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
Keyword(s):  
Molecular Conformation ◽  
Two Dimensional ◽  
Molecular Assemblies

On the formation of ordered two-dimensional molecular assemblies

Langmuir ◽  
1992 ◽  
Vol 8 (3) ◽  
pp. 894-897 ◽  
Author(s):  
Abraham Ulman ◽  
Raymond P. Scaringe
Keyword(s):  
Two Dimensional ◽  
Molecular Assemblies

scholarly journals Molecular conformation of gonadoliberin using two-dimensional NMR spectroscopy

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

Two-dimensional rigid molecular network with elastic boundaries for constructing hybrid molecular assemblies

2009 ◽  
Vol 19 (10) ◽  
pp. 1490 ◽  
Author(s):  
Xiaojing Ma ◽  
Yibao Li ◽  
Xiaohui Qiu ◽  
Keqing Zhao ◽  
Yanlian Yang ◽  
...  
Keyword(s):  
Molecular Network ◽  
Two Dimensional ◽  
Molecular Assemblies

scholarly journals Ethyl (4-{[(diethylcarbamothioyl)sulfanyl]methyl}-2-oxo-2H-chromen-7-yl)carbamate

2014 ◽  
Vol 70 (2) ◽  
pp. o219-o220
Author(s):  
K. R. Roopashree ◽  
K. Mahesh Kumar ◽  
B. R. Anitha ◽  
A. J. Ravi ◽  
H. C. Devarajegowda
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonds ◽  
Molecular Conformation ◽  
Ring System ◽  
Two Dimensional ◽  
Aromatic Rings ◽  
Compound C ◽  
Centroid Distance ◽  
Ring Motif ◽  
Chromene Ring

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].

Tailored charge transfer complex based on two-dimensional molecular assemblies

1994 ◽  
Vol 1 (1) ◽  
pp. 33-38 ◽  
Author(s):  
M. Shimomura ◽  
S. Aiba ◽  
S. Oguma ◽  
M. Oguchi ◽  
M. Matsute ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Charge Transfer Complex ◽  
Two Dimensional ◽  
Molecular Assemblies

"Crystal Engineering" Based on Two-Dimensional Molecular Assemblies. Relation between Chemical Structure and Molecular Orientation in Cast Bilayer Films

Langmuir ◽  
1995 ◽  
Vol 11 (3) ◽  
pp. 969-976 ◽  
Author(s):  
Masatsugu Shimomura ◽  
Satoshi Aiba ◽  
Nobuyoshi Tajima ◽  
Noriko Inoue ◽  
Kenji Okuyama
Keyword(s):  
Crystal Engineering ◽  
Molecular Orientation ◽  
Chemical Structure ◽  
Two Dimensional ◽  
Molecular Assemblies ◽  
Bilayer Films

A combined electro- and photo-chemical approach to repeatedly fabricate two-dimensional molecular assemblies

2017 ◽  
Vol 246 ◽  
pp. 823-829
Author(s):  
Yu Wang ◽  
Yibin Sun ◽  
Xiaobing Ding ◽  
Jinghong Liang ◽  
Xiaoyu Cao ◽  
...  
Keyword(s):  
Two Dimensional ◽  
Molecular Assemblies ◽  
Chemical Approach

Supramolecular Chemistry at the Liquid/Solid Interface a Scanning Tunneling Microscopy Approach

2007 ◽  
Vol 121-123 ◽  
pp. 369-372
Author(s):  
S. de Feyter ◽  
A. Miura ◽  
H. Uji-i ◽  
P. Jonkheijm ◽  
A.P.H.J. Schenning ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Scanning Tunneling Microscopy ◽  
Supramolecular Chemistry ◽  
Organic Molecules ◽  
Molecular Conformation ◽  
Scanning Tunneling ◽  
Conjugated Oligomers ◽  
Two Dimensional ◽  
Tunneling Microscopy ◽  
Solid Interface

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.

Sign in / Sign up

Export Citation Format

Share Document