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Ligand Tris (ligand + tri)
Selected AbstractsCytotoxic Rhodium(III) Polypyridyl Complexes Containing the Tris(pyrazolyl)methane Coligand: Synthesis, DNA Binding Properties and Structure,Activity RelationshipsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 25 2009Ruth Bieda Abstract The RhIII complexes of the type [RhCl(pp)(tpm)]2+ [pp = bpy, bpm, phen, tap, dpq, dppz] 4,9 have been prepared by stepwise treatment of RhCl3·3H2O or mer,cis -[RhCl3(DMSO-,S)2(DMSO-,O)] with the appropriate polypyridyl ligand (pp) followed by the tripodal ligand tris(pyrazolyl)methane (tpm). Intermediates of the type [RhCl3(CH3OH)(pp)] 1,3 with pp = bpy, phen, dpq were also characterized but exhibit either low (3) or no (1, 2) cytotoxicity. X-ray structural analyses of [RhCl(bpy)(tpm)][PF6]24 and [RhCl(phen)(tpm)][PF6]26 were performed, and the interaction of complexes 4,9 with DNA was investigated by CD and UV/Vis spectroscopy and by gel electrophoresis. CD and viscosity studies confirm strong intercalation of dppz complex 9 into DNA. Complexes 8 and particularly 9 (IC50 = 0.43, 0.37 ,M) are potent cytotoxic agents towards the human cancer cell lines MCF-7 and HT-29, whereas respectively little (complex 6) or no activity (complexes 4, 5, 7) is observed for the other members of the series. Our findings indicate that the cytotoxicity is dependent on the hydrophobicity of both the polypyridyl and the facial coligand in these and other half-sandwich RhIII complexes. Irradiation of bpy compound 4 in the presence of plasmid pBR322 for 30 min at 311 nm at a molar ratio of r = 0.1 leads to total conversion of the supercoiled form into the nicked version. Although dppz complex 9 also functions as a photonuclease under these conditions, the degree of cleavage is much lower. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Developing the Kharasch Reaction in Aqueous Media: Dinuclear Group 8 and 9 Catalysts Containing the Bridging Cage Ligand Tris(1,2-dimethylhydrazino)diphosphane,EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 5 2008Alba E. Díaz-Álvarez Abstract The dinuclear complexes [{RuCl2(,6 - p -cymene)}2(,-THDP)] (4) and [{MCl(,4 -cod)}2(,-THDP)] [M = Rh (5), Ir (6)], containing the bridging cage-type ligand tris(1,2-dimethylhydrazino)diphosphane (THDP), have been synthesized in high yields (89,95,%) by treatment of dimers [{RuCl(,-Cl)(,6 - p -cymene)}2] (1) and [{M(,-Cl)(,4 -cod)}2] [M = Rh (2), Ir (3)] with one equivalent of THDP. The structure of the (,6 -arene)ruthenium(II) derivative 4 has been unequivocally confirmed by means of X-ray diffraction methods. All these complexes have been found to be active catalysts for the atom-transfer radical addition of bromotrichloromethane to olefins (Kharasch reaction) in heterogeneous aqueous media under mild conditions (room temp.).(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] Synthesis and Characterization of Copper Complexes Containing the Tripodal N7 Ligand Tris{2-[(pyridin-2-ylmethyl)amino]ethyl}amine (=N,-(Pyridin-2-ylmethyl)- N,N -bis{2-[(pyridin-2-ylmethyl)amino]ethyl}ethane-1,2-diamine): Equilibrium, Spectroscopic Data, and Crystal Structures of Mono- and Trinuclear Copper(II) ComplexesHELVETICA CHIMICA ACTA, Issue 9 2005Christian Gérard The stability constants of the CuII chelates with the tripodal heptadentate ligand tris{2-[(2-pyridylmethyl)amino]ethyl}amine (=N,-(pyridin-2-ylmethyl)- N,N -bis{2-[(pyridin-2-ylmethyl)amino]ethyl}ethane-1,2-diamine; tpaa), determined by potentiometry and UV spectrometry, show the formation of [Cu(tpaaH)]3+ and [Cu(tpaa)]2+ species. In the solid state, two mononuclear CuII compounds, [Cu(tpaa)](PF6)2 (1) and [Cu(tpaaH)](ClO4)3,H2O (2), and one trinuclear [Cu3(tpaa)2(ClO4)2](ClO4)4,2,H2O (3) complex were isolated and characterized by IR, UV/VIS, and EPR spectroscopy. An X-ray structure of the mononuclear protonated complex 2 shows that the Cu2+ ion has a distorted square-pyramidal geometry (,=0.21). and the proton is bound to the secondary-amine function of one uncoordinated arm of the tripod ligand (Fig.,4). The crystal lattice for 2 is stabilized by the H-bonds between the N-atom of the free pyridinyl group with the proton of the free secondary-amine function of the neighboring molecule. The linear trinuclear complex 3 consists of two entities of the pyramidal mononuclear complex 1 bound to the third central Cu2+ ion by the free unprotonated arms of the ligands in equatorial position (Fig.,5). The octahedral geometry of the third CuII atom is achieved by two perchlorate anions in the axial positions. The redox properties of 1,3 compounds was examined by cyclic voltammetry. [source] Phosphorus dendrimers and dendrons functionalized with the cage ligand tris(1,2-dimethylhydrazino)diphosphaneHETEROATOM CHEMISTRY, Issue 5 2010Lara-Isabel Rodríguez The synthesis of a new phosphorus dendrimer peripherally functionalized with the cage ligand tris(1,2-dimethylhydrazino) diphosphane is described. In addition, dendrons (dendritic wedges) containing the same cage ligand at the focal point are also reported along with their corresponding ruthenium derivatives, which are thought to be potential catalysts in aqueous media. © 2010 Wiley Periodicals, Inc. Heteroatom Chem 21:290,297, 2010; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20611 [source] Copper Complexes with Neutral N4 Tripodal Ligands: Influence of the Number of Nitrogen Donors on Their Structures, Properties, and Reactivity,EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 26 2009Kiyoshi Fujisawa Abstract Copper coordination complexes of the neutral tetradentate nitrogen-containing ligands tris(3,5-dimethylpyrazol-1-ylmethyl)amine (L0N4) and tris(3,5-diisopropylpyrazol-1-ylmethyl)amine (L1N4), namely the copper(II) chlorido complexes [CuII(L0N4)Cl2] (1) and [CuII(L1N4)Cl2] (2), the copper(II) nitrato complexes [CuII(L0N4)(NO3)](NO3) (3) and [CuII(L1N4)(NO3)](NO3) (4), and the copper(II) sulfato complexes [CuII(L0N4)(SO4)] (5) and [CuII(L1N4)(SO4)] (6), and the copper(I) complexes [CuI(L0N4)](PF6) (7) and [CuI(L0N4)(PPh3)](ClO4) (8), have been systematically synthesized in order to investigate the influence of the number of nitrogen donors on their structures, properties, and reactivity. All copper(II) complexes were fully characterized by X-ray crystallography and by IR/far-IR, UV/Vis absorption, and ESR spectroscopy. Although the structure of 7 was not determined by X-ray crystallography, this complex and the structurally characterized copper(I) triphenylphosphane complex 8 were fully characterized by IR/far-IR and NMR spectroscopy. A comparison of the copper(II) complexes with two tris(pyrazol-1-ylmethyl)amine ligands with different bulkiness of the pyrazolyl rings has allowed us to evaluate the second coordination sphere effects of the ligands. Moreover, the structures and physicochemical properties of these complexes are compared with those of related complexes containing the neutral tridentate tris(pyrazolyl)methane ligand and the neutral bidentate bis(pyrazolyl)methane ligand. Finally, the relative stability of the copper(I) complexes is discussed. The influence of the number of nitrogen donors in copper complexes is observed from these systematic results.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] | ||||||||||