@article {2060,
	title = {Scalarane-based metabolites isolated from the antimitotic extract of the marine sponge Hyrtios erectus},
	journal = {Natural Product Research},
	volume = {22},
	number = {15},
	year = {2008},
	note = {ISI Document Delivery No.: 378PRTimes Cited: 1Cited Reference Count: 9Diaz-Marrero, Ana R. Matainaho, Teatulohi van Soest, Rob Roberge, Michel Andersen, Raymond J.},
	pages = {1304-1309},
	type = {Article},
	abstract = {Two novel sesterterpenes, 1 and 3, containing a scalarane-based framework, have been isolated from the sponge Hyrtios erectus collected in Papua New Guinea. Their structures and relative stereochemistry have been elucidated by analysis of their spectroscopic data.},
	keywords = {AGENTS, ANTICANCER DRUGS, cell-based assay, CYTOTOXIC SESTERTERPENES, cytotoxicity, scalarane framework, seterterpenoids},
	isbn = {1478-6419},
	url = {<Go to ISI>://000261336900003},
	author = {Diaz-Marrero, A. R. and Matainaho, T. and Van Soest, R. and Roberge, M. and Andersen, R. J.}
}
@article {1600,
	title = {Metal complexes in medicinal chemistry: new vistas and challenges in drug design},
	journal = {Dalton Transactions},
	number = {6},
	year = {2006},
	note = {ISI Document Delivery No.: 014YVTimes Cited: 60Cited Reference Count: 44},
	month = {Feb},
	pages = {761-764},
	type = {Article},
	abstract = {An overview is presented of selected metal-bases! pharmaceuticals, either diagnostic or therapeutic, with emphasis on specific attributes and in vivo interactions of these compounds relevant to their use in medicinal applications. Both the advantages and the challenges of this approach are outlined, with possibilities for future developments accentuated.},
	keywords = {AGENTS, BINDING CONSTANTS, BIS(MALTOLATO)OXOVANADIUM(IV), GLUCOSE, HUMAN-SERUM TRANSFERRIN, MODULATION, therapy, TRANSPORT},
	isbn = {1477-9226},
	url = {<Go to ISI>://000235520000001},
	author = {Thompson, K. H. and Orvig, Chris}
}
@article {1153,
	title = {Pre-treatments applied to oxidized aluminum surfaces to modify the interfacial bonding with bis-1,2-(triethoxysilyl)ethane (BTSE) - Part II. Anodized 7075-T6 Al alloy},
	journal = {Applied Surface Science},
	volume = {252},
	number = {5},
	year = {2005},
	note = {ISI Document Delivery No.: 993WHTimes Cited: 6Cited Reference Count: 46},
	month = {Dec},
	pages = {1305-1312},
	type = {Article},
	abstract = {The methods of X-ray pbotoelectron spectroscopy (XPS), secondary-ion mass spectrometry (SIMS), and scanning electron microscopy (SEM) have been used to investigate aspects of the bonding of bis-1,2-(triethoxysilyl)ethane (BTSE) onto anodized samples of 7075-T6 aluminum alloy that have been subjected to the various pre-treatments considered in Part I. The oxide layer thins when this sample is subjected to a Forest Products Laboratory (FPL) treatment; topographical changes are detected by SEM after only 5 min, and the "scallop structures" increase in size for longer times of the FPL treatment. These 7075-Al surfaces adsorb more BTSE than the high-purity Al samples considered in Part I, although the interfacial bonding indicated by the [AlOSi](+)/[Al2O](+) SIMS ratios measured for the former samples are constant for different times of FPL treatment, unlike the situation for high-purity Al. Heating anodized 7075-Al samples, either before or after FPL treatment, has no significant effect on the subsequent BTSE adsorption, but a H-2 plasma treatment can enhance the interfacial Al-O-Si bonding with a decrease in the total BTSE polymerization. (c) 2005 Elsevier B.V. All rights reserved.},
	keywords = {2024-T3, AGENTS, aluminum, corrosion, COUPLING, ESCA, HYDROXIDES, silane adsorption, SIMS, SPECTROSCOPY, surface pre-treatment, THIN-FILMS, X-ray photoelectron, XPS, XPS INVESTIGATIONS, ZIRCONIUM-OXIDE},
	isbn = {0169-4332},
	url = {<Go to ISI>://000233985900015},
	author = {Kim, J. and Teo, M. and Wong, P. C. and Wong, K. C. and Mitchell, K. A. R.}
}
@article {758,
	title = {Boon and bane of metal ions in medicine},
	journal = {Science},
	volume = {300},
	number = {5621},
	year = {2003},
	note = {ISI Document Delivery No.: 675WDTimes Cited: 99Cited Reference Count: 30},
	month = {May},
	pages = {936-939},
	type = {Review},
	abstract = {In biological systems metal ions promote responses that range from deficiency to toxicity. Some, such as iron and zinc, have a known optimal intake range for normal, healthy individuals. Metal ions contained within well-designed molecules already constitute a great boon for the medicinal pharmacopoeia. However, whether essential or not, the threshold for toxicity can be very low. One of the challenges of designing metal-based drugs is to balance the potential toxicity of an active formulation with the substantial positive impact of these increasingly common therapeutic and diagnostic aids.},
	keywords = {AGENTS, COMPLEXES, RADIOPHARMACEUTICALS},
	isbn = {0036-8075},
	url = {<Go to ISI>://000182719800043},
	author = {Thompson, K. H. and Orvig, Chris}
}
@article {569,
	title = {dlf complexes with uniform coordination geometry: Structural and magnetic properties of an LnNi2 core supported by a heptadentate amine phenol ligand},
	journal = {Inorganic Chemistry},
	volume = {42},
	number = {5},
	year = {2003},
	note = {ISI Document Delivery No.: 653EVTimes Cited: 20Cited Reference Count: 37},
	month = {Mar},
	pages = {1576-1583},
	type = {Article},
	abstract = {The synthesis and physical characterization of a series of lanthanide (Ln(III)) and nickel (Ni-II) mixed trimetallic complexes with the heptadentate (N4O3) amine phenol ligand H(3)trn [tris(2{\textquoteright}-hydroxybenzylaminoethyl)amine] has been accomplished in order to extend our understanding of how amine phenol ligands can be used to coaggregate d- and f-block metal ions and to investigate further the magnetic interaction between these ions. The one-pot reaction in methanol of stoichiometric amounts of H(3)trn with NiX2.6H(2)O (X = ClO4, NO3) followed by addition of the corresponding LnX(3).6H(2)O salt, and then base, produces complexes of the general formula [LnNi(2)(trn)(2)]X.nH(2)O.The complexes were characterized by a variety of analytical techniques. Crystals of five of the complexes were grown from methanol solutions and their structures were determined by X-ray analysis: [PrNi2(trn)(2)(CH3OH)]ClO4.4CH(3)-OH.H2O, [SmNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.2H(2)O, [TbNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.3H(2)O, [ErNi2(trn)(2)(CH3OH)]-NO3.6CH(3)OH, and [LuNi2(trn)(2)(CH3OH)]NO3.4.5CH(3)OH.1.5H(2)O. The [LnNi(2)(trn)(2)(CH3OH)](+) complex cation consists of two octahedral Ni-II ions, each of which is encapsulated by the ligand trn(3-) in an N4O2 coordination sphere with one phenolate O atom not bound to Ni-II. Each [Ni(trn)](-) unit acts as a tridentate ligand toward the Ln(III) ion via two bridging and one nonbridging phenolate donors. Remarkably, in all of the structurally characterized complexes, Ln(III) is seven-coordinate and has a flattened pentagonal bipyramidal geometry. Such uniform coordination behavior along the whole lanthanide series is rare and can perhaps be attributed to a mismatch between the geometric requirements of the bridging and nonbridging phenolate donors. Magnetic studies indicate that ferromagnetic exchange occurs in the Ni-II/Ln(II) complexes where Ln = Gd, Tb, Dy, Ho, or Er.},
	keywords = {AGENTS, BLOCK, CRYSTAL-STRUCTURE, DY, EXCHANGE, IONS, LANTHANIDE COMPLEXES, METAL, MOLECULES},
	isbn = {0020-1669},
	url = {<Go to ISI>://000181423000026},
	author = {Bayly, S. R. and Xu, Z. Q. and Patrick, B. O. and Rettig, S. J. and Pink, M. and Thompson, R. C. and Orvig, Chris}
}
@article {569,
	title = {dlf complexes with uniform coordination geometry: Structural and magnetic properties of an LnNi2 core supported by a heptadentate amine phenol ligand},
	journal = {Inorganic Chemistry},
	volume = {42},
	number = {5},
	year = {2003},
	note = {ISI Document Delivery No.: 653EVTimes Cited: 20Cited Reference Count: 37},
	month = {Mar},
	pages = {1576-1583},
	type = {Article},
	abstract = {The synthesis and physical characterization of a series of lanthanide (Ln(III)) and nickel (Ni-II) mixed trimetallic complexes with the heptadentate (N4O3) amine phenol ligand H(3)trn [tris(2{\textquoteright}-hydroxybenzylaminoethyl)amine] has been accomplished in order to extend our understanding of how amine phenol ligands can be used to coaggregate d- and f-block metal ions and to investigate further the magnetic interaction between these ions. The one-pot reaction in methanol of stoichiometric amounts of H(3)trn with NiX2.6H(2)O (X = ClO4, NO3) followed by addition of the corresponding LnX(3).6H(2)O salt, and then base, produces complexes of the general formula [LnNi(2)(trn)(2)]X.nH(2)O.The complexes were characterized by a variety of analytical techniques. Crystals of five of the complexes were grown from methanol solutions and their structures were determined by X-ray analysis: [PrNi2(trn)(2)(CH3OH)]ClO4.4CH(3)-OH.H2O, [SmNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.2H(2)O, [TbNi2(trn)(2)(CH3OH)]NO3.4CH(3)OH.3H(2)O, [ErNi2(trn)(2)(CH3OH)]-NO3.6CH(3)OH, and [LuNi2(trn)(2)(CH3OH)]NO3.4.5CH(3)OH.1.5H(2)O. The [LnNi(2)(trn)(2)(CH3OH)](+) complex cation consists of two octahedral Ni-II ions, each of which is encapsulated by the ligand trn(3-) in an N4O2 coordination sphere with one phenolate O atom not bound to Ni-II. Each [Ni(trn)](-) unit acts as a tridentate ligand toward the Ln(III) ion via two bridging and one nonbridging phenolate donors. Remarkably, in all of the structurally characterized complexes, Ln(III) is seven-coordinate and has a flattened pentagonal bipyramidal geometry. Such uniform coordination behavior along the whole lanthanide series is rare and can perhaps be attributed to a mismatch between the geometric requirements of the bridging and nonbridging phenolate donors. Magnetic studies indicate that ferromagnetic exchange occurs in the Ni-II/Ln(II) complexes where Ln = Gd, Tb, Dy, Ho, or Er.},
	keywords = {AGENTS, BLOCK, CRYSTAL-STRUCTURE, DY, EXCHANGE, IONS, LANTHANIDE COMPLEXES, METAL, MOLECULES},
	isbn = {0020-1669},
	url = {<Go to ISI>://000181423000026},
	author = {Bayly, S. R. and Xu, Z. Q. and Patrick, B. O. and Rettig, S. J. and Pink, M. and Thompson, R. C. and Orvig, Chris}
}
@article {769,
	title = {Spirastrellolide A, an antimitotic macrolide isolated from the Caribbean Marine Sponge Spirastrella Coccinea},
	journal = {Journal of the American Chemical Society},
	volume = {125},
	number = {18},
	year = {2003},
	note = {ISI Document Delivery No.: 675FLTimes Cited: 52Cited Reference Count: 14},
	month = {May},
	pages = {5296-5297},
	type = {Article},
	keywords = {AGENTS, PACLITAXEL, PEPTIDES, TUBULIN},
	isbn = {0002-7863},
	url = {<Go to ISI>://000182682700025},
	author = {Williams, D. E. and Roberge, M. and Van Soest, R. and Andersen, R. J.}
}
@article {701,
	title = {Synthesis and antimitotic/cytotoxic activity of hemiasterlin analogues},
	journal = {Journal of Natural Products},
	volume = {66},
	number = {2},
	year = {2003},
	note = {ISI Document Delivery No.: 652JHTimes Cited: 45Cited Reference Count: 37},
	month = {Feb},
	pages = {183-199},
	type = {Article},
	abstract = {The antimitotic sponge tripeptide hemiasterlin (1) and a number of structural analogues have been synthesized and evaluated in cell-based assays for both cytotoxic and antimitotic activity in order to explore the SAR for this promising anticancer drug lead. One synthetic analogue, SPA110 (8), showed more potent in vitro cytotoxicty and antimitotic activity than the natural product hemiasterlin (1), and consequently it has been subjected to thorough preclinical evaluation and targeted for clinical evaluation. The details of the synthesis of hemiasterlin (1) and the analogues and a discussion of how their biological activities vary with their structures are presented in this paper.},
	keywords = {(-)-HEMIASTERLIN, AGENTS, ALPHA-AMINO-ACIDS, ASYMMETRIC-SYNTHESIS, AZIDATION, CYTOTOXIC PEPTIDES, ELEUTHEROBIN, TRIPEPTIDE, TUBULIN},
	isbn = {0163-3864},
	url = {<Go to ISI>://000181375700005},
	author = {Nieman, J. A. and Coleman, J. E. and Wallace, D. J. and Piers, E. and Lim, L. Y. and Roberge, M. and Andersen, R. J.}
}
@article {5233,
	title = {Lanthanide chemistry with bis{[bis(carboxymethyl)amino]methyl}phosphinate: What does an extra phosphinate group do to EDTA?},
	journal = {Inorganic Chemistry},
	volume = {40},
	number = {15},
	year = {2001},
	note = {ISI Document Delivery No.: 452MHTimes Cited: 9Cited Reference Count: 34},
	month = {Jul},
	pages = {3734-3738},
	type = {Article},
	abstract = {H5XT (bis{[bis(carboxymethyl)amino]methyl}phosphinic acid) is an EDTA(4-)-like ligand containing an extra phosphinate group. [Co-II(XT)](3-), [Co-III(XT)](2-), and a series of [Ln(XT)](2-) complexes have been prepared. The phosphinate group is not coordinated in the Co complexes but is bound in the lanthanide complexes. Solid state and solution behaviors of Ln-XT species are consistent: both monoprotonated and nonprotonated species have been found. Protonation of the metal complex does not lead to dissociation of a carboxylate; rather, the proton distributes around the molecular ion. The pM values of Ln-XT are comparable to those of Ln-EDTA but are higher than those of Ln-TMDTA. The inclusion of a phosphinate eases the selectivity of an EDTA-type ligand for late lanthanides.},
	keywords = {ACID, AGENTS, AMINE PHENOL LIGANDS, ANTIBODY, COMPLEXES, CRYSTAL-STRUCTURES, DERIVATIVES, IONS},
	isbn = {0020-1669},
	url = {<Go to ISI>://000169861800011},
	author = {Xu, L. and Rettig, S. J. and Orvig, Chris}
}
@article {5024,
	title = {Synthetic transformations of eleutherobin reveal new features of its microtubule-stabilizing pharmacophore},
	journal = {Journal of the American Chemical Society},
	volume = {123},
	number = {35},
	year = {2001},
	note = {ISI Document Delivery No.: 467XNTimes Cited: 21Cited Reference Count: 13},
	month = {Sep},
	pages = {8632-8633},
	type = {Article},
	keywords = {AGENTS, COMMON PHARMACOPHORE, PACLITAXEL, TAXOL, TUBULIN},
	isbn = {0002-7863},
	url = {<Go to ISI>://000170729200037},
	author = {Britton, R. and De Silva, E. D. and Bigg, C. M. and McHardy, L. M. and Roberge, M. and Andersen, R. J.}
}
@article {4775,
	title = {Antimitotic diterpenes from Erythropodium caribaeorum test pharmacophore models for microtubule stabilization},
	journal = {Organic Letters},
	volume = {2},
	number = {3},
	year = {2000},
	note = {ISI Document Delivery No.: 282UXTimes Cited: 36Cited Reference Count: 17},
	month = {Feb},
	pages = {257-260},
	type = {Article},
	abstract = {[GRAPHICS] Six new antimitotic diterpenes, 2-7, have been isolated from the Caribbean octocoral Erythropodium caribaeorum, Structural variations encountered in this group of natural products test recently proposed pharmacophore models for microtubule stabilizing compounds.},
	keywords = {AGENTS, ELEUTHEROBIN, TAXOL, TUBULIN},
	isbn = {1523-7060},
	url = {<Go to ISI>://000085238900007},
	author = {Cinel, B. and Roberge, M. and Behrisch, H. and van Ofwegen, L. P. and Castro, C. B. and Andersen, R. J.}
}
@article {3266,
	title = {POTENTIOMETRIC, CALORIMETRIC, AND SOLUTION NMR-STUDIES OF A TRIDENTATE LIGAND WHICH HAS A MARKED PREFERENCE FOR FORMATION OF BIS(LIGAND) VERSUS MONO(LIGAND) LANTHANIDE COMPLEXES AND WHICH EXHIBITS HIGH SELECTIVITY FOR HEAVIER LANTHANIDES},
	journal = {Journal of the American Chemical Society},
	volume = {117},
	number = {45},
	year = {1995},
	note = {ISI Document Delivery No.: TE739Times Cited: 69Cited Reference Count: 59},
	month = {Nov},
	pages = {11230-11238},
	type = {Article},
	abstract = {A new water-soluble N4O3 tripodal amine phenol ligand, tris(((2-hydroxy-5-sulfobenzyl)amino)ethyl)amine (H(3)TRNS) has been synthesized, and its complexation properties with six lanthanide(III) ions (Ln, Nd, Gd, Ho, Yb, Lu) have been probed. In water, the ligand coordinates in a tridentate fashion through the three phenolate oxygen atoms to give mono- and bis(ligand) complexes. The bis complexes are proposed to be 7-coordinate containing one bound water as evinced by O-17 NMR experiments on the Dy3+ complex. while the mono complexes are proposed to have a coordination number of eight or nine. The stepwise formation constants for the 1:1 and 2:1 (L:M) complexes have been measured at 25 degrees C (mu = 0.16 M NaCl) for Nd3+ (log K-1 = 6.41, log K-2 6.34), Gd3+ (log K-1 = 6.67, log K-2 = 7.69), Ho3+ (log K-1 = 7.67, log K-2 = 8.75), and Yb3+ (log K-1 = 8.53, log K-2 = 9.73). The formation constants show an increasing affinity and an unprecedented selectivity for the heavier lanthanides (beta(2(yb)) - beta(2(Nd)) = 10(5.5)). Furthermore, the stepwise stability constant for the 2:1 complex is increasingly greater than that for the 1:1 complexes of Gd3+, Ho3+, and Yb3+, while K-1 and K-2 for the 1:1 and 2:1 complexes of Nd3+ are approximately the same. Solution calorimetry shows that the selectivity for the heavier lanthanides is an enthalpic effect (Delta H-beta 2 = -45.11 (Yb) and -13.71 kJ . mol(-1) (Nd)), while the anomalous behavior in formation constants (K-2 > K-1) is predominantly entropic (Delta S-2 > Delta S-1) and is rationalized in terms of salvation of the complexes, Lanthanum(III) forms only the 1:1 complex (log K = 5.65) which precipitates from solution.},
	keywords = {AGENTS, AMINE PHENOL LIGANDS, AQUEOUS, BIOLOGICAL-SYSTEMS, CHEMISTRY, EXCHANGE, HEPTADENTATE LIGANDS, METAL-IONS, NUCLEAR MAGNETIC-RESONANCE, probes, SHIFT-REAGENTS, WATER},
	isbn = {0002-7863},
	url = {<Go to ISI>://A1995TE73900021},
	author = {Caravan, P. and Hedlund, T. and Liu, S. and Sjoberg, S. and Orvig, Chris}
}
@article {3021,
	title = {CHARACTERIZATION OF TRIS(N-SUBSTITUTED-2-METHYL-3-HYDROXY-4-PYRIDINONATO)TECHNETIUM(IV) CATIONS},
	journal = {Inorganic Chemistry},
	volume = {33},
	number = {24},
	year = {1994},
	note = {ISI Document Delivery No.: PU080Times Cited: 14Cited Reference Count: 20},
	month = {Nov},
	pages = {5607-5609},
	type = {Note},
	keywords = {3-HYDROXY-4-PYRIDINONES, AGENTS, aluminum, CHEMISTRY, COMPLEXES, gallium, INVIVO, RADIOPHARMACEUTICALS, TC-99M, technetium},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1994PU08000042},
	author = {Edwards, D. S. and Liu, S. and Poirier, M. J. and Zhang, Z. H. and Webb, G. A. and Orvig, Chris}
}
@article {7273,
	title = {GENERAL-METHOD FOR THE SYNTHESIS OF TRISHYDROXAMIC ACIDS},
	journal = {Tetrahedron Letters},
	volume = {33},
	number = {14},
	year = {1992},
	note = {ISI Document Delivery No.: HM426Times Cited: 11Cited Reference Count: 19},
	month = {Mar},
	pages = {1827-1830},
	type = {Article},
	abstract = {Triscarboxylic acids, when treated with hydroxylamines in the presence of water-soluble carbodiimide in THF-H2O, at pH approximately 4.8, yield the corresponding trishydroxamic acids in good yields.},
	keywords = {AGENTS, iron, SIDEROPHORES, TRIHYDROXAMATE ANALOGS},
	isbn = {0040-4039},
	url = {<Go to ISI>://A1992HM42600006},
	author = {Karunaratne, V. and Hoveyda, H. R. and Orvig, Chris}
}
@article {6969,
	title = {HEPTADENTATE LIGANDS FOR THE LANTHANIDES - THE 1ST STRUCTURALLY CHARACTERIZED EXAMPLE OF A LANTHANIDE HEPTADENTATE LIGAND COMPLEX - (TRIS(3-AZA-4-METHYL-6-OXOHEPT-4-EN-1-YL)AMINE)YTTERBIUM(III)},
	journal = {Journal of the American Chemical Society},
	volume = {113},
	number = {7},
	year = {1991},
	note = {ISI Document Delivery No.: FD837Times Cited: 55Cited Reference Count: 29},
	month = {Mar},
	pages = {2528-2532},
	type = {Article},
	abstract = {{Several binary heptacoordinate-N4O3-ligand LnL complexes of the lanthanides have been prepared and characterized. The heptadentate ligands are the Schiff base condensation products of tris(2-aminoethyl)amine with 3 equiv of either acetylacetone (to form H-3trac) or a hydroxyacetophenone (to form H-3hatren or H-3datren). The complexes hydrolyze easily but most of the Ln(trac) complexes are stable enough to sublime. Crystals of Yb(trac) were isolated by sublimation, and its structure has been solved; it is the first structurally characterized example of a lanthanide heptadentate ligand complex. Crystals of Yb(trac) are monoclinic},
	keywords = {AGENTS, COORDINATION CHEMISTRY, CRYSTAL, MOLECULAR-STRUCTURE},
	isbn = {0002-7863},
	url = {<Go to ISI>://A1991FD83700029},
	author = {Berg, D. J. and Rettig, S. J. and Orvig, Chris}
}
@article {7073,
	title = {SYNTHESIS AND CHARACTERIZATION OF A PENTADENTATE SCHIFF-BASE N3O2 LIGAND AND ITS NEUTRAL TECHNETIUM(V) COMPLEX - X-RAY STRUCTURE OF (N,N{\textquoteright}-3-AZAPENTANE-1,5-DIYLBIS(3-(1-IMINOETHYL)-6-METHYL-2H-PYRAN-2,4(3H )-DIONATO)(3-)-O,O{\textquoteright},N,N{\textquoteright},N{\textquoteright}{\textquoteright})OXOTECHNETI},
	journal = {Inorganic Chemistry},
	volume = {30},
	number = {26},
	year = {1991},
	note = {ISI Document Delivery No.: GX615Times Cited: 19Cited Reference Count: 35},
	month = {Dec},
	pages = {4915-4919},
	type = {Article},
	abstract = {{Preparations of a potentially pentadentate ligand, N,N{\textquoteright}-3-azapentane-1,5-diylbis(3-(1-iminoethyl)-6-methyl-2H-pyran-2,4-(3H )-dione) (H3apa), and its neutral technetium(V) complex, [TcO(apa)], are described. The C-13 and H-1 NMR, infrared, optical, and mass spectra of the pentadentate ligand and its technetium(V) complex are reported. The X-ray structure of [TcO(apa)] has been determined. Crystals are orthorhombic, space group Pbca, with a = 12.833 (2) angstrom},
	keywords = {<TC=N>2+ CORE, AGENTS, CHEMISTRY, CRYSTAL-STRUCTURE, DONOR-ATOM SET, gallium, OXOTECHNETIUM(V) COMPLEXES, REACTIVITY, RHENIUM(V) OXO-COMPLEXES, S-METHYL DITHIOCARBAZATE},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1991GX61500013},
	author = {Liu, S. and Rettig, S. J. and Orvig, Chris}
}
