@article {2169,
	title = {Serendipitous syntheses of Rh(H)(2)Cl(PRPh2)(3) complexes, and their crystal structures, where R = Me, Cy (cyclohexyl)},
	journal = {Inorganica Chimica Acta},
	volume = {361},
	number = {7},
	year = {2008},
	note = {ISI Document Delivery No.: 304ETTimes Cited: 4Cited Reference Count: 40Lorenzini, Fabio Patrick, Brian O. James, Brian R.},
	month = {May},
	pages = {2123-2130},
	type = {Article},
	abstract = {Reactions of RhCl(cod)(THP) (cod = 1,5-cyclooctadiene; THP = P(CH2OH)(3)) with PMePh2 or PCyPh2 (Cy = cyclohexyl) in acetone/MeOH solution under H-2 surprisingly form the complexes cis,mer-Rh(H)Cl-2(PRPh2)(3) (R = Me or Cy); both complexes are characterized by crystallography (the first structures in which the hydride ligands of such dihydrido-chloro-trisphosphine complexes have been located), and by detailed H-1 and P-31 NMR spectroscopy. The key role of the THP in the observed chemistry is discussed. (C) 2007 Elsevier B.V. All rights reserved.},
	keywords = {CRYSTALLOGRAPHY, ETHYLENE, EXCHANGE, HOMOGENEOUS CATALYTIC HYDROGENATION, hydride, hydride complexes, NMR, PARAHYDROGEN-INDUCED POLARIZATION, PHOSPHINE COMPLEXES, rhodium, RHODIUM(I), SPECTROSCOPY, TERTIARY PHOSPHINES, WATER, WILKINSONS CATALYST},
	isbn = {0020-1693},
	url = {<Go to ISI>://000256093500040},
	author = {Lorenzini, F. and Patrick, B. O. and James, Brian R.}
}
@article {Funk2004,
	title = {X-ray magnetic circular dichroism of Pseudomonas aeruginosa nickel(II) azurin.},
	journal = {J. Am. Chem. Soc.},
	volume = {126},
	number = {18},
	year = {2004},
	pages = {5859{\textendash}66},
	abstract = {We show that X-ray magnetic circular dichroism (XMCD) can be employed to probe the oxidation states and other electronic structural features of nickel active sites in proteins. As a calibration standard, we have measured XMCD and X-ray absorption (XAS) spectra for the nickel(II) derivative of Pseudomonas aeruginosa azurin (NiAz). Our analysis of these spectra confirms that the electronic ground state of NiAz is high-spin (S = 1); we also find that the L(3)-centroid energy is 853.1(1) eV, the branching ratio is 0.722(4), and the magnetic moment is 1.9(4) mu(B). Density functional theory (DFT) calculations on model NiAz structures establish that orbitals 3d(x2-y2) and 3d(z2) are the two valence holes in the high-spin Ni(II) ground state, and in accord with the experimentally determined orbital magnetic moment, the DFT results also demonstrate that both holes are highly delocalized, with 3d(x2-y2) having much greater ligand character.},
	keywords = {Azurin, Azurin: chemistry, circular dichroism, Circular Dichroism: methods, copper, Copper: chemistry, CRYSTALLOGRAPHY, LIGANDS, Magnetics, models, MOLECULAR, Molecular Conformation, NICKEL, Nickel: chemistry, PDF, Pseudomonas aeruginosa, Pseudomonas aeruginosa: chemistry, X-RAY, X-Rays},
	issn = {0002-7863},
	doi = {10.1021/ja036218d},
	url = {http://www.ncbi.nlm.nih.gov/pubmed/15125678},
	author = {Funk, Tobias and Kennepohl, Pierre and Di Bilio, Angel J and Wehbi, William a and Young, Anthony T and Friedrich, Stephan and Arenholz, Elke and Gray, Harry B and Cramer, Stephen P}
}
@article {617,
	title = {Dinuclear organometallic dinitrogen complexes of niobium},
	journal = {Inorganica Chimica Acta},
	volume = {345},
	year = {2003},
	note = {ISI Document Delivery No.: 653EUTimes Cited: 4Cited Reference Count: 30},
	month = {Mar},
	pages = {53-62},
	type = {Article},
	abstract = {{The niobium(III) chloride precursors (R)[P2N2]NbCl stabilized by the bis-(amidophosphine) macrocycle (where (R)[P2N2] RP(CH2SiMe2NSiMe2CH2)(2)PR},
	keywords = {ACTIVATION, amidophosphine ligands, AZOBENZENE, CLEAVAGE, CRYSTAL-STRUCTURE, CRYSTALLOGRAPHY, DINITROGEN COMPLEXES, END-ON, FIXATION, fluxionality, macrocycle, macrocycles, N-2, NIOBIUM, NITRIDE, SIDE-ON},
	isbn = {0020-1693},
	url = {<Go to ISI>://000181422900008},
	author = {Fryzuk,Michael D. and Kozak, C. M. and Patrick, B. O.}
}
@article {4647,
	title = {The structures of the neurotrophin 4 homodimer and the brain-derived neurotrophic factor/neurotrophin 4 heterodimer reveal a common Trk-binding site},
	journal = {Protein Science},
	volume = {8},
	number = {12},
	year = {1999},
	note = {ISI Document Delivery No.: 266RPTimes Cited: 24Cited Reference Count: 45},
	month = {Dec},
	pages = {2589-2597},
	type = {Article},
	abstract = {The neurotrophins are growth factors that are involved in the development and survival of neurons. Neurotrophin release by a target tissue results in neuron growth along the neurotrophin concentration gradient, culminating in the eventual innervation of the target tissue. These activities are mediated through trk cell surface receptors. We have determined the structures of the heterodimer formed between brain-derived neurotrophic factor (BDNF) and neurotrophin 4 (NT4), as well as the structure of homodimer of NT4. We also present the structure of the Neurotrophin 3 homodimer, which is refined to higher resolution than previously published. These structures provide the first views of the architecture of the NT4 protomer. Comparison of the surface of a model of the BDNF homodimer with the structures of the neurotrophin homodimers reveals common features that may be important in the binding between the neurotrophins and their receptors. In particular, there exists an analogous region on the surface of each neurotrophin that is likely to be involved in trk receptor binding. Variations in sequence on the periphery of this common region serve to confer trk receptor specificity.},
	keywords = {BDNF, CELLS, CRYSTAL-STRUCTURE, CRYSTALLOGRAPHY, DIFFERENTIATION, nerve growth factor, NERVE GROWTH-FACTOR, NGF, PURIFICATION, RECEPTOR, RECEPTORS, RECOGNITION, SPECIFICITY},
	isbn = {0961-8368},
	url = {<Go to ISI>://000084314100005},
	author = {Robinson, R. C. and Radziejewski, C. and Spraggon, G. and Greenwald, J. and Kostura, M. R. and Burtnick, L. D. and Stuart, D. I. and Choe, S. and Jones, E. Y.}
}
@article {4061,
	title = {The structure of the Pd(111)-(root 7x root 7)R19.1 degrees-S surface: comparison with the corresponding P/Rh(111) surface},
	journal = {Surface Science},
	volume = {393},
	number = {1-3},
	year = {1997},
	note = {ISI Document Delivery No.: YP959Times Cited: 15Cited Reference Count: 35},
	month = {Dec},
	pages = {L119-L125},
	type = {Letter},
	abstract = {The structure of the Pd(lll)-(root 7 x root 7)R19.1<degrees-S surface has been determined by low-energy electron diffraction and has been shown to involve a reconstructed topmost metal layer based on a packed arrangement of Pd pentagons and triangles, with S atoms at 3/7 monolayer coverage occupying eight-coordinate sites at the centre of each Pd pentagon. Comparisons are made with the structure recently determined for the corresponding P/Rh(lll) system. In both cases, the atomic density in the reconstructed layer increases to five metal atoms and three chemisorbed atoms for every seven atoms in the regular metal surface. Some details are closely similar between the two systems, but an intriguing difference is also indicated. In S/Pd(lll), four metal atoms in each pentagonal ring appear close to hcp-type three-fold sites, while the other is close to a fee-type three-fold site. This contrasts with the situation for the topmost layer of the P/Rh(lll) system, for which the reversed lateral registry has been reported (i.e. the atoms of each pentagonal ring occupy three-fold sites where four are of the fee type and one of the hcp type). (C) 1997 Elsevier Science B.V.},
	keywords = {ADSORBATE STRUCTURE, ARRANGEMENT, chemisorption, CRYSTAL SURFACES, CRYSTALLOGRAPHY, ENERGY-ELECTRON-DIFFRACTION, LEED INTENSITY ANALYSIS, low energy electron diffraction crystallography, LOW INDEX SINGLE, METAL-SURFACES, palladium, PD(111) SURFACE, RECONSTRUCTION, SULFUR, sulphur, surface structure},
	isbn = {0039-6028},
	url = {<Go to ISI>://000071333200009},
	author = {Liu, W. and Mitchell, K. A. R. and Berndt, W.}
}
@article {3749,
	title = {An investigation of structural details for the Cu(110)-((22)(-11))-P reconstructed surface},
	journal = {Surface Review and Letters},
	volume = {3},
	number = {2},
	year = {1996},
	note = {ISI Document Delivery No.: VC948Times Cited: 5Cited Reference Count: 10},
	month = {Apr},
	pages = {1247-1252},
	type = {Article},
	abstract = {An exhaustive tensor LEED study for the half monolayer (ML) structure formed by P at the (110) surface of copper confirms the reconstruction reported earlier [Chem. Phys. 198, 235 (1995)]. All P atoms occupy identical six-coordinate sites; the reconstruction involves 0.25 ML of {\textquoteright}{\textquoteright}added Cu{\textquoteright}{\textquoteright} atoms at hollow sites, each bonded to two neighboring P atoms, which line up along the [<(1)over bar12>] direction. Appreciable relaxations, both vertical and lateral, are identified for atoms in the first four layers. The new feature found here is that the displacements indicated by tensor LEED for individual atoms appear to follow trends that are broadly consistent with reasonable structural chemical principles.},
	keywords = {CRYSTALLOGRAPHY, LEED},
	isbn = {0218-625X},
	url = {<Go to ISI>://A1996VC94800004},
	author = {Liu, W. and Mitchell, K. A. R.}
}
@article {7398,
	title = {PHYSICAL AND STRUCTURAL STUDIES OF N-CARBOXYMETHYL-3-HYDROXY-2-METHYL-4-PYRIDINONE AND N-(PARA-METHOXYPHENYL)-3-HYDROXY-2-METHYL-4-PYRIDINONE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {70},
	number = {3},
	year = {1992},
	note = {ISI Document Delivery No.: JD670Times Cited: 15Cited Reference Count: 40},
	month = {Mar},
	pages = {763-770},
	type = {Article},
	abstract = {{3-Hydroxy-1-carboxymethyl-2-methyl-4-pyridinone (Hcmp) and 3-hydroxy-1-(p-methoxyphenyl)-2-methyl-4-pyridine (Hpap) have been prepared and studied by single crystal X-ray diffraction. Crystals of Hcmp are monoclinic},
	keywords = {2-DIMETHYL-3-HYDROXYPYRID-4-ONE L1, 3-HYDROXY-4-PYRIDINONE, 3-HYDROXY-4-PYRIDINONES, aluminum, CHELATOR 1, COMPLEXES, CONSTANT, CRYSTALLOGRAPHY, gallium, hydrogen bonding, indium, iron, LONG-TERM TRIAL, protonation, solid state, zwitterion},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1992JD67000010},
	author = {Zhang, Z. H. and Rettig, S. J. and Orvig, Chris}
}
