Molecular Orientation, Aggregation, and Order in Rhodamine Films at the Fused Silica/Air Interface

1999 ◽  
Vol 103 (7) ◽  
pp. 1124-1133 ◽  
Author(s):  
Tanya Kikteva ◽  
Dmitry Star ◽  
Zhihong Zhao ◽  
Tammy L. Baisley ◽  
Gary W. Leach
1995 ◽  
Vol 413 ◽  
Author(s):  
Xiaoguang Yang ◽  
Laura Smilowitz ◽  
C. Thomas Buscher ◽  
Duncan McBranch ◽  
Jeanne Robinson ◽  
...  

ABSTRACTSelf-assembled molecular architechtures of nonlinear optical (NLO) chromophores and their super-chromophores are discussed. The chromophores are derivatives of azobenzene sulfonates and the super chromophores are derivatives of calix[4]stilbazole and calix[4]stilbazolium. The studies of azobenzene sulfonates are aimed at understanding the surface coverage and molecular orientation in polar self-assembled monolayers (SAMs). The optimized molecular orientation was found to be 32±3 degree and the maximum surface coverage is approximately 2–4 molecules per nm2 depending on the molecular cross-section. The calixarene chromophores are macrocyclic compounds consisting of four simple D-π-A units bridged by methylene groups. These molecules were synthesized such that four D-π-A units of the calix[4]arene were aligned along the same direction with the calixarene in a cone conformation. Both simple and super-chromophores were subsequently fabricated into covalently bound selfassembled monolayers on the surfaces of fused silica and silicon. Spectroscopic second harmonic generation (SHG) measurements were carried out to determine the absolute value of the dominant element of the second-order nonlinear susceptibility, d33 = 60 pm/V at a fundamental wavelength of 890 nm. Furthermore, SHG imaging was employed to investigate the pattemed SAMs of NLO super chromophores.


1994 ◽  
Vol 50 (1) ◽  
pp. 614-617 ◽  
Author(s):  
Akihiko Sugimura ◽  
Mitsumasa Iwamoto ◽  
Ou-Yang Zhong-can

2015 ◽  
Vol 17 (36) ◽  
pp. 23559-23564 ◽  
Author(s):  
Yuki Nagata ◽  
Taisuke Hasegawa ◽  
Ellen H. G. Backus ◽  
Kota Usui ◽  
Seiji Yoshimune ◽  
...  

We examine the temperature dependence of the interfacial molecular structure at the water–air interface by combining experimental and simulated sum-frequency generation (SFG) spectroscopy.


1996 ◽  
Vol 54 (6) ◽  
pp. 6537-6540 ◽  
Author(s):  
Mitsumasa Iwamoto ◽  
Akihiko Sugimura ◽  
Ou-Yang Zhong-can

2000 ◽  
Vol 661 ◽  
Author(s):  
Keshav S. Gautam ◽  
Ali Dhinojwala

ABSTRACTMolecular orientation of octadecyl alkyl side chains at the poly (vinyl octadecyl carbamates-co-vinyl acetate) polymer-air interface has been studied using surface sensitive sum frequency generation (SFG) spectroscopy. At 280C, below the side chain crystalline transition temperature, the SFG spectra show strong methyl vibrations indicating ordered alkyl side chains at the polymer-air interface. In the liquid state (980C), the SFG spectra show higher contributions from the methylene vibrations indicating higher gauche defects at the interface. This surface order to disorder transition is gradual and spans over a broad temperature range (50-900C), where the bulk is in the smectic liquid crystalline state.


Sign in / Sign up

Export Citation Format

Share Document