heteroaromatic molecule
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Graphene hydrogels functionalized non-covalently by fused heteroaromatic molecule for asymmetric supercapacitor with ultra-long cycle life

2019 ◽  
Vol 317 ◽  
pp. 437-448 ◽  
Author(s):  
Shanshan Li ◽  
Xiaotong Wang ◽  
Lijie Hou ◽  
Xinyuan Zhang ◽  
Yi Zhou ◽  
...  
Keyword(s):  
Cycle Life ◽  
Asymmetric Supercapacitor ◽  
Long Cycle ◽  
Long Cycle Life ◽  
Heteroaromatic Molecule

Reversible multi-electron redox chemistry of π-conjugated N-containing heteroaromatic molecule-based organic cathodes

Nature Energy ◽  
2017 ◽  
Vol 2 (7) ◽  
Author(s):  
Chengxin Peng ◽  
Guo-Hong Ning ◽  
Jie Su ◽  
Guiming Zhong ◽  
Wei Tang ◽  
...  
Keyword(s):  
Redox Chemistry ◽  
Heteroaromatic Molecule

N,N′-Fused Bisphosphole: Heteroaromatic Molecule with Two-Coordinate and Formally Divalent Phosphorus. Synthesis, Electronic Structure, and Chemical Properties

2014 ◽  
Vol 53 (6) ◽  
pp. 3243-3252 ◽  
Author(s):  
Alexander N. Kornev ◽  
Vyacheslav V. Sushev ◽  
Yulia S. Panova ◽  
Olga V. Lukoyanova ◽  
Sergey Yu. Ketkov ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Chemical Properties ◽  
Heteroaromatic Molecule ◽  
And Chemical Properties

Synthesis of a novel benzodifuran derivative and its molecular recognition of poly rA RNA

2013 ◽  
Vol 394 (9) ◽  
pp. 1235-1239 ◽  
Author(s):  
Giovanni N. Roviello ◽  
Valentina Roviello ◽  
Domenica Musumeci ◽  
Carlo Pedone
Keyword(s):  
Nucleic Acid ◽  
Chemical Synthesis ◽  
Conformational Changes ◽  
Cd Spectroscopy ◽  
Synthetic Approach ◽  
Stoichiometric Ratio ◽  
Dna And Rna ◽  
Nmr Characterization ◽  
Cd Studies ◽  
Heteroaromatic Molecule

Abstract In this manuscript, we describe a synthetic approach to a novel benzodifuran derivative as well as CD studies regarding its ability to interact with DNA and RNA. After the chemical synthesis and ESI-MS and NMR characterization, this heteroaromatic molecule was investigated by CD spectroscopy in order to evaluate it as a potential nucleic acid binder. Interestingly, the benzodifuran compound was found to be able to induce conformational changes in both DNA and RNA homoadenine molecules forming in the latter case a complex with a 6:1 benzodifuran/nucleobase stoichiometric ratio, as evidenced by CD titration experiments.

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