Interplay between Hydrogen Bonding, Epitaxy, and Charge Transfer in the Self-Assembly of Croconic Acid on Au(111) and Ag(111)

2015 ◽  
Vol 119 (47) ◽  
pp. 26429-26437 ◽  
Author(s):  
J. Hooper ◽  
D. A. Kunkel ◽  
E. Zurek ◽  
A. Enders
Keyword(s):  
Hydrogen Bonding ◽  
Charge Transfer ◽  
Self Assembly ◽  
The Self

Recording the Self-Assembly Behavior of Nanomaterials Directed by Hydrogen Bonding

2021 ◽  
Author(s):  
Ganghuo Pan ◽  
Jie Leng ◽  
Liye Deng ◽  
Liwen Xing ◽  
Rui Feng
Keyword(s):  
Hydrogen Bonding ◽  
Self Assembly ◽  
The Self ◽  
Assembly Behavior

Self-Assembly of Alkali Lignin in Tetrahydrofuran

2012 ◽  
Vol 550-553 ◽  
pp. 57-61
Author(s):  
Hao Li ◽  
Yong Hong Deng ◽  
Kai Huang
Keyword(s):  
Charge Transfer ◽  
Electrostatic Interaction ◽  
Self Assembly ◽  
The Self ◽  
Charge Transfer Complexes ◽  
Layer By Layer ◽  
Alkali Lignin ◽  
Higher Temperature ◽  
Effects Of Temperature

Alkali lignin (AL) was used as a polyanion to form layer-by-layer self-assembled film with PDAC as a polycation. The effects of temperature and concentration on the adsorption characteristics of AL were investigated. Iodine was added into AL solutions to study the role of π-π interaction in self-assembly of AL and PDAC. Results show that the self-assembly of AL/PDAC is mainly driven by π-π interaction and electrostatic interaction. A higher temperature or a larger concentration can enhance the aggregation of lignin. I2 can form lignin–iodine charge–transfer complexes with AL to reduce the degree of aggregation of AL, so the adsorbed amount of AL decreases significantly with increasing iodine contents.

scholarly journals Influence of the hydrophobic domain on the self-assembly and hydrogen bonding of hydroxy-amphiphiles

2019 ◽  
Vol 21 (21) ◽  
pp. 11242-11258
Author(s):  
Valery Andrushchenko ◽  
Walter Pohle
Keyword(s):  
Hydrogen Bonding ◽  
Ir Spectroscopy ◽  
Self Assembly ◽  
Supramolecular Assemblies ◽  
The Self ◽  
Hydrophobic Domain

IR spectroscopy paired with calculations reveals that structurally similar amphiphiles ODA and DOG form very different supramolecular assemblies.

Cooperative self-assembly and gelation of organogold(i) complexes via hydrogen bonding and aurophilic Au⋯Au interactions

2017 ◽  
Vol 53 (84) ◽  
pp. 11552-11555 ◽  
Author(s):  
Jiangjun Chen ◽  
Zhongxin Zhang ◽  
Chengming Wang ◽  
Zhao Gao ◽  
Zongchun Gao ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Self Assembly ◽  
The Self ◽  
Self Assembled

Organogold(i)-based fibers and gels have been successfully constructed, which involve Au⋯Au interactions in the self-assembled structures.

Charge-Assisted Hydrogen Bonding and Other Noncovalent Interactions in the Self-Assembly of the Organometallic Building Block [(η6-hydroquinone)Rh(P(OPh)3)2]+with a Range of Counteranions

2006 ◽  
Vol 25 (22) ◽  
pp. 5276-5285 ◽  
Author(s):  
Seung Uk Son ◽  
Jeffrey A. Reingold ◽  
Gene B. Carpenter ◽  
Paul T. Czech ◽  
Dwight A. Sweigart
Keyword(s):  
Hydrogen Bonding ◽  
Self Assembly ◽  
Building Block ◽  
Noncovalent Interactions ◽  
The Self

Mastering nanostructured materials through H-bonding recognitions at interfaces

2010 ◽  
Vol 82 (4) ◽  
pp. 917-929 ◽  
Author(s):  
Stefan Mohnani ◽  
Anna Llanes-Pallas ◽  
Davide Bonifazi
Keyword(s):  
Hydrogen Bonding ◽  
Electronic Properties ◽  
Nanostructured Materials ◽  
Self Assembly ◽  
The Self ◽  
Memory Storage ◽  
Technological Application ◽  
Storage Devices ◽  
Hydrogen Bonding Interactions ◽  
Fundamental Research

The controlled engineering of functional architectures composed of π-systems with unusual opto-electronic properties is currently being investigated intensively from both fundamental research and technological application viewpoints. In particular, the exploitation of the supramolecular approach for the facile construction of multidimensional architectures, featuring cavities capable of hosting functional molecules, could be used in several applications, such as nanomedicine, molecular-based memory storage devices, and sensors. This paper highlights our recent strategies to use hydrogen-bonding interactions to prepare nanostructured functional architectures via the self-assembly of organic molecular modules studied at different interfaces.

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.

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