Toward efficient nanoporous catalysts: Controlling site-isolation and concentration of grafted catalytic sites on nanoporous materials with solvents and colorimetric elucidation of their site-isolation

Krishna K. Sharma, Abhishek Anan, Robert P. Buckley, Wayne Ouellette, Tewodros Asefa

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118 Citations (Scopus)

Abstract

We report that the polarity and dielectric constants of solvents used for grafting organosilanes on mesoporous materials strongly affect the concentration of grafted organic groups, the degree of their site-isolation, and the catalytic properties of the resulting materials. Polar and nonpolar organosilanes as well as polar-protic, dipolar-aprotic, and nonpolar solvents were investigated. Polar-protic solvents, which have high dielectric constants, resulted in smaller concentrations (∼1-2 mmol/g) of polar organic groups such as 3-aminopropyl groups, higher surface area materials, site-isolated organic groups, and more efficient catalytic properties toward the Henry reaction of p-hydroxybenzaldehyde with nitromethane. On the other hand, dipolar-aprotic and nonpolar solvents resulted in larger concentrations (∼2-3 mmol/g) of grafted polar functional groups, lower-to-higher surface area materials, more densely populated catalytic groups, and poor-to-efficient catalytic properties toward the Henry reaction. Both the polar-protic and dipolar-aprotic solvents resulted in significantly lower concentration of grafted groups for nonpolar organosilanes such as (3-mercaptopropyl) trimethoxysilane compared to corresponding grafting of the polar amino-organosilanes. The relationship between the solvent properties and the percentage and degree of site-isolation of the grafted functional groups was attributed to differences in solvation of the organosilanes and silanols in various solvents and possible hydrogen-bonding between the organsilanes and the solvents. The degree of site-isolation of the amine groups, which affect the material's catalytic properties, was elucidated by a new colorimetric method involving probing of the absorption maxima (λmax) on the d-d electronic spectrum of Cu2+ complexes with the amine-functionalized materials and the colors of the samples. The absorption λmax and the colors of the materials were found to be uniquely dependent on the type of solvents used for grafting the organoamines. For instance, the monoamine- and diamine-functionalized samples grafted in methanol resulted in pale blue and light purple colors with λmax at ∼720 and 650 nm, respectively. These correspond to CuNO5 and CuN2O 4 structures, respectively, which are indicative of the presence of site-isolated organoamines in samples grafted in methanol. The monoamine and diamine samples grafted in toluene resulted in purple and deep purple colors with λmax at ∼590 and 630 nm, respectively. These correspond to CuN2O4 and CuN4O2, which are indicative of the presence of closely spaced organoamines in samples grafted in toluene. The samples grafted in isopropanol gave colors and λmax intermediate between those of samples grafted in toluene and methanol.

Original languageEnglish
Pages (from-to)218-228
Number of pages11
JournalJournal of the American Chemical Society
Volume130
Issue number1
DOIs
Publication statusPublished - Jan 9 2008

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

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