scholarly journals Proximity Effect and Multiple Andreev Reflections in Gold Atomic Contacts

2001 ◽  
Vol 86 (2) ◽  
pp. 284-287 ◽  
Author(s):  
E. Scheer ◽  
W. Belzig ◽  
Y. Naveh ◽  
M. H. Devoret ◽  
D. Esteve ◽  
...  
2002 ◽  
Vol 65 (18) ◽  
Author(s):  
P. Samuelsson ◽  
G. Johansson ◽  
Å. Ingerman ◽  
V. S. Shumeiko ◽  
G. Wendin

2007 ◽  
Vol 79 (5) ◽  
pp. 57008 ◽  
Author(s):  
A Shailos ◽  
W Nativel ◽  
A Kasumov ◽  
C Collet ◽  
M Ferrier ◽  
...  

2013 ◽  
Author(s):  
Kimberly Schweitzer ◽  
Scott Freng ◽  
Sean McCrea

2013 ◽  
Vol 133 (12) ◽  
pp. 954-960 ◽  
Author(s):  
Akihiro Ametani ◽  
Kazuki Kawamura ◽  
Asha Shendge ◽  
Naoto Nagaoka ◽  
Yoshihiro Baba

2020 ◽  
Vol 59 (12) ◽  
pp. 126502
Author(s):  
Moataz Eissa ◽  
Takuya Mitarai ◽  
Tomohiro Amemiya ◽  
Yasuyuki Miyamoto ◽  
Nobuhiko Nishiyama

1990 ◽  
Vol 55 (8) ◽  
pp. 2027-2032 ◽  
Author(s):  
Jan Schraml ◽  
Robert Brežný ◽  
Jan Čermák

29Si and 13C NMR spectra of five 4-substituted 2,6-dimethoxytrimethylsiloxybenzenes were studied with the aim to elucidate the nature of the deshielding proximity effects observed in the spectra of ortho substituted trimethylsiloxybenzenes. The sensitivity of 29Si chemical shifts to para substitution is in the studied compounds essentially the same as in mono ortho methoxytrimethylsiloxybenzenes. The deshielding proximity effect of the ìsecondî methoxy group is somewhat smaller than that of the ìfirstî group. The present results indicate that the two methoxy groups assume coplanar conformations with the benzene ring and are turned away from the trimethylsiloxy group which is not in the benzene plane. It is argued that in mono ortho methoxytrimethylsiloxybenzenes the two substituent groups adopt the same conformations as in the compounds studied here.


2019 ◽  
Vol 3 (8) ◽  
Author(s):  
Joost Ridderbos ◽  
Matthias Brauns ◽  
Ang Li ◽  
Erik P. A. M. Bakkers ◽  
Alexander Brinkman ◽  
...  

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