2006
DOI: 10.1002/pola.21424
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Immobilization of Ti(OiPr)4 onto silicon oxide surfaces and surface‐initiated polymerization of ϵ‐caprolactone

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Cited by 7 publications
(6 citation statements)
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“…From that perspective, a solid-supported system is very important. Although some metal complexes might be grafted onto a silica or alumina support, 13,[20][21][22][23] the regeneration and recycle was unsuccessful. 20 From the perspective of green chemistry, further development of a recoverable polymer-supported catalyst is desired.…”
Section: Introductionmentioning
confidence: 99%
“…From that perspective, a solid-supported system is very important. Although some metal complexes might be grafted onto a silica or alumina support, 13,[20][21][22][23] the regeneration and recycle was unsuccessful. 20 From the perspective of green chemistry, further development of a recoverable polymer-supported catalyst is desired.…”
Section: Introductionmentioning
confidence: 99%
“…A wide variety of oxo-bridged titanium organometallic complexes have been reported to function as materials for photovoltaic applications, [27] as catalysts for ring-opening polymerizations, [28][29][30] and as photocatalyst materials. [31] Generally, the synthesis of titanium dinuclear complexes, containing more than two different bridging groups including an oxo-bridging group, is extremely difficult because the highly oxophilic nature of Ti metal causes the generation of oxo-bridged di-or multinuclear titanium complexes.…”
Section: Resultsmentioning
confidence: 99%
“…The EDS spectra showed the existence of half-titanocenes in the formed precatalysts: the Ti K a peak was observed at 4.56 keV for 1 and 2, and the Cl K a peak at 2.63 keV for 1 and at 2.66 keV for 2, respectively (see Supporting Information (SI)). The XPS data (see SI) also showed Ti peaks at 458.2 eV (Ti 2p3/2) and 463.9 eV (Ti 2p 1/2 ) for 1, and at 458.5 eV (Ti 2p 3/2 ) and 463.9 eV (Ti 2p 1/2 ) for 2, [26] indicating successful immobilization of the half-titanocenes onto the MWCNTs. After activation of the precatalysts with methylalumoxane (MAO), ethylene polymerization was carried out for 1 h with ethylene gas at a pressure of 1.01 Â 10 5 Pa. We obtained extremely high molecular weight (M w ) PEs from the 1/dried MAO system (M w ¼ 2 273 000 g mol À1 at polymerization temperature T p ¼ 30 8C, and M w ¼ 989 600 g mol À1 at T p ¼ 50 8C, Table 1).…”
mentioning
confidence: 90%