Palladium catalyzed coupling reactions for the functionalization of Si surfaces: superior stability of alkenyl monolayers

Typeset version

 

TY  - JOUR
  - Collins, G.; O’Dwyer, C.; Morris, M. A.; Holmes, J. D.
  - 2013
  - September
  - Langmuir
  - Palladium catalyzed coupling reactions for the functionalization of Si surfaces: superior stability of alkenyl monolayers
  - Published
  - ()
  - 29
  - 38
  - 11950
  - 11958
  - Palladium-catalyzed Suzuki, Heck, and Sonogashira coupling reactions were studied as reaction protocols for organic modification of Si surfaces. These synthetically useful protocols allow for surface modification of alkene, alkyne, and halide terminated surfaces. Surface oxidation and metal contamination were assessed by X-ray photoelectron spectroscopy. The nature of the primary passivation layer was an important factor in the oxidation resistance of the Si surface during the secondary functionalization. Specifically, the use of alkynes as the primary functionalization layer gave superior stability compared to alkene analogues. The ability to utilize Pd-catalyzed coupling chemistries on Si surfaces opens great versatility for potential molecular and nanoscale electronics and sensing/biosensing applications.
  - Washington DC, USA
  - na
  - na
  - http://pubs.acs.org/journal/langd5
  - dx.doi.org/10.1021/la402480f |
DA  - 2013/09
ER  - 
@article{V231168190,
   = {Collins, G. and  O’Dwyer, C. and  Morris, M. A. and  Holmes, J. D.},
   = {2013},
   = {September},
   = {Langmuir},
   = {Palladium catalyzed coupling reactions for the functionalization of Si surfaces: superior stability of alkenyl monolayers},
   = {Published},
   = {()},
   = {29},
   = {38},
  pages = {11950--11958},
   = {{Palladium-catalyzed Suzuki, Heck, and Sonogashira coupling reactions were studied as reaction protocols for organic modification of Si surfaces. These synthetically useful protocols allow for surface modification of alkene, alkyne, and halide terminated surfaces. Surface oxidation and metal contamination were assessed by X-ray photoelectron spectroscopy. The nature of the primary passivation layer was an important factor in the oxidation resistance of the Si surface during the secondary functionalization. Specifically, the use of alkynes as the primary functionalization layer gave superior stability compared to alkene analogues. The ability to utilize Pd-catalyzed coupling chemistries on Si surfaces opens great versatility for potential molecular and nanoscale electronics and sensing/biosensing applications.}},
   = {Washington DC, USA},
  issn = {na},
   = {na},
   = {http://pubs.acs.org/journal/langd5},
   = {dx.doi.org/10.1021/la402480f |},
  source = {IRIS}
}
AUTHORSCollins, G.; O’Dwyer, C.; Morris, M. A.; Holmes, J. D.
YEAR2013
MONTHSeptember
JOURNAL_CODELangmuir
TITLEPalladium catalyzed coupling reactions for the functionalization of Si surfaces: superior stability of alkenyl monolayers
STATUSPublished
TIMES_CITED()
SEARCH_KEYWORD
VOLUME29
ISSUE38
START_PAGE11950
END_PAGE11958
ABSTRACTPalladium-catalyzed Suzuki, Heck, and Sonogashira coupling reactions were studied as reaction protocols for organic modification of Si surfaces. These synthetically useful protocols allow for surface modification of alkene, alkyne, and halide terminated surfaces. Surface oxidation and metal contamination were assessed by X-ray photoelectron spectroscopy. The nature of the primary passivation layer was an important factor in the oxidation resistance of the Si surface during the secondary functionalization. Specifically, the use of alkynes as the primary functionalization layer gave superior stability compared to alkene analogues. The ability to utilize Pd-catalyzed coupling chemistries on Si surfaces opens great versatility for potential molecular and nanoscale electronics and sensing/biosensing applications.
PUBLISHER_LOCATIONWashington DC, USA
ISBN_ISSNna
EDITIONna
URLhttp://pubs.acs.org/journal/langd5
DOI_LINKdx.doi.org/10.1021/la402480f |
FUNDING_BODY
GRANT_DETAILS