Journal of the American Chemical Society, Vol.127, No.46, 16129-16135, 2005
Evidence for a two-step mechanism in electronically selective single-walled carbon nanotube reactions
Covalent and noncovalent chemistries that are selective to single-walled carbon nanotubes of a particular electronic type have become increasingly important for electronic structure separation and on-chip modification of nanoelectronic devices. By monitoring transient Raman spectroscopy and photoluminescence (PL) during a reaction with 4-chlorobenzene diazonium in aqueous solution, evidence for a characteristic two-step mechanism with two distinct time constants is uncovered. A long-lived intermediate selectively and noncovalently binds and partially dopes the nanotube surface (iota = 2.4 min). A slower, covalent reaction is tracked using the time-dependent increase in the disorder mode in Raman (iota = 73 min). The transient Raman and PL data are well described using a series of two first-order reactions. The covalent bonding step can be deactivated by changing the structure of the surfactant adsorbed phase, further supporting the mechanism.