Nickel-containing MCM-41 molecular sieves have been synthesized hydrotherma
lly using cetyltrimethylammonium chloride as a template. The stabilization
of Ni(I) in NiMCM-41 is minimal. The various NI(I) species formed by reduct
ion and adsorbate interactions in NiAlMCM-41 in which Ni(II) is incorporate
d into a framework position by addition of Ni(II) into the synthesis mixtur
e and in Ni-AlMCM-41 where Ni(II) is incorporated into extraframework posit
ions by liquid state ion exchange were studied by electron spin resonance (
ESR) and electron spin-echo modulation. Dehydration at elevated temperature
or thermal reduction by hydrogen produces Ni(I) species in Ni-AlMCM-41 whi
ch are detectable by ESR. By contrast, in NiAIMCM-41 neither dehydration at
high temperature nor hydrogen reduction is effective in producing N(1). Ni
(1) is obtained in NiAIMCM-41 by gamma-irradiation at 77 K. Both NiAlMCM-41
and Ni-AlMCM-41 show differences in their ESR characteristics after reduct
ion and adsorption of D2O, CO, and ethylene. D2O adsorption forms Ni(I)-(O-
2)(n) indicating water decomposition in both materials. CO adsorption onto
Ni-AlMCM-41 and NiAlMCM-41 produces Ni(I)-(CO)(3) and Ni(I)-(CO)(2), respec
tively. The interaction between NL(I) and ethylene seems weaker in NiAlMCM-
41 than in Ni-AlMCM-41. The contrasting characteristics of Ni(I) in NiAlMCM
-41 and Ni-AlMCM-41 suggest that Ni(I) is in a framework site in NiAlMCM-4
1. The differentiation between extraframework and framework sites is confir
med by the effect of sodium ethylenediaminetetraacetate on removing nickel
ions from ion-exchanged Ni-AlMCM-41 but not from synthesized NiAIMCM-41.