Isotope scrambling in the formation of cyanopolyynes by laser ablation of carbon particles in liquid acetonitrile Original Research Article

Cyanopolyynes, H(Ctriple bond; length of mdashC)nCtriple bond; length of mdashN (n = 3–6), were formed by laser ablation of carbon particles in liquid acetonitrile. The molecules were separated according to the size n and characterized by UV absorption spectroscopy, mass spectroscopy in combination with gas-chromatographic separation, and nuclear magnetic resonance (NMR) spectroscopy. For the study of nascent carbon cluster distribution during the growth of the long carbon chain molecules, isotopomer distribution was analyzed by NMR spectroscopy for the product molecules. Two cyanopolyynes of HC7N and HC9N were isolated from solutions after laser ablation of isotope-enriched carbon powder (99% 13C) in liquid acetonitrile, CH3CN, of natural isotopic abundance (1.1% 13C). With the observed chemical shift, δ, and spin–spin coupling constants, JCH and JCC, spectral simulation was made to determine relative abundance of possible isotopomeric forms for HC9N. We found that the isotope of 12C, mostly from solvent molecules, contributes substantially for the part of carbon in the cyano group, –Ctriple bond; length of mdashN, in HC9N. The isotopomer distribution observed for the sequence of H–Ctriple bond; length of mdashC–Ctriple bond; length of mdashC– was fairly explainable by a binomial, random distribution of the two carbon isotopes of 12C and 13C, reducing the concentration of 13C to 76–55%.