4.5 Article

Small Heterocyclic D-π-D-π-A Push-Pull Molecules with Complex Electron Donors

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2021, 期 22, 页码 3223-3233

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.202100137

关键词

DFT calculations; Heteroaromatic donors; N; N'-dibutyl-2-thiobarbituric acid; Optoelectronic properties; Small push-pull chromophores

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This study designed and synthesized a series of small push-pull chromophores based on electron-withdrawing N,N'-dibutylthiobarbituric acid. The relationship between structure and properties, especially focusing on the type of pi-linker and donor, was elucidated through experimental and theoretical methods.
A large series of small push-pull chromophores based on electron-withdrawing N,N'-dibutylthiobarbituric acid has been designed and successfully synthesized. The electron donating part involves common mesomeric donors such as methoxy, N,N-dimethylamino, N,N-diphenylamino, and piperidin-1-yl groups. Five-membered heteroaromatics, namely thiophene, N-methylpyrrole, and furan have been employed as electron rich pi-linkers and auxiliary donors. Structural analogues bearing aromatic 1,4-phenylene linker were also synthesized for comparison. Fundamental thermal and optoelectronic properties were studied by differential scanning calorimetry, cyclic voltammetry, and absorption spectroscopy. Thorough structure-property relationships were elucidated, focusing mostly on type of the used pi-linker and donor. All experimental conclusions are corroborated by theoretical calculations. The study has shown that a complex donor moiety may be built by properly combining mesomeric and auxiliary donors. Whereas strong mesomeric donor (amino) suppresses the donating effect of auxiliary donors/pi-linkers, a combination of weak donor (methoxy) appended at a five-membered heterocycle pronounces the donating ability of the latter.

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