In situ Structural Characterization of Metal−Molecule−Silicon Junctions Using Backside Infrared Spectroscopy

2008 ◽  
Vol 112 (36) ◽  
pp. 14021-14026 ◽  
Author(s):  
Adina Scott ◽  
Christina A. Hacker ◽  
David B. Janes
Author(s):  
Shabana Noor ◽  
Richard Goddard ◽  
Fehmeeda Khatoon ◽  
Sarvendra Kumar ◽  
Rüdiger W. Seidel

AbstractSynthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes with the formula [ZnLn(HL)(µ-OAc)(NO3)2(H2O)x(MeOH)1-x]NO3 · n H2O · n MeOH [Ln = Pr (1), Nd (2)] and the crystal and molecular structure of [ZnNd(HL)(µ-OAc)(NO3)2(H2O)] [ZnNd(HL)(OAc)(NO3)2(H2O)](NO3)2 · n H2O · n MeOH (3) are reported. The asymmetrical compartmental ligand (E)-2-(1-(2-((2-hydroxy-3-methoxybenzylidene)amino)-ethyl)imidazolidin-2-yl)-6-methoxyphenol (H2L) is formed from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation, resulting in a peripheral imidazoline ring. The structures of 1–3 were revealed by X-ray crystallography. The smaller ZnII ion occupies the inner N2O2 compartment of the ligand, whereas the larger and more oxophilic LnIII ions are found in the outer O2O2’ site. Graphic Abstract Synthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes (Ln = Pr, Nd) bearing an asymmetrical compartmental ligand formed in situ from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation are reported.


1982 ◽  
Vol 36 (4) ◽  
pp. 361-368 ◽  
Author(s):  
Larry F. Wieserman ◽  
David M. Hercules

This study compares the properties of γ-alumina, silica, and titania using ESCA and in situ FT-IR. The FWHM's of the O1s and metal 2p ESCA peaks increased systematically from titania to γ alumina; the O1s/metal 2p ESCA peak area ratios were nearly equal for γ-alumina and silica. For titania, however, the value was half that obtained for γ-alumina. In situ FT-IR showed hydroxyl bands with increasing frequencies from titania to silica. Alumina and titania form carbonate-type structures after exposure to CO at elevated temperatures. Silica exhibited no additional bands after CO treatment that could be assigned to physically adsorbed CO or carbonate-type structures. At 100°C, there is a direct correlation between the specific surface area and the intensity of infrared absorbance of the free-hydroxyl and the hydrogen-bonded hydroxyl bands for silica. The intensities of the infrared bands due to matrix modes were not affected by surface area.


2012 ◽  
Vol 544 ◽  
pp. 34-38 ◽  
Author(s):  
T. Hosokai ◽  
A. Hinderhofer ◽  
A. Vorobiev ◽  
C. Lorch ◽  
T. Watanabe ◽  
...  

1990 ◽  
Vol 112 (12) ◽  
pp. 4821-4830 ◽  
Author(s):  
David R. Corbin ◽  
L. Abrams ◽  
G. A. Jones ◽  
M. M. Eddy ◽  
W. T. A. Harrison ◽  
...  

2013 ◽  
Vol 52 (12) ◽  
pp. 6788-6797 ◽  
Author(s):  
Mengqiang Zhu ◽  
Brendan W. Puls ◽  
Cathrine Frandsen ◽  
James D. Kubicki ◽  
Hengzhong Zhang ◽  
...  

2019 ◽  
Vol 5 (4) ◽  
pp. 457-467 ◽  
Author(s):  
Francisco M. Braz Fernandes ◽  
Edgar Camacho ◽  
Patrícia F. Rodrigues ◽  
Patrick Inácio ◽  
Telmo G. Santos ◽  
...  

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