Nanostructuring of Hybrid Silicas through a Self-Recognition Process

被引:13
作者
Arrachart, Guilhem [2 ]
Creff, Gaelle [3 ]
Wadepohl, Hubert [4 ]
Blanc, Christophe [3 ]
Bonhomme, Christian [1 ]
Babonneau, Florence [1 ]
Alonso, Bruno [5 ]
Bantignies, Jean-Louis [3 ]
Carcel, Carole [2 ]
Moreau, Joel J. E. [2 ]
Dieudonne, Philippe [3 ]
Sauvajol, Jean-Louis [3 ]
Massiot, Dominique [6 ]
Man, Michel Wong Chi [2 ]
机构
[1] Univ Paris 06, CNRS, UPMC, LCMCP,UMR 7574, F-75252 Paris 05, France
[2] ENSCM, CNRS, UMII, AM2N ICGMontpellier,UMI,UMR 5253, F-34296 Montpellier, France
[3] Univ Montpellier 2, Lab Verres & Colloides Nanostruct, UMR 5587, F-34095 Montpellier 05, France
[4] Heidelberg Univ, Inst Anorgan Chem, D-69120 Heidelberg, Germany
[5] ENSCM, CNRS, UMII, MACS ICGMontpellier,UMI,UMR 5253, F-34296 Montpellier, France
[6] CNRS, CEMHTI Lab, F-45071 Orleans 2, France
关键词
hydrogen bonds; hybrid materials; molecular recognition; solid-state structures; LAMELLAR BRIDGED SILSESQUIOXANES; SOLID-STATE; PHOTOLUMINESCENCE; TRANSCRIPTION; COMBINATION; GELS;
D O I
10.1002/chem.200802748
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A study was conducted to demonstrate nanostructuring of hybrid silicas through a hybrid self-recognition process. The self-recognition model was investigated for nanostructing these materials. The model was based on the dimerization properties of a single monosilylated compound that was distinct from the complementary system which involved two different monosilylated compounds. The study demonstrated the formation of a structured bridged silsesquioxane in bulk form using a silylated ureidopyrimidinone derivative. The hydrolysis and polycondensation of the silylated ureidopyrimidinone derivative was characterized at room temperature by in situ optical microscopy measurement to monitor the early stages of the formation of the hybrid material. It was observed that a complete dissolution of the precursor occurred in the solvent mixture at room temperature in test tubes.
引用
收藏
页码:5002 / 5005
页数:4
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