• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

硅上接枝的可光致变色的亚甲基间隔氟化芳基偶氮苯单层

A photoswitchable methylene-spaced fluorinated aryl azobenzene monolayer grafted on silicon.

机构信息

Department of Chemistry, Mokwon University, Daejon 302-729, Republic of Korea.

出版信息

Chem Commun (Camb). 2010 Aug 7;46(29):5232-4. doi: 10.1039/c0cc00521e. Epub 2010 May 26.

DOI:10.1039/c0cc00521e
PMID:20505874
Abstract

Aryldiazonium-terminated methylene-spaced trifluoromethylazobenzene derivatives have been synthesized. Their self-assembled monolayers (SAMs) on a silicon surface allow for a stable and reversible molecular photoswitch.

摘要

芳基重氮末端亚甲基间隔三氟甲基偶氮苯衍生物已经被合成。它们在硅表面的自组装单分子层(SAMs)允许分子光开关稳定且可逆。

相似文献

1
A photoswitchable methylene-spaced fluorinated aryl azobenzene monolayer grafted on silicon.硅上接枝的可光致变色的亚甲基间隔氟化芳基偶氮苯单层
Chem Commun (Camb). 2010 Aug 7;46(29):5232-4. doi: 10.1039/c0cc00521e. Epub 2010 May 26.
2
Correlation between the structure and wettability of photoswitchable hydrophilic azobenzene monolayers on silicon.硅基上光致变色亲水性偶氮苯单层的结构与润湿性的相关性。
Langmuir. 2011 Aug 2;27(15):9403-12. doi: 10.1021/la201526u. Epub 2011 Jun 30.
3
Controlling binding affinities for anions by a photoswitchable foldamer.通过光致变色的分子折叠体控制阴离子的结合亲和力。
Org Lett. 2010 Aug 20;12(16):3630-3. doi: 10.1021/ol1014043.
4
Light-driven molecular switches in azobenzene self-assembled monolayers: effect of molecular structure on reversible photoisomerization and stable cis state.光驱动偶氮苯自组装单层中的分子开关:分子结构对可逆光致异构化和稳定顺式态的影响。
Chem Commun (Camb). 2010 May 28;46(20):3598-600. doi: 10.1039/b921801g. Epub 2010 Apr 8.
5
Self-Assembled Monolayers of an Azobenzene Derivative on Silica and Their Interactions with Lysozyme.二氧化硅上偶氮苯衍生物的自组装单分子层及其与溶菌酶的相互作用
Langmuir. 2015 Dec 22;31(50):13543-52. doi: 10.1021/acs.langmuir.5b03603. Epub 2015 Dec 10.
6
Photoactive diazoketo-functionalized self-assembled monolayer for biomolecular patterning.用于生物分子图案化的光活性重氮酮官能化自组装单分子层
Langmuir. 2009 Aug 18;25(16):8888-93. doi: 10.1021/la901870a.
7
Controlled amino-functionalization by electrochemical reduction of bromo and nitro azobenzene layers bound to Si(111) surfaces.通过电化学还原结合在Si(111)表面的溴代和硝基偶氮苯层实现可控氨基功能化。
Phys Chem Chem Phys. 2014 Sep 28;16(36):19258-65. doi: 10.1039/c4cp02464h.
8
Reversible photoswitching of azobenzene-based monolayers physisorbed on a mica surface.基于偶氮苯的单层分子在云母表面物理吸附的可逆光致变色。
Langmuir. 2010 Jan 19;26(2):943-9. doi: 10.1021/la902411h.
9
Enhanced selective immobilization of biomolecules onto solid supports coated with semifluorinated self-assembled monolayers.
Biomaterials. 2008 Jan;29(2):204-14. doi: 10.1016/j.biomaterials.2007.09.013. Epub 2007 Oct 17.
10
Novel mesogenic azobenzene dimer at air-water and air-solid interfaces.新型介晶偶氮苯二聚体在气-水和气-固界面的情况。
Langmuir. 2009 Jan 20;25(2):839-44. doi: 10.1021/la8030733.

引用本文的文献

1
Unraveling the surface properties of PMMA/azobenzene blends as coating films with photoreversible surface polarity.揭示聚甲基丙烯酸甲酯/偶氮苯共混物作为具有光可逆表面极性的涂膜的表面性质。
RSC Adv. 2021 Apr 26;11(25):15428-15437. doi: 10.1039/d1ra01192h. eCollection 2021 Apr 21.
2
A Low-Temperature Heat Output Photoactive Material-Based High-Performance Thermal Energy Storage Closed System.一种基于低温热输出光活性材料的高性能热能存储封闭系统。
Materials (Basel). 2021 Mar 16;14(6):1434. doi: 10.3390/ma14061434.
3
Tailoring Pore Size and Chemical Interior of near 1 nm Sized Pores in a Nanoporous Polymer Based on a Discotic Liquid Crystal.
基于盘状液晶的纳米多孔聚合物中近1纳米尺寸孔的孔径和化学内部结构的定制
Macromolecules. 2017 Apr 11;50(7):2777-2783. doi: 10.1021/acs.macromol.7b00013. Epub 2017 Mar 23.
4
Photo-switchable molecular monolayer anchored between highly transparent and flexible graphene electrodes.光致变色分子单层固定在高透明和柔性的石墨烯电极之间。
Nat Commun. 2013;4:1920. doi: 10.1038/ncomms2937.