Structural and Functional Models for the Dinuclear Copper Active Site in Catechol Oxidases:  Syntheses, X-ray Crystal Structures, Magnetic and Spectral Properties, and X-ray Absorption Spectroscopic Studies in Solid State and in Solution

1996 ◽  
Vol 35 (11) ◽  
pp. 3409-3419 ◽  
Author(s):  
Frank Zippel ◽  
Friedhelm Ahlers ◽  
Rüdiger Werner ◽  
Wolfgang Haase ◽  
Hans-Friedrich Nolting ◽  
...  
Biochemistry ◽  
1995 ◽  
Vol 34 (20) ◽  
pp. 6649-6659 ◽  
Author(s):  
Lijin Shu ◽  
Yu-Min Chiou ◽  
Allen M. Orville ◽  
Marcia A. Miller ◽  
John D. Lipscomb ◽  
...  

Biochemistry ◽  
1992 ◽  
Vol 31 (19) ◽  
pp. 4596-4601 ◽  
Author(s):  
Robert A. Scott ◽  
Shengke Wang ◽  
Marly K. Eidsness ◽  
Aidas Kriauciunas ◽  
Charles A. Frolik ◽  
...  

2001 ◽  
Vol 79 (3) ◽  
pp. 263-271
Author(s):  
Paul K Baker ◽  
Michael GB Drew ◽  
Deborah S Evans

Reaction of [WI2(CO)3(NCMe)2] with two equivalents of 1-phenyl-1-propyne (MeC2Ph) in CH2Cl2, and in the absence of light, gave the bis(1-phenyl-1-propyne) complex [WI2(CO)(NCMe)(η2-MeC2Ph)2] (1) in 77% yield. Treatment of equimolar quantities of 1 and NCR (R = Et, i-Pr, t-Bu, Ph) in CH2Cl2 afforded the nitrile-exchanged products, [WI2(CO)(NCR)(η2-MeC2Ph)2] (2-5) (R = Et (2), i-Pr (3), t-Bu (4), Ph (5)). Complexes 1, 2, and 5 were structurally characterized by X-ray crystallography. All three structures have the same pseudo-octahedral geometry, with the equatorial sites being occupied by cis and parallel alkyne groups, which are trans to the cis-iodo groups. The trans carbon monoxide and acetonitrile ligands occupy the axial sites. In structures 1 and 2, the methyl and phenyl substituents of the 1-phenyl-1-propyne ligands are cis to each other, whereas for the bulkier NCPh complex (5), the methyl and phenyl groups are trans to one another. This is the first time that this arrangement has been observed in the solid state in bis(alkyne) complexes of this type.Key words: bis(1-phenyl-1-propyne), carbonyl, nitrile, diiodo, tungsten(II), crystal structures.


2007 ◽  
Vol 46 (19) ◽  
pp. 7742-7748 ◽  
Author(s):  
Ingmar Persson ◽  
Emiliana Damian Risberg ◽  
Paola D'Angelo ◽  
Simone De Panfilis ◽  
Magnus Sandström ◽  
...  

2006 ◽  
Vol 70 (18) ◽  
pp. A573 ◽  
Author(s):  
T.M. Seward ◽  
C.M.B. Henderson ◽  
O.M. Suleimenov ◽  
J.M. Charnock

1980 ◽  
Vol 35 (2) ◽  
pp. 237-238 ◽  
Author(s):  
Martin Jansen

Abstract K3NO3 and RbsNO3 were prepared by solid state reaction of equimolar mixtures of K2O/KNO2 and Rb20/RbN02, respectively. According to X-ray powder photographs their crystal structures are derived from the perovs-kite structure. K3NO3 is isostructural with Na3NO3 (a = 521.7 pm, Z = 1), Rb3NO3 represents a tetragonally distorted variant with a = 770.5, c = 550.8 pm and Z = 2.


1998 ◽  
Vol 275-276 ◽  
pp. 150-158 ◽  
Author(s):  
Ian Harvey ◽  
Richard W. Strange ◽  
Ralf Schneider ◽  
Carol A. Gormal ◽  
C. David Garner ◽  
...  

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