Amines

Organometallic chemistry: synthesis and applications of cyclometallated compounds
Mass, IR and NMR spectra of selected compounds
Amines

benzylamine: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K). ¹H (300 MHz, CD₃CO₂D, 293 K). ¹H (400 MHz, dmso-d₆, 293 K).
biphenyl-2-ylamine: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K). ¹H (300 MHz, CD₃CO₂D, 293 K). IR (KBr, 4000-400 cm^-1).
ethane-1,2-diamine: ¹H (200 MHz, CDCl₃, SiMe₄, 2938 K).
4-methoxybenzylamine: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
methyl 4-aminobenzoate: ¹H (400 MHz, CDCl₃, SiMe₄, 293 K).
(R)-1-(1-naphthyl)ethylamine: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
1-naphthylamine:¹H (400 MHz, CDCl₃, SiMe₄, 293 K), IR (KBr, 4000-400 cm^-1).
4-nitroaniline: ¹H (400 MHz, dmso-d₆, 293 K), IR (KBr, 4000-400 cm^-1).
phenylamine: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K). ¹H (400 MHz, CDCl₃+ py-d₅, SiMe₄, 293 K). ¹H (400 MHz, dmso-d₆, 293 K). IR (NaCl, windows, 4000-400 cm^-1).
(S)-1-phenylethylamine: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
2-phenylethylamine: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
2,4,6-trimethylaniline: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).