Organised structures of flexible bolaamphiphiles with trisiloxane spacers: three- and two-dimensional molecular assemblies with different molecular conformation

Soft Matter ◽  
2006 ◽  
Vol 2 (2) ◽  
pp. 157 ◽  
Author(s):  
Norihiro Mizoshita ◽  
Takahiro Seki
Langmuir ◽  
1992 ◽  
Vol 8 (3) ◽  
pp. 894-897 ◽  
Author(s):  
Abraham Ulman ◽  
Raymond P. Scaringe

1986 ◽  
Vol 158 (2) ◽  
pp. 323-332 ◽  
Author(s):  
Kandala V. R. CHARY ◽  
Sudha SRIVASTAVA ◽  
Ramakrishna V. HOSUR ◽  
Kunal B. ROY ◽  
Girjesh GOVIL

2009 ◽  
Vol 19 (10) ◽  
pp. 1490 ◽  
Author(s):  
Xiaojing Ma ◽  
Yibao Li ◽  
Xiaohui Qiu ◽  
Keqing Zhao ◽  
Yanlian Yang ◽  
...  

2014 ◽  
Vol 70 (2) ◽  
pp. o219-o220
Author(s):  
K. R. Roopashree ◽  
K. Mahesh Kumar ◽  
B. R. Anitha ◽  
A. J. Ravi ◽  
H. C. Devarajegowda

In the title compound, C18H22N2O4S2, the 2H-chromene ring system is essentially planar (r.m.s. deviation = 0.012 Å). The molecular conformation is stabilized by a C—H...O hydrogen bond. In the crystal, N—H...S and C—H...O hydrogen bonds occur, the former enclosing anR22(22) ring motif, and lead to the formation of a two-dimensional slab-like network lying parallel to (10-1). π–π interactions are observed between inversion-related aromatic rings [shortest centroid–centroid distance = 3.6300 (11) Å].


1994 ◽  
Vol 1 (1) ◽  
pp. 33-38 ◽  
Author(s):  
M. Shimomura ◽  
S. Aiba ◽  
S. Oguma ◽  
M. Oguchi ◽  
M. Matsute ◽  
...  

Langmuir ◽  
1995 ◽  
Vol 11 (3) ◽  
pp. 969-976 ◽  
Author(s):  
Masatsugu Shimomura ◽  
Satoshi Aiba ◽  
Nobuyoshi Tajima ◽  
Noriko Inoue ◽  
Kenji Okuyama

2017 ◽  
Vol 246 ◽  
pp. 823-829
Author(s):  
Yu Wang ◽  
Yibin Sun ◽  
Xiaobing Ding ◽  
Jinghong Liang ◽  
Xiaoyu Cao ◽  
...  

2007 ◽  
Vol 121-123 ◽  
pp. 369-372
Author(s):  
S. de Feyter ◽  
A. Miura ◽  
H. Uji-i ◽  
P. Jonkheijm ◽  
A.P.H.J. Schenning ◽  
...  

With scanning tunneling microscopy (STM), the intramolecular conformational and intermolecular ordering aspects have been investigated of a variety of organic molecules physisorbed at the liquid-solid interface. By balancing the interplay between intramolecular and intermolecular interactions (hydrogen bonding), leading to control of the molecular conformation, foldamers were created which order into well-defined two-dimensional crystals. The nature of the hydrogen bonding groups in conjugated oligomers leads to the formation of infinite stacks and cyclic multimers, expressing the chiral nature of the molecules.


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