2011
DOI: 10.1039/c1jm10426h
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Si–C attachment points during sol–gel synthesis of organosilicas from 2,8-bis-silylated Tröger's base as building block precursor

Abstract: The porous organosilica framework containing Tr€ oger's base (TB) prepared by mild sol-gel synthesis from 2,8-bis-silylated TB precursor contains a mixture of two point attached TB and one point attached TB units, resulting from unexpected partial Si-C bond cleavage as demonstrated by 29 Si MAS NMR spectroscopy and by selective chemo-desorption of the anchored organic part of the hybrid material.

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Cited by 3 publications
(3 citation statements)
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“…36 The Si-C hydrolysis was reported to occur during the preparation of hybrid phenylene-bridged materials, when the sol-gel reaction was performed under hydrothermal conditions in basic media, i. e., a methodology similar to the one followed in the present study. 53,54,55 On the other hand, the preparation of layered hybrid materials, LHM-TEMS, by combination of organosilane and monosilane precursors resulted in hybrid materials containing standard tetrahedral silicon units Si(nAl) in their framework from TEOS. One additional chemical shift around -85 ppm, together with T-type silicon species due to the presence of silyl-ethylendiamino and silyl-methyl groups from BTMN and TEMS precursors can be observed ( Figure 6 and Table 2 (Table 2).…”
Section: Spectroscopic Characterizationmentioning
confidence: 99%
“…36 The Si-C hydrolysis was reported to occur during the preparation of hybrid phenylene-bridged materials, when the sol-gel reaction was performed under hydrothermal conditions in basic media, i. e., a methodology similar to the one followed in the present study. 53,54,55 On the other hand, the preparation of layered hybrid materials, LHM-TEMS, by combination of organosilane and monosilane precursors resulted in hybrid materials containing standard tetrahedral silicon units Si(nAl) in their framework from TEOS. One additional chemical shift around -85 ppm, together with T-type silicon species due to the presence of silyl-ethylendiamino and silyl-methyl groups from BTMN and TEMS precursors can be observed ( Figure 6 and Table 2 (Table 2).…”
Section: Spectroscopic Characterizationmentioning
confidence: 99%
“…The latter family of materials has been used for catalytic processes involving the formation of CC bonds . The advances in the routes of preparing hybrid materials made by the Corma group offer the opportunity to simultaneously integrate, in the same mesoporous framework, strong acid centers, derived from sulfonic groups, together with highly selective strong bases, derived from Tröger’s base , or protonic sponges . Their high catalytic activity for the S-arylation and azide–alkyne cycloaddition reactions confirm the validity of the multifunctional hybrid materials to be used as effective heterogeneous catalysts with similar or even higher performances than their homogeneous counterparts .…”
Section: Synthesis and Applications Of Hybrid Organic–inorganic Mater...mentioning
confidence: 89%
“…The incorporation of photoresponsive precursors into the sol-gel matrix as organic building blocks can be a powerful tool for developing new fluorescent organosilicas for optical applications such as photostabilizers, waveguides, laser materials, and organic light emitting diodes (OLEDs). [1][2][3][4][5][6][7][8][9][10] In particular, selfassembly of bridged silsesquioxanes represents a typical and efficient approach to design and fabricate silica-based hybrid materials based on a sol-gel process. 11 The concept of selfdirected assembly in sol-gel derived bridged silsesquioxane hybrid materials was first presented by Moreau et al, 12 where new hybrid materials were reported with helical morphology via H-bond mediated hydrolysis of a single chiral precursor.…”
Section: Introductionmentioning
confidence: 99%