RESUMO
The functionalization of single-walled carbon nanotubes (SWNTs) is an effective method for controlling a local band gap, resulting in photoluminescence (PL) in the near-infrared region. Herein, SWNTs were functionalized using a series of bromoalkanes and dibromoalkanes to evaluate the effects of their length on the nanotube PL properties. When bromoalkanes (Cn H2n+1 Br) or dibromoalkanes (Cn H2n Br2 ) with tether lengths of six or more were utilized for six different semiconducting SWNTs, the obtained SWNT adducts exhibited two new PL peaks, whereas dibromoalkanes with tether lengths of 3-5 (Cn H2n Br2 : n=3-5) produced single peaks. Combined with theoretical calculations, the results suggested that the tether length of reagents changes the formation mechanism of functionalized adducts, that is, Cn H2n Br2 (n=3-5) tends to result in kinetic products.
RESUMO
We conducted the chiral separation of functionalized single-walled carbon nanotubes (SWNTs) with dibromopropane derivatives. Depending on their chirality and diameter, the thermal treatment of functionalized SWNTs leads to a shift in the emission radiation to longer wavelengths owing to rearrangement reaction in competition with elimination reaction.