SOMC grafting of vanadium oxytriisopropoxide (VO(O i Pr) 3 ) on dehydroxylated silica; analysis of surface complexes and thermal restructuring mechanism

Vanadium oxytriisopropoxide (VO(O Pr) ), 1, was grafted on highly dehydroxylated silica (SiO : aerosil silica treated at 700 °C under high vacuum) to generate compound 2 following the concepts and methodology of surface organometallic chemistry (SOMC). The resulting compound was analyzed by elementa...

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Bibliographic Details
Published in:RSC advances 2018, Vol.8 (37), p.20801-20808
Main Authors: Högerl, Manuel P, Serena Goh, Li Min, Abou-Hamad, Edy, Barman, Samir, Dachwald, Oliver, Pasha, Farhan Ahmad, Pelletier, Jeremie, Köhler, Klaus, D'Elia, Valerio, Cavallo, Luigi, Basset, Jean-Marie
Format: Article
Language:English
Subjects:
Chemistry
Grafting
Heat treatment
High vacuum
Infrared radiation
NMR
Nuclear magnetic resonance
Organic chemistry
Organometallic compounds
Propylene
Silicon dioxide
Vanadium
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Summary:Vanadium oxytriisopropoxide (VO(O Pr) ), 1, was grafted on highly dehydroxylated silica (SiO : aerosil silica treated at 700 °C under high vacuum) to generate compound 2 following the concepts and methodology of surface organometallic chemistry (SOMC). The resulting compound was analyzed by elemental analysis, FT-IR, H, C and V solid state (SS) NMR, Raman and EPR spectroscopies. The grafting reaction of 1 to generate 2 was found to lead to the formation of a monopodal surface complex [([triple bond, length as m-dash]Si-O-)V(O)(O Pr) ], 2m, as well as bipodal [([triple bond, length as m-dash]Si-O-) V(O)(O Pr)], 2b, formed along with ([triple bond, length as m-dash]Si-O- Pr) moieties as an effect of the classical rearrangement of 2m with strained siloxane bridges. Upon controlled thermal treatment at 200 °C under high vacuum, 2m and 2b were found to mainly rearrange to tetrahedral VO moieties [([triple bond, length as m-dash]Si-O-) V(O)] (3) with formation of propylene whereas the ([triple bond, length as m-dash]Si-O- Pr) groups were preserved. The mechanism of the thermal rearrangement of the isopropoxide groups was investigated by a DFT approach revealing the occurrence of a concerted γ-H-transfer and olefin elimination mechanism.
ISSN:2046-2069
2046-2069
DOI:10.1039/c8ra02419g