1999
DOI: 10.1002/(sici)1099-0739(199904)13:4<287::aid-aoc844>3.3.co;2-g
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Silsesquioxanes as models of silica supported catalyst I. [3‐(Diphenylphosphino)propyl]‐hepta[propyl]‐[octasilsesquioxane] and [3‐mercapto‐propyl]‐hepta[propyl]‐[octasilsesquioxane] as ligands for transition‐metal ions

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Cited by 8 publications
(33 citation statements)
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“…The organoalkoxysilanes of the type R n Si(OR′) 4-n with various R organic functional groups and OR′ alkoxy groups are well known as precursors for the preparation of silica-based organic-inorganic hybrids. Like gel permeation chromatography, DOSY NNR showed a plateau between 70 to 100 hours in the growth of the oligomers, a time at which, according to 29 Si NMR spectroscopy, the well-defined octakis(3-mercaptopropylsilsesquioxane) is the major species. [5] A number of studies were carried out on different organically modified alkoxysilanes in which the pre-hydrolysis step usually initiated the network formation.…”
Section: Introductionmentioning
confidence: 99%
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“…The organoalkoxysilanes of the type R n Si(OR′) 4-n with various R organic functional groups and OR′ alkoxy groups are well known as precursors for the preparation of silica-based organic-inorganic hybrids. Like gel permeation chromatography, DOSY NNR showed a plateau between 70 to 100 hours in the growth of the oligomers, a time at which, according to 29 Si NMR spectroscopy, the well-defined octakis(3-mercaptopropylsilsesquioxane) is the major species. [5] A number of studies were carried out on different organically modified alkoxysilanes in which the pre-hydrolysis step usually initiated the network formation.…”
Section: Introductionmentioning
confidence: 99%
“…[24,25] As we reported recently, NBB synthesis is achievable under strictly controlled conditions by exploiting in situ water production (ISWP) provided by the esterification reaction between a carboxylic acid and an alcohol. This starting precursor with its thiol function is interesting for different applications that range from the immobilization on the hybrid surface of biomolecules, such as enzymes or proteins [28] and transition metals, [29] to the development of biosensing [30] and peptide separation [31] devices. [26,27] In this paper we report on the structural development and growth mechanisms of NBBs prepared by the ISWP route from 3-mercaptopropyltrimethoxysilane (McPTMS).…”
Section: Introductionmentioning
confidence: 99%
“…Confirmation of the POSS-M24 structure is provided by the 13 C NMR spectrum, which exhibits, exclusively, sharp signals for carbon belonging to the fully converted vinyl groups in the MPTMS addition to octavinyloctasilsesquioxane (Fig. 3).…”
Section: Hsmentioning
confidence: 64%
“…1 H, 13 C and 29 Si nuclear magnetic resonance NMR spectra were recorded with a Brucker AVANCE III DRX-500 MHz spectrometer using CDCl 3 or C 6 D 6 as solvents. Spectrometer operating frequencies were 500.…”
Section: Methodsmentioning
confidence: 99%
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