Carbonyl compounds

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

anthracen-9-carbaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

benzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
benzophenone:¹H (400 MHz, CDCl₃, SiMe₄, 293 K), IR (KBr, 4000-400 cm^-1).

2-bromobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

2-chlorobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

4-chlorobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

2,6-dichlorobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

2,6-difluorobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
4-dimethylaminobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
fluorenone: ¹H (400 MHz, CDCl₃, SiMe₄, 293 K).
4-hydroxybenzaldehyde: ¹H (400 MHz, dmso-d₆, 293 K), IR (KBr, 4000-400 cm^-1).

4-methoxybenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K), IR (ATR diamond, 4000-400 cm^-1 ).
1-naphthaldehyde: ¹H (400 MHz, CDCl₃, 293 K).
4-nitrobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

pentafluorobenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

2,4,6-trimethylbenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).

2,4,6-trimethoxybenzaldehyde: ¹H (200 MHz, CDCl₃, SiMe₄, 293 K).
3,4,5-trimethoxybenzaldehyde: ¹H (400 MHz, CDCl₃, SiMe₄, 293 K)