@article {2494,
	title = {N,O-Chelates of Group 4 Metals: Contrasting the Use of Amidates and Ureates in the Synthesis of Metal Dichlorides},
	journal = {European Journal of Inorganic Chemistry},
	number = {18},
	year = {2009},
	note = {ISI Document Delivery No.: 467LNTimes Cited: 5Cited Reference Count: 69Leitch, David C. Beard, J. David Thomson, Robert K. Wright, Vincent A. Patrick, Brian O. Schafer, Laurel L.},
	month = {Jun},
	pages = {2691-2701},
	type = {Article},
	abstract = {A series of dichloride complexes of titanium and zirconium with amidate and ureate ancillary ligands have been prepared, Three examples of bis(amidate)dichlorotitanium and zirconium complexes were effectively synthesized through salt metathesis with metal tetrachloride as starting materials. Optimum results were achieved using sodium amidate salts formed from sodium bis(trimethylsilyl)amide and neutral amide proligands, while other methods were ineffective. Use of electron-donating ureate ligands in lieu of amidates enables preparation through alternate routes. Protonolysis of Ti(NMe2)(2)Cl-2 and Zr(NMe2)(2)Cl-2(dme) with urea proligands leads to dichlorobis(ureate) complexes in good yield. Using a tethered bis(ureate) ligand eliminates the fluxional behaviour and coordination isomerism observed for both bis(amidate) and bis(ureate) zirconium complexes. ((C) Wiley-VCH Verlag GmbH \& Co. KGaA, 69451 Weinheim, Germany, 2009)},
	keywords = {amidate, BIS(AMIDATE) TITANIUM PRECATALYST, CATALYTIC, Chelates, COORDINATION CHEMISTRY, EARLY, GUANIDINATE LIGANDS, HYDROAMINATION, INTERMOLECULAR HYDROAMINATION, N, O ligands, OLEFIN POLYMERIZATION, SOLUTION DYNAMICS, STRUCTURAL-CHARACTERIZATION, TITANIUM, TRANSITION-METALS, Ureate, ZIEGLER-NATTA POLYMERIZATION, ZIRCONIUM},
	isbn = {1434-1948},
	url = {<Go to ISI>://000267740500015},
	author = {Leitch, D. C. and Beard, J. D. and Thomson, R. K. and Wright, V. A. and Patrick, B. O. and Schafer, L. L.}
}
@article {2063,
	title = {Chiral Ligand Design: A Bidentate Ligand Incorporating an Acyclic Phosphaalkene},
	journal = {Angewandte Chemie-International Edition},
	volume = {47},
	number = {42},
	year = {2008},
	note = {ISI Document Delivery No.: 360YLTimes Cited: 7Cited Reference Count: 71Dugal-Tessier, Julien Dake, Gregory R. Gates, Derek P.},
	pages = {8064-8067},
	type = {Article},
	keywords = {ALKYLATION, ALLYLIC, BEARING DIPHOSPHINIDENECYCLOBUTENE LIGANDS, BIPHOSPHININE COMPLEXES, CATALYZED ASYMMETRIC, CLAISEN REARRANGEMENT, COORDINATION PROPERTIES, ENANTIOSELECTIVE ISOMERIZATION, ETHYLENE POLYMERIZATION, HIGHLY-ACTIVE CATALYSTS, HYDROGENATION, IRIDIUM, ligand design, N, P-ligands, PHOSPHAALKENES, PHOSPHORUS, PI-ACCEPTOR LIGANDS},
	isbn = {1433-7851},
	url = {<Go to ISI>://000260094600016},
	author = {Dugal-Tessier, J. and Dake, G. R. and Gates, D. P.}
}
@article {2259,
	title = {Rare-earth amidate complexes. Easily accessed initiators for epsilon-caprolactone ring-opening polymerization},
	journal = {Inorganic Chemistry},
	volume = {47},
	number = {18},
	year = {2008},
	note = {ISI Document Delivery No.: 346UBTimes Cited: 8Cited Reference Count: 76Stanlake, Louisa J. E. Beard, J. David Schafer, Laurel L.},
	month = {Sep},
	pages = {8062-8068},
	type = {Article},
	abstract = {{The direct synthesis of yttrium amidate complexes using the simple reaction of amide proligands and Y(N(SiMe3)(2))(3) results in the high-yielding preparation and isolation of crystalline, monomeric materials. The complex, tris(N-2{\textquoteright},6{\textquoteright}-diisopropylphenyl(naphthyl)amidate)yttrium mono(tetrahydrofuran) (4), was structurally determined to be a 7-coordinate C, symmetric structure, maintaining one bound tetrahydrofuran molecule. Compound 4 (C12H17[NCO]C10H1)(3)Y(C4H8O) crystallized in the monoclinic space group P2(1)/c with a = 13.7820(11) angstrom},
	keywords = {BETA-DIKETIMINATE, BIS(AMIDATE) TITANIUM PRECATALYST, CATALYTIC-ACTIVITY, COMPLEXES, LANTHANIDE, METHYL-METHACRYLATE, MOLECULAR-STRUCTURES, N, ORGANOLANTHANIDE, PHENYL ISOCYANATE, RAY CRYSTAL-STRUCTURES, SIGMA-BOND},
	isbn = {0020-1669},
	url = {<Go to ISI>://000259093700022},
	author = {Stanlake, L. J. E. and Beard, J. D. and Schafer, L. L.}
}
@article {729,
	title = {Synthesis and molecular structure of 4-methoxyphenyl-2 {\textquoteright}-pyrrolylthione and its rhenium complex},
	journal = {Inorganica Chimica Acta},
	volume = {349},
	year = {2003},
	note = {ISI Document Delivery No.: 692RBTimes Cited: 4Cited Reference Count: 17},
	month = {Jun},
	pages = {58-64},
	type = {Article},
	abstract = {{A bidentate monoanionic N,S-ligand, 4-methoxyphenyl-2{\textquoteright}-pyrrolylthione (1) was synthesised via an oxygen-to-sulphur exchange in the corresponding ketone and then fully characterised. A trinuclear complex (2) of rhenium with this compound was obtained in a reaction of KReO4 with 1 in the presence of a reducing agent in aqueous ethanol, followed by slow precipitation from chloroform-hexane. The structure of compound 2 corresponds to the formula [Re3O4(C12H10NOS)(6)](+1)[ReO4](-1).2CH(3)CH(2)OH. A single crystal X-ray diffraction study was performed for this complex. The following crystal data were obtained for 2: M-r = 2262.556, monoclinic, space group C2/c},
	keywords = {4-methoxyphenyl-2 {\textquoteright}-pyrrolylthione, CRYSTAL-STRUCTURE, LIGAND, N, S-ligand, X-ray diffraction study},
	isbn = {0020-1693},
	url = {<Go to ISI>://000183673100008},
	author = {Selivanova, S. V. and Dolphin, D. and van Lier, J. E. and Kudrevich, S. V.}
}
@article {553,
	title = {Facile synthesis of N,N {\textquoteright}-dimethylated N-confused porphyrins},
	journal = {Tetrahedron},
	volume = {58},
	number = {44},
	year = {2002},
	note = {ISI Document Delivery No.: 608QCTimes Cited: 4Cited Reference Count: 8},
	month = {Oct},
	pages = {9111-9116},
	type = {Article},
	abstract = {N-Confused tetraarylporphyrins react with CH3I in the presence of Na2CO3 to give, in high yield, N,N{\textquoteright}-dimethylated N-confused porphyrin salts, which are mixtures of structural isomers. The structures of the major isomers were determined by X-ray diffraction and NMR spectroscopic analyses. These N,N{\textquoteright}-dimethylated N-confused tetraarylporphyrin salts generate singlet oxygen when irradiated at long wavelengths in the visible region, and therefore, are potential sensitizers for photodynamic therapy. (C) 2002 Elsevier Science Ltd. All rights reserved.},
	keywords = {ISOMER, METHYLATION, N, N {\textquoteright}-dimethylated N-confused porphyrin, N-confused porphyrin, RING, singlet oxygen, TETRAPHENYLPORPHYRIN},
	isbn = {0040-4020},
	url = {<Go to ISI>://000178857300026},
	author = {Xiao, Z. W. and Dolphin, D.}
}
@article {3928,
	title = {Effect of pyridyl donors in the chelation of aluminum(III), gallium(III), and indium(III)},
	journal = {Inorganic Chemistry},
	volume = {36},
	number = {7},
	year = {1997},
	note = {ISI Document Delivery No.: WQ490Times Cited: 18Cited Reference Count: 62},
	month = {Mar},
	pages = {1306-1315},
	type = {Article},
	abstract = {{A new preparation of N,N{\textquoteright}-bis(2-pyridylmethyl)ethylenediamine-N,N{\textquoteright}-diacetic acid (H(2)bped) is reported, and its properties of complexation with Al(III), Ga(III), In(III), and Co(III) are investigated. The molecular structure of the cobalt(III) complex [Co(bped)]PF6 . CH3CN . H2O (C20H25CoF6N5O5P) has been solved by X-ray methods; the complex crystallizes in the triclinic space group P (1) over bar, with a = 10.611(2) Angstrom},
	keywords = {AQUEOUS-SOLUTION, BINDING CONSTANTS, COMPLEXES, COORDINATION, CRYSTAL-STRUCTURES, LIGANDS, METAL-IONS, MULTINUCLEAR MAGNETIC-RESONANCE, N, N{\textquoteright}-BIS(2-HYDROXYBENZYL)ETHYLENEDIAMINE-N, N{\textquoteright}-DIACETIC ACID, STABILITY},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1997WQ49000006},
	author = {Caravan, P. and Rettig, S. J. and Orvig, Chris}
}
@article {7397,
	title = {POTENTIAL GA-67 RADIOPHARMACEUTICALS FOR MYOCARDIAL IMAGING - TRIS(1-ARYL-3-HYDROXY-2-METHYL-4-PYRIDINONATO)GALLIUM(III) COMPLEXES},
	journal = {Nuclear Medicine and Biology},
	volume = {19},
	number = {3},
	year = {1992},
	note = {ISI Document Delivery No.: HL213Times Cited: 36Cited Reference Count: 33},
	month = {Apr},
	pages = {327-335},
	type = {Article},
	abstract = {A series of highly lipophilic complexes of 1-aryl-3-hydroxy-2-methyl-4-pyridinones with gallium(III)-67 has been evaluated in vitro and in vivo as potential radiopharmaceuticals. The pyridinones have different substituents at the para -position of the phenyl ring: R = H, CH3, OCH3 and NO2. Biodistribution studies of Ga-67 complexes have been carried out in rabbits, mice, rats and a dog. High heart uptake of the radionuclide has been shown in rabbits and the dog. The different biodistribution patterns in mice and rats indicate that there is a species difference in the biodistribution of these complexes. Rabbits and the dog show rapid heart uptake and blood clearance. The speciation of the Ga3+ ion in vivo is simulated in vitro with a simple blood plasma model based on the available thermodynamic data.},
	keywords = {3-HYDROXY-4-PYRIDINONES, aluminum, BIODISTRIBUTION, CHELATING LIGAND, CHEMISTRY, gallium, INDIUM COMPLEXES, MULTIDENTATE LIGANDS, N, N{\textquoteright}-DIACETIC ACID, N{\textquoteright}-DIPYRIDOXYLETHYLENEDIAMINE-N, TRIVALENT METAL-IONS},
	isbn = {0883-2897},
	url = {<Go to ISI>://A1992HL21300012},
	author = {Zhang, Z. H. and Lyster, D. M. and Webb, G. A. and Orvig, Chris}
}
