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231226s2022 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.2c01076
|2 doi
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|a pubmed24n1143.xml
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|a eng
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|a Yan, Qi
|e verfasserin
|4 aut
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|a Co-assembly Behaviors of Flavonol Derivatives Induced by a Pyridine Derivative on HOPG via Hydrogen Bonding and Van der Waals Forces
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|c 2022
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|a ƒa Online-Ressource
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|a Date Revised 19.07.2022
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a In this paper, two new flavonol derivatives, 2-(4-(dodecyloxy)phenyl)-3-hydroxyflavone (DHF) and 2-(3,5-bis(dodecyloxy)phenyl)-3-hydroxyflavone (BDHF), were synthesized to investigate the respective self-assembly behaviors at the liquid/solid interface by scanning tunneling microscopy. In addition, a linear pyridine derivative with acetylene groups called BisPy was added to regulate the assembly of DHF and BDHF, individually. However, only BDHF molecules successfully co-assembled into grid structures with BisPy molecules. Furthermore, the assembly and co-assembly behavior mechanism of flavonol derivatives and BisPy molecules were further studied by density functional theory calculations. This work will lay a foundation for investigating the self-assembly of flavonol derivatives and the co-assembly regulated by pyridine derivatives at the liquid-solid interface
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|a Journal Article
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|a Meng, Ting
|e verfasserin
|4 aut
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|a Luo, Wendi
|e verfasserin
|4 aut
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|a Sun, Lei
|e verfasserin
|4 aut
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|a Zeng, Qingdao
|e verfasserin
|4 aut
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|a Xu, Haijun
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 38(2022), 28 vom: 19. Juli, Seite 8651-8656
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|x 1520-5827
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|g volume:38
|g year:2022
|g number:28
|g day:19
|g month:07
|g pages:8651-8656
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|u http://dx.doi.org/10.1021/acs.langmuir.2c01076
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