@article {5127,
	title = {An aurophilicity-determined 3-D bimetallic coordination polymer: using [Au(CN)(2)](-) to increase structural dimensionality through gold center dot center dot center dot gold bonds in (tmeda)Cu[Au(CN)(2)](2)},
	journal = {Chemical Communications},
	number = {03},
	year = {2001},
	note = {ISI Document Delivery No.: 396KHTimes Cited: 68Cited Reference Count: 24},
	pages = {259-260},
	type = {Article},
	abstract = {A coordination polymer with the [Au(CN)(2)](-) building block has been prepared and it exhibits weak Au(I)-mediated ferromagnetic interactions; the structure illustrates that aurophilicity is a powerful tool to increase dimensionality, generating a three-dimensional system from a 1-D polymer.},
	keywords = {BUILDING-BLOCKS, CHEMISTRY, COMPONENT, CRYSTAL-STRUCTURE, LIGANDS, MAGNETIC-PROPERTIES, NETWORK},
	isbn = {1359-7345},
	url = {<Go to ISI>://000166635200017},
	author = {Leznoff, D. B. and Xue, B. Y. and Patrick, B. O. and Sanchez, V. and Thompson, R. C.}
}
@article {5128,
	title = {Synthesis, structure and magnetic properties of 3D interpenetrating nets of M(pyrazine)[Au(CN)(2)](2) (M = Cu, Ni, Co) supported by aurophilic interactions},
	journal = {Polyhedron},
	volume = {20},
	number = {11-14},
	year = {2001},
	note = {ISI Document Delivery No.: 451LWTimes Cited: 46Cited Reference Count: 517th International Conference on Molecule-Base Magnets (ICMM 2000)SEP 16-21, 2000SAN ANTONIO, TX},
	month = {May},
	pages = {1247-1254},
	type = {Proceedings Paper},
	abstract = {{New inorganic coordination polymers of the form M(pyrazine)[Au(CN)(2)](2) (M = Cu (1); Ni (2); Co (3)) have been prepared and the copper(II) analogue structurally characterised. The X-ray analysis revealed two 3D interpenetrating alpha -polonium networks consisting of 1D chains of Cu-pyrazine units connected by [Au(CN)(2)] bridges. The two networks are connected via weak aurophilic interactions (Au-Au: 3.4729(2) Angstrom). Thermogravimetric analysis of all three compounds indicated the robust nature of these 3D systems, with decomposition beginning at 260 (1), 406 (2) and 360 degreesC (3). The magnetic susceptibility of 1 shows a maximum in chi (M) at 5.0 K; these data could be fitted to the theoretical expressions for either a 1D or a 2D Heisenberg antiferromagnetic array (J = -2.74 cm(-1)},
	keywords = {ANTIFERROMAGNET, aurophilic, COMPLEXES, COMPONENT, coordination polymers, CRYSTAL-STRUCTURE, Cu(II) complexes, cyanide ligands, DICYANOAURATE(I), FERROMAGNET, interactions, interpenetration, MAGNETIC PROPERTIES, NITRATE, NITROXIDE, Pyrazine},
	isbn = {0277-5387},
	url = {<Go to ISI>://000169804400021},
	author = {Leznoff, D. B. and Xue, B. Y. and Stevens, C. L. and Storr, A. and Thompson, R. C. and Patrick, B. O.}
}
@article {5128,
	title = {Synthesis, structure and magnetic properties of 3D interpenetrating nets of M(pyrazine)[Au(CN)(2)](2) (M = Cu, Ni, Co) supported by aurophilic interactions},
	journal = {Polyhedron},
	volume = {20},
	number = {11-14},
	year = {2001},
	note = {ISI Document Delivery No.: 451LWTimes Cited: 46Cited Reference Count: 517th International Conference on Molecule-Base Magnets (ICMM 2000)SEP 16-21, 2000SAN ANTONIO, TX},
	month = {May},
	pages = {1247-1254},
	type = {Proceedings Paper},
	abstract = {{New inorganic coordination polymers of the form M(pyrazine)[Au(CN)(2)](2) (M = Cu (1); Ni (2); Co (3)) have been prepared and the copper(II) analogue structurally characterised. The X-ray analysis revealed two 3D interpenetrating alpha -polonium networks consisting of 1D chains of Cu-pyrazine units connected by [Au(CN)(2)] bridges. The two networks are connected via weak aurophilic interactions (Au-Au: 3.4729(2) Angstrom). Thermogravimetric analysis of all three compounds indicated the robust nature of these 3D systems, with decomposition beginning at 260 (1), 406 (2) and 360 degreesC (3). The magnetic susceptibility of 1 shows a maximum in chi (M) at 5.0 K; these data could be fitted to the theoretical expressions for either a 1D or a 2D Heisenberg antiferromagnetic array (J = -2.74 cm(-1)},
	keywords = {ANTIFERROMAGNET, aurophilic, COMPLEXES, COMPONENT, coordination polymers, CRYSTAL-STRUCTURE, Cu(II) complexes, cyanide ligands, DICYANOAURATE(I), FERROMAGNET, interactions, interpenetration, MAGNETIC PROPERTIES, NITRATE, NITROXIDE, Pyrazine},
	isbn = {0277-5387},
	url = {<Go to ISI>://000169804400021},
	author = {Leznoff, D. B. and Xue, B. Y. and Stevens, C. L. and Storr, A. and Thompson, R. C. and Patrick, B. O.}
}
@article {4486,
	title = {Clq binding to liposomes is surface charge dependent and is inhibited by peptides consisting of residues 14-26 of the human ClqA chain in a sequence independent manner},
	journal = {Biochimica Et Biophysica Acta-Biomembranes},
	volume = {1418},
	number = {1},
	year = {1999},
	note = {ISI Document Delivery No.: 189EWTimes Cited: 20Cited Reference Count: 36},
	month = {Apr},
	pages = {19-30},
	type = {Article},
	abstract = {Complement activation by anionic liposomes proceeds by antibody-independent, C1q-initiated activation of the classical pathway. Purified C1q bound to anionic liposomes in an acidic lipid concentration-dependent manner. Saturation binding, but not the apparent association constant, was enhanced by increasing the cardiolipin content of the liposomes or decreasing either the pH or ionic strength of the reaction mixture. These observations indicate the involvement of electrostatic factors in the binding. A highly cationic region in the collagen-like domain of C1q comprised of residues 14-26 of the C1qA polypeptide chain was assessed for involvement in liposome binding. This region has previously been shown to mediate C1q binding to other immunoglobulin-independent activators of the classical pathway of complement. Peptides containing residues 14-26 of C1qA, denoted C1qA(14-26), inhibited C1q binding to and complement activation by anionic liposomes. The inhibitory capacity of these cationic peptides had no sequence or conformation specificity. Rather, the amount of positive charge on the peptides was the determining factor. When present in excess, peptides with five cationic residues inhibited C1q binding and complement activation; however, C1q peptides with only two cationic residues did not. In addition to the C1qA(14-26) region, other parts of C1q that contain cationic residues may also be involved in C1q binding to anionic liposomes. (C) 1999 Elsevier Science B.V. All rights reserved.},
	keywords = {1ST, ACTIVATES COMPLEMENT, C1Q A-CHAIN, CLASSICAL COMPLEMENT PATHWAY, CLEARANCE, Clq binding, COLLAGEN, COMPONENT, liposome clearance, liposome-mediated complement activation, PHAGOCYTOSIS, PROTEINS, SERUM, SYSTEM},
	isbn = {0005-2736},
	url = {<Go to ISI>://000079892300002},
	author = {Bradley, A. J. and Brooks, D. E. and Norris-Jones, R. and Devine, D. V.}
}
