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Title: Surface organometallic chemistry of tin: Reactivity of tetraalkyltin complexes and tributyltin hydride toward silica

Journal Article · · Journal of the American Chemical Society; (United States)
DOI:https://doi.org/10.1021/ja00055a049· OSTI ID:6567625
; ; ; ;  [1];  [2]
  1. Universite Cl. Bernard, Villeurbanne (France)
  2. Institut Francais du Petrole, Rueil Malmaison (France)

Tetraalkyltin complexes, SnR[sub 4] (R = Me, Et, i-Pr, Bu), and tributylhydridotin were reacted with the surface of partially dehydroxylated silica. Interaction between the complexes and the silica surface was followed by IR and [sup 13]C and [sup 119]Sn MAS NMR spectroscopies and analysis of the evolved gases. At room temperature, all the studied complexes are physisorbed: a hydrogen-type bonding between the terminal methyl group of the alkyl ligands and/or the hydride ligand and the surface silanol groups is evidenced. Above 100[degrees]C, with silica dehydroxylated at 500[degrees]C (SiO[sub 2](500)), a reaction occurs, leading to the formation at 200[degrees]C of essentially one surface complex,-SiO-SnR[sub 3] (1) with evolution of 1 mol of alkane per mol of surface tin. 1 is already formed at room temperature by reaction of silica with Bu[sub 3]SnH; the reaction is slow and liberates 1 mol of H[sub 2]/mol of surface Sn. At low surface coverage, and for R [ne] Me, the alkyl ligands of 1 are folded toward the surface, interacting with it via hydrogen-type bonding. The same interaction and reaction are observed when the surface of silica is less dehydroxylated, SiO[sub 2](200): nevertheless 1 is less stable, probably due to the availability of surface silanol groups in the neighborhood of 1. 28 refs., 9 figs., 1 tab.

OSTI ID:
6567625
Journal Information:
Journal of the American Chemical Society; (United States), Vol. 115:2; ISSN 0002-7863
Country of Publication:
United States
Language:
English