Molecular Recognition on a Cavitand-Functionalized Silicon Surface

被引:58
作者
Biavardi, Elisa [1 ,2 ]
Favazza, Maria [3 ,4 ]
Motta, Alessandro [3 ,4 ]
Fragala, Ignazio L. [3 ,4 ]
Massera, Chiara [5 ]
Prodi, Luca [6 ]
Montalti, Marco [6 ]
Melegari, Monica [1 ,2 ]
Condorelli, Guglielmo G. [3 ,4 ]
Dalcanale, Enrico [1 ,2 ]
机构
[1] Univ Parma, Dipartimento Chim Organ & Ind, I-43100 Parma, Italy
[2] INSTM UdR Parma, I-43100 Parma, Italy
[3] Univ Catania, Dipartimento Sci Chim, I-95100 Catania, Italy
[4] INSTM UdR Catania, I-95100 Catania, Italy
[5] Univ Parma, Dipartimento Chim Gen & Inorgan, I-43100 Parma, Italy
[6] Univ Bologna, Latemar Unit, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
关键词
RAY-PHOTOEMISSION-SPECTROSCOPY; HYDROGEN-TERMINATED SILICON; CONFIGURATIONAL ANALYSIS; ALKYL MONOLAYERS; COMPLEXES; HOST; HYDROSILATION; PRINTBOARDS; PHOSPHONATE; CHEMISTRY;
D O I
10.1021/ja901678b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A Si(100) surface featuring molecular recognition properties was obtained by covalent functionalization with a tetraphosphonate cavitand (Tiiii), able to complex positively charged species. Tiiii cavitand was grafted onto the Si by photochemical hydrosilylation together with 1-octene as a spatial spectator. The recognition properties of the Si-Tiii surface were demonstrated through two independent analytical techniques, namely XPS and fluorescence spectroscopy, during the course of reversible complexationguest exchange-clecomplexation cycles with specifically designed ammonium and pyridinium salts. Control experiments employing a Si(100) surface functionalized with a structurally similar, but complexation inactive, tetrathiophosphonate cavitand (TSiiii) demonstrated no recognition events. This provides evidence for the complexation properties of the Si-Tiiii surface, ruling out the possibility of nonspecific interactions between the substrate and the guests. The residual Si-O- terminations on the surface replace the guests' original counterions, thus stabilizing the complex ion pairs. These results represent a further step toward the control of self-assembly of complex supramolecular architectures on surfaces.
引用
收藏
页码:7447 / 7455
页数:9
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