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Ultra stable self-assembled monolayers of N-heterocyclic carbenes on gold.
Crudden, Cathleen M; Horton, J Hugh; Ebralidze, Iraklii I; Zenkina, Olena V; McLean, Alastair B; Drevniok, Benedict; She, Zhe; Kraatz, Heinz-Bernhard; Mosey, Nicholas J; Seki, Tomohiro; Keske, Eric C; Leake, Joanna D; Rousina-Webb, Alexander; Wu, Gang.
Afiliação
  • Crudden CM; 1] Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada [2] Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8602, Japan.
  • Horton JH; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada. jhh@queensu.ca
  • Ebralidze II; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
  • Zenkina OV; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
  • McLean AB; Queen's University, Department of Physics, Engineering Physics and Astronomy, Stirling Hall, Kingston, Ontario K7L 3N6, Canada.
  • Drevniok B; Queen's University, Department of Physics, Engineering Physics and Astronomy, Stirling Hall, Kingston, Ontario K7L 3N6, Canada.
  • She Z; 1] Department of Physical and Environmental Sciences, University of Toronto Scarborough, Toronto, Ontario M1C 1A4, Canada [2] Department of Chemistry, University of Toronto, Toronto M5S 3H6, Canada.
  • Kraatz HB; 1] Department of Physical and Environmental Sciences, University of Toronto Scarborough, Toronto, Ontario M1C 1A4, Canada [2] Department of Chemistry, University of Toronto, Toronto M5S 3H6, Canada.
  • Mosey NJ; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
  • Seki T; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
  • Keske EC; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
  • Leake JD; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
  • Rousina-Webb A; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
  • Wu G; Queen's University, Department of Chemistry, Chernoff Hall, Kingston, Ontario K7L 3N6, Canada.
Nat Chem ; 6(5): 409-14, 2014 May.
Article em En | MEDLINE | ID: mdl-24755592
ABSTRACT
Since the first report of thiol-based self-assembled monolayers (SAMs) 30 years ago, these structures have been examined in a huge variety of applications. The oxidative and thermal instabilities of these systems are widely known, however, and are an impediment to their widespread commercial use. Here, we describe the generation of N-heterocyclic carbene (NHC)-based SAMs on gold that demonstrate considerably greater resistance to heat and chemical reagents than the thiol-based counterparts. This increased stability is related to the increased strength of the gold-carbon bond relative to that of a gold-sulfur bond, and to a different mode of bonding in the case of the carbene ligand. Once bound to gold, NHCs are not displaced by thiols or thioethers, and are stable to high temperatures, boiling water, organic solvents, pH extremes, electrochemical cycling above 0 V and 1% hydrogen peroxide. In particular, benzimidazole-derived carbenes provide films with the highest stabilities and evidence of short-range molecular ordering. Chemical derivatization can be employed to adjust the surface properties of NHC-based SAMs.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ouro / Compostos Heterocíclicos / Metano Idioma: En Revista: Nat Chem Assunto da revista: QUIMICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ouro / Compostos Heterocíclicos / Metano Idioma: En Revista: Nat Chem Assunto da revista: QUIMICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão