Pressure dependence of the electronic spectra of quasi-one-dimensional Pt2X semiconductors

1989 ◽  
Vol 111 (1) ◽  
pp. 66-72 ◽  
Author(s):  
Mary Ann Stroud ◽  
Harry G. Drickamer ◽  
Miriam Heinrichs Zietlow ◽  
Harry B. Gray ◽  
Basil I. Swanson
ChemInform ◽  
1989 ◽  
Vol 20 (13) ◽  
Author(s):  
M. A. STROUD ◽  
H. G. DRICKAMER ◽  
M. H. ZIETLOW ◽  
H. B. GRAY ◽  
B. I. SWANSON

2008 ◽  
Vol 27 (21) ◽  
pp. 5441-5445 ◽  
Author(s):  
Shohei Sase ◽  
Yoen-Seok Cho ◽  
Atsushi Kawachi ◽  
Atsushi Wakamiya ◽  
Shigehiro Yamaguchi ◽  
...  

2003 ◽  
Vol 58 (12) ◽  
pp. 727-734 ◽  
Author(s):  
Hirokazu Kobayashi ◽  
Takahiro Ueda ◽  
Keisuke Miyakubo ◽  
Taro Eguchi

The pressure dependence of the 129Xe chemical shift tensor confined in the Tris(o-phenylenedioxy) cyclotriphosphazene (TPP) nanochannel was investigated by high-pressure 129Xe NMR spectroscopy. The observed 129Xe spectrum in the one-dimensional TPP nanochannel (0.45 nm in diameter) exhibits a powder pattern broadened by an axially symmetric chemical shift tensor. As the pressure increases from 0.02 to 7.0 MPa, a deshielding of 90 ppm is observed for the perpendicularcomponent of the chemical shift tensor δ⊥, whereas a deshielding of about 30 ppm is observed for the parallel one, δ‖. This suggests that the components of the chemical shift tensor, δ‖ and δ⊥, are mainly dominated by the Xe-wall and Xe-Xe interaction, respectively. Furthermore, the effect of helium, which is present along with xenon gas, on the 129Xe chemical shift is examined in detail. The average distance between the Xe atoms in the nanochannel is estimated to be 0.54 nm. This was found by using δ⊥ at the saturated pressure of xenon, and comparing the increment of the chemicalshift value in δ⊥ to that of a β -phenol/Xe compound.


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