scholarly journals Frontispiece: Macrocyclic Complexes Derived from Four cis ‐L 2 Pt Corners and Four Butadiynediyl Linkers; Syntheses, Electronic Structures, and Square versus Skew Rhombus Geometries

2021 ◽  
Vol 27 (39) ◽  
Author(s):  
Brenna K. Collins ◽  
Melissa Clough Mastry ◽  
Andreas Ehnbom ◽  
Nattamai Bhuvanesh ◽  
Michael B. Hall ◽  
...  
2017 ◽  
Vol 46 (44) ◽  
pp. 15301-15310 ◽  
Author(s):  
Hanusha Bhakhoa ◽  
Lydia Rhyman ◽  
Edmond P. Lee ◽  
Daniel K. W. Mok ◽  
Ponnadurai Ramasami ◽  
...  

Metal-cyclen complexes have a number of important applications. In this work, the electronic structures and preparative conditions are investigated for some Group 1 metal (M), [M(Me4cyclen)L]+ complexes.


1984 ◽  
Vol 19 (6) ◽  
pp. 593-598
Author(s):  
I. P. Beletskii ◽  
K. B. Yatsimirskii

Author(s):  
Dawn A. Bonnell ◽  
Yong Liang

Recent progress in the application of scanning tunneling microscopy (STM) and tunneling spectroscopy (STS) to oxide surfaces has allowed issues of image formation mechanism and spatial resolution limitations to be addressed. As the STM analyses of oxide surfaces continues, it is becoming clear that the geometric and electronic structures of these surfaces are intrinsically complex. Since STM requires conductivity, the oxides in question are transition metal oxides that accommodate aliovalent dopants or nonstoichiometry to produce mobile carriers. To date, considerable effort has been directed toward probing the structures and reactivities of ZnO polar and nonpolar surfaces, TiO2 (110) and (001) surfaces and the SrTiO3 (001) surface, with a view towards integrating these results with the vast amount of previous surface analysis (LEED and photoemission) to build a more complete understanding of these surfaces. However, the spatial localization of the STM/STS provides a level of detail that leads to conclusions somewhat different from those made earlier.


1992 ◽  
Author(s):  
Mark van Schilfgaarde

1995 ◽  
Vol 60 (4) ◽  
pp. 527-536 ◽  
Author(s):  
Martin Breza ◽  
Alena Manová

Using semiempirical MNDO method of quantum chemistry the optimal geometries and corresponding electronic structures of [Pb3(OH)n]6-n model systems as well as of their hydrated [Pb3(OH)n(H2O)8-n]6-n analogues (n = 4, 5) are investigated. The most stable trinuclear lead(II) complexes present in aqueous solutions correspond to cyclo-(μ3-OH)(μ2-OH)3Pb32+, Pb(μ-OH)2Pb(μ-OH)2Pb2+, cyclo-(μ3-OH)2(μ2-OH)3Pb3+, Pb(OH)(μ-OH)2Pb(μ-OH)Pb(OH)+ and Pb(OH)(μ-OH)2Pb(μ-OH)2Pb+ systems. The key role of OH bridges (by vanishing direct Pb-Pb bonds) on the stability of individual isomers is discussed.


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