Rotational transitions of SO, SiO, and SiS excited by a discharge in a supersonic molecular beam: Vibrational temperatures, Dunham coefficients, Born–Oppenheimer breakdown, and hyperfine structure

2003 ◽  
Vol 119 (22) ◽  
pp. 11715-11727 ◽  
Author(s):  
M. Eugenia Sanz ◽  
Michael C. McCarthy ◽  
Patrick Thaddeus
1953 ◽  
Vol 91 (6) ◽  
pp. 1403-1408 ◽  
Author(s):  
B. P. Fabricand ◽  
R. O. Carlson ◽  
C. A. Lee ◽  
I. I. Rabi

1953 ◽  
Vol 91 (6) ◽  
pp. 1395-1403 ◽  
Author(s):  
Charles A. Lee ◽  
B. P. Fabricand ◽  
R. O. Carlson ◽  
I. I. Rabi

2013 ◽  
Vol 8 (0) ◽  
pp. 1402066-1402066 ◽  
Author(s):  
Linge ZANG ◽  
Nobuhiro NISHINO ◽  
Tohru MIZUUCHI ◽  
Shinsuke OHSHIMA ◽  
Masaki TAKEUCHI ◽  
...  

1988 ◽  
Vol 152 (1) ◽  
pp. 87-93 ◽  
Author(s):  
K. McMillan ◽  
D. Bender ◽  
M. Eliades ◽  
D. Danzeiser ◽  
B.A. Wofford ◽  
...  

2021 ◽  
Vol 92 (4) ◽  
pp. 043539
Author(s):  
Guoliang Xiao ◽  
Jiao Yin ◽  
Chengyuan Chen ◽  
Beibin Feng ◽  
Wulyu Zhong ◽  
...  

1993 ◽  
Vol 48 (12) ◽  
pp. 1219-1222 ◽  
Author(s):  
U. Kretschmer ◽  
H. Dreizler

Abstract We investigated the 33S nuclear quadrupole coupling of thiazole- 33S in natural abundance by molecular beam Fourier transform microwave spectroscopy. In addition the 14N nuclear quadrupole coupling could be analyzed with high precision. We derived the rotational constants A = 8529.29268 (70) MHz, B = 5427.47098 MHz, and C = 3315.21676 (26) MHz, quartic centrifugal distortion constants and the quadrupole coupling constants of 33S χaa = 7.1708 (61) MHz and χbb= -26.1749 (69) MHz and of 14N χ aa = -2.7411 (61) MHz and χbb = 0.0767 (69) MHz.


2001 ◽  
Vol 3 (4) ◽  
pp. 223-227 ◽  
Author(s):  
A. Giardini Guidoni ◽  
S. Piccirillo ◽  
D. Scuderi ◽  
M. Satta ◽  
T. M. Di Palma ◽  
...  

One and two-color, mass selected R2PI spectra of theS1←S0transitions in the bare(+)-(R)- 1-phenyl-1-ethanol(ER) and its complexes with different solvent molecules (solv) (-)-(R)-2-butanol(BR) or(+)-(S)-2-butanol(BS), (—)-(R)-2-pentanol (TR) or(+)-(S)-2-pentanol(TS) and(-)-(R)-2-butylamine(AR) or(+)-(S)-2-butylamine(AS), have been recorded after a supersonic molecular beam expansion. The one-color R2PI excitation spectra of the diastereomeric complexes are characterized by significant shifts of their band origin relative to that of bareER. The extent and the direction of these spectral shifts are found to depend upon the structure and the configuration ofsolvand are attributed to different short-range interactions in the ground and excited states of the complexes. In analogy with other diastereomeric complexes, the phenomenological binding energy of the homochiral cluster is found to be greater than that of the heterochiral one. Preliminary measurements of excitation spectrum of(+)-(R)-1-Indanol(IR) is also reported.


RSC Advances ◽  
2016 ◽  
Vol 6 (44) ◽  
pp. 37982-37993 ◽  
Author(s):  
Roberta Tatti ◽  
Lucrezia Aversa ◽  
Roberto Verucchi ◽  
Emanuele Cavaliere ◽  
Giovanni Garberoglio ◽  
...  

High kinetic energy impacts between inorganic surfaces and molecular beams seeded by organics represent a fundamental tool in materials science, particularly when they activate chemical–physical processes leading to nanocrystals' growth.


2007 ◽  
Vol 98 (7) ◽  
Author(s):  
Yu Wu ◽  
Tullio Toccoli ◽  
Norbert Koch ◽  
Erica Iacob ◽  
Alessia Pallaoro ◽  
...  

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