38720-30-8

Basic information

• Product Name: tricarbonyl[(1-4-η)-4-(4-methoxyphenyl)-1-phenyl-1-azabuta-1,3-diene]iron
• CAS NO: 38720-30-8
• Molecular Weight: 377.179
• Mol File: 38720-30-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tricarbonyl[(1-4-η)-4-(4-methoxyphenyl)-1-phenyl-1-azabuta-1,3-diene]iron(CAS DataBase Reference)
• NIST Chemistry Reference: tricarbonyl[(1-4-η)-4-(4-methoxyphenyl)-1-phenyl-1-azabuta-1,3-diene]iron(38720-30-8)
• EPA Substance Registry System: tricarbonyl[(1-4-η)-4-(4-methoxyphenyl)-1-phenyl-1-azabuta-1,3-diene]iron(38720-30-8)

Safety Data

• Hazardous Substances Data: 38720-30-8(Hazardous Substances Data)

Upstream product

• 15321-51-4 diiron nonacarbonyl 

Downstream Products

• 12152-72-6 (cyclohexa-1,3-diene)iron tricarbonyl 

Relevant articles and documents

Synthesis, Molecular Structure, Fluxional Behavior, and Tricarbonyliron Transfer Reactions of (η4-1-Azabuta-1,3-diene)tricarbonyliron Complexes

The η4-1-azabuta-1,3-diene)tricarbonyliron complexes 10 are easily prepared in high yield by condensation of the corresponding arylamines 7 with the cinnamaldehydes 8 and subsequent ultrasound-promoted complexation of the resulting 1-azabuta-1,3-dienes 9 with nonacarbonyldiiron. The complexes 10 are shown to represent excellent reagents for the transfer of the tricarbonyliron fragment onto cyclohexa-1,3-diene (1a). The structural characterization for the complexes 10 is achieved by IR, 1H-NMR, and 13C-NMR spectroscopy, as well as X-ray crystallography of 10b, 10c, and 101. Using variable temperature 13C-NMR spectroscopy the fluxionality of the complexes 10a, 10b, 10c, 10e, and 2 is investigated and the activation barrier for the turnstile rotation of the tricarbonyliron fragment is determined. The transfer reaction and the structural factors influencing the transfer of the tricarbonyliron fragment are extensively investigated.