Raman band shapes and dynamics of molecular motion for SF6in the supercritical dense fluid region

1981 ◽  
Vol 75 (4) ◽  
pp. 1612-1622 ◽  
Author(s):  
T. W. Żerda ◽  
J. Schroeder ◽  
J. Jonas
Keyword(s):  
Molecular Motion ◽  
Raman Band ◽  
Dense Fluid

Molecular motion ofn‐alkane chains in urea inclusion adducts studied by analysis of Raman band profiles

1990 ◽  
Vol 93 (7) ◽  
pp. 4659-4672 ◽  
Author(s):  
Masamichi Kobayashi ◽  
Hiroshi Koizumi ◽  
Yonhae Cho
Keyword(s):  
Molecular Motion ◽  
Raman Band ◽  
Urea Inclusion

Molecular motion in the van der Waals solid C6H6:C6F6

1992 ◽  
Vol 89 ◽  
pp. 1755-1766 ◽  
Author(s):  
JH Williams ◽  
RP White
Keyword(s):  
Molecular Motion ◽  
Van Der Waals

VIBRATIONAL SPECTROSCOPY, RESONANCE FRACTION AND MOLECULAR MOTION

1974 ◽  
Vol 35 (C6) ◽  
pp. C6-131-C6-137 ◽  
Author(s):  
Y. HAZONY ◽  
R. H. HERBER
Keyword(s):  
Vibrational Spectroscopy ◽  
Molecular Motion

Evidence of Molecular Motion

2019 ◽  
Vol 087 (04) ◽  
Author(s):  
Arthur Odom ◽  
Clare Bell
Keyword(s):  
Molecular Motion

Visualization and Manipulation of Molecular Motion in Solid State through Photo-Induced Clusteroluminescence

2019 ◽  
Author(s):  
Haoke Zhang ◽  
Lili Du ◽  
Lin Wang ◽  
Junkai Liu ◽  
Qing Wan ◽  
...  
Keyword(s):  
Quantum Mechanics ◽  
Excited State ◽  
Solid State ◽  
Light Source ◽  
Molecular Motion ◽  
Molecular Machine ◽  
Conjugated Molecules ◽  
Time Resolved ◽  
Packing Structure ◽  
New Strategy

<p>Building molecular machine has long been a dream of scientists as it is expected to revolutionize many aspects of technology and medicine. Implementing the solid-state molecular motion is the prerequisite for a practical molecular machine. However, few works on solid-state molecular motion have been reported and it is almost impossible to “see” the motion even if it happens. Here the light-driven molecular motion in solid state is discovered in two non-conjugated molecules <i>s</i>-DPE and <i>s</i>-DPE-TM, resulting in the formation of excited-state though-space complex (ESTSC). Meanwhile, the newly formed ESTSC generates an abnormal visible emission which is termed as clusteroluminescence. Notably, the original packing structure can recover from ESTSC when the light source is removed. These processes have been confirmed by time-resolved spectroscopy and quantum mechanics calculation. This work provides a new strategy to manipulate and “see” solid-state molecular motion and gains new insights into the mechanistic picture of clusteroluminescence.<br></p>

RAMAN SPECTRA OF TITANIUM DI-, TRI-, AND TETRA-CHLORIDES

2001 ◽  
Vol 15 (28n30) ◽  
pp. 3865-3868 ◽  
Author(s):  
H. MIYAOKA ◽  
T. KUZE ◽  
H. SANO ◽  
H. MORI ◽  
G. MIZUTANI ◽  
...  
Keyword(s):  
Force Constant ◽  
Raman Spectra ◽  
Normal Mode ◽  
Raman Band ◽  
Normal Mode Analysis ◽  
Force Constants ◽  
Mode Analysis ◽  
Oxidation Number

We have obtained the Raman spectra of TiCl n (n= 2, 3, and 4). Assignments of the observed Raman bands were made by a normal mode analysis. The force constants were determined from the observed Raman band frequencies. We have found that the Ti-Cl stretching force constant increases as the oxidation number of the Ti species increases.

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