Near-Silence of Isothiocyanate Carbon in C NMR Spectra: A Case Study of Allyl Isothiocyanate

نویسندگان

  • Rainer Glaser
  • Roman Hillebrand
  • Wei Wycoff
  • Cory Camasta
چکیده

H and C NMR spectra of allyl isothiocyanate (AITC) were measured, and the exchange dynamics were studied to explain the near-silence of the ITC carbon in C NMR spectra. The dihedral angles α = ∠(C1−C2−C3−N4) and β = ∠(C2−C3−N4−C5) describe the conformational dynamics (conformation change), and the bond angles γ = ∠(C3−N4−C5) and ε = ∠(N4−C5−S6) dominate the molecular dynamics (conformer flexibility). The conformation space of AITC contains three minima, Cs-M1 and enantiomers M2 and M2′; the exchange between conformers is very fast, and conformational effects on C chemical shifts are small (νM1 − νM2 < 3 ppm). Isotropic chemical shifts, ICS(γ), were determined for sp, sp, and sp N-hybridization, and the γ dependencies of δ(N4) and δ(C5) are very large (10−33 ppm). Atom-centered density matrix propagation trajectories show that every conformer can access a large region of the potential energy surface AITC(γ,ε,...) with 120° < γ < 180° and 155° < ε < 180°. Because the extreme broadening of the C NMR signal of the ITC carbon is caused by the structural flexibility of every conformer of AITC, the analysis provides a general explanation for the near-silence of the ITC carbon in C NMR spectra of organic isothiocyanates.

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تاریخ انتشار 2015