110412-86-7Relevant academic research and scientific papers
Solution Behaviour, Kinetics and Mechanism of the Acid-Catalysed Cyclopalladation of Imines
Gomez, Montserrat,Granell, Jaume,Martinez, Manuel
, p. 37 - 44 (2007/10/03)
The cyclometallation reactions of N-benzylidene-benzylamines, -anilines and -propylamine with palladium acetate have been studied in acetic acid solution.Carbon-hydrogen electrophilic bond activation occurs to produce different types of metallacycles, given the polyfunctional nature of the ligands selected.The cyclometallated compounds formed indicate that the stability of the final species is, with respect to the activated C-H bond, in the order: five-membered aromatic endo > six-membered aliphatic endo > five-membered aromatic exo, >>> five-membered exo, four-membered.The nature of the final cyclometallated compounds in acetic acid solution has been ascertained via 1H NMR spectroscopy; as a whole the spectra are complex, indicating that the nature of the cyclometallated species in solution is not simple, and that a wide variety of compounds is present depending on the imine used.The metallation reactions have been monitored kinetically via UV/VIS spectroscopy at different temperatures and pressures in order to establish the mechanism through which these acid-assisted reactions occur.Although the thermal activation parameters cover a wide range of values (ΔH(excit.) = 49 to 73 kJ mol-, ΔS(excit.) = -52 to -138 J K-1 mol-1), the activation volume is in a very narrow range, -15 +/- 3 cm3 mol-1.The results are interpreted as the formation of a highly ordered four-centred transition state, involving the C-H and Pd-O (acetato) bonds, which is found to be very sensitive to the presence of any protons that could enhance the leaving-group characteristics of the MeCO2H ligand, converting it into its protonated MeCO2H2+ form.
Variable-temperature and -pressure kinetics and mechanism of the cyclopalladation reaction of imines in aprotic solvent
Gómez, Montserrat,Granell, Jaume,Martinez, Manuel
, p. 2539 - 2546 (2008/10/08)
The cyclometalation reactions of benzylidenebenzylamines, -anilines, and -propylamine with palladium acetate have been studied in toluene solution. The cyclometalated compounds are formed via C-H electrophilic bond activation to produce different types of metallacycles, depending upon the polyfunctional nature of the ligand selected. If a five-membered endo metallacycle is possible, it is formed via aromatic C-H bond activation. Formation of a five-membered exo metallacycle only takes place when endo cyclometalation requires the formation of a six-membered compound via aliphatic C-H bond activation or when the steric hindrance affects the planarity of the imine in an important way. The activation of aliphatic C-H bonds has been achieved for endo six-membered metallacycles only when the alternative aromatic C-H bond activation would produce a four-membered exo compound; no activation of aliphatic C-H bonds to form exo five-membered complexes has been observed. The reactions have been monitored kinetically at different temperatures and pressures in order to establish the mechanism through which these spontaneous reactions occur. Three different sets of activation parameters are apparent from the results obtained: those related to the benzylamines and propylamine (ΔH? = +4S/+67 kJ mol-1, ΔS? = -100/-180 J K-1 mol-1, ΔV? = -11/-17 cm3 mol-1), those related to the aniline derivatives (ΔH? = +66/+75 kJ mol-1, ΔS? = -96/-123 J K-1 mol-1, ΔV? = -21/-25 cm3 mol-1), and finally those related to the imines producing aliphatic bond activation (ΔH? = +487+49 kJ mol-1, ΔS? = -167/-177 J K-1 mol-1, ΔV? = -20/-24 cm3 mol-1). The results are interpreted as the formation of a highly ordered four-center transition state, involving the C-H and Pd-O(acetato) bonds, which is found to be very sensitive to the flexibility and steric hindrance of the imine ligands and very insensitive to electronic changes of the C-H bonds.
Ligand Exchange Reactions in Cyclopalladated Complexes of Benzylideneanilines. Crystal Structure of
Granell, Jaume,Sainz, Daniel,Sales, Joaquim,Solans, Xavier,Font-Altaba, Manuel
, p. 1785 - 1790 (2007/10/02)
The ligand exchange reactions between and the free imines p-RC6H4CH=NC6H5 (R = H, Cl, NMe2, or NO2)(NCH) in acetic acid have been studied.The substitution process is favoured when the incoming ligand contains electron-withdrawing substituents
