2009
DOI: 10.1002/anie.200901636
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Reversible Metal‐Free Carbon Dioxide Binding by Frustrated Lewis Pairs

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Cited by 722 publications
(510 citation statements)
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“…Easily-reversible binding of carbon dioxide requires the formation of weak interactions between the Lewis acid and the base, and there are already examples of FLPs that bind CO2 and release it at remarkably low temperatures (~ −20°C). 108,111 Drawing useful comparisons between FLP systems is quite difficult as there simply are not enough complexes of a single 'type' to reliably identify trends. For instance, a bridged-FLP, (Me3C6H2)2P-CH2CH2-B(C6F5)2, was found to bind CO2 but released it above −20°C in dichloromethane.…”
Section: Carbamato and Carboxylato Complexesmentioning
confidence: 99%
See 1 more Smart Citation
“…Easily-reversible binding of carbon dioxide requires the formation of weak interactions between the Lewis acid and the base, and there are already examples of FLPs that bind CO2 and release it at remarkably low temperatures (~ −20°C). 108,111 Drawing useful comparisons between FLP systems is quite difficult as there simply are not enough complexes of a single 'type' to reliably identify trends. For instance, a bridged-FLP, (Me3C6H2)2P-CH2CH2-B(C6F5)2, was found to bind CO2 but released it above −20°C in dichloromethane.…”
Section: Carbamato and Carboxylato Complexesmentioning
confidence: 99%
“…For instance, a bridged-FLP, (Me3C6H2)2P-CH2CH2-B(C6F5)2, was found to bind CO2 but released it above −20°C in dichloromethane. 108 Meanwhile, another bridged-FLP not dissimilar in structure, tBu2P-CH2-BPh2, was stable to CO2 loss even at 100°C under vacuum. 109 The increased stability of the latter was attributed to its smaller bite angle (one less carbon in the P-(CH2)x-B chain), but the borane fragment was also not fluorinated.…”
Section: Carbamato and Carboxylato Complexesmentioning
confidence: 99%
“…This centres on the activation of H 2 by so-called frustrated Lewis pairs in specifically designed, organometallic complexes (Mömming et al 2009). The critical issues for this methanol cycle (figure 8) therefore centre on the following points: -The separation (and hence availability) of CO 2 at high (volume) concentrations, for example, in large industrial plants.…”
Section: Synthetic Methanol-a Sustainable Organic Fuel For Transportmentioning
confidence: 99%
“…These have been used to activate CO 2 , for example, Stephan used B(C 6 F 5 ) 3 and PtBu 3 to trap CO 2 (C in Chart 1). 10 Such activation of CO 2 using FLPs has allowed subsequent reduction to methanol and methane. 11,12 There are few, but an increasing number, of transition metal FLP type systems which can activate CO 2 X-ray quality single crystals of 1 were grown by slow diffusion of hexane into a concentrated benzene solution at 298 K over five days.…”
mentioning
confidence: 99%