期刊文献+

Fluoride-Responsive Organogel Based on Hydrazide Derivatives

Fluoride-Responsive Organogel Based on Hydrazide Derivatives
下载PDF
导出
摘要 <div style="text-align:justify;"> An organogelator named N-[3-(hydroxy)-4-(dodecyloxy)-benzoyl]-N’ (4’-nitro-benzoyl) hydrazide (D12) was synthesized. It could form stable gels in some of the tested organic solvent. SEM images revealed that the molecules self- assembled into fibrous aggregates in the xerogels. The X-ray diffraction analysis showed that the xerogel exhibited a layered structure. FT-IR studies confirmed that intermolecular hydrogen bonding between C=O and N-H groups was the major driving force for gelation of organic solvents. The gel exhibited gel-sol transition and color change upon addition of F<span style="font-size:10px;"><sup>- </sup></span>. An extended conjugated system formed through the phenyl group and a five-membered ring based on intramolecular hydro-gen bonding between the oxygen atom near the deprotonation nitrogen atom and the other NH, which is responsible for the dramatic color change upon addition of <span style="text-align:justify;white-space:normal;">F</span><span style="font-size:10px;text-align:justify;white-space:normal;"><sup>- </sup></span>. </div> <div style="text-align:justify;"> An organogelator named N-[3-(hydroxy)-4-(dodecyloxy)-benzoyl]-N’ (4’-nitro-benzoyl) hydrazide (D12) was synthesized. It could form stable gels in some of the tested organic solvent. SEM images revealed that the molecules self- assembled into fibrous aggregates in the xerogels. The X-ray diffraction analysis showed that the xerogel exhibited a layered structure. FT-IR studies confirmed that intermolecular hydrogen bonding between C=O and N-H groups was the major driving force for gelation of organic solvents. The gel exhibited gel-sol transition and color change upon addition of F<span style="font-size:10px;"><sup>- </sup></span>. An extended conjugated system formed through the phenyl group and a five-membered ring based on intramolecular hydro-gen bonding between the oxygen atom near the deprotonation nitrogen atom and the other NH, which is responsible for the dramatic color change upon addition of <span style="text-align:justify;white-space:normal;">F</span><span style="font-size:10px;text-align:justify;white-space:normal;"><sup>- </sup></span>. </div>
作者 Guanghui Lv Lirong Lin Xinyang Chen Chaoran Chen Lei Huang Hong Xin Guanghui Lv;Lirong Lin;Xinyang Chen;Chaoran Chen;Lei Huang;Hong Xin(College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, China;School of Computer Science and Technology, Xidian University, Xi’an, China)
出处 《Journal of Materials Science and Chemical Engineering》 2020年第12期8-17,共10页 材料科学与化学工程(英文)
关键词 ORGANOGEL Hydrazine Derivatives Fluoride Response Hydrogen Bonding Organogel Hydrazine Derivatives Fluoride Response Hydrogen Bonding
  • 相关文献

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部