scholarly journals Induced Axial Chirality by a Tight Belt: Naphthalene Chromophores Fixed in a 2,5-Substituted Cofacial para-Phenylene-Ethynylene Framework

2021 ◽  
Author(s):  
Eric Sidler ◽  
Juraj Malinčík ◽  
Alessandro Prescimone ◽  
Marcel Mayor
Keyword(s):  
Phenylene Ethynylene ◽  
Axial Chirality

We report the design of a synthetically easy accessible axial chirality-inducing framework for a chromophore of choice. The scaffold consists of two basic para-phenylene-ethynylene backbones separated by laterally placed corner...

Sterically Crowded Heterocycles. VII. Reduction of Some (Z)-1,3-Diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)prop-2-en-1-ones as Their Axial Chirality Probe

1996 ◽  
Vol 61 (7) ◽  
pp. 1018-1026 ◽  
Author(s):  
Richard Kubík ◽  
Stanislav Böhm ◽  
Josef Kuthan
Keyword(s):  
Hydroxy Derivative ◽  
Borohydride Reduction ◽  
Axial Chirality ◽  
Pm3 Calculations

Borohydride reduction of titled ketones 1a-1g gave diastereoisomeric mixtures of (Z)-1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)prop-2-en-1-ols 2a-2g and 3a-3g in which the former ones prevailed. Only individual racemic products were obtained after borohydride reduction of (E)-1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)-prop-2-en-1-one 4 to corresponding 1-hydroxy derivative 5 and by conversion of (Z)-1-oxo derivative 1a to 1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)propan-1-one (6) with sodium hydrogenselenide. Diastereoselectivity of the borohydride reduction is discussed using the PM3 calculations of the molecules 1a, 2a, 2b, 3a, 3b, 4, 5, and 6.

Self-assembly of chiral oligo(methylene-p-phenylene-ethynylene)s into vesicle-like particles independent of hydrophobicity/hydrophilicity of side chains and solvents

Soft Matter ◽  
2021 ◽  
Author(s):  
Zhiqiang Zhao ◽  
Zheng Bian ◽  
Yu Chen ◽  
Chuanqing Kang ◽  
Lianxun Gao ◽  
...  
Keyword(s):  
Self Assembly ◽  
Molecular Design ◽  
The Self ◽  
Side Chains ◽  
Phenylene Ethynylene

Chiral oligo(methylene-p-phenyleneethynylene)s can form vesicular assemblies no matter whether side chains and solvents are hydrophilic or hydrophobic. The self-assembly processes are highly independent of molecular design and chemical environments.

N‐Heterocyclic Carbene‐Catalyzed Atroposelective Annulation for Access to Thiazine Derivatives with C−N Axial Chirality

2021 ◽  
Vol 60 (17) ◽  
pp. 9362-9367
Author(s):  
Tingting Li ◽  
Chengli Mou ◽  
Puying Qi ◽  
Xiaolin Peng ◽  
Shichun Jiang ◽  
...  
Keyword(s):  
Axial Chirality

Naphthalimide-containing conjugated polyelectrolytes with different chain configurations

2019 ◽  
Vol 17 (10) ◽  
pp. 2635-2639 ◽  
Author(s):  
Yu Chen ◽  
Ying Tan ◽  
Chunyan Tan ◽  
Yunpeng Lu ◽  
Yuzong Chen ◽  
...  
Keyword(s):  
Polymer Chain ◽  
Photophysical Properties ◽  
Phenylene Ethynylene ◽  
Conjugated Polyelectrolytes

Different polymer chain configurations along the main chains of poly(naphthalimide and phenylene ethynylene)s lead to dramatic differences in polymer conformations and photophysical properties.

scholarly journals Asymmetric Alkenyl Catellani Reaction for the Construction of C–N Axial Chirality

2021 ◽  
Author(s):  
Qianghui Zhou ◽  
Chenggui Wu ◽  
Yong Shang ◽  
Chang Liu ◽  
Ze-Shui Liu ◽  
...  
Keyword(s):  
Axial Chirality

Advancing conjugated polymers into nanometer-scale devices

2006 ◽  
Vol 78 (10) ◽  
pp. 1803-1822 ◽  
Author(s):  
Wenping Hu ◽  
Hiroshi Nakashima ◽  
Erjing Wang ◽  
Kazuaki Furukawa ◽  
Hongxiang Li ◽  
...  
Keyword(s):  
Conjugated Polymers ◽  
Molecular Level ◽  
Nanometer Scale ◽  
Transport Mechanisms ◽  
Phenylene Ethynylene ◽  
Polymer Molecules ◽  
Polymer Electronics ◽  
End Groups

In this article, we review the possibility of combining conjugated polymers with nanometer-scale devices (nanodevices), in order to introduce the properties associated with conjugated polymers into such nanodevices. This approach envisages combining the highly topical disciplines of polymer electronics and nanoelectronics to engender a new subdirection of polymer nanoelectronics, which can serve as a tool to probe the behavior of polymer molecules at the nanometer/molecular level, and contribute to clarifying transport mechanisms in conjugated polymers. In this study, we exemplify this combination, using a family of linear and conjugated polymers, poly(p-phenylene-ethynylene)s (PPEs) with thiolacetate-functionalized end groups.

A poly(p-phenylene ethynylene vinylene) with pendant fullerenes

2001 ◽  
Vol 119 (1-3) ◽  
pp. 171-172 ◽  
Author(s):  
A. Marcos Ramos ◽  
M.T. Rispens ◽  
J.C. Hummelen ◽  
R.A.J. Janssen
Keyword(s):  
Phenylene Ethynylene
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