Molecular titanium-hydroxamate complexes as models for TiO2 surface binding

Bradley J. Brennan, Jeffrey Chen, Benjamin Rudshteyn, Subhajyoti Chaudhuri, Brandon Q. Mercado, Victor S. Batista, Robert H. Crabtree, Gary W Brudvig

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14 Citations (Scopus)

Abstract

Hydroxamate binding modes and protonation states have yet to be conclusively determined. Molecular titanium(iv) phenylhydroxamate complexes were synthesized as structural and spectroscopic models, and compared to functionalized TiO2 nanoparticles. In a combined experimental-theoretical study, we find that the predominant binding form is monodeprotonated, with evidence for the chelate mode.

Original languageEnglish
Pages (from-to)2972-2975
Number of pages4
JournalChemical Communications
Volume52
Issue number14
DOIs
Publication statusPublished - 2016

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ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Ceramics and Composites
  • Electronic, Optical and Magnetic Materials
  • Surfaces, Coatings and Films
  • Materials Chemistry
  • Metals and Alloys

Cite this

Brennan, B. J., Chen, J., Rudshteyn, B., Chaudhuri, S., Mercado, B. Q., Batista, V. S., Crabtree, R. H., & Brudvig, G. W. (2016). Molecular titanium-hydroxamate complexes as models for TiO2 surface binding. Chemical Communications, 52(14), 2972-2975. https://doi.org/10.1039/c5cc09857b