Donor–acceptor interaction-driven folding of linear naphthalene–glycol oligomers templated by a rigid bipyridinium rod

2015 ◽  
Vol 2 (12) ◽  
pp. 1578-1583 ◽  
Author(s):  
Tian-Guang Zhan ◽  
Ben-Ye Lu ◽  
Feng Lin ◽  
Tian-You Zhou ◽  
Xin Zhao ◽  
...  
Keyword(s):  
Self Assembly ◽  
Supramolecular Structures ◽  
The Self ◽  
Acceptor Interaction ◽  
Donor Acceptor ◽  
Rigid Rod ◽  
Glycol Oligomers

The construction of folded and helical supramolecular structures through the self-assembly of a series of flexible linear oligomers induced by a rigid rod-like template has been demonstrated.

Role of the deposition temperature on the self-assembly of the non-planar molecule benzene-1,3,5-triphosphonic acid (BTP) at the liquid–solid interface

2016 ◽  
Vol 18 (35) ◽  
pp. 24219-24227 ◽  
Author(s):  
Doan Chau Yen Nguyen ◽  
Lars Smykalla ◽  
Thi Ngoc Ha Nguyen ◽  
Michael Mehring ◽  
Michael Hietschold
Keyword(s):  
Self Assembly ◽  
Deposition Temperature ◽  
Supramolecular Structures ◽  
The Self ◽  
Solid Interface ◽  
Planar Molecule ◽  
Hydrogen Bonded

Hydrogen-bonded supramolecular structures of BTP at the undecanol–graphite interface were studied by STM in dependence on the deposition temperature.

Bis-naphthalimides bridged by electron acceptors: optical and self-assembly characteristics

RSC Advances ◽  
2016 ◽  
Vol 6 (75) ◽  
pp. 71638-71651 ◽  
Author(s):  
Ankita Saini ◽  
K. R. Justin Thomas
Keyword(s):  
Self Assembly ◽  
Organic Molecules ◽  
Vital Role ◽  
Electron Acceptors ◽  
Supramolecular Structures ◽  
The Self ◽  
Small Organic Molecules

The self-assembly of small organic molecules into molecular stacks plays a vital role in the construction of stable supramolecular structures.

scholarly journals {N 1-[2-(Butylselanyl)benzyl]-N 2,N 2-dimethylethane-1,2-diamine}dichloridomercury(II)

2018 ◽  
Vol 74 (8) ◽  
pp. 1151-1154
Author(s):  
Pushpendra Singh ◽  
Harkesh B. Singh ◽  
Ray J. Butcher
Keyword(s):  
Hydrogen Bonding ◽  
Solid State ◽  
Self Assembly ◽  
Title Compound ◽  
Supramolecular Assembly ◽  
Molecular Geometry ◽  
The Self ◽  
Intermolecular Hydrogen Bonding ◽  
Hydrogen Bonding Interactions ◽  
Donor Acceptor

In the title compound, [HgCl2(C16H28N2Se)], the primary geometry around the Se and Hg atoms is distorted trigonal–pyramidal and distorted square-pyramidal, respectively. The distortion of the molecular geometry in the complex is caused by the steric demands of the ligands attached to the Se atom. The Hg atom is coordinated through two chloride anions, an N atom and an Se atom, making up an unusual HgNSeCl2 coordination sphere with an additional long Hg...N interaction. Intermolecular C—H...Cl interactions are the only identified intermolecular hydrogen-bonding interactions that seem to be responsible for the self assembly. These relatively weak C—H...Cl hydrogen bonds possess the required linearity and donor–acceptor distances. They act as molecular associative forces that result in a supramolecular assembly along the b-axis direction in the solid state of the title compound.

scholarly journals Design directed self-assembly of donor–acceptor polymers

2016 ◽  
Vol 52 (73) ◽  
pp. 10938-10947 ◽  
Author(s):  
Tomasz Marszalek ◽  
Mengmeng Li ◽  
Wojciech Pisula
Keyword(s):  
Molecular Weight ◽  
Self Assembly ◽  
The Self ◽  
Side Chain ◽  
Structural Factors ◽  
Chemical Design ◽  
Donor Acceptor

This review discusses the role of chemical design on the self-assembly of donor–acceptor polymers on surfaces. Three major structural factors are highlighted including molecular weight, side chain engineering and backbone curvature of the polymers.

Electrochemical probing of hydrogelation induced by the self-assembly of a donor–acceptor complex comprising pyranine and viologen

2017 ◽  
Vol 53 (15) ◽  
pp. 2371-2374 ◽  
Author(s):  
Sougata Datta ◽  
Nilanjan Dey ◽  
Santanu Bhattacharya
Keyword(s):  
Self Assembly ◽  
Methyl Viologen ◽  
Electrochemical Analysis ◽  
The Self ◽  
Acceptor Complex ◽  
Two Component ◽  
Donor Acceptor

We report the electrochemical analysis of a donor–acceptor type two-component hydrogelation by an electroactive co-assembly of pyranine and n-dodecyl methyl viologen.

Donor–acceptor interaction-driven self-assembly of amphiphilic rod–coil molecules into supramolecular nanoassemblies

Nanoscale ◽  
2017 ◽  
Vol 9 (45) ◽  
pp. 17975-17982 ◽  
Author(s):  
Shengsheng Yu ◽  
Yuntian Yang ◽  
Tie Chen ◽  
Jingzhe Xu ◽  
Long Yi Jin
Keyword(s):  
Charge Transfer ◽  
Self Assembly ◽  
Acceptor Interaction ◽  
Donor Acceptor ◽  
Spherical Micelles

Pyrene-based amphiphiles self-assemble into nanofibers, spherical micelles and multilayer nanotubes. The addition of TNF allowed polymerization of these objects through charge-transfer interactions to form various supramolecular nanoassemblies.

Planarization of tetracarboxamides: tuning the self-assembly of polycyclic aromatic hydrocarbons

2019 ◽  
Vol 55 (43) ◽  
pp. 6070-6073
Author(s):  
Yeray Dorca ◽  
Cristina Naranjo ◽  
Patricia Delgado-Martínez ◽  
Rafael Gómez ◽  
Luis Sánchez
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Self Assembly ◽  
Supramolecular Structures ◽  
The Self ◽  
Supramolecular Polymers ◽  
Self Assembling ◽  
Π Stacking ◽  
Polycyclic Aromatic

The geometry-dependent self-assembling features of two PAHs, 1 and 2, is reported. The more planar 1 forms H-type supramolecular polymers, in a highly cooperative fashion by combination of H-bonding and π-stacking, with rod-like morphology. However, the highly distorted 2 interacts only by means of H-bonding yielding lamellar supramolecular structures.

Self-assembly of Hydrazide-based Heterodimers Driven by Hydrogen Bonding and Donor-Acceptor Interaction†

2006 ◽  
Vol 24 (9) ◽  
pp. 1200-1208 ◽  
Author(s):  
Dai-Jun Feng ◽  
Peng Wang ◽  
Xiao-Qiang Li ◽  
Zhan-Ting Li
Keyword(s):  
Hydrogen Bonding ◽  
Self Assembly ◽  
Acceptor Interaction ◽  
Donor Acceptor
Sign in / Sign up

Export Citation Format

Share Document