The principal optical polarisabilities of the naphthalene molecule

1935 ◽  
Vol 1 (7) ◽  
pp. 425-430 ◽  
Author(s):  
M. Ramanadham
Keyword(s):  
Naphthalene Molecule ◽  
Optical Polarisabilities

Ring current model of the naphthalene molecule

1997 ◽  
Vol 92 (3) ◽  
pp. 609-617 ◽  
Author(s):  
RICCARDO ZANASI ◽  
PAOLO LAZZERETTI
Keyword(s):  
Ring Current ◽  
Current Model ◽  
Naphthalene Molecule

scholarly journals Guest-induced fluorescence property of macrocyclic boronic ester

2014 ◽  
Vol 70 (a1) ◽  
pp. C672-C672
Author(s):  
Haruki Sugiyama ◽  
Kohei Johmoto ◽  
Hidehiro Uekusa ◽  
Yuji Kikuchi ◽  
Hiroki Takahagi ◽  
...  
Keyword(s):  
Crystal Packing ◽  
Uv Light ◽  
Condensation Reaction ◽  
Fluorescence Property ◽  
Channel Structure ◽  
Diffusion Method ◽  
Blue Color ◽  
Guest Molecules ◽  
One Dimensional ◽  
Naphthalene Molecule

Macrocyclic boronic esters (1) are obtained as a self-assembled molecule by condensation reaction between rac-tetrol (2) and 1,4-naphthalenediboronic acid (3) in the presence of toluene molecule [1]. In the crystal, this macrocyclic molecules form a charasteristic one dimensional channel structure that accommodates various small molecules. Interestingly, reversible desorption / absorption phenomena of guest molecules is observed without significant crystal packing change, meaning this crystal may have guest storage, separation, and catalytic abilities. In the course of exploring further functional aspects of the molecule, we give fluorescence property to this crystal by inclusion of acene molecules into this robust one dimensional channel structure. Naphthalene inclusion crystal was obtained by the diffusion method. The crystal structure is isostructural to known crystals, that is, a naphthalene molecule is included in a channel and sandwiched by two naphthalene moieties of the macrocyclic molecule (inter planar distance is about 3.6 angstrom). Under UV light, a blue color fluorescence observed in this crystal, suggesting the guest naphthalene molecule contributes the fluorescence property. After heating by 200 degrees C, the naphthalene was released to leave isostructural apohost crystal without fluorescence property. However, by naphthalene vapor exposure to the apohost crystal, the fluorescence property was recovered, which means naphthalene desorption and absorption are possible in crystalline state. Moreover Anthracene and Tetracene inclusion crystal were obtained, and they also showed light blue and yellow color fluorescence under UV light, respectively. Thus, the fluorescence function was successfully realized by inclusion of acene molecule in the one dimensional channel of the crystals, and furthermore the fluorescent color can be controlled by changing acene molecules.

Doppler-free high resolution laser spectroscopies of the naphthalene molecule

2002 ◽  
Vol 283 (1-2) ◽  
pp. 237-247 ◽  
Author(s):  
M.H. Kabir ◽  
S. Kasahara ◽  
W. Demtröder ◽  
Y. Tatamitani ◽  
M. Okubo ◽  
...  
Keyword(s):  
High Resolution ◽  
Naphthalene Molecule

Vibrational Dynamics of the Neutral Naphthalene Molecule from a Tight-Binding Approach

2002 ◽  
Vol 106 (43) ◽  
pp. 10144-10151 ◽  
Author(s):  
Nguyen-Thi Van-Oanh ◽  
Pascal Parneix ◽  
Philippe Bréchignac
Keyword(s):  
Tight Binding ◽  
Vibrational Dynamics ◽  
Naphthalene Molecule

An electron diffraction investigation of the peri -bonds in perylene

1965 ◽  
Vol 283 (1395) ◽  
pp. 557-575 ◽  
Keyword(s):  
Molecular Structure ◽  
Electron Diffraction ◽  
Bond Length ◽  
Bond Distance ◽  
Diffraction Method ◽  
Vapour Phase ◽  
Electron Diffraction Investigation ◽  
Carbon Bond ◽  
Carbon Carbon Bond ◽  
Naphthalene Molecule

The molecular structure of perylene has been studied in the vapour phase by the sector electron diffraction method. The average carbon-carbon bond distance in perylene apart from the peri -bonds was found to be about 0·010 Ǻ longer than the average carbon-carbon bond distance in the naphthalene molecule. The peri -bond length was determined to be 1·493 ± 0·015 Ǻ.

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