C. A. and Mikata, Y. and Adam,Michael J. and Yano, S. and Orvig, Chris}
}
@article {2863,
	title = {HIGHLY FLEXIBLE CHELATING LIGANDS FOR GROUP 13 METALS - DESIGN AND SYNTHESIS OF HEXADENTATE (N3O3) TRIPODAL AMINE PHENOL LIGAND COMPLEXES OF ALUMINUM, GALLIUM, AND INDIUM},
	journal = {Inorganic Chemistry},
	volume = {32},
	number = {9},
	year = {1993},
	note = {ISI Document Delivery No.: KZ801Times Cited: 48Cited Reference Count: 38},
	month = {Apr},
	pages = {1756-1765},
	type = {Article},
	abstract = {{New, potentially hexadentate (N3O3) amine phenol ligands (H3IIa = 1,1,1-tris(((2{\textquoteright}-hydroxybenzyl)amino)methyl)ethane; H3IIb = 1,1,1-tris(((5{\textquoteright}-chloro-2{\textquoteright}-hydroxybenzyl)amino)methyl)ethane; H3IIC = 1,1,1-tris(((5{\textquoteright}-bromo-2{\textquoteright}-hydroxybenzyl)amino)methyl)ethane; H3IId = 1,1,1-tris(((3{\textquoteright},5{\textquoteright}-dichloro-2{\textquoteright}-hydroxybenzyl)amino)methyl)ethane) have been prepared and characterized by various spectroscopic methods (IR, FAB-MS, NMR). The N3O3 amine phenols are KBH4 reduction products of the corresponding Schiff bases derived from the condensation reactions of 1,1,1-tris(2-aminomethyl)ethane (tame) with 3 equiv of either salicylaldehyde or ring-substituted salicylaldehydes. Neutral binary metal complexes, [M(L)] (M = Al, Ga, In; L = IIa, IIb, IIc, IId) were obtained from the reactions of Al3+, Ga3+, or In3+ With N3O3 amine phenols in the presence of 3 equiv of a base (acetate or hydroxide). The molecular structures of [AI(IIc)]4[Na(H2O)]2)(ClO4)2.6.2H2O, [Ga(IIa)].4.4H2O, and [In(IIa)].4.6H2O were determined by X-ray methods. Crystals of [Al(IIc)]4[Na(H2O)]2(ClO4)2.6.2H2O are orthorhombic, Pbcn},
	keywords = {FE(III), GA(III), HEXAKIS(THIOETHER) COORDINATION, IN(III), IONS, Iron(III), MOLECULAR-STRUCTURE, STABILITIES, TRIDENTATE},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1993KZ80100036},
	author = {Liu, S. and Wong, E. and Karunaratne, V. and Rettig, S. J. and Orvig, Chris}
}
