Toward Single-Site Functional MaterialsPreparation of Amine-Functionalized Surfaces Exhibiting Site-Isolated Behavior
Source abstract
Abstract
A well-defined amine-functionalized silica surface displaying evidence of isolated amine sites is prepared using a molecular patterning technique. A tritylimine patterning agent is used to spatially position the amine sites a minimum distance from each other, resulting in an organic loading of 0.345 mmol of NH 2 /g of solid. The amine-functionalized silica and its precursors were characterized by multiple techniques including thermogravimetric analysis, nitrogen physisorption, FT-Raman spectroscopy, and 13 C and 29 Si cross-polarization magic-angle spinning (CPMAS) NMR spectroscopy. The reactivity of the amine surfaces are further characterized using probe reactions. All of the amine sites in the patterned material are observed to react uniformly, unlike amine-functionalized silicas prepared using traditional techniques. Furthermore, the patterned aminosilica showed evidence of site isolation, whereas a densely loaded amine-functionalized silica synthesized by traditional methods did not.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Molecular Junctions and Nanostructures · Surface Chemistry and Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering, Georgia Institute of Technology, 311 Ferst Drive, Atlanta, Georgia 30332
References (21)
Show source-provided references
1. For · Appl. Catal., A · 2000 · 201 · 25310.1016/S0926-860X(00)00446-4 ↗
2. For · Chem. Commun. · 2001 · 2420
3. For · J. Chromatogr. · 1990 · 521 · 2910.1016/0021-9673(90)85062-Z ↗
4. Kallury K. M. R. · Langmuir · 1994 · 10 · 49210.1021/la00014a025 ↗
5. Fowler C. E. · Chem. Commun. · 1997 · 176910.1039/a704644h ↗
6. Juvaste H. · J. Mol. Catal. A · 1999 · 150 · 110.1016/S1381-1169(99)00200-9 ↗
7. Timonen S. · J. Organomet. Chem. · 1999 · 582 · 27310.1016/S0022-328X(99)00063-7 ↗
8. Juvaste H. · Organometallics · 2000 · 19 · 172910.1021/om990741c ↗
9. Kanan S. M. · Langmuir · 2002 · 18 · 662310.1021/la0203133 ↗
10. Wulff G. · J. Am. Chem. Soc. · 1986 · 108 · 108910.1021/ja00265a045 ↗
11. Wulff G. · React. Polym. · 1987 · 6 · 299
12. Hwang K.-O. · Mater. Sci. Eng. C · 1995 · 3 · 13710.1016/0928-4931(95)00117-4 ↗
13. Hwang K.-O. · J. Mater. Sci. · 1998 · 8 · 2153
14. Katz A. · Nature · 2000 · 403 · 28610.1038/35002032 ↗
15. Pangborn A. B. · J. Organometallics · 1996 · 15 · 151810.1021/om9503712 ↗
16. Cha J. S. · Bull. Korean Chem. Soc. · 1999 · 20 · 400
17. Zhao D. · J. Am. Chem. Soc. · 1998 · 120 · 602410.1021/ja974025i ↗
18. Engelhardt G. · 1988
19. Sindorf D. W. · J. Am. Chem. Soc. · 1983 · 105 · 376710.1021/ja00350a003 ↗
20. Sudholter E. J. R. · J. Colloid Interface Sci. · 1984 · 103 · 55410.1016/0021-9797(85)90130-4 ↗
21. Baranska H. · 1987