Formation of stable second‐sphere adducts between a water‐soluble organometallic complex and a cyclodextrin (CD) is possible by finely designing the structure of the water‐soluble phosphane. The key point to obtain such adducts was the synthesis of a water‐soluble phosphane which possesses a tert‐butylphenyl group recognized by the CD and separated from the phosphorus atom by a phenyl ring to avoid phosphane decoordination during the molecular recognition process between the organometallic complex and the CD. These adducts are able to catalyze the cleavage of water‐insoluble carbonate in a biphasic system.
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Caron et al. (2004) studied this question.
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