2018
DOI: 10.1016/j.mcat.2018.09.003
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CO2 cycloaddition to epoxides promoted by bis-thioether-phenolate Fe(II) and Fe(III) complexes

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Cited by 34 publications
(17 citation statements)
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“…We have reported a simple method to prepare a series of unsymmetrical iron­(II) bispincer-type complexes (Scheme ) via selective coupling of 2,6-dibromopyridine with amines to unsymmetrical pyridine-bridged pincer-type imidazolium salts, followed by coordination between the unsymmetrical ligands and iron­(II) salts . The majority of iron-based catalysts for cycloaddition produced in the past few years were accomplished using the Fe­(III), with only a few examples of iron-based catalysts in the Fe­(II) that were developed by Rieger et al, Capacchione et al, Abu-Surrah et al, van Leeuwen et al, and our group . Moreover, the catalytic efficiency of iron­(II) catalysts has been successfully investigated in the coupling of epoxides with CO 2 by our group. , …”
Section: Resultsmentioning
confidence: 99%
“…We have reported a simple method to prepare a series of unsymmetrical iron­(II) bispincer-type complexes (Scheme ) via selective coupling of 2,6-dibromopyridine with amines to unsymmetrical pyridine-bridged pincer-type imidazolium salts, followed by coordination between the unsymmetrical ligands and iron­(II) salts . The majority of iron-based catalysts for cycloaddition produced in the past few years were accomplished using the Fe­(III), with only a few examples of iron-based catalysts in the Fe­(II) that were developed by Rieger et al, Capacchione et al, Abu-Surrah et al, van Leeuwen et al, and our group . Moreover, the catalytic efficiency of iron­(II) catalysts has been successfully investigated in the coupling of epoxides with CO 2 by our group. , …”
Section: Resultsmentioning
confidence: 99%
“…These findings were rationalized by DFT calculations showing that the rate-limiting step was the ring-opening of the epoxide that took place in the presence of two iron centers: one acted as the Lewis acid and the other one, as metallate, furnished the nucleophile (Figure 16). Lately, we also developed a new family of tridentate bisthioether phenolate ligands that supported both Fe(II) and Fe(III) centers [71]. It is worth noting that the both Fe(II) and Fe(III) The ferrate species 21 was also isolated and characterized both starting from the chloroderivative 20 and the bromo-derivative 22 by reaction with two and one equivalent of TBAB, respectively ( Figure 17 Lately, we also developed a new family of tridentate bisthioether phenolate ligands that supported both Fe(II) and Fe(III) centers [71].…”
Section: Iron-based Systemsmentioning
confidence: 99%
“…Lately, we also developed a new family of tridentate bisthioether phenolate ligands that supported both Fe(II) and Fe(III) centers [71]. It is worth noting that the both Fe(II) and Fe(III) The ferrate species 21 was also isolated and characterized both starting from the chloroderivative 20 and the bromo-derivative 22 by reaction with two and one equivalent of TBAB, respectively ( Figure 17 Lately, we also developed a new family of tridentate bisthioether phenolate ligands that supported both Fe(II) and Fe(III) centers [71]. It is worth noting that the both Fe(II) and Fe(III) Figure 17.…”
Section: Iron-based Systemsmentioning
confidence: 99%
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“…Later, the same research group reported on a system based on Fe(II) and Fe(III) complexes supported by new bis‐thioether phenolate ligands (Figure ), with the intention to clarify the effect of the oxidation state on the catalytic behaviour . Different from systems 22 and 23 (Figure and Figure ), the Fe(II) complexes 24a – c and the Fe(III) complexes 25a – c were found to be dinuclear or mononuclear depending on the ligand's bulkiness.…”
Section: Phenoxy‐based Ligandsmentioning
confidence: 99%